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GE Healthcare
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Technical
Publication
Direction 5275600-100
Revision 3
GE Healthcare
Medical Diagnostic Radiography XR 6000
Pre-Installation
Copyright © 2007~2008 by General Electric Company, Inc.

All rights reserved.
GE HEALTHCARE
DIRECTION 5275600-100, REVISION 3 XR 6000 PRE-INSTALLATION
Published by the GE Company, Inc.

Engineering/Technical: Erna Yan
Page 2
GE HEALTHCARE
LEGAL NOTES
TRADEMARKS
All other products and their name brands are trademarks of their respective holders.
COPYRIGHTS
All Material, Copyright © 2007~2008 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

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This page is intentionally left blank.
Page 4 Legal Notes

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Important Precautions
LANGUAGE
ПРЕДУПРЕЖДЕНИЕ • ТОВА УПЪТВАНЕ ЗА РАБОТА Е НАЛИЧНО САМО НА АНГЛИЙСКИ ЕЗИК.

(BG) • АКО ДОСТАВЧИКЪТ НА УСЛУГАТА НА КЛИЕНТА ИЗИСКА ЕЗИК,
РАЗЛИЧЕН ОТ АНГЛИЙСКИ, ЗАДЪЛЖЕНИЕ НА КЛИЕНТА Е ДА ОСИГУРИ
ПРЕВОД.
• НЕ ИЗПОЛЗВАЙТЕ ОБОРУДВАНЕТО ПРЕДИ ДА СТЕ СЕ КОНСУЛТИРАЛИ
И РАЗБРАЛИ УПЪТВАНЕТО ЗА РАБОТА.
• НЕСПАЗВАНЕТО НА ТОВА ПРЕДУПРЕЖДЕНИЕ МОЖЕ ДА ДОВЕДЕ ДО
НАРАНЯВАНЕ НА ДОСТАВЧИКА НА УСЛУГАТА, ОПЕРАТОРА ИЛИ
ПАЦИЕНТ В РЕЗУЛТАТ НА ТОКОВ УДАР ИЛИ МЕХАНИЧНА ИЛИ ДРУГА
ОПАСНОСТ.
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 ANGLAIS.

ATTENTION
• SI LE TECHNICIEN DU CLIENT A BESOIN DE CE MANUEL DANS UNE
(FR)
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.
ΠΡΟΕΙΔΟΠΟΙΗΣΗ • ΤΟ ΠΑΡΟΝ ΕΓΧΕΙΡΙΔΙΟ ΣΕΡΒΙΣ ΔΙΑΤΙΘΕΤΑΙ ΣΤΑ ΑΓΓΛΙΚΑ ΜΟΝΟ.
(EL) • ΕΑΝ ΤΟ ΑΤΟΜΟ ΠΑΡΟΧΗΣ ΣΕΡΒΙΣ ΕΝΟΣ ΠΕΛΑΤΗ ΑΠΑΙΤΕΙ ΤΟ ΠΑΡΟΝ

ΕΓΧΕΙΡΙΔΙΟ 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
ΕΓΧΕΙΡΙΔΙΟ ΣΕΡΒΙΣ.
• ΕΑΝ ΔΕ ΛΑΒΕΤΕ ΥΠΟΨΗ ΤΗΝ ΠΡΟΕΙΔΟΠΟΙΗΣΗ ΑΥΤΗ, ΕΝΔΕΧΕΤΑΙ ΝΑ
ΠΡΟΚΛΗΘΕΙ ΤΡΑΥΜΑΤΙΣΜΟΣ ΣΤΟ ΑΤΟΜΟ ΠΑΡΟΧΗΣ ΣΕΡΒΙΣ, ΣΤΟ ΧΕΙΡΙΣΤΗ
Ή ΣΤΟΝ ΑΣΘΕΝΗ ΑΠΟ ΗΛΕΚΤΡΟΠΛΗΞΙΑ, ΜΗΧΑΝΙΚΟΥΣ Ή ΑΛΛΟΥΣ
ΚΙΝΔΥΝΟΥΣ.
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.

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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.
• 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。

GE HEALTHCARE
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.
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.

GE HEALTHCARE
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.

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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.

GE HEALTHCARE
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.
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.

GE HEALTHCARE
OMISSIONS & ERRORS

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

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 is 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 indicate 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, or could 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 is 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 injuries 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 TO BE LIMITED TO THE MOST EXTREME SITUATIONS.
WARNING - INDICATES A POTENTIALLY HAZARDOUS SITUATION WHICH, IF NOT
AVOIDED, COULD RESULT IN DEATH OR SERIOUS INJURY.
Preface Page 15
GE HEALTHCARE
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.
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 may 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 16 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.
Preface Page 17
GE HEALTHCARE
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.
Figure 1 Component Identification
Headers and footers in this publication are designed to allow you to quickly identify your location.
The document part number and revision number appear in every header on every page. Odd
numbered page footers indicate the current chapter, its title and current page number. Even
numbered page footers show the current section and its title, as well as the current page number.
2.3 Computer Screen Output/Input Text Character Styles

Within this publication, mono-spaced character styles (fonts) are used to indicate computer text that
is either screen input or 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.
Page 18 Preface
GE HEALTHCARE
Example: This paragraph’s font represents computer generated screen “fixed” output.
Fixed Output Its output is fixed from the sense that it does not vary from application
to application. It is 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 is 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: This paragraph’s font represents fixed input. It is computer input that
Fixed Input is 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: A power switch ON/OFF or a keyboard key like ENTER is indicated by applying a character style
Hard Keys that uses both over and under-lined bold text. This is a hard key.
Example: Whereas the computer MENU button that you would click with your mouse or touch with your hand
Soft Keys uses over and under-lined regular text. This is a soft key.
Preface Page 19
GE HEALTHCARE
Page 20 Preface
GE HEALTHCARE
Table of Contents
Preface
Publication Conventions ...................................................................................... 15
Section 1.0
Safety & Hazard Information ........................................................................... 15
1.1 Hazard Messages............................................................................................................ 15
1.2 Text Format of Signal Words ........................................................................................... 15
1.3 Symbols and Pictorials Used ........................................................................................... 16
Section 2.0
Publication Conventions ................................................................................. 17
2.1 General Paragraph and Character Styles........................................................................ 17
2.2 Page Layout..................................................................................................................... 18
2.3 Computer Screen Output/Input Text Character Styles .................................................... 18
2.4 Buttons, Switches and Keyboard Inputs (Hard & Soft Keys) ........................................... 19
Chapter 1 - Introduction........................................................................................ 25
Section 1.0
Objective and Scope of this Manual............................................................... 25
Section 2.0
Avoiding Unnecessary Expenses and Delays............................................... 25
Section 3.0
An Overview of the Pre-Installation Process................................................. 25
Section 4.0
Responsibility of Purchaser/Customer .......................................................... 26
Section 5.0
Contract Changes ............................................................................................ 26
Section 6.0
Responsibilities of the Purchaser .................................................................. 27
Section 7.0
What You Will Receive (System Components).............................................. 27
Chapter 2 - Room Requirements.......................................................................... 31

Section 1.0
Environmental Requirements ......................................................................... 31
1.1 Relative Humidity and Temperature ................................................................................ 31
1.2 Altitude and Atmospheric Pressure ................................................................................. 32
1.3 Heat Output ..................................................................................................................... 32
1.4 Acoustic Output ............................................................................................................... 33
1.5 Light Specification............................................................................................................ 33
1.6 Radiation Protection ........................................................................................................ 33
Table of Contents Page 21

GE HEALTHCARE
Section 2.0
Structural Requirements.................................................................................. 33
2.1 Door Size Requirements ................................................................................................. 33
2.2 Floor Requirements......................................................................................................... 33
2.2.1 Floor Requirements when using provided Floor Anchors .................................. 33
2.2.1.1 Table............................................................................................... 34
2.2.1.2 Wall Stand ...................................................................................... 34
2.2.1.3 Console Pedestal (Option).............................................................. 35
2.2.2 Service Access Requirements ........................................................................... 36
Chapter 3 - Planning Electrical Connections ..................................................... 37

Section 1.0
Routing Cables ................................................................................................. 37
1.1 General ........................................................................................................................... 37
1.2 Conduit............................................................................................................................ 37
1.3 Electrical Ducts ............................................................................................................... 37
1.4 Power Distribution ........................................................................................................... 39
Section 2.0
Master Interconnect System (MIS) .................................................................. 39
Chapter 4 - System Facility Power & Grounds ................................................... 41

Section 1.0
Introduction....................................................................................................... 41
1.1 Power Quality.................................................................................................................. 41
1.2 Electrical Requirements .................................................................................................. 42
1.2.1 System Electrical Requirements ........................................................................ 42
1.2.1.1 System Power Specifications ......................................................... 42
1.2.2 Recommended Power Supply............................................................................ 43
1.2.3 Recommended Wall “Circuit-Breaker” Ratings ................................................. 44
1.2.4 Wiring Electrical Power and Disconnects........................................................... 45
1.2.4.1 Room Power Supply ....................................................................... 45
1.2.4.2 Multiple Emergency “OFF” Switches .............................................. 46
1.2.4.3 Customer-supplied Electrical Outlet ............................................... 46
Section 2.0
Electrical Grounds............................................................................................ 47
2.1 System and Facility Grounds .......................................................................................... 47
2.2 Recommended Ground Wire Sizes................................................................................. 47
2.3 Final Checks, Before System Installation Can Begin...................................................... 47
Chapter 5 - Product Characteristics .................................................................... 51

Section 1.0
Overview............................................................................................................ 51
Section 2.0
System Components Dimensions and Weights ............................................ 51
2.1 Dimensions ..................................................................................................................... 51
2.2 Dimensioned Figures and Drawings ............................................................................... 52
Page 22 Table of Contents

GE HEALTHCARE
2.2.1 System................................................................................................................ 52
2.2.2 Operator Console ............................................................................................... 54
2.2.3 Integrated Table.................................................................................................. 55
2.2.3.1 Table ............................................................................................... 58
2.2.3.2 Tube Stand...................................................................................... 60
2.2.4 Wall Stand .......................................................................................................... 61
2.2.5 Dolly.................................................................................................................... 63
Section 3.0
Positioning and Mounting Equipment............................................................ 64
3.1 Floor Loading and Recommended Mounting Methods.................................................... 64
Chapter 6 - Room Layout...................................................................................... 65

Section 1.0
Radiation Production ....................................................................................... 65
Section 2.0
Clinical Access ................................................................................................. 65
Section 3.0
Peripheral Equipment ...................................................................................... 65
Section 4.0
Room Layout Drawings ................................................................................... 66
Chapter 7 - Planning Aids..................................................................................... 67

Section 1.0
Shipping Dimensions and Weights................................... 67
Section 2.0
Installation Tools and Materials Required ..................................................... 68
2.1 Tools and Materials Checklist.......................................................................................... 68
Section 3.0
Preparing the Delivery Route .......................................................................... 69
Section 4.0
Pre-Installation Checklist ................................................................................ 70
Chapter 8 - System Cable Information ................................................................ 73

Section 1.0
Introduction ...................................................................................................... 73
Section 2.0
Cable Information............................................................................................. 74
2.1 Cable Lengths and Characteristics ............................................. 74
Section 3.0 - System Master Interconnect Schematic (MIS) ........................ 75
Table of Contents Page 23

GE HEALTHCARE
Appendix A - Electromagnetic Compatibility (EMC) .......................................... 77
Section 1.0
Compliance Statement ..................................................................................... 77
Section 2.0
Compatibility Tables......................................................................................... 78
2.1 Electromagnetic Emission............................................................................................... 78
2.2 Electromagnetic Immunity............................................................................................... 79
Section 3.0
Use Recommendations .................................................................................... 81
Section 4.0
Installation Recommendations........................................................................ 82
4.1 Cable Shielding & Grounding.......................................................................................... 82
4.2 Subsystem & Accessories Power Supply Distribution ................................................... 82
4.3 Stacked Components & Equipment ................................................................................ 82
4.4 Low Frequency Magnetic Field ....................................................................................... 82
4.5 Electrostatic Discharge Environment & Recommendations............................................ 82
Appendix B - Revision History............................................................................. 83
Appendix C - List of Effected Pages ................................................................... 84
Page 24 Table of Contents

GE HEALTHCARE
Chapter 1 - Introduction
Section 1.0
Objective and Scope of this Manual
This document is intended as a guide and informational resource for planning and properly
preparing a location for the installation of a XR 6000 system.
Section 2.0
Avoiding Unnecessary Expenses and Delays
To avoid unnecessary expenses and delays, use the “Pre-Installation” checklist located in Chapter
7 to determine if you are ready for the installation to begin. Once you believe that your room/location
is ready for installation to begin, complete the “Pre-Installation” checklist. The checklist is an
important tool that helps verify that nothing has been missed. The checklist summarizes the
preparations and allows you to record a permanent record of the activities that have taken place.
Section 3.0
An Overview of the Pre-Installation Process
Pre-installation is a co-operative effort between the customer/purchaser and GE Healthcare
(GEHC). Complete the checklists contained in this manual. They are an important part of the pre-
installation process. The checklists summarize the required preparations and verify the completion
of the pre-installation procedures.
Figure 1-1 outlines the information in this document and its place in the pre-installation process.
Chapter 1 - - Introduction Page 25

GE HEALTHCARE
Site Data Consultants:

Collected Radiation
Chapter 2 - - from Field Seismic
Room Room Structure
Requirements Requirements
Chapter 5 - -
Product System
Characteristics Componets Site Planning
Chapter 6 - - and layout
Room Layout Information
Order Cable Lengths
Chapter 3 - -
Planning Electrical Electrical
Connections Information
Chapter 4 - -
System Facility
Power & Grounds Pre-installation Site Plan
Documentation Drawings
Installation
Tools
Checklist
Chapter 7 - - Pre-installation Pre-Installation Checklists and

No
Planning Aids Checklist Site Work Survey Complete?
Yes
Delivery
Route
Delivery
Survey/Map
and
Installation
Figure 1-1 Pre-Installation Overtable
Section 4.0
Responsibility of Purchaser/Customer
To ensure that the installation of a XR 6000 system meets the purchaser or Customer expectations,
it is important to determine who will take responsibility for various items in the course of the system
installation process. To aid you in determining these responsibilities, review the following checklists
with the customer and assign responsibilities as appropriate:
• Tools and Equipment Checklist (see page 68)
• Pre-Installation Checklist (see page 70)
Section 5.0
Contract Changes
Be sure to inform the customer that the cost of any alterations or modifications not specified in the
sales contract are the responsibility of the customer.
Page 26 Section 4.0 - Responsibility of Purchaser/Customer

GE HEALTHCARE
Section 6.0
Responsibilities of the Purchaser
The purchaser is responsible for completion of “Pre-Installation”. This includes the procurement and
installation of all required materials and services to get the room ready for installation of the product.
This responsibility includes providing:
• A clean and safe work environment for installation of the product (finished floor, ceiling, walls,
and proper room lighting).
• A location suitable for the installation of the product. See Chapter 2 - - Room Requirements.
- Suitable support structures in the floor, walls, or ceiling necessary for the mounting of the
product and/or its components.
- Installation of conduit, ducts and/or raceways necessary to route cables safely. See
Chapter 4 - - System Facility Power & Grounds and Chapter 5 - - Product Characteristics.
- Electrical power and grounds of specified quality and reliability. See Chapter 4 - - System
Facility Power & Grounds.
* Electrical power of the required voltage, including an emergency-off safety switch in
the room. Power and ground cables to the PDU.
* Properly installed and sized junction boxes, including covers and fittings at locations
required and called out in architectural drawings.
• A location suitable for operation of the product. See Chapter 6 - - Room Layout.
• Installation of non-electric services.
Section 7.0
What You Will Receive (System Components)
The XR 6000 system may consist of the following main components (See Figure 1-2 and Table 1-
1):
- Radiographic Table
- Standard Integrated Tube Stand
- Standard Wall Stand
- Operator Console
- Generator
- PDU
- E7843X X-Ray Tube
- Collimator

GE HEALTHCARE
Standard
3
1 4
Cabinet
Operator Console WLS
Standard
The XR 6000 is divided into basic components:

1. Operator Console (Console Stand - Optional)
2. Integrated Table Standard
3. Cabinet
4. Wall Stand Standard (Optional)
5. 50kW X-ray Tube - Toshiba E7843X
6. Collimator
Figure 1-2 XR 6000 System Component Identification
Page 28 Section 7.0 - What You Will Receive (System Components)

GE HEALTHCARE
Item Component Model Number

1a Console 5194507
1b Console Pedestal (Option) 5192392
2 Standard Integrated Table 5180891
2a Standard Integrated Tube Stand 5183392
3a Generator (VR Jedi 50 R1T) 2212259-2
3b PDU 5220653
4 Standard Wall Stand 5194508
5 X-ray Tube - E7843X 5192454
6 Manual Collimator 5189248
Table 1-1 XR 6000 System Component Identification
Note: Please ask customer to provide a support for the console if the console pedestal is not ordered.

GE HEALTHCARE
Page 30 Section 7.0 - What You Will Receive (System Components)

GE HEALTHCARE
Chapter 2 - Room Requirements
Section 1.0
Environmental Requirements
1.1 Relative Humidity and Temperature
PRODUCT OR RELATIVE HUMIDITY TEMPERATURE

COMPONENT (Non-Condensing)
IN-USE STORAGE IN-USE STORAGE
MIN. MAX. MIN. MAX. MIN. MAX. MIN. MAX.
Integrated Table 20% 85% 20% 95% +10° F 40° C -18° C +70° C
(50° F) (104° F) (-4° F) (158° F)
Wall Stand 20% 85% 20% 95% +10° F 40° C -18° C +70° C
(50° F) (104° F) (-4° F) (158° F)
Generator 30% 75% 10% 100% -10° F 40° C -40° C +70° C
(14° F) (104° F) (-40° F) (158° F)
PDU 20% 85% 20% 95% +10° F 40° C -18° C +70° C
(50° F) (104° F) (-4° F) (158° F)
Operator Console 30% 80% 20% 90% +10° F 40° C -20° C +70° C
(50° F) (104° F) (-4° F) (158° F)
X-ray Tube 30% 85% 20% 90% +10° F 40° C -20° C +70° C
(50° F) (104° F) (-4° F) (158° F)
Table 2-1 Environmental Requirements (Relative Humidity & Temperature)
Limits for rates of change:

In-Use Storage
< 10 degree C / hour < 20 degree C / hour
< 30% / hour < 30% / hour
Note: STORAGE values only refer to equipment that is still in shipping containers. If the equipment is
partially or completely installed, refer to IN-USE values.
Chapter 2 - - Room Requirements Page 31

GE HEALTHCARE
1.2 Altitude and Atmospheric Pressure
PRODUCT OR ALTITUDE ATMOSPHERIC PRESSURE

COMPONENT IN-USE STORAGE IN-USE STORAGE
MIN. MAX. MIN. MAX. MIN. MAX. MIN. MAX.
Integrated Table -100 m (- 3000 m -100 m (- 15000 m 10 psi 15.4 psi 7 psi (48 15.4 psi
328 ft.) (9842 ft.) 328 ft.) (49212 ft.) (69 kPa) (106 kPa) kPa) (106 kPa)
Wall Stand -100 m (- 3000 m -100 m (- 15000 m 10 psi 15.4 psi 7 psi (48 15.4 psi
Generator -100 m (- 3000 m -100 m (- 15000 m 10 psi 15.4 psi 7 psi (50 15.4 psi
PDU -100 m (- 3000 m -100 m (- 15000 m 10 psi 15.4 psi 7 psi (48 15.4 psi
Operator Console -100 m (- 3000 m -100 m (- 15000 m 10 psi 15.4 psi 7 psi (50 15.4 psi
X-ray Tube -100 m (- 3000 m -100 m (- 15000 m 10 psi 15.4 psi 7 psi (50 15.4 psi
Table 2-2 Environmental Requirements - (Altitude & Atmospheric Pressure)
Limits for rates of change:

In-Use Storage
< 1.8 hPA / hour < 76 hPA / hour
Note: STORAGE values only refer to equipment that is still in shipping containers. If the equipment is
partially or completely installed, refer to IN-USE values.
1.3 Heat Output
The continuous and peak power consumption of this system is as follows:
• 6kW Continuous Power
• 75kW Peak Power
PRODUCT OR HEAT OUTPUT HEAT OUTPUT

COMPONENT (BTU/hr.) (WATTS)
IN-USE IN-USE
Generator 891.36 261
PDU 500 145
Operator Console 20 6
X-ray Tube 1089.44 319
Total System Output 2500.80 731
Table 2-3 Heat Outputs by Component
Page 32 Section 1.0 - Environmental Requirements

GE HEALTHCARE
1.4 Acoustic Output
SOUND OUTPUT (dBA)

COMPONENT IN-USE (measured 1m from any STAND-BY (measured 1m from any
point in system) point in system)
System < 60 < 55
Table 2-4 XR 6000 Acoustic Output
1.5 Light Specification

The monitor screen is adjusted for an optimum ambient light level of 50 lux.
1.6 Radiation Protection

Because X-ray equipment produces radiation, special precautions may need to be taken or special
site modifications may be required. The General Electric Company does not make
recommendations regarding radiation protection. It is the purchasers responsibility to consult a
radiation physicist for advice on radiation protection in X-ray rooms.
Section 2.0
Structural Requirements
2.1 Door Size Requirements
Minimum door sizes also apply to hallway and elevator. See Chapter 5 “- Product Characteristics”
on page 51., for additional details.
Door Height: The minimum door height to accommodate the Tube Stand is 225 cm.
Door Width:
• The minimum door width to accommodate the Table is: 100 cm.
• The minimum door width is calculated based on a straight-in approach requiring a 2.5 m wide
corridor. Minimum widths will change based on narrower corridors.
2.2 Floor Requirements

The preferred method of installing the table and standard wall stand is to use the provided floor
anchors.
2.2.1 Floor Requirements when using provided Floor Anchors
Potential for Injury and/or Equipment Damage:

Anchors must be a minimum of 75mm from any concrete edge including ducts and cracks.
In addition, the general condition of the concrete in the immediate mounting area should be
inspected to ensure that anchors will be set in good quality concrete.

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2.2.1.1 Table
The Table Assembly is placed on the floor, which must accpet the weight and the weight/area
defined in Chapter 5, Section 3.1 - Floor Loading and Recommended Mounting Methods.
• The weight of the complete table is 240 kg.
• The ground surface must be approximately level.
• The XR 6000 Table system must be attached to the floor.
The floor bearing the XR 6000 system must be concrete and the thickness to be determined by a
Structural Engineer to properly support the equipment loads. The supplied anchors require a
minimum embedment of 55 mm into the concrete. If the floor thickness is less than 75 mm, it is
recommended that the unit be secured using a through-bolt method with a reinforcement plate on
the back side. For additional details, see Chapter 5, Section 3.1 - Floor Loading and Recommended
Mounting Methods.
PP
Ȼ[
PP
PP
Figure 2-1 Floor Mounting - Table Assembly
2.2.1.2 Wall Stand

The Wall Stand Assembly is placed on the floor, which must accpet the weight and the weight/area
defined in Chapter 5, Section 3.1 - Floor Loading and Recommended Mounting Methods.
• The weight of the complete standard wall stand is 106.5 kg.
• The XR 6000 Wall Stand system must be attached to the floor.
Concrete area for wall stand installation should be 0.1 m2.
the back side. For additional details, see Chapter 5, Section 3.1 - Floor Loading and
Recommended Mounting Methods.
Page 34 Section 2.0 - Structural Requirements

GE HEALTHCARE
PP
PP
PP
Ȼ[
PP
Figure 2-2 Floor Mounting - Wall Stand
2.2.1.3 Console Pedestal (Option)

The Console Pedestal Assembly is placed on the floor, which must accpet the weight and the
weight/area defined in Chapter 5, Section 3.1 - Floor Loading and Recommended Mounting
Methods.
• The weight of the console with pedestal is 6.0 kg.
• The XR 6000 Console Pedestal must be attached to the floor.
Concrete area for console pedestal installation should be 0.2 m2.
the back side. For additional details, see Chapter 5, Section 3.1 - Floor Loading and
Recommended Mounting Methods.

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PP PP
PP
Ȼ[
PP
Figure 2-3 Floor Mounting - Console Pedestal
2.2.2 Service Access Requirements

Allow appropriate space for service access of equipment, per country and regional requirements.
Page 36 Section 2.0 - Structural Requirements

GE HEALTHCARE
Chapter 3 - Planning Electrical Connections
Section 1.0
Routing Cables
1.1 General
High voltage and power cables must be separated from other cables. Use a separate trough in the
duct system, or use a separate conduit. Minimize cable length between the line disconnect and the
System Cabinet power unit to reduce voltage regulation problems and wiring costs.
For information about the cables supplied with your system, please refer to Chapter 8 - - System
Cable Information.
1.2 Conduit
Separate conduits must be used for power and signal wires. These wires must be kept separated
from each other.
Using conduit imposes some important considerations when used with this system. Of primary
concern, the majority of cables used are pre-terminated. Pre-termination greatly simplifies
interconnection but makes cable-pulling difficult because of the added dimensions of the
connectors.
Conduit must be large enough to pass the cable and connector through with all other cables already
in the conduit. Also, the size of conduit chosen must allow for future growth. There is the possibility
of additional cables being added later as the system is developed and options are added.
The use of conduit is recommended for cables running overhead between rooms, especially when
a diagonal run provides the shortest cable path.
1.3 Electrical Ducts

It’s important that electrical ducts have separate compartments for power and signal wires. These
wires must be kept separated from each other for proper system operation.
Electrical ducts have advantages, when used with a single room or two adjacent rooms. Electrical
ducts combine cabling in a neat and functional appearance, with accessibility and room for
expansion.
Chapter 3 - - Planning Electrical Connections Page 37

GE HEALTHCARE
Figure 3-1 System Electrical Ducts
&0
&0
Figure 3-2 Table Electrical Ducts
Page 38 Section 1.0 - Routing Cables

GE HEALTHCARE
1.4 Power Distribution
XR 6000 system power distribution consists of two major components that must either be customer
supplied or GE Healthcare supplied. These are:
• Feeder power from Hospital distribution center to the XR 6000 System Cabinet load power unit
(SKL).
• Power distribution from the XR 6000 System Cabinet load power unit (SKL) to all the
components in the XR 6000 system room.
Usually the feeder power from the Hospital distribution center is customer supplied and the power
distribution within the XR 6000 system is supplied by GEHC.
Note: For hospital facility feeder power and ground requirements to the XR 6000 system power unit, refer
Additional to: Chapter 4 - - System Facility Power & Grounds.
Reference For XR 6000 system power distribution from the System Cabinet power unit, refer to XR 6000 MIS
Material Exists Map, see Chapter 8 - - System Cable Information.
Section 2.0
Master Interconnect System (MIS)
System interconnect cables are described in MIS (Master Interconnect System) documents
shipped with the system. These documents specify all interconnections between components
within the system and its options.
Note: For specific XR 6000 system interconnect maps and connection details, please refer to Chapter 8
Additional - - System Cable Information.
Reference
Material Exists
Chapter 3 - - Planning Electrical Connections Page 39

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Page 40 Section 2.0 - Master Interconnect System (MIS)

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Chapter 4 - System Facility Power & Grounds
Section 1.0
Introduction
The purpose of this chapter is to ensure that the product is properly powered and grounded, thus
ensuring the proper operation of the product installed. The information in this chapter should be
adhered to, unless there are written deviations approved by GE Healthcare.
This chapter gives the sizes and procedures on how to power and ground your system. If these
power and grounding instructions are not adhered to, proper operation cannot be guaranteed. Any
cost associated and found to be a result of non-conformity, as stated in this chapter, may result in
additional cost charged back to the institution and/or their contractor.
All XR 6000 system and sub-system power connections shall be made ONLY to power
outlets that are connected to the XR 6000 system.
All XR 6000 system component power connections must be made in accordance with the XR 6000
MIS Map, see Chapter 8 - - System Cable Information.
1.1 Power Quality

The electrical power, from its origination to the system, must adhere to the wire size and transformer
sizes as prescribed in the installation drawings. The feeder voltage-drops, as well as the supplying
power, must be within the given parameters. Sizing for feeder is usually calculated for a maximum
of 2% voltage drop at the minimum voltage range. The actual feeder sizing may vary from the
installation drawing for a facilities voltage.
Calculate feeder losses before you begin. Total feeder losses must be calculated to ensure that the
losses are less than those specified in the installation drawings. Calculating the recommended
minimum transformer sizing for feeding a system ensures the transformer losses are less than half
of the maximum regulation for the system.
Regulation is the calculated voltage losses for the entire power distribution system (No-Load
Voltage minus Full-Load Voltage) divided by the no-load voltage minus the system losses (Full-
Load Voltage):
NoLoadVoltage – FullLoadVoltage
Regulation = ---------------------------------------------------------------------------------------------------- × 100
FullLoadVoltage
In the X-ray room, there must be a lockable facility power disconnect. It must be installed electrically
before the equipment, for the purpose of locking out the power. This must be done before service
to the high voltage system is performed.
Chapter 4 - - System Facility Power & Grounds Page 41

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1.2 Electrical Requirements
In China, all cables used to provide system power and ground must be CCC
certified.
Only WYE connected power source are currently permitted, due to current system
(generator) design.
All system components obtain their power from the Power Distribution Unit (PDU). The Generator
and PDU are both in the table Providing power and ground wires to the PDU are the
responsibility of the customer. As an aid, wire sizes for various lengths of the power supply cable
are shown in the following tables.
PE CABLES SHALL HAVE THE DIAMETER NOT LESS THAN THE POWER SUPPLY
CONDUCTOR, AND SHALL HAVE AN IMPEDENCE NOT MORE THAN 0.1 OHMS.
1.2.1 System Electrical Requirements
1.2.1.1 System Power Specifications
PARAMETER JEDI GENERATOR - 50kW

Input Voltage 380/400/440/480 VAC WYE 3-Phase and ground without neutral
Required Power Source WYE Distribution
Daily Voltage variations +/- 10% (VAC) In this range, the generator will operate without any de-
rating in accuracy.
Line Impedance The apparent line impedance guaranteed by the customer should be
equal or less than the values indicated below, according to the voltage
value and the commercial power of the generator.
Voltage range (V) Line Impedance (ohms)
3 phase 50kW
380 0.15
415 0.18
440 0.20
480 0.24
Note: 400-480 VAC impedance values are based on IEC 601-2-7
standard. Values are interpolated from values in standard.
HV cable length 8m
HV cable type IB EEC: 22 mm cable de Lyon (<=150 pF/m)
USA: 22 mm DSI (<=165pF/m)
EEC: 16 mm Claymount (<=165 pF/m)
HV cable connector = Federal standard
Ground Wire #8 AWG
Table 4-1 System Power Specifications
Page 42 Section 1.0 - Introduction

GE HEALTHCARE
PARAMETER JEDI GENERATOR - 50kW
Inrush current 600 A
Normal Frequency 50/60Hz
Daily frequency variation 47~63Hz
Table 4-1 System Power Specifications
1.2.2 Recommended Power Supply

PDU Power Supply cable has to be provided by the customer, and also can be ordered from GE
(S3922KG). Wire size for various lengths of the Power Supply cable are shown in Table 4-5.
Note: Power cable should be flexible enough to allow generator to roll back into table.
PARAMETER THREE PHASE GENERATOR - 50kW

Input Voltage
Wire Size 380 VAC 400 VAC 415VAC 440 VAC 460 VAC 480 VAC
Length
15 m (50 ft.) 10 (#8 10 (#8 10 (#8 10 (#8 10 (#8 10 (#8
mm 2 AWG) mm 2 AWG) mm 2 AWG) mm 2 AWG) mm 2 AWG) mm AWG)
2
30 m (150 ft.) 16 (#6 16 (#6 16 (#6 16 (#6 16 (#6 16 (#6

mm2 AWG) mm2 AWG) mm2 AWG) mm2 AWG) mm2 AWG) mm2 AWG)
46 m (200 ft.) 22 (#5 22 (#5 22 (#5 22 (#5 22 (#5 22 (#5
2 AWG) 2 AWG) 2 AWG) 2 AWG) 2 AWG) 2 AWG)
mm mm mm mm mm mm
60 m (100 ft.) 30 (#3 30 (#3 30 (#3 30 (#3 30 (#3 30 (#3
2 AWG) 2 AWG) 2 AWG) 2 AWG) 2 AWG) 2 AWG)
mm mm mm mm mm mm
Table 4-2 Minimum Wire Size 50 kW
Phase 3 3 3 3
Nominal Line Voltage (Vac) 380 400 440 480
Voltage Range (Vac) +/- 10% +/- 10% +/- 10% +/- 10%
Momentary Line Current (Amp) 110 105 95 88
Continuous Line Current (Amp) 7 6.7 6 5.5
Power Demand (kVA) 70 70 70 70
Frequency 47/53Hz and 57/63Hz
Table 4-3 kVA Load Characteristics 50 kW

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1.2.3 Recommended Wall “Circuit-Breaker” Ratings
Power / Voltage 32 kW 50 kW
380 V 70 A / 600 V 110 A / 600 V
400 V 66 A / 600 V 105 A / 600 V
440 V 60 A / 600 V 95 A / 600 V
480 V 55 A / 600 V 88 A / 600 V
Table 4-4 Wall Breaker Parameter (Theoretical Current Values)
Note: The main circuit breaker supplied by the customer must be sized in accordance to local regulations.
Shunt trip circuit
breaker
required.

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1.2.4 Wiring Electrical Power and Disconnects
This section provides additional data regarding power circuits the customer must provide, and
internal electrical circuits necessary to supply the correct power to the XR 6000 system. Figure 4-
1 shows the room power supply installed.
1.2.4.1 Room Power Supply

Connect the Customer supplied breaker box
to the Emergency "OFF" button using Customer
supplied wires.
3 Phase & GND Use either normally "closed" or normally "open"
contacts, depending on the box.
1 Emergency Shutoff
(obtain from GE)
Customer supplied
breaker box 600 V max AC/DC 10 amp
Breaker box E/O

Normally
closed
CB
CIRCUIT
BREAKER
Normally
open
1 Connect to normally
closed switch using
cable supplied with
Emergency Shutoff
TM1
(System Cabinet)
Jedi
DLK
1 2 4 6
Customer supplied switch
Cable supplied with
Emergency Shutoff -
(See Note 1 below)
24 VDC
Warning Light
XRL
220VAC / 110VAC 8Amp
Figure 4-1 Room Power Supply (see Table 4-5 for Legend)

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Key for Description

Figure 4-1
CB Circuit breaker with remote trip (shunt) capabilities supplied by customer.
DLK Open-door detector (per local regulations). SKL provides 24 VDC.
(see note below)
XRL Yellow X-ray emission indicator lamp above the room access door. 220 V in
Europe/120 V in USA with 25 W max. bulb (per local regulations). Wires and light
fixtures supplied by customer.
Note: Use only a multi conductor, shielded, PVC/PVC, UL TYPE CM cable. Alpha Wire.
CQA10210637. This wire is found in GE Catalog Item A8091JH as a “bulk” roll of wire (60 Meters).
Material consists of two 16 AWG (19/0.0117 strand) conductors. Shields must be grounded at
both ends.
Table 4-5 Legend for Figure 4-1 and Figure
1.2.4.2 Multiple Emergency “OFF” Switches

Figure 4-2 shows how multiple emergency “OFF” switches could be wired.
E/O1
Normally
closed
Circuit
Breaker
E/O2
Normally
closed
1) If using the normally

"closed" contacts, connect
multiple EPOs in series.
2) If using the normally "open"
contacts, connect multiple Connect to normally closed
EPOs in parallel. switch only. For multiple
EPOs, connect in series only!
Figure 4-2 Wiring Multiple “Emergency OFF” (E/O) Switches
1.2.4.3 Customer-supplied Electrical Outlet

Customer must provide an electrical outlet of appropriate voltage rating within 0.91 meters of the
System Cabinet.

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Section 2.0
Electrical Grounds
2.1 System and Facility Grounds
The ground for this system must originate at the system’s power source and be continuous (i.e.,
transformer or first access point of power into a facility, and be continuous to the system power
disconnect in the room). Ground connection at the power source must be at the grounding point of
the “Neutral/Ground” if a “Wye” transformer is used, or typical grounding points of a separately
derived system. In the case of an external facility, it must be bonded to the facility ground point at
the electrical service entrance.
The “system” ground can be spliced using “High Compression Fittings” but must be properly
terminated at each distribution panel it passes through. When it is terminated, it must be connected
into an approved grounding block. Incoming and outgoing grounds must terminate at this same
grounding block. Grounds must only be terminated to approved grounding blocks. Grounds must
never connect directly to the panels, frames or other materials in a cabinet or distribution panel
(refer to Figure 4-3).
2.2 Recommended Ground Wire Sizes

The ground wire must be copper and never smaller than 8 AWG.
The ground wire impedance from the system disconnect (including the ground rod) measured to
earth, must not exceed 2 ohms (as measured by one of the applicable techniques described in
Section 4 of ANSI/IEEE Standard 142 - 1982). Refer to Figure 4-3 and Figure 4-4 for typical
equipment and methods to measure the different portions of the 2 ohm impedance.
Note: For general system grounding requirements and information on establishing an equi-potential
Additional grounding system, refer to:
Reference • Direction 46-014505, Electrical Safety - Equipment Grounding
Material Exists
• Direction 46-014546, Electrical Safety - Leakage Currents
For specific XR 6000 system grounding maps and connection details, refer to Chapter 8 - - System
Cable Information.
2.3 Final Checks, Before System Installation Can Begin

The customer must provide GE Healthcare or its representative (installation specialist) evidence
that grounds and electrical power meet GE Healthcare' specifications.
Prior to product installation, a local service or installation specialist, to be determined by GEHC, will
do a physical walk through of the exam suite to ensure the following:
1.) Ground wires are of the same size as the power feeder or 8 AWG, whichever is larger.
2.) Grounds at junction points are connected properly and securely to an approved ground bus.
3.) Grounds within an enclosure are tied together by copper wire or to an appropriate buss bar
(i.e., separate buss bars within an enclosure must be tied together with copper wire of
appropriate size).
4.) Grounds originate at the power source (i.e., transformer or entrance panel into facility).
5.) Ground wires measure less than 2 ohms to earth.

GE HEALTHCARE
You may use the following form to record the results of that inspection.
GROUND IMPEDANCE MEASURED TO BE OHMS

Inspector’s Name and Date:
Customer’s Name and Date:
DISTRIBUTION PANEL
L1
L2
INCOMING L3 OUTGOING
GROUNDING
BLOCK
GROUND WIRES MUST APPROVED FOR
ATTACH TO THE SAME WIRE TYPE USED
GROUNDING BLOCK
Figure 4-3 Ground Connection at Distribution Panel
Page 48 Section 2.0 - Electrical Grounds

GE HEALTHCARE
ECOS 2300
To ensure proper measurement of
the ground rod, the grounding con-
ductor from a facility must be re-
moved. Since this wire may be car-
rying amounts of current, this proce-
dure should only be performed by a
qualified person.
GROUND AUXILIARY AUXILIARY

ELECTRODE POTENTIAL CURRENT
UNDER TEST ELECTRODE ELECTRODE
X Y Z
62% D
ESTABLISHED
62%
CLEARANCE
BAND
DISTANCE
Figure 4-4 Ground Rod Impedance Test

GE HEALTHCARE
Page 50 Section 2.0 - Electrical Grounds

GE HEALTHCARE
Chapter 5 - Product Characteristics
Section 1.0
Overview
Refer to this section for dimensional drawings for the components of the XR 6000 system. These
components include:
• System - Figure 5-1 through Figure 5-2
• Operator Console - Figure 5-3.
• Integrated Table - Figure 5-4 through Figure 5-6.
• Radiographic Table - Figure 5-7 through Figure 5-8.
• Integrated Tube Stand - Figure 5-9.
• Standard Wall Stand - Figure 5-10 through Figure 5-12.
• Dolly - Figure 5-13.
Note: Drawings are not to scale. Dimensions are called out on each drawing.
Section 2.0
System Components Dimensions and Weights
2.1 Dimensions
PRODUCT OR DIMENSIONS
References
COMPONENT Width Depth Height
Operator Console:
Console 340 mm 240 mm 110 mm Figure 5-3
Console Pedestal 352 mm 300 mm 950 mm
Standard Integrated Table 2300 mm 1115 ~ 1335 mm 2240 mm See Figure 5-4 through
Figure 5-6
Radiographic Table 2300 mm 850 mm 695 mm Figure 5-7 through
Figure 5-8
Standard Wall Stand 651 mm 284.5 mm 2060 mm See Figure 5-10 through
Figure 5-12
*Showing: Mounting Holes, Cable Entrance, Air Vents, Service Access, Center of Gravity
Table 5-1 Product Physical Characteristics (Width / Depth / Height)
Chapter 5 - - Product Characteristics Page 51

GE HEALTHCARE
2.2 Dimensioned Figures and Drawings
2.2.1 System
PP
1300mm
PP
PP
PP
5500
PP
PP
mm
PP
D
610

325 mm
mm

Figure 5-1 System Views
Page 52 Section 2.0 - System Components Dimensions and Weights

GE HEALTHCARE
Note: If wall stand use only 180 cm SID a < 2640 mm
If wall stand use both 100 cm and 180 cm SID a < 1840 mm
Note: "a" refers to the distance between the tube center and the front panel of wall stand.
2240 mm
PP
PP
1100 mm
PP
PP
PP
PP
PP
PP

PP
PP
Figure 5-2 System Views

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2.2.2 Operator Console
&DEOH (QWUDQFH
PP
PP 130mm
PP
PP PP
Figure 5-3 Console Dimensions

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2.2.3 Integrated Table
Cable Entrence
Figure 5-4 Integrated Table Side View

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)RFXV WR JURXQG GLVWDQFH
)RFXV WR JURXQG GLVWDQFH
Figure 5-5 Integrated Table Front View

GE HEALTHCARE
2300
2100
210
850
1115~1335
1200~1310
Figure 5-6 Integrated Table Top View

GE HEALTHCARE
2.2.3.1 Table
PP
PP
PP
PP
PP
Figure 5-7 Table Dimensions

GE HEALTHCARE
PP
850mm
PP
Figure 5-8 Table Top Dimensions

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2.2.3.2 Tube Stand
Figure 5-9 Standard Tube Stand

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2.2.4 Wall Stand
PP PP
PP
PP
PP
PP
&DEOH (QWUDQFH
PP
Figure 5-10 Standard Wall Stand Plan View

GE HEALTHCARE
360
80
209
284.5
70
600
651
Figure 5-11 Standard Wall Stand Top View
2-
Figure 5-12 Standard Wall Stand Template

GE HEALTHCARE
2.2.5 Dolly
560
2- 11 170
30
110
250
660
676
140
63
Figure 5-13 XR 6000 Dolly (Table/Wall Stand)

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Section 3.0
Positioning and Mounting Equipment
3.1 Floor Loading and Recommended Mounting Methods
PRODUCT OR WEIGHT LOAD WEIGHT/OCCUPIED RECOMMENDED
COMPONENT kg BEARING AREA MOUNTING
AREA INFORMATION
kg/m2
m2
Operator Console Floor mounting
Recommendations:
Console 2 kg
(4) M6 X 65 mm anchors
Console on Pedestal 6 kg 0.105 m2 57.14 kg/m2 (supplied)
(option)
Standard Radiographic 240 kg 1.25 m2 192 kg/m2 Floor mounting
Table Recommendations:
Max. Patient Load is
180 kg (4) M10 X 95 mm anchors
(supplied)
Standard Wall Stand 106.5 kg 0.0735 m2 1448.98 kg/m2 Floor mounting
Recommendations:
(4) M10 X 95 mm anchors
(supplied)
Table 5-2 Product Physical Characteristics (weight)
Page 64 Section 3.0 - Positioning and Mounting Equipment

GE HEALTHCARE
Chapter 6 - Room Layout
Section 1.0
Radiation Production
Because X-ray equipment produces radiation, you may need to take special precautions or make
special site modifications. The General Electric Company does not make recommendations
regarding radiation protection. It is the purchasers responsibility to consult a radiation physicist for
advisement on radiation protection in X-ray rooms.
Section 2.0
Clinical Access
Make sure that you plan the room with the following clinical access requirements:
• Provide emergency egress path out of the room for patient, operators and service personal,
per country and regional requirements.
• Provide easy access to the patient table. Stretchers and other mobile hospital equipment must
reach the table quickly.
• Clinicians at the patient table must be able to communicate with assistants in the control area.
• Operators in the control area must have easy access to the Operator Console. However,
position the controls (including handswitches) so the operator cannot take exposures while
looking around or standing outside the control booth's lead glass window.
• Consult customer on the number and location of nonelectrical lines (air, oxygen, vacuum,
water, etc.) in the radiographic room.
• Provide easy access to the Wall Stand.
• Ensure there is enough space between the table and the Wall Stand to perform standing
ankles, knees, etc.
• For the wallstand, ensure that the room layout is such that the tube can be centered on top of
the horizontal detector.
Note: The generally accepted practice is to load the patient laterally. In case of room layout designed for
longitudinal patient loading, some modifications must be brought to the table.
Section 3.0
Peripheral Equipment
Consult hospital personnel regarding additional space requirements for the following types of
hospital equipment:
• Storage Cabinet
• Sinks
• Oxygen Stations
• Monitoring Equipment
• Crash Cart
Chapter 6 - - Room Layout Page 65

GE HEALTHCARE
Section 4.0
Room Layout Drawings
See Figure 6-1 through Figure 7-1 for typical XR 6000 system room layouts.
Note: The room layout shows the minimum room size that system needs, but customers should be
required to prepare a room according with local regulatory requirements.
Note: You will notice that a minimum of 2200 mm of clearance is shown from the table frame to either end
of the table; this is to allow the table top to be installed.
Figure 6-1 Typical Room Layout
Item Component
1 Radiographic Table
2 Standard Wall Stand
3 Operator Console
Table 6-1 System Components
LENGTH WIDTH CEILING

Recommended Minimum Recommended Minimum Recommended Minimum
6.0 m 5.5 m 6.0 m 5.0 m 3.0 m 2.5 m
(19.7 ft.) (17.6 ft.) (19.7 ft.) (14.0 ft.) (9.8 ft.) (8.2 ft.)
Table 6-2 System Recommended and Minimum Room Size Dimension
Page 66 Section 4.0 - Room Layout Drawings

GE HEALTHCARE
Chapter 7 - Planning Aids
Section 1.0
Shipping Dimensions and Weights
SHIPPING DATA
SHIPPING DIMENSIONS (APPROX.) GROSS NET SHIPPING SHIPPING
PRODUCT OR SHIPPING WEIGHT METHOD
COMPONENT WEIGHT (approx.)
(approx.)
LENGTH (cm) WIDTH (cm) HEIGHT (cm) (kg) (kg)
Table 244 122 120 640 440 box 1#
including
"FIRST
OPEN ME"
box
Tube Stand 244 61 84 230 130 box 2#
Wall Stand 219 80 85 220 120 box 3#
or or or or or or
Basic Wall Stand 196 53 52 160 70
Table 7-1 Shipping Data
Chapter 7 - - Planning Aids Page 67

GE HEALTHCARE
Section 2.0
Installation Tools and Materials Required
2.1 Tools and Materials Checklist
The following tools and materials are needed for installation, but are not shipped with the product: Completed
Assorted hardware for termination of electrical connections (solder-less ring lug terminals and butt
splices, AWG 2-18)
Tie wraps, electrical tape and wire markers
Tags for labelling incomplete work in accordance to OSHA and regulatory requirements
Tag and lock-out equipment
Assorted 12-point sockets (SAE and metric), drives, wrenches and torque wrench (Nm and ft.-lbs)
Electric and hammer drill. Assorted masonry and high-speed bits in both metric and SAE sizes
Assorted sizes of tongue and grove pliers, hammers, hex wrenches (metric and SAE), screw drivers
and metal files
Assorted sizes of wire cutters and strippers, ratchet and standard crimpers (42,400 mm2 and
upwards), and a 75 watt soldering iron
Heat and electrical tape
Chalk line
Digital multimeter
4 ft. level (or two standard levels)
Page 68 Section 2.0 - Installation Tools and Materials Required

GE HEALTHCARE
Section 3.0
Preparing the Delivery Route
1.) Step One – Sketch out the Route
Begin preparing Route Survey by sketching the area of the hospital or clinic which will receive
the equipment. Include all areas on the delivery route from outside of building to destination.
See sample sketch below.
Reference Numbers Numbers in circles refer to the Route Survey data. The Route
Survey is a form on which site data is listed (step 2).
Floor 1 Floor 2
3
1 2
4 7
5
Ramp 6
8
Elevator
9 10
Destination
Figure 7-1 Sample Route
2.) Step Two – Survey the Route

Record all loading capacities, corridor widths, door openings, turning radii, flooring materials,
elevator sizes, obstructions and so on for reference.
3.) Step Three – Check the Route
Verify equipment can actually be transported via the route determined in step 1.

GE HEALTHCARE
Section 4.0
Pre-Installation Checklist
Delivery Date: Sales Person:

Customer: FDO No.: Room #
Equipment:
Physical Requirements of Site Completed

1.) Room size adequate for intended equipment configuration?
2.) Floor is strong enough for intended equipment and mounting methods
approved – seismic regulatory codes considered?
3.) Delivery route accommodates all intended equipment?
4.) Radiation physicist consulted?
5.) Necessary alterations made to circumvent obstructions?
6.) Modifications to room finished?
7.) Supports, platforms been provided?
8.) Support structures installed for floor, and wall mounted equipment?
9.) Has floor been modified for cable ducts?
10.) Electrical service in place - at the ratings specified in pre-installation

documentation?
11.) Power available to operate power tools?
12.) All non-electrical lines (air, water, oxygen, vacuum) installed?
Interconnections Completed
1.) Signal cable, power and grounding plans produced?
2.) Necessary interconnection hardware, such as junction boxes, conduit or

raceways, and fittings provided?
3.) Interconnection hardware installed?
4.) Flexible, stranded wire provided for System input power connection?
5.) System “feeder” power cables pulled and sufficient length available at
disconnect box for connections?
6.) Interconnecting cables continuity checked, and labeled?
7.) All high voltage cable lengths verified?
8.) Interface information available for equipment?
Page 70 Section 4.0 - Pre-Installation Checklist

GE HEALTHCARE
General Completed
1.) Walls, and floor clear of all obstructions?
2.) Walls finished?
3.) Finished floor installed?
4.) Room lights installed?
5.) Dust-creating work completed?
6.) Old equipment within room removed?
7.) Component positions clearly marked on floor?
8.) Space available to store equipment?
9.) Lock on door, or locked room available?
10.) Room IP Addresses for DICOM and Broadband identified?
11.) Have all fire/safety inspections for occupancy been completed?
Comments:
Inspection Date(s):
Installation Project Manager Signature

GE HEALTHCARE
Page 72 Section 4.0 - Pre-Installation Checklist

GE HEALTHCARE
Chapter 8 - System Cable Information
Section 1.0
Introduction
The following information is provided as an aid to make the physical installation of system cables
easy and efficient. In the tables that follow, the physical characteristics of each cable and its
associated connectors is provided. Thus making it easier to plan cable paths and clearances in
advance. Physical characteristics are given for each available cable length. Review cable lengths
carefully and choose lengths appropriate for your installation prior to the equipment arriving, to
avoid unnecessary installation delays.
Remember, it is up to you to make sure that all cables are routed and connected in accordance with
all regulatory laws that may apply.
Chapter 8 - - System Cable Information Page 73

Section 2.0
Page 74
DIRECTION 5275600-100, REVISION 3

GE HEALTHCARE
Cable Information
2.1 Cable Lengths and Characteristics
Item Cable Number or Voltage Length Usable Length Diameter Cable Specification Connector Plug Size Connector Plug Size
Name (V) (M) (M) (M) One End One End The Other The Other
End End
1 System Console 5 15 13 10 UL2464#22*6P TAV J1 55mm x System 55mm x
Communication Cable 17mm Console J4 17mm
(5182354)
2 System Console 24 15 13 10 UL2464#18*10C PDU TM3 - System 24mm
Power Cable Console J3 (diameter)
Section 2.0 - Cable Information
(5183903)
3 Main Power Cable 380 15 17 UL 600 Main - PDU TM1 -
(5245375) - optional Power
4 Main Grounding Cable 0 15 8 UL 600 Main - PDU TM1 -
(5245422) - optional Power
XR 6000 PRE-INSTALLATION
Section 3.0 - System Master Interconnect Schematic (MIS)

GE HEALTHCARE
1 2 3 4 5 6 7 8
A A
Grounding
B Grounding
B
Tube Stand
System Cabinet
Power Supply Tube
P1 P1 24 VDC Console
PDU
P2 TM2
C Hospital Power P2
24 VDC C
P3 P3 Terminal
Supply
Chapter 8 - - System Cable Information
Grounding
GND GND P1 P2 P3
Stud
3 Phase Stud
TM3 Ele-Magnetic
Brakes
Rotor/Tube fan/Pressure SW
P1 P2 P3 J2/J3 Tube
HV +
HV + HV +
D D
HV -
HV - HV -
Xray-On Light J6
24 VDC
Generator Collimator
Door Interlock J6
Jedi
Table
Switches
E 24 VDC
E
AEC2
AEC1
EM Brakes
J8
J9
TM1
5166493
RS232
Ion-Chamber
RTL
RS485/
RS232
5166654
Ion-Chamber
F Wallstand F
Serial RS485 / RTL

24VDC/PSW
AC Power Line
J3 J4 Handswtich
DC Power Line
G HV Line G
Serial / RTL
Grounding Line
Others System Cosole
J1
H TITLE
Pioneer System Architecture

REV H
FIRST MADE FOR: Pioneer
2
GEHL MEDICAL SYSTEMS 51888818 BLK SHT/CONT ON
1/2
1 2 3 4 5 6 7 8
Page 75
GE HEALTHCARE
1 2 3 4 5 6 7 8
A A
Service Laptop
Handswtich 5194292/
J1
Console J2 5241079 Serial port
B 5194507
B
J4 J3
5184620
5182354
5183903
C Hospital Main Power 380 C
3 phase PDU TM3
5193110 GND
GND AEC2
5183465 Stud
Stud
LU 5197678 5193105
LV TM1 GND
LW J1 TAV Stud
Chapter 8 - - System Cable Information
5197679 5182285
GND GND J1 J1 5193607
Stud Stud GND
TM1 Stud
TM2 Wallstand
5194508
D D
5196643
5182354
5196454
Table
UVW
laptop
console
E E
GND
Stud GND 5183561
Stud
TM1
Stud
GND
TM1
DOOR Interlock AEC1
5166493
AEC1
Room Light J6
F F
5193106
5193103
Jedi R1T 50
2212259-2/4
J2
XP105
Stud
GND
5195936 Rotation
J3 Anode
HV +
2269002-5
HV +
G HV -
2269002-5 HV -
Tube Stand G
5183392/
5184093
5166654
AEC2
H TITLE
Pioneer 500 System Architecture

REV H
FIRST MADE FOR: Pioneer 500
2
GEHL MEDICAL SYSTEMS 51888818 BLK SHT/CONT ON
2/2
1 2 3 4 5 6 7 8
Page 76
GE HEALTHCARE
Appendix A - Electromagnetic Compatibility

(EMC)
Section 1.0
Compliance Statement
This equipment complies with IEC60601-1-2 Edition 2 (2001) EMC standard for medical devices.
This equipment generates, uses, and can radiate radio frequency energy. The equipment may
cause radio frequency interference to other medical and non-medical devices and radio
communications.
To provide reasonable protection against such interference, this product complies the radiated
emission as per CISPR11 Group1 Class A standard limits.
However, there is no guarantee that interference will not occur in a particular installation.
If this equipment is 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 this equipment. 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.
The XR 6000 is predominantly 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 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 XR 6000. Further detailed data & requirements are described in the Use Recommendations
and Installation Recommendations sections.
Appendix A - Electromagnetic Compatibility (EMC) Page 77

GE HEALTHCARE
Section 2.0
Compatibility Tables
This equipment complies with IEC60601-1-2 Edition 2 (2001) EMC standard for medical devices.
The XR 6000 is suitable to be used in an electromagnetic environment, as per the limits &
recommendations described in the tables hereafter:
• Emission Compliance level & limits (Table 1).
• Immunity Compliance level & recommendations to maintain equipment clinical utility (see
Table 2 and Table 3).
Note: This system complies 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
Guidance and manufacturer’s declaration – Electromagnetic Emissions

The XR 6000 is intended for use in the electromagnetic environment specified below. The
customer or the user of the XR 6000 should assure that it is used in such an environment.
Emissions Test Compliance Electromagnetic Environment Guidance
RF emission, Group 1 The XR 6000 uses RF energy only for its internal
CISPR 11 function. Therefore, its RF emissions are very low and
are not likely to cause any interference in nearby
electronic equipment.
RF emissions, Class A The XR 6000 is suitable for use in non-domestic
CISPR 11 environments, and not directly connected to the Public
Harmonic emissions, Not applicable Mains Network. The XR 6000 is predominantly intended
IEC 61000-3-2 for use (e.g. in hospitals) with an appropriate power
supply (see operation manual) and the recommended
Voltage fluctuations/ Not applicable shielding for portable use.
flicker emissions,
IEC 61000-3-3
Table 1 XR 6000 Electromagnetic Emission
Page 78 Section 2.0 Compatibility Tables

GE HEALTHCARE
2.2 Electromagnetic Immunity
Guidance and Manufacturer’s declaration – electromagnetic immunity.

The XR 6000 is intended for use in the electromagnetic environment specified below. The customer or the user
of the XR 6000 should assure that it is used in such an environment.
Immunity Test IEC 60601-1-2 Test Level Compliance Level Electromagnetic Environment
Guidance
Electrostatic +/− 6 kV contact. +/− 6 kV contact. Floors should be wood,
discharge (ESD), +/− 8 kV air. +/− 8 kV air. concrete, or ceramic tile. If floors
IEC 61000-4-2 are covered with synthetic
material, the relative humidity
should be at least 30%.
Electrical fast +/− 2 kV for power supply +/− 2 kV for power supply Mains power quality should be
transient/burst, lines. lines. that of a typical commercial or
EC 61000-4-4 +/− 1 kV for input/output +/− 1 kV for input/output hospital environment
lines. lines.
Surge, +/− 1 kV differential mode. +/− 1 kV differential mode. Mains power quality should be
IEC 61000-4-5 +/− 2 kV common mode. +/− 2 kV common mode. that of a typical commercial or
hospital environment.
Voltage dips, short < 5% UT, (> 95% dip in UT) 0% UT for 5 sec. Mains power quality should be
interruptions and for 0.5 cycle. that of a typical commercial or
voltage variations on 40% UT (60% dip in UT) hospital environment. If the user
power supply input of the XR 6000 requires
for 5 cycles.
lines, IEC 61000-4- continued operation during
11 70% UT (30% dip in UT) for power mains interruptions, it is
25 cycles. recommended that the XR 6000
< 5% UT, (> 95% dip in UT) be powered from an
for 5 sec. uninterruptible power supply or a
battery.
Power frequency (50/ 3 A/m 3 A/m Power frequency magnetic fields
60 Hz) magnetic field, should be at levels characteristic
IEC 61000-4-8 of a typical location in a typical
commercial or hospital
environment.
Note: These are guidelines. Actual conditions may vary.
Table 2 XR 6000 Electromagnetic Immunity

GE HEALTHCARE
Guidance and Manufacturer’s declaration - electromagnetic immunity. The XR 6000 is suitable for use in the specified
electromagnetic environment. The customer or the user of the XR 6000 should assure that it is used in an
electromagnetic environment as described below.
Immunity Test IEC 60601-1-2 Compliance Electromagnetic Environment Guidance
Test Level Level
Conducted RF, 3 Vrms, 150 kHz to V1 = 3Vrms Portable and mobile RF communications equipment
IEC 61000-4-6 80 MHz should be used no closer to any part of the XR 6000,
Radiated RF 3 V/m, 80 MHz to E1 = 3V/m including cables, than the recommended separation
IEC 61000-4-3 2.5 GHz distance calculated from the equation appropriate for the
frequency of the transmitter.
Recommended Separation Distance
d = 1.2
d = 1.2 80 MHz to 800 MHz
d = 2.3 800 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:
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 the XR 6000 is used exceeds the applicable
RF compliance level above, the XR 6000 should be observed to verify normal operation. If abnormal performance is
observed, additional measures may be necessary, such as re-orienting or relocating the XR 6000.
b Over the frequency range 150 kHz to 80 MHz, field strengths should be less than [V1] V/m.
These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection
from structures, objects, and people.
Table 3 XR 6000 Electromagnetic Immunity (Continued)
Page 80 Section 2.0 Compatibility Tables

GE HEALTHCARE
Recommended separation distances between portable and mobile RF communications equipment and the XR 6000
The XR 6000 is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled.
The customer or the user of the XR 6000 can help prevent electromagnetic interference by maintaining a minimum
distance between portable and mobile RF communications equipment (transmitters) and the XR 6000 as
recommended below, according to the maximum output power of the communications equipment.
Rated Maximum Output Power (P) Separation distance according to frequency of transmitter
of Transmitter Watts (W)
150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.5 GHz
d = 1.2 d = 1.2 d = 2.3

Separation Distance Separation Distance Separation Distance
meters meters meters
0.01 (10 mW) 0.12 0.12 0.23
0.1 (100 mW) 0.38 0.38 0.74
1 1.2 1.2 2.3

10 3.8 3.8 7.3
100 12 12 23
For transmitters rated at a maximum output power not listed above, the separation distance can be estimated using
the equation in the corresponding column, where P is the maximum output power rating of the transmitter in
watts (W) according to the transmitter manufacturer. V1 and V2 are the COMPLIANCE LEVELS for the IEC 61000-
4-6 test and E1 is the COMPLIANCE LEVEL for the IEC 61000-4-3 test. V1 and V2 are in V and E1 is in V/m.
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 absorption and
reflection from structures, objects, and people.
Table 4 Recommended Separation Distances
Section 3.0
Use Recommendations
This product complies with IEC 60601-1-2 Edition 2 (2001) EMC standard for medical devices and
with radio frequency emission requirements per CISPR11 Group1 Class A standard limits. The XR
6000 is predominantly 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 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
by continuing to safely acquire controlled radiological X-ray exposures in a mobile radiography
environment.
For example, a 1W mobile phone (800 MHz to 2.5 GHz carrier frequency) shall be put 2.3 meters
apart from the XR 6000 (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 XR 6000.
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
This system complies with above mentioned EMC standard when used with supplied cables.
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 XR
6000, must have all AC power supplied by the same power distribution panel & line.
4.3 Stacked Components & Equipment

The XR 6000 should not be used adjacent to or stacked with other equipment; if adjacent or stacked
use is necessary, the XR 6000 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 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.
Page 82 Section 4.0 Installation Recommendations

GE HEALTHCARE
Appendix B - Revision History

Revision Date Reason for change
1 June 20, 2007 First Release
2 Nov. 5, 2007 Update subsystem drawings and room layout, add console cables’ usable lengths
3 Feb. 15, 2008 Remove "LING LONG"
Revision History Page 83

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Appendix C - List of Effected Pages

PAGES REVISION PAGES REVISION
1 to 84 1
1 to 84 2
1 to 84 3
Page 84 List of Effected Pages

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

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Copyright © 2007~2008 by General Electric Company, Inc.

Published by the GE Company, Inc.

Legal Notes Page 3

Page 4 Legal Notes

ПРЕДУПРЕЖДЕНИЕ • ТОВА УПЪТВАНЕ ЗА РАБОТА Е НАЛИЧНО САМО НА АНГЛИЙСКИ ЕЗИК.

VÝSTRAHA • TENTO PROVOZNÍ NÁVOD EXISTUJE POUZE V ANGLICKÉM JAZYCE.

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.

Page 6 Important Precautions

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

WARNUNG • DIESE SERVICEANLEITUNG EXISTIERT NUR IN ENGLISCHER SPRACHE.

ΠΡΟΕΙΔΟΠΟΙΗΣΗ • ΤΟ ΠΑΡΟΝ ΕΓΧΕΙΡΙΔΙΟ ΣΕΡΒΙΣ ΔΙΑΤΙΘΕΤΑΙ ΣΤΑ ΑΓΓΛΙΚΑ ΜΟΝΟ.

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

FIGYELMEZTETÉS • EZEN KARBANTARTÁSI KÉZIKÖNYV KIZÁRÓLAG ANGOL NYELVEN ÉRHETŐ

Important Precautions Page 7

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.

ADVARSEL • DENNE SERVICEHÅNDBOKEN FINNES BARE PÅ ENGELSK.

Important Precautions Page 9

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.

Page 12 Important Precautions

CERTIFIED ELECTRICAL CONTRACTOR STATEMENT

Important Precautions Page 13

OMISSIONS & ERRORS

Page 14 Important Precautions

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:

Publication Part Number & Revision Number Publication Title

Figure 1 Component Identification

2.3 Computer Screen Output/Input Text Character Styles