Manual de Servicio RX San Francisco PDF

GE Medical Systems
Technical
Publications
Direction 2229351-100
Revision 19
Silhouette VR System
Service Manual
0459
Copyrights 1998~2008 By General Electric Co.

Service Documentation
GE MEDICAL SYSTEMS
SILHOUETTE VR SYSTEM
REV 19
DIRECTION 2229351-100
,
,
.

,

.
(ZH-CN)
TENTO PROVOZN NVOD EXISTUJE POUZE V ANGLICKM

JAZYCE.
V PPAD, E EXTERN SLUBA ZKAZNKM POTEBUJE

NVOD V JINM JAZYCE, JE ZAJITN PEKLADU DO
ODPOVDAJCHO JAZYKA KOLEM ZKAZNKA.
NESNATE SE O DRBU TOHOTO ZAZEN, ANI BYSTE SI

PEETLI TENTO PROVOZN NVOD A POCHOPILI JEHO
OBSAH.
V PPAD NEDODROVN TTO VSTRAHY ME DOJT

K PORANN PRACOVNKA PRODEJNHO SERVISU,
OBSLUNHO PERSONLU NEBO PACIENT VLIVEM
ELEKTRICKHOP PROUDU, RESPEKTIVE VLIVEM
MECHANICKCH I JINCH RIZIK.
ADVARSEL
DENNE SERVICEMANUAL FINDES KUN P ENGELSK.
(DA)
HVIS EN KUNDES TEKNIKER HAR BRUG FOR ET ANDET SPROG

END ENGELSK, ER DET KUNDENS ANSVAR AT SRGE FOR
OVERSTTELSE.
FORSG IKKE AT SERVICERE UDSTYRET MEDMINDRE

DENNE SERVICEMANUAL HAR VRET KONSULTERET OG ER
FORSTET.
MANGLENDE OVERHOLDELSE AF DENNE ADVARSEL KAN

MEDFRE SKADE P GRUND AF ELEKTRISK, MEKANISK ELLER
ANDEN FARE FOR TEKNIKEREN, OPERATREN ELLER
PATIENTEN.
(BG)
VSTRAHA
(CS)
GE MEDICAL SYSTEMS
REV 19
DEZE ONDERHOUDSHANDLEIDING IS ENKEL IN HET ENGELS

VERKRIJGBAAR.
ALS HET ONDERHOUDSPERSONEEL EEN ANDERE TAAL

VEREIST, DAN IS DE KLANT VERANTWOORDELIJK VOOR DE
VERTALING ERVAN.
PROBEER DE APPARATUUR NIET TE ONDERHOUDEN

VOORDAT DEZE ONDERHOUDSHANDLEIDING WERD
GERAADPLEEGD EN BEGREPEN IS.
INDIEN DEZE WAARSCHUWING NIET WORDT OPGEVOLGD,

ZOU HET ONDERHOUDSPERSONEEL, DE OPERATOR OF EEN
PATINT GEWOND KUNNEN RAKEN ALS GEVOLG VAN EEN
ELEKTRISCHE SCHOK, MECHANISCHE OF ANDERE GEVAREN.
THIS SERVICE MANUAL IS AVAILABLE IN ENGLISH ONLY.
IF A CUSTOMER'S SERVICE PROVIDER REQUIRES A

LANGUAGE OTHER THAN ENGLISH, IT IS THE CUSTOMER'S
RESPONSIBILITY TO PROVIDE TRANSLATION SERVICES.
DO NOT ATTEMPT TO SERVICE THE EQUIPMENT UNLESS

THIS SERVICE MANUAL HAS BEEN CONSULTED AND IS
UNDERSTOOD.
FAILURE TO HEED THIS WARNING MAY RESULT IN INJURY TO

THE SERVICE PROVIDER, OPERATOR, OR PATIENT FROM
ELECTRIC SHOCK, OR FROM MECHANICAL OR OTHER
HAZARDS.
KESOLEV TEENINDUSJUHEND ON SAADAVAL AINULT INGLISE

KEELES.
KUI KLIENDITEENINDUSE OSUTAJA NUAB JUHENDIT INGLISE

KEELEST ERINEVAS KEELES, VASTUTAB KLIENT
TLKETEENUSE OSUTAMISE EEST.
RGE RITAGE SEADMEID TEENINDADA ENNE EELNEVALT

KESOLEVA TEENINDUSJUHENDIGA TUTVUMIST JA SELLEST
ARU SAAMIST.
KESOLEVA HOIATUSE EIRAMINE VIB PHJUSTADA

TEENUSEOSUTAJA, OPERAATORI VI PATSIENDI VIGASTAMIST
ELEKTRILGI, MEHAANILISE VI MUU OHU TAGAJRJEL.
VAROITUS
TM HUOLTO-OHJE ON SAATAVILLA VAIN ENGLANNIKSI.
(FI)
JOS ASIAKKAAN HUOLTOHENKILST VAATII MUUTA KUIN

ENGLANNINKIELIST MATERIAALIA, TARVITTAVAN
KNNKSEN HANKKIMINEN ON ASIAKKAAN VASTUULLA.
L YRIT KORJATA LAITTEISTOA ENNEN KUIN OLET

VARMASTI LUKENUT JA YMMRTNYT TMN HUOLTOOHJEEN.
MIKLI TT VAROITUSTA EI NOUDATETA, SEURAUKSENA VOI

OLLA HUOLTOHENKILSTN, LAITTEISTON KYTTJN TAI
POTILAAN VAHINGOITTUMINEN SHKISKUN, MEKAANISEN
VIAN TAI MUUN VAARATILANTEEN VUOKSI.
WAARSCHUWING
(NL)
WARNING
(EN)
HOIATUS
(ET)
ii
GE MEDICAL SYSTEMS
REV 19
ATTENTION
CE MANUEL DE SERVICE N'EST DISPONIBLE QU'EN ANGLAIS.
(FR)
SI LE TECHNICIEN DU CLIENT A BESOIN DE CE MANUEL DANS

UNE AUTRE LANGUE QUE L'ANGLAIS, C'EST AU CLIENT QU'IL
INCOMBE DE LE FAIRE TRADUIRE.
NE PAS TENTER D'INTERVENIR SUR LES QUIPEMENTS

TANT QUE LE MANUEL SERVICE N'A PAS T CONSULT ET
COMPRIS
LE NON-RESPECT DE CET AVERTISSEMENT PEUT ENTRANER

CHEZ LE TECHNICIEN, L'OPRATEUR OU LE PATIENT DES
BLESSURES DUES DES DANGERS LECTRIQUES,
MCANIQUES OU AUTRES.
DIESE SERVICEANLEITUNG EXISTIERT NUR IN ENGLISCHER

SPRACHE.
FALLS EIN FREMDER KUNDENDIENST EINE ANDERE SPRACHE

BENTIGT, IST ES AUFGABE DES KUNDEN FR EINE
ENTSPRECHENDE BERSETZUNG ZU SORGEN.
VERSUCHEN SIE NICHT DIESE ANLAGE ZU WARTEN,

OHNE DIESE SERVICEANLEITUNG GELESEN UND
VERSTANDEN ZU HABEN.
WIRD DIESE WARNUNG NICHT BEACHTET, SO KANN ES ZU

VERLETZUNGEN DES KUNDENDIENSTTECHNIKERS, DES
BEDIENERS ODER DES PATIENTEN DURCH STROMSCHLGE,
MECHANISCHE ODER SONSTIGE GEFAHREN KOMMEN.
(EL)

,

.
,

,
, .
WARNUNG
(DE)
iii
GE MEDICAL SYSTEMS
REV 19
EZEN KARBANTARTSI KZIKNYV KIZRLAG ANGOL

NYELVEN RHET EL.
HA A VEV SZOLGLTATJA ANGOLTL ELTR NYELVRE

TART IGNYT, AKKOR A VEV FELELSSGE A FORDTS
ELKSZTTETSE.
NE PRBLJA ELKEZDENI HASZNLNI A BERENDEZST,

AMG A KARBANTARTSI KZIKNYVBEN LERTAKAT NEM
RTELMEZTK.
EZEN FIGYELMEZTETS FIGYELMEN KVL HAGYSA A

SZOLGLTAT, MKDTET VAGY A BETEG RAMTS,
MECHANIKAI VAGY EGYB VESZLYHELYZET MIATTI
SRLST EREDMNYEZHETI.
AVRUN
ESSI JNUSTUHANDBK ER EINGNGU FANLEG ENSKU.
(IS)
EF A JNUSTUVEITANDI VISKIPTAMANNS ARFNAST

ANNAS TUNGUMLS EN ENSKU, ER A SKYLDA
VISKIPTAMANNS A SKAFFA TUNGUMLAJNUSTU.
REYNI EKKI A AFGREIA TKI NEMA A ESSI

JNUSTUHANDBK
HEFUR VERI SKOU OG SKILIN.
BROT SINNA ESSARI AVRUN GETUR LEITT TIL MEISLA

JNUSTUVEITANDA, STJRNANDA EA SJKLINGS FR
RAFLOSTI, VLRNU EA RUM HTTUM.
IL PRESENTE MANUALE DI MANUTENZIONE E DISPONIBILE

SOLTANTO IN INGLESE.
SE UN ADDETTO ALLA MANUTENZIONE ESTERNO ALLA GEMS

RICHIEDE IL MANUALE IN UNA LINGUA DIVERSA, IL CLIENTE E
TENUTO A PROVVEDERE DIRETTAMENTE ALLA TRADUZIONE.
SI PROCEDA ALLA MANUTENZIONE DELL'APPARECCHIATURA

SOLO DOPO AVER
CONSULTATO IL PRESENTE MANUALE ED AVERNE COMPRESO
IL CONTENUTO
IL NON RISPETTO DELLA PRESENTE AVVERTENZA POTREBBE

FAR COMPIERE OPERAZIONI DA CUI DERIVINO LESIONI
ALL'ADDETTO ALLA MANUTENZIONE, ALL'UTILIZZATORE ED AL
PAZIENTE PER FOLGORAZIONE ELETTRICA, PER URTI
MECCANICI OD ALTRI RISCHI.
FIGYELMEZTETS
(HU)
AVVERTENZA
(IT)
iv
GE MEDICAL SYSTEMS
REV 19
(KO)
(JA)
,
,
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GE MEDICAL SYSTEMS
REV 19
BRDINJUMS
APKALPES ROKASGRMATA IR PIEEJAMA TIKAI ANGU

VALOD.
JA KLIENTA APKALPES SNIEDZJAM NEPIECIEAMA

INFORMCIJA CIT VALOD, NEVIS ANGU, KLIENTA
PIENKUMS IR NODROINT TULKOANU.
NEVEICIET APRKOJUMA APKALPI BEZ APKALPES

ROKASGRMATAS IZLASANAS UN SAPRAANAS.
BRDINJUMA NEIEVROANA VAR RADT ELEKTRISKS

STRVAS TRIECIENA, MEHNISKU VAI CITU RISKU IZRAISTU
TRAUMU APKALPES SNIEDZJAM, OPERATORAM VAI
PACIENTAM.
IS EKSPLOATAVIMO VADOVAS YRA PRIEINAMAS TIK ANGL

KALBA.
JEI KLIENTO PASLAUG TIEKJAS REIKALAUJA VADOVO KITA

KALBA NE ANGL, NUMATYTI VERTIMO PASLAUGAS YRA
KLIENTO ATSAKOMYB.
NEMGINKITE ATLIKTI RANGOS TECHNINS PRIEIROS,

NEBENT ATSIVELGTE EKSPLOATAVIMO VADOV IR J
SUPRATOTE.
JEI NEATKREIPSITE DMESIO PERSPJIM, GALIMI

SUALOJIMAI DL ELEKTROS OKO,
MECHANINI AR KIT PAVOJ PASLAUG TIEKJUI,

OPERATORIUI AR PACIENTUI.
ADVARSEL
DENNE SERVICEHNDBOKEN FINNES BARE P ENGELSK.
(NO)
HVIS KUNDENS SERVICELEVERANDR TRENGER ET ANNET

SPRK, ER DET KUNDENS ANSVAR SRGE FOR
OVERSETTELSE.
IKKE FORSK REPARERE UTSTYRET UTEN AT DENNE

SERVICEHNDBOKEN ER LEST OG FORSTTT.
MANGLENDE HENSYN TIL DENNE ADVARSELEN KAN FRE TIL

AT SERVICELEVERANDREN, OPERATREN ELLER
PASIENTEN SKADES P GRUNN AV ELEKTRISK STT,
MEKANISKE ELLER ANDRE FARER.
NINIEJSZY PODRCZNIK SERWISOWY DOSTPNY JEST

JEDYNIE W JZYKU ANGIELSKIM.
JELI DOSTAWCA USUG KLIENTA WYMAGA JZYKA INNEGO

NI ANGIELSKI, ZAPEWNIENIE USUGI TUMACZENIA JEST
OBOWIZKIEM KLIENTA.
NIE PRBOWA SERWISOWA WYPOSAENIA BEZ

ZAPOZNANIA SI I ZROZUMIENIA NINIEJSZEGO PODRCZNIKA
SERWISOWEGO.
NIEZASTOSOWANIE SI DO TEGO OSTRZEENIA MOE

SPOWODOWA URAZY DOSTAWCY USUG, OPERATORA LUB
PACJENTA W WYNIKU PORAENIA ELEKTRYCZNEGO,
ZAGROENIA MECHANICZNEGO BD INNEGO.
(LV)
SPJIMAS
(LT)
OSTRZEENIE
(PL)
vi
GE MEDICAL SYSTEMS
REV 19
ATENO
ESTE MANUAL DE ASSISTNCIA TCNICA S SE

ENCONTRA DISPONVEL EM INGLS.
SE QUALQUER OUTRO SERVIO DE ASSISTNCIA

TCNICA, QUE NO A GEMS, SOLICITAR ESTES
MANUAIS NOUTRO IDIOMA, DA RESPONSABILIDADE
DO CLIENTE FORNECER OS SERVIOS DE TRADUO.
NO TENTE REPARAR O EQUIPAMENTO SEM TER

CONSULTADO E
COMPREENDIDO ESTE MANUAL DE ASSISTNCIA
TCNICA
O NO CUMPRIMENTO DESTE AVISO PODE POR EM

PERIGO A SEGURANA DO TCNICO, OPERADOR OU
PACIENTE DEVIDO A CHOQUES ELTRICOS,
MECNICOS OU OUTROS.
ESTE MANUAL DE ASSISTNCIA TCNICA S SE

ENCONTRA DISPONVEL EM INGLS.
SE QUALQUER OUTRO SERVIO DE ASSISTNCIA

TCNICA, QUE NO A GEMS, SOLICITAR ESTES
MANUAIS NOUTRO IDIOMA, DA RESPONSABILIDADE
DO CLIENTE FORNECER OS SERVIOS DE TRADUO.
NO TENTE REPARAR O EQUIPAMENTO SEM TER

CONSULTADO E
COMPREENDIDO ESTE MANUAL DE ASSISTNCIA
TCNICA
O NO CUMPRIMENTO DESTE AVISO PODE COLOCAR

EM PERIGO A SEGURANA DO TCNICO, DO
OPERADOR OU DO PACIENTE DEVIDO A CHOQUES
ELCTRICOS, MECNICOS OU OUTROS.
ACEST MANUAL DE SERVICE ESTE DISPONIBIL NUMAI

N LIMBA ENGLEZ.
DAC UN FURNIZOR DE SERVICII PENTRU CLIENI

NECESIT O ALT LIMB DECT CEA ENGLEZ, ESTE
DE DATORIA CLIENTULUI S FURNIZEZE O
TRADUCERE.
NU NCERCAI S REPARAI ECHIPAMENTUL DECT

ULTERIOR CONSULTRII I NELEGERII ACESTUI
MANUAL DE SERVICE.
IGNORAREA ACESTUI AVERTISMENT AR PUTEA DUCE

LA RNIREA DEPANATORULUI, OPERATORULUI SAU
PACIENTULUI N URMA PERICOLELOR DE
ELECTROCUTARE, MECANICE SAU DE ALT NATUR.
(PT-BR)
ATENO
(PT-PT)
ATENIE
(RO)
vii
GE MEDICAL SYSTEMS
REV 19

,
- ,
.

,
,
,

.
OVO SERVISNO UPUTSTVO JE DOSTUPNO SAMO NA

ENGLESKOM JEZIKU.
AKO KLIJENTOV SERVISER ZAHTEVA NEKI DRUGI

JEZIK, KLIJENT JE DUAN DA OBEZBEDI
PREVODILAKE USLUGE.
NE POKUAVAJTE DA OPRAVITE UREAJ AKO NISTE

PROITALI I RAZUMELI OVO SERVISNO UPUTSTVO.
ZANEMARIVANJE OVOG UPOZORENJA MOE DOVESTI

DO POVREIVANJA SERVISERA, RUKOVAOCA ILI
PACIJENTA USLED STRUJNOG UDARA ILI MEHANIKIH
I DRUGIH OPASNOSTI.
TENTO NVOD NA OBSLUHU JE K DISPOZCII LEN V

ANGLITINE.
AK ZKAZNKOV POSKYTOVATE SLUIEB VYADUJE

IN JAZYK AKO ANGLITINU, POSKYTNUTIE
PREKLADATESKCH SLUIEB JE ZODPOVEDNOSOU
ZKAZNKA.
NEPOKAJTE SA O OBSLUHU ZARIADENIA SKR,

AKO SI NEPRETATE NVOD NA OBLUHU A
NEPOROZUMIETE MU.
ZANEDBANIE TOHTO UPOZORNENIA ME VYSTI

DO ZRANENIA POSKYTOVATEA SLUIEB,
OBSLUHUJCEJ OSOBY ALEBO PACIENTA
ELEKTRICKM PRDOM, DO MECHANICKHO ALEBO
INHO NEBEZPEENSTVA.
(RU)
UPOZORENJE
(SR)
UPOZORNENIE
(SK)
viii
GE MEDICAL SYSTEMS
REV 19
ATENCION
ESTE MANUAL DE SERVICIO SOLO EXISTE EN INGLES.
(ES)
SI ALGUN PROVEEDOR DE SERVICIOS AJENO A GEMS

SOLICITA UN IDIOMA QUE NO SEA EL INGLES, ES
RESPONSABILIDAD DEL CLIENTE OFRECER UN
SERVICIO DE TRADUCCION
NO SE DEBERA DAR SERVICIO TECNICO AL EQUIPO,

SIN HABER CONSULTADO Y COMPRENDIDO ESTE
MANUAL DE SERVICIO
LA NO OBSERVANCIA DEL PRESENTE AVISO PUEDE

DAR LUGAR A QUE EL PROVEEDOR DE SERVICIOS, EL
OPERADOR O EL PACIENTE SUFRAN LESIONES
PROVOCADAS POR CAUSAS ELCTRICAS, MECNICAS
O DE OTRA NATURALEZA.
VARNING
(SV)
DEN HR SERVICEHANDBOKEN FINNS BARA

TILLGNGLIG P ENGELSKA.
OM EN KUNDS SERVICETEKNIKER HAR BEHOV AV ETT
ANNAT SPRK N ENGELSKA ANSVARAR KUNDEN
FR ATT TILLHANDAHLLA
VERSTTNINGSTJNSTER.
FRSK INTE UTFRA SERVICE P UTRUSTNINGEN
OM DU INTE HAR LST OCH FRSTR DEN HR
SERVICEHANDBOKEN.
OM DU INTE TAR HNSYN TILL DEN HR VARNINGEN
KAN DET RESULTERA I SKADOR P
SERVICETEKNIKERN, OPERATREN ELLER PATIENTEN
TILL FLJD AV ELEKTRISKA STTAR, MEKANISKA
FAROR ELLER ANDRA FAROR.
DKKAT
(TR)
BU SERVS KILAVUZUNUN SADECE NGLZCES

MEVCUTTUR.
EER MTER TEKNSYEN BU KILAVUZU NGLZCE
DIINDA BR BAKA LSANDAN TALEP EDERSE, BUNU
TERCME ETTRMEK MTERYE DER.
SERVS KILAVUZUNU OKUYUP ANLAMADAN
EKPMANLARA MDAHALE ETMEYNZ.
BU UYARIYA UYULMAMASI, ELEKTRK, MEKANK VEYA
DER TEHLKELERDEN DOLAYI TEKNSYEN,
OPERATR VEYA HASTANIN YARALANMASINA YOL
AABLR.
ix
GE MEDICAL SYSTEMS
REV 19
THIS PAGE INTENTIONALLY LEFT BLANK.
GE MEDICAL SYSTEMS
REV 19
Direction 2229351-100
Revision 19
Silhouette VR System
Service Manual
IMPORTANT! . . . XRAY PROTECTION

Xray equipment if not properly
used
may
cause
injury.
Accordingly, the instructions
herein contained should be
thoroughly
read
and
understood by everyone who
will use the equipment before
you attempt to place this
equipment in operation. The
General
Electric
Company,
Medical Systems Group, will be
glad to assist and cooperate in
placing this equipment in use.
Although
this
apparatus
incorporates a high degree of
protection against xradiation
other than the useful beam, no
practical design of equipment can
provide complete protection. Nor
can any practical design compel

the operator to take adequate
precautions
to
prevent
the
possibility
of
any
persons
carelessly exposing themselves or
others to radiation.
It is important that everyone
having anything to do with x
radiation be properly trained and
fully
acquainted
with
the
recommendations of the National
Council on Radiation Protection
and Measurements as published
in NCRP Reports available from
NCRP
Publications,
7910
Woodmont Avenue, Room 1016,
Bethesda, Maryland 20814, and of
the International Commission on
Radiation Protection, and take
xi
adequate steps to protect against

injury.
The equipment is sold with the
understanding that the General
Electric
Company,
Medical
Systems Group, its agents, and
representatives
have
no
responsibility for injury or damage
which may result from improper
use of the equipment.
Various protective material and
devices are available. It is urged
that such materials or devices be
used.
CAUTION: United States Federal
law restricts this device to use by
or on the order of a physician.
GE MEDICAL SYSTEMS
REV 19
If you have any comments, suggestions or corrections to the information in this document, please
write them down, include the document title and document number, and send them to:
GENERAL ELECTRIC HUALUN MEDICAL SYSTEMS Co. Ltd
ENGINEERING DEPARTMENT
BEIJING ECONOMIC & TECHNOLOGICAL DEVELOPMENT AREA
BEIJING PRC 100176
CERTIFIED ELECTRICAL CONTRACTOR STATEMENT

All electrical installations that are
preliminary to positioning of the
equipment at the site prepared for
the equipment shall be performed
by licensed electrical contractors.
In addition, electrical feeds into
the Power Distribution Unit shall
be
performed
by
licensed
electrical
contractors.
Other
connections between pieces of
electrical equipment, calibrations,
and testing shall be performed by

qualified GE Medical personnel.
The products involved (and the
accompanying
electrical
installations)
are
highly
sophisticated,
and
special
engineering
competence
is
required.
In
performing
all
electrical work on these products,
GE will use its own specially
trained field engineers. All of GEs
electrical work on these products

will comply with the requirements
of the applicable electrical codes.
The purchaser of GE equipment
shall
only
utilize
qualified
personnel
(i.e.,
GEs
field
engineers, personnel of third
party service companies with
equivalent training, or licensed
electricians) to perform electrical
servicing on the equipment.
DAMAGE IN TRANSPORTATION
All packages should be closely
examined at time of delivery. If
damage
is
apparent,
have
notation damage in shipment
written on all copies of the freight
or express bill before delivery is
accepted or signed for by a
General Electric representative or
a
hospital
receiving
agent.
Whether noted or concealed,
damage MUST be reported to the
carrier
immediately
upon
discovery, or in any event, within

14 days after receipt, and the
contents and containers held for
inspection by the carrier. A
transportation company will not
pay a claim for damage if an
inspection is not requested within
this 14 day period.
Call Traffic and Transportation,
Milwaukee, WI (414) 827-3449/
8*285-3449 immediately after
damage is found. At this time be
xii
ready to supply name of carrier,

delivery date, consignee name,
freight or express bill number,
item damaged and extent of
damage.
Complete instructions regarding
claim procedure are found in
Section S of the Policy &
Procedure Bulletins.
GE MEDICAL SYSTEMS
REV 19
REGULATORY REQUIREMENTS
This product conforms with the requirements of Council Directive 93/42/EEC concerning
medical devices when it bears the following CE marking of conformity:
0459
xiii
GE MEDICAL SYSTEMS
REV 19
Electromagnetic Compatibility (EMC)

This product conforms with IEC 60601-1-2:2001+A1:2004 EMC standard for medical devices.
Note:
This equipment generates, uses, and can radiate radio frequency energy. The
equipment may cause or subject to radio frequency interference with other
medical and nonmedical devices and radio communications. To provide
reasonable protection against such interference, the Silhouette VR System
complies with emissions limits for a Group 1, Class A Medical Devices and has
applicable immunity level as stated in IEC 60601-1-2:2001+A1:2004.
However, there is no guarantee that interference will not occur in a particular
installation. Special precautions and other information regarding EMC provided in
the accompanying documents of this equipment shall be observed during
installation and operation of this equipment.
Note:
WARNING
Note:
If this equipment is found to cause interference (which may be determined by

switching the equipment on and off), the user (or qualified service personnel)
should attempt to correct the problem by one or more of the following measure(s):
Reorient or relocate the affected device(s).
Increase the separating space between the equipment and the affected
device.
Power the equipment from a source different from that of the affected
device.
Consult the point of purchase or service representative for further

suggestions.
Use of accessories, transducers, cables and other parts other than those
specified by the manufacturer of this equipment may result in increased
emissions or decreased immunity of the equipment. The manufacturer is not
responsible for any interference caused either by the use of interconnect cables
other than those recommended, or by unauthorized changes or modifications to
this equipment. Unauthorized changes or modifications could void the users
authority to operate the equipment.
To comply with the regulations applicable to an electromagnetic interface for a
Group 1, Class A Medical Device, and to minimize interference risks, the
following requirements shall apply:
All interconnect cables to peripheral devices must be shielded and

properly grounded. Use of cables not properly shielded and grounded
may result in the equipment causing radio frequency interference in
violation of the European Union Medical Device directive and FCC
regulations.
All of those recommended

environment shall be followed.
xiv
guidance
regarding
electromagnetic
GE MEDICAL SYSTEMS
REV 19
Note:
Do not use devices which intentionally transmit RF signals (Cellular Phones,

Transceivers, or Radio Controlled Products) in the vicinity of this equipment as it
may cause performance outside the published specifications. Keep the power to
these type devices turned off when near the equipment. The medical staff in
charge of this equipment is required to instruct technicians, patients, and others.
Guidance and manufacturers declaration Electromagnetic Emissions

The Silhouette VR system is suitable for use in the specified electromagnetic environment.
The purchaser or user of the Silhouette VR system should assure that it is used in an electromagnetic environment as described below:
Emissions Test
Compliance
Electromagnetic Environment
RF Emissions
CISPR11
Group1
RF Emissions
CISPR11
Class A
Harmonic emissions
IEC 61000-3-2
Voltage fluctuations/
flicker emissions
IEC 61000-3-3
Not
applicable
Not
applicable
The Silhouette VR system uses RF energy only for

its internal function. Therefore, its RF emissions are
very low and are not likely to cause any interference
in nearby electronic equipment.
The Silhouette VR system is suitable for use in all
establishments other than domestic and those
directly connected to the public low-voltage power
supply network that supplies buildings used for
domestic purposes.
Guidance and manufacturers declaration - Electromagnetic Immunity (1)

The Silhouette VR system is suitable for use in the specified electromagnetic environment. The
purchaser or user of the Silhouette VR system should assure that it is used in an electromagnetic
environment as described below:
Immunity Test
IEC 60601-1-2
Compliance
Test Level
Level
Electrostatic
Floors are wood, concrete, or ceramic
6 kV contact
6 kV contact
discharge (ESD)
tile, or floors are covered with synthetic
8 kV air
8 kV air
IEC 61000-4-2
material and the relative humidity is at
least 30 %.
2 kV for power
2 kV for
Electrical fast
supply lines
power supply
transient/burst
Mains power quality is that of a typical
lines
IEC 61000-4-4
commercial and/or hospital environment
1 kV for
input/output
1 kV for
input/output
lines
lines
1 kV differential
1 kV
Surge
mode
differential
IEC 61000-4-5
commercial and/or hospital environment.
mode
2 kV common
mode
2 kV common
mode
Voltage dips,
short
< 5 % UT
0 % UT for 5
commercial and/or hospital environment.
(> 95 % dip in UT)
interruptions
sec
If the user of the Silhouette VR system
for 0.5 cycle
and voltage
requires continued operation during
power mains interruptions, it is
variations on
recommended that the Silhouette VR
40 % UT
power supply
input lines
(60 % dip in UT)
system
be
powered
from
an
xv
GE MEDICAL SYSTEMS
REV 19
IEC 61000-4-11
for 5 cycles
uninterruptible power supply or a battery.
70 % UT
(30 % dip in UT)
< 5 % UT
(> 95 % dip in UT)
for 5 s
Power
frequency
(50/60 Hz)
magnetic field
IEC 61000-4-8
3 A/m
Power frequency magnetic fields are at

levels characteristic of a typical location
in a typical commercial and/or hospital
environment.
3 A/m
Note: These are guidelines. Actual conditions may vary.
Guidance and manufacturers declaration - Electromagnetic Immunity (2)

The Silhouette VR system is suitable for use in the specified electromagnetic environment. The
purchaser or user of the Silhouette VR system should assure that it is used in an electromagnetic
environment as described below:
Immunity
IEC 60601-1-2
Compliance
Test
Test Level
Level
Portable and mobile RF communications
equipment are used no closer to any part of the
[EQUIPMENT and/or SYSTEM], including cables,
than the recommended separation distance
calculated from the equation appropriate for the
frequency of the transmitter.
Recommended separation distance
Conducted RF
IEC 61000-4-6
3V
150 kHz to
80 MHz
Radiated RF
IEC 61000-4-3
3 V/m
80 kHz to
800 MHz
[V1 =] 3 V
d= 1.2
[E1=] 3 V/m
d= 1.2
80 MHz to 800 MHz
d= 2.3
800 MHz to 2,5 GHz
Note: P is the power rating of the transmitter in

watts (W) according to the transmitter manufacturer and d is the recommended separation distance in meters (m).
Field strengths from fixed RF transmitters, as
determined by an electromagnetic site survey,*
are less than the compliance level in each frequency range.**
Interference may occur in the vicinity of equipment marked with the following symbol:
xvi
GE MEDICAL SYSTEMS
REV 19
NOTE 1 At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption
and reflection from structures, objects and people.
*Field strengths from fixed transmitters, such as base stations for cellular telephones and land mobile radios,
amateur radio, AM and FM radio broadcast, and TV broadcast cannot be estimated accurately. To assess the
electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be performed. If
the measured field strength exceeds the RF compliance level above, observe the Silhouette VR system to
verify normal operation in each use location. If abnormal performance is observed, additional measures may be
necessary, such as re-orienting or relocating the [EQUIPMENT and/or SYSTEM].
**Over the frequency range 150 kHz to 80 MHz, field strengths are less than 3 V/m.
The Recommended Separation Distances are listed in the next table.

Recommended Separation Distances for Portable and Mobile RF Communications Equipment

and the Silhouette VR system
Frequency of
Transmitter
150KHz to 80 MHz
80 MHz to 800 MHz
800 MHz to 2,5 GHz
Equation
d= 1.2
Rated Power of
Transmitter
(W)
0.01
0.1
1
10
100
d= 1.2
DISTANCE
(meters)
0.12
0.38
1.2
3.8
12
DISTANCE
(meters)
0.12
0.38
1.2
3.8
12
d= 2.3
DISTANCE
(meters)
0.23
0.73
2.3
7.3
23
For transmitters rated at a power not listed above, the DISTANCE can be estimated using the
equation in the corresponding column, where P is the power rating of the transmitter in watts (W)
according to the transmitter manufacturer.
Product Essential Performance
xvii
GE MEDICAL SYSTEMS
REV 19
Level
System
Name
VR system
Fix exposure
Subsystem
AEC
Subsystem
Positioner
movement
Subsystem System console
Subsystem
Power
Distribution Unit
Essential Performance
Exposur; Exposure parameter
display and set; Positioner
movement.
Prob./Appl. Severity
of Failure of Failure
See below
See below
Test
Reqd
Test Methord
Yes
See subsystems below
Pass/Fail Criteria
See subsystems below
Acquire expectant dose
MEDIUM
MEDIUM
Yes
No unintended exposure;
Monitor exposure
No Incorrect exposure the
parameter that displaied
exposure results is not meet
on system console.
product registration standard
Table electromagnetic lock

(EM-lock) function.
MEDIUM
LOW
Yes
Check EM-lock after

immunity test.
The EM-lock function work as

intended after immunity test.
No exposure parameter change
during immunity test;
Exposure parameter set as
intended after immunity test.
System able to turn on and boot
up successfully after immunity
test.
Exposure parameter display

Exposure parameter set .
Provide power to sub-systems.
MEDIUM
LOW
Yes
Observance Exposure
parameter; Set exposure
parameter after Immunity
Test.
LOW
LOW
Yes
Turn on and boot up.
xviii
GE MEDICAL SYSTEMS
REV 19
TABLE OF CONTENTS
CHAPTER
PAGE
BEFORE YOU START

SECTION 1 INTRODUCTION
SECTION 2 OBJECTIVE AND SCOPE OF THIS MANUAL
2-1
Installation Plan
2-2
Interconnection
2-3
Presentation
SECTION 3 ON-SITE REQUIREMENTS
3-1
Tools and Test Equipment
3-2
Documentation
SECTION 4 DESCRIPTION OF SYSTEM
PHYSICAL INSTALLATION
SECTION 1 PHYSICAL INSTALLATION SEQUENCE GUIDE
SECTION 2 INSTALLATION JOB CARD
Installation Preparation
Table Installation
Wall stand Installation
Column Installation
X-Ray Tube Installation
Control box Installation
Collimator Installation
Cable Installation
Spanish Language Labels
AEC Board Option Installation
Table Ion Chamber Option Installation
Wall Stand Ion Chamber Installation
Grid Assembly
Warning Label
xix
1-1
1-1
1-1
1-1
1-2
1-2
1-2
1-2
1-2
1-3
2-1
2-1
2-3
2-3
2-4
2-6
2-11
2-15
2-16
2-17
2-19
2-35
2-37
2-40
2-42
2-43
2-44
GE MEDICAL SYSTEMS
REV 19
TABLE OF CONTENTS (contd.)

CHAPTER
PAGE
CONFIGURATION AND CALIBRATION

SECTION 1 JOB CARDS
Collimator Calibration
HHS Test Calibration
Software Installation
Tube Configuration
Receptor Programming
Automated AEC Calibration
Checksum Validation
Backup and Restore Database Parameters
3-1
3-1
3-1
3-4
3-5
3-15
3-17
3-25
3-37
3-41
FUNCTIONAL CHECK
SECTION 1 INTRODUCTION
SECTION 2 TOOLS AND TEST EQUIPMENT
SECTION 3 OPERATIONAL CHECKS
3-1
System Power up
3-2
Silhouette VR System Mechanical Movement
SECTION 4 PERFORMANCE CHECKS
4-1
Generator Parameter Accuracy
4-2
Post Display Initialization
4-3
Accuracy Checks
4-4
Procedure
4-5
Reproducibilty and Linearity of exposures
4-6
Coefficients of Variation and Linearity
4-7
Automatic Exposure Control (AEC) Reproducibilty
4-8
AEC Maximum mAs
4-9
AEC Minimum Exposure Time
4-10 JEDI Performance Chacks
4-11 Final System Installation
4-1
4-1
4-3
4-4
4-4
4-4
4-6
4-6
4-6
4-7
4-7
4-7
4-9
4-10
4-10
4-11
4-17
4-19
JEDI GENERATOR THEORY AND FUNCTIONAL DESCRIPTION

SECTION 1 THEORY
1-1
Glossary
SECTION 2 THEORY PRESENTATION
2-1
Introduction
2-2
Standard Features
2-3
Applications
2-4
Architecture
xx
5-1
5-1
5-1
5-5
5-5
5-5
5-6
5-7
GE MEDICAL SYSTEMS
REV 19
2-5
A Packaging Architecture
xxi
5-9
GE MEDICAL SYSTEMS
REV 19

CHAPTER
6
PAGE
EXCEPTION HANDLING AND ERROR CODES

SECTION 1 EXCEPTION HANDLING
1-1
Diagnostics
1-2
Power-On Diagnostics
1-3
Live Diagnostics
1-4
Error Code Structure
1-5
Simplified Error Code Definition
1-6
Generator Phase Definition
1-7
Error Class Definition
1-8
Error Code Definition
1-9
Data Associated With The Error Code
1-10 Number Of Occurrences
1-11 Date & Time
SECTION 2 ERROR CODES, DIAGNOSTICS, AND TROUBLESHOOTING
2-1
Introduction
2-2
Power On Diagnostics
2-3
Error Code List
2-4
Error Reporting
2-5
Diagnostics
2-6
Detailed Error Description & Troubleshooting Guide
2-7
Warning Errors
2-8
Other Failures
2-9
Heating Function diagnostics
2-10 Rotation function Diagnostics
2-11 Inverter in Short Circuit Diagnostics
2-12 AEC Diagnostics
2-13 No Load HV Diagnostics
2-14 Inverter Gate Command Diagnostics
xxii
6-1
6-1
6-1
6-1
6-1
6-2
6-2
6-3
6-3
6-4
6-4
6-4
6-4
6-5
6-5
6-5
6-7
6-10
6-11
6-11
6-28
6-29
6-32
6-33
6-34
6-37
6-39
6-40
GE MEDICAL SYSTEMS
REV 19

CHAPTER
PAGE
PLANNED MAINTENANCE
SECTION 1 PREVENTIVE MAINTENANCE ACTION LIST
SECTION 2 PREVENTIVE MAINTENANCE JOB CARDS
RENEWAL PARTS
SECTION 1 SILHOUETTE VR SYSTEM RENEWAL PARTS LIST
SECTION 2 JEDI GENERATOR RENEWAL PARTS
2-1
Introduction
2-2
JEDI Generator Renewal Parts List
2-3
FRU Information
2-4
Jedi 50 R 1T Structure
2-5
Renewal Parts
2-6
Cables
SECTION 3 JEDI GENERATOR DISASSEMBLY/REASSEMBLY
3-1
Introduction
3-2
Tools
HV Tank, 1Tube, 1-3 Phase
Inverter Mid Power Assembly
I/F Board RAD
KV Board RAD
EMC Board 3 Phases
AC/DC 3PH Mid Power Assembly
Inverter Coil Mid Power Assembly
Capacitor Inverter Assembly
LV Power Supply 3 Phase Board
Filament Board 1 INV
Rotor Board High Speed
AEC Board Options
xxiii
7-1
7-1
7-3
8-1
8-1
8-12
8-12
8-12
8-13
8-14
8-15
8-18
8-20
8-20
8-20
8-21
8-27
8-37
8-39
8-43
8-47
8-51
8-57
8-63
8-67
8-71
8-75
GE MEDICAL SYSTEMS
REV 19

CHAPTER
PAGE
SERVICE TOOL JOB CARDS

Software Download/Upgrade
Tube Replacement Software Procedure
9-1
9-1
9-5
10
SCHEMATICS
SECTION 1 SILHOUETTE VR MIS MAP
1-1
Jedi 50 R 1T Cabling
SECTION 2 CENTRAL LISTINGS
2-1
kv Measure Board
2-2
Filament Board 1 Inv.
2-3
Rotation Board High Speed
2-4
LV Power Supply 3 PH Board
2-5
Gate Command Board
2-6
Dual Snub Board
2-7
kV Control Board
2-8
AC/DC 3 Phase board
2-9
I/F Board RAD V1
2-10 I/F Board RAD v2
2-11 AEC Board
2-12 AEC Board V2
2-13 Test Points
SECTION 3 SCHEMATICS
3-1
I/F Board RAD Electrical Schematics
xxiv
10-1
10-1
10-3
10-7
10-7
10-9
10-11
10-13
10-15
10-17
10-19
10-21
10-23
10-25
10-27
10-29
10-29
10-31
10-37
GE MEDICAL SYSTEMS
REV 19
REVISION HISTORY
REV
DATE
A
B
C
0
1
2
Nov. 9, 1998
Nov. 30, 1998
Dec. 10, 1998
Dec. 20, 1998
Jan. 28, 1999
Apr. 14, 1999
3
4
June 24, 1999

Jan. 13, 2000
5
6
Feb. 3, 2000
Feb. 16, 2000
7
8
8
Aug. 25, 2000

May. 15, 2001
June. 26, 2001
Jan. 23, 2003
10
Sept. 16, 2003
11
Oct. 29, 2004
12
Feb.15, 2006
13
14
15
16
16
16
16
16
Jun.20, 2006
Jan.30, 2007
Preliminary release.
Reformat manual to follow GEMS-A document conventions.
General updates.
Initial release.
Revised chapter 6.
Revised chapters 2, 3, 4, 5, 6, 8 and 10. Added Ion Chamber installation
and Invasive mA Measurement.
Revised chapters 2, 3, 4, 7, 10 based on pilot unit installation comments.
Added Console display malfunction to troubleshooting table
in Ch. 6, Sec. 2-8.
Added collimator model number 2226682-1.
Revised job cards IST002, IST004, IST007, IST008. Added pages 2-35 and
2-36. Revised sequence of Other Failures in chapter 6. Revised Renewal
Parts List in chapter 8.
Revised page 2-3, Jobcard IST003, chapter 3.
Revised Jobcard IST003, chapter 2. Add wall stand renewal part, chapter 8.
Revised PDU schematics, chapter 10,
Change Transformer part number to 050-1018, chapter 8
Add note of apply loctite to screws when mounting collimator in page 2-15.
Change renewal part Item #59 in page 8-2.
Add Job Card for Spanish Language Labels, chapter 2
Revised column installation, chapter 2
Update FRU List
Update regulatory requirements and add pictures of cassette tray in renewal
parts.
Change the requirements of warning labels.
Add AID Ion Chamber description.
Update warning label to meet HHS requirements in 2-45.
Add MMS Collimator descriptions.
Jan 16, 2008

Jul 25, 2008
Jul 25, 2008
Jul 25, 2008
Jul 25, 2008
Jul 25, 2008
Aug 19, 2011
May 25, 2012
Oct. 30, 2014
Add detailed safety door and door light connection and collimator screws PM.
Add Note in Chapter 2-17.
Remove Chinese Label Attachment Instruction in Installation in Chapter 2.
Add HHS to SM in Chapter 3.
Updated Language Statement.
Add HHS to SM in Chapter 3.
Revise EMC standard version
Add Caution in Chapter 2-27.
Add apply Loctite 242 requirements in P2-11, P2-15, P2-16, P2-17, P7-2.
17
18
19
REASON FOR CHANGE
xxvi
GE MEDICAL SYSTEMS
REV 19
LIST OF EFFECTIVE PAGES

PAGE
NUMBER
Title Page
2-1 and 2-36
5-1 thru 5-10
8-1 thru 8-74
Back Page
8-1
2-11, 2-35 thru 2-37
8-9
8-2, 8-7, and 8-9
2-16
xxiii thru xxiv
8-1 thru 8-2
i-x
3-4
REVISION
NUMBER
7
7
7
7
-
8
10
11
12
13
14
14
16
16
PAGE
NUMBER
REVISION
NUMBER
7
3-1 thru 3-44
7
6-1 thru 6-44
7
9-1 thru 9-10
7
8
2-5 thru 2-9
10-31
8
8-2, 8-4, 8-6 thru 8-8 10
xvii thru xviii
12
xvii thru xviii
13
i thru viii
14
2-35 thru 2-36
14
8-10 thru 8-11
14
2-17
16
2-27
18
i thru xiv
xxvii
PAGE
NUMBER
REVISION
NUMBER
1-1 and 1-4

4-1 thru 4-20
7-1 thru 7-24
10-1 thru 10-37
8-2 and 8-9
2-15 and 8-2
v thru ix
2-45
2-45
xx
7-2
2-32
2-37
2-11, 2-15, 2-16, 2-17, 7-2
7
7
7
7
8
9
11
12
13
14
14
15
16
19
GE MEDICAL SYSTEMS
REV 19
CHAPTER 1 - BEFORE YOU START

SECTION 1
INTRODUCTION
The goal of this document is to guide the service representative through an entire
X-ray room installation and to provide Diagnostic and Calibration information for
troubleshooting and repair.
The following On-site Requirements must be accounted for prior to beginning
installation of the system.
SECTION 2
OBJECTIVE AND SCOPE OF THIS MANUAL
This direction will lead you in a correct sequence through the manuals needed to
install the equipment. Following the suggested sequence will result in an orderly
installation. However, extenuating circumstances may dictate a deviation from
the recommended sequence. Feel free to deviate, but keep track of your
progress by checking off the tasks in the flowchart as you complete them.
Check equipment according to the packing list (Product Delivery Instructions) for
your system.
2-1
Installation Plan
The main steps in the installation plan are easily seen by looking at the Table of
Contents for Chapters 1 through 4. The plan objectives are to:
1. Give a logical installation order which recognizes mechanical and electrical
interface areas
2. Test and adjust each subsystem independently.
To obtain a good overall view of how these objectives are to be achieved review
the Table of Contents for this document before beginning the installation work.
Then, if it is necessary to deviate from the stated plan, you will be aware of the
essential interface areas. This will give you the information required to make
another effective plan which applies to your particular situation.
1-1
GE MEDICAL SYSTEMS
REV 19
2-2
Interconnection
Interconnection of products by furnished cables or contractor supplied wiring is
indicated by numbered MIS runs in the installation sections. Run interconnect
charts are available which describe the connection and function of each wire.
For Silhouette VR system, refer to the following:
2-3
Silhouette VR system Cable Maps (Chapter 8)
Presentation
The procedures in this manual are presented in job card format.
SECTION 3
ON-SITE REQUIREMENTS
3-1
Tools and Test Equipment

There are additional tools and test equipment besides the standard service
representative tool kit which must be available before installing the Silhouette VR
System. Refer to the subsystem sections of this manual for details.
3-2
Documentation
Directions are necessary for correct installation of the Silhouette VR system.
Procedures from each document will be used and reflect the latest information
available at this time.
Not all procedures in this manual apply to all sites. Before you begin installation,
cross out the procedures that do not apply to your site.
1-2
GE MEDICAL SYSTEMS
REV 19
SECTION 4
DESCRIPTION OF SYSTEM
The Silhouette VR System is divided into seven basic subsystems:
1)
2)
3)
4)
Console
Table Assembly
Wall Stand
Collimator
5) X-ray Tube
6) Generator
7) PDU (No Compliance Plate)
See Table.
TABLE 1
SILHOUETTE VR SYSTEM IDENTIFICATION AND COMPLIANCE PLATES
ITEM
COMPONENT
MODEL NUMBER
PLATE TYPE
Console
2226519
Identification and Compliance
Table Assembly
2226517
XJ-2 Wall Stand
2226683
Identification
MS-18SN Collimator
220-0115
or
or
MMS Collimator
5129405
E7240X X-ray Tube (32KW)
2226679
RAD-12 X-ray Tube (50KW)
2226680
Generator
2212259-X
1-3
GE MEDICAL SYSTEMS
REV 19
1-4
GE MEDICAL SYSTEMS
REV 19
CHAPTER 2 - PHYSICAL INSTALLATION

SECTION 1
PHYSICAL INSTALLATION SEQUENCE GUIDE
Each system is installed in the sequence that will ensure the safest and most
time efficient installation. The installation sequence performed at most sites is as
follows:
DONE
STEP
1
RECEPTION
CHECK,
UNPACKING
HANDING
PERFORM IST 001 JOB CARD
INSTALLING
THE TABLE
STEP
3
INSTALLING
THE
WALL STAND
STEP
4
INSTALLING
THE
COLUMN
STEP
5
INSTALLING
THE
X-RAY TUBE
STEP
6
INSTALLING
THE
CONTROL BOX
STEP
7
INSTALLING
THE
COLLIMATOR
STEP
2
STEP
8
INSTALLING
THE
CABLES AND
WIRES
2-1
GE MEDICAL SYSTEMS
REV 19
STEP
9
STEP
10
Note:
APPLY
SPANISH
LABELS
APPLY
CHINESE
SYSTEM
LABEL
If your country requires the product rating plate label to be in the

language of that country, follow the instructions on document
#45474336. Paste the appropriate language label over the English
rating plate. The rating plate labels are: 2379361 (Spanish),
2379361-2 (German), 2379361-3 (French), 2379361-4 (Italian).
2-2
GE MEDICAL SYSTEMS
REV 19
SECTION 2
INSTALLATION JOB CARD
SILHOUETTE VR
1/1
IST 001
subassembly:
purpose: Prepare for installation
version no. 1
date: 20/10/98
NF No.
Production date
Serial No.
Personnel:2
from
from
Time:2h
to
to
PREINSTALLATION CHECK
1. Verify all required cable duct work, conduits, and raceways are installed according to Site plans.
Ensure customer supplied cables and wires are in place for connection to the system.
Ensure that High Voltage and power cables are separated from signal cables as much as
possible.
Verify that 3 phase power and ground can be placed in the same trough or conduit.
2. Mark exact positions of components on the floor, wall and/or ceiling.

UNPACKING
The SILHOUETTE VR System is shipped in four crates to facilitate transport and installation. Crate dimensions
and weights are shown in the table below.
Crate and Dimensions and Weight
Content
Height
Width
Length
Net Weight(kg) Gross Weight(kg)
mm(inch)
mm(inch)
mm(inch)
kg (lb)
kg (lb)
Table Top and Base
930 (366)
1060(417)
2520(992)
200kg
350kg
Tube Stand
740(291)
740(291)
2250(886)
160kg
250kg
Wall Stand
700(276)
900(354)
1400(551)
120kg
170kg
Generator with PDU
550(217)
720(283)
2250(886)
80kg
130kg
Do not discard any packing material such as envelopes, boxes, bags until all parts are
accounted for, compared to the packing list.
Check the mechanical condition and external appearance of all parts for possible damage or
missing items.
The distribution center or factory must be notified immediately of any damage or shortage of
parts.
2-3
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
1/2
IST 002
subassembly:
purpose: Install the table
NF No.
Production date
from /
/
to
/
/
version no. 1
date: 20/10/98
Serial No.
from
to
Personnel:4
Time: 1h
TABLE ORIENTATION AND INSTALLATION

1. Move the table to position required.
Note:
When positioning the table base, please keep the dimension shown in
following drawing.
1.
For removing the table top, ensure a is larger than 2600mm(minimum

distance).
2. If wall stand use only 180cm SID

If wall stand use both 100cm and 180cm SID
a
b<2640mm.
b<1840mm.
Note:
For more dimension, refer to Silhouette VR PIM (Dir:2229353-100)
2. Unpack table base.
3. Remove front cover (2), and the table top from table base (1).
4. Install anchors in the table-base anchor holes (3). Use anchors from anchor bolts
supplied in shipping bag. Drill holes with M8 drill bit for supplied anchor bolts.
5. Move the table base in position over its anchor holes and secure it to the floor
anchor bolts. Leave the bolts loose for leveling and shimming later.
6. Install left-side anchor bolts then install the right-side bolts (3).
2-4
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
2/2
IST 002
1. Unpack table base. Level the table base and shim as necessary with shims. If possible place shims
close to the anchor bolts. Check longitudinal and transversal leveling with an extended level (such
as a 3-foot or 1 meter level) placed over the table top bearing and film carriage. Do not place level
over bearings at foot end of table. For longitudinal leveling, place the level over the inside portion of
the bearings.
2. After the table base leveling is verified, tighten the anchor bolts, then re-check leveling again and
make final adjustments.

Note:
The tabletop bearings are factory adjusted. Make sure the table base is
shimmed to provide a level tabletop frame before making any
adjustments to the table bearings.
3. If the table top is not level, adjust the table top bearings position by a provided spanner.
Bearing
Provided spanner
2-5
Bearing
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
1/5
IST 003
subassembly: Wall Stand

version no. 2
date: 04/06/01
purpose: Install wall stand

NF No.
Production date
from /
/
Serial No.
from
to
to
Personnel:2
Time: 2h
Left side wall stand modification

The wall stand factory setting is right side. If the site needs left side wall stand, please
follow this instruction.
Note: If the site doesnt have the Ion-chamber, follow the step 1,2,3,6,7,8,9,14,15,16.
1. Lay down the wall stand on a rack.

2. Remove the front panel of wall stand.
3. Demount grid.
4. Demount the Ion-chamber and pull out the Ion-chamber cable.
2-6
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
2/5
5. Demount the cable-connecting box.

6. Remove the four screws retaining to the frame, and
then turn the frame 180.
Cable-connecting box
Frame
7. Mount the frame onto the column.
8. Move the chin rest from the bottom to the top.
2-7
IST 003
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
3/5
9. Move the 2 blocks along diagonal to the other

side.
10. Mount the cable-connecting box.

Note: Make sure the cable-connecting box is in
the correct position as shown.
11. Insert the cable, and then connect the cables in the
cable-connecting box.
12. Mount the cable-connecting box cover.
2-8
IST 003
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
4/5
IST 003
13. Mount the Ion-chamber.

Note: Make sure the Ion-chamber and the chin rest are
kept in the same centerline.
Make sure the Ion-chamber is in the correct
position as shown.
14. Mount the grid and clamps.

Note: If the site doesnt need the Ion-chamber, turn
over the clamps first, and then mount the grid and
clamps.
Clamp
Note: If the site has the Ion-chamber, make sure the

right-hand edge of the grid is closed tightly to the
right-hand edge of the Ion-chamber.
Left
15. Mount the front panel.
Top
16. Exchange lock and plastic block.
2-9
Right
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
5/5
IST 003
Wall Stand Installation Procedure

1. Erect the wall stand.
2. Open the back cover of the wall stand.
3. Remove the transport bolts of the counterweights.
4. If ion chamber is installed, connect the ground wire to the wall stand.
5. Fix the foot panel on the ground with the provided expanding bolts.
DANGER
THE WALL STAND IS HEAVY. AT LEAST TWO PEOPLE ARE REQUIRED

TO MOVE AND ERECT IT TO PREVENT PERSONAL INJURY OR
EQUIPMENT DAMAGE.
THE FLOOR WHERE THE WALL STAND IS INSTALLED MUST BE FLAT
AND LEVEL TO PREVENT THE WALL STAND FROM FALLING DOWN.
6. Install the cassette tray.

7. Balance the counter weight of the cabinet.
8. Assemble the back cover.
Transpor
t Bolts
Foot panel
2-10
Ground Point
for grounding
wire
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
1/4
IST 004
subassembly: Column
version no. 2
date: 11/09/03
purpose: Install the Column

NF No.
Production date
Serial No.
Personnel:2
from
from
Time: 30m
to
to
Note:
In order to let the tube forks keep from damaging during transportation, the tube
forks are disconnected from the tube arm before transportation and should be
installed during the fieldwork.
Warning:
Check calibration due date of Torque wrench and shelf-life of Loctite before usage.
Warning:
In order to ensure to meet the security needs, apply the Loctite 242(or 243) to the
three screws and tighten these 3 screws to 24 N-m (17.7 lbs-ft) with the torque
wrench is the step must be performed, while installation and FRU replace.
1. Put the tube forks (19) into the tube stand arm (18)
2.
3.
4.
5.
6.
7.
Apply Loctite 242(or 243) to the three screws assembling the tube fork (19) with tube stand arm (18)
Tighten these 3 screws to 24 N-m (17.7 lbs-ft) with the torque wrench.
Open the column back cover.
Remove the press plate and other stuffing together from the column.
Remove the top cover (1) from vertical column (11).
Remove the upper stopper (13) of vertical column. Install the tube arm (6) out of the Vertical
Column from the top end of the column and align with outer rail (12).
8. Reassemble the upper stopper with vertical column and reinstall the pulley assembly.
9. Insert the stop bar (17).
2-11
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
2/4
IST 004
10. Route the steel ropes (4) and pass through the holes of pulley assembly (3) and fix the end on the
tube arm. Place the steel ropes around the pulleys securely.
Screw the bolt into tube arm.
Keep 25 -28 mm bolt outside the tube arm.
Fix the bolt with tube arm by provided nut.
The torque screw the nut should between 20.5 - 27.5 N-m.
11. Reassemble the top cover (1) with vertical column. At the same time install the HV Support (9) with
holder (8) by two screws (7).
12. Raise the top end of the vertical column (11) slightly to ensure the counter weight container (5) has
dropped down and check that the steel ropes have enough tension.
13. If you need to move the column, please put the vertical column onto the special
column dolly (See following) for easy movement.
BEFORE ERECTING THE TUBE STAND, YOU MUST INSERT
THE STOP BAR FOR SAFETY. PLACING THE TUBE STAND IN
DANGER
THE UPRIGHT POSITION CAN BE HAZARDOUS BECAUSE IT
IS VERY HEAVY AND AWKWARD TO HANDLE. AT LEAST
TWO PEOPLE ARE REQUIRED TO ERECT THE TUBE STAND.
ONCE VERTICAL, DO NOT LEAVE UNATTENDED AS IT CAN
BE EASILY TIPPED.
2-12
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
3/4
IST 004
Bolt
18
Nut
19
17
2-13
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
4/4
IST 004
1. Remove the end stop (1) and (2) of the longitudinal side rail (3), then align and install the tube stand
(4) into the rail engaging the upper and lower bearings with the rail bearing guides.
2. Lower or raise the tube stand arm (18) as necessary.
3. Re-assemble the end stop with longitudinal support (3).
4. Fasten the steel ropes with tube arm by hexagon head screw (15) until both of the ropes
tension force is balanced.
5. Slide the tube stand along the entire longitudinal movement and ensure its movement is smooth.
Note:
After installing the column, the end stop of the rail must be screwed
down.
4
5
2-14
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
1/1
IST 005
subassembly: X-ray tube

purpose: Install the X-ray tube
NF No.
version no. 1
date: 20/10/98
Production date
Serial No.
Personnel:2
from
from
Time: 15m
to
to
WARNING: CHECK CALIBRATION DUE DATE OF TORQUE WRENCH AND SHELF-LIFE OF LOCTITE
BEFORE USAGE.
WARNING: IN ORDER TO ENSURE TO MEET THE SECURITY NEEDS, THE LOCTITE 242 (OR 243) TO THE
SCREWS AND TIGHTEN SCREWS TO 9.9 N-M (7.3 LBS-FT) WITH THE TORQUE WRENCH IS
THE STEP MUST BE PERFORMED, WHILE INSTALLATION AND FRU REPLACE.
1. Loosen the lock mechanism (5) of the upper clamp (2) of the tube fork.
2. Remove the upper clamp of the tube fork.
3. Put the X-ray tube (4) on lower support (1) of the tube fork.
4. Reinstall the upper clamp (2) of the tube fork.
a. Apply Loctite 242(or 243) to the four screws assembling the upper clamp (2) with lower support (1)
before mounting.
b. Tighten these four screws (3) to 9.9 N-m (7.3 lbs-ft) with the torque wrench.
5. Puts the tube into normal position (Collimator facing downward) using level gauge. Paste the center
mark onto X-ray tube. Make the tube center marks aiming at 0 degrees of the angle indication label.
Then tighten the lock mechanism.
Note:
After installation of the tube, balance the tube arm again.
Center
mark
2-15
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
1/1
IST 006
subassembly: Control box

purpose: Install Control box
NF No.
version no. 1
date: 20/10/98
Production date
Serial No.
Personnel:2
from
from
Time: 15m
to
/
/
to
WARNING: CHECK CALIBRATION DUE DATE OF TORQUE WRENCH AND SHELF-LIFE OF LOCTITE
BEFORE USAGE.
WARNING: IN ORDER TO ENSURE TO MEET THE SECURITY NEEDS, APPLY THE LOCTITE 242 (OR
243) TO THE SCREWS AND TIGHTEN SCREWS TO 9.9 N-M (7.3 LBS-FT) WITH THE
TORQUE WRENCH IS THE STEP MUST BE PERFORMED, WHILE INSTALLATION AND FRU
REPLACE.
1. Open the front cover (1) of the control box.

2. Install the control box (2) with L shape support (3).
3. Remove collimator adaptor from collimator by removing two C-clamps.
4. Install L shape support (3) with collimator adapter (4) and additional filter (5) into X-ray tubes (6)
window.
5. Apply Loctite 242 (or 243) to the four screws (7)
6. Tighten these four screws to 9.9 N-m (7.3 lbs-ft) with the torque wrench.
adapter
2-16
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
1/2
IST 007
subassembly: Collimator
purpose: Install Collimator
NF No.
version no. 1
date: 20/10/98
Production date
Serial No.
Personnel:2
from
from
Time: 15m
to
/
/
to
Warning: Check calibration due date of Torque wrench and shelf-life of Loctite before usage.
Warning: In order to ensure to meet the security needs, apply the Loctite 242 (or 243) to the
screws and Tighten screws to 9.9 N-m (7.3 lbs-ft) with the torque wrench is the step must
be performed, while installation and FRU replace.
1. Rotate the tube (1) so the collimator interface plate (bottom side of tube) is facing up.
2. Put the collimator (2) on the collimator adapter.
3. Apply Loctite 242 (or 243) to the four screws (4).
4. Mount collimator (3) onto the collimator adapter using the two stop plates, and tighten these four
screws (4) to 9.9 N-m (7.3 lbs-ft) with the torque wrench.
Apply loctite on the screws.
Note: Screws,spring washers

and flat washers used
here should get from the
collimator instead of the
tube.
5. Put the X-ray tube back into position.

6. Put a level gauge on the side of the collimator to check level and shim the table is needed.
SILHOUETTE VR
2/2
2-17
IST 007
GE MEDICAL SYSTEMS
REV 19
2-18
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
1/16
IST 008
subassembly: Cable
purpose: Connect wires and cables
version no. 1
date: 20/10/98
NF No.
Production date
Serial No.
Personnel:1
from
from
Time: 3h
to
to
PREPARING CABLES FOR CONNECTION
1. Place the JEDI Generator on the dolly.

2. Position the dolly at the right side in front of the table at about 200mm (8 inches) distance.
Note:
Jedi generator with the dolly is very heavy, so please use the provided
tool to move it. When pushing the dolly into the table, make sure that the
dolly motion route is straight and pay attention not to scrape lacquer on
the table.
If system is equipped with AEC option, perform Job Card 41-2 before
continuing. Job Card 41-2 is located immediately following this Job Card.
3. Use a pair of tools hook the dollys holes across the side of the dolly underpan, then you can move
the Jedi generator assembly conveniently.
CAUTION
Before hooking the dollys side hole, disassemble the Jedi-PDU

upper cover, because it may pinch your hand between the cover
and the hooks handle.
Jedi
Generator
Dolly
2-19
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
2/16
CONTROL BOX CABLE CONNECTION
1. Open the cover of the control box.

2. Plug cables into the corresponding ports.
3. Connect the cables to the junction board.
1. Collimator power
2. X-ray tube rotation
3. Tube arm
movement
4. Column movement
control cables
Column movement
Control cable
2-20
IST 008
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
3/16
IST 008
DANGER
PDU HAS 120V POWER EVEN WHEN THE CONSOLE

POWER IS TURNED OFF BUT CIRCUIT BREAKER IS IN
THE ON POSITION.
5. Table power
supply cable
Table power
supply cable
2-21
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
4/16
IST 008
ANODE ROTATION STARTUP CABLE CONNECTION

Note:
Both cables in table side and tube side must be grounded.
6. Anode rotation
startup cable
Hot
protection
cable
Ground place
Note:
According different X-ray tube, the anode rotation startup cable

connection style at the tube side is different. See following.
32KW (TOSHIBA X-RAY TUBE)

Anode rotation
Tube anode
startup cable
connector
Mark
Mark
C
1
M
2
A
3
SW
5
SW
6
E
Housing Ground
Shield
Housing Ground
50KW (VARIAN X-RAY TUBE)

Anode rotation
Tube anode
startup cable
connector
Mark
Mark
C
5
M
4
A
3
SW
1
SW
2
E
Housing Ground
Shield
Housing Ground
VARIAN
X-RAY TUBE
TOSHIBA
X-RAY TUBE
Ground place
Anode rotation
startup cable
2-22
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
5/16
IST 008
GENERATOR, CONSOLE COMMUNICATION CABLE CONNECTION
7. Console
communication
connector
Generator
communication
connector
Note:
Affix proper language X-ray Warning label, if required, to front of

console.
2-23
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
6/16
CONSOLE POWER CABLE CONNECTION
8.
Console power
cable connector
Console
power cable
connection
2-24
IST 008
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
7/16
AEC1 CABLE CONNECTION
9. AEC1
10. AEC2 (optional)
2-25
IST 008
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
8/16
IST 008
H.V. CABLE CONNECTION (GENERATOR SIDE)

Note:
Apply silicon grease on both sides of plugs before connecting the high
voltage plug!!
Use special high voltage cable spanner wrench to tighten the high
voltage connector plugs.
Make sure plugs are secure and will not loosen!
Note:
Do not use supplied O-rings (black) on the high voltage transformer end.
O-ring is integrated in the high voltage tank.
Note:
Do not use the supplied cable end gasket with the 3 holes. Only use
silicone grease for insulation.
2-26
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
9/16
IST 008
H.V. CABLE CONNECTION (TUBE SIDE)
1. Power up SILHOUETTE VR.

2. Press the VERT or ALL button on the Control box to lower the cross arm on the table top, then
release the button to lock the cross arm into position.
3. Plug in and tighten the H.V. cable of the X-ray tubes anode.
4. Plug in and tighten the H.V. cable of the X-ray tubes cathode.
CAUTION
1. Pay attention to the polarity of the X-ray tube. Incorrect

connection will destroy the tube.
2. The tube model shown below is Toshiba E7240X, the right side is
anode and the left side is cathode.
3. For Varian RAD-12, the right side is cathode and the left side is
anode.
Cathode cable
Anode cable
2-27
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
10/16
IST 008
SYSTEM POWER CABLE CONNECTION

Note:
PDU power cable is supplied by customer.
1. If incomming power cable wire is 10 mm or smaller in diameter, connect

incomming power cables to PDU TM1 DIN connector.
If incomming power cable wire is larger than 10 mm in diameter, connect the
incomming power cables to the top of the main circuit breaker.
CAUTION
Ensure power settings on PDU are set correctly to match wall

power. Incorrect settings may damage equipment. Refer to PDU
schematics (Chapter 8) for details.
2. Set the line voltage taps on T1 and T2 on the back of the PDU. Ensure to set
both T1 and T2 to the voltage that is closest to the incomming line voltage.
2-28
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
11/16
WALL STAND GROUNDING CABLE CONNECTION
2-29
IST 008
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
12/16
INSTALL HAND SWITCH
15. Hand Switch

Connector
2-30
IST 008
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
13/16

Note:
This cable must be bound separately from the other cables.
Table power
supply cable
2-31
IST 008
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
14/16
IST 008
CABLE BINDING
1. Check that all cables are connected correctly, including room interfaces to room door and X-ray on
light. For safety door: connect connector J7s pin1 and pin2; for door light: connect connector J7s
pin4 and pin6; Maximum Ratings for Door Light Power: 250V/2A. See schematic on page 10-1 for
details on plug J7.
2. Bind all cables in the down position.
3. Cover the PDU.
Mounting
Plate
Roller
2-32
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
15/16
IST 008

Note:
Collimator and rotational brake cables must be bound separately from
other cables.
1. Install cables into cable hanger.

2. Wrap H.V., rotation, and collimator cables together with cable tie.
3. Ensure the cross arm and tube rotate movement is smooth.
cable
hanger
2-33
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
H.V. CABLE ALIGNMENT
Note:
16/16
IST 008
The excess cable should be put out of the table and put in proper place.
If needed, coil the excess cable. For safety and maintenance, all cables
should be wrapped and fixed securely.
2-34
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
1/3
IST 009
subassembly: Spanish Language Labels

purpose: Field paste Spanish label
version no. 0
date: 16/06/03
NF No.
Production date
Serial No.
Personnel: 1
from
from
Time: 15min
to
/
/
to
Note:
For Systems installed at Spain, the Spanish language labels must be applied on sites to cover
the English description area on the English labels attached at the factory.
1. Pick up the plastic package marked 2382369 from Accessories crate #4, box 4-1.
2. Attach the Spanish labels to cover the description area of the English labels on the subassemblies according
to the forms below.
Form1 Spanish Label Package (Part No. 2382369) Contents
Note:
For backup, the quantity of the labels are more than the least number needed to be
applied.
Item
Label Part
Quantity
Applied Subassembly
#
Number
1
2382338
9
Table
Wall Stand
PDU
System Console
2
2382342
2
Collimator
3
2382343
2
X-ray Tube (RAD12)
4
2382345
2
X-ray Tube (Toshiba)
5
2382344
2
System
6
5212873
2
MMS Collimator
Form2 Spanish Label Designation
DESIGNATION
SPANISH LANGUAGE
LABELS PART NO.
LOCATION OF NAME PLATE
Table
2382338
Wall Stand
2382338
LOCATION OF SPAIN
LANGUAGE LABELS
2-35
PDU
2382338
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
DESIGNATION
SPANISH LANGUAGE
LABELS PART NO.
2/3
System console
2382338
Collimator /
MMS Collimator
2382342 / 5212873
X-ray Tube (Toshiba)

2382345
System
2382344
LOCATION OF SPAIN
LANGUAGE LABELS
DESIGNATION
SPANISH LANGUAGE
LABELS PART NO.
LOCATION OF SPAIN
LANGUAGE LABELS
2-36
IST 009
X-ray Tube (RAD12)
2382343
GE MEDICAL SYSTEMS
REV 19
JOB CARD IST JEDI 41-2 - AEC BOARD OPTION INSTALLATION

Time: 0 h 20 min - Personnel: 1 field engineer
1 of 3
SUPPLIES
The following items are supplied:
AEC board
1 flat cable
6 screws
TOOLS
5.5 mm nut driver or socket wrench with ratchet.
SAFETY PRECAUTIONS
DANGER
BEFORE ANY MANUAL INTERVENTION, ENSURE THE MAIN POWER IS OFF.

APPLY LOCK OUT - TAG OUT PROCEDURE FOR YOUR OWN SAFETY WHEN
MANIPULATING INSIDE THE EQUIPMENT IS REQUIRED.
To protect the circuit boards, do not forget to wear the antistatic bracelet.
PREREQUISITES
Remove the generator from the table and put it on its bottom side on the floor or on a work bench.
WARNING
THE WHOLE GENERATOR WEIGHTS 63 KILOGRAMS (139 POUNDS). TWO

PEOPLE ARE REQUIRED TO CARRY IT.
2-37
GE MEDICAL SYSTEMS
REV 19
DISASSEMBLY
5-1
Remove the Auxiliary Unit
1.. Disconnect the connectors J2 and J3 and the ground cable on

the top of the generator 1 .
2.. Remove four 5.5 mm hex head securing screws 2 holding the
Auxiliary Unit 4 on the support plate 5 .
3.. Disconnect the flat ribbon cable 3 , without tearing, between the
Auxiliary Unit 4 and the Interface Unit 6 .
4.. Remove the Auxiliary Unit 4 .
5.. After removing the Auxiliary Unit, the Interface Unit appears.
Release the flat ribbon cable 7 , making it sliding along the
cover panel 8 of the Interface Unit.
6.. Unscrew twelve 5.5 mm screws that retain the cover
panel and remove this one 8 .
5-2
AEC Board Installation
1. Mount the AEC board to the plate with six screws

2. Connect the flat cable to connector J5 on the AEC board
and to J3 on the I/F RAD Board.

3. Join connector J1 on AEC board to AEC 2 on bracket
4. Join connector J2 on AEC board to AEC1 on bracket
5. Join connector 6,35 to TP1 on AEC board
2-38
2 of 3
GE MEDICAL SYSTEMS
REV 19
3 of 3
6. Join connector 6,35 to TP2 on AEC board

7. Remember to connect cable from ionization chambers to AEC1 and AEC 2.
AEC board
J5
J1
J2
Rad I/F board
TP1
TP2
REASSEMBLY
Remount the Auxiliary Unit. Reverse the disassembly procedure (refer to section 51).
2-39
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
1/2
subassembly:
Ion
purpose: Ion Chamber Option Installation
NF No. Production date
Serial No.
from /
/
from
to
/
/
to
Chamber version no. 1

date: 20/10/98
Personnel:2
Time: 30min.
1. Unpack the table top.

2. Loosen the screw (1) and remove the pressing plate (2), the grid (3) and the cassette tray.
3. Install the Pre-amplifier and the cable.
Note:
Pay attention to the assembling direction of the ion chamber. The correct
direction is shown as below.
Pre-
Filt
2-40
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
2/2
subassembly:
Ion
purpose: Ion Chamber Option Installation
Serial No.
from /
/
from
to
/
/
to
Cahmber version no. 1

date: 20/10/98
Personnel:2
Time: 30min.
4. Install the ion chamber (4).

5. Reassemble the cassette tray, grid, pressing plate and tighten the screw.
6. Reassemble the tabletop.
2-41
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
1/1
subassembly: Wall Stand Ion Chamber

purpose: Wall Stand Ion Chamber Installation
Serial No.
from /
/
from
to
/
/
to
version no. 1
date: 20/10/98
Personnel: 1
Time: 1 hour
1. Open the front cover of the cassette tray.

2. Remove the cassette tray and grid.
3. Connect the ion chamber pre-amplifier according to the following picture.
Cable Entrance
4. Install the cassette tray.

5. Reassemble Ion chamber and grid.
Note:
Pay attention to the direction of the ion chamber.
6. Install as Job card IST003 steps 3 to 8.
2-42
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
subassembly: Grid
purpose: Assembly grid
from /
/
to
/
/
1/1
version no. 1
date: 20/10/98
Personnel: 1
Time: 20 min.
Serial No.
from
to
1. Loosen the screws fixed left and right clamps.

2. Put the grid under the clamps.
Note:
Ensure the grid direction is parallel with the patient support center line.
3. Make the grid upside clsoe up the baffle and the left side close up the bar under the left clamp, then
push the right clamp towards the grid to clamp it.
4. Fasten the screws again.
Baffle
Grid
Left clamp
Right clamp
2-43
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
1/1
subassembly:
Warning
purpose: Field paste warning label
Serial No.
from /
/
from
to
/
/
to
Note:
Label version no. 3

date: 20/6/2006
Personnel: 1
Time: 2 min.
Silhouette VR is sold to different country, so field engineer need to paste

warning label according to local regulation.
There are three type of warning labels delivered as accessories. They apply to different
countries. See following:
Paste the warning label to the right bottom of the console as shown below
Warning label example
Warning label
2-44
GE MEDICAL SYSTEMS
REV 19
CHAPTER 3 - CONFIGURATION AND CALIBRATION

SECTION 1
JOB CARD CONTENT
Job card
Number
CAL 001
CAL 002
SW JEDI 7-1
SW JEDI 5-1
SW JEDI 8-4
SW JEDI 8-2
SW JEDI 8-5
Content
Collimator Calibration
HHS Test Calibration
Service Software User Guide
Tube Configuration
Receptor Programming
Automated AEC Calibration
Checksum Validation
Version
Page
0
0
0
0
0
0
0
3-1
3-4
3-5
3-15
3-17
3-25
3-37
SECTION
JOB CARDS
SILHOUETTE VR
subassembly: Collimator Calibration
purpose:
NF
No.
1/3
Production date
Serial No.
version no. A
date: 15/10/98
Personnel:1
from
from
Time:15m
to
to
SUPPLIES
None.
TOOLS
SAFETY PRECAUTIONS
Not applicable.
PREREQUISITES
None
3-1
CAL 001
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
2/3
CAL 001
COLLIMATOR CALIBRATION
Note:
For a newly installed Silhouette VR system, the center of Projection of

the Collimator Orientation board compared to the center of the chest
cassette may be not the same. In this case (Illustration 1), the orientation
board of the collimator should be calibrated to the right place.
Projection
Center
Windage
Cassette
Illustration 1 Projection of the Collimator Orientation board
3-2
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
3/3
CAL 001
PROCEDURE
Adjustment of the Collimator Orientation Board
See Illustration 2
Illustration 2 Collimator Orientation Board Assembly
1. Rotate the Collimator to the Chest Stand.

2. Light the Collimator lamp.
3. Loosen the press plate.
4. Adjust the Collimator Orientation board to the right direction.
Adjust the projection center and the cassette center to one point
Adjust the windage angulation to 0.
5. Screw down the press plate again.
3-3
GE MEDICAL SYSTEMS
REV 19
1/1
CAL002
SILHOUETTE VR
subassembly: HHS Test Calibration
Purpose:
Version no. 1
Date: 07/25/2008
NF
No.
Production
date
from /
/
Serial No.
Personnel:1
from
Time:30m
to
to
Installers must indicate that the combination of installed HHS Certified Components is compatible on Form F3382
provided in Direction 46-013894, System Field-Test For HHS.
Silhouette VR HHS Compliance Compatibility List
PRODUCT
CATEGORY
PRODUCT DESCRIPTION
MODEL NUMBER
SYSTEM CONSOLE
2226519
Generator
2212259-X
E7240X X-ray Tube (32KW)

RAD-12 X-ray Tube (50KW)
2226679
2226680
MS-18SN Collimator
2226682
Or
Or
MMS Collimator
5129405
X-RAY CONTROL
X-RAY TUBE
ASSEMBLY
HOUSING
(CASING)
BEAM LIMITING
DEVICE
3-4
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
subassembly: Service Software User Guide
purpose: Software Installation
NF
No.
1/10
SW JEDI 7-1
version no. 0
Production
date
from /
/
Serial No.
date: 11/23/98
Personnel:1
from
Time:15m
to
to
SUPPLIES
None.
TOOLS
-
Service Terminal with floppy drive

Service tools Part No. 2228546-X
- JEDI service software
- 9-wire service cable
SAFETY PRECAUTIONS
Not applicable.
PREREQUISITES
Basic knowledge of PC based computer laptop, DOS and usage of Microsoft WINDOWS.
3-5
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SILHOUETTE VR
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SW JEDI 7-1
PROCEDURE
LOADING SERVICE SOFTWARE ON SERVICE LAPTOP
The Service software is a DOS application. It can operate under DOS or Windows; but for software
download or database backup, it is required to run ASIAN.exe under DOS to avoid
communication problem (with the mouse, click on START, SHUTDOWN, RESTART COMPUTER
UNDER DOS MODE; see Software Download / Upgrade JobCard).
To load the software on to the hard drive:
Power ON Service laptop. Under Windows, run the File Manager (Explorer))
Create a new directory (e.g.: JEDISVC) under C:\
Insert the Service Software floppy delivered with the equipment in the Service Tool set into the floppy drive.
Copy all the files from the floppy to your hard drive.
(Double click on A:\, drag and drop on C:\ JEDISVC or whatever name of your directory.)
Double click the file JEDP424B expanding the software to your hard drive.
The service software is installed and ready for use.
USING SERVICE SOFTWARE
Connect Service terminal as follows:
Use the 9 pin Service cable, part N 2207478, to connect serial line of Service terminal to connector XJ8
on the I/F board.
Switch on the Service terminal.
To run the program:
Under Windows:
-
Exit Windows. Restart computer in MS-DOS mode.
select Disk Drive from where you want to run the program: C: [enter]
change to the new directory
type: ASIAN [enter] to run the program
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SILHOUETTE VR
3/10
SW JEDI 7-1
The following screen appears:
Power ON the generator
Press function key F1

The software will load the help screen information contained in Asiane .msg file.
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SW JEDI 7-1
Wait or press space bar to jump to screen.
The Application screen will appear:
Note:
If the serial line to the generator is not operating (e.g.: cable not correctly
connected, I/F or kV Control board down, Generator not ready or
powered OFF), further screens will not be displayed and no function keys
will operate. Correct this problem before continuing.
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SW JEDI 7-1
TYPICAL SCREEN DESCRIPTION
: Area for Parameters, Error codes. Controlled by JEDI Software.
Display of exposure parameters setup in Application mode, depending on technique selection: kV,
mAs, mA, Exposure time. (max. number of exposure in sequence, not used on Rad product.)
Specific display in Maintenance Mode (Alt S or Alt D).
2 : Status area. Displayed by Service Software, Enlighten or blinking key
controlled by JEDI Software.
Display of function keys usable with menu displayed. Commands are remembered in help area 4
Right arrow: Increase kV

F1: Set 2 points mode
F2: Set 3 points mode
F3: Increase mA or mAs (3 points or 2
points)
F5: Increase Exposure Time
Left arrow: Reduce kV
F9: Darkness correction + (w/t AEC Cell)
F0 (F10): Darkness correction - (w/t

AEC Cell)
Error or impossible
selection
Lit during exposure
Lit during exposure
F4: Decrease mA or mAs (3 points or 2

points)
F6: Decrease Exposure Time
Lit when thermal

limit is reached
Lit when ready for
exposure
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SILHOUETTE VR
6/10
3
SW JEDI 7-1
: Select Technique, Screen film pairs, AEC cell, ...
Keys always displayed, but will be active depending on configuration and technique selection.
Includes help command.
1...4: Select workstation, whenever programmed in service menu TECH.
0: select Large focus
9: select Small focus
A, B, C: Select screen film pair (Whenever programmed)

A: Slow speed
B: Medium speed
C: High speed
D, E, F: Select cell in AEC (Whenever programmed)

D: Left cell
E: Central cell
F: Right cell
R: to Reset whenever error

occurs
U: Toggle fast or normal kV change.
Z: to display in area (1) the measured exposure parameters when DISP in menu 5 is set ON.
APR valid: enlighten when the display in area (1) is valid for recording in Customized protocols. (Not
used in RAD)
4
: Area for Static Help, related to screen in Service Mode.
Displayed by Service Software.

Selecting Maintenance and Application Mode; major keys
FROM
PROCEDURE
TO
APPLICATION MODE
Type <ALT> - <S > (Together)
SETUP/MAINTENANCE MODE
MENU 3
APPLICATION MODE
Type <ALT> - <D > (Together)
SETUP/MAINTENANCE MODE
LAST MENU OR SUB-MENU
selected.
SETUP/MAINTENANCE
MODE
From any menu, type <R > (several APPLICATION MODE

times if necessary) or <Q >
[Q]
[R]
[W]
[ALT] & [S] (Together)
[ALT] & [D]
[
] and [
]
[F1] to [F0]
Other keys
Return to application mode

Return to a higher level menu
Validate
Calibration mode (Menu 3)
Calibration mode (Last menu called)
In maintenance mode, to move through menus
Function keys with action based on context.
Based on context. Main function recalled in the
screen and also in JobCards wherever used.
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GE MEDICAL SYSTEMS
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SILHOUETTE VR
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SW JEDI 7-1
Service Menu Tree Breakdown
Type [ALT] & [S] (Together) to go to Maintenance Menus (MENU 3)
Type [
] and [
] keys to select a menu.
Illustration 1 shows the relationship between the Maintenance Mode menus and the function keys used to
access those menus.
To return to a higher level, key in [R]
The darkened menus are used for Generator and room setup (Configuration and Calibration): menu 3,
4, 5.
Menu 3 is used to Configure the system
Menu 4 is used to calibrate AEC mode (Automatic Exposure Control)
Menu 5 is used to perform Checksum
Menu 1 is used to perform generator test and diagnostics.

Menu 2 is used to enter Date and Time, view/clear error log, and view/clear tube and generator
recorded tracking Data.
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GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
Illustration 1 -
8/10
SW JEDI 7-1
Service Menu Tree Breakdown

MENU 1
[F1]
[F3]
[F5]
ANOD
HEAT
AUTO,
3,4,5
[F7]
HIGH
AEC
AUTO,
3k, 9k
GATE
CD
Tst
NoLD
ShC
INV
Tst
MENU 2
[F3]
[F5]
LIST
[F7]
NEXP
DATE
MENU 3
[F1]
[F5]
TECH
MODE
MENU 4
[F7]
[F5]
AEC
[F1]
[F3]
KG
KVEF
CAL
[F5]
KTIME
[F9]
KF
MENU 5
[F1]
[F7]
RAMS
[F1]
CKS
Vx Px.x
[F3]
MCL
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GE MEDICAL SYSTEMS
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SW JEDI 7-1
Sub-Menu Summary Description

1.. Configuration - MENU3
TECH: programming workstation, technique parameters.

MODE: Select Renard or Normal scale for kV selection.
(See Workstation Parameter JobCard).
2.. Calibration - MENU4
AEC: To set parameters if known, or modify them manually.

CAL: To calibrate Automatic Exposure Control, for each AEC chamber and Screen-film
combination.
(See JobCard Automated AEC calibration)
3.. Ram - MENU5
RAMS: NVRAm operation & display:

- CKSM: To update Checksum after configuration, calibration, parameter change. (See Job
Card Checksum Validation)
- MCLR: Clear NVRam memory. Normally not to be used, unless specifically instructed.
Note:
Do not use if Data Base backup has not been performed previously.
Vx Px.x: Display generator software version (e.g. P3.3)

DSPL: In Maintenance Mode, to display parameter after exposure using key [Z]
4.. Utilities - MENU2
LIST: To display last recorded error codes (up to 64)

-
Last error is viewed with Date and Time
Function keys allow to scroll down and up
[Z] to get back to the last recorded error
Same consecutive error are counted Up in the same line
[^H ], and [W] to clear error log
NEXP: To view/clear tube and generator recorded tracking Data. Clear must be performed only
when replacing X-Ray tube. Meaning of each parameter is found in Tube Replacement
JobCard.
DATE: To enter / modify the date and time.
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SW JEDI 7-1
5.. Diagnostics - MENU1
HEAT: To exercise Heater/filament function.

- Auto: run fixed current on both filament (if 2 filaments) in sequence on selected tube (If
more than 1).
- L or S: run 3, 4, or 5 Amps on Large or Small Focus.
ANOD: To exercise Rotor function.
- Auto: run rotation cycle in Low Speed then High Speed (If allowed by configuration) on
selected tube. (If more than 1)
- 3k: run one cycle acceleration, hold, break in Low Speed on selected tube (If more than 1)
- 9k: run one cycle acceleration, hold, break in High Speed (If allowed by configuration) on
selected tube (If more than 1)
HIGH: To exercise High Voltage function.
- NoLD: To troubleshoot HV problem, without mA nor rotation with or without X-Ray tube.
Test is run from 80 to max. kV, adjustable from 1 to 60 sec.
- Gate CD Test: to verify operation of the gate command board on the Inverter. Test is run
during 10 sec. At 0 kV.
Note:
Requires manual set up. Read related information in diagnostics section.
- ShC INV Tst: To verify operation of inverter with inverter in short circuit. Test is run during
100 msec. At 0 kV.
Note:
Requires manual set up. Read related information in diagnostics section.
AEC: To verify operation of AEC board. Refer to diagnostics section.
3-14
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
subassembly: Tube Configuration
purpose:
NF
No.
1/2
IST JEDI 5-1
version no. 0
Production
date
from /
/
Serial No.
date: 11/23/98
Personnel:1
from
Time:15m
to
to
SUPPLIES
None.
TOOLS
-
Service Terminal with floppy drive.
Service tools Part No. 2228546-X

-
JEDI Service Software
9-wire Service cable
SAFETY PRECAUTIONS
Not applicable.
PREREQUISITES
The service terminal must be configured and software installed (refer to Service Software User Guide
Job Card).
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IST JEDI 5-1
PROCEDURE
Load Software according to tube present in the installation
Two database are available on the JEDI Service Software supplied in Service Tools:
-
one for 32 kW tube: type DRX 1724, File = E32_1724.mx

one for 50 kW tube: type RAD 12,
File = E50RAD12.mx
Load the file corresponding to the tube present in the installation from Service Terminal. Refer to Job
Card Back-up and Restore Database Setup Parameters.
Verify
According to the tube used in the installation, verify:

1.. If 32 kW database loaded for tube DRX 1724
The maximum mA displayed on the console must be 400 mA for 80 kV.

2.. If 50 kW database loaded for tube RAD 12
- The maximum mA displayed on the console must be 630 mA for 80 kV.
-
WARNING
DO NOT USE 32 KW DATABASE FOR 50 KW TUBE OR 50 KW

FOR 32 KW TUBE.
3-16
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
subassembly: Receptor Programming
purpose: Receptor Parameters
NF
No.
1/8
CAL JEDI 8-4
version no. 0
Production
date
from /
/
Serial No.
date: 11/23/98
Personnel:1
from
Time:15m
to
to
Note:
The word Workstation is incorrectly used and displayed in the JEDI

software screens. Workstation actually refers to the word Receptor.
SUPPLIES
None.
TOOLS
-
Service Terminal with floppy drive
JEDI service software
9-wire service cable
SAFETY PRECAUTIONS
The JEDI is factory preprogrammed. Therefore, even if the data appears to correspond to the preprogramming, it must be confirmed. For example, AEC enable, wall bucky enable must be confirmed.
PREREQUISITES
Service terminal must be configured and software installed. Refer to Software Job Card Service
Software User Guide.
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PROCEDURE
Introduction
Receptor programming uses function keys indicated on screen for the following :
receptor select,
tube select,
define nominal number of exposures for 2-point mode operation,
AEC : types of chamber and number of pickup fields in each,
screen-film combination select, (if only one Select A).
Calling the Subroutine
Call TECH (setup mode, menu 3, function key [F1]).
MENU3 TECH
->
MODE
F5
F1
<-
R : Return
Q : Exit
**************
TECH :
MODE :
MENU3
**************
Select Workstation
Renard
Illustration 1 -
Setup Mode, Menu 3
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CAL JEDI 8-4
GE MEDICAL SYSTEMS
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CAL JEDI 8-4
Parameter Selection
Note:
Any new parameters created must be stored in the installation report (same as Illustration 3).
1.. Receptor Selection
OFF
No selection
SPE * Anatomic (for RF room)
DIR* Anatomic (for RAD room)
POMU Wall-mounted Bucky (i.e. SG50 or SG70)
SETE Spot-film device technique on remote-controlled table (i.e. Prestilix 1600)
TOPO Tomography Bucky
TOSE Tomography spot-film device technique
POTA Table-mounted Bucky
PULM Pulmorapid
CHAN Film changer
TOCO Special tomographic applications
SECO Spot-film device technique on conventional table
NUME Digital mode
TONU Digital tomography
Use the [
] and [
] keys to select.
* For RAD
TECH 1 = DIR
TECH 2 = POTA (TABLE BUCKY with moving grid) or DIR (if fixed grid).
TECH 3 = POMU (with moving grid) or DIR (if fixed grid) or OFF (if no Wall Bucky)
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Illustration 2 -
CAL JEDI 8-4
receptor Menu
2.. Tube Selection
T1 Tube 1 only
3.. Select the number of nominal exposures for 2-point mode operation.
Suggested values are given below:

DIR N = 2
POMU N = 2
POTA N = 2
Use function keys [F5] and [F6] to select.

4.. Selection of Exposure Chamber
IN1
IN2
Ionization chamber 1 (for Table Bucky Receptor POTA).

Ionization chamber 2 (for Wall Bucky Receptor on - POMU).
Select AEC in or out using function keys [F7] et [F8]. Each chamber corresponds to a specific
technique, i.e. POMU and POTA.
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CAL JEDI 8-4
5.. Control Console Function Key assignment
Function keys are assigned using the alphanumeric keyboard ([1] corresponds to function key 1,
etc., up to 8). Use the shift key for numbers 0 to 9.
With the RAD Console only four techniques are available.
The technique selected is shown in reverse video in zone 3.
6.. Selection of screen-film combination used
Keys [A], [B] and [C] are used to select the first, second and third screen-film combinations,
respectively.
The combination selected is displayed in reverse video in zone 2.
Press the key again to cancel a selection.
One combination is always selected. Select Key A for the RAD used screen film combination.
7.. Selection of Number of Pickup Fields
The number of pickup fields of the exposure chamber selected for AEC Mode with ionizing chamber
or II must be keyed in:
[D] middle pick-up field (one),
[F] three pick-up fields.
The number of pick-up fields is displayed in reverse video in zone 3.
8.. Validation
Use [W] to validate all values for a given function appearing on the screen.
Renard or Normal Scale for kV Selection
1.. Go to Service Mode, and call Menu 3 using the arrows on the keyboard.
2.. Call MODE by pressing F5.
3.. Select NORMAL or RENARD Scale by pressing F5.
4.. Hit W to confirm.
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CAL JEDI 8-4
Date & Time

To enter the Date and Time:
1.. Go to Service Mode, and call Menu 2 using the arrows on the keyboard.
2.. Call DATE by pressing F7.
3.. Enter date (MM DD YYYY) via numeric keypad.
5.. Hit F1.
6.. Enter time (HH MM) via numeric keypad.
When replacing the battery in the CPU Board, clear the yearcounter display on the righthand side via
F7 and F9 to confirm.
NOTICE
Anytime programming is modified, checksum must be

validated (refer to Calibration Job Card Checksum
Validation).
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CAL JEDI 8-4
RECEPTOR SELECT
FUNCTION
RECEPTOR
DIR
POTA
POMU
OFF
OFF
OFF
OFF
OFF
TUBE
T1
T1
T1
OUT
IN1
IN2
NO
NO
NO
NUMBER OF
EXPOSURES IN
2-POINT MODE
TOMOGRAPHIC
UNIT USED:
Y1
T1
Y2
T2
Y3
T3
Y4
T4
Y5
T5
TYPE
OF
CHAMBER
mA PLATEAU
TIME FOR
1-POINT MODE
EXTERNAL
RECEPTOR
COMMAND*
SCREEN-FILM
COMBINATIONS
1
2
3
NUMBER OF
PICK-UP
FIELDS
MODE
Illustration 3 -
Number of cells used

in AEC
RENARD OR NORMAL kV SELECTION
Receptor Parameters (Example for RAD with Wall Bucky and two ionisation chambers)
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3-24
CAL JEDI 8-4
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
subassembly: Automated AEC Calibration
purpose:
NF
No.
Production
date
from /
/
to
/
/
1/12
CAL JEDI 8-2
version no. 0
date: 11/23/98
Personnel:1
Serial No.
from
to
Time:1h
SUPPLIES
None.
TOOLS
-
sensitometer
densitometer
set of five plexiglass plates (5 cm x 25 cm x 25 cm)
For 5 cm, it is 2 inches
OR
-
a plastic bucket with a minimum height of 25 cm (for water)
Service Terminal with Floppy Drive

-
JEDI service software Part No. 2216253.
9-wire service cable Part No. 2207478.
SAFETY PRECAUTIONS
Standard precautions for work with ionizing radiation.
PREREQUISITES
-
Working knowledge of service terminal and installed software (see Calibration Job Card Setup
for Generator Calibration),
Service terminal must be configured and software installed,
Workstation configuration done (see Calibration Job Card Workstation Parameter),
AEC option must be installed (refer to AEC board installation Job Card).
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SILHOUETTE VR
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CAL JEDI 8-2
PROCEDURE
Development Equipment
Check development Equipment
-
Check that the automatic processor is available
Check that solution concentrations and temperatures comply with the manufacturers
specifications.
Plot a sensitometrics curve to determine the gamma value of the film and to assess solution
quality
All the gray scale levels should be visible, and the base fog should not exceed 0.2 for the
development equipment to be correct.
Note:
This procedure normally requires a sensitometer. If this is not available, proceed as follows :
run 2 exposures, using the same screen-film combination but with different mAs settings, mAs(f1)
and mAs(f2).
develop and measure the density d of each, d(f1) and d(f2). (Measured optical densities must be
between 1.0 and 2.0)
use the formula below to determine gamma :
gamma = ( d(f2) - d(f1) ) / log10 (mAs(f2)/mAs (f1))
if gamma is not between 2 and 3 change or renew the solution
Preliminary Remarks
1.. All calibrations must be performed with a source to image receptor distance between 0.8m and
1.2m.
2.. Center the phantom over the middle pickup tube field.
3.. A calibration procedure has to be performed for each combination of ionization chamber and
screen-film.
4.. If the same screen-film combinations are used for several ionization chambers (e.g. positionner and
bucky), adjust the positionner chamber first, and adust KG only for the other chambers.
For known screen-film combination or ionization chamber, KVEF, KT and KG could be entered with
MENU4 AEC (F5 key). REFER to Calibration JOB card "SERVICE SOFTWARE USER GUIDE .
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GE MEDICAL SYSTEMS
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CAL JEDI 8-2
Principle
The automation of this calibration is to use the optical density entered after one exposure or four
exposures to predict and propose the parameter for the next exposures. This leads to a reduction in the
number of exposures to run to find mAs, kV and reference AEC for a given optical density.
INIT
KVEF acquisition screen
Select ionization chamber

Select screen-film combination
Run kvef calibration

Select screen-film combination
If needed run
Ktime calibration
Run kvef calibration
If needed run
Ktime calibration
If needed run
Format calibration
other screen-film ?
(2more possible)
other screen-film ?
Yes
No
Other ionization chamber ?
(3 more possible)
Yes
No
Yes
Select ionization chamber
No
Run grid calibration
Other ionization chamber ? Yes

No
END
Note:
If an error occurs during exposure, reset by pressing key Z - redo the exposure.
- To redo an exposure after entering the optical density, enter o for optical density and
redo the exposure.
- To clear optical density, press and hold down the CTRL key, press the H key and enter
the new optical density.
Note:
You should back-up the database after all calibration have been done. Refer to Jobcard "Back
up and Restore ".
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CAL JEDI 8-2
KVEF Adjustment
Initialisation
KVEF is the main compensation coefficient for film darkening : its value varies significantly with kV
The MENU4 F7 key of the laptop service enters the calibration menu.
AEC1 1 0,00V L 80kV 10mAs 15cm OD= 0,00

Ionization
Chamber
Focus Kilovolt mAs Plexi or Water Optical

Exposure AEC
Thickness Density
Number Reference
In this step, the available keys have the following function :

- <- or -> keys to select the ionization chamber to be calibrated
-
F1/F2 keys to select the exposure number
F3/F4 keys to select the focus (generally Large Focus)
F5/F6 keys to select the kV
F7/F8 keys to select the mAs in Renard scale
F9/F10 keys to select plexi or water thickness
0 to 9 keys to enter the optical density (target or measured)
A, B or C key to select screen film type(slow, medium, fast) (if only one screen-film, select A key)
T key to select and modify target density

The first proposed exposure is 80kV, 10mAs, 15cm of plexi or water thickness. Exposure time is
calculated to be closest as possible from 100ms, according to the thermal status.
The selected screen/film key flicker.
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KVEF Parameter Acquisition
Refer to the flow diagrams in Illustration 1, Illustration 2 and Illustration 3.

Press Key F7 in Menu 4
Choose screen film to be calibrated with Key A, B or C
Key A, B or C flickers
Operator : Enter a targeted optical

density (generally 1), with key T
and validate with W key
A
Illustration 1 -
KVEF Parameter Acquisition flow diagram
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CAL JEDI 8-2
GE MEDICAL SYSTEMS
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SILHOUETTE VR
6/12
CAL JEDI 8-2
A
Software : first kV step 80kV or next kV step (selected by Key F5-F6
(steps are 80kV, 100kV, max kV, 40kV and 60kV)
Operator : Start a serie of exposures for this kV step
Keys a & B are flickering
Software : thickness proposal for the serie
Operator : Insert plexi thickness in the XRAY beam
Software : mAs proposal

(Operator : Can modify mAs according
to the sensitivity/mAs chart)
Operator : Insert casset (24x30) in spot film
Operator : Perform exposure

Operator : After having performed the
exposure, process the film and
measure the resultant optical density
Operator : Enter the resultant optical density

for each exposure and validate with W key
Software :Try to calculate mAs0 for targeted optical

density. When found, with previous exposure
recorded, V key flickers and screen film keylights ON
NO
Is V flickering ?
YES
Operator : Valid the kV step with V key when flickered
Operator : Display final values kvref, kV,

mAS, thickness, target optical density
NO
Illustration 2 -
Screen key light on?
YES
KVEF Parameter Acquisition flow diagram (continued)
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GE MEDICAL SYSTEMS
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CAL JEDI 8-2
B
End of kvef calibration. If first screen-film
calibration , select, if needed, time
See descriptions of time and grid

calibrations below
next screen-filmcalibration
Illustration 3 -
KVEF Parameter Acquisition flow diagram (continued)
1. Press T key and input Destination Density, then validates it with W key. Pressing T key deselect
Destination Density. Run the first exposures proposed by the software, develop the films and
measure the optical density. For each exposure, the software records the AEC signal from the
ionization chamber. The operator then selects the exposure number with F1/F2 keys, enters the
associated read optical density with key pad, and validates it with W key.
Note: There is no Beep during the exposure! The laptop Icon will light during X-ray.
2. When the optical densities have been entered, the software calculate the parameters for the next
exposure regarding the result of the previous ones (AEC signal from ionization chamber and optical
density).
3. The operator should run the next exposure proposed by the software, develop the film and measure
the optical density. The operator then selects the exposure number with F1/F2 keys and enters the
associated read optical density with the keypad, and validates it with the W key. The software
records the AEC signal from the ionization chamber. At each optical density entered, the software
evaluates if those values permit it to find the mAs0, which provides the target density for this
screen-film combination and the kV. When the mAs0 is found, the software calculates the KVEF
associated, then the V key starts to flicker to ask the operator to validate the calibration by pressing
the V keystroke.
4. Select another kV and repeat the previous operation for all kV steps
Note: Dont forget to change the phantom thickness when changing kV settings!
When all kV values are calibrated, the software extend the result and calculates the equivalent mAs (for
an optical density equal to the target value) to the kV,mA plan.
At the end of the first screen-film KVEF calibration , the operator selects the KT time calibration with the
V key after the V key has been illuminated.
3-31
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
8/12
CAL JEDI 8-2
K Time Parameter Acquisition (Exposure Time Correction)
AEC1 1 0,00V L 80kV 10mAs 15cm OD= 0,00

Ionization
Chamber
Exposure AEC
Focus Kilovolt mAs Plexi or Water Optical
Number Reference
Thickness Density

- F1/F2 keys to select the exposure number
-
0 to 9 keys to enter the optical density (target or measured)
The operator could by-pass this calibration in depressing V key again.

The software uses the KVEF calibration to find the thickness for the first KTIME exposures : if the mAs
for 80kV, 15cm of plexi or water thickness are lower than 32mAs, the software calculates the necessary
plexi or water thickness to obtain more than 32 mAs. The calculated plexi or water thickness is
displayed.
1. Set the plexi or water thickness indicated on the Service Terminal display
2. Run the proposed exposures (0.5s) develop the film and measure the optical density for each image.
The operator then selects the exposure number with F1/F2/ keys, and enters the associated read
optical density with key pad, and validates it with W key. Repeat the operation for the other proposed
exposures (1s, 2s, 3.2s)
3. If the mAs for 80kV, 15cm of plexi or water thickness is greater than 2.5mAs, the software calculates
the necessary plexi or water thickness to obtain less than 2.5 mAs. The calculated plexi or water
thickness is displayed..
4. Set the the plexi or water thickness indicated on the Service Terminal display
5. Run the proposed exposure (10ms), develop the film, measure the optical density, enter and validate
the value with W key.
The software calculate Ktime parameters.
5. The operator validates the Ktime calibration with V key. For the first screen-film calibration, the
software then proposes the KF calibration. By_pass it with V key again.
3-32
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
9/12
CAL JEDI 8-2
KG Parameter Acquisition (Grid Correction)
This KG procedure has to be followed if the same film/screen combination is used on the second
ionisation chamber.
If no second ionization chamber is present, press key R (end of calibration).
For a multiple ionization chamber, the operator runs the previous calibration (KVEF, KTIME for each
film screen combination for one ionization chamber) and runs the KG calibration for the other ionization.
AEC2
0.00V L 80kV xx mAs 15cm OD = 0,00
Ionization AEC Focus Kilovolt mAs

Chamber Reference
Plexi or Water
Optical density
Thickness

- 0 to 9 keys to enter the optical density.
STEP 1
Select the ionization chamber with the arrow keys (AEC2).
Set the SID at the same distance used for KVEF on AEC1. If not possible, go to STEP 3.
STEP 2
Run the proposed exposure, develop the film, measure the optical density and enter the value with
keys 0 to 9.
Repeat the same operations for the next proposed exposures until the V key flickers.
When the V key flickers, press the V key (end of calibration).
Press the R key.
STEP 3
Hit key R and return to Application Mode.
Put 15 cm plexiglass in front of Wall Stand (AEC2)
Set 2 Point Mode
Set KV to 80
For mAs :
Calculate the mAs according to :

mAs = mAs0 * (SID)2
mAs0 => mAs at 80 kV for AEC1 found during Autocalibration
SID = new SID
Example :
mAs0 = 5mAs
SID = 1.4
mAs = 5 * (!.4)2 = 10 mAs
3-33
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
10/12
Set mAs to 16 for backup.

Run exposure in AEC
Develop the film and measure the density
If the density is not equal to 1, go to MENU 4 AEC (F5)
Select KG (Key F3)
Select Grille 2 (Key F5/F6)
Enter a KG parameter :
CAL JEDI 8-2
If density is greater than 1, decrease KG value
If density is smaller than 1, increase KG value
Redo the same exposure and correct KG if density is not equal to 1.
Checksum Validation
The checksum must be validated at the end of the calibration. See Calibration Job Card Checksum
Validation.
AEC Repetition Test
Make a series of 10 exposures in 2-point AEC (exposure time : aproximatively 10ms) and check mAs
accuracy (+-10%) for each exposure.
3-34
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
11/12
CAL JEDI 8-2
Set KVEF, KT, KG
Call the AEC menu (setup mode, menu4, function key [F5])
AEC
KVEF KG KTIME
KF
Set KVEF
-
use the function key F1 to select sub-routine KVEF
AECV 40KV 1
KV step
a.bc
screen-film
combination
1,2 or 3
KVEF
select screen-film combination with A, B or C keys
select kV step 40, 60, 80, 100, or kVmax with F3/F4 keys
set KVEF to known value with key pad
validate each new setting with W key
press the R key when settings have been completed.
Set KT
-
use function key F5 to select sub-routine KG
AEC T N = 0 T = 0.5 1 a.bc

Time step #
Time
screen-film
combination
1,2 or 3
KTIME
use the following keys to select the screen-film combination : A for combination 1, B for
combination 2, C for combination3. The screen-film combination selected is displayed in reverse
video
select time step number with F1/F2 keys. (N = 0 T = 10ms, N = 1 T = 100ms, N = 2 T = 500, N
= 3 T = 1s, N = 4 T = 2s, N = 5 T = 3.2s)
f necessary, select time with F3/F4 keys
set KTIME to the known value with F9/F10 keys
validate each new setting with the W key
press the R key when the settings have been completed.
3-35
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
12/12
CAL JEDI 8-2
Set KG
-
use the function key F3 to select sub-routine KG
AEC G GRILLE 1 KG = a.b

grid no (from 1 to 4)
KG 0.8 to 2
use the function keys F5/F6 to scroll grid (grid number corresponds to the ionization chamber
number). Set KG to the known value using F9/F10 keys
validate each new setting with the W key
press the R key when settings have been completed.
Checksum Validation
The checksum must be validated after settings have been completed; refer to Calibration Job Card
Checksum Validation.
3-36
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
subassembly: Checksum Validation
purpose:
NF
No.
1/4
CAL JEDI 8-5
version no. 0
Production
date
from /
/
Serial No.
date: 11/23/98
Personnel:1
from
Time:5m
to
to
SUPPLIES
None.
TOOLS
-
Service Terminal with Floppy Drive

-
SAFETY PRECAUTIONS
Not applicable.
PREREQUISITES
Service terminal must be configured and software installed (refer to Service Software User Guide Job
Card).
3-37
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
2/4
CAL JEDI 8-5
PROCEDURE
Preliminary Remarks
NOTICE
Checksums must be validated at end of generator setup or

whenever a parameter is changed.
In the checksum validation process, the processor computes a number which is a function of all the
setup parameters. When the generator is powered up, this number is computed, i.e. the sum
is checked.
If the two numbers differ, the generator displays an error code, indicating that one or more parameters
have been changed since the last time the sums were checked, or that a RAM-related fault has
occurred.
Note:
X-ray generation is inhibited if there is a checksum error.
Note:
The display Va .
board EPROMS.
b on menu 5 is for the software version in the CPU
3-38
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
3/4
CAL JEDI 8-5
Checksum Validation
Call RAMS (setup mode, menu 5, function key [F1]
Resulting display :
RAMS
CKSM
MCLR
Enter function key [F1] and [V] simultaneously.

A buzzer will sound, indicating that the sums have been checked
and OK on display screen.
NOTICE
MCLR is used to erase all setup parameters. Function key

[F3] corresponding to this function should not be used.
3-39
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
4/4
3-40
CAL JEDI 8-5
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
subassembly: Backup and Restore Database Parameters
purpose:
NF
No.
Production
date
from /
/
to
/
/
Serial No.
from
to
1/4
CAL JEDI 8-6
version no. 0
date: 11/23/98
Personnel:1
Time:15m
SUPPLIES
None.
TOOLS
-
Service Terminal
-
SAFETY PRECAUTIONS
Not applicable.
PREREQUISITES
1. The service terminal must be configured and the software installed (refer to Service Software
User Guide Job Card)
2. All calibrations must have been completed.
3-41
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
2/4
CAL JEDI 8-6
APPLICABILITY
Setup parameters must be logged after the setup procedure has been completed, or whenever these
parameters are changed. This enables service engineers to key in parameters rapidly, i.e. when
changing the KV Control Board in the event of a battery outage.
PROCEDURE
CPU MEMORY BACKUP
The generator must be in application mode. The control console push buttons will be inactive during
the transfer.
-
Connect service terminal to XJ8 on the I/F Board.
Power up.
Insert the calibration floppy disk with write protection off.
From Laptop Dos, A: (It can also be run from Service Laptop Hard Disk Drive but in DOS mode).
Type JEDI on the terminal.
Hit [F6] to save memory.
The system asks for a file name. Default file name is A:\sv_var.mx.
-
Type a file name or hit [ENTER].
During transfer, the number of frames sent is displayed.

When transfer ends, the message Transfer successful is displayed.
If any error is detected, the transfer stops and an error message is displayed.
See list of error messages in this Job Card.
Note:
It is recommended that the floppy disk be protected by setting

write protection to on, once successful transfer is completed.
3-42
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
3/4
CAL JEDI 8-6
CPU Memory Restore
All parameters stored in CPU NVRAM memory must have been saved previously on calibration floppy
disk.
The procedure is the same as Memory backup except: Hit [F7] to restore memory.
This procedure is also used to down load new software (File type for Database or Software is
automaticaly recognised).
Note:
Calibration floppy disk may be write protected to prevent erasure of data.
Note:
Errors during memory restore may cause unpredictable results. A new

transfer is required.
If generator is locked, cycle power and repeat the entire memory restore
procedure.
Error Messages
MESSAGE
ERROR
Cannot open file
- No floppy disk.
- Floppy write protected during attempt to backup.
File contains data.

Delete old (y,n):
The file already exists (backup).

If you answer y, the existing file will be erased.
Error time out
- Generator OFF.
- Terminal not connected to generator..
Error communication
Error during transfer. Try a new transfer from the beginning.

Note:
Ensure ASIAN.exe software running under DOS and

not under WINDOWS.
3-43
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
4/4
3-44
CAL JEDI 8-6
GE MEDICAL SYSTEMS
REV 19
CHAPTER 4 - FUNCTIONAL CHECK

SECTION 1
INTRODUCTION
Functional Checks describes the procedures necessary to determine whether the
Silhouette VR system (Refer to Illustration 1) is operating correctly and
performing within specifications.
All the Silhouette VR system functions should conform to safety regulations, local
codes or other applicable standards.
Operational Checks
Performance Checks
Operational Checks may be performed by the customer or trained personnel.

These checks only indicate that the unit is functioning correctly at an operational
level. They do not indicate that the unit is performing within specifications.
Performance Checks must be performed by trained personnel only. These
checks verify that the unit is performing to specification. It is recommended to
complete these checks during and after installation, during periodic maintenance,
and when the equipment is replaced or modified.
Before performing Functional Checks all System Configuration and Calibrations
must be completed. (Refer to Chapter 3).
4-1
GE MEDICAL SYSTEMS
REV 19
ILLUSTRATION1
SILHOUETTE VR System
1. COLUMN
2. TUBE ARM
3. X-RAY TUBE
4. TABLE TOP
5. LONGITUDINAL SUPPORT
6. TABLE BASE
7. FOOT PEDAL
8. CASSETTE TRAY
9. COLLIMATOR
10.CONTROL BOX
4-2
GE MEDICAL SYSTEMS
REV 19
SECTION 2
TOOLS AND TEST EQUIPMENT
In addition to the standard service tool kit the following tools and test equipment
will be necessary to perform the functional checks described in this chapter:
DVM
Metric Tape Measure
KEITHLEY 35080A kV peak meter (or equivalent)
RADCAL MDH2025 dosimeter (or equivalent) with 20x5-60 probe
4-3
GE MEDICAL SYSTEMS
REV 19
SECTION 3
OPERATIONAL CHECKS
Operational Checks are used to verify that the Silhouette VR system is operating
correctly. These simple checks are generally performed using the control pedals,
press-button on the Cassette Tray and the Cassette Tray handle.
3-1
System Power up
Note:
Before this step, all electrical cables must be connected and

examined.
Power up the Silhouette VR system, verify that all corresponding LEDs displayed
are correct (see pg 6-5).
3-2
Silhouette VR System Mechanical Movement

All mechanical operations of the Table Assembly are controlled by the Control
Box located at the front end of cross arm. Vertical, longitudinal, angulation
movements of the table assembly are performed by pressing the corresponding
buttons on the control panel.(Refer to Illustration 2).
ILLUSTRATION 2
CONTROL BOX PANEL
1. Vertical Travel Control Switch.

2. Longitudinal Travel Control Switch.
3. Angular Indicator.
4. All Moving Function Control Switch.
5. Angulation rotating Control Switch.
6. Handle.
4-4
GE MEDICAL SYSTEMS
REV 19
3-2-1
Tube Stand Longitudinal Movement
1. Pressing the corresponding switch on the control box and moving the Tube
Stand via the handle verifies that the Tube Stand movement is operating
smoothly and uniformly.
2. Verify that the operation of the Tube Stand along with the Cassette Tray
moves smoothly all the way to the end of the table.
3-2-2
Tube Stand Rotation

Push the control boxs handle to drive the tube arm to the left or to the right for
rotation and verify that the Tube Stand can be rotated.
3-2-3
Tube Arm Vertical Movement

Press down the vertical button on the control box and verify the tube arm can
move smoothly up and down.
3-2-4
X-Ray Tube Angulation

Press down the angulation switch and verify that the X-ray tube can be angulated
to the 90 and 180 degree detent position about the Tube Arms horizontal axis.
3-2-5
Table Top Movement Checks

1. With the Silhouette VR system switched off, verify that the table top can be
moved in longitudinal direction freely.
2. Power the Silhouette VR system on and verify that the table top is locked in
position.
3. Check the horizontal movements of the table top by pressing the control
pedals:
3-2-6
a. Press the control pedals to the downward position, the table top is free
for both longitudinal and transverse movement.
b. Verify that all movements are smooth.
c. Release the control pedal, the table top will automatically lock into place.
Cassette Tray Movement Check
The Cassette Tray is normally coupled with the tube stand. A handle on the
Bucky carriage can lock or unlock them.
1. In coupled state:
The Cassette Tray should move together with the Tube Stand.
2. Uncoupled state:
a. Press the push button on the Bucky carriage. Verify that the Cassette
Tray can be moved longitudinally without the Tube Stand.
b. Release the push button, the Cassette Tray is locked into position.
4-5
GE MEDICAL SYSTEMS
REV 19
3-2-7
Collimator Rotation
1. Loosen set screw.
2. Rotate the collimator.
3. Verify the collimator can be rotated.
4. Secure set screw
SECTION 4
PERFORMANCE CHECKS
4-1
Generator Parameter Accuracy

For these performance checks, standard precautions for work with ionizing
radiation must be followed and all calibrations must be completed. Tools needed
are: Service tool Part No. 2228546, KEITHLEY 35080A kV peak meter, RADCAL
MDH 2025 dosimeter with 20x5-60 probe.
The precision of all parameters (kVp, mA, exposure times, mAs) is checked at
variable settings of kVp, first in Three Point mode and then in Two Point mode.
Note:
4-2
kVp values are measured using kV peak meter Keithley 35080A.
Post Display Initialization

Values for mA, exposure times and mAs are displayed on the Service Terminal
after each exposure.
To enable this display, the Post Display must first be initialized, using the
following procedure:
1. Connect Service Laptop.
2. Go to Calibration Mode.
3. Select Menu 5 via the control keys.
4. Press [F7] to select DSPL.
5. Press [F1] to select DISPLAY ON.
6. Press Q to quit the program and return to Application Mode.
7. The POST DISPLAY now remains operational until the generator is
powered down.
After each exposure, the parameters used may be displayed on the Service
Terminal, by pressing the Z key.
4-6
GE MEDICAL SYSTEMS
REV 19
4-3
Accuracy Checks
4-3-1
Summary
Test exposures are made at specified settings, first in Three Point mode, then in
Two Point mode, (without the use of AEC, Automatic exposure Control). The
values of parameters read during the exposure are noted and compared with
specified limits.
In each mode, exposures are made first with the small focal spot, then with the
large focal spot, at kVp values of 60, 80, and 130 kVp.
In Three Point mode, each exposure is made at 20 mAs, and exposures are
made with different values of mA and exposure time at each kVp value.
In Two Point mode, exposures are made with different values of mAs at each
kVp value.
The parameters to be set for each exposure are specified in Tables 1, 2, 3, and 4
of this document.
4-4
Procedure
Refer to Tables 1, 2, 3, and 4. Make a series of exposures corresponding to the
values specified in the tables, and note the actual parameters displayed for each
exposure in the spaces provided.
For each parameter and each exposure, the tables specify acceptable high and
low values.
CAUTION
The measurements of mA, mAs and ms must be made using

the post display of the Service Terminal. For kVp values, use
the Keithley 35080A.
4-5
Reproducibilty and Linearity of exposures
4-5-1
Summary
Reproducibility and linearity are checked by making a series of exposures,
measuring the actual dose produced in each case. The results are used to
calculate
coefficients
of
variation
(C)
and
linearity
(L).
Record values in Table 5.
Measurements are made using a RADCAL MDH 2025 dosimeter with the probe
(20x5-60) positioned at 100 cm (39 inches) from the focal spot.
CAUTION
The measurements of mAs must be made using the post

display of the Service Terminal.
4-7
GE MEDICAL SYSTEMS
REV 19
4-5-2
Reproducibility checks - Procedure

1. Position the probe as specified above.
2. Make ten exposures with the following conditions:
Note:
Three Point mode,
no AEC
Large focal spot
70 kVp
200 mS
100 mA
Take care not to saturate the ionization cell. The maximum output dose
permitted with the 20x5-60 probe is 3.3 mR/ms.
3. For each exposure, note the measured dose (mR), and the mAs value
shown on the POST DISPLAY in the space provided in Table 5.
4-5-3
Linearity checks - Procedure

1. Position the probe as specified above.
2. Make ten exposures with the following conditions:
Note:
Three Point mode,
no AEC
Large focal spot
70 kVp
200 mS
125 mA
3. For each exposure, note the measured dose (mR), and the mAs value
shown on the POST DISPLAY in the space provided in Table 5.
4-8
GE MEDICAL SYSTEMS
REV 19
4-6
Coefficients of Variation and Linearity
4-6-1
Reproducibility - Coefficient of Variation C

The coefficient of Variation, C, is defined as:
C=
1
Rm
( Ri Rm)
n 1
i =1
n
where:
Ri = dose measured during exposure i
Rm = average dose measured over ten successive exposures taken
under the same conditions in less than an hour
n = number of exposures (ten)
Make the calculation and enter it into Table 5.
4-6-2
Coefficient of linearity L
The coefficient of Variation, L, is defined as:
L=
Rm1
Xm1 Xm2
Rm2
; Xm1 =
and Xm2 =
A1
A2
Xm1 + Xm2
where:
Rm1 = average dose measured over ten successive exposures taken
under the same conditions (in particular with the same value of mA,
here 100 mA), in less than an hour
Rm2 = average dose measured over ten successive exposures taken
under the same conditions (in particular with the same value of mA,
here 125 mA), in less than an hour
A1 = the mAs value used during the exposures used to measure Rm1
(here 20 mAs)
A2 = the mAs value used during the exposures used to measure Rm2
(here 25 mAs)
Make the calculation and enter it into Table 5.
4-6-3
Acceptance Criteria
The results should give:
-
Reproducibility C < 0.05
Linearity L < 0.1
4-9
GE MEDICAL SYSTEMS
REV 19
4-7
Automatic Exposure Control (AEC)
Reproducibilty
Reproducibilty is checked in Two Point and Three Point modes of operation. In
each case, ten exposures are made and the doses are recorded. A coefficient of
variation is calculated, as defined in section 4-6.
4-7-1
Two Point Mode

1. Select a receptor which uses AEC.
2. Select the large focal spot
3. Using two point mode, set the kVp to 120 kVp, mAs to 20 mAs.
4. Select the central measurement cell.
5. Center a phantom under the X-ray tube (10 to 20 cm (4 to 8 inches) of
Plexiglass or water).
6. Center the probe (20x5-60) of a RADCAL MDH 2025 dosimeter 100 cm (39
inches) from the focal spot.
7. Make ten exposures. After each exposure note the dose (mR) in the space
provided in Table 6.
Note:
4-7-2
Three Point Mode

Repeat the complete procedure specified above for Two Point mode, but use
Three Point mode at 70 kVp, 100 mA, and 100 ms.
4-8
AEC Maximum mAs

This procedure checks the limitation on maximum mAs. When kVp is equal to or
greater than 50 kVp, the mAs value should not exceed 600 mAs.
1. Select a receptor which uses AEC.
3. Use Three Point mode, using values of 80 kVp, 160 mA, and 4000 ms (640
mAs).
4. Close the collimator.
5. Make an exposure.
6. Check that the exposure is interrupted after about four seconds; the buzzer
should sound and the Inhibit indicator
should light.
7. Press the z key on Service Terminal to display the exposure parameters;

check that the value for mAs is 600 mAs or less.
Pass
Note:
Fail
If the test fails, run diagnostics to troubleshoot.
4-10
GE MEDICAL SYSTEMS
REV 19
4-9
AEC Minimum Exposure Time
This procedure checks that the minimum exposure time is less than 16 ms.
1. Select a workstation which uses AEC.
3. Use Three Point mode, using values of 150 kVp, maximum mA, and 0.1 s.
4. Set the SID to approximately 1 m (39 inches).
5. Open the collimator.
6. Select each of the three measurement cell in turn. For each one:
-
Center the X-ray tube on the chosen measurement cell.
Make an exposure.
Press the
key on Service Terminal to display the exposure
parameters; check that the value for exposure time is less than 16
ms.
Pass
Note:
Fail
If the test fails, run diagnostics to troubleshoot.
4-11
GE MEDICAL SYSTEMS
REV 19
TABLE 1
JEDI 50 R 1T ACCURACY - SMALL FOCAL SPOT - RADIOGRAPHY - 3 POINTS - TUBE:
60 kVp
mA
54.55
65.45
80 kVp
Data
mA
limits
Data
ms
limits
Data
mAs
limits
20
1000
15.87
73.65
130 kVp
Data
mA
limits
Data
ms
limits
Data
mAs
limits
Data
mA
limits
Data
ms
limits
Data
mAs
limits
20
20
1000
20
20
1000
20
945
17.28
15.87
945
17.28
15.87
945
17.28
---
---
---
---
---
---
---
---
---
24.12
1055
22.72
24.12
1055
22.72
24.12
1055
22.72
50
400
20
50
400
20
50
400
20
43.56
377
18.24
43.56
377
18.24
43.56
377
18.24
---
---
---
---
---
---
---
---
---
56.44
423
21.76
56.44
423
21.76
56.44
423
21.76
100
200
20
100
200
20
100
200
20
88.14
188.18
18.26
88.14
188.18
18.26
88.14
188.18
18.26
---
---
---
---
---
---
---
---
---
111.86
211.82
21.74
111.86
211.82
21.74
111.86
211.82
21.74
160
125
20
160
125
20
160
125
20
140.64
117.31
18.16
140.64
117.31
18.16
140.64
117.31
18.16
---
---
---
---
---
---
---
---
---
179.36
132.69
21.84
179.36
132.69
21.84
179.36
132.69
21.84
86.35
121.4
138.6
20
---
---
---
50
---
---
---
100
---
---
---
*160
---
CAUTION
---
---
for tube RAD 12 only
1- kVp values are measured using kV peakmeter Keithkey

35080A.
2- mA, time and mAs measurements must be made using the
post display of the Service Terminal.
4-12
GE MEDICAL SYSTEMS
REV 19
TABLE 2
JEDI 50 R 1T ACCURACY - LARGE FOCAL SPOT - RADIOGRAPHY - 3 POINTS - TUBE:
60 kVp
mA
54.55
65.45
80 kVp
Data
mA
limits
Data
ms
limits
Data
mAs
limits
20
1000
15.87
73.65
130 kVp
Data
mA
limits
Data
ms
limits
Data
mAs
limits
Data
mA
limits
Data
ms
limits
Data
mAs
limits
20
20
1000
20
20
1000
20
945
17.28
15.87
945
17.28
15.87
945
17.28
---
---
---
---
---
---
---
---
---
24.12
1055
22.72
24.12
1055
22.72
24.12
1055
22.72
50
400
20
50
400
20
50
400
20
43.56
377
18.24
43.56
377
18.24
43.56
377
18.24
---
---
---
---
---
---
---
---
---
56.44
423
21.76
56.44
423
21.76
56.44
423
21.76
100
200
20
100
200
20
100
200
20
88.14
188.18
18.26
88.14
188.18
18.26
88.14
188.18
18.26
---
---
---
---
---
---
---
---
---
111.86
211.82
21.74
111.86
211.82
21.74
111.86
211.82
21.74
200
100
20
200
100
20
200
100
20
177.07
93.68
18.27
177.07
93.68
18.27
177.07
93.68
18.27
---
---
---
---
---
---
---
---
---
222.93
106.31
21.73
222.93
106.31
21.73
222.93
106.31
21.73
320
64
20.48
320
64
20.48
320
64
20.48
283.44
59.66
18.72
283.44
59.66
18.72
283.44
59.66
18.72
---
---
---
---
---
---
---
---
---
356.56
68.34
22.24
356.56
68.34
22.24
356.56
68.34
22.24
86.35
121.4
138.6
20
---
---
---
50
---
---
---
100
---
---
---
200
---
---
---
* 320
---
---
for tube RAD 12 only
4-13
---
GE MEDICAL SYSTEMS
REV 19
TABLE 3
JEDI 50 R 1T ACCURACY SMALL FOCAL SPOT - RADIOGRAPHY 2 POINTS - TUBE:
mAs
60 kVp
80 kVp
130 kVp
Displays
mAs
mAs
mAs
0.26
0.26
0.26
0.74
0.74
0.74
18.28
18.28
18.28
21.72
21.72
21.72
46
46
46
54
54
54
0.5
20
50
TABLE 4
JEDI 50 R 1T ACCURACY LARGE FOCAL SPOT - RADIOGRAPHY 2 POINTS - TUBE:
mAs
60 kVp
80 kVp
130 kVp
Displayed
mAs
mAs
mAs
0.26
0.26
0.26
0.74
0.74
0.74
18.28
18.28
18.28
21.72
21.72
21.72
73.72
73.72
73.72
86.28
86.28
86.28
0.5
20
80
4-14
GE MEDICAL SYSTEMS
REV 19
TABLE 5
REPRODUCIBILITY AND LINEARITY OF EXPOSURES IN 3 POINT MODE - TUBE:
70 kVp - 200 ms
20 mAs (100 mA)
mR (R1)
mAs (A1)
25 mAs (125 mA)

mR (R2)
mAs (A2)
1
2
3
4
5
6
7
8
9
10
Rm
Xm
C
(< 0.05)
L
(< 0.1)
Refer to section 4-6 for C and L calculation formula.
CAUTION
Measurement of mAs must be made using the post display of

the Control Console.
4-15
GE MEDICAL SYSTEMS
REV 19
TABLE 6
AEC: REPRODUCIBILITY OF EXPOSURES
MODE
2POINT
3POINT
kVp =120
kVp = 70
mAs = 20
mA = 250
ms = 1000
DOSE
cGy (mR)
cGy (mR)
1
2
3
4
5
6
7
8
9
10
Rm
C
(< 0.05)
Refer to section 4-6 for C calculation formula.
4-16
GE MEDICAL SYSTEMS
REV 19
4-10
JEDI Performance Checks
JOB CARD JEDI 382 - Performance checks

Time: 0 h 15 min (Mechanical handling only) - Personnel: 1 field engineer
1 of 2
SUPPLIES
Not applicable.
TOOLS
A multimeter and an oscilloscope with a filtering capability. There is a red 8 inch multimeter probe
supplied.
SAFETY PRECAUTIONS
PREREQUISITES
DANGER
BEFORE ANY MANUAL INTERVENTION, ENSURE THE MAIN POWER IS OFF.

APPLY LOCK OUT - TAG OUT PROCEDURE FOR YOUR OWN SAFETY WHEN
MANIPULATING INSIDE THE EQUIPMENT IS REQUIRED.
Disassembly
1.. Remove the twelve 5.5mm hex head screws which secure the right cover of the Power Unit.
Remove the cover (refer to Job Card D/R JEDI17-24).
4-17
GE MEDICAL SYSTEMS
REV 19
2 of 2
1
1
HV Tank
KV Measure Board
J6
HV+
J2
KV+ measure
sh4
5ohms
1%
sh3
5 ohms
1%
3
To KV Control Board
45
2
HV-
46
KV- measure
Measurement tool
(multimeter or oscilloscope)
mA= V/(sh3//sh4)= V/5ohms
2.. Put a probe inside the generator on the shunt SH3 (right side of the resistor) of KV Measure board
on HV Tank 1 .
3.. Connect a second probe on the mechanical ground 2 .
4.. Check the resistor value with a multimeter: it should be 5 Ohms (+/- 0.05).
mA measurement
1.. Power on the generator

2.. Use a multimeter for mA 50mA with a exposure time set to 1s minimum.
3.. Use an oscilloscope for other mA, the signal must be filtered at f 10kHz.
4-18
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
1/2
IST 009
subassembly: Final System Installation

purpose:
NF No.
version no. 1
date: 20/10/98
Production date
Serial No.
Personnel:2
from
from
Time: 15m
to
to
Final System Installation
Note:
If this is the initial installation of the system, then perform all steps in this
Job Card.
If system was previously installed, then only perform the steps necessary
to return the system to operating condition.
1. Remove Service Laptop connection.

2. Cover JEDIs assembly coping.
3. Roll generator into position under table.
4. Secure generator with two bolts.
5. Install front cover.
4-19
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
2/2
IST 009
1. Unpack the table top (1) then remove end-of-travel stops (2) from one end.
DANGER
THE TABLE TOP IS LARGE AND HEAVY (APPROX. 50KG). TWO

PEOPLE ARE REQUIRED TO MOVE AND INSTALL IT TO PREVENT
PERSONAL INJURY OR EQUIPMENT DAMAGE.
2. Align the end of the table top (end with stops removed) with the end of the table base, then slide the
table top into position.
3. Re-install the end stop screw (3) & (4).
CAUTION
Ensure that the table top clears the longitudinal locks when
sliding it over the bearings.
4. To ensure the table tops 4-way moving (longitudinal & lateral) capabilities operate smoothly, place
the longitudinal (5) and transversal (6) levels on table top to verify and ensure table top is level.
4-20
GE MEDICAL SYSTEMS
REV 19
CHAPTER 5 - JEDI GENERATOR THEORY

AND FUNCTIONAL DESCRIPTION
SECTION 1
THEORY
1-1
Glossary
Glossary of terms used in this document:

Term
Definition
ABC
Automatic Brightness Control. Regulation loop which makes the measured

brightness equal to brightness demand
AEC
Automatic Exposure Control. Exposure cut off technique which uses the
brightness signal to cut the exposure
CAN
Controller Area Network. A network used for localized control.
CPU
Control Processor Unit. Microprocessor and peripherals which run the

software/firmware
EPLD
Erasable Programmable Logic Device.
EMC
Electro Magnetic Compatibility. The EMC function prevents the generator

from polluting the power source.
FPGA
Field Programmable Gate Array. It is programmed by the CPU core after the
reset and handles all the exposure control logic including the system interface
realtime lines.
HV Ripple
High voltage variations due to inverter current pulses. Typically a few percent.
State Machine
Software or hardware function which handles the state of a system and

authorize to go to the next state upon reception of specific events.
IGBT
Insulated gate bipolar transistor. A type of power switch
Ilp
HV power inverter parallel resonant current; current in the parallel inductor
Ilr
HV power inverter serial resonant current; current in the serial inductor.
MOS
Metal Oxide Semiconductor. A type of power switch
OGP
On Gantry Processor. Unit which drives the generator in CT systems
PDU
Power Distribution Unit
RMS
Root Mean Square
5-1
GE MEDICAL SYSTEMS
REV 19
5-2
GE MEDICAL SYSTEMS
REV 19
JEDI HIGH LEVEL BLOCK DIAGRAM

ILLUSTRATION 1
JEDI GENERATOR / FUNCTIONAL ARCHITECTURE
5-3
GE MEDICAL SYSTEMS
REV 19
5-4
GE MEDICAL SYSTEMS
REV 19
SECTION 2
THEORY PRESENTATION
2-1
Introduction
Jedi is the engineering name for a family of compact high frequency X-Ray
generators. This generator family covers a wide range of applications from
mobile equipment up to vascular systems:
2-2
JEDI 12-25 kW: Mobile applications
JEDI 24-48 kW: CT applications
JEDI 32-50 kW: RAD applications
JEDI 50-65-80 kW: RF applications
JEDI 100 kW: VASCULAR applications
Standard Features
Jedi is a family of 150 kV generators operating from 12 kW up to 100 kW for all
the major radiological, fluoroscopic and CT applications. The family handles 1 ms
to continuous exposures with tube currents ranging from 0mA up to 1000 mA.
The generators feature the very latest technology available:
Constant potential independent of line voltage variations
Power generation by a high-frequency converter (High voltage ripple: 40

kHz-140 kHz)
Distributed micro-processor controlled functions (CAN bus)
Other features include:
Single phase, three phase or battery power source
Very low kV and mA ripple, excellent accuracies and dose reproducibility
Compatible with a wide range of tubes, high speed or low speed, can supply
up to 3 different tubes. Thermal load interactive integrator ensuring optimum
use of the heat protection curve of the x-ray tube
Available in various packaging configurations: gantry, under-table, cabinet
Serviceability: high reliability, fast installation (no generator calibration),

application error codes ensure fast troubleshooting
Meets CE marking (and in particular EMC), IEC, UL, CSA, MHW regulations
(if required)
Optional pulsed fluoroscopy
5-5
GE MEDICAL SYSTEMS
REV 19
2-3
Applications
RAD
Surgery
x
x
x
3 Points Mode
2 Points Mode
1 Point Mode
0 Point Mode
x
x
x
AEC
Tomography
AET
Continuous/Pulsed Fluoroscopy
x
x
x
Rad Exposures
Cinema 30 fr/s
RF
x
x
x
x
x
x
x
x
Vascular/
Cardiac
x
x
x
x
x
Cinema 90 fr/s
ABC
CT
x
x
x
x
Variable mA Scans
Low mA Fluoroscopy
Legend:
-
AEC - Automatic Exposure Control
AET - Automatic Tomographic Exposure
ABC - Automatic Brightness Control in fluoroscopy
5-6
GE MEDICAL SYSTEMS
REV 19
2-4
Architecture
Refer to Illustration 19: Jedi Generator / Functional Architecture
The Jedi family is composed of 3 elements:
2-4-1
A Kernel
High voltage chain composed of kV control, HV power inverter and HV tank
Anode rotation function
Tube filaments heater function
Control bus for communication between the functions
DC bus for power distribution to each function
Input voltage to DC conversion: AC/DC function
Low voltage power supply
Application software, running on the kV control board
These functions are the Jedi core. They are present in all versions of the
generator.
A function can be unique for all products, or can have several different releases
based on product specification.
Examples:
The anode rotation function is available in 2 releases:
low speed rotation for applications where the tube has a max rotation of
3000 rpm
high speed/low speed rotation for applications where at least one of the
tubes can use
8000-10000 rpm
The control bus is unique.

2-4-2
Options Depending on the Application
A System Interface which can be:

-
CT interface
RAD interface (console interface, room interface, AEC management

present or not)
ATLAS interface
EMC function
Grid function (RF, vascular)
Bias function (RF, vascular)
Tube management (2 tubes or 3 tubes option)

5-7
GE MEDICAL SYSTEMS
REV 19
ILLUSTRATION 2
JEDI GENERATOR/FUNCTIONAL ARCHITECTURE
5-8
GE MEDICAL SYSTEMS
REV 19
2-5
A Packaging Architecture
The packaging architecture consists in a set of boxes which can be put together
in several ways to make Jedi fit either in a cabinet, or a console foot, or a table
foot. The boxes can also be split in 2 units distant of several meters (example:
CT gantry). Refer to Illustration 20.
The boxes normally consist of the following:
2-5-1
Auxiliaries Box
Rotation function
Heater function
Low voltage power supply (which can also be in the AC/DC box)
This box is always present.

2-5-2
Power Box
HV tank
HV power inverter
kV control
System interface (for the less complex system interface)

2-5-3
AC/DC Box
MC filter (optional)
AC/DC function
Low voltage power supply (which can also be in the auxiliaries box)

2-5-4
System Interface Box
RAD interface
AEC interface
This box is present in the RAD product.

2-5-5
Optional Boxes
Tube selection
Grid/Bias control
5-9
GE MEDICAL SYSTEMS
REV 19
ILLUSTRATION 3
JEDI GENERATOR / PACKAGING ARCHITECTURE
Inverter
LVPS Board
(for TIGER)
Dual Snub
Tube
HV
Gate
Board
+-
KV Measure
CT
Inter
face
AC/DC
Board
HV Tank
Rectifier
Block
KV Control
Board
EMC Filter
(Optional)
AC/DC Box
Power Box
LVPS Board
(for NP and
Emperor)
RAD
Interface
AEC
Interface
Heater Board
System Interface
Box for the rad
product
Rotation
Board
Tube
Selection
Rotation
Capacitor
Grid/Bias
Control
Rotation
Capacitor
(optional)
Auxiliaries
Box
Optional
Boxes
5-10
GE MEDICAL SYSTEMS
REV 19
CHAPTER 6 - EXCEPTION HANDLING AND ERROR CODES

SECTION 1
EXCEPTION HANDLING
JEDI software performs auto-test at power up and continuously monitors the
correct operation of its functions during application. Any malfunction is stored in
the JEDI error log. Errors found can only be reported if the generator is powered
on and functional.
1-1
Diagnostics
There are different levels of diagnostics.
1-2
Power-On Diagnostics
At power-up the kV control performs its own initialisation, checks its memory
integrity (checksum of program and NVRAM) and starts the communication with
its peripherals as well as the system. Communication is permanently checked
afterwards. It then initialises the Rotation board and Heater board with their
respective database parameters and loads kV control FPGA.
Eight LEDs (S7..S0) on the kV control board show the software status.
During power-on, the Heater board and the Rotation board CPUs are initialised
and check their memory integrity and hardware. If a problem is encountered, a
PRD error is reported to the kV control.
1-3
Live Diagnostics
1. Under application faults will be reported through an error code on the
Service Laptop. Some are straightforward and convey the root cause. Refer
to the recommended action in the error list.
2. Diagnostics run separately:
heating function
rotation function
inverter gate command diagnostic
inverter in short circuit diagnostic
no load HV function diagnostics
3. Manual Diagnostics
Through a troubleshooting guide based on an error message or when the
generator does not reply.
6-1
GE MEDICAL SYSTEMS
REV 19
1-4
Error Code Structure
The error code structure described in this chapter applies to JEDI error detection
and logging. The JEDI error log file can be accessed from the system through the
system console or a laptop (JEDI error log upload functionality).
When an error is detected, it is logged in the JEDI error log file. The file contains
a maximum of sixty four error logs.
Each log shows the following structure:
Simplified
error code
Generator
Phase
Error Class
Error Code
Data
Number of
associated
occurrences
with the error
code
Date & time
The fields are described in the following paragraphs.

1-5
Simplified Error Code Definition

The simplified error code is a grouping of the JEDI error codes. This field gives a
rapid understanding of which part of JEDI is faulty.
Simplified Error Code

30
40
50
60
70
80
90
100
110
10
20
25
27
Description
Tube spits errors
Rotation errors
Heater errors
Exposure errors (HV inverter + mA measure + exposure control
Power supply errors (low voltage + DC bus)
Hardware errors (internal communications + cables)
Application errors (saved RAM + software)
External communication errors
Thermal errors
Rotation warnings (engineering use)
Heater warnings (engineering use)
LVPS warnings (engineering use)
Application warnings (mainly saved RAM battery change)
6-2
GE MEDICAL SYSTEMS
REV 19
1-6
Generator Phase Definition
The generator phase field contains the state of the generator when the error
occurred.
Generator Phase
0
1
2
3
4
5
6
1-7
Description
idle: entered in diagnostic mode
powered up; waiting for configuration
Stand by: configuration completed, waiting for a preparation command
Preparation in progress: JEDI gets ready to take X-rays
Ready for exposures (rotation at speed; filament; HV inverter drive ready;
no errors): waiting for an exposure command
High voltage on
Error detected and not yet cleared
Error Class Definition

There are five classes of errors that correspond to different levels of impact to the
system. The class of errors correspond to the seriousness of the errors.
Class
1
Description
Errors which have no impact on the system operation.
Errors detected in background diagnostics during application. They are referred
as Warning errors, to monitor drifts and used for engineering tracking.
The generator phase remains unchanged.
Errors are stored in the JEDI error log.
Errors which are detected by JEDI and that are recoverable automatically without
noticeable effect on the system, such as error related to recovered tube spits.
The generator phase remains unchanged.
Errors which usually occur during exposure.
Errors detected by JEDI during exposure. They stop the exposure and revert the
generator into a safe state.
Error will be reset on Exposure Command release. It will require another Exposure
Command to restart the sequence.
The generator phase is set to error until the error is cleared.
Errors which are related to any hardware failures, software application or
communication errors.
JEDI will revert to a safe state.
If preparation is in progress, it is stopped.
Errors are cleared either by a reset error action from the system (for system having a
reset error mechanism) or by a prep release or by a new prep command.
Application cannot work if errors are persistent.
These codes may appear when the generator or tube temperature limits are reached.
The application waits until the thermal information disappears. The error information is
temporary.
6-3
GE MEDICAL SYSTEMS
REV 19
1-8
Error Code Definition
Each error code comprises two fields (which cannot be generated and used
separately);
the first field describes the JEDI function which is faulty (referred to as
the function code)
the second field describes the error detected.
Example: error code 0306 means:
03: high voltage generation function;
06: no kV feedback on anode.
Function Codes List
Function Code
01
02
03
04
05
06
07
08
09
10
11
12
13
14
Description
Rotation
heater
High voltage generation
mA control
Power supplies
System interface
Software
Application
Tube control
Tube management
Grid
Bias
AEC
Hardware
1-9
Data Associated With The Error Code

The field data associated with the error code shows detailed information over
the state of the generator when the error occurred.
Examples: rotation high speed acceleration state, small focus preheat, tube
number 1 selected.
1-10
Number Of Occurrences
The field number of occurrences is used to log the same error occurring several
times consecutively. Instead of filling the error log file with the same error which
has occurred consecutively several times, the first error is logged and successive
errors are recorded through increasing the number of occurrences field.
Date & Time
1-11
The field date & time stores the date and time when the error occurred. This is
the JEDI internal date and time which may be different from the system date and
time. In the case of logging the same error the date/time is of the most recent
entry.
6-4
GE MEDICAL SYSTEMS
REV 19
SECTION 2
ERROR CODES, DIAGNOSTICS, AND TROUBLESHOOTING
2-1
Introduction
This diagnostics section is to introduce the JEDI generator with the following
information:
2-2
Power-On diagnostics LED indication.
List all the potential error codes that can be issued by JEDI Generator.
Provide error code explanation, potential cause and recommended action.
List of diagnostics aids and explanation of diagnostics.
Power On Diagnostics
Refer to theory of operation for power-on sequence. This paragraph in this
section is to provide meaning of boards LED status. The LED display status is
offering useful information at a glance to proceed to error code based
troubleshooting. Whenever in doubt, a simple step is to watch the LED status
display on the kV control board, than the Rotation and Heater.
kV control LED status:

- During Power On Diagnostics :
kV control board
S0..................S7
_
oooo
S0.........................S7
' ' ' ' ' ' o'

The 8 LEDs (S0...S7) are lit successively in both directions (Scrolling as indicated by the arrows): the power up
diagnostics are completed, kV control board is up and running.
S0.....................S7
o ' o ' o ' o '
One out of two is lit: Data base checksum problem. An error code is logged. Refer to error code description.
S0.....................S7
'
' o oo
S7, S6, S5 are lit along with either S0 or S1 or S2 (depending of the type of FPGA downOne out of two is lit: Data
base checksum problem. An error code is logged. Refer to error code description.
6-5
GE MEDICAL SYSTEMS
REV 19
When an application error occurs (Not PRD)
'
'
'
'
K ' K '
e.g: No communication
The simplified error code is displayed on the Leds. They blink; when the error is
cleared (by a return to the standby mode for example), the 8 LEDs are lit
successively.
Heater board LED status: (See central listing)
After the power on diagnostics, heater board LEDs DS1 and DS2 are lit
successively. Any different status correspond to an abnormal situation. An error
code is logged. Refer to error code description.
Rotation board LED status: (See central listing)
After the power on diagnostics, rotation board LED DS5 is blinking. Any different
status correspond to an abnormal situation. An error code is logged. Refer to
error code description.
6-6
GE MEDICAL SYSTEMS
REV 19
2-3
Error Code List
The error code list and associated short description is presented below.
simplified
error
code
30
Description
Error
Error
Code
Description
Class
Tube Spits
2
2
2
2
2
0301H
0302H
0303H
0304H
0305H
Tube spit (kV+ and kV- dropped)

Tube spit (kV+ has dropped)
Tube spit (kV- has dropped)
Tube spit (kV regulation error)
FPGA problem (restarting safety signal)
40
Rotation Error
4
4
4
4
4
4
4
4
4
4
4
4
0101H
0102H
0103H
0104H
0105H
0106H
0107H
0108H
0109H
0110H
0111H
0149H
No CAN message received within 5 secs

Database not correct
Rotation current overload
Rotation Openload
Rotation Phases unbalanced
Rotation Phases error
Rotation Inverter permanent overcurrent
Rotation command error
MAINS_DROP has failed
PRD error
F0 main frequency problem
Unknown Rotation error
50
Heater Error
4
4
4
4
4
4
4
4
4
4
4
4
4
4
4
4
0201H
0203H
0204H
0205H
0206H
0207H
0208H
0209H
0210H
0211H
0212H
0213H
0214H
0215H
0216H
0221H
0222H
0223H
0224H
0248H
0249H

Heater inverter permanent overcurrent
Filament permanent open circuit
Heater Inverter permanent short circuit
Filament too high for Pre-heat
Filament too high for Boost
Filament too high for Heat
Heater command error
Current under estimated fork
Current over estimated fork
MAINS_DROP detected
PRD error
Stay too long in Boost
Filament selection error
Measured current while inverter OFF
Filament Database not correct
Unknown Heater error
6-7
GE MEDICAL SYSTEMS
REV 19
simplified
error
code
60
70
Description
Error
Error
Description
0306H
No kV Feedback on anode
3
3
3
3
3
3
3
3
3
3
3
3
3
3
3
3
2
3
3
3
3
3
3
3
3
3
0307H
0308H
0309H
0310H
0311H
0312H
0313H
0314H
0316H
0317H
0318H
0319H
0320H
0323H
0401H
0402H
0403H
0504H
0801H
0802H
0803H
1406H
1407H
1408H
1409H
1410H
No kV Feedback on cathode
No kV Feedback on anode and cathode
kV detected during kV diag
kV max detected
ILP current not OK
ILR current not OK
ILR max current detected
ILR current timeout
Spit Max error
Spit Ratio error
kV did not reach 75% after 20ms
kV unbalanced detected
FPGA problem (safety signal)
ILP and ILR currents not OK
No mA feedback
mA scale error
mA accuracy exceeded 5%
Inverter Gate Power Supply failed
Exposure backup mAs exceeded
Exposure backup time exceeded
Exp cmd while gene not ready
time counter error
mAs counter error
AEC counter error
mAs meter saturated
FPGA Locked
0501H
DC bus out of range
4
4
4
4
4
4
4
4
4
4
4
0503H
Inverter Gate Power Supply error
0505H Mains power supply has dropped during exposure
0506H
DC bus 1 phase precharge error
0507H
DC bus 1 phase discharge error
0549H
Unknown LVPS error
0553H
Detected +160V too high
0557H
Detected +160V too low
0563H
0567H
0573H
Detected -15V too strong
0577H
Detected -15V too weak
Class
Exposure
errors
Power Supply
errors
6-8
GE MEDICAL SYSTEMS
REV 19
simplified
Description
Error Error
error
Class
code
4
0180H
80
Hardware error
4
0181H
4
0280H
4
0281H
4
0321H
4
0322H
4
0601H
4
0602H
4
0902H
4
1402H
4
1403H
4
1404H
4
1405H
90
100
Application
errors
Communication
errors
Description
Rotor board communication problem

Rotor board has reset
Heater board communication problem
Heater board has reset
kV conversion error
kV ref ADC / DAC failed
RTL error
External CAN bus off
tube Fan supply error
Internal CAN bus off
Connectic Fault
FPGA configuration problem
Tank sensor problem
0701H
Saved RAM checksum pb
4
4
4
0702H
0703H
0704H
Software problem
Watchdog reset has just occurred
Rotor/Heater hold too long
0603H
Debug screen com error
4
4
4
4
0604H
0605H
0606H
1301H
Database download error

TAV communication error
MPC/Madrid communication error
AEC communication error
110
Thermal error
5
5
0804H
0903H
Tank Thermal Error

Tube exceeded 70degC
10
Rotor Warning
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
0151H
0152H
0153H
0154H
0155H
0156H
0157H
0158H
0159H
0160H
0161H
0162H
0163H
0164H
0199H
CAN Domain command number error

CAN Domain request with no transfer init
CAN Domain Toggle bit error
CAN Domain : less than 2 data to download
CAN Domain Abort received & applied
Bad index in config upload
Tube switch while rotor not off
Acceleration cmd while no tube selected
Acceleration cmd while database not OK
Database download while rotor speeding
Acceleration command not OK
Rotor acceleration while in error
Rotation Inverter overcurrent (< 3 times)
Unknown rotation warning
6-9
GE MEDICAL SYSTEMS
REV 19
simplified
Description
Error Error
error
Class
code
1
0251H
20
Heater Warning
1
0252H
1
0253H
1
0254H
1
0255H
1
0256H
1
0257H
1
0258H
1
0259H
1
0260H
1
0261H
1
0262H
1
0263H
1
0299H
25
27
2-4
Low Voltage
Power supply
Warnings
Application
warnings
Description
Received command is not OK

Heater command not OK
Heater inverter overcurrent (inverter1) (<3 times)
Filament open circuit (inverter1) (<3 times)
Heater Inverter short circuit (inverter1) (<3times)
Tube switch while filaments not OFF
Database download while heater not cut
Unknown Heater warning
0550H
No more warn +160V too low or too gigh
1
1
1
1
1
1
1
1
1
0551H
0555H
0560H
0561H
0565H
0570H
0571H
0575H
0599H

No more warn +15V too low or too high
No more warn -15V too low or too high
Unknown LVPS warning
1401H
Saved RAM power supply limit reached
Error Reporting
The control console only displays the simplified error code from the Jedi
generator.
Whenever a generator error is displayed on the operator console, the Jedi
errorlog upload functionality is available to get more detailed information about
the error .This function is performed from the service laptop.
The simplified error code is used to find the Jedi error code in the Jedi errorlog
file.
With this information, look at the Jedi trouble shooting table to find the FRU to
replace.
6-10
GE MEDICAL SYSTEMS
REV 19
2-5
Diagnostics
This chapter describes diagnostics tools based on error codes and specific
diagnostics.
This chapter describes diagnostics tools based on error codes and specific
diagnostics.
Before any manual intervention, ensure the main power is off.

Apply lock out-tag out procedure for your own safety when
manipulating inside the equipment is required.
WARNING
2-6
Detailed Error Description & Troubleshooting

Guide
The table below provides guidelines to troubleshoot Generator problems based
on error code.
For each code, there is:
Associated message and additional explanation related to the error

occurrence.
List potential cause, in the order of expected probability.
Recommended action, with, in some cases, link to some more information

as indicated where cases apply, such as to run some specific diagnostics.
Codes are sorted by ascending order both for simplified code and error code.
Refer to the theory of operation for error code structure.
Information about associated data structure is located at the end of each error
code subset whenever it applies.
Whenever wiring, cabling, LED check is mentioned in the recommended actions,
refer to the central listing or to Illustration 1.
6-11
6-12
K1
EMC Flt.
"VCC": +5V
3ph, 380 - 480 VAC
+ 15 V
- 15 V
+
AC/DC
DS 1
F1
NE 1
+ 15V
- 15V
LVPS
Rotor
Board
DS 7
DS 3, 2, 1
+5, -15, +15
DS 2
DC bus, 160V
(120 to 200V)
DS 3
Heater Board
REV 19
CB1
PDU
+ 15 V
- 15 V
kV ctrl
-15V, +15V
DS 1, 2
+ M
DC bus, 400 ... 800 V
N1 (230 V)
I/F
PUPTor
DS7-6
DS 300
Console
Gate Command Board
INVERTER. & LLC. Circuit
DC bus, 400 ... 800 V
Neon's
AEC
DS 1
LEDs
GE MEDICAL SYSTEMS
ILLUSTRATION?1
JEDI VISUAL POWER SUPPLY DISTRIBUTION FOR SILHOUETTE VR
GE MEDICAL SYSTEMS
REV 19
2-6-1
Errors
Tube spits detection Errors (Code 30)

Class 2
Error code
Message/explanation
Potential cause
300301H
Tube spit (kV+ and kV- dropped)

kV drop/spit detected
x-ray tube spit.
300302H
Tube spit (kV+ has dropped)

1. Anode side Tube spit.
kV drop/spit detected on Anode side 2. Anode HV cable
3. HV tank
300303H
Tube spit (kV- has dropped)

1. Cathode side Tube spit.
kV drop/spit detected on cathode side 2. Cathode HV cable
3. HV tank
300304H
kV regulation error
This is a slow speed safety circuit in
case of smooth spits.
300305H
Re-starting safety. (unknown reason) 1. External unknown cause.

Error occurring on safety line, while 2. kV control board.
No root error present at the error
inputs (Err 0301 to 0304). This is
probably due to transient interference
(Spikes).
1 smooth HV tube spits

2 kV control board (HV regulation
problem)
3 too much line impedance
4 half of AC/DC capacitors open
5 Inverter (parallel inductor or filtering
capacitors)
6 HV tank
6-13
GE MEDICAL SYSTEMS
REV 19
Anode Rotation errors (Code 40)

Class 4
Error code
Message/explanation
Potential cause
400101H
No CAN message received within 5

secs
The rotation board has not received
any signal from the kV control main
software for the last 5 sec.,
interpreted as a loss of
communication
1. kV Control main software lost

2. kV control or Rotation board driver
failure
3. Bad contact on one of the pin on
the CAN bus line connector
400102H
Database not correct.

The firmware of the rotation board
has detected that the Database
received from the kV control board
has wrong data.
1. Wrong kV control Database. It can

only happen at power up.
400103H
Rotation current overload

1. Rotation board
Rotation board has detected Main or 2. Wrong Database (improbable)
auxiliary rotation current too high
compared to the max. Tube motor
current.
400104H
Rotation current openload

Rotation board detected that no
current is flowing to the motor.
400105H
Rotation phases unbalanced

1. One rotation wire missing
2. Rotation board
The amplitude difference of the
current bwtween main and auxiliary is 3. Wrong tube configuration database
too large.
400106H
Rotation phase error

1. Rotation board
The rotation board has detected that
the current in the anode stator does
not show the correct phase shift
between main and auxiliary.
1. Tube stator winding is open circuit:

x-ray tube
2. Incorrect wiring (Open)
3. No DC bus on Rotation board
4. Rotation board
6-14
GE MEDICAL SYSTEMS
REV 19
Error code
Message/explanation
Potential cause
400107H
Rotation Inverter permanent

1. Rotation board
overcurrent
2. Tube stator winding in short circuit > x-ray tube
An overcurrent has been detected
3. Wiring incorrect (shorted)
and 3 restart have been tried
unsuccessfully within a single rotation
state
400108H
Rotation command error.

No hardware failure
Rotation board has informed kV
control board that the command was
erroneous; this is a DEBUG error.
400109H
MAINS_DROP has failed

1. Interference (spikes)
The firmware of the rotation board 2. Mains drop
has detected the mains_drop signal 3. Cable or connector contact in DC
bus between power unit and
activation and transmitted error to kV
control
auxiliary unit
4. Rotation board
400110H
PRD error
Rotation board
Firmware checksum, RAM test and
EPLD access are performed at power
up or reset.
400111H
F0 main frequency problem.

EPLD has not applied the inverter
start command.
400149H
Unknown Rotation error.

Software problem
The main software received an error
from rotation board with no error code
assocxiated.
Rotation board
Associated data structure:

PRD error:
component failure:
0001H=RAM
0002H=RAM stack
0200H=EPLD
8000H=program checksum
6-15
GE MEDICAL SYSTEMS
REV 19
rotation database error :

2 bytes data, each value points to a specific parameter found as being erroneous
other errors:
rotation state:
0=inverter OFF
1=acceleration 0 to low speed
2=acceleration 0 to high speed
3=acceleration low speed to high
4=low speed run
5=high speed run
6=high speed to low speed brake
7=brake reverse
8=brake DC
6-16
GE MEDICAL SYSTEMS
REV 19
Filament Heater errors (Code 50)

Class 4
Error code
Message/explanation
Potential cause
500201H
No CAN message received within 5

secs
The Heater board has not received
any command from the kV control
main software for the last 5 sec.,
interpreted as a loss of
communication
1. kV Control main software lost

2. kV control or Heater board driver
failure
3. Bad contact on one of the pin on
the CAN bus line connector
500203H
Heater inverter permanent

1. Heater board
overcurrent. (SW limit)
Issued by the heater board when an
overcurrent has been detected and 3
restarts have been tried without
success within 100 ms
500204H
Filament permanent open circuit.

Issued by the heater board when an
open has been detected and 3
500205H
Heater Inverter permanent short

1. Heater board
circuit (HW limit)
Issued by the heater board when a
short circuit has been detected and 3
500206H
Filament current too high on inverter

1 for Pre-Heat
This is the result of an integrated
value of the RMS current
measurement on Heater board
comparison with max. Tube value in
Database.
1.
2.
3.
4.
X-ray tube filament open

Heater to HV tank cable
Cathode HV cable or pin contacts
Open circuit in filament transformer
inside HV Tank.
1. Tube Database or calibration

2. Heater board
6-17
GE MEDICAL SYSTEMS
REV 19
Error code
Message/explanation
Potential cause
500207H

1 for Boost
Same as above

2. Heater board
500208H

1 for Heat
Same as above

2. Heater board
500209H
Heater command error

No hardware failure
Heater board has informed kV control
board that the command was
erroneous; this is a DEBUG error.
500210H
Current under estimated fork/range

Heater board
RMS filament current measurement
(every 0.5 msec.) on heater board is
too high
500211H
Current under estimated fork range

1. Open circuit
RMS filament current measurement 2. Heater board
(every 0.5 msec.) on heater board is
too low
500212H
MAINS_DROP detected.
1. Interference (spikes)
The firmware of the Heater board has 2. Mains drop
3. Cable or connector contact in DC
detected the mains_drop signal
bus between AC/DC and auxiliary
activation and has transmitted error to
kV control
unit
4. Heater board
500213H
PRD error
1. Heater board
Firmware checksum, RAM test and 2. No -15V on Heater board
EPLD access are performed at power
up or reset.
500214H
Boost too long on inverter 1.

Boost command stayed longer than
400 ms
May be a loss of communication during

boost.
6-18
GE MEDICAL SYSTEMS
REV 19
Error code
Message/explanation
Potential cause
500215H
Filament selection error.

Heater board
The relay on the Heater board
selecting the filament is in the wrong
position with respect to the selection
500216H
Measured current while inverter OFF

Inverter current has been measured
while the inverter was not
commanded
500221H
0222H
0223H
0224H
Filament Database not correct

1. Wrong kV control Database. It can
only happen at power up.
The firmware of the heater board has
detected that the Received Database
from kV control contains erroneous
data for Tube 1, 2, 3, or 4.
500248H
0249H
Unknown heater error

Software problem.
The main software received an error
from heater board with no error code
associated.
Heater board
Associated data structure:

PRD error:
component failure:
0001H=RAM
0002H=RAM stack
0200H=EPLD
8000H=program checksum
Filament database error:

2 bytes bitmap (LSByte=small focus, MSByte=large focus)
Each bit points to an erroneous parameter
other errors:
1 byte bitmap with the following structure:
bit7 (MSB)
focus selected
0=small focus selected
1=large focus selected
bit6
bit5
bit4
tube selected
1=tube 1 selected
2=tube 2
3=tube 3
4=tube 4
bit3
bit2
small focus state
0=inverter OFF
1=preheat
2=boost
3=heat
6-19
bit1
bit0 (LSB)
large focus state
0=inverter OFF
1=preheat
2=boost
3=heat
GE MEDICAL SYSTEMS
REV 19
Exposure errors (Code 60)

Class 3
Error code
Message/explanation
Potential cause
600306H
No kV feedback on anode side

1. HV cable short circuit
2. HV tank
kV measured <12 kV 0,5 ms after
start of exposure on anode side only 3. kV control board (less probable)
600307H
No kV feedback on cathode side

1. HV cable short circuit
kV measured <12kV 0,5ms after start 2. HV tank
3. kV control board (less probable)
of exposure on cathode side only
600308H
No kV Feedback (on anode and

1. HV tank
2. kV control board
cathode)
kV measured <12 kV 0,5 ms after
start of exposure on both anode and
cathode.
600309H
kV detected during kV diagnostics.

KV measured during inverter
diagnostics while no kV must be
generated.
Improper setup before the diagnostic is

run.
600310H
kV MAX detected
kV reached 160 kV during exposure
kV control
600311H
ILP current not OK.

The current in the parallel resonant
circuit of the inverter did not rise at
the beginning of the exposure.
1. Inverter LC resonant circuit

(Inverter coil assy, capa inverter
assy.)
2. Inverter
3. kV control
600312H
ILR current not OK

The current in the serial resonant
circuit of the inverter did not rise at
the beginning of the exposure.
See above
600313H
Inverter max. ILR current detected.

This is a hardware detection of
maximum current in serial resonant
circuit.
1 HV tank
2 kV control
600314H
ILR Current time out.

The current resonant frequency is
lower than expected
1. kV control
2. Inverter
3. Current measurement circuit.
6-20
GE MEDICAL SYSTEMS
REV 19
Class 3
Error code
Message/explanation
Potential cause
600316H
Spit Max error.

kV control has detected the number
of tube spits during exposure has
reached the limit (see theory of
operation, software section)
reasonably x-ray tube
600318H
kV did not reach 75% after 20 ms.

Indicates that there were no HV ON
signal generated for exposure time
count-up
1. kV control
600319H
kV unbalanced detected.
HV tank
Detects that there is more than 12 kV
difference between kV+ and kV -
600320H
FPGA problem; Safety hit with

1. This may be due to transient
unknown reason
interference (Spikes).
No error at the inputs while checking 2. SW bug
for error source.
600323H
ILP and ILR current not OK

No inverter current measures at the
beginning of the exposure
600401H
No mA feedback
1. HV tank
2. kV control board
mA measurement function:
3. x-ray tube (filament open)
kV control has detected no mA
feedback 20 ms after the beginning of
the exposure.
600402H
mA scale error
1. kV control board
mA has been measured to be either 2. default filament currents not
correctly adjusted
too low or too high with respect to mA
demand 20 ms after the beginning of 3. HV Tank (improbable)
the exposure
1. Inverter LC resonant circuit.

(Inverter coil assy, capa inverter
assy, cabling)
2. Inverter
3. kV control board
601. tube spit

mA accuracy exceeded 5%
0403H
Measured mA every 50 msec
(Class 2 error)
exceeded 5% of mA demand.
This error is logged, but does not stop
the exposure.
600504H

gate supply voltage has dropped
below the level required to drive the
IGBTs properly
600801H
Exposure backup mAs exceeded

1. Esposure command line stuck to
the active state
The exposure command last so long
that the maximum mAs allowed has 2. kV control board
3. Heater board
been reached.
1. Inverter (gate command board)

2. kV control board
3. Generator input voltage too low or
line impedance too high
6-21
GE MEDICAL SYSTEMS
REV 19
Class 3
Error code
Message/explanation
Potential cause
600802H
Exposure backup time exceeded.

1. System
The exposure command last longer 2. System-Generator cable
than the duration that was loaded by 3. I/F board: exposure line stuck to the
active state
the system (Backup time + 5%.)
600803H
Exp cmd while gene not ready.

generator received an exposure
command while not in ready state
1. Software bug/problem
2. Cable / communication
problem
3. External cause (Spikes)
601406H
Time counter error.

Error found in verifying the counter
normal operation.
kV control board
601407H
mAs counter error

Error found in verifying the counter
normal operation.
kV control board
601408H
AEC counter error

If there is no AEC feedback in AEC
station exposure.
1.
2.
3.
4.
601409H
mAs meter saturated.

A check is done on mAs counter
operation at the beginning of
exposure and found the mAs meter
with unrealistic value.
1. kV control
601410H
FPGA locked.
FPGA detected an error and did not
allow start exposure after exposure
command symbol was received
1. Software problem
2 kV control
6-22
ION chamber
AEC cable, connection
AEC board
kV control
GE MEDICAL SYSTEMS
REV 19
Power supply (Code 70)

Class 4
Error code
Message/explanation
Potential cause
700501H
DC bus out if range (<400 or >850)
1. mains problem (Too low or too

high)
2. One phase missing at Generator
input
700503H

(checked at prep)
1.
2.
3.
4.
700505H
Mains power supply has dropped

During exposure
unknown
700549H
Unknown LVPS error

Software problem
The main software received an LVPS
error with no error code associated.
700553H
Detected +160 V too high

+160 V is higher than 225 V
(measured on heater board)
1. LVPS
2. Heater board
700557H
Detected +160 V too low

+160 V is lower than 110 V
1. LVPS
2. Heater board
700563H
Detected +15 V too high

+15 V is higher than 17.3 V
1. LVPS open circuit

2. Heater board
700567H
Detected +15 V too low

+15 V is lower than 13 V (measured
on heater board)

2. Heater board
3. rotation (short circuit)
kV control (short circuit) (improbable)
700573H
Detected -15 V too high

-15 V is lower than -17.3 V

2. Heater board
700577H
Detected -15 V too low

1. LVPS (open circuit)
-15 V is higher than -13 V (measured 2. Heater board
on heater board)
3. rotation (short circuit)
4. kV control (short circuit)
(improbable)
6-23
Mains
Cable pb
Gate command board (Inverter)
kV control
GE MEDICAL SYSTEMS
REV 19
Hardware errors (Code 80)

Class 4
Error code
Message/explanation
Potential cause
800180H
Rotation board communication

problem.
kV control board communication
Watch Dog with Rotation board
popped up because it did not get
reply from Rotation board.
1. Rotation board
2. Control bus cable
3. kV control
800181H
Rotation board has reset.

1. Rotation board
kV control has detected the Rotation 2. Interference (Spikes)
board has reset. KV control will
reload Rotation Database.
800280H
Heater board communication problem 1. Heater board

kV control board communication
Watch Dog with Heater board popped 3. kV control
up because it did not get reply from
Heater board.
800321H
KV conversion error
KV feedback measured while no KV
generated
KV control board
800322H
kV ref ADC / DAC failed

kV control DAC and ADC capability
are permanently tested for
coherency.
KV control board
800601H
RTL error (+ associated data to check 1. system communication power

which of the 4 RTL lines)
supply (for isolated
communications)
Real Time Lines show a wrong state.
RTLs are tested on a regular basis in 2. system communication cable
3. system interface board
stand by.
4. system interface to kV control flat
cable
5. kV control board
800602H
External CAN bus off
1. system communication power

supply (for isolated
communications)
2. system communication cable
3. system interface board
4. system interface to kV control flat
cable
5. kV control board
800902H
Tube Fan supply error.

Rotation board has detected that a
wrong voltage is applied to the tube
fan
1. No 115 V tube cooling supply

2. Rotation board
801402H
Internal CAN bus off

3. kV control
Can device on kV control board
detected abnormal level on its 2 line 3. Heater or Rotation
and sent error to the CPU
6-24
GE MEDICAL SYSTEMS
REV 19
Class 4
Error code
Message/explanation
Potential cause
801403H
Connection Fault
Multiple, but likely improbable.
One of the flat cable connector is not
connected in Generator.
801404H
FPGA configuration problem.

kV control board.
Detected during power up. The kV
control main software cannot load the
FPGA.
801405H
Tank temperature sensor problem.

kV control
Means that t value of the HV tank is HV tank
< 10C
6-25
GE MEDICAL SYSTEMS
REV 19
Application errors (Code 90)

Class 4
Error code
Message/explanation
Potential cause
900701H
NV RAM checksum pb.

Generator kV control board has
detected corruption in the NV Ram
verification (After power up)
1. Database problem
2. External cause (Spikes)
3. kV control
900702H
Software problem.
1. Software or Database problem.

2. kV control board failure.
900703H
Watchdog reset has just occurred.

1. Software or Database problem.
This error is logged when the CPU of 2. kV control board failure.
the kV control board is reset by its
Watch Dog timer.
900704H
Rotation/Heater hold too long.

Software problem.
Will pop up if preparation command
from the system is maintained longer
than 3 minutes.
6-26
GE MEDICAL SYSTEMS
REV 19
Communication errors (code 100)

Class 4
Error code
Message/explanation
Potential cause
1000603H
Debug screen com. error
Engineering use
1000604H
Database download error

Generator has detected a problem
during Database download
1. Database file incorrect

2. Transmission problem
1000605H
TAV communication error.

1. Software / laptop problem
2. Cable problem
Generator has detected a
communication problem between the
I/F and the service laptop (When
generator is controlled by the laptop)
1000606H
MPC/Madrid
Communication error.
No reply from the console.
(This error message can be seen
using the service laptop)
1. Cable, connection problem between

Generator and the console.
2. Interface board
3. kV control board
4. Cabling between kV control board
and IF board
5. Console problem
1001301H
AEC communication error

KV Control has detected a
communication problem with AEC
board.
1.
2.
3.
4.
AEC board
I/F board
kV control
Wiring
Thermal errors (code 110)

Class 5
Error code
Message/explanation
Potential cause
1100804H
Tank Thermal Error

HV tank temperature measurement
has reached 60 degree C
1. HV tank too hot; normal error

2. HV tank
3. kV control
1100903H
70 degree C thermal safety error

70 loop detected open
1.
2.
3.
4.
6-27
X-ray tube too hot; normal error

Wiring problem
Sensor problem (Tube)
rotation board
GE MEDICAL SYSTEMS
REV 19
2-7
Warning Errors
Warning errors are the result of automated and regular background monitoring
for either software events or voltages exceeding thresholds.
Those errors are merely for engineering usage and do not indicate any hardware
error failure.
However, as they are logged into the Generator Err_log file, just as the previous
list of errors, they are listed here to help error review. If many are seen when
viewing error log, we recommend reporting this with a CQA, since the equipment
is still operating.
10
20
Rotation Warning 0151H

0152H
0153H
0154H
0155H
0156H
0157H
0158H
0159H
0160H
0161H
0162H
0163H
0164H
0199H
Heater Warning
0251H
0252H
0253H
0254H
0255H
0256H
0257H
0258H
0259H
0260H
0261H
0262H
0263H
0299H

Bad index in config upload
Tube switch while rotor not off
Acceleration cmd while no tube selected
Acceleration cmd while database not OK
Database download while rotor speeding
Acceleration command not OK
Rotor acceleration while in error
Rotation Inverter overcurrent (< 3 times)
Unknown rotation warning
Received command is not OK
Heater command not OK
Heater inverter overcurrent (inverter1) (<3 times)
Filament open circuit (inverter1) (<3 times)
Heater Inverter short circuit (inverter1) (<3times)
Tube switch while filaments not OFF
Database download while heater not cut
Unknown heater warning
6-28
GE MEDICAL SYSTEMS
REV 19
25
27
2-8
Low Voltage
Power Supply
Warnings
Application
warnings
0550H
0555H
0560H
0561H
0565H
0570H
0571H
0575H
0599H

No more warn -15V too low or too high
Unknown LVPS warning
1401H
Saved RAM power supply limit reached

This message is the result of a computation that is
made by the software based on the Date for a
period of approximately 7 years
Other Failures
Error
Message /
code
explanation
System GENERATOR
does not reply to
the system
3 phases CB1
breaker trips in
PDU
Software or Data
base corrupt
Potential cause
1. No power on Generator
2. EMC filter
3. AC/DC- Diode bridge
4. Cable between AC/DC and LVPS
5. LVPS down
6. CAN cable problem
7. kV control
8. CT interface
9. Rotation board
10. Heater board
11. Inverter in short circuit
12. Generator to system cable
1. Short circuit on Generator :
IGBT in short circuit
ACDC or bridge rectifier in short circuit
EMC filter in short circuit
1. After software download:
-Incorrect or uncompleted download
-Checksum problem
6-29
GE MEDICAL SYSTEMS
REV 19
OTHER FAILURES
Error
code
Message /
explanation
Potential cause
Recommended action Troubleshooting guide
Console CONSOLE
boot up error
Console power supply is not Locate the Switch Power DSP1 on the back of
correct
PDU, then adjust VR1 to make 5V terminal out put
5.50.05V.
System GENERATOR
does not reply
to the system
1. No power on the
Generator
2. EMC filter
3. AC/DC- Diode bridge
4. Cable between AC/DC
and LVPS
5. LVPS down
6. CAN cable problem
7. kV control
8. RAD interface
9. AEC board
10. Rotation board
11. Heater board
12. Inverter in short circuit
13. Generator to system
cable
6-30
Perform the troubleshooting in the following way:

1/ kV control Leds S0-S7 are lit successively: refer
to system communication errors (code 06xx H)
2/ Leds S0-S7 show a specific pattern: refer to
PRD errors section
3/ Led RESET is lit: board is maintained in reset
either by the system or by a system I/F failure or
kV control failure
4/ Led HALT is lit: replace kV control
5/ No Led is lit: verify that +5 V on kV control
board (J6, pin 2).is present. If yes, replace kV
control. If no:
6/ Verify if +15 V/-15 V is present (Leds DS1/DS2).
If yes:
Verify that mains_drop line is not stopping the kV
control software (mains_drop active):
6_1/ Check if DS1 LED on LVPS board is lit. If yes,
replace LVPS board.
6_2/ Disconnect Heater board control bus cable.
Check if kV control software starts. If yes,
replace Heater board.
6_3/ Disconnect Rotation board control bus cable
and connect it directly to LVPS board. Check if
kV control software starts. If yes, replace
rotation board.
6_4/ If AEC existing, disconnect AEC cable (J5)
from IF board (J3) cable. Check if kV control
software starts. If yes, disconnect AEC
chambers and connect AEC board to IF board.
If kV control starts, check AEC chambers, else
replace AEC board.
6_5/ Disconnect IF board cable (J10). Check if kV
control software starts. If yes, replace IF
board, else: replace kV control board.
if no:
7/ Verify if +15 V/-15 V is present on rotation board
(DS1/DS2) and the 160 V is present on the
heater board (DS3). If yes: check the control
bus cable to the kV control board. If no error,
change the kV control board. If no:
GE MEDICAL SYSTEMS
REV 19
Error
code
Message /
explanation
Potential cause
Recommended action Troubleshooting guide
GENERATOR
does not reply
to the system
(Condt)
8/ Verify if the LVPS DC input is right. If no, check

AC/DC fuse and input line
If yes:
9/ disconnect all output cables from the LVPS
board. Verify the +15 V/-15 V/160 V output. If
right: reconnect each board successively to find
the one stucking the 15V to ground. If wrong,
replace LVPS board
3 phases CB1
breaker trips
in PDU
1/ Disconnect DC bus cables between AC/DC and

1. Short circuit on
inverter (on AC/DC side)
Generator:
- IGBT in short circuit
2/ Check if these cables are in short circuit. If yes,
- ACDC or bridge rectifier in
replace inverter
short circuit
if no,
- EMC filter in short circuit
3/ Remove ACDC board
4/ Check between outputs pins then between
inputs of ACDC board. If short circuit, replace
AC/DC FRU
if no:
5/ Check bridge rectifier, between outputs, if yes,
replace ACDC FRU (including rectifier bridge)
if no:
6/ Check bridge rectifier, between inputs, if yes,
replace ACDC FRU (including rectifier bridge)
if no:
7/ Disconnect AC line input from EMC board.
Check EMC for short circuit between phases. If
short circuit, replace EMC board.
Software or
Data base
corrupt
1. After software download: Retry download

- Incorrect or uncompleted
download
- Checksum problem
Console
display
malfunction
Console power does not

reach the specification
PDU DPS1:V1 output should be +5V. Adjust the

potentiometer if needed.
6-31
GE MEDICAL SYSTEMS
REV 19
2-9
Heating Function diagnostics
HEATING FUNCTION DIAGNOSTICS

Purpose:
The purpose of this test is to drive the heater inverter(s) on both filaments and all the tubes connected
to the Generator in order to identify a faulty heater FRU or a wrong connection between heater board,
HV Tank and tube(s).
Pre-requisites:
kV control board alive and running: S0-S7 Leds are lit successively or a combination of them blink
heater board alive and running: DS1 and DS2 Leds are lit successively
heater DC supply present: DS3 Led is lit
Test type: No manual interaction

Sequence:
Select the tube to run the test on, start the diagnostic.
The following sequence runs on the small focus and then on the large focus:
5 seconds preheat
0,4 s boost
5 s heat (focal spot max current - 1Amp)
There is 10 s stop time between each focal spot run

During the test, the heater safeties are checked the same way than in application mode.
Error codes reporting:
Refer to the troubleshooting table.
6-32
GE MEDICAL SYSTEMS
REV 19
2-10
Rotation Function diagnostics
ROTATION FUNCTION DIAGNOSTICS

Purpose:
The purpose of this test is to drive the rotation inverter(s) in high speed mode (for application
supporting high speed mode) and low speed mode on all the tubes connected to the Generator in order
to identify a faulty rotation FRU or a faulty dephasing capacitors FRU or a wrong connection between
rotation board and tube.
Pre-requisites:
rotation board alive and running: DS5 Led blinking
rotation DC supply present: DS7 neon is lit
cabling between rotation board and tube checked
Test type:
No manual interaction, no loop on
Sequence:
Select the tube to run the test on, start the diagnostic.
The following sequence runs in low speed mode and then in high speed mode (if high speed mode
allowed):
acceleration (time depends on tube type)
2 s run
brake (time depends on tube type)
There is 2 s stop time between each speed mode.

During the test, the rotation safeties are checked the same way than in application mode.
Error code
Associated data
Conclusion
0103H
0104H
0105H
0106H
Associated data points only to high

speed mode
Power-off. Check if rotation board K2 relay is short

circuiting the rotor capacitors. If yes replace the rotation
board. If no replace the rotation capacitors
0103H
0104H
0105H
0106H
Associated data points to both high

speed and low speed mode
Replace the rotation board
For the other error codes, refer to the troubleshooting table.
6-33
GE MEDICAL SYSTEMS
REV 19
2-11
Inverter in Short Circuit Function diagnostics
INVERTER IN SHORT CIRCUIT DIAGNOSTICS

Purpose:
The purpose of this test is to verify that the HV power inverter is working properly. The inverter is
commanded at a fixed frequency and is loaded with a short circuit. Verification is made that the inverter
currents are correctly set. At the same time verification is made that no High voltage is measured. This
test is performed without connecting the HV Tank to the inverter so that no Xray is generated. Anode
rotation and filament drive are not activated during this test.
Pre-requisites:
Generator input line in an acceptable range (380 V-10% to 480 V+10% for 3-phase AC input)
inverter gate_cmd board DC supply present: DS300 neon is lit
inverter dual snubber board DC supply present: DS1 neon is lit
Inverter gate command diagnostic passed without failure
Test type: Manual operation is required.

Sequence:
1.. Disconnect the HV Tank primary cables from the inverter (see HV Tank D/R job card).
Take care not to disconnect at the same time the parallel inductor cable which is tightened with the HV
Tank primary cables
Put the short circuit cable (included in the first aid kit) between the two capacitors as shown:
Check that the parallel inductor cable do not remain unscrewed.

6-34
GE MEDICAL SYSTEMS
REV 19
2.. Power on the Generator

3.. Verify that the DS1 neon on inverter dual snubbers board is lit
4.. Verify that the DS300 neon on inverter gate_cmd board is lit
5.. Start the diagnostic and verify that no error is reported on the operator console
6.. Press the exposure switch (500 ms exposure is taken)
7.. Release the exposure switch
8.. Verify error reported on the console
9.. After exiting the test, power off the Generator
10..Remove the short circuit cable, reconnect the HV Tank primary cables (see HV Tank D/R job card).
11..Verify that the parallel inductor cable is connected.
Error reporting:
error
Conclusion
DS1 neon off
Check that DC bus cables between AC/DC and inverter
DS300 neon off
Check the gate_cmd supply cable between AC/DC and gate_cmd

board
0301/0302/0303/0304/0309/
0310/0319 (H)
Check that HV Tank primary cables have been removed.

If yes, replace kV control board
0311
No Ilp current detected. See note 2
0312
No Ilr current detected. See note 3
0313
replace kV control board
0314
Ilr current resonant frequency is lower than expected. See note 4
0320
if problem persists, replace kV control board
0323
Both Ilr and Ilp currents not detected. See note 1
0501
kV control or inverter can be faulty
0503
0504
0505
Isolation fault between inverter components and ground. Check inverter

inductors. If no faulty component, kV control or inverter can be faulty
note 1: Ilp and Ilr currents not detected

1.. Check the -15 V (Led DS1) on kV control board (see central listing).
If it is not lit, refer to other failures section. Else:
2.. Power off the Generator. Wait until all neons are off
3.. Check that the currents transformers (capacitor set) to gate_cmd board cable is correctly connected.
If yes:
4.. Check that the inverter inductors are correctly connected. If yes:
5.. Check that the gate_cmd to HV Tank cable and HV Tank to kV control cables are correctly
connected.
If yes, replace the inverter
6.. Reconnect all the cables
note 2: Ilp current not detected
6-35
GE MEDICAL SYSTEMS
REV 19
2.. Check that the parallel inductor is correctly connected. If yes:
3.. Check that the parallel inductor impedance is 0 Ohms. If no: replace inverter. If yes:
4.. Check that inverter capacitors (capacitors set) are not broken. If yes, replace the capacitor set. Else:
5.. Disconnect the currents transformers to gate_cmd board cable. Check that the parallel current
transformer impedance is 0. If no: replace the capacitor set. Else:
connected. If yes:
7.. Disconnect the HV Tank to kV control cable. Check that the impedance between pin 20 and pin 21
of J2 of HV Tank is 3,3 Ohms. If no replace the inverter. If yes replace kV control board.
8.. Reconnect all the cables.
note 3: Ilr current not detected
2.. Check that the inductors are correctly connected. If yes:
3.. Disconnect the currents transformers to gate_cmd board cable. Check that the serial current
transformer impedance is 0. If no: change capacitor set. Else:
4.. Check that inverter capacitors (capacitors set) are not broken. If yes, replace the capacitor set. Else:
connected. If yes:
6.. Disconnect the HV Tank to kV control cable. Check that the impedance between pin 20 and pin 21
of J2 of HV Tank is 5 Ohms. If no replace iverter. If yes replace kV control board.
note 4: Ilr current resonant frequency is lower than expected
2.. Check that the inductors are correctly connected. If yes:
3.. Check that the inverter capacitors (capacitors set) are not broken. If yes: replace the capacitor set.
Else:
4.. Disconnect the currents transformers to gate_cmd board cable. Check that the parallel current
transformer impedance is 0. If no: change the capacitor set. Else: replace kV control board.
6-36
GE MEDICAL SYSTEMS
REV 19
2-12
AEC diagnostics
AEC DIAGNOSTICS
Purpose:
The purpose of this test is to drive the AEC function in order to identify a faulty AEC, IF or kV control
board FRU or the wrong connection between the AEC board and ion chambers.
Pre-requisites:
application mode without AEC mode is running properly
kV Control board alive and running: S0-S7 LEDs are lit successively or a combination of them blink
cabling between IF board, AEC board and ionization chambers checked.
Test type:
Automated, with the use of Service Laptop
Sequence:
Select AEC function in menu 1 on Service Laptop.
Press V to run the test.
AEC function is verified through a series of 7 tests as follows:
AEC return measurement test:
A voltage reference is switched to one input of the AEC select multiplex.

Nominal value of return voltage = 5.24 V
Test 1 is OK if: 4 V < measured value < 6 V
This test is also performed at lower frequency count up:
Test 2 is OK if:
4 V < measured value < 6 V.
Switching Gain test (x10):
A voltage reference is switched to one input of the AEC select multiplex and count up gain is applied.
Nominal value of return volatge = 4.76 V
Test 3 is OK if:
4 V < measured value < 6 V.
AEC ion chamber HV power supply test:
A portion of HV power supply is switched to one input of the AEC select multiplex:
-
No cell selected, Test 4 is OK if return voltage measurement is 0 V.
Select respectively one of the three cells, left, right, middle.
6-37
GE MEDICAL SYSTEMS
REV 19
Test 5, 6, 7 are OK if: 1 V < measured value < 3 V.

Error Code
1111111
(*)
Associated Data
Conclusion
None
Test OK
Any combination
None
Test KO = test failed; replace AEC

board
0001000
None
Communication error:
- Replace AEC board
- If same problem, apart from a DOA
board, suspect IF board then KV
Control board.
(*) except for AEC board with serial number: 2184569-X: the resulting error code must be 0001111 (test
is OK on this board the HV power supply test is not performed).
For the other error codes, refer to the troubleshooting table.
6-38
GE MEDICAL SYSTEMS
REV 19
2-13
No Load HV diagnostics
NO LOAD HV DIAGNOSTICS
Purpose:
The purpose of this test is to verify that the HV power inverter and HV tank are working properly. The
exposure is taken as in application mode except that no filament drive nor anode rotation is running.
Verification is made that the inverter currents are correctly set and that kV regulation is operating
properly. As no filament drive is applied, no XRays are generated.
This test also allow to separate Generator from HV cable or x-ray tube problem by running it with or
without the HV cables plugged on the HV tank.
Pre-requisites:
Generator input line in an acceptable range (380 V -10% to 480 V +10% for 3-phase AC input)
inverter dual snubber board DC supply present: DS1 neon is lit
Inverter gate command diagnostic passed without failure
Inverter in short circuit diagnostic passed without failure
(*) HV Receptacles must be filled with oil if HV cables are removed.

Sequence:
1.. Power on the Generator
2.. Start the diagnostic and verify:
-
error reported on the operator console
inverter gate_cmd board Leds DS101, DS102, DS201, DS202 are lit: IGBTs gate drive supply is
working properly
3.. Select kV (default = 80 kV) and exposure time (default = 1 sec.).

4.. Press the exposure switch
5.. During the exposure, verify:
-
6.. Release the exposure switch

7.. Power off the Generator
Error reporting:
See Troubleshooting Table.
6-39
GE MEDICAL SYSTEMS
REV 19
2-14
Inverter Gate Command diagnostics
INVERTER GATE COMMAND DIAGNOSTICS

Purpose:
The purpose of this test is to verify that the HV power inverter drive is working properly. The IGBTs gate
drive supply and the IGBTs gate drive is verified. At the same time verification is made that no inverter
currents nor High voltage are measured. This test is performed without DC voltage applied to the
inverter so that no Xray is generated. Anode rotation and filament drive are not activated during this test.
Pre-requisites:
generator input line in an acceptable range (380V-10% to 480V+10% for 3-phase AC input)

Sequence:
1/ Switch the system OFF. Ensure there is no voltage on AC/DC board
2/ FOR SILHOUETTE VR:
- Remove DC BUS cable going to Inverter (refer to Inverter Mid Power Assembly
Disassembly/Reassembly procedure, section - 1 ).
-
Remove the EMC cover (refer to Inverter Mid Power Assembly Disassembly/Reassembly
procedure, section 1 ).
Refer to Central Listing to GATE COMMAND BOARD and to DUAL SNUB BOARD for leds
location.
3/ Power on the Generator

4/ Verify that the DS1 neon on inverter dual snubbers board is not lit
5/ Start the diagnostic and verify:
inverter gate_cmd board Leds DS101, DS102, DS201, DS202 are lit: IGBTs gate drive supply is
working properly
6/ Press the exposure switch (10 s exposure is taken after a 10 sec. delay)
7/ During the exposure, verify:
inverter gate_cmd board Leds DS100 and DS200 are lit: IGBTs gate drive is working properly
8/ Release the exposure switch

9/ Power off the Generator
10/ Reconnect the 2 DC bus cables from the AC/DC board (see Central Listing).
6-40
GE MEDICAL SYSTEMS
REV 19
Error reporting:
Error
Conclusion
DS1 neon lit
Check that DC bus cables have been removed
DS300 neon off
Check the gate_cmd supply cable between AC/DC and gate_cmd

board
0301/0302/0303/0304/0309/
0310/0311/0312/0313/0314/
0319/0323 (H)
Check that DC bus cables have been removed.

If yes, replace kV control board
0320
if problem persists, replace Kv control board
0501
kV control or inverter fault, replace inverter first
0503
0504
one of
DS101/DS102/DS201/DS202
LEDs off while no error
reported
Replace inverter
DS100 and/or DS200 LEDs

off
Check cabling between kV control, HV Tank and gate_cmd board.

If cabling is right, kV control or inverter fault, replace inverter first
6-41
GE MEDICAL SYSTEMS
REV 19
6-42
GE MEDICAL SYSTEMS
REV 19
CHAPTER 7 - PLANNED MAINTENANCE

SECTION 1
PREVENTIVE MAINTENANCE ACTION LIST
The following table lists the required planned maintenance activities and the associated Job Card for each task.
OPERATION
FREQUENCY
JOB CARD
DESCRIPTION
GENERAL
General cleaning and
painting
As required
PM 001
Keep all surfaces clean and touch-up paint chips
Visual inspection
12 months
PM 002
Check for debris that would indicate abnormal wear
Functional checks
12 months
PM 003
Perform the tasks described in Chapter 4, Functional Checks
Control pedals and

movement inhibition
buttons
12 months
PM 004
Check condition and functioning; ensure pedals and buttons

have free play without any obstruction
SID display meter
12 months
Check that the SID display shows the real SID
Electrical cables
12 months
Check condition of cable sheathing and correct routing
Power and ground

connections
12 months
Check condition and connections
Connector panel and

cable connectors
12 months
Check condition and connections
TABLE BASE
PATIENT SUPPORT
Surface finish
12 months
PM 005
Longitudinal bearings
12 months
Check condition and lubricate with grease
Longitudinal bearing
tracks and rails
12 months
Clean and wipe with light machine oil
Transversal rods and

bearings
12 months
Check condition; clean and wipe with light machine oil and
lubricate with grease
Rubber bumper end stops 12 months

(Longitudinal &
transversal)
Check condition and clean
Check condition of stops and tightness of anchoring
CASSETTE TRAY AND CARRIAGE

Electrical connector and
cable
12 months
PM 006
Ensure connector is in good condition and making good

contact; check condition of cable sheathing
Cassette handle
assembly, push button &
hand holder
12 months
Ensure handle and push button have free play without any
obstruction
Bearings and tracks

(front and rear)
12 months
Check condition; clean and wipe with light machine oil and
lubricate with grease
Rubber bumper end stops 12 months
Check condition of stops and tightness of anchoring
Tray
12 months
Check general condition of the tray
Cassette size marker and

locking assembly
12 months
Check condition; clean and wipe with light machine oil
7-1
GE MEDICAL SYSTEMS
REV 19
OPERATION
FREQUENCY
JOB CARD
DESCRIPTION
TUBE STAND
Counterweight Cable
12 months
PM 007
Inspect and grease length of chains; replace if required
Carriage roller bearing

inspection
12 months
Clean roller bearings and tracks
Vertical lock
12 months
Clean and inspect
Check longitudinal
bearing and rail mounting
screws
12 months
If the longitudinal bearing and rail mounting screws are loose,

below steps must be performed while installation or
replacement:
1. Apply Loctite 242 (or 243) to the screws.
2. Tighten M8 screws to 24 N-m (17.7lbs-ft) with the torque
wrench; Tighten M10 screws to 48 N-m (35.4 lbs-ft) with the
torque wrench.
ACCESSORIES
Compression band
12 months
Patient hand grips
12 months
PM 008
Check condition
Check condition
GENERATOR
Check generator
functions
12 months
Replace NonVolatile RAM Every 8 Years

on the kV Control Board
PM 009
1.
2.
3.
4.
5.
PM JEDI 15-2 1.
2.
3.
Test exposure, including AEC if present

Record last error codes
Record result on counters
Check technique factors
Tighten terminals and remove dust
Upload database
Battery replacement
Download database
MMS Collimator
Mirror
6 months
Wipe off the dust with clean cloth
Cross marked plate
3 months
Wipe off the dust with antielectro-static agent
Movable parts
Once per 18000

operation cycles
Adjustment and lubrication (grease etc ) and checking

movable mechanical parts by service engineer
Check of difference of
light field and x-ray field
12 months
Upon replacement of lamp by service engineer
Check the collimator

mounting screws
12 months
Check the flange and stop plate, if mounting screws are loose,
below steps must be performed while installation or
replacement:
1. Apply Loctite 242 (or 243) to the screws
2. Tighten screws to 9.9 N-m (7.3lbs-ft) with the torque wrench
Tube
Check the tube mounting
screw
12 months
Remove tube covers, Check tube fork and tube arm, if

mounting screws are loose, below steps must be performed
while installation or replacement:
1. Apply Loctite 242 (or 243) to the screws.
2. Tighten M6 screws to 9.9 N-m (7.3lbs-ft) with the torque
wrench; Tighten M8 screws to 24 N-m (17.7lbs-ft) with the
torque wrench;
WALL STAND (Optional component)

General cleaning and
painting
As required
PM 001
Keep all surfaces clean and touch-up paint chips
7-2
GE MEDICAL SYSTEMS
REV 19
OPERATION
FREQUENCY
JOB CARD
DESCRIPTION
Visual inspection
12 months
PM 002
Check for defects that would indicate abnormal wear
Functional checks
12 months
PM 003
Perform the tasks described in Chapter 4, Functional Checks
Counterweight Cable
12 months
PM 007
Carriage roller bearing

inspection
12 months
Clean roller bearings and tracks
Vertical lock
12 months
Clean and inspect
Inspect and grease length of chains; replace if required
7-3
GE MEDICAL SYSTEMS
REV 19
SECTION 2
PREVENTIVE MAINTENANCE JOB CARDS
The following pages list the preventive maintenance Job Card detailed activities.
7-4
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
1/1
subassembly: General Cleaning and Painting

purpose: Maintenance
NF No.
version no. A
date: 05-Dec-98
Procedure
Production date
Serial No.
Personnel: 1
from
from
Time:15 min
to
to
SUPPLIES
Cleaning liquids and compounds.
Touch-up paint.
TOOLS
None.
SAFETY PRECAUTIONS
Remove power from the system before beginning work.
Check that the power is off.
prerequisites
None.
PROCEDURE
1) Remove power from the system.
2) Carefully clean all surfaces of the system. Note any paint damage as you clean the system.
3) Apply touch-up paint to any paint-damage areas.
4) Reapply power to the system.
7-5
PM 001
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
1/1
PM 002
subassembly: Visual Inspection

NF No.
version no. A
date: 05-Dec-98
Procedure
Production date
Serial No.
Personnel: 1
from
from
Time:15 min
to
to
SUPPLIES
None.
TOOLS
None.
SAFETY PRECAUTIONS
PREREQUISITES
None.
PROCEDURE
1) Remove power from the system.
2) Visually check around the moving parts of the system for any debris, wear or damage. This includes tabletop,
tube stand, XRT mount, collimator moving parts and the wall stand if present.
3) If any debris, wear or damage is observed, replace or repair the affected areas.
4) Reapply power to the system.
7-6
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
1/1
subassembly: Functional Checks

NF No.
version no. A
date: 05-Dec-98
Procedure
Production date
Serial No.
Personnel: 1
from
from
Time: 45 min
to
to
SUPPLIES
None.
TOOLS
None.
SAFETY PRECAUTIONS
No specific precautions.
PREREQUISITES
None.
PROCEDURE
Follow the functional checks specified in Chapter 4 of this Service Manual.
7-7
PM 003
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
1/2
subassembly: Table Base Maintenance

NF No.
version no. A
date: 05-Dec-98
Procedure
Production date
Serial No.
Personnel: 1
from
from
Time: 45 min
to
to
SUPPLIES
None.
TOOLS
Measuring tape.
SAFETY PRECAUTIONS
Remove power from the system before beginning work as indicated in the procedure steps .
prerequisites
None.
7-8
PM 004
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
2/2
PM 004
PROCEDURE
A) Control Pedals and Movement Inhibition Buttons

1) Confirm the control pedal unlocks the table top when depressed and locks the table top in place
when released. Adjust the locks as required if there is inappropriate table motion.
2) Confirm that each of the 4 movement inhibit buttons on the control panel release the appropriate lock
when depressed and locks the relevant motion when released. Adjust the locks as required if there is
inappropriate motion.
B) SID display meter

1) Position SID to lowest level
2) Note position indicated on SID display
3) Measure physical SID with measuring tape
4) Confirm SID display is correctand adjust SID display as needed
5) Repeat steps 2-4 with SID at highest level
C) Electrical cables
1) Remove power from system
2) Check condition of all cables including cable sheathing, connectors and overall condition;
if any cable damage is noted, replace or repair affected cable
3) Confirm that the cables are correctly routed
D) Power and ground cables

1) Check that power is removed from system
2) Check condition of all power and ground cables including cable sheathing, connections and
overall condition; if any cable damage is noted, replace or repair affected cable
E) Connector panel and cable connectors

1) Check that power is removed from system
2) Check condition of all interconnection cables including cable sheathing, connections and
overall condition; if any cable damage is noted, replace or repair affected cable
4) Reapply power when complete
7-9
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
subassembly: PATIENT SUPPORT MAINTENANCE
NF No.
1/2
version no. A
date: 05-Dec-98
Procedure
Production date
Serial No.
Personnel: 1
from
from
Time: 45 min
to
to
SUPPLIES
Grease.
Light Machine Oil.
TOOLS
None.
SAFETY PRECAUTIONS
PREREQUISITES
None.
7-10
PM 005
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
2/2
PM 005
PROCEDURE
A) Surface finish
Remove the dust from the table top and table topside rails.
B) Longitudinal bearingsRemove the dust.
C) Longitudinal bearing tracks and rails

Remove the dust from the bearing tracks and rails. Add the light machine oil on the tracks and rails.
D) Transversal rods and bearings

Remove the dust.
E) Rubber bumper end stops (longitudinal and transversal)

Verify the bumper stops have no cracks and one fixed tightly.
7-11
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
1/2
subassembly:Cassette Tray And Carriage Maintenance

NF No.
version no. A
date: 05-Dec-98
Procedure
Production date
Serial No.
Personnel: 1
from
from
Time: 45 min
to
to
SUPPLIES
Grease.
Light Machine Oil.
TOOLS
None.
SAFETY PRECAUTIONS
PREREQUISITES
None.
7-12
PM 006
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
2/2
PROCEDURE
A) Electrical connector and cable

Confirm properly connected.
B) Cassette handle assembly, push button and hand holder

Check the push button function. Check the movement with the handle functions.
C) Bearings and tracks (front and rear)

Remove the dust and add grease or light machine oil.
D) Rubber bumper and stops

Confirm the bumper and stops have no cracks and are fixed tightly.
E) Tray
Confirm the pull-in and pull-out movement is smooth.
F) Cassette size marker and locking assembly

Check the cassette size marker is firmly set and the cassette locking assembly is functional.
7-13
PM 006
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
1/2
subassembly: Tube Stand And Wall Stand Maintenance

NF No.
version no. A
date: 05-Dec-98
Procedure
Production date
Serial No.
Personnel: 1
from
from
Time: 45 min
to
to
SUPPLIES
Grease.
Light Machine Oil.
TOOLS
None.
SAFETY PRECAUTIONS
PREREQUISITES
None.
7-14
PM 007
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
2/2
PROCEDURE
A) Counterweight chain (Tube stand)

Check the chain is fixed tightly.
B) Carriage roller bearing inspection

Corresponding movement operates smoothly.
C) Vertical lock
Confirm proper function.
D) Longitudinal bearing and rail mounting screws
Check longitudinal bearing and rail mounting screws. Confirm screws no loose
7-15
PM 007
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
1/2
subassembly: ACCESSORIES MAINTENANCE

NF No.
version no. A
date: 05-Dec-98
Procedure
Production date
Serial No.
Personnel: 1
from
from
Time: 15 min
to
to
SUPPLIES
None.
TOOLS
None.
SAFETY PRECAUTIONS
PREREQUISITES
None.
7-16
PM 008
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
2/2
PROCEDURE
A) Compression band
Mount and remove the compression band on the table top.
B) Patient hand grips

Mount and remove the hand grips on the table top rails.
7-17
PM 008
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
1/6
subassembly: GENERATOR FUNCTIONAL CHECKS

NF No.
version no. A
date: 05-Dec-98
Procedure
Production date
Serial No.
Personnel: 1
from
from
Time: 60 min
to
to
SUPPLIES
Film.
Error-code recording form.
X-ray counter recording form.
TOOLS
Laptop.
SAFETY PRECAUTIONS
PREREQUISITES
None.
7-18
PM 009
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
2/6
PM 009
PROCEDURE
1.1
Test exposure
Post display initialization:
Connect the service Laptop
Run the service software
Go to calibration mode by using keys ALT and S
Go to MENU 5 with arrow keys
Press (F7) to select DSPL
Press (F1) to select Display ON
Press Q to quit the program and return to application mode
1.2
and
mA accuracy
Run the exposures in table below and check if the mA value on post display (Z key) is between the min
max value.
If not , run the same exposure 10 times with exposure time set to 12.5ms and then check again.
1.3
Focus
Parameter
mA results
(Post Display)
Small
Small
Small
Large
Large
Large
40 kV 100mA 50ms
80kV 100mA 50ms
120kV 100mA 50ms
40 kV 200mA 50ms
80kV 200mA 50ms
120kV 200mA 50ms
min and max

value
90-110
90-110
90-110
180-220
180-220
180-220
AEC functionality check (if existing)

Put 15cm of Plexiglas or a plastic bucket with 15 cm of water on the table top
Select Two point mode (mAs)
Set kV to 80 kV and mAs to 600
Run the exposure
Develop the film
Check that the density is 1 +/-10%.If not redo AEC calibration. (See Job card in chapter 3)
7-19
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
2.
3/6
PM 009
Record last error codes

Press (F3) to select LIST
Press (F5) to select the first error code
Fill the chart below with the error code number
Then use F5 key for following error code.
Refer to diagnostic section (Chapter 6) for fix if necessary.
Simplified Error Error
Generator
Error
Data associated with
Code
Code
Phase
Class
the Error Code
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
28
29
30
Refer to diagnostic section (Chapter 6) for fix error (if necessary).
Number of
occurrences
Clear the Error Log after checking. (Use CTRL and H keys, then confirm with W key).
7-20
Date and
Time
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
3.
4/6
PM 009
Record results on counters

Press (F5) to select NEXP(Number of EXPosures)
Press (F5) to select the first counter
Fill the chart below with the counter number
Then use F5 key for following counter.
Counter name
No WARM-UP
RX GSF
RXGLF
RXSCOP
ROTANOD
NEXPSF
NEXPLF
N100%SF
Data
Dont care
N100%LF
Dont care
NAMOR
KJSF
KJLF
TIME ON
N EXP G
H
H
Dont care
H
Dont care
E
E
H
Explanation
Number of skipped warm-up (N/A)
Cumulated exposure time on Small Focus
Cumulated exposure time on Large Focus
Cumulated exposure time in Fluoro (N/A)
Cumulated anode rotation time
Cumulated number of exposure on Small Focus
Cumulated number of exposure on Large Focus
Cumulated number of exposure on Small Focus at
100% (N/A)
Cumulated number of exposure on Large Focus at
100% (N/A)
Cumulated Number of spits
Cumulated dissipated power on Small Focus
Cumulated dissipated power on Large Focus
Total Generator Power On (not erasable)
Total generator number of exposure (not erasable)
7-21
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
4.
5/6
PM 009
Check technique factors

Run the Accuracy checks in Functional Check procedure in Chapter 4.
Make a copy of illustrations 3, 4, 5, and 6 and fill it with the results you get.
5.
Tighten terminals and remove dust

-
Tighten the inputs connections on generator, located near the labels on AC/DC module
(refer to illustration in disassembly / reassembly section).
Tighten the DC bus connections on generator located on the upper side of the
generator (refer to illustration in disassembly / reassembly section).
Verify if all connectors are correctly plugged in.
Remove dust by using a vacuum cleaner.
7-22
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
6/6
7-23
PM 009
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
1/2
subassembly: Replace Generator NonVolatile Parameters RAM

purpose: Replacement
NF No.
version no. B
date: 15/10/98
Procedure
Production date
Serial No.
Personnel:1
from
from
Time:45m
to
to
SUPPLIES
None.
TOOLS
5.5 nut driver or socket wrench with ratchet.
SAFETY PRECAUTIONS
PREREQUISITES
Upload the database that is stored in the RAM before starting the replacement procedure
refer to JobCard Backup & Restore Database Setup Parameters
7-24
PM JEDI 15-2
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
2/2
PM JEDI 15-2
Remove and Replace the RAM

On the kV Control board, note the direction that the RAM faces. Insert the tip of a small screw driver underneath
left side of U32 and lever gently, then grasp it between your thumb and forefinger and pull it directly away from its
support on the board.
Insert the new Nonvolatile Parameters RAM in its place. Be careful to insert it facing in the same direction.
U32
kV control Board
Refer to Central Listing section for more details.
CAUTION
This NV RAM contains a LITHIUM CARBON MonoFlouride

(LiCFx) battery, used to provide the battery backup for the
static RAM and the time keeper device.Electrical
Characteristics: 3 V - 49 mAh type BR 1225.Resend the former
component to your local GEMS representative for recycling.
Download Database
Reapply power.
Download the database (refer to Job Card Backup & Restore Database Setup Parameters).
7-25
GE MEDICAL SYSTEMS
REV 19
CHAPTER 8 - RENEWAL PARTS

SECTION 1
SILHOUETTE VR SYSTEM RENEWAL PARTS LIST
Item
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
Note:
Refer to Section 2 for information regarding JEDI Generator Renewal

Parts.
Note:
Refer to the next several pages for illustrations of the parts listed below:
GPCP Part#
2226325
050-1018
2226325-3
2226325-4
2226325-5
2226325-6
2226325-7
2226325-8
2226325-9
2226325-10
2226325-11
2226325-12
2226325-13
2226325-14
2226325-15
2226325-16
2226325-17
2226325-18
2226325-19
2226325-20
612-2202
2226325-22
2259298-111
2226325-24
2226325-25
2226325-26
2226325-27
2226325-28
2226325-29
2226325-30
2226325-31
2226325-32
2226325-33
2226325-34
2226325-35
2226325-36
2226325-37
2226679
220-0115
2275895
2226325-40
2226325-41
2212259-2
2226680
2226519
2226687
2259298-76
2252611-2
Name
Transformer
Transformer
Contactor
No Fuse Breaker
Relay
Relay
Noise filter
Spark killer
Fuse
Fuse
Fuse
Fuse
SW power supply
Bridge
Capacitor
Resistor
EM lock(1)
EM lock(2)
EM lock(3)
EM lock(4)
EM lock(5)
Cassette tray assembly
Steel string assembly
Lamp for power indicator
Switch
Micro switch
Micro switch
Push switch
Bearing
Bearing
Bearing
Bearing
Bearing
Bearing
Bearing
Linear bearing
Bearing
X-ray tube
Collimator
Knob of Collimator
Collimator lamp
Console CPU Board
Generator
X-ray tube
Console
Grid
Tube Forks
Ion chamber
Description
250VA, input:380V, output:100V,
300VA, input:380V, output:24V,
SK-50, 50A, 600V
NF-SF50, 50A, 480V
MY4, AC100V
LY2, DC12V
ZGB2202-01U
CR-30151
61NM, 2.5A/250V
61NM, 5A/250V
61NM, 8A/250V
RS414-033, 2A/500V
HKT-75-525
S25VB600
SME 100LGSN2200MB
RHA25-G1J
Cassette tray & Tube stand longitudinal travel
Tube rotation
Tube arm vertical travel
Table top longitudinal movement
Table top lateral movement
DGR-3
JS606
Z-15G1308
VS10N061-C2
PB-307A
GB278 80301
GB278 80017
GB278 80200
GB278 80201
GB278 60203
GB278 80101
GB278 80027
LB254058
NAKD 30
E7240X
MS-18SN
MS-18N-01-1
150W, AC24V
Modified MPC board
Jedi
RAD-12
Operator Console
For Table
For Table
8-1
Quantity/unit
1
1
1
1
1
1
1
1
1
1
1
2
1
1
1
1
2
1
1
4
4
1
2
1
4
1
1
1
2
1
4
4
2
2
2
2
2
1
1
1
1
1
1
1
1
1
1
1
GE MEDICAL SYSTEMS
REV 19
Item
49
50
51
52
53
54
55
56
57
58
59
60
61
62
63
64
65
66
GPCP Part#
2259298-78
2259298-79
2259298-97
2259298-81
2259298-82
2259298-83
2259298-84
2226325-23
2259298-86
2259298-91
2351400
612-2510
2384229
2382369
613-1006
2377851
5167409
5167409-1
Name
Pulling rod
Joint axle
Table side cover (pair)
Spring for foot pedal
Foot pedal
Table top bumper
Table tray bumper
Column spring
Hand switch assembly
Console key switch
Table Top
Table top frame assembly
Rotating plate assembly
VR Spanish Label Kit
Hand Shank
Switch Power Supply
AID Ion Chamber
AID Ion Chamber with 4
meters cable
MMS Collimator
MMS Collimator Lamp
Description
Pulling the rod to move the cassette tray
Connected with pulling rod
67
68
Wall
Stand
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
5129405
5136302
2259298-100
2259298-101
2259298-102
2259298-103
2259298-104
2226325-42
2259298-105
2259298-106
2259298-107
2259298-108
2259298-109
2385418
2259298-75
2252611-3
615-2103
5167409
5167409-2
Bearing
Slide block
Bearing
Limiting rubber block
Steel string assembly
Cassette tray
Cassette tray
Wall stand panel
Wall stand panel
Decorative washer
Handle
Handle Seat Assembly
Grid
Ion chamber
Nut
AID Ion Chamber
AID Ion Chamber with 24
meters cable
Used for steel string assembly

Used for side rail
Used for side rail
Cable
1
2
3
4
2259298-85
2259298-87
2259298-88
2259298-89
5
6
2259298-90
2259298-98
5166493
5166654
9
10
610-2021
610-2022
HV cable
PDU-Table cable
Console Power Cable
Console Communication
Cable
Rotation Cable
Chest stand grounding
Cable
4m Interconnecting cable for For Table
AID Chamber
24m Interconnecting cable
For Wall Stand
for AID Chamber
Table cable assembly 1
Table cable assembly 2
For Table
Quantity/unit
1
1
1 pair
1
1
4
2
2
1
1
1
1
1
1
1
1
1
1
1
1
Single side load

Double side load
Single side load
Double side load
Used for panel
For Wall Stand

For Wall Stand
For Wall Stand
For Wall Stand
8-2
2
4
8
2
2
1
1
1
1
4
2
1
1
1
2
1
1
2
1
1
1
1
1
1
1
1
1
GE MEDICAL SYSTEMS
REV 19
ILLUSTRATION 1
PDU (FRONT) ILLUSTRATED PARTS
8-3
GE MEDICAL SYSTEMS
REV 19
ILLUSTRATION 2
PDU (REAR) ILLUSTRATED PARTS
Item #52
Item #53
8-4
GE MEDICAL SYSTEMS
REV 19
ILLUSTRATION 3
SYSTEM ILLUSTRATED PARTS
Item #58
Item #57
Item# 41
Item# 24
Item# 25
Item #43
Item #42
Item #39
Item# 40
Item# 38
Item #44
8-5
GE MEDICAL SYSTEMS
REV 19
ILLUSTRATION 4
CASSETTE TRAY ASSEMBLY ILLUSTRATED PARTS
Item # 63
8-6
GE MEDICAL SYSTEMS
REV 19
ILLUSTRATION 5
TABLE ASSEMBLY ILLUSTRATED PARTS
Item #50
Item #54
Item #32
Item #35
Item #60
Item #49
Item #55
Item #66
Item #51
TBD
Item #21
Item
TBD #20
Item #36
Item #48
Item #46
8-7
Item #59
GE MEDICAL SYSTEMS
REV 19
ILLUSTRATION 6
TUBE ARM ILLUSTRATED PARTS
Item #47
Item #18
Item #56
Item #61
Item #62
8-8
GE MEDICAL SYSTEMS
REV 19
ILLUSTRATION 7
WALL STAND PARTS
Item #3
Item #1
Item #2
Item #15
Item #10
Item #12
Item #8,9
Item #11
Item #13
Item #6,7
Item #5
Item #7
Item #6
Item #4
Item #17
8-9
GE MEDICAL SYSTEMS
REV 19
Replace Collimator Lamp

WARNING
ONLY THE LAMP OFFERED BY GEHL OR SPECIFIED IN THE MANUAL CAN BE USED
AS REPLACED PART. OTHERWISE IT MAY CAUSE ISSUE OF LIGHT ILLUMINANCE,
EDGE CONTRAST OR LIGHT/X-RAY FIELD ALIGNMENT.
1. Removing the defective lamp

Remove the collimator rear cover (refer to Figure 1)
Unplug the connector of the lamp
Tape Scale
Lamp
Angle Plate
Rear Cover
Inside
Rear Cover
Outside
Figure 1 Collimator Lamp Exchange Cover
Screw
Figure 2 Collimator Lamp Exchange
8-10
GE MEDICAL SYSTEMS
REV 19
WARNING
IF THE LAMP OF THE LIGHT LOCALIZER REMAINS ILLUMINATED FOR A LONGER
PERIOD OF TIME, THE CLOSING MAY HEAT UP. PLEASE AVOID TOUCHING THE
LAMP HOLDER UNTIL IT COOLS DOWN. MUST WEAR CLEAN GLOVE AND AVOID
ANY STAIN ON THE LAMP BULB AND BE CAUTIOUS SO AS NOT BREAK BULB TO
HURT HAND OR EYES.
2. Mount new lamp

Insert new lamp to the position (to make the bulb conductor contact with the lamp socket.
Verify if there is misalignment . Usually, the lamp and mirror doesnt need adjusting. So if
misalignment occur, loosen the two screws (part 1 of Figure 3)to adjust lamp socket slightly
to compensate the misalignment in transverse direction, adjust the mirror(part 2 of Figure 3)
angle to compensate the misalignment in longitude direction (refer to Figure 3) by loosening
the screw(part 1 of Figure 3) after removing the center cross window.
WARNING
WHEN ADJUST THE MIRROR ANGLE, NEVER CONTACT IT DIRECTLY BY HAND TO

AVOID LEAVING ANY STAIN ON THE MIRROR. THIS SHALL BE DONE BY QUALIFIED
FIELD ENGINEER WITH CLEAN GLOVE. OTHERWISE, IT WOULD LEAD TO THE
DETERIORATING FOR PERFORMANCE OF MIRROR.
Screw
Mirror
Figure 3 Mirror Angle Adjustment
8-11
GE MEDICAL SYSTEMS
REV 19
SECTION 2
JEDI GENERATOR RENEWAL PARTS
2-1
Introduction
This Section provides information for the identification of Renewal Parts for the
JEDI 50 R 1T generator.
2-2
JEDI Generator Renewal Parts List
GPCP Part Number
Name
Description
Quantity/
Unit
2216578
PWB
Heater Board JEDI Program V2.02
2214605-3
PWB
Rotation Board JEDI Program V3.02
2212166
Transformer
LVPS 3PH V3
2215814
Inverter
Mid Power Inverter Assy
2214606-2
PWB
Programmed kV Control Board P 3.2
2214995
PS Assy
AC/DC 3PH Board Assy
2209840
Filter
EMC Filter
2217057
Spare
First Aid Spare
2214527
HV Transformer
HV Tank (ref: 2186730 FRU order is 2214527)
2184567-4
PWB
RAD I/F Board
2184569-2
PWB
AEC Board
8-12
GE MEDICAL SYSTEMS
REV 19
2-3
FRU Information
Information shown for each FRU (Field Replaceable Unit) is explained below.
Wherever possible, the FRU or its position is illustrated for easy identification.
FRU name
Part number for
Inverter PW Assembly2187001
FRU: 1
Job Card D/Rxxx
Inverter Capa Assembly

2203900
FRU: 2
Job Card D/Rxxx
FRU Codes:
1 Critical (Spare available in stock)
2 Not Critical (Not in stock, but may be
ordered)
FRU: Not Available (Not a field replaceable unit)
Repairable
Notes: The quantity is 1 if not specified. The FRU
is not repairable if not specified.
FRU:
FRU:
Notes. These may include:

Reference to an illustration with more information
Reference to a relevant Disassembly/Reassembly Job
Card Items included with the FRU etc.
Items shown in this way are included in

immediately above, but may also be
8-13
GE MEDICAL SYSTEMS
REV 19
2-4
Jedi 50 R 1T Structure
JEDI 50 R 1T
2212259-2
JEDI STD HV Tank

2214527
Power Unit HLB

2214447-2
Module Auxiliaries 50 R 1T
2215808
System cable
2214511
Module Power 50 R 1T
2229597
CAN Cable
2221983
Equipped AC/DC 50 R 1T
2221722
Service Tools
2228546
Interface Module 50 R 1T
2205629-2
First Aid Spares
2217057
AEC Board (option)

2204112-2
AEC I/F Cable

2202419
8-14
GE MEDICAL SYSTEMS
REV 19
2-5
Renewal Parts
ILLUSTRATION 7
JEDI 50 R 1T GENERATOR LOCATION OF MAIN ASSEMBLIES
Miscellaneous Items:
First aid spares:
Services tools
1 short circuit cable

1 fuse 15 A 700 VDC
2207478
1 fuse 10 A 250 V
10 M48 mm screws,
10 tiewraps
2217057
FRU: 1
Service software, No. 2227656

9-wire service cable, No.
2228546
FRU: 2
8-15
GE MEDICAL SYSTEMS
REV 19
ILLUSTRATION 8
JEDI 50 R 1T AC/DC UNIT, INTERFACE UNIT & AUXILIARY UNIT
AC/DC 3 Phase Mid Power

Assy (Board & Rectifier
+ 2 cables)
2214995
FRU: 1
Job Card D/R JEDI 17-30
EMC Filter Board

2209840
FRU: 1
AC/DC Unit
AEC Board V1
2184569-2
AEC Board V22222253
FRU: 1
RAD I/F Board V1

2184567-4
RAD I/F Board V2
2226456FRU: 1
Interface Unit
Rotor Board High Speed

2214605-3
FRU: 1
LV Power Supply 3 Ph Board

2212166
FRU: 1

2214604
FRU: 1
Auxiliary Unit
8-16
GE MEDICAL SYSTEMS
REV 19
ILLUSTRATION 9
JEDI 50 R 1T POWER UNIT
Inverter Coils Mid Power Assy

2200700
FRU: 2
Capa Inverter Assy

2229505
FRU: 2
A
Non-Volatile parameters
RAM
2159419
FRU: 2
Job Card PM JEDI 15-2
Programmed kV Control
Board
2214606-2
FRU: 1
Inverter Mid Power Assy

2215814FRU: 1
A
Jedi Standard HV Tank
2214527
FRU: 1
8-17
GE MEDICAL SYSTEMS
REV 19
2-6
Cables
DC_BUS N to INVERTER
DC_BUS P to INVERTER
DC_BUS to Auxiliary
Unit (Rotation Board)
88
J1
Not Used
9pts
AEC Board
J4
Not Used
Not Used
Room Door
Interface
9
pts
J7
9
pts
J5
9
pts
J6
9
pts
J8
25
pts
J9
DC_BUS+
DC_BUS-
PH3 PH2 PH1

16
pts J5
J3
DC_BUS to
Power Unit
(Gate Command
Board)
J1 J2 J3
DC_BUS M
PH1
PH2
W22
Service
Laptop
Console
J2&TP2 J1&TP1
PH3
9pts 9pts
EMC Board
AC/DC Board
I/F Board
64
pts
J10
J3
16
pts
1
1
2
2
AC/DC Unit
33
AEC1
9
pts
AEC2
9
pts
Interface Unit
THREE PHASES
+ Ground from PDU
From
KV Control
board
Keyed
Connections
1
1
I/F RAD - AEC cable (option)
55
2202419
FRU: 2
22
Assy AEC cable
2198185
FRU: 2
6
6
2208000
FRU: 2
33
KV control - I/F RAD cable
CAN cable
KV Measure - KV Control cable

2198191
FRU: 2
77
2202418
FRU: 2
44
KV Measure - Gate Command cable
ROT / LVPS / Heater cable

2215903
FRU: 2
8
8
System cable
2221983
2214511
FRU: 2
FRU: 2
8-18
GE MEDICAL SYSTEMS
REV 19
88
DC_BUS N
70 o C
DC_BUS P
DC_BUS to ACDC Unit J1
DC_BUS to ACDC Unit J3
to Tube
Rotor
to Tube
NP
anode
cathode
11
J2
26
pts J1
grey
HV Tank
red
J1
J3
- + L0S
F F
1 -+ ACP
J3
J1A
J2A
CF-N CF-P
KV Measure
Board
J1
34
pts
26pts
J2
J2
J3
J2
CAN
CAN
55
J1
CF1 CF2
26 pts
7
7
66
J1
KV Control
Board
LVPS
Board
CF3 CF4
50pts
to IF Board
26pts
J4
Gate
Command1
34
Board
pts
3
3
Rotation Board
High Speed
ILr ILp
blue
6 5 4 3
Power Unit
Inverter
grey
44
50pts
26pts
CF1 CF2
J2
J3
1
26
pts
Auxiliary Unit
64
pts
Keyed
Connections
1
1
I/F RAD - AEC cable (option)
55
2202419
FRU: 2
22
Assy AEC cable
2198185
FRU: 2
6
6
2208000
FRU: 2
33
KV control - I/F RAD cable
CAN cable
KV Measure - KV Control cable

2198191
FRU: 2
77
2202418
FRU: 2
44
KV Measure - Gate Command cable
ROT / LVPS / Heater cable

2215903
FRU: 2
8
8
System cable
2221983
2214511
FRU: 2
FRU: 2
8-19
GE MEDICAL SYSTEMS
REV 19
SECTION 3
JEDI GENERATOR DISASSEMBLY/REASSEMBLY
3-1
Introduction
This section provides information to dismount and remount FRU (Field
Replaceable Unit).
3-2
Tools
Serviceability of Jedi Generator requires the following tools:
Digital Multimeter
(A)
Phillips Screwdriver
(B)
Allen Key
(C)
Screwdriver With Interchangeable Socket Head
(D)
Long Extension for Ratchet Wrench
(E)
Short Extension for Ratchet Wrench
(F)
Cutting Pliers
(G)
High Voltage Wrench
(H)
Ratchet Wrench
(I)
Socket Wrench
(J)
Hexagonal Head Socket Set
(K)
8-20
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
subassembly: HV Tank, 1 Tube, 1-3 Phase
purpose: Replacement Procedure
NF
No.
1/6
D/R JEDI 17-3
Production date
Serial No.
version no. 0
date: 11/23/98
Personnel:1
from
from
Time:1h 30m
to
to
SUPPLIES
None
TOOLS

3 mm Allen wrench.
13 mm socket with ratchet.
Cclamp for HV connections.
SAFETY PRECAUTIONS
DANGER
BEFORE ANY MANUAL INTERVENTION, ENSURE THE MAIN

POWER IS OFF. APPLY LOCK OUT - TAG OUT PROCEDURE
FOR YOUR OWN SAFETY WHEN MANIPULATING INSIDE THE
EQUIPMENT IS REQUIRED.
PREREQUISITES
Upload the database that is stored in the RAM before starting the replacement procedure (refer to
JobCard Backup & Restore Database Setup Parameters).
WARNING
THE WHOLE GENERATOR WEIGHS 63 KILOGRAMS (139

POUNDS). TWO PEOPLE ARE REQUIRED TO CARRY IT.
8-21
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
2/6
D/R JEDI 17-3
DISASSEMBLY
1. To release the Power Unit, follow the instructions of Disassembly / Reassembly procedure of
Inverter Mid Power Assembly.
Observe the Caution relating to dangerous voltages, and the Warning relating to the weight of
the generator!
NOTICE
Do not remove the two EMC panels from the top of the Power
Unit.
2. Disconnect the cable 1 connected to J3 on the KV

Measure Board.
3. Disconnect the short ribbon cable 2 connecting J2 on the
Gate Command board (Inverter Assembly) to J1 on the KV
Measure Board (HV Tank).
4. Disconnect the wider short ribbon cable 3 connecting J2
on the KV Control Board to J2 on the KV Measure board
(HV Tank).
5. Using a 13 mm socket wrench, remove the three

nuts 4 attaching the primary coil flat cables to the
round capacitors located on the shelf just above
the KV Control Board.
6. Remove the two screws 5 on the HV Tank rear
side.
NOTICE
Take great care not to let screws

fall into the HV connector receptacles.
Cover them with plastic caps.
8-22
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
3/6
D/R JEDI 17-3
7. Remove the 5.5 mm screws: three at the front side 6 (two at right,
one at left) and three at the right side 7 .
8. At the rear side, remove the eight 3 mm Allen screws 8 which
secure the heat sink of the Inverter Mid Power Assembly to the HV
Tank.
9. Take off the assembly constitued by five parts: EMC covers, Coils
Inverter Assy, Capa Inverter Assy, Mid Power Assy and KV
Control Board. The HV Tank is now free 9 .
8-23
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
4/6
D/R JEDI 17-3
REASSEMBLY
Reverse the disassembly procedure to reassemble and replace the unit.

1. Mount the flat cable J1 on the kV Measure Board of the new HV Tank (refer to (refer to
Disassembly section 2 ).
2. Reassemble the HV Tank with the other elements of the Power Unit (refer to Disassembly section
9 ).
3. Mount the eight 3 mm Allen screws to secure the heat sink of the Inverter Mid Power Assembly to
the HV Tank. (refer to section Disassembly 8 ).
Tighten to torque 8 N.m (80 kg.cm).
4. Put back the 3 front 5.5 mm hex head screws (refer to section Disassembly 6 ), one at the left side,
two at the right side.
Tighten them between 1.5 to 2 N.m (15 to 20 kg.cm).
5. Reconnect the short ribbon cable from J1 on the KV Measure board to J2 on the Gate Command
board (refer to section Disassembly 2 ).
6. Using the 13 mm socket wrench, connect the primary coil flat cables to the three capacitors 1 ).
CAUTION
The two flat cables with white bands on them go both

together on the middle capacitor with the parallel resonant
cable (refer to section Reassembly 2 ).
8-24
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
5/6
DR JEDI 17-3
7. Reconnect the cable to J3 on the KV Measure Board (refer to section Disassembly 1 ).

Tighten the nuts to 8 N.m (80 kg.cm).
8. Reconnect the wider short ribbon cable from J2 on the kV Control board to J2 on the kV Measure
Board (refer to section Disassembly 3 ).
9. Mount the two 5.5 hex head screws securing the cover to the HV Tank on the HV outlet side (refer
to section Disassembly 5 ) and the three screws on the other side (refer to section Disassembly 7 ).
8-25
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
6/6
D/R JEDI 17-3
Tighten the screws between 1.5 to 2 N.m (15 to 20 kg.cm).

10. Mount the Power Unit on the support plate.
THE POWER UNIT WEIGHTS 30 KG (66 POUNDS).
WARNING
11. Refer to Disassembly / Reassembly procedure of Inverter Mid Power Assembly to complete
reassembly of the Unit.
12. Put 5 cl of oil into the HV receptacles. Reconnect the HV cables.
VERIFY
Connect the service laptop (refer to Service Software User Guide JOB CARD) and proceed to HV no
load diagnostics to ensure correct operation.
Skip steps Gate Command and Inverter in Short Circuit diagnostics.
8-26
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
subassembly: Inverter Mid-Power Assembly
NF
No.
1/10
D/R JEDI 17-24
Production date
Serial No.
version no. 0
date: 11/23/98
Personnel:1
from
from
Time:2h
to
to
SUPPLIES
None.
TOOLS

3 mm Allen wrench.
13 mm socket wrench with ratchet.
Cclamp for HV connections.
SAFETY PRECAUTIONS
DANGER
CAUTION

LOOK THROUGH THE FRONT OF THE POWER UNIT;

OBSERVE LEDS DS 1 AT THE TOP OF THE DUAL SNUB
BOARD AND DS 300 AT THE RIGHT HAND END OF THE
GATE COMMAND BOARD. IF EITHER IS LIT, WAIT UNTIL
BOTH ARE OFF BEFORE PROCEEDING FURTHER. THESE
LEDS INDICATE THE PRESENCE OF DANGEROUS VOLTAGE
ON THE POWER SUPPLY CAPACITORS.
PREREQUISITES
THE WHOLE GENERATOR WEIGHTS 63 KILOGRAMS (139
WARNING
8-27
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
2/10
D/R JEDI 17-24
DISASSEMBLY
JEDI 50 R 1T Generator general view
FRONT VIEW
1 AC/DC UNIT
2 POWER UNIT
3 INTERFACE UNIT
4 AUXILIARY UNIT
5 SUPPORT PLATE
REAR view
TABLE BUCKY
WALL BUCKY
DOOR
LAP TOP
CONSOLE
AEC2
AEC1
8-28
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
3/10
1. Disconnect the connectors J2 and J3 and the ground

cable on the top of the generator 1 .
2. Remove four 5.5 mm hex head securing screws
holding the Auxiliary Unit on the support plate 2 .
3. Disconnect the flat ribbon cable 3 , without tearing,
between the Auxiliary Unit and the Interface Unit.
4. Remove the Auxiliary Unit.
Remove the Interface Unit
1. The Interface Unit appears after removing the

Auxiliary Unit. Release the flat ribbon cable 1 ,
making it sliding along the cover panel 2 of the
Interface Unit.
2. Unscrew twelve 5.5 mm screws that retain the
cover panel and remove this one 2 .
3. On the I/F Rad Board, disconnect the flat wide
ribbon cable J10 3 linked to the KV Control Board.
WARNING
THE POWER UNIT WEIGHTS

30 KILOGRAMS (66 POUNDS).
DO NOT TRY TO LIFT IT
WITHOUT ASSISTANCE.
8-29
D/R JEDI 17-24
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
4/10
4. Unscrew twelve 5.5 mm screws securing the

Interface Unit box to the Power box.
5. Taking care of the flat wide ribbon cable 3 ,
remove the Interface Unit box. The components of
the Power Unit appear: coils assembly, capacitors
assembly, KV Control Board.
Remove the AC/DC Unit and the support plate
1. On the top of the generator, the two connectors 1 are fixed

mecanically on the support plate. Unscrew connectors
screws in order to release the 4 power cables 2 coming
from the Power Unit and the AC/DC Unit.
2. Remove the screw securing the ground cable 3 on the
AC/DC Unit. Disconnect the cable linking the AC/DC Unit
and the Power Unit 4 .
3. Remove the four screws 5 on the support plate in order to
release the Power Unit. This one is then free.
8-30
D/R JEDI 17-24
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
5/10
Remove the Inverter Mid Power Assembly
1. Remove the 5.5 mm hex head screws which

secure the two EMC cover panels 1 at each side
of the Power Unit; remove the panels.
2. With a 10 mm socket wrench with ratchet 2 ,

remove the three hex head screws securing the
cables Q100C, Q100E and Q200C 3 on the
8-31
D/R JEDI 17-24
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
6/10
D/R JEDI 17-24
3. Disconnect flat ribbon cables from J1 and J3 on the Gate

Command Board 4 and disconnnect J4 at the right hand side of
the board.
4
4. With 10 mm wrench, disconnect the parallel Coil connection from

the Current Transformer pass through 5 and with 13 mm wrench
the other connection from the Capacitor Assembly 6 .
5. Remove the eight 3 mm Allen screws 7 which secure the Inverter

Mid Power Assembly to the HV Tank.
6. Remove the Inverter Mid Power Assembly 8 .
8-32
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
7/10
D/R JEDI 17-24
REASSEMBLY
1. Present the new Inverter assembly. Put back the eight 3 mm Allen screws to secure the Inverter Mid
Power assembly to the HV Tank (refer to section Remove the Inverter Mid Power Assembly 7 ).
Tighten them firmly to torque 2 N.m (20 kg.cm).
2. Remount all cables that were removed:
1. Remount the three Coil cables on the Inverter IGBTs with three 5.5 mm screws.
Tighten them firmly to torque 3 N.m (30 kg.cm).
WARNING
RESPECT THE ORIENTATION OF THE CABLES TO THE

IGBTS CONNECTIONS TO AVOID CABLE CONTACT WITH
TOP COVER.
2. Reconnect the short flat cable between the HV Tank and the Gate Command board (J3), and
the inverter current feedback cable (J1) on the Gate Command board (refer to section Remove
the Inverter Mid Power Assembly 4 ).
8-33
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
8/10
D/R JEDI 17-24
3. Reconnect the DC bus cable to J4 to the right hand side of the Gate Command board.
Top J4
4. With the 10 mm screw and flat and lock washer, reconnect the shorter cable of the parallel coil
on the Inverter assembly onto the right hand side current transformer (Ti1/100) pass throug A .
Tighten to 3 N.m (30 kg.cm) torque.
5. With the 13 mm screw, with flat and lock washer, reconnect the longer cable of the coil on the
central capacitor (C3UF) of the Capacitor assembly, together with the two primary HV
Transformer flat wires (the two with a white ring) B .
Tighten to 8 N.m (80 kg.cm) torque.
3. Perform an overall inspection before proceeding. Use the following illustration to check the
connections are right.
8-34
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
9/10
D/R JEDI 17-24
4. Remount the two EMC panels on the top of Power Unit with the 5.5 hex head screws.
Tighten all the cover screws to torque between 1.5 to 2 N.m (15 to 20 kg.cm)
5. Assemble the Power Unit with the AC/DC Unit on the support plate with 5.5 mm hex head screws.
Put back in place the disconnected cables: ground, DC bus (refer to section Remove the Inverter
Mid Power Assembly ).
6. Remount the Interface Unit on the support plate then the Auxiliary Unit. Follow the inverse
procedure indicated in the sections and .
7. Remount the generator inside the table.
8-35
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
10/10
D/R JEDI 17-24
VERIFY
Run HV LOAD DIAGNOSTIC Inverter in Short Circuit Diagnostics and Inverter Gate Command
Diagnostic are not pre-requested.
Verify correct operation on the whole application range.
8-36
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
1/2
subassembly: I/F Board RAD

NF
No.
D/R JEDI 17-25
Production date
Serial No.
version no. 0
date: 11/23/98
Personnel:1
from
from
Time:15m
to
to
SUPPLIES
None.
TOOLS
SAFETY PRECAUTIONS
DANGER

PREREQUISITES
WARNING

8-37
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
2/2
D/R JEDI 17-25
DISASSEMBLY
The I/F Board Rad is situed in the Interface Unit. To reach this Unit, the Auxiliary Unit has to be
released from the generator. Follow the instructions of Disassembly / Reassembly procedure of
Inverter Mid Power Assembly (refer to sections and to ).
Remove the I/F Board Rad
1. Disconnect the flat ribbon cable 1 and the two cables 2 , if

existing, coming from the AEC Board (option).
2. Disconnect the flat wide ribbon cable J10 coming from the KV
Control Board 3 .
3. Remove the four screws of connectors J8 and J9 4 .
4. Remove the ten 5.5 mm screws 5 securing the Interface

Board Rad; remove the board.
3
REASSEMBLY
1. Reverse the disassembly procedure to reassemble the unit. Tighten screws to torque between 1.5
and 2 N.m (15 to 20 kg.cm).
2. Power the system on and verify that the system functions properly.
8-38
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
1/4
subassembly: KV Board RAD

NF
No.
D/R JEDI 17-26
Production date
Serial No.
version no. 0
date: 11/23/98
Personnel:1
from
from
Time:45m
to
to
SUPPLIES
None.
TOOLS

10 mm Allen wrench.
SAFETY PRECAUTIONS

DANGER
PREREQUISITES
Remove the generator from the table and put it on its botttom side on the floor or
on a work bench.
WARNING

The KV Control board contains a saved memory Database with essentially the following parameters:
Tube configuration parameters, AEC calibration parameters, and Room configuration

(workstation, AEC, screen film pairs).
Filament aging variable

Error Log
Recorded parameter data
If it is possible, backup database first. Else, the diagram hereafter helps you to determine the action to
take for your situation.
8-39
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
2/4
D/R JEDI 17-26
First
Configura*
tion
Calibration
Upload
Database
Yes
Save Non
Volatile RAM
Database
KV Control
Out of Order
DB
Upload
Possible?
Is
original DB
saved?
(*)
No
No
Yes
SW
OK?
Replace
KV Control
Replace
KV Control
Replace
KV Control
No
Download
Software
Yes
Yes
Download
Database
SW
OK?
Yes
No
No
Download
Software
Download
Software
Download
Original
Database
(*)
Configura*
tion if
applicable
Calibrate if
applicable
Reset
Database:
* Date
* Time
* Clear Error
log
Operational
Checks
Save Non
Volatile RAM
Database
(*) or most recent
END
8-40
SW
OK?
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
3/4
D/R JEDI 17-26
DISASSEMBLY
NOTICE
The KV Control board spare is pre-loaded with NP/NP+

software.
It will be required to download the software that is on site.
DATABASE RESTORE IS MANDATORY.
Remove the Auxiliary Unit as described in Inverter Mid Power Assembly Disassembly/Reassembly
procedure.
Remove the Interface Unit
Remove the Interface Unit as described in Inverter Mid Power Assembly Disassembly/Reassembly
procedure.
Remove the kV Control Board
1. Disconnect the cables from J1, J2 and J3 on the kV

Control Board 1 .
2. Remove the seven 5.5 mm hex head screws which
secure the kV Control Board; remove the board 2 .
REASSEMBLY
Reverse the disassembly procedure to reinstall the KV Control board and the Interface Unit.
Tighten 5.5 mm screws to torque between 1.5 and 2 N.m (15 to 20 kg.cm).
8-41
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
4/4
D/R JEDI 17-26
VERIFY
1. Connect the Service Laptop (refer to Service Software User Guide JOB CARD)
2. Reapply power and verify that the 8 LEDs on KV Control board are scrolling.
3. Verify software version (service floppy, menu 5)
If it corresponds to the software version on the floppy delivered with the equipment (or upgraded
by FMI), proceed to Database Restore (refer to Backup & Restore Database Setup Parameters
Calibration JobCard).
If not, download the software and proceed to Software Download / Upgrade JobCard.
4. Restore Database (refer to Backup & Restore Database Setup Parameters Calibration JobCard)
Up-to-date database if available

Most recent or originally saved Data Base if available
Default one from the floppy delivered with the equipment in the Service Tool set.
Alternately, you may try to swap the NVRAM chip (U32) from the former to the new KV Control board
to keep all the parameters. Refer to Replace Non Volatile Parameters RAM JobCard. If this chip is not
involved in the failure or the cause for replacement, it will allow to keep up-to-date data.
5. Calibrate:
Perform several exposures on both focus in several workstation, with exposure time longer than
12.5 ms
If default database was restored, it is necessary to resume room set up (refer to Workstation
parameter Calibration JobCard) and AEC calibration (if present) (refer to Automated AEC Calibration
JobCard). Then perform the checksum (refer to Checksum Validation JobCard).
6. Save Database on the service floppy delivered with the equipment (refer to Backup & Restore
Database Setup Parameters JobCard).
8-42
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
1/4
subassembly: EMC Board 3 Phases

NF
No.
D/R JEDI 17-29
Production date
Serial No.
version no. 0
date: 11/23/98
Personnel:1
from
from
Time:45m
to
to
SUPPLIES
None.
TOOLS
SAFETY PRECAUTIONS
DANGER

PREREQUISITES
WARNING

8-43
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
2/4
DISASSEMBLY
Remove the AC/DC Unit
1. On the top of the generator, disconnect the

connectors J1 and J2 1 .
2. On the support plate, unscrew connectors screws
in order to release the 2 power cables coming
from the AC/DC Unit 2 .
3. Disconnect the ground cable 3 .
4. Remove the four 5.5 mm screws securing the
AC/DC Unit to the support plate 4 . The AC/DC
Unit is now free 5 .
Remove the EMC Board
1. Remove ten 5.5 mm hex head screws which

retain the cover. Remove that one.
2. Remove the three nuts 1 securing the phase
cables and three screws 2 retaining the EMC
board to the rectifier block.
3. Unscrew nine 5.5 mm hex head screws 3 and
remove the EMC Board 4 .
8-44
D/R JEDI 17-29
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
3/4
D/R JEDI 17-29
REASSEMBLY
Reverse the disassembly procedure to reinstall the EMC board.

Tighten 5.5 mm screws to torque between 1.5 and 2 N.m (15 to 20 kg.cm).
CAUTION
Ensure that U1 screw is tighten to the torque between 1.5 and

2 N.m (15 to 20 kg.cm). Refer to section d
Disassembly 5 .
Remount the generator inside the table.
VERIFY
Reapply power and verify the presence of 3 phases.

Verify that the system functions correctly.
8-45
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
4/4
8-46
D/R JEDI 17-29
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
1/4
subassembly: AC/DC 3 PH Mid Power Assembly

NF
No.
D/R JEDI 17-230
Production date
Serial No.
version no. 0
date: 11/23/98
Personnel:1
from
from
Time:45m
to
to
SUPPLIES
None.
TOOLS
5.5 mm socket, with ratchet if possible (to remove cover and board)
10 mm socket with ratchet (to remove DC and rectifier cables)
Large Philips screw driver (to remove cables from the rectifier block).
SAFETY PRECAUTIONS
DANGER

1. Insure that the neon (orange) indicator light on the board has gone out.
2. Be careful touching components on this board; some become very hot.
3. To protect the circuit boards, do not forget to wear the antistatic bracelet.
PREREQUISITES
WARNING

8-47
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
2/4
D/R JEDI 17-230
DISASSEMBLY
Note:
The AC/DC 3 Phases Mid Power Assembly is made up of two main elements: AC/DC Board 3
Phases and Rectifier Block 3 Phases.
Remove the AC/DC Unit
1. On the top of the generator, disconnect the

connectors J1 and J2 1 .
2. On the support plate, unscrew connectors screws
in order to release the 2 power cables coming
from the AC/DC Unit 2 .
3. Disconnect the ground cable 3 .
4. Remove the four 5.5 mm screws securing the
AC/DC Unit to the support plate 4 . The AC/DC
Unit is now free 5 .
Remove the AC/DC Board
1. Remove fourteen 5.5 mm hex head screws which

retain the cover. Remove that one.
2. Remove the two DC cables fastened with 10 mm
nuts on the board
3. Remove two screws retaining the AC/DC

board to the rectifier block
4. Remove seven 5.5 mm hex head screws 3 and

lift out the AC/DC Board 4 .
8-48
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D/R JEDI 17-230
Remove the Rectifier Block
1. The Rectifier Block 1 appears after removing the EMC

Board (refer to EMC Board 3 Phases
Disassembly/Reassembly Job Card ) and the AC/DC
Board
2. With the Allen key 3 mm, unscrew the 2 screws 2 holding
the rectifier to the chassis and remove the block.
REASSEMBLY
1. Reverse the disassembly procedure to reinstall the AC/DC 3 PH Mid Power Assembly and the EMC
Board.
2. Tighten the 10 mm cable retaining nuts to 3 N.m (30 kg.cm), and the 5.5 mm hex head screws to
1.5 to 2 N.m (15 to 20 kg.cm).
Ensure cable terminals are repositioned as noticed before
CAUTION
CAUTION
Verify that the + and - DC Bus cables are not reversed to prevent
1
damage to the Inverter (Refer to section Disassembly ).
CAUTION
The Rectifier Block has to be placed with the two poles in regard of
1
the AC/DC Board (Refer to section Disassembly ).
CAUTION
Be careful to preserve the special grease that is spread between the

Rectifier Block and the chassis. This grease, called: Conductive
Surface Compound, provides both thermal and electrical
conductivity that is important in reducing failure of the rectifier.
3. Remount the generator inside the table.

VERIFY
Reapply power and verify that the system functions correctly.
8-49
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SILHOUETTE VR
4/4
8-50
DR JEDI 17-230
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
1/6
subassembly: Inverter Coil Mid Power Assembly

NF
No.
D/R JEDI 17-31
Production date
Serial No.
version no. 0
date: 11/23/98
Personnel:1
from
from
Time:2h
to
to
SUPPLIES
None.
TOOLS

3 mm Allen wrench.
SAFETY PRECAUTIONS
DANGER

PREREQUISITES
WARNING

8-51
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
2/6
D/R JEDI 17-31
DISASSEMBLY
DANGER
RESPECT THE CAUTION RELATING TO DANGEROUS

VOLTAGE.
Remove the Auxiliary Unit and the Interface Unit
Remove these Units as described in Disassembly / Reassembly procedure for Inverter Mid Power
Assembly.
Remove the AC/DC Unit and the support plate as described in Disassembly / Reassembly procedure
for Inverter Mid Power Assembly.
WARNING
THE POWER UNIT IS NOW FREE BUT IT WEIGHTS 30

KILOGRAMS (66 POUNDS). DO NOT TRY TO LIFT IT
WITHOUT ASSISTANCE.
Remove the Inverter Coil Mid Power Assembly
1. On the Power Unit, remove the 5.5 mm hex head

screws 1 which secure the L-shaped EMC cover
panel 2 ; remove this one.
2. With a 10 mm socket wrench with ratchet 3 ,
remove the three hex head screws 4 securing
the cables Q100C, Q100E and Q200C on the
8-52
GE MEDICAL SYSTEMS
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SILHOUETTE VR
3/6
D/R JEDI 17-31
3. Remove the 10 mm screw 5 on the left current transformer Ti1/40 pass through, top of the
Capacitor assembly. Retain the washers and release the cable.
4. Disconnect the two cables linking coils to capacitors at right and left 6 . Use a socket wrench to
remove screws.
5. On each side 7 , remove one 5.5 mm screw holding the coils support.
6. Remove the Inverter Coil assembly 8 .
8-53
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
4/6
D/R JEDI 17-31
REASSEMBLY
1. Present the new Inverter Coil assembly and mount one 5.5 mm hex head screw on each side of the
frame to hold the Coil assembly (refer to section Remove the Inverter Coil Mid Power Assembly 7 ).
Tighten to torque between 1.5 to 2 N.m (15 to 20 kg.cm)
2. Remount all cables that were removed:
1. Remount the three Coil cables on the Inverter Mid Power Assembly (IGBTS) with three screws
1 . There is a locking washer between the screws and the cable.
Tighten firmly to torque 3 N.m (30 kg.cm).
WARNING
RESPECT THE ORIENTATION OF THE CABLES TO THE

IGBTS CONNECTIONS TO AVOID CABLE CONTACT WITH
TOP COVER.
2. With the 10 mm screw, with flat and lock

washer, remount the remaining cable from the
right coil (of the Coil assembly) onto the upper
left current transformer Ti1/40 pass through 2
(refer to section Disassembly 5 ).
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GE MEDICAL SYSTEMS
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SILHOUETTE VR
5/6
D/R JEDI 17-31
Tighten firmly to torque 3 N.m (30 kg.cm).

3. Using a socket wrench, connect the two
cables linking coils to capacitors at right and
left (refer to section Disassembly 6 ).
Tighten to torque between 1.5 to 2 N.m (15 to 20 kg.cm).
3. Refer to Disassembly / Reassembly procedure for Inverter Mid Power Assembly.
VERIFY
It is recommended to perform the No load HV diagnostics test. INVERTER GATE and INVERTER
in Short Circuit diagnostics are not pre-requested.
Verify correct operation on the whole application range.
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GE MEDICAL SYSTEMS
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SILHOUETTE VR
6/6
8-56
D/R JEDI 17-31
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
1/6
subassembly: Capacitor Inverter Assembly

NF
No.
D/R JEDI 17-32
Production date
Serial No.
version no. 0
date: 11/23/98
Personnel:1
from
from
Time:3h
to
to
SUPPLIES
None.
TOOLS

10 mm allen wrench.
SAFETY PRECAUTIONS
DANGER

ENSURE THERE IS NO VOLTAGE ON THE DC BUS CABLE
WARNING
PREREQUISITES
WARNING

8-57
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
2/6
D/R JEDI 17-32
DISASSEMBLY
DANGER
RESPECT THE CAUTION RELATING TO DANGEROUS

VOLTAGE.
Remove the Auxiliary Unit and the Interface Unit
Remove these Units as described in Disassembly / Reassembly procedure for Inverter Mid Power
Assembly .
Remove the AC/DC Unit and the support plate together as described in Disassembly / Reassembly
procedure for Inverter Mid Power Assembly.
WARNING
THE POWER UNIT IS NOW FREE BUT IT WEIGHTS 30 KILOGRAMS

(66 POUNDS). DO NOT TRY TO LIFT IT WITHOUT ASSISTANCE.
Remove the Capacitor Inverter Assembly
1. On the Power Unit, remove the 5.5 mm hex head

screws 1 which secure the L-shaped EMC cover
panel 2 ; remove this one.
2. Remove the cable from connector J1 3 on the
Gate Command Board.
8-58
GE MEDICAL SYSTEMS
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SILHOUETTE VR
3/6
D/R JEDI 17-32
3. Disconnect the Filament cable J3 4 from the HV Tank.
4. Remove the 10 mm 5 and 13 mm screws 6 on the top side , and the 13 mm screws 7 on the
lower side of the Capacitor assembly. Release the cables.
5. Remove the four left and right 5.5 mm screws 8 holding the Capacitor assembly.
6. Remove the Capacitor Inverter Assembly 9 .
8-59
GE MEDICAL SYSTEMS
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SILHOUETTE VR
4/6
D/R JEDI 17-32
REASSEMBLY
1. Present the new capacitor assembly.

2. Mount two 5.5 mm hex head screws to hold the Capacitor assembly (refer to section Disassembly
8 ).
3. Reconnect the cable J1 on the Gate Command Board (refer to section Disassembly 3 )
4. Attach the shorter cable (parallel coil) on the upper right current transformer (Ti1/100) pass
through with a 10 mm screw 1 and its washers (refer to section Disassembly 5 ). Tighten to torque
3 N.m (30 kg.cm).
5. Remount the DC+ cable and the corresponding serial coil cable together on the upper left side
of the capacitor assembly with a 13 mm screw and its washers (refer to section Disassembly 6 ).
Tighten to torque 8 N.m (80 kg.cm).
6. Remount the DC- cable and the corresponding serial coil cable together on the upper right
side of the capacitor assembly with a 13 mm screw and its washers (refer to section Disassembly
6 ). Tighten to torque 8 N.m (80 kg.cm).
7. Remount the remaining serial coil cable to the upper left current transformer (Ti1/40) pass
through with a 10 mm screw 1 and its washers (refer to section Disassembly 5 ). Tighten to torque
3 N.m (30 kg.cm).
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GE MEDICAL SYSTEMS
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SILHOUETTE VR
5/6
DR JEDI 17-32
8. Run the INVERTER IN SHORT CIRCUIT diagnostic:
WARNING
Note:
HV TANK PRIMARY CABLES ARE DISCONNECTED AND

ISOLATED.
Connect the short circuit cable (included in the first aid kit) between the left capacitor
and the central capacitor (see picture in Inverter In Short Circuit diagnostics).
1. Tighten one extremity of the short circuit on the left capacitor with a 13 mm screw and its
washers. Tighten to torque 8 N.m (80 kg.cm),
2. Mount the longer wire (Parallel Coil) and the other extremity of the short circuit on the central
capacitor (C3UF) with a 13 mm screw and its washers. Tighten to torque 8 N.m (80 kg.cm),
Use the illustration below to check the connections are right:
3. Reassemble the Power Unit with AC/DC Unit, Interface Unit and Auxiliary Unit (refer to Inverter
Mid Power Assembly Disassembly/Reassembly Job Card).
4. RUN INVERTER SHORT CIRCUIT DIAGNOSTICS.
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DR JEDI 17-32
9. After INVERTER SHORT CIRCUIT diagnostics, disassemble the Auxiliary Unit and the Interface
Unit (see section Disassembly). Remove the short circuit cable.
10. On the central capacitor (C3UF), attach together the two flat wires of the primary coils of the HV
transformer that have a white ring 2 and the longer wire of Parallel Coil with a 13 mm screw and
its washers. Tighten to torque 8 N.m (80 kg.cm)
11. Mount the two remaining flat cables 3 from the HV Tank with 13 mm screws and their washers
underneath the capacitor assembly, one on the left side, one on the right side.
12. Reconnect the Filament cable J3 on the HV Tank (refer to section Disassembly 4 ).
13. Mount the two last remaining 5.5 mm hex head screws on the left and right side of the frame (refer
to section Disassembly 4 ).
Tighten to torque 1.5 to 2 N.m (15 to 20 kg.cm)
14. Reassemble the Power Unit. Mount it with the AC/DC Unit, the Interface Unit and the Auxiliary Unit
on the support plate (Refer to Disassembly / Reassembly procedure for Inverter Mid Power
Assembly).
VERIFY
It is recommended to perform the No load HV diagnostics test. Verify correct operation on the whole
application range.
8-62
GE MEDICAL SYSTEMS
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SILHOUETTE VR
1/4
subassembly: LV Power Supply 3 Phase Board

NF
No.
DR JEDI 17-33
Production date
Serial No.
version no. 0
date: 11/23/98
Personnel:1
from
from
Time:15m
to
to
SUPPLIES
None.
TOOLS
5.5 mm hex nut driver or socket wrench with ratchet.
SAFETY PRECAUTIONS
DANGER

1. Insure that the Neon N1 (orange) indicator light on the LVPS Board has gone out.
2. Be careful touching components on the LVPS Board. Some become very hot.
PREREQUISITES
WARNING

8-63
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2/4
DISASSEMBLY
1. Disconnect the connectors J2 and J3 and the ground cable on the

top of the generator 1 .
2. Remove four 5.5 mm hex head securing screws 2 holding the
3. Disconnect the flat ribbon cable 3 , without tearing, between the
Remove the LV Power Supply Board
1. The Auxiliary Unit being free, unscrew ten 5.5 hex

head screws and remove its cover.
2. Disconnect the 3 cables
Power Supply 3 Phases board
3
4
from the LV
.
3. Unscrew the six 5.5 mm hex head screws and

remove the LV Power Supply 3 Phase Board
8-64
DR JEDI 17-33
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
3/4
DR JEDI 17-33
REASSEMBLY
Reverse the disassembly procedures to reinstall the LV Power Supply 3 Phases Board.
CAUTION
Verify that the following cables are not reversed before power
ON (refer to section Remove the LV Power Supply Board:
1. Cables CF2 (+DC BUS) and CF1 (- DC BUS)

2. Cables CF4 (160 V) and CF3 (0 V)
Tighten the 5.5 mm hex head screws to 1.5 to 2 N.m (15 to 20 kg.cm).
Remount the cover. Tighten the 5.5 mm hex head screws to 1.5 to 2 N.m (15 to 20 kg.cm).
Remount the auxiliary unit on the generator support plate.
VERIFY
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SILHOUETTE VR
4/4
8-66
DR JEDI 17-33
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
1/4
subassembly: Filament Board 1 INV

NF
No.
D/R JEDI 17-34
Production date
Serial No.
version no. 0
date: 11/23/98
Personnel:1
from
from
Time:15m
to
to
SUPPLIES
None.
TOOLS
SAFETY PRECAUTIONS
DANGER

1. Insure that the Neon DS3 (green) indicator light on the Filament Board has gone out.
2. Be careful touching components on the Filament Board . Some become very hot.
PREREQUISITES
WARNING

8-67
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2/4
DISASSEMBLY
1. Disconnect the connectors J2 and J3 and the ground cable on the

top of the generator 1 .
Remove the Filament Board

2. Disconnect the ribbon cable

Filament Board
Disconnect
between the
and the LVPS Board

3
and the connector J2
3. Unscrew the six 5.5 mm hex head screws and

remove the Filament Board 1 INV
8-68
D/R JEDI 17-34
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
3/4
D/R JEDI 17-34
REASSEMBLY
Reverse the disassembly procedures to reinstall the Filament Board 1 INV.

2
CAUTION
Verify that cables CF4 (160 V) and CF3 (0 V)

are not
reversed before power ON (refer to section Remove the
Filament Board).
VERIFY

Run Heater Function Diagnostics.
8-69
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
4/4
8-70
D/R JEDI 17-34
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
1/4
subassembly: Rotor Board High Speed

NF
No.
D/R JEDI 17-35
Production date
Serial No.
version no. 0
date: 11/23/98
Personnel:1
from
from
Time:15m
to
to
SUPPLIES
None.
TOOLS
SAFETY PRECAUTIONS
DANGER

1. Insure that the Neon DS7 (orange) indicator light on the Rotor Board has gone out.
2. Be careful touching components on the Rotor Board. Some become very hot.
PREREQUISITES
WARNING

8-71
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SILHOUETTE VR
2/4
D/R JEDI 17-35
DISASSEMBLY
1. Disconnect the connectors J2 and J3 and the

ground cable on the top of the generator 1 .
2. Remove four 5.5 mm hex head securing screws
2 holding the Auxiliary Unit 4 on the support
plate 5 .
3. Disconnect the flat ribbon cable 3 , without tearing,
between the Auxiliary Unit 4 and the Interface
Unit 6 .
Remove the Rotor Board

2. Disconnect the ribbon cable
Board High Speed
between the Rotor
and the LVPS Board
Disconnect cables CF1 and CF2
3. Unscrew two 5.5 mm hex head screws that are in

3
holes
below the surface of the board and that
secure an IGBT.
4. Unscrew the eight 5.5 mm hex head screws and
remove the Rotor Board High Speed
CAUTION
Be careful to preserve the special grease that is spread

between the IGBT and a heat sink under the Rotation Board.
This grease, called Conductive Surface Compound,
provides both thermal and electrical conductivity that are
important in reducing failure of the IGBT.
8-72
GE MEDICAL SYSTEMS
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3/4
D/R JEDI 17-35
REASSEMBLY
Reverse the disassembly procedure to reinstall the Rotor Board High Speed.
CAUTION
Ensure that cables are correctly connected. Ensure that

marks on the cables match the marks on the board.
VERIFY

Run Heater Function Diagnostics.
8-73
GE MEDICAL SYSTEMS
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SILHOUETTE VR
4/4
8-74
D/R JEDI 17-35
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
1/3
subassembly: AEC Board (Option)

NF
No.
D/R JEDI 17-36
Production date
Serial No.
version no. 0
date: 11/23/98
Personnel:1
from
from
Time:10m
to
to
SUPPLIES
None.
TOOLS
SAFETY PRECAUTIONS
DANGER

PREREQUISITES
WARNING

8-75
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
2/3
D/R JEDI 17-36
DISASSEMBLY

1
1. Disconnect the connectors J2 and J3 and the ground cable on

the top of the generator 1 .
2


4. Remove the Auxiliary Unit 4 .

4
Remove the AEC Board
1. After removing the Auxiliary Unit, the Interface Unit

appears. Release the flat ribbon cable 1 , making it
sliding along the cover panel 2 of the Interface Unit .
2. Unscrew twelve 5.5 mm screws that retain the cover

panel and remove this one 2 .
8-76
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3/3
D/R JEDI 17-36
3. Disconnect the flat ribbon cable from J5 3 between the I/F Board RAD 7 and the AEC Board 8 .
4. Disconnect the connectors J2 4 and J1 5 , and Test Points TP1 and TP2 6 on the AEC Board.
5. Remove the six 5.5 mm screws securing the AEC Board 8 .
REASSEMBLY
Reverse the disassembly procedure to reassemble the unit. Tighten screws to torque between 1.5 and
2 N.m (15 to 20 kg.cm).
VERIFY
Reapply power.
Proceed to AEC diagnostics to ensure correct operation.
8-77
GE MEDICAL SYSTEMS
REV 19
8-78
GE MEDICAL SYSTEMS
REV 19
CHAPTER 9 - SERVICE TOOL JOB CARDS

SILHOUETTE VR
subassembly: Software Download/Upgrade
purpose:
NF
No.
1/4
version no. 0
Production
date
from /
/
Serial No.
date: 11/23/98
Personnel:1
from
Time:15m
to
to
SUPPLIES
None.
TOOLS
-
SW JEDI 7-2

-
JEDI Service Software
9-wire Service cable
SAFETY PRECAUTIONS
Not applicable.
PREREQUISITES
Database backup must have been performed.
9-1
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
2/4
SW JEDI 7-2
PROCEDURE
Load Software File on Service Laptop
The service software can operate under DOS, Windows 95 or Windows 3.1.
If you do not have it on the laptop, refer to Service Software User Guide
JobCard.
Power ON service laptop

Under Windows, run the File Manager (Explore)
Create a specific directory (e.g. : JEDISVC) under C:\
Insert into the floppy drive the floppy delivered with the equipment in the service tool set (or with the
upgrade)
Copy the all files from the floppy disk to that directory
(Double click on A:\, drag and drop on C:\ JEDISVC or whatever name of your
directory)
Unzip software file

The floppy drive supplied with the equipment (or the upgrade kit) contains Autozipped files.
It is necessary to load those files on the hard disk drive and run them; they will
unzip and create other files that you will use.
Double click on the JEDP424B.exe file, and verify that the new file is created.
Software download
1.. Connect Service terminal as follows:
Use the 9-wire service cable, to connect serial line of service terminal to
connector XJ8 on the I/F board.
2.. Restart the computer in DOS mode (for software download or database backup, it is required to run
ASIAN.exe under DOS to avoid communication problem).

With the mouse, click on START, SHUTDOWN, RESTART COMPUTER UNDER
DOS MODE.
3.. Run the program:
Under DOS:
-select Disk drive from where you want to run the program:
C: enter
-key in : ASIAN enter
9-2
GE MEDICAL SYSTEMS
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3/4
SW JEDI 7-2
4.. From the laptop software main screen, type F7: restore memory.
5.. Type appl.mx, then enter (or C:\JEDI\appl.mx)
Wait for the count to start. It may take 20 seconds before starting. The software
code transfer will take about 20 minutes. Download is complete when all the
LEDs on kV Control board are ON and laptop indicates download is complete.
Normally, the kV Control board will reset at the end of transfer and all the LEDs
will scroll.
If not, reset the kV Control board.
9-3
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4/4
SW JEDI 7-2
6.. Verify the software version is P3.2, behind RAM text (or P3.X in case of new software)
From the main screen, type F1, then ALT S and go to menu 5.
7.. Select menu 2 with the arrows, select LIST, and clear generator error log. (^H, then W)
8.. To exit program, press Q, or R to return then ESC, or ESC twice.
9-4
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
subassembly: Tube Replacement Software Procedure
purpose:
NF
No.
Production
date
from /
/
to
/
/
Serial No.
from
to
1/6
version no. 0
date: 11/23/98
Personnel:1
Time:15m
SUPPLIES
None.
TOOLS
-
SW JEDI 7-3

- JEDI Service Software
- 9-wire service cable
SAFETY PRECAUTIONS
Not applicable.
PREREQUISITES
Knowledge of Service Software (refer to Service Software User Guide Job Card).
9-5
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
2/6
SW JEDI 7-3
PROCEDURE
Perform a Database backup
Refer to JobCard Backup & Restore Database Setup Parameters.
1.. Connect Service terminal as follows:
Use the 9 pin Service cable, to connect serial line of Service terminal to connector XJ8 on the
I/F board.
2.. Restart the computer in DOS mode (for software download or database backup, it is required to run
ASIAN.exe under DOS to avoid communication problem).
With the mouse, click on START, SHUTDOWN, RESTART COMPUTER UNDER DOS MODE.
3.. Run the program:
select Disk Drive from where you want to run the program: C: enter
key in : ASIAN enter
4.. Save memory
From the laptop software main screen, type F6: save memory.
9-6
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
3/6
SW JEDI 7-3
Reset Tube Data tracking counter and error log.

1.. Type ALT-S to jump to Service Menu.
2.. Select menu 2 with the arrows.
3.. Type F5 to select NEXP
Note:
Before resetting all the memory, it is advised to record them on table Generator Counter
Reading Record, found at the end of this Job Card.
9-7
GE MEDICAL SYSTEMS
REV 19
SILHOUETTE VR
4/6
SW JEDI 7-3
4.. Enter ^H, press W to confirm.

All the tube related Data will be erased; only Generator related Data will be kept.
The filament ageing parameter will be reset to default value.
5.. Type Q to go back to main screen.

Verify new tube operation, clear error log
1.. Press F1 to jump to application screen.
2.. Run a dozen of exposures from low kv, mA, to high kV, mA in direct workstation.
3.. Verify correct operation of the system.
4.. Go in menu 2, LIST (F3); Clear the Error log.
5.. Exit from laptop service software.
6.. Run exposures from the Operating console.
7.. Take necessary steps to ship the replaced tube. Include filled out table with tube information.
9-8
GE MEDICAL SYSTEMS
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SW JEDI 7-3
Generator Counter Reading Record
Date of reading:
Address of
installation:
GENERATOR COUNTER READING RECORD

Date of putting into service:
Generator identification:
Serial number:
Software version:
Options: (AEC)
X-Ray system
description:
Counter name
NO WARMUP
RXGSF
RXGLF
RXSCOP
ROTANOD
NEXPSF
NEXPLF
N100%SF
N100%LF
NAMOR
KJSF
KJLF
TIME_ON
N_EXP_G
Tube data
H
H
H
H
.
.
E
E
H
H
Explanation
Number of skipped Warm-up (N/A on Tiger)
Cumulated exposure time on small focus
Cumulated exposure time on large focus
Cumulated exposure time in fluoro (N/A on RAD.)
Cumulated Anode rotation time
Cumulated Number of exposure on small focus
Cumulated Number of exposure on large focus
Cumulated Number of exposure on small focus at 100 % Power
(N/A on Tiger)
Cumulated Number of exposure on large focus (N/A on Tiger)
Cumulated Number of spits
Cumulated dissipated power on Small focus
Cumulated dissipated power on Large focus
Total generator Power On time (Not erasable)
Total generator number of exposure (Not erasable)
9-9
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6/6
9-10
SW JEDI 7-3
GE MEDICAL SYSTEMS
REV 19
CHAPTER 10 - SCHEMATICS
SECTION 1
SILHOUETTE VR MIS MAP
Factory
installed
220-0111
220-0110
J7
J8
Laptop
Service
1
2
4
Door
interlock
switch
220VAC
110VAC
24VAC
6
610-2024
Room Warning
Light
220-0112
Tube stand
220-0358
46-832751G7
220-0114
Table
Base
Control
box
220-0115
10-1
GE MEDICAL SYSTEMS
REV 19
10-2
GE MEDICAL SYSTEMS
REV 19
1-1
Jedi 50 R 1T Cabling
ILLUSTRATION 1
JEDI 50 R 1T CABLING (1/2)
10-3
GE MEDICAL SYSTEMS
REV 19
10-4
GE MEDICAL SYSTEMS
REV 19
ILLUSTRATION 2
JEDI 50 R 1T CABLING (2/2)
10-5
GE MEDICAL SYSTEMS
REV 19
10-6
GE MEDICAL SYSTEMS
REV 19
SECTION 2
CENTRAL LISTINGS
2-1
kv Measure Board
CAUTION
This board forms part of the oil seal of the High Voltage Tank. It can
only be removed at the factory. The Field Replaceable Unit (FRU) is
the complete HV Tank.
ILLUSTRATION 3
KV MEASURE BOARD
10-7
GE MEDICAL SYSTEMS
REV 19
10-8
GE MEDICAL SYSTEMS
REV 19
2-2
HIGH VOLTAGE: DO NOT GO INTO GENERATOR UNTIL INDICATOR
DS3 GOES OUT.
DANGER
ILLUSTRATION 4
FILAMENT BOARD 1 INV.
DC
160v
LF Common
SF
DS3 - Green - +160v

DC present
160v
DS4 - Yellow - Inverter

Output Running
DC
0
SF_LF - Yellow - Small

Focus / Large Focus
Relay Feedback
ON - Yellow - Inverter
Command ON
RST - Red - Board being

reset or powered up
DS2 - Yellow - Status

LED
DS1 - Yellow - Status

LED
10-9
GE MEDICAL SYSTEMS
REV 19
10-10
GE MEDICAL SYSTEMS
REV 19
2-3
Rotation Board High Speed
DS6
AND DS7 (NEON-ORANGE) GO OUT.
DANGER
ILLUSTRATION 5
ROTATION BOARD HIGH SPEED
Auxiliary
DC bus
DS6
DC bus
10-11
Common
Main
GE MEDICAL SYSTEMS
REV 19
2-3-1
Indicators
INDICATOR
2-3-2
COLOR
INDICATES:
RESET
RED
BOARD BEING RESET OR POWERED UP
INV_ON
YELLOW
THE INVERTER IS RUNNING
DS1
GREEN
PRESENCE OF +15 V SUPPLY
DS2
GREEN
PRESENCE OF -15 V SUPPLY

PRESENCE OF +5 V SUPPLY
DS3
GREEN
DS4-DS5
YELLOW
BOARD STATUS
DS6
NEON
(ORANGE)
FAN VAC POWER SUPPLY PRESENT
DS7
NEON
(ORANGE)
DC BUS PRESENT
J2 Wiring
10
11
12
13
14
15
16
115V
sense
Fan, 115V AC
Line input
Fan*, 115V AC
Line output
X-ray tube
Thermal safety
* used in application with fan cooling
10-12
GE MEDICAL SYSTEMS
REV 19
2-4
LV Power Supply 3 PH Board
DANGER
HIGH VOLTAGE AND HOT SURFACE: DO NOT TOUCH

BOARD UNTIL INDICATOR NE1 (NEON - ORANGE)
GOES OUT.
ILLUSTRATION 6
LV POWER SUPPLY 3 PH BOARD
NE1 - Orange - indicates presence of DC Bus
+ 400
DC bus
- 400
160V
DC
0
DS2 - Green - 160 VDC
DS1 - Red - Mains

Drop
10-13
GE MEDICAL SYSTEMS
REV 19
10-14
GE MEDICAL SYSTEMS
REV 19
2-5
Gate Command Board
HIGH VOLTAGE: DO NOT TOUCH BOARD UNTIL DS300 ON THIS
BOARD AND DS1 ON DUAL SNUB BOARD ARE OUT.
DANGER
CAUTION
Hot surface on transformer T300 and heat sink.
ILLUSTRATION 7
GATE COMMAND BOARD
DS300
DC bus
DS300 - Neon (Orange) Presence of voltage on DC

bus for Flyback Converter to
create power supplies for
both Gate Commands
DS200 - Yellow - High

IGBT* (Q200) Gate
Command running
DS200
DS201 - Green - Presence

of +20 V Supply on high
IGBT* Gate Command
DS201 DS202
DS202 - Green - Pres

ence of -10 V Supply on
high IGBT* Gate Command
Inverter
ILP
current
feedback
ILR
DS100 -Yellow-Low IGBT*

(Q100) Gate Command run ning
DS100
DS102
DS101 - Green - Presence of

+20 V Supply on low IGBT*
Gate Command
DS102 - Green - Presence

of -10 V Supply on low
IGBT* Gate Command
DS101
* Insulated Gate
Bipolar Transistor
10-15
GE MEDICAL SYSTEMS
REV 19
10-16
GE MEDICAL SYSTEMS
REV 19
2-6
Dual Snub Board
DANGER

DS1 (NEON - ORANGE) GOES OUT.
ILLUSTRATION 8
DUAL SNUB BOARD
DS1 - Neon (Orange) - Indicates presence of voltage on DC Bus
10-17
GE MEDICAL SYSTEMS
REV 19
10-18
GE MEDICAL SYSTEMS
REV 19
2-7
kV Control Board
ILLUSTRATION 9
KV CONTROL BOARD
10-19
GE MEDICAL SYSTEMS
REV 19
2-7-1
2-7-2
2-7-3
Switches and Jumpers
SWITCH OR
JUMPER
FUNCTION
RST
RESET PUSH BUTTON
Indicators
INDICATOR
COLOR
INDICATES:
CONF
RED
FIELD PROGRAMMABLE GATE ARRAY (FPGA)

CONFIGURATION NOT ACCOMPLISHED
OK
YELLOW
INVERTER GATE POWER SUPPLY OK
TX_TAV
YELLOW
TRANSMIT TO SERVICE LAPTOP
RX_TAV
YELLOW
RECEIVE FROM SERVICE LAPTOP
TX_CONS
YELLOW
TRANSMIT TO CONSOLE (IF EXISTING)
RX_CONS
YELLOW
RECEIVE FROM CONSOLE (IF EXISTING)
T_CAN_X
YELLOW
SYSTEM CAN BUS TRANSMIT
R_CAN_X
YELLOW
SYSTEM CAN BUS RECEIVE
HALT
RED
MICROPROCESSOR HALTED
RESET
RED
BOARD BEING RESET
S0 TO S7
YELLOW
STATUS LED
IN APPLICATION MODE THESE LEDS FLASH IN
SEQUENCE CONTINUOUSLY
DS1
GREEN
-15V SUPPLY
DS2
GREEN
+15V SUPPLY
Non Volatile RAM

REFERENCE
DESIGNATION
U32
NON VOLATILE PARAMETERS RAM (BATTERY INCLUDED)
10-20
GE MEDICAL SYSTEMS
REV 19
2-8
AC/DC 3 Phase board
DANGER
HIGH VOLTAGE: DO NOT GO INTO GENERATOR UNTIL DS1 (NEON

- ORANGE) GOES OUT.
Some components on this board can become very hot.
CAUTION
ILLUSTRATION 10
AC/DC 3 PHASE BOARD
10-21
GE MEDICAL SYSTEMS
REV 19
10-22
GE MEDICAL SYSTEMS
REV 19
2-9
I/F Board RAD V1
ILLUSTRATION 11
I/F BOARD RAD V1
N1 - Orange (neon) Indicates presence of 100

VAC for the
ON & VAC
Pin 9
Table Bucky
Pin 1
Pin 9
Wall Bucky
Pin 1
Pin 9
Room Door & Light
Pin 1
Service Laptop
TUBE
Presence of strap
Console
PUPT - Yellow Data being sent to the console
Serial Link Configuration

(RS422)
10-23
GE MEDICAL SYSTEMS
REV 19
10-24
GE MEDICAL SYSTEMS
REV 19
2-10
I/F Board RAD V2
ON & VAC
N1 - Orange (neon) Indicates presence of

100 VAC for the Bucky
Pin 9
Table Bucky
Pin 1
Pin 9
Wall Bucky
Pin 1
Room Door & Light I/F
To AEC board
Pin 9
Pin 1
DS4:
CAN TRANSMIT
(yellow)
DS5:
EXT.CAN
TRANSMIT (yellow)
Service Laptop
DS6: Receive Data
from console (yellow)
Console
OPTIONAL
DS7: DATA being sent to

console (TRANSMIT)
(yellow)
No strap (engineering
use)
Presence of strap TUBE 1
DS3:
Reset led (red)
DS1, DS2: Status micro

processor (yellow)
10-25
GE MEDICAL SYSTEMS
REV 19
10-26
GE MEDICAL SYSTEMS
REV 19
2-11
AEC Board
ILLUSTRATION 12
AEC BOARD
2-11-1 Test Points

TESTPOINT
MEASUREMENT
SIGNAL
RANGE
TP1
230 VDC
230 VDC _5%
TP2
230 VDC
230 VDC _5%
TP3
230 VDC
230 VDC _5%
TP4
230 VDC
230 VDC _5%
R10V
10 VDC (REFERENCE)
10 VDC _1%
10-27
GE MEDICAL SYSTEMS
REV 19
10-28
GE MEDICAL SYSTEMS
REV 19
2-12
AEC Board V2
ILLUSTRATION 13
AEC BOARD V2
AEC4
2-13
AEC3
AEC1
AEC2
N1 - Orange (neon) Presence of 230 VDC
Test Points
TESTPOINT
TP1
TP2
TP3
TP4
TP5
TP6
TP7
TP8
TP9
TP10
TP11
MEASUREMENT
SIGNAL
RANGE
230 VDC
230 VDC
230 VDC
230 VDC
AEC assignment reference
10 VDC (reference)
AEC return voltage
AEC1 return voltage
AEC2 return voltage
AEC3 return voltage
AEC4 return voltage
230 VDC _5%

230 VDC _5%
230 VDC _5%
230 VDC _5%
0 to 10 V
10 VDC _1%
10-29
GE MEDICAL SYSTEMS
REV 19
10-30
GE MEDICAL SYSTEMS
REV 19
SECTION 3
SCHEMATICS
PDU Connection Diagram
To RAD Interface
J4-1
10-31
GE MEDICAL SYSTEMS
REV 19
Table Base and Tube Stand Power
10-32
GE MEDICAL SYSTEMS
REV 19
A61001C
Total 4 sheets
Console Control Board Circuit Diagram
10-33
GE MEDICAL SYSTEMS
REV 19
10-34
GE MEDICAL SYSTEMS
REV 19
10-35
GE MEDICAL SYSTEMS
REV 19
10-36
GE Medical Systems
GE Medical Systems: Telex 3797371
P.O. Box 414, Milwaukee, Wisconsin 53201 U.S.A.
(Asia, Pacific, Latin America, North America)

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GE Medical Systems

Copyrights 1998~2008 By General Electric Co.

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V PPAD, E EXTERN SLUBA ZKAZNKM POTEBUJE

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THIS SERVICE MANUAL IS AVAILABLE IN ENGLISH ONLY.

IF A CUSTOMER'S SERVICE PROVIDER REQUIRES A

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