Direction 5429484 - CA-1EN Revision 1 GE Healthcare Brivo XR515 Service Manual (Class A)

GE Healthcare
gehealthcare.com
Technical 
Publication
Direction 5429484 -CA-1EN

Revision 1
GE Healthcare
Brivo XR515 Service Manual(Class A)
Copyright © 2013 by General Electric Company, Inc. All Rights Re-

served
GE HEALTHCARE 
DIRECTION 5429484 -CA-1EN, REVISION 6 INSTALLATION MANUAL
Page 2
GE HEALTHCARE 
LEGAL NOTES
TRADEMARKS
All other products and their name brands are the trademarks of their respective holders.
COPYRIGHTS
All Material, Copyright © 2013 by General Electric Company, Inc. All rights reserved. The material
presented and contained herein may not be reproduced in any form or manner, without the written permission
of General Electric Company, Inc.
Legal Notes Page 3

GE HEALTHCARE 
This page is intentionally left blank.
Page 4 Legal Notes

GE HEALTHCARE 
IMPORTANT PRECAUTIONS
LANGUAGE
ПРЕДУПРЕЖДЕНИЕ  ТО В А УП Ъ ТВ А Н Е ЗА РА Б О ТА Е Н А Л И Ч Н О С А М О Н А А Н ГЛ И Й С КИ ЕЗИ К.
(BG)  А КО Д О С ТА В Ч И КЪ Т Н А УС Л УГА ТА Н А КЛ И ЕН ТА И ЗИ С КА ЕЗИ К,
РА З Л И Ч ЕН О Т А Н ГЛ И Й С КИ , ЗА Д Ъ Л Ж ЕН И Е Н А КЛ И ЕН ТА Е Д А О С И ГУРИ
П РЕ В О Д .
 Н Е И ЗП О Л ЗВ А Й ТЕ О Б О РУД В А Н ЕТО П РЕД И Д А С ТЕ С Е КО Н С УЛ ТИ РА Л И
И Р А ЗБ РА ЛИ УП Ъ ТВ А Н ЕТО З А РА Б О ТА .
 Н ЕС П А ЗВ А Н ЕТО Н А ТО В А П Р ЕД УП РЕЖ Д Е Н И Е М О Ж Е Д А Д О В ЕД Е Д О
Н А РА Н Я В А Н Е Н А Д О С ТА В Ч И КА Н А УС ЛУГА ТА , О П ЕРА ТО РА И Л И
П А Ц И ЕН Т В РЕЗ УЛ ТА Т Н А ТО КО В УД А Р И Л И М ЕХА Н И Ч Н А И Л И Д РУГА
О П А С Н О С Т.
警告  本维修手册仅提供英文版本。
(ZH-CN)  如果维修服务提供商需要非英文版本，客户需自行提供翻译服务。
 未详细阅读和完全理解本维修手册之前，不得进行维修。
 忽略本警告可能对维修人员，操作员或患者造成触电、机械伤害或其他形式的伤害。
VÝSTRAHA  TENTO PROVOZNÍ NÁVOD EXISTUJE POUZE V ANGLICKÉM JAZYCE.
(CS)  V PŘÍPADĚ, ŽE EXTERNÍ SLUŽBA ZÁKAZNÍKŮM POTŘEBUJE NÁVOD V

JINÉM JAZYCE, JE ZAJIŠTĚNÍ PŘEKLADU DO ODPOVÍDAJÍCÍHO JAZYKA
ÚKOLEM ZÁKAZNÍKA.
 NESNAŽTE SE O ÚDRŽBU TOHOTO ZAŘÍZENÍ, ANIŽ BYSTE SI PŘEČETLI
TENTO PROVOZNÍ NÁVOD A POCHOPILI JEHO OBSAH.
 V PŘÍPADĚ NEDODRŽOVÁNÍ TÉTO VÝSTRAHY MŮŽE DOJÍT K PORANĚNÍ
PRACOVNÍKA PRODEJNÍHO SERVISU, OBSLUŽNÉHO PERSONÁLU NEBO
PACIENTŮ VLIVEM ELEKTRICKÉHOP PROUDU, RESPEKTIVE VLIVEM
MECHANICKÝCH ČI JINÝCH RIZIK.
ADVARSEL  DENNE SERVICEMANUAL FINDES KUN PÅ ENGELSK.

(DA)  HVIS EN KUNDES TEKNIKER HAR BRUG FOR ET ANDET SPROG END
ENGELSK, ER DET KUNDENS ANSVAR AT SØRGE FOR OVERSÆTTELSE.
 FORSØG IKKE AT SERVICERE UDSTYRET MEDMINDRE
DENNE SERVICEMANUAL HAR VÆRET KONSULTERET OG ER FORSTÅET.
 MANGLENDE OVERHOLDELSE AF DENNE ADVARSEL KAN MEDFØRE
SKADE PÅ GRUND AF ELEKTRISK, MEKANISK ELLER ANDEN FARE FOR
TEKNIKEREN, OPERATØREN ELLER PATIENTEN.
Important Precautions Page 5

GE HEALTHCARE 
WAARSCHUWING  DEZE ONDERHOUDSHANDLEIDING IS ENKEL IN HET ENGELS

VERKRIJGBAAR.
(NL)
 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 PATIËNT GEWOND
KUNNEN RAKEN ALS GEVOLG VAN EEN ELEKTRISCHE SCHOK,
MECHANISCHE OF ANDERE GEVAREN.
• THIS SERVICE MANUAL IS AVAILABLE IN ENGLISH ONLY.

WARNING
• IF A CUSTOMER’S SERVICE PROVIDER REQUIRES A LANGUAGE
(EN) 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, MECHANICAL OR OTHER HAZARDS.
HOIATUS  KÄESOLEV TEENINDUSJUHEND ON SAADAVAL AINULT INGLISE KEELES.

(ET)  KUI KLIENDITEENINDUSE OSUTAJA NÕUAB JUHENDIT INGLISE KEELEST
ERINEVAS KEELES, VASTUTAB KLIENT TÕLKETEENUSE OSUTAMISE EEST.
 ÄRGE ÜRITAGE SEADMEID TEENINDADA ENNE EELNEVALT
KÄESOLEVA TEENINDUSJUHENDIGA TUTVUMIST JA SELLEST ARU
SAAMIST.
 KÄESOLEVA HOIATUSE EIRAMINE VÕIB PÕHJUSTADA TEENUSEOSUTAJA,
OPERAATORI VÕI PATSIENDI VIGASTAMIST ELEKTRILÖÖGI, MEHAANILISE
VÕI MUU OHU TAGAJÄRJEL.
VAROITUS  TÄMÄ HUOLTO-OHJE ON SAATAVILLA VAIN ENGLANNIKSI.
(FI)  JOS ASIAKKAAN HUOLTOHENKILÖSTÖ VAATII MUUTA KUIN

ENGLANNINKIELISTÄ MATERIAALIA, TARVITTAVAN KÄÄNNÖKSEN
HANKKIMINEN ON ASIAKKAAN VASTUULLA.
 ÄLÄ YRITÄ KORJATA LAITTEISTOA ENNEN KUIN OLET VARMASTI LUKENUT
JA YMMÄRTÄNYT TÄMÄN HUOLTO-OHJEEN.
 MIKÄLI TÄTÄ VAROITUSTA EI NOUDATETA, SEURAUKSENA VOI OLLA
HUOLTOHENKILÖSTÖN, LAITTEISTON KÄYTTÄJÄN TAI POTILAAN
VAHINGOITTUMINEN SÄHKÖISKUN, MEKAANISEN VIAN TAI MUUN
VAARATILANTEEN VUOKSI.
Page 6 Important Precautions

GE HEALTHCARE 
• CE MANUEL DE MAINTENANCE N’EST DISPONIBLE QU’EN

ATTENTION 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’INTERVENTION SUR LES ÉQUIPEMENTS TANT
QUE LE MANUEL SERVICE N’A PAS ÉTÉ CONSULTÉ ET COMPRIS.
• LE NON-RESPECT DE CET AVERTISSEMENT PEUT ENTRAÎNER
CHEZ LE TECHNICIEN, L’OPÉRATEUR OU LE PATIENT DES
BLESSURES DUES À DES DANGERS ÉLECTRIQUES, MÉCANIQUES
OU AUTRES.
WARNUNG  DIESE SERVICEANLEITUNG EXISTIERT NUR IN ENGLISCHER SPRACHE.

(DE)  FALLS EIN FREMDER KUNDENDIENST EINE ANDERE SPRACHE BENÖTIGT,
IST ES AUFGABE DES KUNDEN FÜR EINE ENTSPRECHENDE
ÜBERSETZUNG 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 STROMSCHLÄGE, MECHANISCHE ODER SONSTIGE
GEFAHREN KOMMEN.
ΠΡΟΕΙ∆ΟΠΟΙΗΣΗ  ΤΟ ΠΑΡΟΝ ΕΓΧΕΙΡΙ∆ΙΟ ΣΕΡΒΙΣ ∆ΙΑΤΙΘΕΤΑΙ ΣΤΑ ΑΓΓΛΙΚΑ ΜΟΝΟ.
(EL)  ΕΑΝ ΤΟ ΑΤΟΜΟ ΠΑΡΟΧΗΣ ΣΕΡΒΙΣ ΕΝΟΣ ΠΕΛΑΤΗ ΑΠΑΙΤΕΙ ΤΟ ΠΑΡΟΝ

ΕΓΧΕΙΡΙ∆ΙΟ ΣΕ ΓΛΩΣΣΑ ΕΚΤΟΣ ΤΩΝ ΑΓΓΛΙΚΩΝ, ΑΠΟΤΕΛΕΙ ΕΥΘΥΝΗ ΤΟΥ
ΠΕΛΑΤΗ ΝΑ ΠΑΡΕΧΕΙ ΥΠΗΡΕΣΙΕΣ ΜΕΤΑΦΡΑΣΗΣ.
 ΜΗΝ ΕΠΙΧΕΙΡΗΣΕΤΕ ΤΗΝ ΕΚΤΕΛΕΣΗ ΕΡΓΑΣΙΩΝ ΣΕΡΒΙΣ ΣΤΟΝ ΕΞΟΠΛΙΣΜΟ
ΕΚΤΟΣ ΕΑΝ ΕΧΕΤΕ ΣΥΜΒΟΥΛΕΥΤΕΙ ΚΑΙ ΕΧΕΤΕ ΚΑΤΑΝΟΗΣΕΙ ΤΟ ΠΑΡΟΝ
ΕΓΧΕΙΡΙ∆ΙΟ ΣΕΡΒΙΣ.
 ΕΑΝ ∆Ε ΛΑΒΕΤΕ ΥΠΟΨΗ ΤΗΝ ΠΡΟΕΙ∆ΟΠΟΙΗΣΗ ΑΥΤΗ, ΕΝ∆ΕΧΕΤΑΙ ΝΑ
ΠΡΟΚΛΗΘΕΙ ΤΡΑΥΜΑΤΙΣΜΟΣ ΣΤΟ ΑΤΟΜΟ ΠΑΡΟΧΗΣ ΣΕΡΒΙΣ, ΣΤΟ ΧΕΙΡΙΣΤΗ
Ή ΣΤΟΝ ΑΣΘΕΝΗ ΑΠΟ ΗΛΕΚΤΡΟΠΛΗΞΙΑ, ΜΗΧΑΝΙΚΟΥΣ Ή ΑΛΛΟΥΣ
ΚΙΝ∆ΥΝΟΥΣ.

GE HEALTHCARE 
FIGYELMEZTETÉS  EZEN KARBANTARTÁSI KÉZIKÖNYV KIZÁRÓLAG ANGOL NYELVEN ÉRHETŐ

EL.
(HU)
 HA A VEVŐ SZOLGÁLTATÓJA ANGOLTÓL ELTÉRŐ NYELVRE TART IGÉNYT,
AKKOR A VEVŐ FELELŐSSÉGE A FORDÍTÁS ELKÉSZÍTTETÉSE.
 NE PRÓBÁLJA ELKEZDENI HASZNÁLNI A BERENDEZÉST, AMÍG A
KARBANTARTÁSI KÉZIKÖNYVBEN LEÍRTAKAT NEM ÉRTELMEZTÉK.
 EZEN FIGYELMEZTETÉS FIGYELMEN KÍVÜL HAGYÁSA A SZOLGÁLTATÓ,
MŰKÖDTETŐ VAGY A BETEG ÁRAMÜTÉS, MECHANIKAI VAGY EGYÉB
VESZÉLYHELYZET MIATTI SÉRÜLÉSÉT EREDMÉNYEZHETI.
AÐVÖRUN  ÞESSI ÞJÓNUSTUHANDBÓK ER EINGÖNGU FÁANLEG Á ENSKU.

(IS)  EF AÐ ÞJÓNUSTUVEITANDI VIÐSKIPTAMANNS ÞARFNAST ANNAS
TUNGUMÁLS EN ENSKU, ER ÞAÐ SKYLDA VIÐSKIPTAMANNS AÐ SKAFFA
TUNGUMÁLAÞJÓNUSTU.
 REYNIÐ EKKI AÐ AFGREIÐA TÆKIÐ NEMA AÐ ÞESSI ÞJÓNUSTUHANDBÓK
HEFUR VERIÐ SKOÐUÐ OG SKILIN.
 BROT Á SINNA ÞESSARI AÐVÖRUN GETUR LEITT TIL MEIÐSLA Á
ÞJÓNUSTUVEITANDA, STJÓRNANDA EÐA SJÚKLINGS FRÁ RAFLOSTI,
VÉLRÆNU EÐA ÖÐRUM ÁHÆTTUM.
• IL PRESENTE MANUALE DI MANUTENZIONE È DISPONIBILE

AVVERTENZA SOLTANTO IN INGLESE.
(IT)
• SE UN ADDETTO ALLA MANUTENZIONE ESTERNO ALLA GEMS
RICHIEDE IL MANUALE IN UNA LINGUA DIVERSA, IL CLIENTE È
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.

GE HEALTHCARE 
 このサービスマニュアルには英語版しかありません。
(JA)  サービスを担当される業者が英語以外の言語を要求される場合、翻訳作業はその業
者の責任で行うものとさせていただきます。
 このサービスマニュアルを熟読し理解せずに、装置のサービスを行わないでくださ
い。
 この警告に従わない場合、サービスを担当される方、操作員あるいは患者さんが、
感電や機械的又はその他の危険により負傷する可能性があります。
경고  본 서비스 지침서는 영어로만 이용하실 수 있습니다.
(KO)  고객의 서비스 제공자가 영어 이외의 언어를 요구할 경우, 번역 서비스를 제공하는 것
은 고객의 책임입니다.
 본 서비스 지침서를 참고했고 이해하지 않는 한은 해당 장비를 수리하려고 시도하지

마십시오.
 이 경고에 유의하지 않으면 전기 쇼크, 기계상의 혹은 다른 위험으로부터 서비스 제공

자, 운영자 혹은 환자에게 위해를 가할 수 있습니다.
BRĪDINĀJUMS  ŠĪ APKALPES ROKASGRĀMATA IR PIEEJAMA TIKAI ANGĻU VALODĀ.

(LV)  JA KLIENTA APKALPES SNIEDZĒJAM NEPIECIEŠAMA INFORMĀCIJA CITĀ
VALODĀ, NEVIS ANGĻU, KLIENTA PIENĀKUMS IR NODROŠINĀT
TULKOŠANU.
 NEVEICIET APRĪKOJUMA APKALPI BEZ APKALPES ROKASGRĀMATAS
IZLASĪŠANAS UN SAPRAŠANAS.
 ŠĪ BRĪDINĀJUMA NEIEVĒROŠANA VAR RADĪT ELEKTRISKĀS STRĀVAS
TRIECIENA, MEHĀNISKU VAI CITU RISKU IZRAISĪTU TRAUMU APKALPES
SNIEDZĒJAM, OPERATORAM VAI PACIENTAM.
ĮSPĖJIMAS  ŠIS EKSPLOATAVIMO VADOVAS YRA PRIEINAMAS TIK ANGLŲ KALBA.

(LT)  JEI KLIENTO PASLAUGŲ TIEKĖJAS REIKALAUJA VADOVO KITA KALBA – NE
ANGLŲ, NUMATYTI VERTIMO PASLAUGAS YRA KLIENTO ATSAKOMYBĖ.
 NEMĖGINKITE ATLIKTI ĮRANGOS TECHNINĖS PRIEŽIŪROS, NEBENT
ATSIŽVELGĖTE Į ŠĮ EKSPLOATAVIMO VADOVĄ IR JĮ SUPRATOTE.
 JEI NEATKREIPSITE DĖMESIO Į ŠĮ PERSPĖJIMĄ, GALIMI SUŽALOJIMAI DĖL
ELEKTROS ŠOKO.
 MECHANINIŲ AR KITŲ PAVOJŲ PASLAUGŲ TIEKĖJUI, OPERATORIUI AR
PACIENTUI.

GE HEALTHCARE 
ADVARSEL  DENNE SERVICEHÅNDBOKEN FINNES BARE PÅ ENGELSK.

(NO)  HVIS KUNDENS SERVICELEVERANDØR TRENGER ET ANNET SPRÅK, ER
DET KUNDENS ANSVAR Å SØRGE FOR OVERSETTELSE.
 IKKE FORSØK Å REPARERE UTSTYRET UTEN AT DENNE
SERVICEHÅNDBOKEN ER LEST OG FORSTÅTT.
 MANGLENDE HENSYN TIL DENNE ADVARSELEN KAN FØRE TIL AT
SERVICELEVERANDØREN, OPERATØREN ELLER PASIENTEN SKADES PÅ
GRUNN AV ELEKTRISK STØT, MEKANISKE ELLER ANDRE FARER.
OSTRZEŻENIE  NINIEJSZY PODRĘCZNIK SERWISOWY DOSTĘPNY JEST JEDYNIE W JĘZYKU

ANGIELSKIM.
(PL)
 JEŚLI DOSTAWCA USŁUG KLIENTA WYMAGA JĘZYKA INNEGO NIŻ
ANGIELSKI, ZAPEWNIENIE USŁUGI TŁUMACZENIA JEST OBOWIĄZKIEM
KLIENTA.
 NIE PRÓBOWAĆ SERWISOWAĆ WYPOSAŻENIA BEZ ZAPOZNANIA SIĘ I
ZROZUMIENIA NINIEJSZEGO PODRĘCZNIKA SERWISOWEGO.
 NIEZASTOSOWANIE SIĘ DO TEGO OSTRZEŻENIA MOŻE SPOWODOWAĆ
URAZY DOSTAWCY USŁUG, OPERATORA LUB PACJENTA W WYNIKU
PORAŻENIA ELEKTRYCZNEGO, ZAGROŻENIA MECHANICZNEGO BĄDŹ
INNEGO.
ATENÇÃO  ESTE MANUAL DE ASSISTÊNCIA TÉCNICA SÓ SE ENCONTRA DISPONÍVEL

EM INGLÊS.
(PT)
 SE QUALQUER OUTRO SERVIÇO DE ASSISTÊNCIA TÉCNICA, QUE NÃO A
GEMS, SOLICITAR ESTES MANUAIS NOUTRO IDIOMA, É DA
RESPONSABILIDADE DO CLIENTE FORNECER OS SERVIÇOS DE
TRADUÇÃO.
 NÃO TENTE REPARAR O EQUIPAMENTO SEM TER CONSULTADO E
COMPREENDIDO ESTE MANUAL DE ASSISTÉNCIA TÉCNICA
 O NÃO CUMPRIMENTO DESTE AVISO PODE POR EM PERIGO A SEGURANÇA
DO TÉCNICO, OPERADOR OU PACIENTE DEVIDO A CHOQUES ELÉTRICOS,
MECÂNICOS OU OUTROS.
ATENŢIE  ACEST MANUAL DE SERVICE ESTE DISPONIBIL NUMAI ÎN LIMBA ENGLEZĂ.

(RO)  DACĂ UN FURNIZOR DE SERVICII PENTRU CLIENŢI NECESITĂ O ALTĂ
LIMBĂ DECÂT CEA ENGLEZĂ, ESTE DE DATORIA CLIENTULUI SĂ
FURNIZEZE O TRADUCERE.
 NU ÎNCERCAŢI SĂ REPARAŢI ECHIPAMENTUL DECÂT ULTERIOR
CONSULTĂRII ŞI ÎNŢELEGERII ACESTUI MANUAL DE SERVICE.
 IGNORAREA ACESTUI AVERTISMENT AR PUTEA DUCE LA RĂNIREA
DEPANATORULUI, OPERATORULUI SAU PACIENTULUI ÎN URMA
PERICOLELOR DE ELECTROCUTARE, MECANICE SAU DE ALTĂ NATURĂ.

GE HEALTHCARE 
ОСТОРОЖНО!  ДАННОЕ РУКОВОДСТВО ПО ОБСЛУЖИВАНИЮ ПРЕДЛАГАЕТСЯ ТОЛЬКО

НА АНГЛИЙСКОМ ЯЗЫКЕ.
(RU)
 ЕСЛИ СЕРВИСНОМУ ПЕРСОНАЛУ КЛИЕНТА НЕОБХОДИМО
РУКОВОДСТВО НЕ НА АНГЛИЙСКОМ, А НА КАКОМ-ТО ДРУГОМ ЯЗЫКЕ,
КЛИЕНТУ СЛЕДУЕТ САМОСТОЯТЕЛЬНО ОБЕСПЕЧИТЬ ПЕРЕВОД.
 ПЕРЕД ОБСЛУЖИВАНИЕМ ОБОРУДОВАНИЯ ОБЯЗАТЕЛЬНО
ОБРАТИТЕСЬ К ДАННОМУ РУКОВОДСТВУ И ПОЙМИТЕ ИЗЛОЖЕННЫЕ В
НЕМ СВЕДЕНИЯ.
 НЕСОБЛЮДЕНИЕ ТРЕБОВАНИЙ ДАННОГО ПРЕДУПРЕЖДЕНИЯ МОЖЕТ
ПРИВЕСТИ К ТОМУ, ЧТО СПЕЦИАЛИСТ ПО ОБСЛУЖИВАНИЮ, ОПЕРАТОР
ИЛИ ПАЦИЕНТ ПОЛУЧАТ УДАР ЭЛЕКТРИЧЕСКИМ ТОКОМ,
МЕХАНИЧЕСКУЮ ТРАВМУ ИЛИ ДРУГОЕ ПОВРЕЖДЕНИЕ.
UPOZORNENIE  TENTO NÁVOD NA OBSLUHU JE K DISPOZÍCII LEN V ANGLIČTINE.
(SK)  AK ZÁKAZNÍKOV POSKYTOVATEĽ SLUŽIEB VYŽADUJE INÝ JAZYK AKO

ANGLIČTINU, POSKYTNUTIE PREKLADATEĽSKÝCH SLUŽIEB JE
ZODPOVEDNOSŤOU ZÁKAZNÍKA.
 NEPOKÚŠAJTE SA O OBSLUHU ZARIADENIA SKÔR, AKO SI NEPREČÍTATE
NÁVOD NA OBLUHU A NEPOROZUMIETE MU.
 ZANEDBANIE TOHTO UPOZORNENIA MÔŽE VYÚSTIŤ DO ZRANENIA
POSKYTOVATEĽA SLUŽIEB, OBSLUHUJÚCEJ OSOBY ALEBO PACIENTA
ELEKTRICKÝM PRÚDOM, DO MECHANICKÉHO ALEBO INÉHO
NEBEZPEČENSTVA.
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 ELÉCTRICAS, MECÁNICAS O DE
OTRA NATURALEZA.

GE HEALTHCARE 
VARNING  DEN HÄR SERVICEHANDBOKEN FINNS BARA TILLGÄNGLIG PÅ ENGELSKA.

(SV)  OM EN KUNDS SERVICETEKNIKER HAR BEHOV AV ETT ANNAT SPRÅK ÄN
ENGELSKA ANSVARAR KUNDEN FÖR ATT TILLHANDAHÅLLA
ÖVERSÄTTNINGSTJÄNSTER.
 FÖRSÖK INTE UTFÖRA SERVICE PÅ UTRUSTNINGEN OM DU INTE HAR LÄST
OCH FÖRSTÅR DEN HÄR SERVICEHANDBOKEN.
 OM DU INTE TAR HÄNSYN TILL DEN HÄR VARNINGEN KAN DET RESULTERA
I SKADOR PÅ SERVICETEKNIKERN, OPERATÖREN ELLER PATIENTEN TILL
FÖLJD AV ELEKTRISKA STÖTAR, MEKANISKA FAROR ELLER ANDRA
FAROR.
DİKKAT  BU SERVİS KILAVUZUNUN SADECE İNGİLİZCESİ MEVCUTTUR.

(TR)  EĞER MÜŞTERİ TEKNİSYENİ BU KILAVUZU İNGİLİZCE DIŞINDA BİR BAŞKA
LİSANDAN TALEP EDERSE, BUNU TERCÜME ETTİRMEK MÜŞTERİYE DÜŞER.
 SERVİS KILAVUZUNU OKUYUP ANLAMADAN EKİPMANLARA MÜDAHALE
ETMEYİNİZ.
 BU UYARIYA UYULMAMASI, ELEKTRİK, MEKANİK VEYA DİĞER
TEHLİKELERDEN DOLAYI TEKNİSYEN, OPERATÖR VEYA HASTANIN
YARALANMASINA YOL AÇABİLİR.
DAMAGE IN TRANSPORTATION
All packages should be closely examined at time of delivery. If damage is apparent write “Damage
In Shipment” on ALL copies of the freight or express bill BEFORE delivery is accepted or “signed
for” by a GE representative or 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 GEHC Global Parts 1-800-548-3366 and select option 8, immediately after damage is found.
At this time be 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 And
Procedures Bulletins.
14 July 1993
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 Healthcare 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 GE’s electrical work on these products will comply with the requirements of the
applicable electrical codes.

GE HEALTHCARE 
The purchaser of GE equipment shall only utilize qualified personnel (i.e., GE’s field engineers,
personnel of third-party service companies with equivalent training, or licensed electricians) to
perform electrical servicing on the equipment.
IMPORTANT...X-RAY PROTECTION
X-ray 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, Healthcare
Group, will be glad to assist and cooperate in placing this equipment in use.
Although this apparatus incorporates a high degree of protection against x-radiation 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 anyone 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 of any other local authorities, and take adequate steps to protect against
injury.
The equipment is sold with the understanding that the General Electric Company, Healthcare
Group, its agents, and representatives have no responsibility for injury or damage which may result
from improper use of the equipment.
Various protective materials and devices are available. It is urged that such materials or devices be used.
LITHIUM BATTERY CAUTIONARY STATEMENTS
CAUTION Danger of explosion if battery is incorrectly replaced. Replace only with the same or equivalent type
Risk of recommended by the manufacturer. Discard used batteries according to the manufacturer’s
Explosion instructions.
OMISSIONS & ERRORS

Customers, please contact your GE Sales or Service representatives.
GE personnel, please use the GEHC CQA Process to report all omissions, errors, and defects in
this publication.

GE HEALTHCARE 

GE HEALTHCARE 
Revision History
Revision Date Reason for change

1 Apr.18, 2013 First Release
Revision History Page 15

GE HEALTHCARE 
Page 16
GE HEALTHCARE 
Preface
Publication Conventions
Standardized conventions for representing information is a uniform way of communicating information to a
reader in a consistent manner. Conventions are used so that the reader can easily recognize the actions or
decisions that must be made. There are a number of character and paragraph styles used in this publication to
accomplish this task. Please become familiar with them before proceeding forward.
It’s important that you read and understand hazard statements, and not just ignore them.
Section 1.0
Safety & Hazard Information
Proper product safety labeling allows a person to safely use or service a product. The format and style for
safety communications reflected in this publication represents the harmonization of IEC/ISO 3864 and ANSI
Z535 standards.
Within this publication, different paragraph and character styles are used to indicated potential hazards.
Paragraph prefixes, such as hazard, caution, danger and warning, are used to identify important safety
information. Text (Hazard) styles are applied to the paragraph contents that are applicable to each specific
safety statement.
1.1 Hazard Messages

Any action that will, could or potentially cause personal injury will be preceded by the safety alert symbol
and an appropriate signal word. The safety alert symbol is the triangle with an exclamation mark within it.
It’s always used next to the signal word to indicate the severity of the hazard. Together, they are used to
indicate a hazard exists.
Signal words describe the severity of possible human injures that may be encountered. The alert symbol and
signal word are placed immediately before any paragraph they affect. Safety information includes:
1.) Signal Word - The seriousness level of the hazard.
2.) Symbol or Pictorial - The consequence of interaction with the hazard.
3.) Word Message:
a.) The nature of the hazard (i.e. the type of hazard)
b.) How to avoid the hazard.
The safety alert symbol is not used when an action can only cause equipment damage.
1.2 Text Format of Signal Words

DANGER - INDICATES AN IMMINENTLY HAZARDOUS SITUATION WHICH,
IF NOT AVOIDED, WILL RESULT IN DEATH OR SERIOUS INJURY. THIS
SIGNAL WORD IS LIMITED TO THE MOST EXTREME SITUATIONS.
WARNING - INDICATES A POTENTIALLY HAZARDOUS SITUATION WHICH, IF
NOT AVOIDED, COULD RESULT IN DEATH OR SERIOUS INJURY.
Caution - Indicates a potentially hazardous situation which, if not avoided, may result in minor or
moderate injury. It may also be used to alert against unsafe practices.
Preface Page 17
GE HEALTHCARE 
NOTICE - Indicates information or a company policy that relates directly or indirectly to the safety of
personnel or protection of property. This signal word is associated directly with a hazard or hazardous
situation and is used in place of 'DANGER,' 'WARNING,' or 'CAUTION.' It can include:
• Destruction of a disk drive
• Potential for internal mechanical damage, such as to a X-ray tube
1.3 Symbols and Pictorials Used

The following Symbols and Pictorials are be used in this publication. These graphical icons (symbols) may
be used to make you aware of specific types of hazards that could possibly cause harm.
keep_up magnetic biohazard compressgas ppe-hearing
fragile impact corrosive heavyobject ppe-2people
static_elec heat general laser ppe-respitory
keep_dry pinch radiation poisongas ppe-loto
general explosive electrical flammable ppe-eye
torque crush/mechanical tipping Read Manual ppe-gloves
ce instuction poisonmatl entanglement instuction
Page 18 Preface
GE HEALTHCARE 
Section 2.0
Publication Conventions
2.1 General Paragraph and Character Styles
Prefixes are used to highlight important non-safety related information. Paragraph prefixes (such as Purpose,
Example, Comment or Note) are used to identify important but non-safety related information. Text styles
are also applied to text within each paragraph modified by the specific prefix.
EXAMPLES OF PREFIXES USED FOR GENERAL INFORMATION:

Purpose: Introduces and provides meaning as to the information contained within the chapter, section or
subsection (such as used at the beginning this chapter, for example).
Note: Conveys information that should be considered important to the reader.
Example: Used to make the reader aware that the paragraph(s) that follow are examples of information possibly stated
previously.
Comment: Represents “additional” information that may or may not be relevant to your situation.
2.2 Page Layout

Publication Part Number & Revision Number Publication Title
The current section and its title The current chapter and its title
are always shown in the footer of are always shown in the footer of
the left (even) page. the right (odd) page.
An exclamation point in a triangle is used Paragraphs preceeded by a symbol
to indicate important information to the user. (e.g. bullets) contain information that
Paragraphs preceeded by Alphanumeric has no specific order.
characters (e.g. numbers) contain infor-
mation that must be followed in a specific order.
Headers and footers in this publication are designed to allow you to quickly identify your location. The
document part number and revision number appears in every header on every page. Odd numbered page
footers indicate the current chapter, its title and current page number. Even page footers show the current
section and its title, as well as the current page number.
Preface Page 19
GE HEALTHCARE 
2.3 Computer Screen Output/Input Text Character Styles
Within this publication, mono-spaced character styles (fonts) are used to indicate computer text that’s either
screen input and output. Mono-spaced fonts, such courier, are used to indicated text direction. When you type
at your keyboard, you are generating computer input. Occasionally you will see the math operator “greater-
than” and “less-than” symbols used to indicate the start and finish of variable output. When reading text
generated by the computer, you are reading it as computer generated output. In addition to direction,
characters are italicized (e.g. italics) to indicate information specific to your system or site.
Example: Fixed This paragraph’s font represents computer generated screen “fixed” output.
Output Its output is fixed from the sense that it does not vary from application
to application. It’s the most commonly used style used to indicate
filenames, paths and text that do not change from system to system. The
character style used is a fixed width such as courier.
Example: This paragraph’s font represents computer screen output that is
Variable Output “variable”. It’s used to represent output that varies from application to
application or system to system. Variable output is sometimes found placed
between greater-than and less-than operators for clarification. For
example: <variable_ouput> or <3.45.120.3>. In both cases, the < and >
operators are not part of the actual input.
Example: Fixed This paragraph’s font represents fixed input. It’s computer input that is
Input typed-in via the keyboard. Typed input that does not vary from application
to application or system to system. Fixed text the user is required to
supply as input. For example: cd /usr/3p
Example: This paragraph’s font represents computer input that can vary from
Variable Input application to application or system to system. With variable text, the
user is required to supply system dependent input or information. Variable
input sometimes is placed between greater-than and less-than operators.
For example: <variable_input>. In these cases, the (<>) operators would
be dropped prior to input. For example: ypcat hosts | grep <3.45.120.3>
would be typed into the computer as:
ypcat hosts | grep 3.45.120.3
without the greater-than and less-than operators.
2.4 Buttons, Switches and Keyboard Inputs (Hard & Soft Keys)
Different character styles are used to indicate actions requiring the reader to press either a hard or soft button,
switch or key. Physical hardware, such as buttons and switches, are called hard keys because they are hard
wired or mechanical in nature. A keyboard or on/off switch would be a hard key. Software or computer
generated buttons are called soft keys because they are software generated. Software driven menu buttons are
an example of such keys. Soft and hard keys are represented differently in this publication.
Example: Hard A power switch ON/OFF or a keyboard key like ENTER is indicated by applying a character style that uses
Keys both over and under-lined bold text that is bold. This is a hard key.
Example: Soft Whereas the computer MENU button that you would click with your mouse or touch with your hand uses
Keys over and under-lined regular text. This is a soft key.
Page 20 Preface
GE HEALTHCARE 
Table of Contents
Preface
Publication Conventions ..................................................................................................... 17
Section 1.0
Safety & Hazard Information........................................................................................ 17
1.1 Hazard Messages ............................................................................................................................ 17
1.2 Text Format of Signal Words ......................................................................................................... 17
1.3 Symbols and Pictorials Used .......................................................................................................... 18
Section 2.0
Publication Conventions................................................................................................. 19
2.1 General Paragraph and Character Styles ........................................................................................ 19
2.2 Page Layout .................................................................................................................................... 19
2.3 Computer Screen Output/Input Text Character Styles ................................................................... 20
2.4 Buttons, Switches and Keyboard Inputs (Hard & Soft Keys) ........................................................ 20
Chapter 1 - Safety and Service ........................................................................................... 29

Section 1.0
Lock-Out & Tag-Out (LOTO)....................................................................................... 29
1.1 System Power ................................................................................................................................. 29
1.2 LOTO Procedure for System Power ............................................................................................... 30
Section 2.0
Applying System Power.................................................................................................. 31
2.1 System Preparation for Energizing Power...................................................................................... 31
2.2 Energizing System .......................................................................................................................... 31
Section 3.0
De-Energizing System..................................................................................................... 32
Section 4.0 
Equipment Safety - Electrostatic Discharge (ESD) ..................................................... 32
4.1 Generating Static............................................................................................................................. 32
4.2 Personal Grounding Methods and Equipment ................................................................................ 33
4.3 Grounding the Work Area .............................................................................................................. 33
4.4 Recommended Materials and Equipment ....................................................................................... 34
Chapter 2 System Component............................................................................................ 35
Chapter 3 - System Installation Guide .............................................................................. 37

Section 1.0
Installation ....................................................................................................................... 37
Section 2.0 Installation Checklist .................................................................................. 39
Table of Contents Page 21

GE HEALTHCARE 
Chapter 4 - Before You Begin ............................................................................................ 41
Chapter 5 - Mechanical Installation and Cable Connection .......................................... 43

Section 1.0
Arm Component ............................................................................................................. 43
1.1 Unpacking and Positioning ............................................................................................................. 43
1.2 Installation....................................................................................................................................... 55
Section 2.0 Detector Housing Component .................................................................... 57
2.1 Unpacking ....................................................................................................................................... 57
2.2 Installation....................................................................................................................................... 57
2.3 Cable connection............................................................................................................................. 61
Section 3.0
X-ray Tube and Collimator ........................................................................................... 67
3.1 Unpacking ....................................................................................................................................... 67
3.2 Installation....................................................................................................................................... 69
3.3 Cable connection............................................................................................................................. 73
Section 4.0 Top Box ........................................................................................................ 78
4.1 Unpacking ....................................................................................................................................... 78
4.2 Installation....................................................................................................................................... 79
4.3 Cable Connection............................................................................................................................ 79
Section 5.0
Cabinet Electrical Connections .................................................................................... 81
Chapter 6 - Workstation ..................................................................................................... 85

Section 1.0
Computer ......................................................................................................................... 85
Section 2.0
Mouse and Keyboard...................................................................................................... 85
Section 3.0
Console & Handswitch ................................................................................................... 86
Section 4.0
LCD Monitor................................................................................................................... 86
Section 5.0
Bar Code Reader (Purchased Option) .......................................................................... 87
Section 6.0
Workstation Cable Connections.................................................................................... 88
Chapter 7 Table Installation.............................................................................................. 89

Section 1.0 Unpacking ................................................................................................... 89
Page 22 Table of Contents

GE HEALTHCARE 
Section 2.0 Installation .................................................................................................. 90
Chapter 8 - Alignment between Collimator and Detector.............................................. 91
Chapter 9 - Column Cover Installation............................................................................. 95

Section 1.0 Unpack Column Covers ............................................................................. 95
Section 2.0 Install Column covers ................................................................................. 95
Chapter 10Column Support Installation .......................................................................... 97
Chapter 11 - System Check ................................................................................................ 99

Section 1.0 Operational Checks ..................................................................................... 99
1.1 U-Arm Longitudinal Movement ..................................................................................................... 99
1.2 Positioner SID Adjustment ............................................................................................................. 99
1.3 Tube Rotation ................................................................................................................................. 99
1.4 Detector Housing Rotation ............................................................................................................. 99
1.5 Collimator Rotation ........................................................................................................................ 99
Section 2.0 Functional Checks ....................................................................................... 99
2.1 Image quality test............................................................................................................................ 99
2.2 Image artifact check (Optional) .................................................................................................... 100
2.3 Acqisition Test .............................................................................................................................. 100
2.3.1 Digital Wallstand Mode Test.......................................................................................... 100
2.3.2 Digital Table Mode Test................................................................................................. 100
2.3.3 Digital Cassette Mode Test ............................................................................................ 100
Chapter 12 - Labels and Rating Plates ............................................................................ 103
Chapter 13 - Installation Checklist .................................................................................. 105
Chapter 14 - Final Steps.................................................................................................... 107

Section 1.0 Final Installation and Admin Tasks ........................................................ 107
Chapter 15 - Counterweight ............................................................................................. 109
Chapter 16 - Illustrated Renewal Parts.......................................................................... 111

Section 1.0 Illustrated Renewal parts ........................................................................ 111
1.1 Service Tool .................................................................................................................................. 111
1.2 Table ............................................................................................................................................. 111
1.3 Image Chain .................................................................................................................................. 112
1.4 Control Room ............................................................................................................................... 113
1.5 PDU .............................................................................................................................................. 114
1.5.1 MIS Cable....................................................................................................................... 115
1.5.2 U-Arm............................................................................................................................. 115

GE HEALTHCARE 
1.5.3 JEDI Generator ............................................................................................................... 121
1.6 JEDI Generator Renewal Parts ..................................................................................................... 121
1.6.1 Introduction .................................................................................................................... 121
1.6.2 JEDI Generator Renewal Parts List................................................................................ 121
1.6.3 FRU Information ............................................................................................................ 122
Chapter 17 Part Replacement .......................................................................................... 125

Section 1.0Detector replacement ................................................................................. 125
Section 2.0Grid-in Switch in Detector Housing ......................................................... 126
Section 3.0Grid Detent Replacement .......................................................................... 127
Section 4.0X-Ray Tube/Collimator replacement ....................................................... 128
Section 5.0Detector Power Supply Replacement ....................................................... 129
Section 6.0150w Power Supply .................................................................................... 130
Section 7.0Spine PCB board Replacement(5430961) ................................................ 130
Section 8.0Spring on Tube Support Replacement ..................................................... 131
Section 9.0PDU Unit Replacement .............................................................................. 132
Section 10.0Collimator Lamp (5136302) Replacement ............................................. 133
Chapter 18 System Data Backup and Restore................................................................ 135

Section 1.0 System Backup’s Coverage....................................................................... 135
Section 2.0 Backup ........................................................................................................ 136
2.1 Before You Begin ......................................................................................................................... 136
2.2 Procedure ...................................................................................................................................... 136
Section 3.0 Restore ........................................................................................................ 137
3.1 Before You Begin ......................................................................................................................... 137
3.2 Procedure ...................................................................................................................................... 137
Chapter 19 Complete System Software Load and/or Upgrade..................................... 141

Section 1.0 Personnel Requirements ........................................................................... 141
Section 2.0 Overview..................................................................................................... 141
Section 3.0 Preliminary Requirements ....................................................................... 142
3.1 Tools and Test Equipment ............................................................................................................ 142
3.2 Consumables ................................................................................................................................. 142
3.3 Safety ............................................................................................................................................ 142
3.4 Required Conditions ..................................................................................................................... 142
Section 4.0 Procedure ................................................................................................... 142
Section 5.0 Finalization................................................................................................. 152

GE HEALTHCARE 
Chapter 20 System Configuration .................................................................................. 153
Section 1.0 When to Perform System Configuration................................................. 153
1.1 During System Installation ........................................................................................................... 153
1.2 Missing or Lost System Backups.................................................................................................. 153
1.3 Addition of Purchased Options..................................................................................................... 154
Section 2.0 Starting the System Configuration Tool ................................................. 154
Section 3.0 System Configuration Tool Parameters .................................................. 154
3.1 Site Parameters ............................................................................................................................. 154
3.2 General Parameters ....................................................................................................................... 155
3.3 Positioner ...................................................................................................................................... 157
3.4 Options Parameters ....................................................................................................................... 157
3.5 Insite.............................................................................................................................................. 157
3.6 Product Network Filters................................................................................................................ 158
3.7 NTP Settings ................................................................................................................................. 158
3.8 HIPAA Configuration................................................................................................................... 158
3.9 Generator Time ............................................................................................................................. 158
Section 4.0 Network Connection (DICOM) Configuration ...................................... 158
4.1 Network Hosts .............................................................................................................................. 158
4.1.1 Host Tab ......................................................................................................................... 158
4.1.2 Preference Tab................................................................................................................ 159
4.2 Printers .......................................................................................................................................... 161
4.2.1 Agfa Drystar 3000 Printer ............................................................................................. 161
4.2.1.1 Printer Parameters..................................................................................... 161
4.2.1.2 Print Layouts............................................................................................. 162
4.2.2 Agfa Drystar 5500 .......................................................................................................... 163
4.2.2.1 Printer Parameters..................................................................................... 163
4.2.2.2 Print Layouts............................................................................................. 165
4.2.3 Fuji FM DPL Print Parameters....................................................................................... 166
4.2.4 Fuji DryPix 1000 Print Parameters ................................................................................ 167
4.2.5 Fuji DryPix 3000 Print Parameters ................................................................................ 169
4.2.6 Fuji DryPix 7000 Printer Parameters ............................................................................. 171
4.2.7 Kodak 8200 Print Parameters......................................................................................... 172
4.2.11 Codonics Horizon Print Parameters ............................................................................... 178
4.3 Query Modality............................................................................................................................. 180
4.3.1 Changing the Query Modality to “CR” .......................................................................... 180
4.3.2 Changing the Query Modality to “DX”.......................................................................... 180
Section 5.0 Install Demo Images .................................................................................. 180
Section 6.0 Operator’s Manual (OM) Installation..................................................... 180
Section 7.0 Data, Time and NTP settings.................................................................... 181
7.1 NTP Setting................................................................................................................................... 181
Section 8.0 Jedi Time Sync with System Time ........................................................... 181
Section 9.0 Adding a Bar Code Reader....................................................................... 182
9.1 Configuration ................................................................................................................................ 182

GE HEALTHCARE 
Section 10.0 System Login (HIPPA)............................................................................ 182
10.1 User Accounts .............................................................................................................................. 182
10.1.1 System Log-in................................................................................................................. 182
10.1.2 About User Accounts...................................................................................................... 183
10.1.3 Default User Accounts.................................................................................................... 183
10.2 Login Feature ................................................................................................................................ 183
10.2.1 Logging In and Out......................................................................................................... 183
10.2.2 Understanding users and groups..................................................................................... 184
10.2.3 Understanding groups and privileges ............................................................................. 184
10.3 Configuring the System ................................................................................................................ 184
Section 11.0 InSite........................................................................................................ 184
11.1 Configuration ................................................................................................................................ 184
11.1.1 Preliminaries ................................................................................................................... 184
11.1.2 Set Modem Configuration .............................................................................................. 186
11.1.3 Set Network Configuration............................................................................................. 187
11.2 Pro Diags Setup............................................................................................................................. 188
11.2.1 Summary......................................................................................................................... 190
11.2.2 Procedure ........................................................................................................................ 190
11.3 InSite Checkout............................................................................................................................. 191
Section 12.0 iLinq user guide ...................................................................................... 193
Section 13.0 Configuring In-House Service (Advanced Service Mode) .................. 193
13.1 Overview of Service Package ....................................................................................................... 193
13.2 Before You Begin ......................................................................................................................... 194
13.3 Enabling Advanced Service Mode of Operation .......................................................................... 194
13.4 Verifying Advanced Service Mode of Operation ......................................................................... 195
Chapter 21System Installation Calibration .................................................................... 197

Section 1.0 Before You Begin...................................................................................... 197
1.1 Service User Interface (SUIF)....................................................................................................... 197
1.2 Calibration Sequence .................................................................................................................... 197
1.2.1 After first installation, those calibrations are needed. Follow the steps below in. ........ 198
1.2.2 Saving Changes .............................................................................................................. 198
1.2.3 Invoking New Calibrations............................................................................................. 198
1.3 Returning the System to the User ................................................................................................. 198
1.4 Temporarily Changing the Measurement System to Calibrations ................................................ 199
1.5 The use of Collimator(XS-1D) tape (Note the difference between SID and OID)....................... 199
Section 2.0 Positioner.................................................................................................... 199
Section 3.0 Tube Warm-up for Accuracy ................................................................... 199
3.1 REQUIREMENTS........................................................................................................................ 199
3.2 Tube Warm-up Procedure for Accuracy ....................................................................................... 199
Section 4.0 AEC Calibration....................................................................................... 201
4.1 Before You Begin ......................................................................................................................... 201
4.2 Table Ion Chamber........................................................................................................................ 201
4.2.1 Before You Begin ........................................................................................................... 201
4.2.2 Procedure ........................................................................................................................ 201
Section 5.0 Detector (Bad Pixels, Gain, CF) Calibration ......................................... 201
5.1 Before You Begin ......................................................................................................................... 201

GE HEALTHCARE 
5.2 Calibration Overview.................................................................................................................... 202
5.3 When should it be performed........................................................................................................ 202
5.4 Procedure ...................................................................................................................................... 202
Section 6.0 Dose Predication - mR/mAs..................................................................... 203
Section 7.0 Image Quality Calibration..................................................................... 203
Section 8.0 Generator Accuracy Test Calibration .................................................... 204
Section 9.0 Monitor Calibration ................................................................................. 204
Section 10.0 PACS / Image Display Test Image ........................................................ 204
10.1 Objectives ..................................................................................................................................... 204
10.2 Simplified Procedure .................................................................................................................... 205
10.3 Results........................................................................................................................................... 207
Section 11.0 Quality Assurance Procedure (QAP) ................................................... 208
11.1 Before You Begin ......................................................................................................................... 208
11.2 When to Perform QAP.................................................................................................................. 208
11.3 Simplified Procedures................................................................................................................... 208
Chapter 22 System Diagnositcs........................................................................................ 209

Section 1.0 diagnostics .................................................................................................. 209
1.1 Diagnostics home page ................................................................................................................. 209
1.2 Communication diagnostics home................................................................................................ 209
1.2.1 The Ethernet diagnostics explain.................................................................................... 209
1.3 Exposure/Acquisition.................................................................................................................... 210
1.3.1 Generator ........................................................................................................................ 210
1.3.1.1 Rotation..................................................................................................... 210
1.3.1.2 Heater........................................................................................................ 212
1.3.1.3 AEC Function ........................................................................................... 213
1.3.2 Detector diagnostics ...................................................................................................... 213
1.3.2.1 Built in Self....................................................................................... test 214
1.3.2.2 PING TEST............................................................................................... 215
1.3.2.3 Ethernet Statistics Test.............................................................................. 216
1.3.2.4 Demtector Temperature Test .................................................................... 216
1.3.2.5 PS Partial Load ......................................................................................... 217
1.3.2.6 PS Fully Loaded .................................................................................... 218
1.4 Positioner ...................................................................................................................................... 219
Chapter 23 - Schematics and Drawings........................................................................... 221

Section 1.0 System Schematics..................................................................................... 221
Section 2.0 System Electric Assembly ......................................................................... 222
Section 3.0 Cable Assembly.......................................................................................... 223
Chapter 24 Troubleshooting............................................................................................ 225

Section 1.0 How to Start Diagnostic Tools.................................................................. 225
Section 2.0 How to change chinese input bar font size? ........................................... 225

GE HEALTHCARE 
Section 3.0 Positioner Troubleshooting ...................................................................... 227
Section 4.0 Using the Enhanced Error Messages....................................................... 231
Section 5.0 Workstation ............................................................................................. 232
5.1 Bar Code Reader ........................................................................................................................... 232
5.1.1 Is the power on? Is the red illumination beam on?........................................................ 232
5.1.2 Is the scanner having trouble reading your symbols?..................................................... 232
5.1.3 Is the bar code displayed but not entered?...................................................................... 232
5.1.4 The scanner won’t read your bar code at all................................................................... 232
5.2 Console.......................................................................................................................................... 233
5.3 LCD Monitor................................................................................................................................. 233
5.3.1 No Picture ...................................................................................................................... 233
5.3.2 Power Button Does Not Respond ................................................................................... 233
5.3.3 Image persistence .......................................................................................................... 233
5.3.4 Message “OUT OF RANGE” is displayed..................................................................... 233
5.3.5 Image is unstable, unfocused or swimming is apparent ................................................. 233
5.3.6 LED on monitor is not lit (no green or amber color can be seen) .................................. 234
5.3.7 Display image is not sized properly ............................................................................... 234
5.3.8 No Video......................................................................................................................... 234
5.3.9 On-Screen Manager ........................................................................................................ 234
Section 6.0 Soft Reset of Software on PC.................................................................... 234
Section 7.0 Engineering Toolkit................................................................................... 235
Section 8.0 QAP Results and Images .......................................................................... 236
Chapter 25 - EMC Conformance Statement................................................................... 239

Section 1.0 Compliance Statement .............................................................................. 239
Section 2.0 Compatibility Tables ................................................................................. 240
2.1 Electromagnetic Emission............................................................................................................. 240
2.2 Electromagnetic Immunity............................................................................................................ 241
Section 3.0 Use Recommendations .............................................................................. 243
Section 4.0 Installation Recommendations ................................................................. 244
4.1 Cable Shielding & Grounding....................................................................................................... 244
4.2 Subsystem & Accessories Power Supply Distribution ................................................................. 244
4.3 Stacked Components & Equipment .............................................................................................. 244
4.4 Low Frequency Magnetic Field .................................................................................................... 244
4.5 Static Magnetic Field Limits......................................................................................................... 244
4.6 Electrostatic Discharge Environment & Recommendations......................................................... 245
Chapter 26 Integrating the Healthcare Enterprise (IHE) Integration Statement....... 247

Section 1.0 - Introduction ............................................................................................. 247
1.1 Overview ....................................................................................................................................... 247
1.2 Important Remarks....................................................................................................................... 247
Section 2.0 - IHE Integration Statement..................................................................... 248

GE HEALTHCARE 
Chapter 1 - Safety and Service
Section 1.0
Lock-Out & Tag-Out (LOTO)
1.1 System Power
Name Of Equipment: System (Workstation, System Cabinet, Table, U-Arm)
Number Of Locks: One per person, working on the system
Title(s) of Employees Authorized to Perform LOTO: Those trained in Lockout Tagout (LOTO)
Title(s) of Affected Employees and How to Notify: Hospital Personnel; notified by verbal
communication.
Location of Energy Isolating

Energy Source Yes No Magnitude of Energy
Means
Electrical X System’s Main “A1” Power 320 - 480VAC, 3 Phase
Disconnect
Pneumatic X
Hydraulic X
Gas/Water/Steam X
Chemical X
Mechanical Motion X
Gravity X
Springs X
Thermal X
Stored Energy X
Air Under Pressure X
Oil Under Pressure X
Water Under Pressure X
Gas Under Pressure X
Steam X
Other X
Type(s) of Equipment and/or Method(s) Selected to Dissipate or Isolate Stored Energy:
Allow 3 minutes for stored energy to dissipate.
Type(s) of Equipment and/or Method(s) Used to Ensure Disconnection’s:
One Lock & Tag for Main “A1” Disconnect
Chapter 1 - - Safety and Service Page 29

GE HEALTHCARE 
1.2 LOTO Procedure for System Power
Name of Equipment: System (Workstation, System Cabinet, Table, U-Arm)
Step Lockout/Tagout Procedure

1 Prepare for shutdown of equipment by notifying affected personnel working in the area that
lockout/tagout is being performed.
2 Bring system software down. See Section 3.0 on page 32 and return to Step 3
3 Locate main power supply (Service) disconnect feeding System Cabinet.
4 Lock Out / Tag Out the main power disconnect.
5 Using an insulated voltmeter, measure the incoming power connection to the system cabinet at the
circuit breaker.
6 If no voltage is present at the system cabinet’s circuit breaker; place the power switch on the PDU
to the OFF position and service equipment as required.
7 After service has been performed, notify affected personnel that equipment will be re-energized
and LOTO devices are being removed.
8 Assure the safety of the area and that all safety devices and guards have been replaced
9 Return system functions to a preset state.
10 Remove Lock-Out Tag-Out equipment from main disconnect.
11 Locate main power supply (Service) disconnect feeding System Cabinet and re-apply power.
12 Perform system startup. See Energizing System on page 31.
Page 30 Section 1.0 - Lock-Out & Tag-Out (LOTO)

GE HEALTHCARE 
Section 2.0
Applying System Power
2.1 System Preparation for Energizing Power
POTENTIAL PERFORM LOTO BEFORE PERFORMING SERVICE OF ANY KIND. See Section 1.0 on
ELECTRICA page 29.
L SHOCK
Follow the steps below to ensure that your system powers up safely, properly and reliably.
Potential for PDU tap settings must match input voltage else there is potential for equipment damage.
Equipment
Damage
2.2 Energizing System

System power-up is controlled by both hardware and software. When power is applied, power is switched
“ON” to each of the subsystems through hardware. Software in the subsystems boot and begin loading their
operating systems and applications. Complete system startup takes approximately 2 minutes.
1.) Prepare the system for energizing, if required. See System Preparation for Energizing Power on page 31.
2.) Remove tag and lock from facility power. See Section 1.2 on page 30
3.) Press the POWER ON button on the console to initiate system start-up.
Figure 1-1 Console Power On Button
4.) System startup is complete when applications screen is displayed on workstation computer.

GE HEALTHCARE 
Section 3.0
De-Energizing System
Shut down is controlled by both software and hardware. When a shutdown is initiated, application and the
operating software execution is terminated. While this takes place, signals are sent to the PDU to shut-off
system hardware. Complete shutdown takes approximately 1 minute.
1.) From the application interface, using the mouse, click on the tools icon. This selects the Service User
Interface.
2.) Now click on SHUT DOWN.
3.) Now tag and lock out facility power to the system, if you wish to perform service. See Section 1.2 on
page 30.
Section 4.0
Equipment Safety - Electrostatic Discharge (ESD)
A sudden discharge of static electricity from your finger or other conductor can destroy static-sensitive
devices or microcircuitry. Often the spark is neither felt nor heard, but damage occurs. An electronic device
exposed to electrostatic discharge (ESD) might not appear to be affected at all and can work perfectly
throughout a normal cycle. The device can function normally for a while, but it has been degraded in the
internal layers, reducing its life expectancy.
Networks built into many integrated circuits provide some protection, but in many cases, the discharge
contains enough power to alter device parameters or melt silicon junctions.
4.1 Generating Static

The following table shows that:
Page 32 Section 3.0 - De-Energizing System

GE HEALTHCARE 
• Different activities generate different amounts of static electricity.
• Static electricity increases as humidity decreases.
Relative Humidity
Event 55% 40% 10%
Walking across carpet 7,500 V 15,000 V 35,000 V
Walking across vinyl floor 3,000 V 5,000 V 12,000 V
Motions of bench worker 400 V 800 V 6,000 V
Removing bubble pack from PCB 7,000 V 20,000 V 26,500 V
Packing PCBs in foam-lined box 5,000 V 11,000 V 21,000 V
Many electronic components are sensitive to ESD. Circuitry design and structure determine the degree of
sensitivity. The following packaging and grounding precautions are necessary to prevent damage to electric
components and accessories.
• Transport products in static-safe containers, such as tubes, bags, or boxes to avoid hand contact.
• Protect all electrostatic parts and assemblies with conductive or approved containers or packaging.
• Keep electrostatic sensitive parts in their containers until they arrive at static-free stations.
• Place items on a grounded surface before removing them from their container.
• When handling or touching a sensitive component or assembly, ground yourself by touching the chassis.
• Avoid contact with pins, leads, or circuitry.
• Place reusable electrostatic-sensitive parts from assemblies in protective packaging or conductive foam.
4.2 Personal Grounding Methods and Equipment

Use the following equipment to prevent static electricity damage to equipment:
• Wrist straps are flexible straps with a maximum of one-megohm +/- 10% resistance in the ground cords.
To provide a proper ground, wear the strap against bare skin. The ground cord must be connected and
fit snugly into the banana plug connector on the grounding mat or workstation.
• Heel straps, toe straps, and boot straps can be used at standing workstations and are compatible with
most types of shoes or boots. On conductive floors or dissipative floor mats, use them on both feet with
a maximum of one-megohm +/- 10% resistance between the operator and ground.
Static Shielding Protection Levels
Method Voltage
Antistatic plastic 1,500
Carbon-loaded plastic 7,500
Metallized laminate 15,000
4.3 Grounding the Work Area

To prevent static damage of components and parts in the work area:
• Cover the work surface with approved static-dissipative material. Provide a wrist strap connected to the
work surface and properly grounded tools and equipment.
• Use static-dissipative mats, foot straps, or air ionizers to give added protection.
• Handle electrostatic sensitive components, parts, and assemblies by the case or PCB laminate.
• Handle components only at static-free work areas.
• Turn off power and input signals before inserting and removing connectors or test equipment.
• Use fixtures made of static-safe materials when fixtures must directly contact dissipative surfaces.

GE HEALTHCARE 
• Keep work area free of non-conductive materials, such as ordinary plastic assembly aids and Styrofoam.
4.4 Recommended Materials and Equipment

Materials and equipment that are recommended for use in preventing static electricity include:
• Antistatic tape, smocks, aprons, or sleeve protectors
• Conductive bins, foam, tabletop workstations with ground cord of one-megohm +/-10% resistance, and
other assembly or soldering aids.
• Static-dissipative table or floor mats with hard tie to ground
• ESD Field service kits
• Static awareness labels
• Wrist straps and footwear straps providing one-megohm +/-10% resistance
• Material handling packages
- Conductive plastic bags, plastic tubes and tote boxes
- Opaque shielding bags
- Transparent metallized shielding bags and shielding tubes
Page 34 Section 4.0 - Equipment Safety - Electrostatic Discharge (ESD)

GE HEALTHCARE 
Chapter 2 System Component

Figure 2-1 Brivo 515 System Component Identification
3 2 4
7
8
Table 2-1 Component Items for Brivo XR515
Item Component Name Part Number
1 Arm 5420592
2 Collimator XS-1D 5429399
3 Detector 5436666
4 Tube 5331186
5 Console 5429246
6 Cabinet(PDU and Generator) 5429116
7 Workstation 5810000-A
8 Monitor 5414707
9 Stretcher table 5428952
Chapter 2 - System Component Page 35

GE HEALTHCARE 
Page 36 -
GE HEALTHCARE 
Chapter 3 - System Installation Guide

The primary tasks are designed to be performed in sequence. Follow the sequence of tasks describe for each primary task in Section
1.0 that follow.
Section 1.0
Installation
1 Receive and Inventory System People Required: 1 Minutes to Complete: 10

Inventory equipment & report discrepancies immediately.
2 Uncrate, Inventory and move them to room People Required: 2 Minutes to Complete: 60
Collect Product Locator Cards and store in a secure location.
Uncrate and Inventory subbox.
Plan route and transport equipment to room.
2 System cabinet positioning and fix Arm People Required: 2 Minutes to Complete: 10
Take out cabinet to the designed position.
fix and position Arm according to designed position
3 Detector component installation and cable connection People Required:2 Minustes to Complete:55
Take out detector housing from shipping container.
Install detector housing to the U-Arm.
Connect and routing cables
Install ion chambor(optional)
install detector.
install the grid(optional)
Tube and collimator installation and cable

4 connection People Required:2 Minutes to Complete:20
Take out Tube support, tube and collimator from shipping container.
Install the tube support to the U-Arm
Put the tube on the tube support
Connect the collimator to the tube
5 Top Box installation People Required: 2 Minutes to Complete: 10

Take out top box from shipping container.
Install the top box on the top of the U-Arm
Chapter 3 - - System Installation Guide Page 37

GE HEALTHCARE 
(Continued)
6 System Cable Routing and Connection People Required: 2 Minutes to Complete: 20

Connect cables to Cabinet.
7 System console and PC installation People Required: 2 Minutes to Complete: 15

Position and connect Workstation computer, Console and accessories. Including any purchased
equipment (i.e.Bar Code Reader) options.
8 Table unpacking and installation People Required: 2 Minutes to Complete: 20

Unpacking the table box and complete installation
9 System Power on People Required:1 Minutes to Complete: 10
10 Alignment between collimator and detector People Required: 1 Minutes to Complete: 20
12 Configuration and calibration People Required: 1 Minutes to Complete: 20

Configure the equipment
Calibrate the equipment
13 Data backup for restore People Required: 1 Minutes to Complete: 30
14 Function Checks People Required: 1 Minutes to Complete: 30

Do system checks after system configuration and calibration.
15 Final cover installation People Required: 2 Minutes to Complete: 30
If necessary, attach Warning Labels and Rating

16 People Required: 1 Minutes to Complete: 15
Plates
Attach all the warning labels and detent marks.
If your country requires the product rating plate to be in the language of that country, follow the
instructions on document #45474336. Paste the appropriate language label over the English rating plate.
17 Cleanup Site People Required: 1 Minutes to Complete: 20

Remove and dispose of shipping materials and tools properly.
18 Customer Turnover People Required: 1 Minutes to Complete: 10

Complete & Return Product (i.e; Locator) Cards.
Perform general house keeping tasks and turn system over to user.
19 Complete Installation Checklist People Required: 1 Minutes to Complete: 10

Field Engineer to fill out installation checklist at completion of installation.
Page 38 Section 1.0 - Installation

GE HEALTHCARE 
Lead is used in this system to provide required radiation shielding, such as in tube, collimator, please pay
attention and do not touch it directly.
Section 2.0 Installation Checklist

Purpose: Installation checklist to confirm that all critical installation steps have been completed.
Item # Item
1.) Power and ground cables connected and tightened:
Power cables (how many?, where?)
Ground cables (how many?, where?)
2.) All signal cables connected and tightened.
3.) Cable shield clamps installed and tightened (how many?, where?).
4.) All mounting bolts installed and tightened (floor and wall).
5.) Collimator alignments done.
6.) Detector installed and connected.
7.) Control room cables properly dressed.
8.) Correct language decal applied to workstation.
9.) All covers installed.
10.) Room cleaned.
11.) Product locator cards collected.
12.) Missing components and/or options:
13.) List of any installation drawing deviations (all deviations should be signed by customer
and reviewed by the installation specialist).
14.) Packing materials disposed of.
15.) Service Tool returned
16.) Detent marks and labels attached.
17.) Have all calibrations been completed?
18.) Have the sample images been installed on the system?
19.) Have purchased options been installed/enabled/configured?
Chapter 3 - - System Installation Guide Page 39

GE HEALTHCARE 
Item # Item
20.) All appropriate regulatory labels installed:
X-ray tube focal spot
Warning labels
Rating plates
21.) InSite checkout completed?
22.) Have functional checks been completed?
23.) Are all covers installed?
24.) Have all protective tape/coverings been removed?
25.) Are there any cosmetic issues?
26.) Are there any system issues?
27.) Are there any functional limitations?
28.) Has system documentation (paper and CDROM) been given to the customer?
29.) Is the hospital scheduling system (HIS/RIS) configured? Does the modality display
MWL (Modality WorkList) responses successfully?
30.) Are printers configured and printer calibrations done on ALL printers?
31.) Are PACS configured and SMPTE and/or test images pushed to system for successful
display (be sure burn/no burn is properly set for PACS)?
32.) Has local physics inspection been completed. Some states/sites may not allow use of
system for patients until this is done.
33.) Has backup of pristine system been performed? (Patient Data Base as well as total
system backup)
34.) Has Field Engineer completed all checklists:
Installation checklist
Page 40 Section 2.0 - Installation Checklist

GE HEALTHCARE 
Chapter 4 - Before You Begin

Purpose:
Check all the crates appearances, preventive collision labels and preventive tilting labels.
If the center of the preventive collision label is GREEN, it means the system is OK without any collision
during shippment.
If the center of the preventive collision label is RED, it means the system is not OK with collision during
shippment. Please open the crates to check system carefully.
Red
Figure 4-1 Preventive Collision Label
If the center of the preventive tilting label is GREEN, it means the system is OK without any tilting during
shippment.
If the center of the preventive tilting label is RED, it means the system is not OK with tilting during shipment.
Please open the crates to check system carefully.
Green
Figure 4-2 Preventive Tilting Label
Prepare standard service toolkit
Chapter 4 - - Before You Begin Page 41

GE HEALTHCARE 
Page 42 Section 2.0 - Installation Checklist

GE HEALTHCARE 
Chapter 5 - Mechanical Installation and Cable

Connection
Section 1.0
Arm Component
1.1 Unpacking and Positioning
Be careful of injured by the nails.
• Do not discard any packing materials such as envelopes, boxes, bags until all parts are accounted for
against the packing list.
• Check the mechanical conditions and external appearances of all parts for possible damages or missing
items.
• The distribution center or factory must be notified immediately for any damage or shortage of parts.
Note: Take out the Operator and Service Documents and CD. Read Manuals carefully before system installation
and calibration.
Chapter 5 - - Mechanical Installation and Cable Connection Page 43

GE HEALTHCARE 
1.) Loosen the corner protectors on the corner of shipping container.
Figure 5-1 Loosen corner protectors
2.) Remove the top and side of shipping container, and Arm is bound on it. See Figure 5-2.
Page 44 Section 1.0 - Arm Component

GE HEALTHCARE 
Figure 5-2 Table Crate with top and side plate Removed

GE HEALTHCARE 
3.) Remove the protective covering with the scissor.
Figure 5-3 Remove the Protective Covering
4.) Take out the wood fixtures and metal fixtures in the crate.
Figure 5-4 Take Out All the fixtures in the crate
5.) Use the service tool to move the U-Arm to the position.

GE HEALTHCARE 
1.) Open the service tool from packing box.
2.) Relax the cords fixed around the service tool.
3.) Brake the casters and lift up the foldable crane
4.) Remove the bolt and axle from the ring in the transport cart.

GE HEALTHCARE 
5.) Fixed the bar back to the cart.
6.) Remove out the bolts from the cart box to take out the lifting rope

GE HEALTHCARE 
7.) Insert the bolt to the hole in the bottom of the column.
8.) Insert the axle trough the hole in the top of the column.
9.) Set the two ropes crossingly from one side in the bottom bolt to another side in the top
axle

GE HEALTHCARE 
10.) Unfold the foldable crane.
* Screw off the bolt from the crane to put down the carrier and then fix back the bolt
to the axis
carrier
* Draw out the pin and Strench out the lifting hook to the number 3 position.
Pin
11.) Adjust the lifting arm height by hold the bar up and down to lift the U-arm off to the
transport cart.

GE HEALTHCARE 
hold the
bar
12.) Block the bottom of the column to the bar on the cart.
13.) Install the ring to the top of the column
14.) Bundle up the Arm and cart together. put the hook under the cart to avoid scrape.

GE HEALTHCARE 
15.) Push the cart with the U-arm to the position.

16.) Rotate the U-arm away from the center and connect the hook on the lift arm to the ring.
17.) Lift up the column by foldable crane.

* If you don’t need to enter the elevator, please go to the step 19.
* If you need to enter the elevator, please go to the step 18.
18.) When the column is lifted up to 45° off the ground, put up the tripot on the cart to support
up the column.
* Remove the bolt on the column.
Slide
* Remove out the pin on the tripot.

GE HEALTHCARE 
* Put up the tripot and fix it to the column by tightening a bolt with a wrench.
* make the bottom of the column off the ground by the bar across the cart.
* Remove off the foldable crane and push the U-arm into or out of the elevator then.
* When reach to the position, connect the foldable crane to the ring on the column and
put down the tripot.
19.) Using the foldable crane to make the column stand on the position.

GE HEALTHCARE 
20.) Lift up the U-Arm off the ground and rotate the column to front
21.) Pull down the lift arm by screw the knob on the foldable crane to disconnect the crane with
the ring on the column.
Knob
6.) Pull the arm down the ground and return to the front.

GE HEALTHCARE 
Figure 5-5 Position the Arm(Take Brivo XR575 as example)
7.) Move the other crate and take out the system accessories
Figure 5-6 Unpacking System accessories crate.

GE HEALTHCARE 
1.2 Installation
1.) Refer to the room layout in Pre-Installation Manual, confirm the location of the column with Arm.
2.) Move out the two fixed plate from the cart to fix the column with the Arm.
3.) Insert the pin hydrant though the column and install the fixed plate to both side of the column.for
safety concern. For Brivo XR575P, the column cover need to be removed firstly.
fixed plate Pin hydrant
4.) Use a center punch or marking pen to mark the location of the 5 mounting holes at the notch of the
column base.
Figure 5-7 Mark the location

GE HEALTHCARE 
5.) Move the column away from the mounting location.
6.) Use a masonry bit and impact drill to drill four 14mm holes for the anchor bolts, M12 X 150 and
then clean the holes of all dust and chips.
Note: Anchors require a minimum engagement of 110 mm into the concrete. If the floor thickness is less
than 110mm it is recommended that the unit should be secured using a through
bolt method with a reinforcement plate on the back side.
7.) Reposition the column over the position and anchor holes.
8.) Insert and screw the anchor bolts into the four holes. Do not tighten the mounting bolts until
the table has been leveled.
Figure 5-8 Insert the anchor bolts into the holes
Section 2.0 Detector Housing Component

2.1 Unpacking
Remove the protective covering and take out detector housing.
2.2 Installation
1.) Screw off the Lock/Release handle of detector housing from the U-Arm
Figure 5-9 Release handle of detector housing

GE HEALTHCARE 
2.) Insert detector housing to U arm.
Figure 5-10 Insert detector housing to U-Arm
3.) Direct the plate on the detector housing to the detent on U-Arm.
Figure 5-11 Direct to the detent
4.) Install the Lock/Release handle of detector housing
Page 58 Section 2.0 - Detector Housing Component

GE HEALTHCARE 
Figure 5-12 Install the Lock/Release handle of detector housing
5.) Make the detector vertical to the floor by release the handle to rotate the detector housing.
Lock
Release
Figure 5-13 rotate the detector housing
Note: When the detector housing is vertical to the arm, the detent will be in fixed position.
6.) To balance the U-Arm, install the tube support.

GE HEALTHCARE 
Tube support
U-Arm
Figure 5-14 Install Tube Support

GE HEALTHCARE 
2.3 Cable connection
1.) Screw off the back cover of the detector housing.
Figure 5-15 screw off the back cover of detector housing (before)
Figure 5-16 screw off the back cover of detector housing (after)
2.) Open the detector housing front cover.

GE HEALTHCARE 
Figure 5-17 Open the detector housing front cover
3.) Insert cables (5428934, 5428629, 5428859, 5433031) from the back of U-arm into detector
housing.And leave the cables out of the detector housing about600mm.
Figure 5-18 Insert cables into detector housing
4.) Connect cable(5428647) to two fans

GE HEALTHCARE 
Figure 5-19 Connect cables to two electric fans
5.) Connect the receptacle plug(5433031 to Grid-in SW) into the micro switch of grid in/out.
Figure 5-20 Plug in grid in/out switch
6.) Put the cable(5433031 to button) in the wire slot under the detector housing.
Figure 5-21 Cable connection to button
7.) Route the other cables in the detector housing.

GE HEALTHCARE 
Figure 5-22 Cable route
8.) Slide in the Ion chambor with the cable inside the housing firstly.
DO NOT put anything onto the detector rail.

a.) Remove the block on the slide.
Bottom block Up block
Ion chambor slide rail
Figure 5-23 Remove the block on the slide rail
b.) Slide in the ion chambor

GE HEALTHCARE 
Figure 5-24 Slide in the ion chambor
c.) Cable conncection(5437495) to the ion chambor
Figure 5-25 Ion chambor cable connection
d.) Screw off the nuts and fix the ground cables on the U-Arm
e.) Fixed back the blocks in the detector housing.

GE HEALTHCARE 
9.) Install the detector
a.) Unpack the detector package.
Figure 5-26 Detector
b.) Move off the block and relax the four clamps
c.) Slide in the detector

d.) Connect the cables (5428934, 5428629,5428859)
Ground Cable
5428859
Figure 5-27 Cable connection to detector
e.) Mount on the block and fix the four clamps

10.) Slide in the grid to the rail in the detector housing
11.) Install back the front cover and connect the cable (5433031 to button)to handle button.
GE HEALTHCARE 
12.) Connect the cable (5433031 to E-stop)to emergency button on the left cover.
13.) Fix covers with screws.
Figure 5-28 finish detector component installation
14.) Route the cables between the detector housing and U-Arm
15.) Wear the cables sleeve.
Figure 5-29 Route the cables
Section 3.0
X-ray Tube and Collimator
3.1 Unpacking
Be careful of injured by the nails.
• Do not discard any packing materials such as envelopes, boxes, bags until all parts are accounted for
against the packing list.
• Check the mechanical conditions and external appearances of all parts for possible damages or missing
items.
• The distribution center or factory must be notified immediately of any damage or shortage of parts.
1.) Loosen the screws on the tube arm, install the tube fork into it, and screw it tightly. And mount the cable

GE HEALTHCARE 
supporting plate. See Figure 5-30.
Figure 5-30 Loosen Fibulaes and Remove Crate
2.) Loosen the screws of the upper clamp of tube fork, and remove the upper clamp of tube fork.
Figure 5-31 Remove the upper clamp of tube fork
3.) Take out X-ray tube from the box.

GE HEALTHCARE 
Figure 5-32 Take out the Tube from the box
3.2 Installation
1.) Put the tube on the tube support.
Figure 5-33 Put the tube on the tube support
Notice the tube installation direction. If the direction is wrong, the tube focal spot will be
inaccurate, and the tube may be falling down if the clamps are loose.
Hold the tube to prevent it from falling down.

2.) Relax the climps beside the fland and remove the flank from the collimator.
Note: Don’t relax the climps off the collimator, just remain it on the collimator for next reinstallation.

GE HEALTHCARE 
Figure 5-34 Remove the flank from the collimator
3.) Install the flank to fix the tube.
At the bottom of the tube support
Figure 5-35 Fix X-ray Tube
4.) Rotate the tube support 180 degrees to make the flank up.
Figure 5-36 Rotate Tube Support 180 Degrees

GE HEALTHCARE 
5.) Mount collimator onto the collimator flange using the two stop plates.
Note: In order to securely mount the collimator, please add Loctite 242 to the screws on the stop plates.
Figure 5-37 Mount Collimator
6.) Rotate tube support back.

7.) Install the Cable support on tube support.

GE HEALTHCARE 
Figure 5-38 cable support on tube support
8.) Install the other cable support on the Arm
Figure 5-39 cable support on the Arm

GE HEALTHCARE 
3.3 Cable connection
1.) Remove the cable support cover.
Figure 5-40 Remove the cable support cover
2.) Route the cable(5428663,5428666,5428637) through cable support to the tube side.
Figure 5-41 route cables through cable support
3.) Prior to the connection of the high-voltage cables, remove the old silicone compound on the plug
surfaces with clean dry cloth and check to verify there are as cracks, flaws, or traces of creeping
discharge on the surfaces.
Note: When the traces of creeping discharge are found, be sure to replace the defective parts. (Grinding off the
traces only will not be effective.)
4.) Coat the tip of the cable plugs with the silicone compound about five to seven grams, that is, to the extent
the tip is hidden under the heaped up compound. At this time, the side of the cable plug should not be
greased.

GE HEALTHCARE 
Figure 5-42 Coating with Silicone Compound
5.) Remove the cap covered the socket of the tube housing and wipe the inside softly with a clean dry cloth.
DO NOT use any chlorinated solvents to clean any parts.
6.) Connect the anode and cathode HV cables (2269002-5) to the X-ray tube.
HV Cable Socket HV Cable

+ (ANODE) +
- (CATHODE) -
Check the polarity of HV cables carefully, and DO NOT connect the two HV cables reversedly.
Connect the HV cables in the correct polarity with sufficient care not to produce clearance
between the cable plug flange and the cable socket at the insertion of the plugs. Presence of such
clearance or incomplete silicone compound coating will cause creeping discharge and normal
operation of tube will be disturbed.
Figure 5-43 Inserting Cable Plug
7.) Tighten the high-voltage cables solidly to the sockets of the tube housing by the threaded cable flange.

GE HEALTHCARE 
The elapse of time and repeated temperature rise of the tube housing may loosen the fastening portion,
it is necessary to fulfill periodical checking and retightening of the fastening after the initiation of the
operation of the X-ray tube. As a periodical maintenance means, the high-voltage plugs and sockets
must be regreased in each period shorter than a year. When regreasing, the operation should be repeated
from the foregoing item 7).
8.) Demount the tube cover on Anode side.
Figure 5-44 Demount Tube Cover
9.) Connect the anode rotation cable (5428666).

Note: Fix the cable with clamp.
Figure 5-45 Anode Rotation Cable Conections
Tube HV Tank Color

1 C White
2 M Black
3 A Red
SW SW Brown
SW SW Yellow
E E Green

GE HEALTHCARE 
10.) Install the HV cables(5393036) to the anode side and cathode side
Figure 5-46 Install Cables to Anode side and Cathode side
11.) Remount the tube cover.

12.) Connect the cable(5428637 to button ) to handle button on tube side .

GE HEALTHCARE 
Note: Don’t make the

cable go through the
axis of the tube
support.
Figure 5-47 Cable connection from spine board to tube side button.
13.) Connect collimator power cable(5428663).
Figure 5-48 connect collimator power cable
14.) Route the cables and package the cable sleeves.

GE HEALTHCARE 
Figure 5-49 Route the cables on tube support
Section 4.0 Top Box

4.1 Unpacking
Remove the protective covering and take out top box.
Figure 5-50 Top Box
Page 78 Section 4.0 - Top Box

GE HEALTHCARE 
4.2 Installation
1.) Install the top box to the top of the U-arm column
Figure 5-51 Install the top box to U-arm column
4.3 Cable Connection

1.) Connect the cable (5447187) to brake on topbox.
2.) Install the cable support to the top box.
Figure 5-52 Install the cable support

GE HEALTHCARE 
3.) Route the cables onto the cable support, open the top box cover
4.) Install the cable clip.Make the cables (5428931,5428934,5428631,5428663,5428665) pass
across the clip and plug them into the related interface.
Cable clip
ground cable 5428665
Figure 5-53 Cable Connection on Top Box
5.) Moute on the top box cover
Page 80 Section 4.0 - Top Box

GE HEALTHCARE 
Figure 5-54 Moute on the top box cover
6.) Route the cables and package the cable sleeve.
Figure 5-55 Take Brivo XR575 as an example
Section 5.0
Cabinet Electrical Connections
For details, please refer to System Schematics and Drawings in Service Manual and Pre-Installation Manual.
Note: The handle on each side of the cabinet only used to lift off the cover. Don’t move the cabinet by the
two handles.

GE HEALTHCARE 
1.) Connect and route System Power Cable and Grounding cable.(hospital provide).
Figure 5-56 Connect and Route System Power Cable
2.) Connect and route cables to Jedi.
Page 82 Section 5.0 - Cabinet Electrical Connections

GE HEALTHCARE 
HV cable 5393036
Jedi X-ray On
Lmp Cable
5432235
IF board to Jedi
Cable 5428664
Ion Chambor(AEC1)
cable 5437495
Tube Rotator
cable 5428666
Figure 5-57 Connect and Route Cables to Jedi
3.) Connect and route cable to PDU

GE HEALTHCARE 
IF Board:
IF powercable to PDU
5428661,
IF board to Jedi
able 5428664,
IF board to Spine
board cable 5428632,
IF board to PC RS232
,
cable 5428628.
IF broad to Console
cable 5428630,
Room-door open switch
cable 5432234
J2+J3:
PC power cable 5428622
J1:U-Arm power cable

5428631
J4:IF power cable

5428661
Room-door open switch

cable 5432234
Jedi X-ray lamp On

cable 5432235
Figure 5-58 Connect and route cable to PDU
4.) Ground cable(5478018) between PDU to PC
Page 84 Section 5.0 - Cabinet Electrical Connections

GE HEALTHCARE 
Chapter 6 - Workstation
Section 1.0
Computer
1.) Placement
2.) Connections(USB/PS2)
5428622
5428628
5428629
cable connected to
monitor
Figure 6-1 Magic PC Connections
Section 2.0
Mouse and Keyboard
1.) Placement
2.) Connections (USB/PS2)
Chapter 6 - - Workstation Page 85

GE HEALTHCARE 
Section 3.0
Console & Handswitch
1.) Placement
2.) Connect IF (System Cabinet) to console(cable 5428630).
3.) Connect Handswitch to console.
Figure 6-2 Console component
IF to Console cable Handswitch cable

5428630
Figure 6-3 Console cables connection
Section 4.0
LCD Monitor
1.) Placement
2.) Connections
a.) Video (DVI)
b.) Power & Ground
Page 86 Section 3.0 - Console & Handswitch

GE HEALTHCARE 
Section 5.0
Bar Code Reader (Purchased Option)
1.) Placement
2.) Connections
Chapter 6 - - Workstation Page 87

GE HEALTHCARE 
Section 6.0
Workstation Cable Connections
Part No. Description Workstation TO References
5428628 PC RS232 cable Magic Com port System IF See Figure 6-1
5428629 PC ethernet cable Magic PC Gb-E Detector See Figure 6-1
card
5428622 Image Monitor power Cable Monitor PDU J2 See Figure 6-1
5428622 Magic PC power cable Magic PC PDU J3 See Figure 6-1
Table 6-1 Workstation to Wall Box
Page 88 Section 6.0 - Workstation Cable Connections

GE HEALTHCARE 
Chapter 7 Table Installation
Section 1.0 Unpacking

1.) Screw off the bolt on top cover of the table box.
Figure 7-1 Unpacking the package of table
2.) Take out all of the table accessories
Figure 7-2 take out table accesories
Chapter 7 - Table Installation Page 89

GE HEALTHCARE 
Section 2.0 Installation

1.) Install the two side brackets on the table top
Figure 7-3 install the table
Page 90 Section 1.0 - Unpacking

GE HEALTHCARE 
Chapter 8 - Alignment between Collimator and

Detector
1.) Power up the system. Check LEDs status.
2.) Open collimator light, confirm the center of the light field projected by the collimator with an article,
such as a screw.
Figure 8-1 Shortest SID
3.) Rotate the Arm to horizontal position. Adjust the SID from 100mm to 180mm to make judge.
Figure 8-2 Longest SID
4.) Make sure the bias of the center is less than 5 mm, and make sure the collimator beam can align the
center point of the detector mark.
Chapter 8 - - Alignment between Collimator and Detector Page 91

GE HEALTHCARE 
Figure 8-3 Collimator Beam Align Detector Center Point
5.) If the requirements above cannot be met, adjust the four screws on the tube fork and insert iron plates
into the tube support to align the collimator.
1.) When all position between 180mm and 100 mm are up or down, adjust four screws of
number 1 as illustrated in Figure 8-4 Align Collimator
2.) When the position is tilt left or right, adjust four screws of number 2 as illustrated in Figure
8-4 Align Collimator
3.) When the position is tilt up or down, relax two screws of number 3 as illustrated in Figure
8-4 Align Collimator,screw the two little bolts of number 4 as illustrated in Figure 8-4 Align
Collimator

GE HEALTHCARE 
1 3
Notch
the position
of wo little
4 olts
Figure 8-4 Align Collimator
6.) Rotate the Arm to 90 degree and conduct collimator alignment under above way.
Chapter 8 - - Alignment between Collimator and Detector Page 93

GE HEALTHCARE 

GE HEALTHCARE 
Chapter 9 - Column Cover Installation
Section 1.0 Unpack Column Covers
Section 2.0 Install Column covers

1.) Relax the three screws on the top of the column to fix the cover.
Figure 9-1 Relax the screws to fix the top cover
2.) Mount on the top cover on it with the three screws. And cover the top plate to it.
top plate
Figure 9-2 top cover installation
Chapter 9 - - Column Cover Installation Page 95

GE HEALTHCARE 
Page 96 Section 1.0 - Unpack Column Covers

GE HEALTHCARE 
Chapter 10Column Support Installation

Purpose: Enhanced fix the column and U-arm to ceiling or wall with either plate enclosed with
package.
1.) Take out the plates from the package. One choice is for connection to ceiling and the other is
for connection to wall.
2.) Install the plate to the topbox.
3.) Use a masonry bit and impact drill to drill six 12mm holes for the anchor bolts, M10 X 100.
Note: Anchors require a minimum engagement of 120 mm into the concrete. If the ceiling or wall
thickness is less than 120mm, it is recommended that the unit should be secured using a through
bolt method with a reinforcement plate on the back side.
Figure 10-1 Connection to ceiling
Figure 10-2 Connection to wall
Chapter 10 - Column Support Installation Page 97

GE HEALTHCARE 
Page 98 Section 1.0 - Unpack Column Covers

GE HEALTHCARE 
Chapter 11 - System Check
Section 1.0 Operational Checks

This section is used to perform the check the mechanical movement.
1.1 U-Arm Longitudinal Movement

• Pressing the Up/Down movement button moving the U-Arm Check the longitudinal movement is
operating smoothly and uniformly
• Release the button, check the housing is locked.
1.2 Positioner SID Adjustment

• Pressing the SID movement button moving the detector housing and tube component. The
positioner shall have a SID range from 1000mm to 1800mm.
• Release the button, check the housing is locked.
1.3 Tube Rotation

Release the lock and hold the operation handle to drive the tube component to the left or to the right for
rotation. Check the Tube component can be rotated not less than +45 degree~ -240
degrees.
1.4 Detector Housing Rotation

Release the lock and hold the operation handle to drive the tube component to the left or to the right for
rotation. Check the Tube component can be rotated not less than +45 degree~
-45 degrees.
1.5 Collimator Rotation

1.) Loosen set screw.
2.) Rotate the collimator.
3.) Check the collimator can be rotated.
4.) Secure set screw
Section 2.0 Functional Checks

2.1 Image quality test
1.) Go to SUIF according to the instruction described above. Then press the “Image Quality” button on the
SUIF.
2.) Then press "Image control tools" to do the QAP. There will be the detail instruction on the
Chapter 11 - - System Check Page 99

GE HEALTHCARE 
screen for each step. The system will tell operator the pass or failed.
3.) Wait until the test result displayed.
Make sure all the items pass the test.
2.2 Image artifact check (Optional)

Please follow below steps to check if there any image artifact may impact clinical diagnostics.
1.) Set exposure mode and technique as: Digital cassette receptor; SF; 80kV; 200mA; Detector position,
SID and FOV same as Digital cassette calibration setup. Insert 20mm Aluminum phantom (5270546)
into the tray on collimator.
2.) Set exposure time to 5ms, and take exposure. After exposure is done, view Raw Image to adjust contrast
to 98% and set brightness to visible level. Zoom the image to 1, pan cross the whole image to observe
the image to make sure there is not any visible artifact.
3.) Set exposure time to 32ms, and take exposure. After exposure is done, view Raw Image to adjust
contrast to 98% and set brightness to visible level. Zoom the image to 1, pan cross the whole image to
observe the image to make sure there is not any visible artifact.
4.) Set exposure time to 80ms, and take exposure. After exposure is done, view Raw Image to adjust
contrast to 98% and set brightness to visible level. Zoom the image to 1, pan cross the whole image to
observe the image to make sure there is not any visible artifact.
The detector calibration can be passed if this check is ok. Otherwise, it needs to redo detector calibration or
mark the bad line.
2.3 Acqisition Test
2.3.1 Digital Wallstand Mode Test

Create a new patient. Select “chest” exam. Select Digital Wallstand receptor, AEC mode. Insert detector into
Wallstand housing. Align the tube to detector. Open a suitable FOV. Check if there no exposure inhibit
displayed.
Press handle switch do an exposure. Check if it can stop exposure automatically by AEC.
Verify it can get a uniform image and this image is cut automatically according collimator FOV.
Draw out detector. Verify the exposure inhibit displayed and it can’t do exposure.
Close the exam.
2.3.2 Digital Table Mode Test

Create a new patient. Select “abdomen” exam. Select Digital Table receptor, AEC mode. Insert detector into
Table housing. Align the tube to detector. Open a suitable FOV. Check if there no exposure inhibit displayed.
Press handle switch do an exposure. Check if it can stop exposure automatically.
Draw out detector. Verify the exposure inhibit displayed and it can’t do exposure.
Close the exam.
2.3.3 Digital Cassette Mode Test

Create a new patient. Select “Hand” exam. Select Digital Cassette receptor, Fix mode. Place the detector on
tabletop. Align the tube to detector. Open a suitable FOV. Check if there no exposure inhibit displayed.
Press handle switch do an exposure. Check if it can stop exposure automatically.
Insert detector into table housing. Verify the exposure inhibit displayed and it can’t do exposure.
Close the exam.
Page 100 Section 2.0 - Functional Checks

GE HEALTHCARE 
Chapter 12 - Labels and Rating Plates

Product identification labels can be found on the tops and sides of the cabinets, the rear of
monitors, and other exterior surfaces on the equipment. The types of system identification
compliance plates are located in below table?Contact service personnel if you can not find
these plates.
Chapter 12 - - Labels and Rating Plates Page 101

GE HEALTHCARE 

GE HEALTHCARE 
Chapter 13 - Installation Checklist

Purpose: Installation checklist to confirm that all critical installation steps have been completed.
Item # Item
1.) Power and ground cables connected and tightened:

• Power cables (how many, where)
• Ground cables (how many, where)
2.) All signal cables connected and tightened.
3.) Cable shield clamps installed and tightened (how many, where).
4.) All mounting bolts installed and tightened (floor and wall).
5.) Mechanical alignments done.
6.) Control room cables properly dressed.
7.) All covers installed.
8.) Room cleaned.
9.) Product locator cards collected.
10.) Missing components and/or options:
11.) List of any installation drawing deviations (all deviations should

be signed by customer).
12.) Packing materials disposed of.
13.) Dollies and crates returned:

• Positioner Table / Standard Wall Stand dolly
14.) Have all calibrations been completed?
15.) Have the sample images been installed on the system?
16.) Have purchased options been installed/enabled/configured?
17.) Have System backup done?
18.) All appropriate regulatory labels installed:

• X-ray tube focal spot
19.) Have functional checks been completed?
20.) Are all covers installed?
21.) Have all protective tape/coverings been removed?
Table 13-1 Installation Checklist
Chapter 13 - - Installation Checklist Page 103

GE HEALTHCARE 
Item # Item
22.) Are there any cosmetic issues?
23.) Are there any system issues?
24.) Are there any functional limitations?
25.) Has system documentation (paper) been given to the customer?
26.) Has local physics inspection been completed? (some states/sites

may not allow use of system for patients until this is done)
27.) Has backup of pristine system been performed? (Patient Data

Base as well as total system backup)
28.) Field engineer has completed all checklists:

• Pre-Installation
• Installation checklist
Table 13-1 Installation Checklist

GE HEALTHCARE 
Chapter 14 - Final Steps
Section 1.0 Final Installation and Admin Tasks

1.) Ready system for normal customer operation.
2.) Install all covers on system equipment. (Refer to above for procedure.)
3.) Remove trash, remove installation equipment and tools, clean up room and store service manuals.
4.) Fill out and return the Product Locator Cards or complete in eGIB.
5.) Record installation time in Service database.
Chapter 14 - - Final Steps Page 105

GE HEALTHCARE 
Page 106 Section 1.0 - Final Installation and Admin Tasks

GE HEALTHCARE 
Chapter 15 - Counterweight
Purpose: The counterweight has been finished before delivery. It usually don’t need to do
this step in fields. Just in case the equipment can’t keep level , adjust the weight of either
side of the Arm and the back of the column under the instructions in this chapter to balance
the equipment.
1.) If the Arm can’t be level in 0°, add or reduce the counterweights in either side of the Arm.
counterweight
counterweight
2.) If the column tilts foreward or backward, move the Arm to top position, open the counterweight
cover on the back of the column, add or reduce the counterweights.
Chapter 15 - - Counterweight Page 107

GE HEALTHCARE 

GE HEALTHCARE 
Chapter 15 - - Counterweight Page 109

GE HEALTHCARE 

GE HEALTHCARE 
DIRECTION 5429484 -CA-1EN, RIVISION 1 ILLUSTRATED PARTS LIST
Chapter 16 - Illustrated Renewal Parts
Section 1.0 Illustrated Renewal parts

Note: If any brake is replaced, please use electric iron to seal the cable.
.
1.1 Service Tool
Part Number Detailed Part Description Quantity
5440377 Galaxy Svc Tool 1
1.2 Table
5456538 CASTOR 4
5457304 Tabletop 1
Chapter 16 - Illustrated Renewal Parts Page 111

GE HEALTHCARE 
5456538 5457304
1.3 Image Chain
5436666 SUPER VALUE RAD 1
5136302 Lamp, 24V 1
5331186 Vamana SVRAD Tube Assembly 1
5429399 Chongqing Hualun XS-1D collimator 1
5429402 Galaxy 40lp grid with frame 1
5429405 Galaxy 70lp grid with frame 1
5270546 20mm Al phantom for Pioneer DR 1
5167409 AID Ion Chamber 1
Page 112 Section 1.0 Illustrated Renewal parts

GE HEALTHCARE 
5136302 5429402/5429405 5270546
5429399 5331186 5167409
1.4 Control Room
5429246 TM:Terminal for exposure handswitch and 1

power on
5439061 Hand switch with RoHs compliance 1
5448740 Handle Switch Support Assembly 1
5417444 FRU 19 Inch VA Medical Color Monitor 1
5810000-4 DVD+/-R/RW/ROM SuperMulti Optical 1

Drive
5810000-8 Single Socket PC 475W Power Supply 1

(Section 4.3)
5810000-10 Single Port Gigabit Ethernet PCI-e Card 1

per Section 7.3
5810000-A GDXR Console Workstation XR Super 1

Value DR
5810000-D 250GB SATA 10K RPM 512e/AF HDD 1

GE HEALTHCARE 
5429246 5439061
5448740
1.5 PDU
5224265 Relay MY2J 24VDC 1
5435232 Transformer 1100VA 1
5435234 Power supply 24W 1
5435236 Relay LY4-D 1
5393006 3P Breaker DZ47 1
5443099 Galaxy PDU fuse kit 1
5443496 Insulation board assembly 1
5393007 Contactor CJX2 5011 1
5428661 IF power cable 1
5428664 IF-Jedi cable 1
5432234 IF room-door open switch cable 1
5432235 Jedi x-ray on lamp cable 1
5429135 Galaxy interface board with firmware 1

GE HEALTHCARE 
5393037
5435234
5393036
5224265
5435236
5443099
5398369
5435232 5443496
1.5.1 MIS Cable
5428622 PC power cable 2
5428628 PC RS232 cable 1
5428630 IF-TM cable 1
1.5.2 U-Arm
021-0144 Pioneer program need PSP Document 8

GB-T276 608-2Z
Bearing
5224265 Relay MY2J 24VDC 1

GE HEALTHCARE 
5393036 WanBo HV cable 12m 2
5394097 Power supply for URP detector 1
5428629 PC ethernet cable 1
5428631 U-ARM power cable 1
5428632 IF Spine cable 1
5428635 Vertical POT cable 1
5428637 Tube-side button cable 1
5428639 SID POT cable 1
5428645 Vertical lock and limit switch cable 1
5428647 Detector fan cable 1
5428663 Collimator power cable 1
5428665 U-ARM main PE cable 1
5428666 Tube rotator cable 1
5428769 Detector fan and lead cable 1
5428858 Handle tansfer cable 1
5428859 Detector housing GND 1
5428931 Spine power cable 1
5428934 Detector power cable 1
5429135 Galaxy interface board with firmware 1
5430959 U1 handle membrane 1
5430961 Spine PWA with Firmware 1
5432235 Jedi x-ray on lamp cable 1
5433031 Detector housing signal cable 1
5435322 Encoder connection cable 1
5435324 rotation lock cable 1
5435327 estop button and lead cable 1
5437495 Ion chamber cable for galaxy 1
5439843 Lock Handle 1
5439844 Spring 1
5443085 Steel rope 2

GE HEALTHCARE 
5444677 Spring 1
5445505 Cable sleeves 1
5445536 gear cover top 1
5446298 Chin rest and frame 1
5446299 power supply of 150w 1
5447915 Brake 1
5447916 patient barrier 1
5448732 Lock Handle 1
5448734 Limit switch, Galaxy 2
5452377 Brake on Arm 1
5452378 V3M11-Tube Handle 1
5452427 gear cover down 1
5453213 Brake on top box 1
5453214 V3M21-Tube Handle 1
5456202 grid detent
5457298 Bearing 8
5458080 safe lock 1
5458806 Grid-in switch used in Galaxy 1
5458808 Handle 1
5459299 The spring of U-arm rotation detent. 1
5461879 Detector housing left part 1
5447187 Manual U-ARM Vertical lock cable 1
5444763 angle meter cover 1

GE HEALTHCARE 
5430961
5443085
5458806
5446298
5444677 5458808
5448732
5439843

GE HEALTHCARE 
5447916 5447915
5435327
5461879
5445536 5430959
5452427
5453214 5452378 5429135

GE HEALTHCARE 
5444763
5428769
5452377
5394097
5453213
5456202
5446299

GE HEALTHCARE 
5459299
5458807
5443085
5458080
5439844
1.5.3 JEDI Generator

Refer to section 1.6.2 JEDI Generator Renewal Parts List.
1.6 JEDI Generator Renewal Parts
1.6.1 Introduction
This Section provides information for the identification of Renewal Parts for the JEDI 50 R 1T
generator.
1.6.2 JEDI Generator Renewal Parts List
Part No. Description Quantity

/Unit
2202419 I/F RAD - AEC cable (option) 1
2214527 JEDI STD HV TANK (SPARE) 1

2217057 FIRST AID SPARES 1

GE HEALTHCARE 
5119911 AEC board 1
5392132-2 PROGRAMMED ROTATION BOARD 5.07 1
5126988-2 LVPS 3PH V5_FRU 1

5126989 INVERTER MID POWER ASSY_FRU 1
5436156 PROGRAMMED KV CONTROL BOARD P5.47 5,59 1
5126997 AC-DC 3PH MID POWER ASSY_FRU 1

5126999 EMC FILTER TRI V2B_FRU 1
2184567-4 RAD I/F Board 1
2409047 FILAMENT BOARD 1 INVERTER V3.01 1

99185290 Fuse 15A 1
2121569 Power bridge 1

2200700 Inverter Coils Mid Power Assy 1
2159419 Non-Volatile parameters RAM 1
2208000 Assy AEC cable 1

2198191 KV Measure - KV Control cable 1
2215903 ROT / LVPS / Heater cable 1
5133341 CAPA INVERTER ASSY 2

2202418 KV control - I/F RAD cable 1
2221983 CAN cable 1
2198185 KV Measure - Gate Command cable 1

2214511 System cable 1
1.6.3 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.
When need to replace the part, please use the standard usual tools.

GE HEALTHCARE 
FRU name
Inverter PW Assembly
2187001 Part number for
 Inverter Capa Assembly ordering
2203900
Notes. These may include:

Items shown in this way are Reference to an illustration with more information
included in the FRU shown Reference to a relevant Disassembly/Reassembly
immediately above, but may also be Job Card Items included with the FRU etc.
ordered separately.

GE HEALTHCARE 

GE HEALTHCARE 
Chapter 17 Part Replacement

Note: After the replacement of all part configured in U-Arm, Calibration execution is necessary.
Section 1.0Detector replacement

1.) Removal
1.) System Power Off
> Shut down the system.
> Switch off the PDU and Conduct LOTO.
> Position the detector component to an appropriate position convenient for
uninstalling the left part of detector housing(5461879) and detector.
2.) Uninstall the detector
> Insert the pin hydrant through the column and install the fixed plate for safety concern.
For Brivo XR575P, the column cover need to be removed firstly.
> Uninstall the back cover of the detector housing and relax the four clips.
> Uninstall the left part of detector housing, and disconnect the E-stop cable.
Chapter 17 Part Replacement Page 125

GE HEALTHCARE 
Figure 17-1 Uninstall the left part of the detector housing
> Disconnect the cables connected with detector(5428934, 5428629, 5428859)

> Remove the block on the slide
> Now you can remove the old detector.
2.) Reinstall the new detector.
1.) Reinstall the new detector according to the Chapter 5 - Mechanical Installation and
Cable Connection -Section 2.0 Detector Housing Component
2.) Install the left part of the detector housing and connect the E-stop cable.
3.) Remove LOTO and energize the system.
4.) Clean the site.
Section 2.0Grid-in Switch in Detector Housing

1.) Removal
> Position the detector component to an appropriate position convenient for
uninstalling patient barrier(5447916) on detector housing.
2.) Uninstall the Grid-in Switch
> Insert the pin hydrant though the column and install the fixed plate for safety concern.
For Brivo XR575P, the column cover need to be removed firstly.
Page 126 Section 1.0 Detector replacement

GE HEALTHCARE 
> Remove the patient barrier on detector housing.
> Put out the receptable plug from the Grid-in switch.
> Remove the Grid-in switch on detector housing.
2.) Reinstall the new Grid-in switch.
1.) Reinstall the new Grid-in switch to the detector housing.
2.) Connect the receptable plug to the Grid-in switch.
3.) Put back the patient barrier to the detector housing.
5.) Clean the site.
Section 3.0Grid Detent Replacement

1.) Removal

GE HEALTHCARE 
> Position the detector housing to an appropriate position
2.) Uninstall the Grid detent.
> Remove the plate with handle on the housing
> Remove the top plate on the housing
> Disclose the grid detent and screw off it from the housing
2.) Reinstall the new grid detent.

1.) Reinstall the new grid detent to the detector housing.
2.) Put back the plates to the detector housing.
4.) Clean the site.
Section 4.0X-Ray Tube/Collimator replacement

1.) Removal
> Position the tube to an appropriate position convenient for uninstalling the tube and
collimator. To see the details, please refer to theChapter 5 - Mechanical
Installation and Cable Connection-Section 3.0 X-ray Tube and Collimator
2.) Uninstall the tube
> Uninstall all the tube cover.
> Remove the tube cover on anode side and disconnected the anode rotation cable
(5428666)

GE HEALTHCARE 
> Disconnect the HV cables.
> Rotate the tube 180 degrees.
> Loosen the two collimator stop plates and remove the collimator. Refer to the
Chapter 5 - Mechanical Installation and Cable Connection-Section 3.0 X-ray
Tube and Collimator
> Now you can remove the old tube.
2.) Reinstall the new tube and collimator
1.) Reinstall the new tube and collimator according to the Chapter 5 - Mechanical Installation
and Cable Connection-Section 3.0 X-ray Tube and Collimator
2.) Install the tube cover.
4.) Clean the site.
Section 5.0Detector Power Supply Replacement

1.) Removal
1.) Shut down the system.
2.) Switch off the PDU and Conduct LOTO.
3.) Seperate the single topbox from the top plate.
4.) Screw off the cables connected in the power supply.
5.) screw off the supply from the box.
2.) Reinstall
1.) Install the new power supply
2.) Install back the topbox
4.) Clean the site.

GE HEALTHCARE 
Section 6.0150w Power Supply
1.) Removal
3.) Seperate the single topbox from the top plate.
4.) Screw off the cables connected in the power supply.
5.) screw off the supply from the box.
2.) Reinstall
1.) Install the new power supply
2.) Install back the topbox
4.) Clean the site.
Section 7.0Spine PCB board Replacement(5430961)

1.) Removal
1.) Move the detector housing to the end of the Arm.
4.) Remove the back cover of the Arm in detector housing side.
5.) Screw off the spine board.

GE HEALTHCARE 
2.) Reinstall
1.) Install the new board
2.) Install back the cover
4.) Clean the site.
Section 8.0Spring on Tube Support Replacement

1.) Removal
3.) Insert the pin hydrant though the column and install the fixed plate for safety concern.
4.) Tied up a cable tie around the spring

GE HEALTHCARE 
5.) Draw off the spring by pliers

2.) Reinstall
1.) Install the new spring
2.) Tied up a cable tie around the spring
3.) Hold the cable tie by plier and draw the spring to the handle under the same way.
5.) Clean the site.
Section 9.0PDU Unit Replacement

1.) Removal
3.) Uninstall the PDU
> Demount PDU cover.
> Disconnect the cables connected on the PDU IF board and remove the IF board.
> Disconnect the system power cable and groud cable.
> Disconnect the Door Light connection beween PDU and Jedi.
> Disconnect Door interlock Cable between PDU and IF board.
> Remove old PDU from the tray by remove the fix screws.
2.) Install
1.) PDU Install
> Demount PDU cover.
> Install the PDU IF board on the new PDU.
> Connect the cables to the IF board according to Chapter 5 - Mechanical
Installation and Cable Connection-Section 5.0 Cabinet Electrical Connections
> Connect and route System Power Cable according to Chapter 5 - Mechanical
> Connect and route the Door Light connection at PDU according to Chapter 5 -
Mechanical Installation and Cable Connection-Section 5.0 Cabinet Electrical
Connections
> Connect and route Door interlock Cables according to Chapter 5 - Mechanical

GE HEALTHCARE 
> Install the PDU cover.
Section 10.0Collimator Lamp (5136302) Replacement

3.) Loose the fix knob, and rotate the collimator to the location which is convenient for operation
4.) Demount the back cover with screws.
Figure 17-2 Collimator Lamp Uninstallation
5.) Replace the collimator lamp.

6.) Remount back cover, rotate collimator back, and tighten the fix knob.
Note: The collimator uses a special Collimator lamp.When the collimator lamp burns out it MUST be
replaced with the replacement lamp listed in the renewal parts section. Part number 5136302 MUST
be used as a replacement lamp. DO NOT use any other lamp as a replacement bulb as X-ray field
to Light field alignment may not meet HHS requirements.

GE HEALTHCARE 

GE HEALTHCARE
DIRECTION 5429484 -CA-1EN, REVISION 1 SOFTWARE INSTALLATIONT
Chapter 18 System Data Backup and Restore
Potential for Data Loss. Archive all protocols, patient files, and backup calibration and
configuration data. It's recommended that a system backup be performed prior to any
installation, upgrade or restoration of software. The installation of software can destroy
existing files, including patient, calibration and configuration files. You might have to
configure and calibrate your system, if you do not have a good backup to restore!
Purpose: Files within the workstation PC and other subsystems need to be saved, if system
software is reload, upgraded or becomes corrupt. After system installation or in the event a
subsystem failure occurs, saved files can be restored in their original condition and location.
Section 1.0 System Backup’s Coverage

The following data is part of a system backup:
1.) All Calibration Files
2.) All Configuration Files.
3.) System Error Log
4.) Image Quality Results
5.) Custom Looks
6.) DICOM Printers/Preferences/Network Configurations.
The following data is not included in a system backup:
1.) Archival of Image Data - The process for archiving image data is found in the operators
manual.
2.) Procedure Protocols - You only need to save the protocol data base (dBase) if you have
made changes to the default values. Defaults are always loaded during an SW
installation. The default protocol dBase is included with each system shipped. See the
Chapter 18 - System Data Backup and Restore Page 135

GE HEALTHCARE 
operators manual for procedures.
Note: The Repeat Reject Analysis Data will not be saved with the System backup. Use the RRA Reporting
Tool to export Repeat Reject Analysis Data if desired.
Section 2.0 Backup

2.1 Before You Begin
The backup utility is used to create a copy of system files, which are stored in various places
(subsystems and directories).
- Workstation PC
- Generator (Jedi)
2.2 Procedure1
1.) From the application desktop, click on the Service Tools icon.
2.) Click on [Launch] button.
3.) Select the Utilities Tab.
4.) Click on the plus sign preceding the System folder ICON, in the navigation frame.
5.) Click on Backup link.
6.) Insert your “Backup” CD into the CD/DVD drive.

7.) Select the media type by clicking on one of the media type buttons.
1.
Page 136 Section 1.0 - System Backup’s Coverage

GE HEALTHCARE
8.) Click on [START].
- To cancel and return to the Tools main screen, press [STOP]
Note: USB Backup cannot be stopped and do not remove USB drive during Backup.
9.) When backup is complete, you will see “System backup success" in the status bar.
10.) Remove and label CD((include current date and time)).
11.) Exit SUIF
Section 3.0 Restore

• After the OS Configuration restore is run, the SUIF will no longer respond because of the files
that have been changed. A system Reset must be performed after restoring the OS
Configuration files to continue using the SUIF.
• Only one selection can be restored by execution of the following procedure. The following
procedure must be repeated for each item you wish to restore. There are nine system items
available to be restored. You must perform the procedure for each item to completely restore
all of the system’s files (calibration & configuration)
Available choices are:
- Digital
- IUI
- System Control
- IP Looks
- Table IDC
- ASTRA
- OS Configuration
• You must have a “good” backup of the files you wish to restore from CD or USB.
Note: The data in system backup/restore CD contains related OS config file.
3.2 Procedure
Potential for Data Loss. DICOM configuration information is not part of the backup. All
DICOM information should be kept written down and kept with system information. Use it
later to manually reconfigure DICOM, after the restore is completed.
If the OS configuration restore needed, please do it at last step.


GE HEALTHCARE 
3.) Select the Utilities Tab.
4.) Click on the plus sign preceding the System folder ICON, in the navigation frame.
5.) Click on Restore link,
6.) Select the media type by clicking on one of the media type buttons.
7.) Click on [START].

- To cancel and return to the Tools main screen, press [CANCEL]
8.) Click on the down-arrow in the drop down box to display a drop down list of items.
9.) Click on the item you wish to restore.

10.) Insert your “Backup” CD into the CD/DVD drive.

GE HEALTHCARE
11.) Click on [CONTINUE] to restore the selected subsystem. To cancel subsystem restore, press
[CANCEL] .
12.) When restore is complete, you will see restore success in the status bar.
13.) Exit SUIF
14.) Reset the system

GE HEALTHCARE 

GE HEALTHCARE
Chapter 19 Complete System Software Load

and/or Upgrade
Note: Configure the Time Zone after software re-installation or upgrade.
Section 1.0 Personnel Requirements

• Required Persons: 1 person
• Preliminary Reqs: 5mins
• Procedure: 75 (Time estimate does not include saving and restoring patient images and/or
protocols files)
• Finalization: 0 min
Section 2.0 Overview

Before You Begin:
• The following times are typical for a complete system LFC:
1.) Five Minutes to backup system files.
2.) Approximately ninety minutes to save and restore images and protocols.
3.) Thirty minutes to install the OS and Applications software.
4.) Thirty Minutes to load generator software
5.) Five Minutes to restore system files.
6.) Five minutes to cleanup and return system to operational readiness.
• Only use this System Software load procedure to re-install and/or upgrade your system
software completely. The following procedure installs both the operating system, application
and Generator software.
• Pay particular attention, if instructed, to system resets. It's important that power be cycled
according to a specified procedure. Cycling power at the wrong time or by the wrong method
can result in a PC's operating file system (Linux) becoming corrupt. If the OS on the PC gets
corrupted, you may have to reload it again or start over.
• What happens when you press and hold the <reset> button on the Console? In less than one
minute, the system cycles all subsystem power “OFF” and then “ON” again:
1.) When the reset button is pressed, the console sends a signal to the I/O board
(Corona) to cycle (reset) system power.
2.) The I/O board then notifies software running on the PC that a shutdown is about to
begin.
3.) Software on the PC begins an immediate and orderly shutdown of software on the
PC.
4.) When 40 seconds has expired, the I/O board sends a command to shutoff all
subsystem power to the PDU.
5.) Within ten seconds after all subsystem power is shut-off, the I/O board turns “ON” all
subsystem power again.
6.) The PC then reboots and the system returns to operational readiness.
Chapter 19 - Complete System Software Load and/or Upgrade Page 141

GE HEALTHCARE 
• The following SW procedure assumes that you are beginning with the System powered “ON”
and application software running (i.e. System Operationally Ready).
Note: Configure the Time Zone after software re-installation or upgrade by refer to Planned
Maintenances.
Section 3.0 Preliminary Requirements

3.1 Tools and Test Equipment
• Linux Operating System Software DVD: 1
• System Applications Software CD-ROM: 1
3.2 Consumables
• Empty/blank CD-R: 2
3.3 Safety
Potential for Data Loss.

• Archive patient images you wish to keep.
• Backup protocols you wish to keep.
• Preform a “Save” of system configuration and calibrations data and label the CD-R.
• Do not press the <RESET> button on the Console, Unless you are instructed.
3.4 Required Conditions

• System must be 100% functional and operationally ready before performing the following
procedure.
• Suggest you unplug the ethernet cable before you begin.
Section 4.0 Procedure

1.) Are you performing a new system installation?
a.) Yes; start the procedure at Step 4.
b.) No; continue on to the next step (Backup System Files).
2.) Backup System Files. Refer to Section 2.0-Procedure on page 136
3.) Backup Protocol Data Base and System Images.
a.) Save Protocol Data Base.
Note: From SUIF/Config/General/Application Language, record the language config. This is because the
database only can be restored at the system configured with the same language enviroment.
I.) From the Worklist screen, click Service Tools icon. The Service Tools screen
Page 142 Section 3.0 - Preliminary Requirements

GE HEALTHCARE
appears.
II.) Select Preferences first and then Protocols, from the menu.
III.) Insert a blank CD into the CD tray and close.
IV.) Click [Back up] .

V.) A message will appear: Press OK to continue with Protocol Database back up.
VI.) Press [OK] after you see the message. The protocol database is saved to the CD-
RW.
VII.)Remove the CD from tray and label it as “Protocol Database” (include the current date
and time).
VIII.)Place the CD in safe location for future use.

b.) Save Images
I.) Open the CD tray.
II.) Insert your blank CD-R into the tray.
III.) entering the Worklist screen and clicking the icon of image management,this is

GE HEALTHCARE 
shown in following picture.
IV.) Now, select the exams you wish to copy.
Note: select some exams with CTRL+LEFT BUTTON

V.) Click on [CD1] on the lower left corner of the screen as the destination. The CD Write
screen will appear with the following options:
• Deselect All - Deselects all exams on the list.
• Store Optimally - Automatically checks if the selected images will fit on the
CD. It will automatically deselect any items that cannot fit onto the CD.
• Write - Begins the copy process.
• Cancel - Closes the screen and returns you to the Image Management
screen.
VI.) Confirm that the exams to be copied are the ones you have chosen. Deselect any
exams you do not want saved to the CD-RW.
VII.)Click on [Write] , using the mouse.
1.) The CD begins copying.
2.) To see the status of the exams being copied, click on located at the
bottom of the Image Management screen.
Page 144 Section 4.0 - Procedure

GE HEALTHCARE
3.) The transfer log screen will appear.
4.) Click on [Close] and return to the Image Management screen.
5.) When copying is complete, the CD tray will open.
VIII.)Remove the CD from tray and label as Image Data (include current date and time).
6.) Perform the “Load from Cold”.
Do not press the RESET button on the Console, unless you are instructed to.
a.) Load Linux Operating System (OS) software.
I.) Place the Linux Operating System DVD into the PC.
II.) Press and hold the RESET button for at least 3 seconds. You will hear a short beep,
and the system will begin to shut down and later reboot.
III.) When a ring is heard,the PC “splash” screen is displayed, press <F9> as instructed
on the screen.
IV.) When the Boot Device Menu is displayed, select to boot from "Optical Drive" and
press the <Enter>key.
V.) When the "Boot: "appears, type: GEHCXR and then press the <Enter>key.
VI.) Be patient, it takes approximately 15 minutes for the Linux Operating System
software to load.
VII.)Remove the Linux Operating System DVD from the PC and close the CD/DVD drive
drawer.
b.) Load Application Software
I.) Insert the Applications CD into the CD/DVD drive.
II.) Open the CDROM, and run the "autorun" file once. It will reboot for installing the
Graphics driver.
III.) After entering the system, open the CDROM and run the "autorun" file again.
IV.) Select “Brivo XR575” for Brivo XR575 model or "Brivo XR515" for Brivo XR515 model
as the product configuration to install Software.
V.) Click the Install tab.
VI.) When the installation of applications software is complete, "Installation is complete"
appear on the screen.
VII.)Click OK.
VIII.)Click [REBOOT]
IX.) The system will reboot and pop up the login screen.
X.) Remove the Applications CD from the CD/DVD drive.
For Brivo XR515 system, 192.168.1.1 and 192.168.1.45 has been used by Magic PC eth0 and
Detector. If these IP addresses also used in hospital network, we need to change Magic PC eth0
and Detector IP. So, if system IP conflict with 192.168.1.1 and 192.168.1.45, please follow the
below procedure.

GE HEALTHCARE 

GE HEALTHCARE
1. click Ctrl+Alt+F5, open a terminal and type:
/sbin/ifconfig, check eth1 IP address
The IP address of eth1 is 192.168.2.1
2. Type:
su
#superxr
3. Run below three commands one by one

chmod u+x changeIp
dos2unix changIp
./changIp
There’s a IP list as below displayed for selection:
2.Type 1 and then click ENTER
3. Software reboot automatically after running the script
4. Log in and start an exam, It should acq successfully.

GE HEALTHCARE 
4.) Login to System
Note: Username and password are case sensitive. Enter them carefully.
a.) Enter username.
Username:insite
b.) Enter password.
Password:2getin
5.) Create User Accounts (Not Required if you have a System Calibration/Configuration Backup
CD)
Enter hospital user names and passwords, if they do not already exist on a system back CD.
6.) Are you performing a new system installation?
a.) Yes, skip to Step 14
b.) No, proceed onto “Selectively Restore System Calibration and Configuration Files” Step 8
7.) Selectively (except Generator dB) Restore System Calibration and Configuration Files.
Note: Do not restore the Generator dB files at this time. You will restore that file after the generator
software is loaded.
a.) From the Application Desktop, click on the Service Tools icon.
b.) Click on the [Launch] button.
c.) Select the Utilities Tab.
d.) Click on the plus (+) sign preceding the System folder icon in the navigation frame.
e.) Click on the [ Restore] link.
f.) Insert your “Cal/Config Backup” CD or USB.

GE HEALTHCARE
g.) Select the media type by clicking on one of the media type buttons.
h.) Click on [START].

* To cancel and return to the Tools main screen, press [STOP]
i.) Click on the arrow that points down, in the drop-down box, to display a list of items that
can be selected.
j.) Restore the Digital files

k.) Restore OS Configuration files
l.) Remove Cal/Config Backup CD.
m.) Press and hold the RESET button for 3 seconds. You will hear a short beep.
You will now re-initialize the system to recognize the restored calibration and
configuration files
n.) Log into the system, when prompted.
o.) Open the Service Desktop.
p.) From the SUIF home page. verify that your current configuration accurately describes the
number of Detectors you have installed. The software load automatically defaults to one
Detector, unless you have done a successful restore and system reset.
8.) Backup System Calibration and Configuration files.
9.) Restore Protocol Data Base
a.) Be assure the system language config are the same with the backuped database. From
the Worklist screen, click the Service Tools icon. The Service Tools screen appears.

GE HEALTHCARE 

Worklist screen
b.) Select [Preferences] and then [ Protocols] .
c.) Insert the CD with the saved protocols database into the CD/DVD drive.
d.) Click the [Retrieve] button.

Service tools screen

GE HEALTHCARE
e.) A message appears: Press OK to continue with Protocol Database retrieve.

f.) Click the [OK] button.The saved protocol database is now loaded onto your system.
g.) Remove the CD from the CD/DVD drive and store it in a safe place.
10.) Restore System Images
a.) Use the [CD1] button to open the CD tray on the PC.
b.) Select Eject CD from the drop-down list. The CD/DVD drive tray will open.
c.) Place the CD with the images onto the tray and close.
d.) Click the [CD1] on the top left corner of the screen. The exam list updates to now show
you the images stored on the CD.
e.) Select the exams you wish to retrieve. using the mouse.
f.) Click the [Local] button as the destination (located on the lower left corner of the screen).
g.) A message appears: Images will be copied to the selected exam. Images will not
automatically be removed from the source exam.
h.) Click [OK] , when it appears.
* If there is a problem and the exams cannot be copied to the selected network host:
1.) A message appears: The network destination is not responding. If the problem
persists contact your network administrator.
2.) Click OK to close the message.
3.) Try copying the exams at a later time.
* To see the status of the exams being copied:
1.) Click [Transfer Log] at the bottom of the Image Management screen.
2.) The Transfer Log screen appears.
3.) Click the [Close] button to close the screen and return to the Image Management
screen.
11.) Reload any applicable software patches.
12.) Re-checkout Insite.
13.) Congratulations, you're finished. Unless, you're installing a new system. Then proceed on to

GE HEALTHCARE 
calibration and configuration tasks.
Section 5.0 Finalization

1.) Plug the ethernet cable.
2.) Perform Detector vertical bar and bad pixel cal.
3.) Perform QAP.
4.) Perform the Data, Time and NTP settings.
5.) Backup the system.
Page 152 Section 5.0 - Finalization

GE HEALTHCARE
DIRECTION 5429484 -CA-1EN, REVISION 1 CONFIGURATION
Chapter 20 System Configuration
Section 1.0 When to Perform System Configuration
Potential for Data Loss:

1.) Always create an up-to-date backup of your system data following product installation
or changes to configuration data.
2.) Upon exiting the Service User Interface (SUIF), for Configuration and Calibration
information to take effect, the system must be reset. This must be done before the
system is used for patient acquisitions.
1.1 During System Installation

Your system is delivered to you configured with default values. You should configure your system
to the values that are appropriate for your particular installation. The items that must be configured
are identified in Step.
Table 20-1 System Configuration Parameters
System Configuration Parameter
Step - Site Parameters on page 154
Step - General Parameters on page 155
Step - Positioner on page 157
Step - Options Parameters on page 157
Step - Insite on page 157
Step - Product Network Filters on page 158
Step - NTP Settings on page 158
Step - HIPAA Configuration on page 158
Step - Generator Time on page 158
1.2 Missing or Lost System Backups

If you perform a software install and do not restore configuration files, you must re-perform all of
configurations listed in , after it’s complete. A software install resets all configuration data. If you
performed a [backup] before you began the software install, you are not required to perform the
configuration and calibrations. Simply [restore] the data saved previously
Chapter 20 - System Configuration Page 153

GE HEALTHCARE 
1.3 Addition of Purchased Options

Installation of purchased options can only be performed by authorized GE sales and service
representatives. If you add purchased options to your system, you should update the system
configuration files immediately and create/save a new backup.
Section 2.0 Starting the System Configuration Tool

1.) Log into the System
a.) Log in as username: insite
b.) Enter the password: 2getin
2.) From the application desktop, click Utility-System-Service icon sequently.
4.) The Home page Summary information shall display.
5.) Click on Configuration icon.
6.) In the left frame, click on the page icon associated with the configuration parameter name you
wish to change.
Section 3.0 System Configuration Tool Parameters

3.1 Site Parameters
The following information can be viewed regardless of service mode. All can be edited, except for
those identified
Table 20-2 Site Parameters
Parameters Definition
Site Name Name of specific location (Hospital, clinic...) where system is installed
(64 characters maximum)
Street Address1 Address of location system is installed (5 lines, and 64 characters

maximum per line)
Street Address2 Address of location system is installed (5 lines, and 64 characters

maximum per line)
City City of system is installed (5 lines, and 64 characters maximum per

line)
State/Province State/Province of location system is installed (5 lines, and 64

characters maximum per line)
PostalCode PostalCode of location system is installed (5 lines, and 64 characters

maximum per line)
Department Name Department name (i.e. Radiology) responsible for equipment

maintenance (64 characters maximum)
Telephone 64 characters maximum
Page 154 Section 1.0 - When to Perform System Configuration

GE HEALTHCARE
Table 20-2 Site Parameters
Parameters Definition
Fax 64 characters maximum
Contact Person Name Customer or person responsible for maintenance of equipment. One
line, and 64 characters maximum.
Contact Person Phone Two lines, and 64 characters maximum per line
System ID System identifier assigned by GE Healthcare following system

installation and prior to customer turnover. (64 characters maximum)
Installation Date Date system installation completed; created by GE Healthcare. (64

characters maximum)
Service Contract Customer licensed Inhouse Service Contract number; created by GE

Number* Healthcare. (64 characters maximum)
Contract Expiration* Licensed Inhouse Service Contract number expiration date; created
by GE Healthcare. (64 characters maximum)
AE Title 16 characters maximum
Port Number 4 characters maximum
IP Address 16 characters maximum
Subnet Mask 16 characters maximum
Default Gateway 16 characters maximum Note: If the customer site does not have a
default gateway, use the default value loaded upon installation. The
field cannot be empty.
3.2 General Parameters
Table 20-3 General Parameters
Parameter Definition
Time Zone Allows the user to choose time zone according to site.
System Clock Allows the user to set the system clock according to site needs.
Data Display Format Allows the user to change/set system date display format. The Date
format is defined as MM-DD-YYYY (default) or DD-MM-YYYY.
Time Display Format Allows the user to change/set system time display format. The time
Format may be kept in a 24 hour format (Military) or 12 hour AM/PM
format: (hh:mm:ss (AM/PM)). The default value is Military
KeyBoard Allows the user to change/set system KeyBoard type.
Measurement System Used to define English or Metric as the system’s measurement

system. The default value is metric.

GE HEALTHCARE 
Table 20-3 General Parameters
Parameter Definition
Application Language Defines the language used for applications screens. The default
value is English. For the site the chinese application wanted, the
Chinese should be selected.
Encoding Defines the language encoding. Encoding must consistent between

system and the RIS/PACS/Printers.
• ISO_IR 100：English encoding
• GB18030:Chinese encoding
• ISO_IR 192:Russian or other languages
QAP Timeout This item determines the interval between QAP test in days. Used to
inform system users that a QAP interval has expired and a QAP test
should be performed. The default value is 7 days.
VA Site This will configure the system for VA options.
Screen Blank Timeout Used to set the period of inactivity (where no user inputs and
processing activity occurs) in which screen blanking can begin. This
feature functions to prolong the life of the monitor, thus preventing a
burn-in. Time is selected in minutes. The default value is 15 minutes.
(4 characters maximum)
Image Mask Adjustment Adjusts the mask that is applied to the acquired image from the
detector. It affect Raw and Processed images.

GE HEALTHCARE
3.3 Positioner
Table 20-4 Positioner Parameter
Parameter Meaning
Mode choose the system work mode;

normal work mode and exhibition mode
Ceiling Height set height of the floor to the roof(unit: cm)
Anti-Collision Yes:open the Anti-collision

No: close the Anti-collision
Motor Mode At Power On Speed:motor runs in constant-speed

Power-assisted:manualoperation runs with the motor running
3.4 Options Parameters

Table 20-5 Options Parameters (Need Service Key)
Parameter Meaning
If customer purchased the option, select Yes to open the

Auto Protocol Assist option, else select No.

AEC option, else select No.

Multi Patient Print option, else select No.

Exam Report Print option, else select No.
HIPPA This was a Non-purchased option. Please select Yes.
DICOM Connectivity This was a Non-purchased option. Please select Yes.
Grid Line Pair Per the user situation,Please select 40 or 70
Remove Patient Orientation This was a Non-purchased option. Please select Yes.
DICOM Tag
3.5 Insite
To configure the system for insite connectivity via broadband or modem.
Please refer to please refer to the Chapter Login Administration in Operator Manual for this setup.
on page 184 for operation steps.
Note: Note: Exit service user interface and reboot system after completion of Insite checkout /
configuration activities.

GE HEALTHCARE 
3.6 Product Network Filters

Configure the Production network fiters,firewall default setting is ON.
3.7 NTP Settings

This parameter allows you to set the Date, Time and Network Time Protocol (NTP) settings for the
system. Please refer to Data, Time and NTP settings on page 181 for operation steps.
3.8 HIPAA Configuration

If you activate this function on Options parameter screen, upon system start-up, a Logon screen will
pop up to protect your system data with entering an username and password. Please refer to
System Login (HIPPA) on page 182 for operation steps.
3.9 Generator Time

This test will execute the Jedi Time Diagnostics and Sync. Please refer to Jedi Time Sync with
System Time on page 181 for operation steps.
Section 4.0 Network Connection (DICOM) Configuration

See the Operator’s Manual for instructions on how to configure DICOM on this system.
The following worksheets should be used to capture and archive your system’s DICOM
configuration for future reference. Records configuration information in the work sheets that follows.
Place worksheets in a safe place so that they may be referenced in the future if needed.
4.1 Network Hosts
4.1.1 Host Tab
Table 20-6 Host Tab
Attribute Host Device 1 Host Device 2 Host Device 3
Host Label = = =
Application Entry Title = = =
Network Address = = =
Port Number = = =
Query Retrieve = = =
Storage Commitment = = =

GE HEALTHCARE
Table 20-6 Host Tab
Attribute Host Device 1 Host Device 2 Host Device 3
Storage Commitment - Application Entity = = =

Title
Storage Commitment - Network Address = = =
Storage Commitment - Port Number = = =
Comments = = =
4.1.2 Preference Tab

Values for each network node are configured on the Workstation PC. Generally, options 1, 2 and 3
are enabled (checked) for remote viewing stations, PACS, etc.
• Option 1 - Check this option if the remote host being configured should be able to Query and
get a response of a list of images on the magic.
• Option 2 - Check this option if the remote host being configured should be able to Retrieve
any of images returned on the image list (pull) from the magic.
• Option 3 - Check this option if the remote host being configured should be able to Send / Push
any of the images in its local database to the magic.
• Option 4 - This option will never be used since the magic does not yet generate multi-frame
images.
• Option 5 - Checking this option will cause the magic to strip out all patient information in the
images being sent to the remote node being configured. Same as de-identify and push
automatically. Some sites may want to check this option for some nodes being configured for
security purposes (if they do not want to divulge any patient info to the folks using this remote
node).
• Options 6- should be checked / enabled based on the procedure that you have from Rich
Warp.
• Options 7 & 8 - will be used only for the HIS / RIS system being configured Option 7 should
be selected for the HIS / RIS system only if it has been configured to accept MPPS messages
from the magic.
• Options 8 - may not be implemented on your system yet. If it has not been implemented,
please ignore.
• Options 9 - DX images send as CR Modality
Table 20-7 Preference Tab
Option Attribute Value
1 Allow this network host to query the =

TERRA_NETWORK
2 Allow this network host to retrieve from the =

TERRA_NETWORK
3 Allow this network host to send images to the =

TERRA_NETWORK
4 This network host accepts multiple frame image. =

GE HEALTHCARE 
Table 20-7 Preference Tab
Option Attribute Value
5 Perform de-identification (anonymous patient =

images) when sending to this network host.
6 Apply “Burn-On-Send” to images when sending to =Burn-On-Send

this network host.
7 Send MPPS N-Create and N-Set notification to this =

network host.
8 Make this network host the HIS/RIS source. (Only =

one host can be designated as the HIS/RIS source.)
9 DX Images sent as CR Modality =

GE HEALTHCARE
4.2 Printers
4.2.1 Agfa Drystar 3000 Printer
4.2.1.1 Printer Parameters
Table 20-8 Printer Tab
Attribute Value Comments
DICOM Printer Label DRYSTAR3000 Or customers preference
Application Entry Title Enter value given by Site Network AE Titles may be site specific, be
Administrator sure to check on-site
IPNetwork Address Enter value given by Site Network

Administrator
Port Number 104 Port number may be site specific, be

sure to check on-site
Pixel Depth 12
Printer Pixel Size (micron) 79.4
Configuration Information PERCEPTION_LUT=LINEAR (no

spaces)
Density Min. = 20, Max. = 300
Magnification Type CUBIC
Smooth Factor 140
Trim NO Not Supported
Polarity NORMAL
Border Density BLACK
Empty Image Density BLACK
Printer Memory Size 40Mbytes
Table 20-9 Layout Tab
Attribute Value
Select the desired layouts allowed for this printer 1:1, 1:2, 2:1, 2:2
Slide formats Not Applicable

GE HEALTHCARE 
Table 20-10 Film Size Tab
Attribute Value Value Comments
8 x 10in Pixel Width = 2388 AGFA Layout - Portrait 9006

Pixel Height = 2972
10 x 12in Pixel Width =

Pixel Height =

Pixel Height =
11 x 14in Pixel Width = 3300 AGFA Layout -Portrait 9014

Pixel Height = 4256

Pixel Height =

Pixel Height = 5174
24 x 24cm Pixel Width =

Pixel Height =

Pixel Height =
General Comments:
- Supports Clear and Blue Film. If medium selected (Clear, Paper) does not match the
printer, the job will be queued until the correct film is loaded.
- AGFA layouts are specific to maximum printable area layouts. Please consult the AGFA
technical representative to install custom layouts
- Only 14x17 film was tested with this printer.
- Trim is not supported by this printer
Note: Avoid print job failures by having printer vendor ensure that the Confirmation Level (DICOM
Connectivity) at the printer is set to ?? (accept all). Failure to set this level on the printer will result
in failed print jobs
4.2.1.2 Print Layouts

For accurate image sizing, a custom layout must be configured by printer vendor/manufacture . In
addition to the above layouts, the following layouts must be installed by the authorized AGFA print
representative:
Table 20-11 Agfa Drystar 3000 Print Layouts
FILM SIZE FORMAT P/L AGFA LAYOUT
14 x 17 1:1 P 2411
14 x 17 1:2 P 9001

GE HEALTHCARE
14 x 17 2:1 P 9000
14 x 17 2:2 P 9002
14 x 17 1:1 L 2511
14 x 17 1:2 L 9003
14 x 17 2:1 L 9004
14 x 17 2:2 L 9005
11 x 14 1:1 P 9014
11 x 14 1:2 P 9102
11 x 14 2:1 P 9103
11 x 14 2:2 P 9104
11 x 14 1:1 L 9018
11 x 14 1:2 L 9202
11 x 14 2:1 L 9203
11 x 14 2:2 L 9204
8 x 10 1:1 P 9006
8 x 10 1:2 P 9009
8 x 10 2:1 P 9008
8 x 10 2:2 P 9010
8 x 10 1:1 L 9007
8 x 10 1:2 L 9012
8 x 10 2:1 L 9011
8 x 10 2:2 L 9013
4.2.2 Agfa Drystar 5500
4.2.2.1 Printer Parameters
DICOM Printer Label DRYSTAR5500 Or customers preference

GE HEALTHCARE 
IP Address Enter value given by Site Network

Administrator
Port Number 104
Pixel Depth 12
Printer Pixel Size (micron) 55
Configuration Information LUT=0.0
Smooth Factor 140
Polarity NORMAL
Attribute Value
8 x 10in Pixel Width = 3852 AGFA Layout - Portrait 9006

Pixel Height = 4300
10 x 12in Pixel Width = 4880

Pixel Height = 5280

Pixel Height =
11 x 14in Pixel Width = AGFA Layout -Portrait 9014

Pixel Height =

GE HEALTHCARE

Pixel Height =

Pixel Height = 7788

Pixel Height =

Pixel Height =
4.2.2.2 Print Layouts

For accurate image sizing, a custom layout must be configured by printer vendor/manufacture . In
addition to the above layouts, the following layouts must be installed by the authorized AGFA print
representative:
14 x 17 1:1 P 2411
14 x 17 1:2 P 9001
14 x 17 2:1 P 9000
14 x 17 2:2 P 9002
14 x 17 1:1 L 2511
14 x 17 1:2 L 9003
14 x 17 2:1 L 9004
14 x 17 2:2 L 9005
11 x 14 1:1 P 9014
11 x 14 1:2 P 9102
11 x 14 2:1 P 9103
11 x 14 2:2 P 9104
11 x 14 1:1 L 9018
11 x 14 1:2 L 9202
11 x 14 2:1 L 9203
11 x 14 2:2 L 9204
8 x 10 1:1 P 9006

GE HEALTHCARE 
8 x 10 1:2 P 9009
8 x 10 2:1 P 9008
8 x 10 2:2 P 9010
8 x 10 1:1 L 9007
8 x 10 1:2 L 9012
8 x 10 2:1 L 9011
8 x 10 2:2 L 9013
4.2.3 Fuji FM DPL Print Parameters
DICOM Printer Label FUJIFMDPL Or customers preference

Administrator
Port Number 104
Pixel Depth 12
Configuration Information CS000
Smooth Factor SHARP
Polarity NORMAL

GE HEALTHCARE
Attribute Value
8 x 10in Pixel Width = 1998 The following configurations

Pixel Height = 2510 must be configured by the Fuji
printer representative to print
10 x 12in Pixel Width = correctly sized images:
Pixel Height = • LUT1 as SAR17 for calling
AE_TITLE.
10 x 14in Pixel Width = • Trim width at 1 pixel for
Pixel Height = calling AE_TITLE.
• Globally configure “a
margin between image” for
Pixel Height = 3600 0 pixels.
14 x 14in Pixel Width = • Globally configure “Image
layout” for spread
Pixel Height =

Pixel Height = 4240

Pixel Height =

Pixel Height =
4.2.4 Fuji DryPix 1000 Print Parameters
DICOM Printer Label DRYPIX1000 Or customers preference

Administrator
Port Number 104 Port numbers may be site specific,

be sure to check on-site

GE HEALTHCARE 
Pixel Depth 12
Smooth Factor SHARP
Polarity NORMAL
Attribute Value

GE HEALTHCARE
Table 20-21 film Size Tab
8 x 10in Pixel Width = 2280 The following configurations

Pixel Height =2877 must be configured by the Fuji
AE_TITLE.-Trim width at 1
10 x 14in Pixel Width = pixel for calling AE_TITLE.
Pixel Height = • Globally configure “a
11 x 14in Pixel Width = 2962 0 pixels.
Pixel Height = 4096 • Globally configure “Image
layout” for spread.
• A densitometer filter (FUJI
Pixel Height = part number 605S0003)
14 x 17in Pixel Width = must be used when
performing printer
Pixel Height = calibration.
Pixel Height =

Pixel Height =
4.2.5 Fuji DryPix 3000 Print Parameters

Administrator

Pixel Depth 12

GE HEALTHCARE 
Smooth Factor SHARP
Polarity NORMAL
Attribute Value
8 x 10in Pixel Width = The following configurations

Pixel Height = must be configured by the Fuji
AE_TITLE.
10 x 14in Pixel Width = • Trim width at 1 pixel for
Pixel Height = calling AE_TITLE.
• Globally configure “a
Pixel Height = 0 pixels.
14 x 14in Pixel Width = • Globally configure “Image
layout” for spread.
Pixel Height =
• A densitometer filter (FUJI
14 x 17in Pixel Width = 4072 part number 605S0003)
Pixel Height = 4972 must be used when
performing printer
24 x 24cm Pixel Width = calibration.
Pixel Height =

Pixel Height =
Note: ONLY 14 x 17 film should be used with this printer. Any other film size used may print films with
incorrect measurements

GE HEALTHCARE
4.2.6 Fuji DryPix 7000 Printer Parameters

Administrator

Pixel Depth 12
Smooth Factor SHARP
Polarity NORMAL
Attribute Value
Slide formats

GE HEALTHCARE 

Pixel Height =4819

Pixel Height =

Pixel Height = 7043

Pixel Height =

Pixel Height =

Pixel Height =

Pixel Height =

Pixel Height =
4.2.7 Kodak 8200 Print Parameters
DICOM Printer Label KODAK8200 Or customers preference

Administrator

Pixel Depth 12
Configuration Information LUT=Wkstn2a.w87,2 (no spaces)

GE HEALTHCARE
Smooth Factor 15
Trim NO
Polarity NORMAL
Select the desired layouts allowed for this printer 1:1, 1:2, 2:1, 2:2 1:2 only valid for portrait 2:1 only
valid for landscape
Slide formats Not applicable Not supported: Do not select
Table 20-30 film Size Tab

Pixel Height =

Pixel Height =

Pixel Height =

Pixel Height =

Pixel Height =

Pixel Height =4277

Pixel Height =

Pixel Height =

GE HEALTHCARE 

Administrator

Pixel Depth 12
Smooth Factor 15
Trim NO
Polarity NORMAL
valid for landscape

GE HEALTHCARE

Pixel Height = must be configured by the
Kodak printer representative:
10 x 12in Pixel Width = • Calling AE_TITLE must be
Pixel Height = declared in 9410 host table
or print will be rejected.
10 x 14in Pixel Width = • Pixel correction turned off.
Pixel Height = • TFT emulation enabled.
Landscape printing will be
functional only if a Kodak
Pixel Height = 8800 is installed.
14 x 14in Pixel Width = Note: User will get incorrect
image sizing if unsupported
Pixel Height = formats (i.e. portrait 2:1 or
14 x 17in Pixel Width = 4096 landscape 1:2) are used.
Pixel Height = 5221

Pixel Height =

Pixel Height =

Administrator

Pixel Depth 12

GE HEALTHCARE 
Smooth Factor 15
Trim NO
Polarity NORMAL
valid for landscape

Pixel Height = must be configured by the
Kodak printer representative:
10 x 12in Pixel Width = • Calling AE_TITLE must be
Pixel Height = declared in 9410 host table
or print will be rejected.
10 x 14in Pixel Width = • Pixel correction turned off.
Pixel Height = • TFT emulation enabled.
Landscape printing will be
functional only if a Kodak
Pixel Height = 8800 is installed.
14 x 14in Pixel Width = Note: User will get incorrect
image sizing if unsupported
Pixel Height = formats (i.e. portrait 2:1 or
landscape 1:2) are used.
14 x 17in Pixel Width=4096
Pixel Height =5221

Pixel Height =

Pixel Height =

GE HEALTHCARE

Administrator

Pixel Depth 12
Configuration Information LUT = Ver693c0.w87,6
Smooth Factor 40
Trim NO
Polarity NORMAL
Select the desired layouts allowed for this printer Check at least one (1on1) or
more as desired
Slide formats

GE HEALTHCARE 
8 x 10in Pixel Width =4742

Pixel Height =6286

Pixel Height = 7342

Pixel Height =

Pixel Height = 8896

Pixel Height = 8662
14 x 17in Pixel Width= 8896

Pixel Height =10612

Pixel Height =

Pixel Height =
4.2.11 Codonics Horizon Print Parameters
DICOM Printer Label HORIZON Or customers preference
Administrator,eg : PRINT_SCP sure to check on-site

Administrator
Port Number Enter value given by Site Network Port numbers may be site specific,
Administrator, eg: 104 be sure to check on-site
Pixel Depth 12
Configuration Information LUT = LINEAR
Magnification Type Replicate

GE HEALTHCARE
Smooth Factor 0 Not supported
Trim NO
Polarity NORMAL
Border Density BLACK Can also pass OD value of (0 - 310)
Empty Image Density BLACK Can also pass OD value of (0 - 310)
Select the desired layouts allowed for this printer
Slide formats
8 x 10in Pixel Width = 2406 1.) Codonics Horizon printer

Pixel Height = 2790 supports Clear Film, Blue
Film and Paper.
10 x 12in Pixel Width = 6286 2.) Only 8 x 10 and 14 x 17
Pixel Height = 7342 Film Formats have been
validated
10 x 14in Pixel Width = 3.) Other Smoothing and
Pixel Height = Sharpening Algorithms for
Magnification Type are
11 x 14in Pixel Width = 3376 supported. Consult
Pixel Height = 4072 CODONICS Technical
representative to install
14 x 14in Pixel Width = custom preferences if
Pixel Height = desired.
14 x 17in Pixel Width= 5322

Pixel Height =5025

Pixel Height =

Pixel Height =

GE HEALTHCARE 
4.3 Query Modality
4.3.1 Changing the Query Modality to “CR”

The default setting for Query Modality is DX, following a LFC. If you change the value of Query
Modality and then perform a system backup, your can recover your new value by performing a
system restore.
1.) On the operator keyboard, press the <CTRL-ALT-F1> keys to bring up a terminal window.
2.) In the terminal window, login as:
- magic login: xruser <enter>
- password: 4$xray<enter>
3.) In the terminal window, type: cd /magichome/xruser/bin <enter>
4.) In the terminal window, type: ./setModalityToCR <enter>
5.) You will see the response: The Querying Modality has been successfully set to CR
6.) In the terminal window, type: exit <enter>
7.) On the operator keyboard, press the <CTRL-ALT-F7> keys to close the terminal window.
4.3.2 Changing the Query Modality to “DX”

1.) On the operator keyboard, press the <CTRL-ALT-F1> keys to bring up a terminal window.
2.) In the terminal window, login as:
- magic login: xruser <enter>
- password: 4$xray<enter>
3.) In the terminal window, type: cd /magichome/xruser/bin <enter>
4.) In the terminal window, type: ./setModalityToDX <enter>
5.) You will see the response: The Querying Modality has been successfully set to DX
6.) In the terminal window, type: exit <enter>
7.) On the operator keyboard, press the <CTRL-ALT-F7> keys to close the terminal window.
8.) Reset the XR/d system for the Monitor Configuration changes to take effect.
Section 5.0 Install Demo Images

Load demo images from CD-ROM provided with the system into the image database. Refer to
Operator’s Manual for procedure to upload images from CD.
Section 6.0 Operator’s Manual (OM) Installation

The operator manual must be installed and the appropriate language selected:
- when the system is initially installed
- following a complete system load from cold
- following a software reload of the workstation PC
The procedure follows:
- Reset the system to clear any inconsistencies.
- Login as insite
- Password 2getin
- Install the operator manual portable media in the host PC

GE HEALTHCARE
- Press the following keys: <Cntrl><Alt><F2> simultaneously, to open a command window.
- At the login prompt, type: xruser
- Enter the password: 4$xray
- Insert Operators manual CD into the CD bay of Workstation PC
- To run the interactive script, at prompt type the following: ./xrdinstall.om
- Choose English as the language to install
- Allow load process to complete.
- Enter exit at the prompt.
- To return to the graphical user interface, press <Cntrl><Alt><F7> keys simultaneously.
- Remove the operator manual portable media from the host PC
- Reset the system using the RCIM reset button
- Login as insite
- Password 2getin
- Launch the Image Management Viewer in Applications
- Click on the Image Tools Button
- Click on the CBT button
Section 7.0 Data, Time and NTP settings

7.1 NTP Setting
1.) Enter SUIF->Configuration->NTP Setting.
2.) On the right screen, Click “Click here” and pop up the date, time and NTP setting screen.
3.) Click the “Region” and “Time Zone Setting” button to select correct option.
4.) Click the “Change” button below “Data & Time” to Setting Data and Time.
* manually input the current time and date
* Synchronize with NTP server
Section 8.0 Jedi Time Sync with System Time

1.) Enter SUIF->Configuration->Generator Time.
2.) Follow the instruction, Click “Start” on the screen. Then “PASSED” result is displayed on the
screen.

GE HEALTHCARE 
Section 9.0 Adding a Bar Code Reader

9.1 Configuration
A User’s Guide is supplied with the bar code reader for configuration. Please refer to the User’s
Guide for additional programming choices.
Make sure the correct keyboard is connected and configured before adding the Bar Code Reader
Setting the bar code reader back to the default state will disable any user-programmed
configurations, such as the addition of the tab character’ and first character stripping.
Section 10.0 System Login (HIPPA)

Note: Usernames and passwords should only be created in conjunction with or in collaboration with the
users system administrator.
10.1 User Accounts
10.1.1 System Log-in

Upon system start-up, you must enter an username and password to enable the full functionality of
the system. When the log in pop-up window is displayed, use the keyboard to enter your username
and password. If you make a mistake, you will be notified to re-enter.
Page 182 Section 7.0 - Data, Time and NTP settings

GE HEALTHCARE
You must be logged in as the insite user to configure the system.
Once logged in, you will have full access to system features and operation you are entitled to by
permissions.
10.1.2 About User Accounts

Additional user accounts can be created to restrict access to system operation and data. Three
account types are supported by this system: xruser, insite and root. When creating a user ID, you
must choose one of these account types.
xrusers- Users with these privileges are allowed access to all system features and operation.
insite - Gives complete control over protocols and user accounts. The insite account includes all of
the privileges defined for a typical Radiologist account. The difference is that the insite account can
also create and maintain user accounts.
root - Can only create user accounts.
User accounts must be created after system installation or whenever system software is installed
or re-installed.
10.1.3 Default User Accounts

When system software is installed, three “protected” user accounts are automatically created:
xruser, insite and root. The user ID “xruser” is assigned Radiologist privileges. User ID “insite” is
assigned Admin/Service privileges. These accounts cannot be deleted.
Log into the Digital system with User ID insite, enter the password ******, for Admin/Service
privileges.
10.2 Login Feature

The login feature requires you to log in to gain access to the system and can be turned “on” or “off”
by the system administrator. How your site uses this feature depends on if your site's policies. Sites
with more than one network are referred to as Enterprise systems. Those without multiple networks
are referred to as stand-alone systems. The login feature can be used withstand-alone or enterprise
networks. Although some features are more applicable to enterprise systems.
10.2.1 Logging In and Out

After a period of inactivity set by your administrator, a splash screen is displayed.
• Logging In
1.) Type in your name and password.
2.) Click [Login]
Note: Logging off does not prohibit other users from logging in. Logout is designed to protect patient
privacy; not to stop approved users from logging in. When you or another user logs back in, the
system returns to its last known state.
• Emergency Login
Your splash screen may or may not display the Emergency login button (2). Turning this option
on or off is set by your system administrator. When using Emergency login, you may be
prompted to enter your name.

GE HEALTHCARE 
Use Emergency login unless you have a valid account set up.
• log in with Admin Privileges
If you have administrator privileges, when you log in you are asked if you to perform
administrative tasks or scan. Do not click the button next to the Enter administrator screen, if
you only want to scan.
• Manual Logout
1.) Move the cursor to a blank area on the screen.
2.) Right-click and select Lock Screen from the menu.
10.2.2 Understanding users and groups

Every person who has permission to use the system is a user. Users are set up by system
administrators. These administrators may be IT personnel in an enterprise environment, or a site
manager or lead tech in stand-alone environments. The administrator adds new users and assigns
the users to a group which dictates the level of privileges a person will have. For example, a person
named Sue Smith could belong to a group called technologists, radiologists, administrators, or any
combination.
10.2.3 Understanding groups and privileges

The group to which a person belongs has privileges. If you do not have an enterprise system, the
assignment of group privileges will probably be limited to those who have administrator privileges
and those who don’t. If your system is set up for enterprise login, your IT person or administrator
will be using more of the features.
10.3 Configuring the System

System administrators can preform a number of tasks that affect what users can do or will see.
please refer to the Chapter Login Administration in Operator Manual for this setup.
Section 11.0 InSite

11.1 Configuration
11.1.1 Preliminaries
1.) Insert the Class “M” service media into the host PC prior to starting the SUIF.
2.) From the applications desktop, click on the tools icon.
3.) From the Tools desktop, click on the [Launch] button. The service Home Tab is now displayed.
Page 184 Section 11.0 - InSite

GE HEALTHCARE
4.) On the SUIF, select the Configuration Tab.
5.) Within the Configuration folder, click the InSite link.

6.) Enter the InSite Network Configuration routine by clicking on start. Then displays the InSite
Interactive Proprietary Agreement Screen.
Figure 20-1 Priority Acknowledgement Screen

GE HEALTHCARE 
7.) From the InSite Interactive Proprietary Agreement page, click on [Accept] three (3) times.
Figure 20-2 Configuration Screen
11.1.2 Set Modem Configuration

1.) Click on the [Device Connection] Tab
2.) In the Device Connection Type drop down list box, choose [Modem]. The screen reloads and
displays to the modem configuration fields.
Figure 20-3 Device Configuration (Connection Type Modem) Screen

GE HEALTHCARE
Note: Check selections before you press [apply]. The Device Connection tab allows you to configure and
set up the serial port and modem for use with InSite. Six (6) items must be set before you [Apply]
the configuration. The items are Dial-out Prefix, Internal Prefix, Modem Type, Country and CPU
Serial Port Name and CPU Serial Port Speed.
3.) Select a Dial-out prefix or enter a site specific one if it is not in the list. Dial-out pre fixes may
be required on some sites to get a line outside of the hospital. “9,1” is the most common and
is the set default. The “,” creates a 3 second delay between numbers. Multiple Comma's can
be used to increase the delay time.
4.) Select a dialing modem of [Tone] or [Pulse]. Tone is selected by default.
5.) Select a supported Modem Type.
6.) Select the Country where your system is located. The Default - All Others is the default
selection, for use in the United States.
7.) The CPU Serial Port Name must be set to /dev/ttyS2.
8.) The CPU Serial Port Speed should remain at its default settings: 38400.
9.) After all selections are made click on the [APPLY] button to set up the serial port and set up
the registers on the modem. In about 25 Seconds the configuration information will disappear
and the status line at the bottom of the screen will now read ProDiags Auto Setup: Completed
Successfully. The InSite checkout screen is then automatically displayed. The [CUSTOM]
button is to display a screen of custom modem selections that are not required in a normal
setup.
11.1.3 Set Network Configuration

1.) Click on the [Device Connection] Tab
2.) In the Device Connection Type drop down list box, choose [Network]. The screen reloads and
displays to the network configuration fields.
Figure 20-4 Device Configuration (Connection Type Network) Screen
3.) Enter the IP address of your system or the gateway IP address as defined by the facilities
network administrator.
4.) Click [Apply] button.

GE HEALTHCARE 
11.2 Pro Diags Setup

This software contains a data collection package that pushes data and basic system configuration
files to the On Line Center’s RDA Database. Two ProDiags tasks (idm and idm_send_data) that
must be configured to match the site’s operational usage.
1.) Select the ProDiags Tab
2.) To enter this section of ProDiags setup, click the Custom button.
Figure 20-5 ProDiags Custom Screens

GE HEALTHCARE

GE HEALTHCARE 
11.2.1 Summary
1.) Click on [Hour] and [Minute] fields of idm_send_data task and select an hour and minute from
the pull down lists that the system is normally “on” (typically between 9am and 5pm). After each
selection, click [Yes] on the Data has been modified. Please confirm it message.
2.) Click on [Hour] and [Minute] fields of idm task and select an hour and minute from the pull down
lists to schedule 5 minutes before the idm_send_data task. After each selection, click [Yes] on
the “Data has been modified. Please confirm it" message.
3.) When idm and idm_send_data hour and minute selections are complete, click on [Apply] to
finalize the schedule updates. Click [Yes] on the Are you sure you want to apply changes?
message.
4.) Close the ProDiags utility browser by clicking on [Close] from the upper left browser window
pull down menu.
11.2.2 Procedure
Use the following sequence to update the scheduled time (Hour and Minute) of the idm and
idm_send_data tasks:
1.) ProDiags idm_send_data Task
a.) Click on the idm_send_data task Hour field.
b.) From the pull down list, select an hour that the system is normally “ON” (typically between
09:00 and 17:00).
c.) On the “Data has been modified. Please confirm it” pop-up message, click on [YES].
d.) Click on the idm_send_data task Minute field.
e.) From the pull down list, select a minute .
f.) On the Data has been modified. Please confirm it pop-up message, click on YES.
2.) ProDiags idm Task

GE HEALTHCARE
a.) Set up the idm task to run five minutes before the idm_send_data task.
b.) Click on the idm task Hour field.
c.) From the pull down list, select an hour that sets the idm task to run five minutes before
the idm_send_data task.
d.) On the Data has been modified. Please confirm it pop-up message, click on [YES].
e.) Click on the idm_send_data task Hour field.
f.) From the pull down list, select a minute that sets the idm task to run five minutes before
the idm_send_data task.
g.) On the Data has been modified. Please confirm it pop-up message, click on [YES].
3.) When completed with the idm and idm_send_data modifications, click on the [APPLY] button
at the bottom of the Schedule Management Tab.
4.) On the Apply change confirmation pop-up message, click [YES].
11.3 InSite Checkout

Figure 20-6 InSite Checkout Screen
Note: Observe the following:

• The entire system must be re-booted before all features of InSite Interactive are available. Re-
boot entire system after InSite Checkout is complete.
• When On-Line center is called, make sure that the model type _D8K_G1 is used to checkout
the system.
1.) Click on the[ InSite Checkout] tab, if not automatically displayed.
2.) Normal operation is to select [checkout now]. The InSite Checkout Tab allows the user to
complete the InSite configuration process. The user has one of three options, [ CHECKOUT
NOW], [DISABLE INSITE] or [AUTO CHECKOUT].
a.) [CHECKOUT NOW] - Selecting this button configures PPP to allow a dial-in connection
from the OnLine Center. The user must call the local OnLine Center to have them

GE HEALTHCARE 
complete the checkout. During this process, the OnLine Center will download an
sclink.cfg configuration file and run ConfigLink to configure PPP to allow only the OnLine
Center to be able to dial and login to the site.
Figure 20-7 Configure InSite Screen
b.) [DISABLE INSITE] - Selecting this button will remove the system configurations that have
been configured during a previously successful checkout.
Note: Open a terminal window and manually remove the sclink.cfg file if necessary from the ~insite
directory.
c.) [AUTO CHECKOUT] - This button can only be used if a sclink.cfg already file exists, (i.e.,
meaning the site has completed a checkout using the [CHECKOUT NOW] button. [AUTO
CHECKOUT] will run ConfigLink, dial the AutoSC, queue a task with the AutoSC to dial
back, and wait for the AutoSC to dial back and leave a file /tmp/autocheckout. The IIP
Configuration Tool will wait only 10 minutes for the for the file to appear. Typically, the
AutoSC will call back in 5-6 minutes.
3.) Wait 10 seconds after the InSite Checkout is complete before touching any workstation buttons
and proceeding with the next step. (The workstation automatically reloads the browser after
InSite configuration is completed. Failure to wait before proceeding will cause the system to
“hang” )
4.) Reset System. A system reset is necessary after exiting Service User Interface for
configuration parameters to be established for use in applications.

GE HEALTHCARE
Section 12.0 iLinq user guide
1. Insure that insite Checkout is done successfully. Below icon will appear in the lower right
corner of screen.
2. Click iLinq icon and open the iLinq web browser.

3. On the left frame list, the iLinq applications - ContactGE, Settings, Messages, TiP Virtual
Assist could be accessed by clicking on the respective buttons.
4. In ContactGE, customer or FE could raises issues to GE OLE. Detail site information could be
added in Settings and uploaded into GE OLE. Messages history could be checked in Messages. Tip
Virtual Assist is a remote desktop tool which supply GE OLE an effective way to support and guide
site customer or FE.
5. Click on the “TiP Virtual Assist” menu item in the Virtual Assist menu on iLinq browser. Then
click on the Change Session Password button in the right window. Enter "testing" in the New
Password and Confirm Password fields.
6. After password has been changed, click on Accept in the window. The Remote Training
window pops up as shown directly below.
7. Please contact related GE OLE and wait for remote connection from GE OLE.
Section 13.0 Configuring In-House Service (Advanced

Service Mode)
13.1 Overview of Service Package
In-House Service is licensed to customers that have purchased an Advanced Service Package
License from GE. To obtain a license, an appropriate RCAT must be purchased. When this
functionality is enabled, users can operate the SUIF in advanced service mode without the need of
a GE Service key.
However, the following functionality is never enabled by a In-house license to allow:

• InSite Configuration.
• In-House Service Configuration or entitlement.
• Purchased Options Configuration.

GE HEALTHCARE 
When the in-House Service Package is received, GE personnel should instruct the end-user on how
to use both the diagnostics and any service materials supplied in the Service materials.

The following information is required to enable the Advanced Service mode of operation on the
system:
• Installation Date: The date the system was initially installed.
• Service Contract Number: As provided by the Service support representative responsible for
administering the service agreement.
• Expiration Date: The date the service agreement expires.
13.3 Enabling Advanced Service Mode of Operation

The procedure to enable the Advanced Service mode of operation follows:
1.) Insert the Class “M” service key into the CD drive, prior to starting the SUIF.
3.) From the Tools desktop, click on the [Launch] button. The service Home Tab is now
displayed.
Page 194 Section 13.0 - Configuring In-House Service (Advanced Service Mode)
GE HEALTHCARE
4.) On the SUIF, click on Configuration Tab.
5.) On the Configuration page, click on [Site] link.

6.) Enter the following information:
- Installation Date
- Service Contract Number
- Expiration Date
Note: If you fail to enter data for any one of the above fields, you will receive an error message.
7.) Press [Commit] .

8.) Exit the SUIF by pressing the Exit Icon.
13.4 Verifying Advanced Service Mode of Operation

1.) Remove the Class “M” service key, prior to entering the SUIF.
3.) From the Tools desktop, click on the [Launch] button. The service Home Tab is now displayed
(see ).
4.) Verify the Home screen displays Advanced Service at the top of the page.
5.) On the SUIF, press the Configuration ICON.
6.) On the Configuration page, press on the [Site] link.

7.) Verify, Installation Date, Service Contract Number and Expiration Date fields cannot be edited.
See .
8.) Exit the SUIF by pressing the Exit Icon.

GE HEALTHCARE 
Page 196 Section 13.0 - Configuring In-House Service (Advanced Service Mode)
GE HEALTHCARE
DIRECTION 5429484 -CA-1EN, REVISION 1 CALIBRATION
Chapter 21System Installation Calibration
Section 1.0 Before You Begin

1.1 Service User Interface (SUIF)
A list of available system calibrations is displayed on the Service User Interface, whenever the
calibration tab is chosen.
Table 21-1 Service User Interface (SUIF) ICONs
Clicking on the plus + to expand each folder.
Click minus - sign to close a folder
Open a calibration by clicking on the page icon.
Be patient when executing commands. Text status messages are generally displayed in status line,
whenever a calibration icon is selected. If you are uncertain whether a command is being executed,
check the status line first. Repeated attempts to execute a command may require you to exit the
SUIF and re-enter to gain control again.
1.2 Calibration Sequence
Potential for Data Loss

• Always create an up-to-date backup of your system data following product installation
or after making any calibrations.
• The system must be reset, upon exiting the Service User Interface for Configuration and
Calibration information to take affect. This must be done before the system is used with
patient acquisitions.
Calibrations must be performed in the order shown on the left hand side of the calibration tab. The
calibration summary screen only displays the date that a specific calibration was last performed.
Chapter 21 - System Installation Calibration Page 197

GE HEALTHCARE 
1.2.1 After first installation, those calibrations are needed. Follow the steps below in.
Table 21-2 First Installation Calibration
Tool Calibration/Task Order
Positioner Calibration U-Arm 1
Collimator Alignment Collimator 2
Tube Warm-up for Accuracy Tube 3
AEC Calibration Table Ion Chambor 4
Detector (Bad Pixels,Gain, CF) Detector 5

Calibration
Dose Predication - mR/mAs Dose Prediction 6
Image Quality Printer 7
Quality Assurance Procedure (QAP) QAP 8
Generator Accuracy Test Spot check generator accuracy 9
You must always calibrate your system before it can be used and remember to restart your system
after the calibration to active the calibration.
1.2.2 Saving Changes

Do backup after calibrations in Chapter 18 - System Data Backup and Restore
1.2.3 Invoking New Calibrations

Press the <reset> button on the Console to invoke calibration changes.
The system must be rebooted if changes are made to calibrations files. This includes the creation
of new calibrations and/or the restoration of calibration files. Applications software running on this
system only reads calibration files during workstation boot-up. Any changes after boot-up are not
detected by the applications software.
1.3 Returning the System to the User

1.) After completing calibrations, delete any New Patients files created during service, and before
turning the system over to the end-user.
2.) Perform a system reset. A system reset must be performed to invoke changes. Application
software and most SUIF tools only reads the system calibration files during boot-up. If you
make changes, they will not be invoked until you reset (reboot) the system.
3.) Perform a system backup following calibration and after the system has reset. In order to
preserve any new calibrations, a system backup must be made.
Page 198 Section 1.0 - Before You Begin

GE HEALTHCARE
1.4 Temporarily Changing the Measurement System to Calibrations
All positioner calibrations and functional checks use metric values (distances). If the applixations
environment uses the English measurement system, the measurement system should be
temporarily changed to Metric until the calibrations are completed.
To change the Measurement System, open the Service Desktop and select Configuration/General/
Measurement System. Click on [English] or [Metric] to select.
1.5 The use of Collimator(XS-1D) tape (Note the difference between SID and
OID)
In the calibration, you need to use collimator tape to measure SID. In the case to measure SID, you
need to consider the effect of OID (Object Image distance) .
To measure the SID when Uarm is at the 90 degree postion, you can use the collimator tape to
measure the distance from tube to patient and record it as length A. Then the SID = length A + OID.
To measure the SID when Uarm is at the 0 degree postion, you can use the collimator tape to
measure the distance from tube to table top and record it as length B. Then the SID = length B +
Table OID.
Section 2.0 Positioner

Apply the instruction on the screen to perform the calibration
Section 3.0 Tube Warm-up for Accuracy

Use the below protocols before checking the Accuracy when a fresh Tube is connected to Jedi and
Database is loaded for the first time.
3.1 REQUIREMENTS
1.) Use the focal spot of the tube specified in the table See Table 21-3,
2.) The operating tube voltage and current should be monitored all exposures during this
operation.
3.) The anode rotation should be utilized at normal speed (3000 or 3600 min-1).
4.) Do not exceed either the generator or the tube ratings.
ALL RADIATION SAFETY RULES MUST BE OBSERVED. IN ORDER TO PROTECT

HUMANBODY FROM HARMFUL X-RAY, CLOSE THE COLLIMATOR OR BLOCK THE TUBE
ASSEMBLY RADIATION PORT WITH AT LEAST A SIX (6) MM THICK PIECE OF LEAD. NO
PATIENT OR PERSONNEL IS ALLOWED IN THE ROOM.
3.2 Tube Warm-up Procedure for Accuracy

Step1: Open an exam, select fixed mode.
Step2: Setup the exposure protocols as below one by one.

GE HEALTHCARE 
Step3: Take required number of exposures for each protocol, wait for one minute between
exposures.
Step4: Close the exam.
Table 21-3 Tube Warm-up Protocol for Accuracy
Filament Mode kV mA mS No. of Exposures
SF 40 50 50 2
40 50 10 2
40 200 50 2
40 200 10 2
80 50 50 2
80 50 10 2
80 200 50 2
80 200 10 2
120 50 50 2
120 50 10 2
120 200 50 2
120 200 10 2
LF 40 50 50 2
40 50 10 2
40 200 50 2
40 200 10 2
80 50 50 2
80 50 10 2
80 200 50 2
80 200 10 2
120 50 50 2
120 50 10 2
120 200 50 2
120 200 10 2

GE HEALTHCARE
Section 4.0 AEC Calibration
The following applies when performing Automatic Exposure Control (AEC) calibrations.
• If additional information on a calibration is not shown below, just follow the instructions
presented on SUIF.
• Before executing any Automatic Exposure Control (AEC) calibration; if you have performed
any positioner calibration you must reset the system by pressing the <reset> button on the
console.
4.2 Table Ion Chamber

Calibrates the Ion chamber to produce the proper amount of output across all three Ion chamber
cells.
4.2.1 Before You Begin

• Flat Field Phantom required.
• Grid Removed
• Tube, generator and collimator shall be calibrated already.
4.2.2 Procedure
Note: It is important that the Grid be removed. If the grid is left in during calibration, the CF value
will be higher than normal. The normal value for CF is approximately 1.2, whereas the value
when the grid is left in is approximately 1.7.
1.) Follow the on-screen instructions as presented by the tool.
Section 5.0 Detector (Bad Pixels, Gain, CF) Calibration
Mechanical risk. Be care of collimator collision. Remember to take flat panel phantom off
from collimator before system power off or reset.

The following applies when performing Detector (Bad Pixels, Gain, CF) calibrations.
presented on SUIF.
• Remove the radiation meter from its case and allow it to warm-up to room temperature before
using.
• If the flat field phantom has any scratches, dents, or other imperfections on the large surfaces,
it must be replaced before calibration.
• The following tools are required:
- Flat Field Phantom
- Dose meter holder

GE HEALTHCARE 
- Dosimeter (Keithley, MDH, or equivalent)
• Bad pixel calibration must be executed before gain calibration is performed.
• The system must be operating without a reboot for ten contiguous minutes or more. The
detector requires ten minutes or more of stable operation before any calibration is performed.
• When making exposures, hold the expose switch when requested for the entire specified
amount of time.
• If the SID, tube angle, or collimator rotation are not correct, an exposure will not be allowed.
5.2 Calibration Overview

There shall be 2 calibrations total for each kind of receptors and each calibration shall be consist of
those parts:
• Bad Pixel Calibration - Used to detect defective pixels. It can be executed independent of the
other calibrations but is not recommended.
The BAD PIXEL calibration routine:
- Acquires images without using X-rays for the first minutes
- Automatically selects and locks default techniques
- Manually sets the collimator blades to 45 cm x 45 cm size (slightly larger than the
detector).
- Displays the Initial Bad Pixel Calibration Screen (Dark Image processing).
• Gain Calibration - Tool is used to calibrate a gain coefficient for each pixel in order to achieve
uniform gain across the detector. Run all kVp/Gain calibrations.
Note: Do all the kVs in GAIN calibration procedure. Make sure that grid is taken out during detector
calibration.
• CF Measurement- Tool is used to update the CF and AEC dose calibration parameters.
- Run all CF measurement routines.
- The measured exposure value must be entered in units of “mR"or “uGy"
5.3 When should it be performed

• During initial system installation.
• Whenever a detector, X-ray tube, Beam quality filtration, Collimator or Ion chamber is
replaced.
• If the Ion chamber is re-calibrated.
• When QAP has failed its isolated defect specification or QAP results have changed by more
than 10% during a two week interval.
• When a pixel or line artifact appears in an image(s).
5.4 Procedure
There are three steps for calibrating an Image Detector. All three steps must be completed in the
following order: Bad Pixel Calibration, Pixel Gain Variation Calibration and CF Measurement.
You are required to do the following:
1.) Follow the on-screen instructions as presented by the tool.
2.) Install the flat field phantom.
3.) Execute Bad Pixel Calibration refer to the screen instruction.
4.) Execute Gain Calibration refer to the screen instruction.

GE HEALTHCARE
- 20 mm flat field phantom must not be installed for the 60 kVp gain calibrations (gain
>3000)
- 20 mm flat field phantom must be installed for 80 and both 120 kVp (and gain >3000)
5.) Execute CF Calibration refer to the screen instruction.
a.) Insert Flat Field Phantom into the X-ray Calibration Fixture.
b.) Locate small chamber probe of Dosimeter between the collimator and the detector. Probe
should be 65 cm from focal spot (measured by collimator tape).
Note: The radiation meter is a very sensitive to temperature. It's important that the meter be at or near
room temperature before making any measurements. The meter must be allowed to thermally
stabilize for a minimum of 20 minutes after removing the meter from the case, especially if it has
been stored outside.
Important precautions follow:
I.) If the meter is not stable and drifts with no exposure, let it stabilize before taking
measurements.
II.) Tape the meter in place to avoid misalignment during the measurement.
III.) Verify that the Dose meter probe positioned properly. (eg: Keithley “Diagnostic side
is facing the collimator.)
IV.) Read the meter BEFORE touching the probe holder. Vibration of the meter will
increase the exposure reading.
V.) Hold the hand switch on prep for 3-5 seconds for each exposure.
VI.) Verify that the aluminum is replaced in the collimator for the 2nd and 3rd exposures.
VII.)Verify the collimator size adjustments are not accidentally bumped when removing
the probe holder.
VIII.)Verify that the grid is not in place before proceeding.
6.) Configure Radiation meter to measure exposure in mR or uGy
7.) Execute CF Measurement Calibration.
8.) Perform QAP and verify that Image Quality (IQ) passes.
Section 6.0 Dose Predication - mR/mAs

The following applies when performing Dose Predication (mR/mAs) calibrations.
presented on SUIF.
Before executing any Dose Predication (mR/mAs) calibration; if you have performed any positioner
calibration you must reset the system by pressing the <reset> button on the Console.
Section 7.0 Image Quality Calibration

The following applies when performing Printer calibrations.
If additional information on a calibration is not shown below, just follow the instructions presented
on SUIF-Calibration-Image Quality-Printer.

GE HEALTHCARE 
Section 8.0 Generator Accuracy Test Calibration

The test provides a means to spot check generator accuracy in the field. you can execute the test
at any step for disgnostic.
If additional information on a calibration is not shown below, just follow the instructions presented
on SUIF
Section 9.0 Monitor Calibration

After system is powered on, please adjust the monitor follow below procedure.
1.) In Image Management UI, click Image Tools - “TG18 Samples” button, create TG18 test
images.
2.) “View” these images. Open the image like below picture.
3.) ->Press MENU once.
4.) ->Select Image menu.
5.) ->Press ">" or "<" to select Auto Balance.
6.) ->Press ">" to readjust color of the image.
7.) ->Press "Menu" twice to exit Image menu.
8.) ->Press ">" and "<" to Select Display menu.
9.) ->Press Enter to select Brightness adjustment.
10.) ->Press ">" and "<" to adjust Brightness, set brightness to 50%.
11.) ->Press ">" or "<" to select Contrast adjustment.
12.) ->Press ">" and "<" to adjust Contrast, set contrast to 50%.
13.) ->Press ">" or "<" to select Hue adjustment.
14.) ->Press ">" and "<" to adjust Hue, set Hue to 50%.
15.) ->Press ">" or "<" to select Saturation adjustment.
16.) ->Press ">" and "<" to adjust Saturation, set Saturation to 50%.
17.) ->Press ">" or "<" to select Black Level adjustment.
18.) ->Press ">" and "<" to adjust Black Level, set Black Level to 50%.
19.) ->Press "Menu" twice to exit Display menu.
20.) ->Press ">" and "<" to select Color menu.
21.) ->Press ">" or "<" to select Gamma, set Gamma to .
22.) ->Press ">" and "<" to select Color Temp, set Color Temp to Natural
23.) ->Press "Menu" three times to save the change automatically and exit OSD MENU.
Section 10.0 PACS / Image Display Test Image

10.1 Objectives
• Simplified Procedure: To determine configuration for Burn-on-Send or No-Burn for each
destination host (PACS).
• Results: To record results from Simplified Procedure and Additional Tests.
• Background: To provide further information about Image Display on PACS.

GE HEALTHCARE
• Additional Tests: To test several Image Display characteristics (Optional).
10.2 Simplified Procedure

1.) Verify All PACS Review Monitors Are Calibrated
Note: Monitor calibration is a critical first step before testing and configuring Image Display.
a.) Verify that the PACS monitor is calibrated according to DICOM Part 14. Each site is
responsible for providing evidence of PACS monitor calibration.
b.) View SMPTE Pattern
I.) Load SMPTE pattern into Patient List by clicking on “Image Tools” then “SMPTE”
II.) Send SMPTE pattern to PACS review workstation.
III.) Verify that 5% and 95% squares are equally visible on PACS.
c.) Record results in Table 21-5, line numbers 1 and 2.
2.) Send PACS Test Images to PACS
a.) Load Images
I.) Load the PACS Test Images onto the acquisition workstation. Either use:
> DICOM-formatted CDROM with images
> Images on system under Image Tools
II.) Patient Name will appear as GE_PACS_Test_Image, Definium
III.) Patient ID will be 1000001
b.) Configure PACS to [ No-Burn]
I.) Click the Utilities icon
II.) Click Network Connections – Edit
III.) Select the Network Host for the PACS to be tested, click Edit
IV.) Click the Preferences tab
V.) Make sure that Apply Burn-on-Send to images… is not checked
c.) Send No-Burn image
I.) Highlight PACS Test Image #1 in the Images list
Note: All images in the GE_DX_Image_Display_Test exam are named "1". In the following steps, when
an Image number (1, 2, 3....) is called out, you should select that image ’position’ from the Images
list. For example: image number 1 is the first image on the list, image 6 is the sixth image on the
list. To verify that you have selected the correct image, the image number can be viewed in the
upper left corner of the image.
II.) Click the appropriate PACS Network Host in the Destination icon list
d.) Configure PACS to Burn-on-Send
I.) Click the Utilities icon, click Network Connections – Edit
II.) Select the Network Host for the PACS to be tested, click Edit
III.) Click the Preferences tab; check the option Apply Burn-on-Send to images…
e.) Send Burn-on-Send image
I.) Highlight PACS Test Image 6 in the Images list
II.) Click the appropriate PACS Network Host in the Destination icon list
f.) Review images on PACS
I.) Bring PACS Test Images 1 and 6 up on the PACS review workstation.
> The images can be identified by the watermark image number next to the GE logo
inside the chest image region.

GE HEALTHCARE 
> Verify (if possible) that Image 1 is displayed with a VOI-LUT, and Image #6 is
displayed with a Linear LUT
II.) If PACS Test Images 1 and 6 appear visually identical (equal number of bright/dark
bands), the PACS supports VOI-LUT. **: Configure PACS as No-Burn
III.) If PACS Test Images 1 and 6 appear visually different (different number of bright/dark
bands), or chest region has saturation in lung or abdomen, the PACS either does not
support VOI-LU or applies it incorrectly. **: Configure PACS as Burn-on-Send
IV.) Record results in Table 21-5, line numbers 3 and 4
** For more information, see Background and In-Depth Instructions below.
3.) Suggested Configurations
Table 21-4 should be used as a guideline in addition to the tests above to determine if a PACS
system should be configured for Burn-on-Send. This table considers only whether a PACS
supports VOI-LUTs.
Table 21-4 Suggested PACS Configurations
No-Burn Burn-on-Send
GE Centricity RA1000 v1.0,v2.0, v2.1 GE Pathspeed v7.12, 8.0
GE Centricity RA600 v6.1, 7.0 GE AW v3.1, 4.0
GE Radworks v5.1 Kodak DirectView v4.3
GE Pathspeed v8.1 or later Kodak DirectView v5.1, 5.2
McKesson HRS v3.3, 3.3.2 Kodak Directview(CEMAX ICON), v4.3
Fuji Synapse v3.0, 3.1 Merge eFilm, v2.0, 2.1.0
Agfa IMPAX v4.5, 5.2 Stentor iSite v3.0, v3.3.1
Philips Siemens Magic View 300
RealTime iPACS Viewer v5.0 VA Vista
GE-IDX-RealTime iPACS Viewer v5.0 Picker
Philips EasyAccess Neusoft v3.0
Sectra v10.2 Thinking Systems
----- AMICAS LightView v4.10.196

GE HEALTHCARE
10.3 Results
Table 21-5 Results from the Simplified and Additional Tests Sections
Category Number Tests Yes / No
1 PACS monitors calibrated according to DICOM
2 SMPTE 5% and 95% squares equally visible on

PACS?
Simplified
3 Images 1 and 6 appear visually identical?
4 PACS configured for Burn-on-Send?
WC = / /
WW = / /
5 DICOM Header on PACS (Image 1 No-Burn)?
VOI-LUT
Tags(Yes/No
WC = / /
DICOM Header on PACS (Image 6 Burn-on- WW = / /

6 Send)?
VOI-LUT
Tags(Yes/No
WC = / /
7 Values Displayed on PACS Viewer (Image 1)?
WW = / /
WC = / /
Additional 8 Values Displayed on PACS Viewer (Image 6)?
Tests WW = / /
9 Saturation visible in Lung or Abdomen region?
Able to see all five squares in Top Band of Image NO

10 6?
Able to see all five squares in Top Band of Image

11 1?
12 Images 1, 4 and 5 appear visually identical?
13 Images 6, 7 and 8 appear visually identical?
14 PACS able to select Normal/Harder/Softer?
DICOM Header on PACS (Image 9 - CR-

Fallback)?
15
VOI-LUT not present; correct WW/WC?

GE HEALTHCARE 
Section 11.0 Quality Assurance Procedure (QAP)
Mechanical risk. Be care of collimator collision. Remember to take flat panel phantom off
from collimator befor system power off or reset.

The following applies when performing Quality Assurance Procedure (QAP).
presented on SUIF
• Before executing any Quality Assurance Procedure; if you have performed any positioner
calibration you must reset the system by pressing the <reset> button on the RCIM
11.2 When to Perform QAP

Perform QAP every time you calibrate the detector (Wall Stand ) and as a final system check
following system installation. See the Operators Manual for the QAP procedure
11.3 Simplified Procedures

1.) Click [Image Quality] button
Figure 21-1 Image Quality button
2.) Click [Quality Control Tools] and [Acquisition] sequently to open QAP screen.
Figure 21-2 Open QAP screen
3.) Perform QAP under the screen instruction

GE HEALTHCARE
DIRECTION 5429484 -CA-1EN, REVISION 1 DIAGNOSTICS
Chapter 22 System Diagnositcs
Section 1.0 diagnostics

1.1 Diagnostics home page
All system diagnostics are located in this section, To run a diagnostic, navigate to the
particular diagnostic in the directory tree the left and click on the diagnostic
1.2 Communication diagnostics home
1.2.1 The Ethernet diagnostics explain

in the following picture, as per instructions finishing the diagnostic of Magic to Hospital
Network
Chapter 22 - System Diagnositcs Page 209

GE HEALTHCARE 
1.3 Exposure/Acquisition
select Exposure/Acquisition folder to see the diagnostics item.
1.3.1 Generator
select the Generator folder to see the Generator diagnostic
1.3.1.1 Rotation
select the Rotation in the Generator folder to see the Rotation Function Test, as per the
procedures to finish the diagnostics.
Page 210 Section 1.0 - diagnostics

GE HEALTHCARE

GE HEALTHCARE 
1.3.1.2 Heater
select the Rotation in the Generator folder to see the Heater Function Test, as per the procedures
to finish the diagnostics.

GE HEALTHCARE
1.3.1.3 AEC Function
select the Rotation in the Generator folder to see the AEC Test, as per the procedures to finish the
diagnostics.
1.3.2 Detector diagnostics

Select item in detector folder to start table detector diagnostics.

GE HEALTHCARE 
1.3.2.1 Built in Self test

GE HEALTHCARE
1.3.2.2 PING TEST

GE HEALTHCARE 
1.3.2.3 Ethernet Statistics Test
1.3.2.4 Demtector Temperature Test

GE HEALTHCARE
1.3.2.5 PS Partial Load

GE HEALTHCARE 
1.3.2.6 PS Fully Loaded

GE HEALTHCARE
1.4 Positioner

GE HEALTHCARE 

GE HEALTHCARE
1 2 3 4 5 6 7 8
A 12VDC A
24VDC
12VDC
24VDC
DIRECTION 5429484 -CA-1EN, REVISION 1
B B
220VAC
RS232 Spine USB
Board
C RS232/12VDC
C
Magic PC
(HP Z400)
Display VGA
Collimator
Section 1.0 System Schematics
card
Xray Tube
Grid
Detector
Note: Only
for 575-P
Ion-Chamber
D Monitor D
9DF
Detector housing
E-Stop PS2
E
USB Keyboard
0(WKHUQHW
Mouse
HV+/-
Rotor
Barcode
USB
E Reader E
Hospital
Network
Ethernet
Chapter 23 - - Schematics and Drawings

COM PWR_In
F F
RS232 220VAC
220VAC
AEC1 Hand
57
9 SW
Pwr PDU 380Vac
Ctrl RT
G IF G
JEDI Xray On lamp E-Stop E Power-On
E
Board TM E Reset
(50kW)
6:VLJQDO
Door lock
Hospital Door For electrical scheme with detail Cable
3P Power
Chapter 23 - Schematics and Drawings
interconncetion , please see 5466426SCH

RS232/RT
REVISIONS APPROVALS YY/MM/DD TITLE REV
H MADE H
REV MADE BY DATE ECR NO. DESCRIPTION Galaxy System Block Diagram
CHECK
1 Li Bidan 07/29/2011 - Initial Draft Release Brivo XR515 2
Spine board, Mini PDU, Cabnet APPR
2 Du Haitao 09/29/2012 SHT/CONT ON
updated, Cable connection added 6515888SCH
OTHER
1/ 1
1 2 3 4 5 6 7 8
Page 221
SCHEMATICS

Page 222
GE HEALTHCARE
-(', &DELQHW 3'8 - 3&021,725

'RRU
7DQN - 3&+267
SFV
*1'
RU SFV ;5D\/LJKW
67$725
DIRECTION 5429484 -CA-1EN, REVISION 1
'&%86 - - - 'RRU/2&.
&RQVROH
ഒ 8
,)3:$ - 9

$(& 31 : 0DLQSRZHU
-
/DSWRS
- - - - *1'

7RSER[ RQFROXPQWRS 3 +DQG6:,7&+

31

3RZHU
6HUYR PRWRU
- -
70&2162/(
3 3 3 3 31

&ROOLPDWRU
31
Section 2.0 System Electric Assembly
Section 1.0 - System Schematics

'HWHFWRU - - - - 5RWDWLRQ/2&.
*ULGLQ 6SLQH3:$
%ULYR3 9HUWLDO327 31
,RQFKDPEHU (VWRS - LQWKH$UP -
EXWWRQ %ULYR 6,'327 31
31
+RXVLQJ )DQ - - - - - RQO\IRU3 $QJOHPHWHU/&'

31
%ULYR3 6,'/2&.

%ULYR 31
˄%ULYR3
%ULYR
%XWWRQ
9HUWLFDOORFN
7XEH &RQVROH/&'
$QGOLPLWVZLWFK
31
1RWH
[[[[[[ FRQQHFWFDEOHDQGSDUWQXPEHU
8$50&RQQHFWLYLW\
3RZHUVXSSO\
SCHEMATICS

Page 223 Chapter 23 - - Schematics and Drawings
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
Approved Document - 5429130ADW_r2.pdf Page 2 of 3
Section 3.0 Cable Assembly
SCHEMATICS DIRECTION 5429484 -CA-1EN, REVISION 1
 GE HEALTHCARE
Section 1.0 - System Schematics Page 224
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
Approved Document - 5429130ADW_r2.pdf Page 3 of 3
SCHEMATICS DIRECTION 5429484 -CA-1EN, REVISION 1
 GE HEALTHCARE
GE HEALTHCARE
DIRECTION 5429484 -CA-1EN, REVISION 1 TROUBLESHOOTING
Chapter 24 Troubleshooting
Section 1.0 How to Start Diagnostic Tools
2.) From the Tools desktop, click on the [Launch] button. The service Home Tab is now
displayed.
3.) Click on Diagnostic icon.
4.) In the left frame, click on the page icon associated with the diagnostic you wish to execute. For
details,refer to Chapter 22 - System Diagnositcs
Section 2.0 How to change chinese input bar font size?

1.) press Ctrl + space , get the Chinese input tool bar and press “SCIM” Icon with mouse right
button from the tool bar
2.) select item “SCIM setup” from the configure menu
3.) select Panel->GTK-> font from the setup UI
Chapter 24 - Troubleshooting Page 225

GE HEALTHCARE 
4.) select the appropriate font family,style, specially the size and press “OK” button. the new font
size for the Chinese input tool will be applied.
Page 226 Section 2.0 - How to change chinese input bar font size?
GE HEALTHCARE
Section 3.0 Positioner Troubleshooting
U-arm introduction-5 movements

1. Arm Vertical : 325~1655mm
2. SID Adjustment:
1000~1800mm
3. Arm Rotation: -30º~+135 º
4. Tube Rotation: -240º~+45º
5. Detector Tilting: -45º~+45º 1
5 3 4
2 2
5/
GE Title or job number /
10/18/2012
Arm vertical movement Limit

Motor/gearbox/POT switch
(only for motorization)
Limit block
Steel rope
Chain and pulley (only

Brake bearing
for motorization)
Synchronous belt (only Vertical

for motorization) carriage
Steel Anti-falling
rope device
Column
Counter Slide way

weight
Limit block
7/
Slide way GE Title or job number /
10/18/2012

GE HEALTHCARE 
SID Adjustment
Chain and
pulley
Joint for chain Chain and

pulley POT
and carriage
Joint for chain
and carriage
Chain and
pulley
Brake
Carriage
Slide way Carriage
Limit block
Slide way
Arm 8/
10/18/2012
Arm Rotation Small Gear

with brake
Fixed big Gear

with Bearing
Detent
U1/U2 Angle
meter
Column
U3 Angle meter Fixed big Gear

with Bearing
Detent
brake Board on ArmGE Title or job number9 //

10/18/2012
GE HEALTHCARE
Tube Rotation
Detent
Handle
U1 Tube Support
with Handle
Rotation Lock Handle

shaft
U2/U3 Tube Support 10 /

with Handle GE Title or job number /
10/18/2012
Detector Tilting
Emergency Detent
stop switch
Limit Board
Slot for
Grid
Rotation
U-arm shaft
handle
Lock Handle
Patient
barrier
V/H indicator
for Detector
Detector
Grid-in
Ion-chamber Sensor
11 /
10/18/2012

GE HEALTHCARE 
Stretcher Table introduction

Trim Tabletop
Handle
Lock castor
Side bracket Lock

12 /
10/18/2012
GE HEALTHCARE
Resolution: Remount the WS to where the least WS SID is 1000mm

2) AEC failed
17. Protocol DB is junk code

Protocal DB restore shall be undergone under the same language as backup.
Resolution: Change the language to the one under which Protocol DB is restored. Reset
system. Change the language to what you need. Reset system.
Section 4.0 Using the Enhanced Error Messages

Enhanced error messages are available to GEHC personnel, when the GEHC restricted service key
is installed. The enhanced error messages contain additional information not found in the system
error log during normal system operation or available to the normal user. These enhanced error
messages contain additional information that aid in fault isolation and choosing the proper
corrective action.
With the service key installed, error messages in the system error log area automatically linked to
the enhanced messages. The complete set of enhanced error messages is contained in a single

GE HEALTHCARE 
HTML file located on the same CD-ROM as the service key. When the CD is installed, you'll notice
that error numbers in the system log are underlined to indicate a hyper-link to the enhanced
message. You use the mouse to clink on the links.
To utilize the enhanced error messages:

1.) Close the SUIF, if it’s open. Applications can only mount the CD-ROM path in Linux, when the
SUIF is closed.
2.) Install the service key CD-ROM into the CD-ROM drive and close the drive.
3.) Launch the SUIF.
4.) Using the mouse, click on the Error Log Tab
5.) Using the mouse, left click on an error number of interest to you. This will launch a browser
and allow you to see the enhanced error message.
6.) To exit, click on the SUIF <close >button and remove the service key CD-ROM.
Section 5.0 Workstation

5.1 Bar Code Reader
The Bar code reader automatically performs self-tests whenever initially turned on. If it’s not
functioning properly, review the following sections to try to isolate the problem or replace the reader.
The barcode reader is not user serviceable (except for cleaning) and must be replaced as a whole
unit (FRU).
If you aren’t sure what programming options have been set, or if you want the factory default
settings restored, scan the “Factory Default Settings”.
5.1.1 Is the power on? Is the red illumination beam on?

If the red illumination beam isn’t illuminated, check that:
1.) The cable is connected properly.
2.) The host system power is on (if external power isn’t used).
3.) The trigger works.
5.1.2 Is the scanner having trouble reading your symbols?

If the scanner isn’t reading symbols well, check that the symbols:
1.) Aren’t smeared, rough, scratched, or exhibiting voids.
2.) Aren’t coated with frost or water droplets on the surface.
3.) Are enabled in the scanner or in the decoder to which the scanner connects.
5.1.3 Is the bar code displayed but not entered?

The bar code is displayed correctly, but you still have to press a key to enter it (the <Enter>/
<Return> key or the <Tab> key, for example). You need to program a suffix. See the reader’s user
guide on setting up suffixes.
5.1.4 The scanner won’t read your bar code at all.

1.) Scan sample bar codes in the user guide. If the scanner reads the sample bar codes, check
GE HEALTHCARE
that “your “bar code is readable.
2.) If the scanner still can’t read the sample bar codes, scan “All Symbologies”.
5.2 Console
When power is first applied to the console, firmware inside the unit turns ON all of the LEDs for 2
seconds and then turns them OFF (LED ON sequence). If the LEDs don’t turn ON and OFF after
power-up, the console needs to be replaced.
5.3 LCD Monitor
5.3.1 No Picture
• The signal cable should be completely connected to the display card/computer.
• The display card should be completely seated in its slot.
• Check the Vacation Switch should be in the ON position.
• Front Power Switch and computer power switch should be in the ON position.
• Check to make sure that a supported mode has been selected on the display card or system
being used.
• Check the monitor and your display card with respect to compatibility and recommended
settings.
• Check the signal cable connector for bent or pushed-in pins.
• Check the signal input, “INPUT 1” or “INPUT 2”.
5.3.2 Power Button Does Not Respond

• Unplug the power cord of the monitor from the AC outlet to turn off and reset the monitor, or
simultaneously press the RESET and Power buttons.
• Check the Vacation Switch on the left side of the monitor.
5.3.3 Image persistence

Image persistence is when a “ghost” of an image remains on the screen even after the monitor has
been turned off. Unlike CRT monitors, LCD monitors’ image persistence is not permanent. To
alleviate image persistence, turn the monitor off for as long as an image was displayed. If an image
was on the monitor for one hour and “ghost” of that image remains, the monitor should be turned
off for one hour to erase the image.
5.3.4 Message “OUT OF RANGE” is displayed

Message “OUT OF RANGE” is displayed (screen is either blank or shows rough images only)
• Image is displayed only roughly (pixels are missing) and OSM? warning “OUT OF RANGE” is
displayed: Either signal clock or resolution is too high. Choose one of the supported modes.
• OSM warning “OUT OF RANGE” is displayed on a blank screen: Signal frequency is out of
range. Choose one of the supported modes.
5.3.5 Image is unstable, unfocused or swimming is apparent

• Signal cable should be completely attached to the computer.
• Use the OSM () Image Adjust controls to focus and adjust display by increasing or decreasing
the fine total. When the display mode is changed, the OSM Image Adjust settings may need
to be readjusted.

GE HEALTHCARE 
• Check the monitor and your display card with respect to compatibility and recommended signal
timings.
• If your text is garbled, change the video mode to non-interlace and use 60Hz refresh rate.
5.3.6 LED on monitor is not lit (no green or amber color can be seen)
Power Switch should be in the ON position and power cord should be connected.
5.3.7 Display image is not sized properly

• Use the OSM Image Adjust controls to increase or decrease the Coarse total.
• Check to make sure that a supported mode has been selected on the display card or system
being used.
5.3.8 No Video
• If no video is present on the screen, turn the Power button off and on again.
• Make certain the computer is not in a power-saving mode (touch the keyboard or mouse).
5.3.9 On-Screen Manager

OSM Trademarks apply to appropriate countries. (On-Screen Manager) control buttons on the front
are used to basic monitor functions. They function as follows:
• To access OSM menu, press any of the control buttons (<,>, –, +).
• To change signal input, press the <SELECT> button. OSM must be closed in order to change
signal input.
Section 6.0 Soft Reset of Software on PC

Problem: System software has hung on the PC.
Solution/Work-Around: There is a hot-key that will allow you to do a soft reset of the PC Software.
After software reset, exposures can be taken.
The procedure for doing a soft reset follows:
1.) Press <Ctrl>+ <Esc>.
Note: Only a hard reset will properly reset the entire system.
2.) When the GUI below appears, select [OK].
3.) The Software will shutdown and restart at the HIPPA Login screen, in about 60 seconds.
GE HEALTHCARE
Section 7.0 Engineering Toolkit
Problem: There are no software tools available if the PC hangs.
Solution/Workaround: There is a hot-key that will allow you to open an engineering user interface
to help diagnose an issue.
Here is the procedure to access this engineering GUI:
1.) Press <Ctrl>+<Shift>+ <F5>.
2.) The following GUI will popup on the screen your mouse cursor is currently on (Left or Right):
3.) Choose one of the following actions:

GE HEALTHCARE 
Section 8.0 QAP Results and Images
Table 24-1
<a> Enter insert mode, the characters typed in will be inserted after the current cursor
position. If you specify a count, all the text that had been inserted will be repeated
that many times.
<h> Move the cursor to the left one character position.
<i> Enter insert mode, the characters typed in will be inserted before the current cursor
position. If you specify a count, all the text that had been inserted will be repeated
that many times.
<j> Move the cursor down one line.
<k> Move the cursor up one line.
<l> Move the cursor to the right one character position.
<r> Replace one character under the cursor. Specify count to replace a number of
characters
<u> Undo the last change to the file. Typing u again will re-do the change.
<x> Delete character under the cursor. Count specifies how many characters to delete.
The characters will be deleted after the cursor.
Table 24-2
<A> Append at the end of the current line. I Insert from the beginning of a line. O
(letter oh) Enter insert mode in a new line above the current cursor position.
<a> Enter insert mode, the characters typed in will be inserted after the current
cursor position. A count inserts all the text that had been inserted that many
times.
<i> Enter insert mode, the characters typed in will be inserted before the current
cursor position. A count inserts all the text that had been inserted that many
times.
<o> Enter insert mode in a new line below the current cursor position.
The QAP results files and images can be found in the following location:
/export/home/insite/server/htdocs/suif/iq/en/iqst/<Receptor Type> where, Receptor Type = Table

or WS
The following is an example of an InSite session:
relay:relay 192.227.61.116 23
Raptor Firewall Secure Gateway.
GE HEALTHCARE
GEHC/CTT Linux 4.3.8
Kernel 2.6.7-2.2smp on an i686
login: insite
Password:
Last login: Tue Mar 1 09:53:58 from 150.2.12.163
Welcome InSite
[insite@magic ~]$ su - xruser
Password: 4$xray
[xruser@magic xruser]$ cd /export/home/insite/server/htdocs/suif/iq
[xruser@magic iq]$ pwd
/export/home/insite/server/htdocs/suif/iq
[xruser@magic iq]$ cd en
[xruser@magic en]$ cd iqst
[xruser@magic iqst]$ ls
Table WS
[xruser@magic iqst]$ cd Table
[xruser@magic Table]$ ls
200502280838P_Details.txt
200502280838P_iqst_Bad_Pixel.jpg
200502280838P_iqst_Conversion_Factor.jpg
200502280838P_iqst_Global_BNU.jpg
200502280838P_iqst_Local_BNU.jpg
200502280838P_iqst_Noise_Power_Spectrum.jpg

GE HEALTHCARE 
200502280838P_iqst_Physical_Test.jpg
200502280838P_iqst_Relative_DQE.jpg
200502280838P_iqst_SNR_Non_Unif.jpg
200502280838P_iqst_System_MTF.jpg
200502280838P_IQST.txt
200502280838P_QAP.txt
Image200502280838Pcomposite.img
Image200502280838Pflatfield1.img
Image200502280838Pflatfield2.img
Imagetimestamp
timestamp
Each time the QAP is run, 15 files are created. Three text result files (details.txt, IQST.txt, and
QAP.txt), nine graphical result jpg file types, and three image files (two flat field and one composite).
The only image files retained are for the last two QAP runs.
In addition, there are two time stamp files “timestamp” which documents when the QAP tests ran,
and “Imagetimestamp”, which documents when the last two sets of QAP images were created).
GE HEALTHCARE
DIRECTION 5429484 -CA-1EN, REVISION 1 EMC CONFORMANCE STATEMENT
Chapter 25 - EMC Conformance Statement
Section 1.0 Compliance Statement
The equipment comply with IEC 60601-1-2 Edition 2.1 (2004-11) EMC standards
for medical devices.
These equipments generate, use, and can radiate radio frequency energy. These
equipments may cause radio frequency interference to other medical and non-
medical devices and radio communications.
To provide reasonable protection against such interference, each product
complies with the radiated emission standard limits as per CISPR11 Group1
Class A standard limits.
However, there is no guarantee that interference will not occur in a particular
installation.
If these equipments are found to cause interference (which may be determined by
turning 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 separation between the equipment and the affected device (see
recommended separation distances)
• 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 by using other
than recommended interconnect cables or by unauthorized changes or
modifications to these equipments. Unauthorized changes or modifications could
void the users' authority to operate the equipment.
All interconnect cables to peripheral devices must be shielded and properly
grounded, except when technologically prohibited. Use of cables not properly
shielded and grounded may result in the equipment causing radio frequency
interference.
Each product is intended for use in non-domestic environments, and not directly
connected to the Public Mains Network that supplies buildings used for domestic
purposes.
The compatible accessories must be used within the recommended operating
conditions outlined in the operation manuals. In addition to calibration and warm-
up, other devices must be reset before and after use to ensure accurate dose
measurements. Sustained exposure to electromagnetic fields (exceeding the test
conditions) may cause false measurements. Failure to follow the recommended
Chapter 25 - - EMC Conformance Statement Page 239

GE HEALTHCARE 
use may cause false measurements.
The magnetic field environment from a MRI device located nearby is a risk of
interference.
All of the above are required to achieve the Electromagnetic Compatibility for a
typical installation of the system. Further detailed data & requirements are
described in the Use Recommendations and Installation Recommendations
sections.
Section 2.0 Compatibility Tables
These equipments comply with IEC 60601-1-2 Edition 2.1 (2004-11) EMC
standards for medical devices.
Each product is suitable to be used in an electromagnetic environment, as per the
limits & recommendations described in the tables hereafter:
• Emission Compliance level & limits (Table 25-1).
• Immunity Compliance level & recommendations to maintain equipment clinical
utility (see Table 25-2 and Table 25-3).
Note: These systems comply with above mentioned EMC standard when used
with supplied cables.If different cable lengths are required, contact a qualified
service representative for advice.
2.1 Electromagnetic Emission

Table 25-1 Guidance and manufacturer’s declaration – electromagnetic emissions
Guidance and manufacturer’s declaration – electromagnetic emissions

Each product is intended for use in the electromagnetic environment specified below. The customer or the user of
each product should assure that it is used in such an environment.
Emissions Test Compliance Electromagnetic environment – guidance
RF emissions, CISPR 11 Each product uses RF energy only for its internal function. Therefore,
Group 1 its RF emissions are very low and are not likely to cause any
interference in nearby electronic equipment.
RF emissions, CISPR 11 Class A Each product is suitable for use in non-domestic environments, and
Harmonic emissions, not directly connected to the Public Mains Network.
Not applicable Each product is intended for use (e.g. in hospitals) with an
IEC 61000-3-2
appropriate power supply (see operation manual) and the
Voltage fluctuations/ recommended shielding for portable use.
flicker emissions, Not applicable
IEC 61000-3-3
Page 240 Section 2.0 - Compatibility Tables

GE HEALTHCARE
2.2 Electromagnetic Immunity
Table 25-2 Guidance and manufacturer’s declaration – electromagnetic immunit
Guidance and manufacturer’s declaration – electromagnetic immunity

Each product is intended for use in the electromagnetic environment specified below. The customer or the user of each product should assure
that it is used in such an environment.
Immunity Test IEC 60601 Test Level Compliance Level Electromagnetic Environment Guidance
Electrostatic discharge +/− 6 kV contact. +/− 6 kV contact. Floors should be wood, concrete, or
(ESD), IEC 61000-4-2 +/− 8 kV air. +/− 8 kV air. ceramic tile. If floors are covered
with synthetic material, the relative
humidity should be at least 30%.
Electrical fast transient/ +/− 2 kV for power supply +/− 2 kV for power Mains power quality should be that
burst, IEC 61000-4-4 lines. supply lines. of a typical commercial or hospital
+/− 1 kV for input/output +/− 1 kV for input/output environment
lines. lines.
Surge, IEC 61000-4-5 ±1 kV differential mode ±1 kV differential mode Mains power quality should be that of a typical
±2 kV common mode ±2 kV common mode commercial or hospital environment.
Voltage dips, short < 5% UT (> 95% dip in UT) 0% UT for 5 sec. Mains power quality should be that of a typical
interruptions and for 0.5 cycle. commercial or hospital environment. If the user
voltage variations on 40% UT , (60% dip in UT) of the system requires continued operation
power supply input for 5 cycles. during power mains interruptions, it is
lines, IEC 61000-4-11 70% UT , (30% dip in UT) recommended that the system be powered from
for 25 cycles. an un-interruptible power supply or a battery.
< 5% UT, (> 95% dip in
UT) for 5 cycles
Power frequency (50/60 3 A/m 3 A/m Power frequency magnetic fields should be at
Hz) magnetic field, levels characteristic of a typical location in a
IEC 61000-4-8 typical commercial or hospital environment.
Note: These are guidelines. Actual conditions may vary.

GE HEALTHCARE 
Table 25-3 Guidance and manufacturer’s declaration – electromagnetic immunity
Guidance and manufacturer’s declaration – electromagnetic immunity

Each product is intended for use in the electromagnetic environment specified below. The customer or the user of each product should assure
that it is used in such an environment.
Immunity Test IEC 60601 Test Level Compliance Level Electromagnetic Environment Guidance
Conducted RF, 3 Vrms, 3Vrms Portable and mobile RF communications equipment
IEC 61000-4-6 150 kHz ~ 80 MHz should be used no closer to any part of each product,
including cables, than the recommended separation
distance calculated from the equation appropriate for
Radiated RF 3V/m 3V/m the frequency of the transmitter.
IEC 61000-4-3
80 MHz~2.5GHz Recommended Separation Distance
80 MHz to 800 MHz
800 MHz to 2.5 GHz

where, P is the maximum output power rating of the
transmitter in watts (W) according to the transmitter
manufacturer and d is the recommended separation
distance in metres (m).
Field strengths from fixed RF transmitters, as
determined by an electromagnetic site surveya, should
be less than the compliance level in each frequency
rangeb.
Interference may occur in the vicinity of equipment
marked with the following symbol:
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.
a Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio,
AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic environment
due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which each
product is used exceeds the applicable RF compliance level above, each product should be observed to verify normal operation. If abnormal
performance is observed, additional measures may be necessary, such as re-orienting or relocating each product.
b Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
Page 242 Section 2.0 - Compatibility Tables

GE HEALTHCARE
Table 25-4 Recommended separation distances between portable and mobile RF
communications equipment and each product – for EQUIPMENT and SYSTEMS that are not
LIFE-SUPPORTING.
Recommended separation distances between portable and mobile RF communications equipment and products
Each product is intended for use in an electromagnetic environment in which radiated RF disturbances are
controlled. The customer or the user of each product can help prevent electromagnetic interference by
maintaining a minimum distance between portable and mobile RF communications equipment
(transmitters) and each product as recommended below, according to the maximum output power of the
communications equipment.
Separation distance according to frequency of transmitter m
150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.5 GHz
Rated Maximum Output Power (P)
of Transmitter Watts (W)
0.01 0.12 0.12 0.23
0.1 0.37 0.37 0.74
1 1.17 1.17 2.33
10 3.69 3.69 7.38
100 11.67 11.67 23.33

For transmitters rated at a maximum output power not listed above, the recommended separation distance d in metres
(m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output
power rating of the transmitter in watts (W) according to the transmitter manufacturer.
NOTE 1 At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by reflection from
structures, objects and people.
Section 3.0 Use Recommendations
These equipments comply with IEC 60601-1-2 Edition 2.1 (2004-11) EMC
standard for medical devices and with radio frequency emission requirements per
CISPR11 Group1 Class A standard limits. The system is intended for use in
hospitals.
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 types of devices turned off when near this equipment.
Adhering to the distance separation recommended in Table 25-4, between 150 kHz
& 2.5 GHz, will reduce disturbances recorded at the image level but may not
eliminate all disturbances. However, when installed and operated as specified
herein, the system will maintain its essential performance including safe X-Ray
acquisition and patient positioning, proper error reporting, and integrity of
patient and image data.
For example, a 1W mobile phone (800 MHz to 2.5 GHz carrier frequency) shall be
put 2.3 meters apart from the system (in order to avoid image interference risks).

GE HEALTHCARE 
The use of accessories, transducers, and cables other than those specified may
result in degraded ELECTROMAGNETIC COMPATIBILITY of the system.
The medical staff in charge of this equipment is required to instruct technicians,
patients, and other people who may be around this equipment to comply fully with
the above equipment requirements.
Section 4.0 Installation Recommendations
These systems comply with above mentioned EMC standard when used with
supplied cables up to maximum lengths referenced in the system Pre-Installation
manual. In order to minimize interference risks, the following requirements shall
apply.
4.1 Cable Shielding & Grounding
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.
4.2 Subsystem & Accessories Power Supply Distribution
All components, accessories subsystems, systems which are electrically

connected to the system, must have all AC power supplied by the same power
distribution panel & line.
4.3 Stacked Components & Equipment
The system should not be used adjacent to or stacked with other equipment; if
adjacent or stacked use is necessary, the system should be tested and verified in
order to ensure normal operation in the configuration in which it will be used.
Consult qualified personnel regarding device/system configurations.
4.4 Low Frequency Magnetic Field
Not applicable.
4.5 Static Magnetic Field Limits
In order to avoid interference on the system, static field limits from the surrounding
environment are specified.
Static field is specified less than <1 Gauss around the unit.
Page 244 Section 4.0 - Installation Recommendations

GE HEALTHCARE
4.6 Electrostatic Discharge Environment & Recommendations
In order to reduce electrostatic discharge interference, install a charge dissipative

floor material to avoid electrostatic charge buildup.
The relative humidity shall be at least 30 percent.
The dissipative material shall be connected to the system ground reference, if
applicable.

GE HEALTHCARE 
Page 246 Section 4.0 - Installation Recommendations

GE HEALTHCARE
DIRECTION 5429484 -CA-1EN, REVISION 1 IHE
Chapter 26 Integrating the Healthcare

Enterprise (IHE) Integration Statement
Section 1.0 - Introduction

1.1 Overview
This IHE Integration Statement describes the intended conformance of this GE

product with the IHE Technical Framework. The IHE Technical Framework
defines a subset of the functional components of the healthcare enterprise, called
IHE Actors, and specifies their interactions in terms of a set of coordinated,
standards-based transactions. These transactions are organized into functional
units called Integration Profiles that highlight their capacity to address specific
clinical needs.
Users familiar with these concepts can use Integration Statements as an aid to
determine what level of integration this product supports with other systems and
what clinical and operational benefits such integration might provide.
Other GE Integration Statements as well as further information on IHE may be

found on Internet at: ge.com/ihe
1.2 Important Remarks
The use of these IHE Integration Statements, by itself, it is not sufficient to ensure
that interoperation will be successful. The user needs to proceed with caution and
ensure that a qualified systems' integration (such as that provided by GE's IT
Professional Services) address at least four issues:
• Integration - The integration of any system into an integrated department or
enterprise requires an analysis of the applications requirements. The design of a
solution that integrates GE systems with non-GE systems is the user's
responsibility and should not be underestimated. Special care should be
exercised in defining the expected workflow, the special conditions, and the
clinical practice to be supported to ensure a safe and effective operation.
• Validation - Testing the complete range of possible interactions between any
GE system and non-GE system, before the integration is declared operational,
should not be overlooked. Therefore, the user should ensure that any non-GE
provider accepts full responsibility for all validation required for their connection
with GE systems. This includes the accuracy of the data once it has crossed the
interface and the stability of the data for the intended applications. Such a
Chapter 26 - Integrating the Healthcare Enterprise (IHE) Integration Statement Page 247
GE HEALTHCARE 
DIRECTION 5429484 -CA-1EN, REVISION 1 IHE
validation is required before any clinical use (diagnosis and/or treatment) is
performed.
• Future Evolution - GE understands that the IHE Technical Framework and the
underlying communication standards will evolve to meet the user's growing
requirements. GE is actively involved in the development of the IHE Technical
Framework and the underlying standards.Such evolutions may require changes to
already installed systems. In addition, GE reserves the right to discontinue or
make changes to product features including those reflected by this IHE Integration
Statement. The user should ensure that any non-GE system that connects with
GE systems also plans for the future evolution of IHE. Failure to do so will likely
result in the loss of function and/or connectivity as the IHE Integration profiles
evolve and GE Products are enhanced to support these changes.
Section 2.0 - IHE Integration Statement
General Electric -IHE Integration Statement Date: NOV 04 2012
Vendor Product Name Version
Galaxy
GE Healthcare All
Brivo XR515
This product implements all transactions required in the IHE Technical Framework to support the IHE
Integration Profiles, Actors and Options listed below:
Actors Implemented Options Implemented
Integration Profiles Implemented
Scheduled Workflow Acquisition Modality Broad Worklist Query Patient

Based Worklist Query
Patient Information Acquisition Modality None

Reconciliation
Internet address for GE Healthcare IHE information:ge.com/ihe
Links to Standards Conformance Statements for the Implementation
HL7 Not Applicable
DICOM ge.com/dicom
Links to general information on IHE
In North America: In Europe: In Japan:

www.rsna.org/ihe www.ihe-europe.org www.jira-net.or.jp/ihe-j
www.himss.org/ihe
Page 248 Section 1.0 - - Introduction

ay
Xr
GE HEALTHCARE
NO.1, YONGCHANG NORTH ROAD
ECONOMIC & TECHNOLOGICAL DEVELOPMENT ZONE
FAX: 86-10-67881850
TELE: 86-10-58068888
250
BEIJING, P. R. CHINA 100176

Direction 5429484 - CA-1EN Revision 1 GE Healthcare Brivo XR515 Service Manual (Class A)

Uploaded by

Document Information

Original Title

Copyright

Available Formats

Share this document

Share or Embed Document

Sharing Options

Did you find this document useful?

Is this content inappropriate?

Copyright:

Available Formats

Direction 5429484 - CA-1EN Revision 1 GE Healthcare Brivo XR515 Service Manual (Class A)

Uploaded by

Copyright:

Available Formats

GE Healthcare

Direction 5429484 -CA-1EN

Copyright © 2013 by General Electric Company, Inc. All Rights Re-

Legal Notes Page 3

Page 4 Legal Notes

VÝSTRAHA  TENTO PROVOZNÍ NÁVOD EXISTUJE POUZE V ANGLICKÉM JAZYCE.

(CS)  V PŘÍPADĚ, ŽE EXTERNÍ SLUŽBA ZÁKAZNÍKŮM POTŘEBUJE NÁVOD V

ADVARSEL  DENNE SERVICEMANUAL FINDES KUN PÅ ENGELSK.

Important Precautions Page 5

WAARSCHUWING  DEZE ONDERHOUDSHANDLEIDING IS ENKEL IN HET ENGELS

• THIS SERVICE MANUAL IS AVAILABLE IN ENGLISH ONLY.

HOIATUS  KÄESOLEV TEENINDUSJUHEND ON SAADAVAL AINULT INGLISE KEELES.

VAROITUS  TÄMÄ HUOLTO-OHJE ON SAATAVILLA VAIN ENGLANNIKSI.

(FI)  JOS ASIAKKAAN HUOLTOHENKILÖSTÖ VAATII MUUTA KUIN

Page 6 Important Precautions

• CE MANUEL DE MAINTENANCE N’EST DISPONIBLE QU’EN

WARNUNG  DIESE SERVICEANLEITUNG EXISTIERT NUR IN ENGLISCHER SPRACHE.

ΠΡΟΕΙ∆ΟΠΟΙΗΣΗ  ΤΟ ΠΑΡΟΝ ΕΓΧΕΙΡΙ∆ΙΟ ΣΕΡΒΙΣ ∆ΙΑΤΙΘΕΤΑΙ ΣΤΑ ΑΓΓΛΙΚΑ ΜΟΝΟ.

(EL)  ΕΑΝ ΤΟ ΑΤΟΜΟ ΠΑΡΟΧΗΣ ΣΕΡΒΙΣ ΕΝΟΣ ΠΕΛΑΤΗ ΑΠΑΙΤΕΙ ΤΟ ΠΑΡΟΝ

Important Precautions Page 7

FIGYELMEZTETÉS  EZEN KARBANTARTÁSI KÉZIKÖNYV KIZÁRÓLAG ANGOL NYELVEN ÉRHETŐ

AÐVÖRUN  ÞESSI ÞJÓNUSTUHANDBÓK ER EINGÖNGU FÁANLEG Á ENSKU.

• IL PRESENTE MANUALE DI MANUTENZIONE È DISPONIBILE

Page 8 Important Precautions

경고  본 서비스 지침서는 영어로만 이용하실 수 있습니다.

 본 서비스 지침서를 참고했고 이해하지 않는 한은 해당 장비를 수리하려고 시도하지

 이 경고에 유의하지 않으면 전기 쇼크, 기계상의 혹은 다른 위험으로부터 서비스 제공

BRĪDINĀJUMS  ŠĪ APKALPES ROKASGRĀMATA IR PIEEJAMA TIKAI ANGĻU VALODĀ.

ĮSPĖJIMAS  ŠIS EKSPLOATAVIMO VADOVAS YRA PRIEINAMAS TIK ANGLŲ KALBA.

Important Precautions Page 9

ADVARSEL  DENNE SERVICEHÅNDBOKEN FINNES BARE PÅ ENGELSK.

OSTRZEŻENIE  NINIEJSZY PODRĘCZNIK SERWISOWY DOSTĘPNY JEST JEDYNIE W JĘZYKU

ATENÇÃO  ESTE MANUAL DE ASSISTÊNCIA TÉCNICA SÓ SE ENCONTRA DISPONÍVEL

ATENŢIE  ACEST MANUAL DE SERVICE ESTE DISPONIBIL NUMAI ÎN LIMBA ENGLEZĂ.

Page 10 Important Precautions

ОСТОРОЖНО!  ДАННОЕ РУКОВОДСТВО ПО ОБСЛУЖИВАНИЮ ПРЕДЛАГАЕТСЯ ТОЛЬКО

UPOZORNENIE  TENTO NÁVOD NA OBSLUHU JE K DISPOZÍCII LEN V ANGLIČTINE.

(SK)  AK ZÁKAZNÍKOV POSKYTOVATEĽ SLUŽIEB VYŽADUJE INÝ JAZYK AKO

ATENCION  ESTE MANUAL DE SERVICIO SOLO EXISTE EN INGLES.

Important Precautions Page 11

VARNING  DEN HÄR SERVICEHANDBOKEN FINNS BARA TILLGÄNGLIG PÅ ENGELSKA.

DİKKAT  BU SERVİS KILAVUZUNUN SADECE İNGİLİZCESİ MEVCUTTUR.

CERTIFIED ELECTRICAL CONTRACTOR STATEMENT

Page 12 Important Precautions

LITHIUM BATTERY CAUTIONARY STATEMENTS

OMISSIONS & ERRORS

Important Precautions Page 13

Page 14 Important Precautions

Revision Date Reason for change

This page is intentionally left blank.

Revision History Page 15

1.1 Hazard Messages

1.2 Text Format of Signal Words

1.3 Symbols and Pictorials Used

keep_up magnetic biohazard compressgas ppe-hearing

fragile impact corrosive heavyobject ppe-2people

static_elec heat general laser ppe-respitory

keep_dry pinch radiation poisongas ppe-loto

general explosive electrical flammable ppe-eye

torque crush/mechanical tipping Read Manual ppe-gloves

ce instuction poisonmatl entanglement instuction

EXAMPLES OF PREFIXES USED FOR GENERAL INFORMATION:

2.2 Page Layout