GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
Important Precautions
• THIS SERVICE MANUAL IS AVAILABLE IN ENGLISH ONLY.
• IF A CUSTOMER’S SERVICE PROVIDER REQUIRES A LANGUAGE OTHER
THAN ENGLISH, IT IS THE CUSTOMER’S RESPONSIBILITY TO PROVIDE
TRANSLATION SERVICES.
WARNING
(EN)
AVERTISSEMENT
(FR)
• 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.
• CE MANUEL DE MAINTENANCE N’EST DISPONIBLE QU’EN ANGLAIS.
• SI LE TECHNICIEN DU CLIENT A BESOIN DE CE MANUEL DANS UNE AUTRE
LANGUE QUE L’ANGLAIS, C’EST AU CLIENT QU’IL INCOMBE DE LE FAIRE
TRADUIRE.
• NE PAS TENTER D’INTERVENTION SUR LES ÉQUIPEMENTS TANT QUE LE
MANUEL SERVICE N’A PAS ÉTÉ CONSULTÉ ET COMPRIS.
• LE NON-RESPECT DE CET AVERTISSEMENT PEUT ENTRAÎNER CHEZ LE
TECHNICIEN, L’OPÉRATEUR OU LE PATIENT DES BLESSURES DUES À DES
DANGERS ÉLECTRIQUES, MÉCANIQUES OU AUTRES.
WARNUNG
(DE)
• DIESES KUNDENDIENST-HANDBUCH EXISTIERT NUR IN ENGLISCHER
SPRACHE.
• FALLS EIN FREMDER KUNDENDIENST EINE ANDERE SPRACHE BENÖTIGT,
IST ES AUFGABE DES KUNDEN FÜR EINE ENTSPRECHENDE ÜBERSETZUNG
ZU SORGEN.
• VERSUCHEN SIE NICHT, DAS GERÄT ZU REPARIEREN, BEVOR DIESES
KUNDENDIENST-HANDBUCH NICHT ZU RATE GEZOGEN UND VERSTANDEN
WURDE.
• WIRD DIESE WARNUNG NICHT BEACHTET, SO KANN ES ZU VERLETZUNGEN
DES KUNDENDIENSTTECHNIKERS, DES BEDIENERS ODER DES PATIENTEN
DURCH ELEKTRISCHE SCHLÄGE, MECHANISCHE ODER SONSTIGE
GEFAHREN KOMMEN.
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GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
• ESTE MANUAL DE SERVICIO SÓLO EXISTE EN INGLÉS.
• SI ALGÚN PROVEEDOR DE SERVICIOS AJENO A GEHC SOLICITA UN IDIOMA
QUE NO SEA EL INGLÉS, ES RESPONSABILIDAD DEL CLIENTE OFRECER UN
SERVICIO DE TRADUCCIÓN.
AVISO
(ES)
• NO SE DEBERÁ DAR SERVICIO TÉCNICO 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.
• ESTE MANUAL DE ASSISTÊNCIA TÉCNICA SÓ SE ENCONTRA DISPONÍVEL EM
INGLÊS.
• SE QUALQUER OUTRO SERVIÇO DE ASSISTÊNCIA TÉCNICA, QUE NÃO A
GEHC, SOLICITAR ESTES MANUAIS NOUTRO IDIOMA, É DA
ATENÇÃO
(PT)
RESPONSABILIDADE DO CLIENTE FORNECER OS SERVIÇOS DE TRADUÇÃO.
• NÃO TENTE REPARAR O EQUIPAMENTO SEM TER CONSULTADO E
COMPREENDIDO ESTE MANUAL DE ASSISTÊNCIA TÉCNICA.
• O NÃO CUMPRIMENTO DESTE AVISO PODE POR EM PERIGO A SEGURANÇA
DO TÉCNICO, OPERADOR OU PACIENTE DEVIDO A‘ CHOQUES ELÉTRICOS,
MECÂNICOS OU OUTROS.
AVVERTENZA
(IT)
HOIATUS
(ET)
• IL PRESENTE MANUALE DI MANUTENZIONE È DISPONIBILE SOLTANTO IN
INGLESE.
• SE UN ADDETTO ALLA MANUTENZIONE ESTERNO ALLA GEHC 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.
• NON TENERE CONTO 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.
• KÄESOLEV TEENINDUSJUHEND ON SAADAVAL AINULT INGLISE KEELES.
• 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.
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GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
• TÄMÄ HUOLTO-OHJE ON SAATAVILLA VAIN ENGLANNIKSI.
• JOS ASIAKKAAN PALVELUNTARJOAJA VAATII MUUTA KUIN
ENGLANNINKIELISTÄ MATERIAALIA, TARVITTAVAN KÄÄNNÖKSEN
HANKKIMINEN ON ASIAKKAAN VASTUULLA.
VAROITUS
(FI)
• ÄLÄ YRITÄ KORJATA LAITTEISTOA ENNEN KUIN OLET VARMASTI LUKENUT
JA YMMÄRTÄNYT TÄMÄN HUOLTO-OHJEEN.
• MIKÄLI TÄTÄ VAROITUSTA EI NOUDATETA, SEURAUKSENA VOI OLLA
PALVELUNTARJOAJAN, LAITTEISTON KÄYTTÄJÄN TAI POTILAAN
VAHINGOITTUMINEN SÄHKÖISKUN, MEKAANISEN VIAN TAI MUUN
VAARATILANTEEN VUOKSI.
ΠΡΟΚΛΗΘΕΙ ΤΡΑΥΜΑΤΙΣΜΟΣ ΣΤΟ ΑΤΟΜΟ ΠΑΡΟΧΗΣ ΣΕΡΒΙΣ, ΣΤΟ ΧΕΙΡΙΣΤΗ Ή
ΣΤΟΝ ΑΣΘΕΝΗ ΑΠΟ ΗΛΕΚΤΡΟΠΛΗΞΙΑ, ΜΗΧΑΝΙΚΟΥΣ Ή ΑΛΛΟΥΣ ΚΙΝΔΥΝΟΥΣ.
FIGYELMEZTETÉS
(HU)
VIÐVÖRUN
(IS)
• EZEN KARBANTARTÁSI KÉZIKÖNYV KIZÁRÓLAG ANGOL NYELVEN ÉRHETŐ
EL.
• 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.
• ÞESSI ÞJÓNUSTUHANDBÓK ER EINGÖNGU FÁANLEG Á ENSKU.
• EF ÞJÓNUSTUAÐILI VIÐSKIPTAMANNS ÞARFNAST ANNARS TUNGUMÁLS EN
ENSKU, ER ÞAÐ Á ÁBYRGÐ VIÐSKIPTAMANNS AÐ ÚTVEGA ÞÝÐINGU.
• REYNIÐ EKKI AÐ ÞJÓNUSTA TÆKIÐ NEMA EFTIR AÐ HAFA SKOÐAÐ OG
SKILIÐ ÞESSA ÞJÓNUSTUHANDBÓK.
• EF EKKI ER FARIÐ AÐ ÞESSARI VIÐVÖRUN GETUR ÞAÐ VALDIÐ MEIÐSLUM
ÞJÓNUSTUVEITANDA, STJÓRNANDA EÐA SJÚKLINGS VEGNA RAFLOSTS,
VÉLRÆNNAR EÐA ANNARRAR HÆTTU.
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GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
• TENTO SERVISNÍ NÁVOD EXISTUJE POUZE V ANGLICKÉM JAZYCE.
•VPŘÍPADĚ, ŽE POSKYTOVATEL SLUŽEB ZÁKAZNÍKŮM POTŘEBUJE NÁVOD
V JINÉM JAZYCE, JE ZAJIŠTĚNÍ PŘEKLADU DO ODPOVÍDAJÍCÍHO JAZYKA
ÚKOLEM ZÁKAZNÍKA.
• NEPROVÁDĚJTE ÚDRŽBU TOHOTO ZAŘÍZENÍ, ANIŽ BYSTE SI PŘEČETLI
VÝSTRAHA
(CS)
TENTO SERVISNÍ NÁVOD A POCHOPILI JEHO OBSAH.
•VPŘÍPADĚ NEDODRŽOVÁNÍ TÉTO VÝSTRAHY MŮŽE DOJÍT ÚRAZU
ELEKTRICKÁM PROUDEM PRACOVNÍKA POSKYTOVATELE SLUŽEB,
OBSLUŽNÉHO PERSONÁLU NEBO PACIENTŮ VLIVEM ELEKTRICKÉHOP
PROUDU, RESPEKTIVE VLIVEM K RIZIKU MECHANICKÉHO POŠKOZENÍ NEBO
JINÉMU RIZIKU.
• DENNE SERVICEMANUAL FINDES KUN PÅ ENGELSK.
• HVIS EN KUNDES TEKNIKER HAR BRUG FOR ET ANDET SPROG END
ENGELSK, ER DET KUNDENS ANSVAR AT SØRGE FOR OVERSÆTTELSE.
ADVARSEL
(DA)
• FORSØG IKKE AT SERVICERE UDSTYRET MEDMINDRE
DENNE SERVICEMANUAL ER BLEVET LÆST OG FORSTÅET.
• MANGLENDE OVERHOLDELSE AF DENNE ADVARSEL KAN MEDFØRE SKADE
PÅ GRUND AF ELEKTRISK, MEKANISK ELLER ANDEN FARE FOR
TEKNIKEREN, OPERATØREN ELLER PATIENTEN.
WAARSCHUWING
(NL)
BRĪDINĀJUMS
(LV)
• DEZE ONDERHOUDSHANDLEIDING IS ENKEL IN HET ENGELS
VERKRIJGBAAR.
• ALS HET ONDERHOUDSPERSONEEL EEN ANDERE TAAL VEREIST, DAN IS DE
KLANT VERANTWOORDELIJK VOOR DE VERTALING ERVAN.
• PROBEER DE APPARATUUR NIET TE ONDERHOUDEN VOORDAT DEZE
ONDERHOUDSHANDLEIDING WERD GERAADPLEEGD EN BEGREPEN IS.
• INDIEN DEZE WAARSCHUWING NIET WORDT OPGEVOLGD, ZOU HET
ONDERHOUDSPERSONEEL, DE OPERATOR OF EEN PATIËNT GEWOND
KUNNEN RAKEN ALS GEVOLG VAN EEN ELEKTRISCHE SCHOK,
MECHANISCHE OF ANDERE GEVAREN.
•ŠĪ APKALPES ROKASGRĀMATA IR PIEEJAMA TIKAI ANGĻU VALODĀ.
• 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 ELEKTRISK
ĀS STRĀVAS
TRIECIENA, MEHĀNISKU VAI CITU RISKU IZRAISĪTU TRAUMU APKALPES
SNIEDZĒJAM, OPERATORAM VAI PACIENTAM.
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GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
• ŠIS EKSPLOATAVIMO VADOVAS YRA IŠLEISTAS TIK ANGLŲ KALBA.
• JEI KLIENTO PASLAUGŲ TEIKĖJUI REIKIA VADOVO KITA KALBA – NE ANGLŲ,
VERTIMU PASIRŪPINTI TURI KLIENTAS.
ĮSPĖJIMAS
(LT)
•NEMĖGINKITE ATLIKTI ĮRANGOS TECHNINĖS PRIEŽIŪROS DARBŲ, NEBENT
VADOVAUTUMĖTĖS ŠIUO EKSPLOATAVIMO VADOVU IR JĮ SUPRASTUMĖTE
• NEPAISANT ŠIO PERSPĖJIMO, PASLAUGŲ TEIKĖJAS, OPERATORIUS AR
PACIENTAS GALI BŪTI SUŽEISTAS DĖL ELEKTROS SMŪGIO, MECHANINIŲ AR
KITŲ PAVOJŲ.
• DENNE SERVICEHÅNDBOKEN FINNES BARE PÅ ENGELSK.
• HVIS KUNDENS SERVICELEVERANDØR TRENGER ET ANNET SPRÅK, ER DET
KUNDENS ANSVAR Å SØRGE FOR OVERSETTELSE.
ADVARSEL
(NO)
• IKKE FORSØK Å REPARERE UTSTYRET UTEN AT DENNE
SERVICEHÅNDBOKEN ER LEST OG FORSTÅTT.
• MANGLENDE HENSYN TIL DENNE ADVARSELEN KAN FØRE TIL AT
SERVICELEVERANDØREN, OPERATØREN ELLER PASIENTEN SKADES PÅ
GRUNN AV ELEKTRISK STØT, MEKANISKE ELLER ANDRE FARER.
OSTRZEŻENIE
(PL)
ATE NŢIE
(RO)
• NINIEJSZY PODRĘCZNIK SERWISOWY DOSTĘPNY JEST JEDYNIE W JĘZYKU
ANGIELSKIM.
•JEŚLI FIRMA ŚWIADCZĄCA KLIENTOWI USłUGI SERWISOWE WYMAGA
UDOSTĘPNIENIA PODRĘCZNIKA W JĘZYKU INNYM NIŻ ANGIELSKI,
OBOWIĄZEK ZAPEWNIENIA STOSOWNEGO TłUMACZENIA SPOCZYWA NA
KLIENCIE.
• NIE PRÓBOWAĆ SERWISOWAĆ NINIEJSZEGO SPRZĘTU BEZ UPRZEDNIEGO
ZAPOZNANIA SI
Ę Z PODRĘCZNIKIEM SERWISOWYM.
• NIEZASTOSOWANIE SIĘ DO TEGO OSTRZEŻENIA MOżE GROZIĆ
OBRAŻENIAMI CIAłA SERWISANTA, OPERATORA LUB PACJENTA W WYNIKU
PORAŻENIA PRĄDEM, URAZU MECHANICZNEGO LUB INNEGO RODZAJU
ZAGROŻEŃ.
• ACEST MANUAL DE SERVICE ESTE DISPONIBIL NUMAI ÎN LIMBA ENGLEZĂ.
• 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.
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GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
ПОЛУЧАТ УДАР ЗЛЕКТРИЧЕСКИМ ТОКОМ, МЕХАНИЧЕСКУЮ ТРАВМУ ИЛИ
ДРУГОЕ ПОВРЕЖДЕНИЕ.
• TÁTO SERVISNÁ PRÍRUČKA JE K DISPOZÍCII LEN V ANGLIČTINE.
• AK ZÁKAZNÍKOV POSKYTOVATEĽ SLUŽIEB VYŽADUJE INÝ JAZYK AKO
ANGLIČTINU, POSKYTNUTIE PREKLADATEĽSKÝCH SLUŽIEB JE
ZODPOVEDNOSŤOU ZÁKAZNÍKA.
UPOZORNENIE
(SK)
• NEPOKÚŠAJTE SA VYKONÁVAŤ SERVIS ZARIADENIA SKÔR, AKO SI
NEPREČÍTATE SERVISNÚ PRÍRUČKU A NEPOROZUMIETE JEJ.
• ZANEDBANIE TOHTO UPOZORNENIA MÔŽE VYÚSTIŤ DO ZRANENIA
POSKYTOVATEĽA SLUŽIEB, OBSLUHUJÚCEJ OSOBY ALEBO PACIENTA
ELEKTRICKÝM PRÚDOM, PRÍPADNE DO MECHANICKÉHO ALEBO INÉHO
NEBEZPEČENSTVA.
VARNING
(SV)
DİKKAT
(TR)
• DEN HÄR SERVICEHANDBOKEN FINNS BARA TILLGÄNGLIG PÅ ENGELSKA.
• 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.
• BU SERVİS KILAVUZU YALNIZCA İNGİLİZCE OLARAK SAĞLANMIŞTIR.
• BU UYARININ GÖZ ARDI EDİLMESİ, ELEKTRİK ÇARPMASI YA DA MEKANİK
VEYA DİĞER TÜRDEN KAZALAR SONUCUNDA TEKNİSYENİN, OPERATÖRÜN
YA DA HASTANIN YARALANMASINA YOL AÇABİLİR.
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GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
(JA)
(ZH-CN)
(KO)
- vii
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GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
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.
CERTIFIED ELECTRICAL CONTRACTOR STATEMENT - FOR USA ONLY
All electrical Installations that are preliminary to position ing of the equipment at the site prepared for the
equipment shall be performed by licensed electrical contractors. Othe r conn ections between pieces o f
electrical equipment, calibrations and testing sha ll be performed by q ualified GE Healthcare person nel.
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.
OMISSIONS & ERRORS
If there are any omissions, errors or suggestions for improving this documentation, please contact the
GE Healthcare Global Documentation Group with specific information listing the system type, manual
title, part number, revision number, page number and suggestion details. Mail the information to:
Service Documentation, 9900 Innovation Drive (RP-2123), Wauwatosa, WI 53226, USA.
GE Healthcare employees should use the iTrak System to report all documentation e rrors or omissions.
SERVICE SAFETY CONSIDERATIONS
DANGER
DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH, ARE PRESENT IN
THIS EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING AND
ADJUSTING.
WARNINGWARNING
Use all Personal Protection Equipment (PPE) such as gloves, safety shoes, safety
glasses, and kneeling pad, to reduce the risk of injury.
For a complete review of all safety requirements, see the Chapter 1, Safety Considerations section in
the Service Manual.
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GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
LEGAL NOTES
The contents of this publication may not be copied or duplicated in any form, in whole or in part, without
prior written permission of GE Healthcare.
GE Healthcare may revise this publication from time to time without written notice.
TRADEMARKS
All products and their name brands are trademarks of their respective holders.
Covers both Vivid 7 and Vivid 7 PRO
Replaces Vivid 7 Service Manual, Part Number FB091202
Updated per BT02-M4 release. Included description for BEP-2.
Updated per BT03-M3 release (software version V 3.0.x).
Updated per RFI release (software version V 3.2.x).
Updated per BT’04-M3 release (software version V4.0.0)
- Removed WLAN from manual. Was removed from product’s spec after the M3 manual was released.
- Added Vivid 7 model for Brazil.
Updated per BT’05-M3 release (software version v5.0.0)
Updated per BT’05-M4 release (software version v5.1.0)
Updated per BT’06-M3 release (software version v6.0.0)
Updated per software version v6.1.0 release
Updated per BT’08 Release (Software version v7.0.0)
Updated due to new/changed service parts. Corrected errors and updated content.
List of Effected Pages
PagesRevisionPagesRevisionPagesRevision
Title Page 12 4-1 to 4-8212 9-1 to 9-11612
Warnings
i to -x
1-1 to 1-7612 6-1 to 6-1412 Back CoverN/A
2-1 to 2-1412 7-1 to 7-7612
3-1 to 3-13612 8-1 to 8-10812
12 5-1 to 5-15412 10-1 to 10-3012
x -
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GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
Changing the Computer Name, AE Title and/or Port Number (Port No.) . . 3 - 44
Set the Scanner’s Network Information - S/W v4.2/v5.2/v6.1/v7.x and later 3 - 47
Set the Scanner’s Network Information - S/W v4.0/v4.1/v5.0/v5.1/v6.0 . . . 3 - 49
GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
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DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
Chapter 1
Introduction
Section 1-1
Overview
1-1-1Purpose of Chapter 1
This chapter describes important issues related to safely servicing this ultrasound machine. The service
provider must read and understand all the information presented here before installing or servicing a
unit.
1-1-2Contents in Chapter 1
Table 1-1 Contents in Chapter 1
SECTIONDESCRIPTIONPAGE NUMBER
1-1
1-2
1-3
1-4
1-5
1-6
1-7
1-8
1-9
1-10
Overview
Service Manual Overview
Important Conventions
Safety Considerations
Labels Locations
Dangerous Procedure Warnings
Lockout/Tagout (LOTO) Requirements
Returning/Shipping Probes and Repair Parts
Electromagnetic Compatibility (EMC)
Customer Assistance
1-1-3Purpose of Service Manual
This Service Manual provides installation and service information for the Vivid 7 Ultrasound Scanning
unit.
1-1
1-2
1-9
1-15
1-20
1-71
1-72
1-72
1-73
1-74
Chapter 1 - Introduction1 - 1
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GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
Section 1-2
Service Manual Overview
The service manual provides installation and service information for the Vivid 7 ultrasound scanning
unit. It is divided in 10 chapters as shown below, in Table 1-2 "Contents in this Service Manual" on
page 1-2.
1-2-1Contents in this Service Manual
The service manual is divided in ten chapters.
In the beginning of the manual, before chapter 1, you will find the language policy for GE Healthcare’s
service documentation, legal information, a revision overview and the Table of Contents (TOC).
An Index has been included after chapter 10.
Table 1-2 Contents in this Service Manual
CHAPTER
NUMBER
1
2Site PreparationsDescribes the site requirements for the Vivid 7 ultrasound scanner
3System SetupContains unpacking and setup procedures
4Functional ChecksContains:
5Components and Functions (Theory) Contains block diagrams and functional explanations of the
6Service AdjustmentsContains instructions on how to make any available adjustments to
7Diagnostics/TroubleshootingProvides procedures for running and diagnostic or related routines
8Replacement ProceduresProvides disassembly procedures and reassembly procedures for all
9Renewal PartsContains a complete list of replacement parts for Vivid 7
10Care & MaintenanceProvides periodic maintenance procedures for Vivid 7
N/A
IntroductionContains content summary and warnings
IndexA quick way to the topic you’re looking for
CHAPTER TITLEDESCRIPTION
- general (frequently used) procedures
- functional checks that must be performed as part of the installation,
or as required during servicing and periodic maintenance
- diagnostics
electronics
the Vivid 7
for the Vivid 7
changeable FRU
1 - 2Section 1-2 - Service Manual Overview
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DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
NOTE:When not otherwise specified, the contents in this manual applies to all Vivid 7 models.
v2.3/v2.4
Chapter 1 - Introduction1 - 5
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DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
1-2-4Product Description
1-2-4-1Overview of the Vivid 7 Ultrasound Scanner
•Vivid 7 is a phased and linear array ultrasound imaging scanner. It also has provisions for analog
input sources like ECG and phono, and a Doppler probe may be connected and used too.
•Real Time 3D (RT 3D) was introduced as an option to VIVID 7 Dimension in 2004 (BT’04).
•The unit can be used for:
-2D Black and White imaging
-2D Color Flow
-M-Mode Black and White imaging
-Color M-Mode
-Doppler
-a number of combinations of the above
-Real Time 3D measurements (4D)
•Vivid 7 is a digital beam forming unit and can handle up to 192 element linear probes by use of
multiplexing.
•Signal flow from the Probe Connector Panel to the Front-End, then to the Mid Processors and BackEnd Processor and finally to the monitor and peripherals.
•System configuration is stored on a hard disk drive (HDD) and all necessary software is loa ded from
the HDD on power up.
1 - 6Section 1-2 - Service Manual Overview
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1-2-4-1 Overview of the Vivid 7 Ultrasound Scanner (cont’d)
CRT MONITOR.
21” LCD MONITOR
- STANDARD FOR BT’08.
- OPTION FOR BT’06
OPERATOR PANEL
(Discontinued 2007)
UPPER PANEL
WITH STEREO
LOUDSPEAKERS
B/W VIDEO PRINTER
PATIENT I/O
MO DRIVE
DVD or CD DRIVE
Figure 1-1 Vivid 7 Major Components
VCR or DVD
RECORDER
DOPPLER (PEDOF)
CONNECTOR
PROBE CONNECTORS
PARKING SLOT
(UNITS WITHOUT 4D)
BRAKE PEDALS
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1-2-4-2History - Hardware/Software Versions
The contents in this sub-section has been moved to chapter 9.
•For Front-End Processor Version 2, please refer to: 9-18-2 "Hardware/Software Versions, Front-
End Processor Version 2 (FEP2)" on page 9-38
•For Front-End Processor Version 1, please refer to: 9-18-4 "Hardware/Software Versions, Front-
End Processor Version 1" on page 9-42
1-2-4-3History - Peripherals/Software Versions
The contents in this sub-section has been moved to chapter 9.
Please refer to:
•9-22-1 "Peripherals Compatibility" on page 9-60
1-2-4-4FRUs for Back-End Processor
The contents in this sub-section has been moved to chapter 9.
Please refer to:
•Section 9-19 "Back-End Processor" on page 9-45
1-2-4-5History - Supported Probes
The contents in this sub-section has been moved to chapter 9.
Please refer to:
•Section 9-26 "Probes" on page 9-74
1-2-4-6How to Turn the Scanner ON and OFF
Please refer to Chapter 4, section 4-2-2 - Power ON/ Boot UP, for a detailed description of how to turn
the scanner ON and to Chapter 4, s ection 4-2- 3 - Power Shut Down for a detailed description of how to
turn the scanner OFF.
1-2-4-7How to Check for Hardware/Software Version, Installed Options
To verify the hardware versions on the boards, please refer to the appropriate table:
•"Hardware/Software Versions, Front-End Processor Version 2 (FEP2)" on page 9-38
•"Hardware/Software Versions, Front-End Processor Version 1" on page 9-42
Please refer to "Software Configuration Checks" on page 4-81 to check the software versions on local
software on the boards.
Please refer to "Functional Checks" on page 4-27 to check for installed options.
1-2-4-8Purpose of Operator Manual(s)
The Operator Manual(s) should be fully read and understood before operating the Vivid 7 and also kept
near the unit for quick reference.
1 - 8Section 1-2 - Service Manual Overview
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Section 1-3
Important Conventions
1-3-1Conventions Used in Book
1-3-1-1Model Designations.
This manual covers the Vivid 7 scanners listed in Table 1-3 on page 1-3.
1-3-1-2Icons
Pictures, or icons, are used wherever they will reinforce the printed message. The icons, labels and
conventions used on the product and in the service information are described in this chapter.
1-3-1-3Safety Precaution Messages
Various levels of safety precaution messages may be found on the equipment and in the service
information. The different levels of concern are identified by a flag word that precedes the precautionar y
message. Known or potential hazards to personal are labeled in one of the following ways:
DANGER
Danger is used to indicate the presence of a hazard that will cause severe
personal injury or death if the instructions are ignored.
WARNINGWARNING
CAUTION
NOTICE
NOTE:Notes provide important information about an item or a procedure.
Warning is used to indicate the presence of a hazard that can cause severe personal
injury and property damage if instructions are ignored.
Caution is used to indicate the presence of a hazard that will or can cause minor personal injury
and property damage if instructions are ignored.
Equipment Damage Possible.
Notice is used when a hazard is present that can cause property damage but has absolutely no
personal injury risk.
Example: Disk drive will crash.
Information contained in a NOTE can often save you time or effort.
Chapter 1 - Introduction1 - 9
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LIGHT
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
1-3-2Standard Hazard Icons
Important information will always be preceded by the exclamation point contained within a
triangle, as seen throughout this chapte r. In addition to text, several differe nt graphical icons (symbols)
may be used to make you aware of specific types of hazards that could possib ly cause har m. Even if a
symbol isn’t used in this manual, it is included for your reference.
Table 1-4 Standard Hazard Icons
ELECTRICALMECHANICALRADIATION
LASERHEATPINCH
LASER
Some others make you aware of specific procedures that should be followed.
Table 1-5 Standard Icons that indicates that a special procedure is to be used
AVOID STATIC ELECTRICITYTAG AND LOCK OUTWEAR EYE PROTECTION
TAG
&
LOCKOUT
Date
Signed
OR
HAND PROTECTIONFOOT PROTECTION
1 - 10Section 1-3 - Important Conventions
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1-3-3Product Icons
The following table describes the purpose and location of safety labels and other impor tant information
provided on the equipment.
Table 1-6 Product Icons sheet 1 of 4
LABEL/SYMBOLPURPOSE/MEANINGLOCATION
Manufacturer's name and address
Identification and Rating Plate
Date of manufacture
Model and serial numbers
Electrical ratings
Rear of console near power inlet
Type/Class Label
IP Code (IPX8/IP68)
Used to indicate the degree of safety or
protection.
Indicates the degree of protection provided
by the enclosure per IEC 529.
IPX8 indicates drip proof and may be used in
an Operating Theater.
The footswitch delivered with Vivid 7 is IP68
rated.
Equipment Type BF (man in the box symbol)
IEC 878-02-03 indicates B Type equipment
having a floating applied part.
Equipment Type CF (heart in the box
symbol) IEC 878-02-05 indicates equipment
having a floating applied part having a
degree of protection suitable for direct
cardiac contact.
DEFIBRILLATOR-PROOF TYPE CF
EQUIPMENT.
Footswitch
Probe connectors including Doppler
probe connector
Probe connectors and ECG connector.
On newer systems also on the rear of
the system.
At the ECG connector on front of
system.
Device Listing/Certification Labels
“CAUTION - This unit weighs...Special
care must be used to avoid...”
“DANGER - Risk of explosion used in...”
Chapter 1 - Introduction1 - 11
Laboratory logo or labels denoting
conformance with industry safety standards
such as UL or IEC.
This precaution is intended to prevent injury
that may result if one person attempt to move
the unit considerable distances or on an
incline due to the weight of the unit.
The system is not designed for use with
flammable anesthetic gases.
The system is not designed for use with
flammable anesthetic gases.
Rear of console
On the console where easily seen
during transport
Rear of console
Rear of console
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Table 1-6 Product Icons (cont’d) sheet 2 of 4
LABEL/SYMBOLPURPOSE/MEANINGLOCATION
Please refer to the Recycling instructions on
the label located outside the Front End Card
Vivid 7 SCANNERS PRODUCED
AFTER SEPTEMBER 2004:
Vivid 7 SCANNERS PRODUCED
BEFORE SEPTEMBER 2004:
Rack’s Cover (Inside the unit),
see Figure 1-20 on page 1-67
and Figure 1-23 on page 1-70.
Vivid 7 SCANNERS PRODUCED AFTER
SEPTEMBER 2004:
“TESTED AND PRODUCTION
MONITORED BY TUV PRODUCT
SERVICE NRTL WITH RESPECT TO
ELECTRICAL SHOCK, FIRE AND
MECHANICAL HAZARDS ONLY IN
ACCORDANCE WITH UL2601-1 AND CAN/
CSA C22.2 NO.601.1”
Products produced before September 2004
will bear the c-UL-us Classification mark,
shown below.
Vivid 7 SCANNERS PRODUCED BEFORE
SEPTEMBER 2004:
“CLASSIFIED BY UNDERWRITERS
LABORATARIES INC WITH RESPECT TO
ELECTRICAL SHOCK, FIRE AND
MECHANICAL HAZARDS ONLY IN
ACCORDANCE WITH UL2601-1 AND CAN/
CSA C22.2 NO.601.1”
REAR OF CONSOLE
REAR OF CONSOLE ON Vivid 7
PRODUCED AFTER SEPTEMBER
2004
REAR OF CONSOLE ON Vivid 7
PRODUCED BEFORE SEPTEMBER
2004
This unit carries the CE mark.
The Vivid 7 unit complies with regulatory
requirements of the European Directive 93/
42/EEC concerning medical devices.
It also complies with emission limits for a
Group 1, Class B Medical Device as stated in
EN 60601-1-2
(IEC 60601-1-2).
(Units produced before 2 May 2002 have the
CE0301 label.)
“CAUTION” The equilateral triangle is
usually used in combination with other
symbols to advise or warn the user.
“ATTENTION - Consult accompanying
documents” is intended to alert the user to
refer to the operator manual or other
instructions when complete information
cannot be provided on the label.
REAR OF CONSOLE
Various
Various
1 - 12Section 1-3 - Important Conventions
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Table 1-6 Product Icons (cont’d) sheet 3 of 4
LABEL/SYMBOLPURPOSE/MEANINGLOCATION
“CAUTION - Dangerous voltage” (the
lightning flash with arrowhead in equilateral
triangle) is used to indicate electric shock
hazards.
Various
“Mains OFF” Indicates the power off position
of the mains power switch.
“OFF/Standby” Indicates the power off/
standby position of the power switch.
CAUTION
This Power Switch DOES NOT ISOLATE
Mains Supply
“Mains ON” Indicates the Power ON position
of the mains power switch.
“ON” Indicates the power on position of the
power switch.
CAUTION
The Power Switch on the Operator Panel
DOES NOT ISOLATE Mains Supply
“Protective Earth” Indicates the protective
earth (grounding) terminal.
“Equipotential”
Indicates the terminal to be used for
connecting equipotential conductors when
interconnecting (grounding) with other
equipment as described in IEC60601-1.
Rear of system adjacent to mains switch
Adjacent to On/Off (Standby) Switch
Used several places inside the scanner.
Rear of console
This symbol indicates that waste electrical
and electronic equipment must not be
disposed of as unsorted municipal waste and
must be collected separately. Please contact
an authorized representative of the
manufacturer for information concerning the
decommissioning of your equipment.
This product consists of devices that may
contain mercury, which must be recycled or
disposed of in accordance with local, state,
or country laws. (Within this system, the
backlight lamps in the monitor display
contain mercury.)
REAR OF THE LCD MONITOR
Rear Panel
REV. 1: USA ONLY
REV.2: USA AND CHINA
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Table 1-6 Product Icons (cont’d) sheet 4 of 4
LABEL/SYMBOLPURPOSE/MEANINGLOCATION
The following product pollution control
information is provided according to SJ/
T11364-2006 Marking for Control of
Pollution caused by Electronic
Information Products.
This symbol indicates the product contains
hazardous materials in excess of the limits
established by the Chinese standard SJ/
T11363-2006 Requirements for
Concentration Limits for Certain Hazardous
Substances in Electronic Information
Products. The number in the symbol is the
Environment-friendly Use Period (EFUP),
which indicates the period during which the
toxic or hazardous substances or elements
contained in electronic information products
will not leak or mutate under normal
operating conditions so that the use of such
electronic information products will not result
in any severe environmental pollution, any
bodily injury or damage to any assets. The
unit of the period is “Year”.
In order to maintain the declared EFUP, the
product shall be operated normally
according to the instructions and
environmental conditions as defined in the
product manual, and periodic maintenance
schedules specified in Product Maintenance
Procedures shall be followed strictly.
Consumables or certain parts may have their
own label with an EFUP value less than the
product. Periodic replacement of those
consumables or parts to maintain the
declared EFUP shall be done in accordance
with the Product Maintenance Procedures.
This product must not be disposed of as
unsorted municipal waste, and must be
collected separately and handled properly
after decommissioning.
Rear Panel
(China)
1 - 14Section 1-3 - Important Conventions
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Section 1-4
Safety Considerations
1-4-1Introduction
The following safety precautions must be observed during all phases of operation, service and repair of
this equipment. Failure to comply with these precautions or with specific warnings elsewhere in this
manual, violates safety standards of design, manufacture and intended use of the equipment.
Chapter 1 - Introduction1 - 15
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1-4-2Human Safety
DANGER
WARNINGWARNING
WARNINGWARNING
WARNINGWARNING
WARNINGWARNING
WARNINGWARNING
DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH, ARE PRESENT IN
THIS EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING AND
ADJUSTING.
WHEN THE TOP CONSOLE IS IN ITS LOCKED POSITION, THE GAS SPRING IS
COMPRESSED AND STORES MECHANICAL ENERGY. DURING NORMAL OPERATION
THE TOP CONSOLE, THE WEIGHT OF THE MONITOR AND THE MECHANICAL FORCE
OF THE GAS SPRING ARE IN BALANCE. TAKE CARE IF/WHEN YOU ACTIVATE THIS
GAS SPRING. PERSONAL INJURY CAN OCCUR AFTER THE PANEL IS REMOVED AND
THE SPRING PRESSURE IS RELEASED. TAKE CARE WHEN YOU REPAIR THE
ELEVATION ASSEMBLY.
TWO PEOPLE SHOULD UNPACK THE UNIT BECAUSE OF ITS WEIGHT. TWO PEOPLE ARE
REQUIRED WHENEVER A PART WEIGHING 16 KG (35 LBS) OR MORE MUST BE LIFTED.
USE ALL PERSONAL PROTECTING EQUIPMENT (PPE) SUCH AS GLOVES, SAFETY
SHOES, SAFETY GLASSES, AND KNEELING PAD, TO REDUCE THE RISK OF INJURY.
BEWARE OF POSSIBLE SHARP EDGES ON ALL MECHANICAL PARTS. IF SHARP
EDGES ARE ENCOUNTERED, THE APPROPRIATE PPE SHOULD BE USED TO
REDUCE THE RISK OF INJURY.
WEAR ALL PPE INCLUDING GLOVES AS INDICATED IN THE CHEMICAL MATERIAL
SAFETY DATA SHEET (MSDS) OR PRODUCT DATA SHEET.
WARNINGWARNING
WARNINGWARNING
WARNINGWARNING
ENSURE THAT THE SYSTEM IS TURNED OFF AND UNPLUGGED. TO VERIFY THAT
THE FRONT END POWER SUPPLY (FEPS) IS IN A ZERO ENERGY STATE, WAIT AT
LEAST 20 SECONDS FOR THE CHARGE ON THE FEP’S OUTPUTS TO BLEED OFF.
WHEN THE UNIT IS RAISED FOR A REPAIR OR MOVED ALONG ANY INCLINE, USE
EXTREME CAUTION SINCE IT MAY BECOME UNSTABLE AND TIP OVER.
TILTING THE CONSOLE REQUIRES TWO PEOPLE IN ORDER TO AVOID INJURY TO
SERVICE PERSONNEL AND DAMAGE TO THE EQUIPMENT.
Operating personnel must not remove the system covers.
Servicing should be performed by authorized personnel only.
Only personnel who have participated in a Vivid 7 Training are authorized to service the equipment.
1 - 16Section 1-4 - Safety Considerations
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1-4-3Mechanical Safety
WARNINGWARNING
PRIOR TO ELEVATING SCANNER, VERIFY THAT THE KEYBOARD IS LOCKED IN ITS
LOWEST POSITION. VERIFY THAT THE FRONT BRAKE IS LOCKED AND THE
SCANNER IS UNABLE TO SWIWEL. VERIFY THAT THE REAR BRAKES ARE IN THE
LOCKED POSITION.
WARNINGWARNING
WARNINGWARNING
WARNINGWARNING
WARNINGWARNING
WARNINGWARNING
CAUTION
WHEN THE UNIT IS RAISED FOR A REPAIR OR MOVED ALONG ANY INCLINE, USE
EXTREME CAUTION SINCE IT MAY BECOME UNSTABLE AND TIP OVER.
ULTRASOUND PROBES ARE HIGHLY SENSITIVE MEDICAL INSTRUMENTS THAT CAN
EASILY BE DAMAGED BY IMPROPER HANDLING. USE CARE WHEN HANDLING AND
PROTECT FROM DAMAGE WHEN NOT IN USE. DO NOT USE A DAMAGED OR
DEFECTIVE PROBE. FAILURE TO FOLLOW THESE PRECAUTIONS CAN RESULT IN
SERIOUS INJURY AND EQUIPMENT DAMAGE.
NEVER USE A PROBE THAT HAS FALLEN TO THE FLOOR. EVEN IF IT LOOKS OK, IT
MAY BE DAMAGED.
REMEMBER: IF THE FRONT CASTER SWIVEL LOCK IS ENGAGED FOR
TRANSPORTATION, PRESSING THE RELEASE PEDAL ONCE DISENGAGES THE
SWIVEL LOCK. YOU MUST DEPRESS THE RELEASE PEDAL A SECOND TIME TO
ENGAGE THE BRAKE.
THE SYSTEM SHOULD NOT BE MOVED WITH THE OPERATOR PANEL EXTENDED.
MOVE THE OPERATOR PANEL TO ITS CENTERED AND LOCKED POSITION. LOWER
THE OPERATOR PANEL AS MUCH AS POSSIBLE BEFORE MOVING THE SYSTEM.
Ensure that nobody touch the console arm/frogleg when moving the Operator Panel (Control
Console).
CAUTION
CAUTION
CAUTION
CAUTION
CAUTION
Do not move the unit if the Operator Panel (Control Console) is in unlocked position.
Always lock the Operator Panel (Control Console) in its parking (locked) position before moving
the scanner around.
Keep the heat venting holes on the monitor unobstructed to avoid overheating of the monitor.
VIVID 7 weighs 190 kg (419 lbs) or more, depending on installed peripherals, when ready for use.
Care must be used when moving it or replacing its parts. Failure to follow the precautions listed
below could result in injury, uncontrolled motion and costly damage.
ALWAYS:
- Be sure the pathway is clear.
- Use slow, careful motions.
- Use two people when moving on inclines or lifting more than 16 kg (35 lbs).
To avoid injury when you move the LCD monitor and the monitor arm, do NOT put your finger,
hand, or object on the joint of the monitor and the monitor arm.
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1-4-3Mechanical Safety (cont’d)
-
CAUTION
CAUTION
CAUTION
CAUTION
CAUTION
CAUTION
CAUTION
Before you move or transport the system, make sure to lock the LCD monitor firmly and flip
down the monitor to prevent damage to the system.
To avoid injury or damage to the monitor, make sure there is nothing within range of the LCD
before moving the monitor and the monitor arm. This includes people as well as things.
Do not transport Vivid 7 in a vehicle without locking the casters (wheels).
Use all Personal Protection Equipment (PPE) such as gloves, safety shoes, safety glasses, and
kneeling pad, to reduce the risk of injury.
Use Protective Glasses during Drilling, Filing and during all other work where eyes need
protection.
Use Safety Shoes when doing work where there is any chance of foot damage.
Use Protective Gloves when drilling and cutting.
NOTE:Special care should be taken when transporting the unit in a vehicle:
•Lock Operator Panel (Control Console) in place.
•Eject any Magneto Optical disk, CD or DVD from their drive.
•Secure the unit in an upright position.
•Lock the casters (wheels) (brake)
•DO NOT use the Operator Panel (Control Console) as an anchor point.
•Place the probes in their carrying case.
1 - 18Section 1-4 - Safety Considerations
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1-4-4Electrical Safety
1-4-4-1Safe Practices
Follow these guidelines to minimize shock hazards whenever you are using the scanner;
•The equipment chassis must be connected to an electrical ground.
•The unit is equipped with a three-conductor AC power cable. This m ust be plugged into an approved
electrical outlet with safety ground.
•The power outlet used for this equipment should not be shared with other types of equipment.
•Both the system power cable and the power co nnector must meet international electrical standards.
WARNINGWARNING
CONNECTING A Vivid 7 SCANNER TO THE WRONG VOLTAGE LEVEL WILL MOST
LIKELY DESTROY IT.
1-4-4-2Probes
Follow these guidelines before connecting a probe to the scanner;
•Inspect the probe prior to each use for damage or degradation to the;
-housing
-cable strain relief
-lens
-seal
•Do not use a damaged or defective probe.
•Never immerse the probe connector or adapter into any liquid.
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Section 1-5
Labels Locations
1-5-1Labels on Front of Monitor and Operator Panel
Table 1-7 Labels on Front of Monitor and Operator Panel
DESCRIPTIONILLUSTRATION
Label, Vivid 7 (Monitor)
(Introduced in 2001)
Label, Vivid 7 (Monitor)
(Introduced in 2002)
Label, Vivid 7 PRO (Monitor)
(Introduced in 2002)
Label, Vivid 7 Dimension (Monitor)
(Introduced 2004)
For Vivid 7 Dimension with LCD screen
(option since 2006)
1 - 20Section 1-5 - Labels Locations
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Table 1-7 Labels on Front of Monitor and Operator Panel (cont’d)
DESCRIPTIONILLUSTRATION
Label, GE Logo
Label, On/Off Switch
(Two versions of the label have been used, the one to the
right is the latest version.)
OR
ON/OFF:
press once
FC314104 03
LABEL POSITION
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1-5-2Labels on Front of LCD Monitor
Table 1-8 Label on Front of LCD Monitor
DESCRIPTIONILLUSTRATION
Label, Vivid 7
Label, GE Healthcare
1-5-3Labels on Rear of LCD Monitor
Table 1-9 Label on Rear of LCD Monitor
DESCRIPTIONILLUSTRATION
Firmware label LCD monitor
1 - 22Section 1-5 - Labels Locations
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Table 1-9 Label on Rear of LCD Monitor (cont’d)
DESCRIPTIONILLUSTRATION
FOR USA ONLY: LCD MONITOR MERCURY HG.
The first version was introduced October 1, 2007
For Global Use: LCD MONITOR MERCURY HG
This version was introduced ultimo October 2007.
(English / Chinese)
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1-5-4Labels on Front Handle
Table 1-10 Labels on Front Handle
DESCRIPTIONILLUSTRATION
Label, Front Handle
Three versions of the label have been used. The lower
one is the latest version.
OR
OR
1 - 24Section 1-5 - Labels Locations
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1-5-5Labels Near Connectors on Front
Table 1-11 Labels Near Connectors on Front
DescriptionIllustration
Label, Probe Connector
(The Label, “Probe Connector” consists of three labels,
named;
- “Main Label Part”,
- “Heart Symbol” and
- “See Manual symbol”.)
Label, Patient I/O Module II
BEP1 ONLY:
Label CD ROM
(introduced April 2002)
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1-5-6Label on External I/O
Table 1-12 Label, External I/O
DESCRIPTIONILLUSTRATION
Marking introduced
late 2002.
(Not In Use)
Label, External. I/O
1 - 26Section 1-5 - Labels Locations
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1-5-7Labels at AC Mains Inlet and Circuit Breaker
Table 1-13 Labels at AC Mains Inlet and Circuit Breaker (used before May 2002)
DESCRIPTIONILLUSTRATION
Label, Warning
System: P/N, Power rating
Label, System: S/N
Label,
C
G E M e d i c a l S y s t e m s
P / N :
C a t . n o . :
P r o d u c t n a m e :
F C 0 0 0 0 3 0
H 5 5 0 0 1 A B
V i v i d 7
2 3 0
5
5 0 / 6 0
V A C
A
H z
F B 0 1 4 9 8 0 0 7
OR
OR
OR
OR
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Table 1-13 Labels at AC Mains Inlet and Circuit Breaker (used before May 2002) (cont’d)
DESCRIPTIONILLUSTRATION
Ground (GND) Label. (Used on 230 VAC Systems and some 100-120 VAC Systems.)
Label, GND-symbol
l
Hospital Grade Ground
Label, GND-symbol., Hospital Grade
(GND) Label. (Used on some
100-120 VAC Systems)
Table 1-14 Labels at AC Mains Inlet and Circuit Breaker (used after May 2002)
DESCRIPTIONILLUSTRATION
Label, AC Controller
1 - 28Section 1-5 - Labels Locations
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1-5-8Label on Rear Cover - Vivid 7 Dimension
Table 1-15 Label on Rear Cover - Vivid 7 Dimension sheet 1 of 3
DESCRIPTIONILLUSTRATION
l
Label, General Info
(Located on rear of system)
Label used for Vivid 7 Dimension after FEB. 2008
Label, General Info
(Located on rear of system)
Label used for Vivid 7 Dimension after OCT. 2005
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Table 1-15 Label on Rear Cover - Vivid 7 Dimension (cont’d) sheet 2 of 3
DESCRIPTIONILLUSTRATION
Label, General Info
(Located on rear of system)
Label used for Vivid 7 Dimension between JUNE 2005 and
OCT. 2005.
l
CISPR11
Group 1 Class B
Groupe 1 Classe B
CLASS I
TYPE CF
FB014970-06
Label, General Info
(Located on rear of system)
Label used for Vivid 7 Dimension
1 - 30Section 1-5 - Labels Locations
Page 69
GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
Table 1-15 Label on Rear Cover - Vivid 7 Dimension (cont’d) sheet 3 of 3
DESCRIPTIONILLUSTRATION
Label, General Info
(Located on rear of system)
Label used for Vivid 7 Dimension,
after September 2004.
Chapter 1 - Introduction1 - 31
Page 70
GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
1-5-9Label on Rear Cover - Vivid 7
Table 1-16 Label on Rear Cover - Vivid 7 sheet 1 of 2
DESCRIPTIONILLUSTRATION
l
Label, General Info
(Located on rear of system)
Label used for Vivid 7
after JUNY 2005
CLASS I
TYPE CF
CISPR11
Group 1 Class B
Groupe 1 Classe B
FC014667-02
Label, General Info
(Located on rear of system)
Label used for Vivid 7
1 - 32Section 1-5 - Labels Locations
Page 71
GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
Table 1-16 Label on Rear Cover - Vivid 7 (cont’d) sheet 2 of 2
DESCRIPTIONILLUSTRATION
Label, General Info
(Located on rear of system)
Label used for Vivid 7 between 2 May 2002 and
September 2004.
l
Label, General Info
(Located on rear of system)
Label used for Vivid 7 before 2 May 2002
Chapter 1 - Introduction1 - 33
Page 72
GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
1-5-10Label on Rear Cover - Vivid 7 PRO
Table 1-17 Label on Rear Cover - Vivid 7 PRO sheet 1 of 3
DESCRIPTIONILLUSTRATION
l
Label, General Info
(Located on rear of system)
Label used for Vivid 7 PRO
introduced FEB. 2008
Label, General Info
(Located on rear of system)
Label used for Vivid 7 PRO
introduced OKT. 2005
1 - 34Section 1-5 - Labels Locations
Page 73
GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
Table 1-17 Label on Rear Cover - Vivid 7 PRO (cont’d) sheet 2 of 3
DESCRIPTIONILLUSTRATION
FC014169-05
Label, General Info
(Located on rear of system)
Label used for Vivid 7 PRO
introduced JUNE 2005
CLASS I
TYPE CF
CISPR11
Group 1 Class B
Groupe 1 Classe B
Label, General Info
(Located on rear of system)
Label used for Vivid 7 PRO
introduced March 2005
Chapter 1 - Introduction1 - 35
Page 74
GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
Table 1-17 Label on Rear Cover - Vivid 7 PRO (cont’d) sheet 3 of 3
DESCRIPTIONILLUSTRATION
Label, General Info
(Located on rear of system)
Label used for Vivid 7 PRO
introduced September 2004
Label, General Info
(Located on rear of system)
Label used for Vivid 7 PRO
before September 2004
1 - 36Section 1-5 - Labels Locations
Page 75
GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
1-5-11Label on Rear Cover - Vivid 7 Dimension for China
Table 1-18 Label on Rear Cover - Vivid 7 Dimension for China sheet 1 of 4
DESCRIPTIONILLUSTRATION
l
Label, General Info
(Located on rear of system)
Label used for Vivid 7 to China
introduced OCTOBER 2007
Label, General Info
(Located on rear of system)
Label used for Vivid 7 to China
introduced FEBRUARY 2007
Chapter 1 - Introduction1 - 37
Page 76
GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
Table 1-18 Label on Rear Cover - Vivid 7 Dimension for China (cont’d) sheet 2 of 4
DESCRIPTIONILLUSTRATION
Label, General Info
(Located on rear of system)
Label used for Vivid 7 to China
introduced OCTOBER 2005
Label, General Info
(Located on rear of system)
Label used for Vivid 7 to China
introduced SEPTEMBER 2005
1 - 38Section 1-5 - Labels Locations
Page 77
GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
Table 1-18 Label on Rear Cover - Vivid 7 Dimension for China (cont’d) sheet 3 of 4
DESCRIPTIONILLUSTRATION
FC014213-04
Label, General Info
(Located on rear of system)
Label used for Vivid 7 to China
introduced JUNE 2005
CLASS I
TYPE CF
Label, General Info
(Located on rear of system)
Label used for Vivid 7 to China
introduced March 2005
Chapter 1 - Introduction1 - 39
Page 78
GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
Table 1-18 Label on Rear Cover - Vivid 7 Dimension for China (cont’d) sheet 4 of 4
DESCRIPTIONILLUSTRATION
Label, General Info
(Located on rear of system)
Label used for Vivid 7 to China
introduced September 2004
1 - 40Section 1-5 - Labels Locations
Page 79
GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
1-5-12Label on Rear Cover - Vivid 7 for China
Table 1-19 Label on Rear Cover - Vivid 7 for China
DESCRIPTIONILLUSTRATION
l
Label, General Info
(Located on rear of system)
Label used for Vivid 7 before 2 May 2002
Label, General Info
(Located on rear of system)
Label used for Vivid 7 to China
before September 2004
Chapter 1 - Introduction1 - 41
Page 80
GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
1-5-13Label on Rear Cover - Vivid 7 PRO for China
Table 1-20 Label on Rear Cover - Vivid 7 PRO for China sheet 1 of 4
DESCRIPTIONILLUSTRATION
l
Label, General Info
(Located on rear of system)
Label used for Vivid 7 PRO to China
introduced OCTOBER 2007
Label, General Info
(Located on rear of system)
Label used for Vivid 7 PRO to China
introduced FEBRUARY 2007
1 - 42Section 1-5 - Labels Locations
Page 81
GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
Table 1-20 Label on Rear Cover - Vivid 7 PRO for China (cont’d) sheet 2 of 4
DESCRIPTIONILLUSTRATION
Label, General Info
(Located on rear of system)
Label used for Vivid 7 PRO to China
introduced OCTOBER 2005
Label, General Info
(Located on rear of system)
Label used for Vivid 7 PRO to China
introduced SEPTEMBER 2005
Chapter 1 - Introduction1 - 43
Page 82
GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
Table 1-20 Label on Rear Cover - Vivid 7 PRO for China (cont’d) sheet 3 of 4
DESCRIPTIONILLUSTRATION
Label, General Info
(Located on rear of system)
Label used for Vivid 7 PRO to China
after JUNY 2005
l
CLASS I
TYPE CF
FC014216-04
Label, General Info
(Located on rear of system)
Label used for Vivid 7 PRO to China
1 - 44Section 1-5 - Labels Locations
Page 83
GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
Table 1-20 Label on Rear Cover - Vivid 7 PRO for China (cont’d) sheet 4 of 4
DESCRIPTIONILLUSTRATION
Label, General Info
(Located on rear of system)
Label used for Vivid 7 PRO to China
after September 2004
Label, General Info
(Located on rear of system)
Label used for Vivid 7 PRO to China
before September 2004
Chapter 1 - Introduction1 - 45
Page 84
GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
1-5-14Label on Rear Cover - Vivid 7 Dimension for Korea
Table 1-21 Label on Rear Cover - Vivid 7 Dimension for Korea
DESCRIPTIONILLUSTRATION
l
Label, General Info
(Located on rear of system)
Label used for Vivid 7 Dimension after DEC. 2006
1 - 46Section 1-5 - Labels Locations
Page 85
GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
1-5-15Label on Rear Cover - Vivid 7 PRO for Korea
Table 1-22 Label on Rear Cover - Vivid 7 PRO for Korea
DESCRIPTIONILLUSTRATION
l
Label, General Info
(Located on rear of system)
Label used for Vivid 7 Dimension after DEC. 2006
Chapter 1 - Introduction1 - 47
Page 86
GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
1-5-16Label on Rear Cover - Vivid 7 - Details Descriptions
Table 1-23 Label on Rear Cover - Vivid 7, Details Descriptions sheet 1 of 2
DESCRIPTIONILLUSTRATION
l
Label on rear side of the Vivid 7.
CLASS I
The Vivid 7 ultrasound unit is a Class I
device, type CF, according to Subclause 14 of IEC60601-1 (1988).
TYPE CF
Equipment Type CF (heart in the box
symbol) IEC 878-02-05 indicates
equipment having a floating applied part
having a degree of protection suitable
for direct cardiac contact.
This symbol indicates that waste
electrical and electronic equipment must
not be disposed of as unsorted
municipal waste and must be collected
separately. Please contact an
authorized representative of the
manufacturer for information concerning
the decommissioning of your equipment.
Please refer to the Recycling
instructions on the label located outside
the Front End Card Rack’s Cover (Inside
the unit), see Figure 1-20 on page 1-67
and Figure 1-23 on page 1-70.
The system is not designed for use with
flammable anesthetic gases.
1 - 48Section 1-5 - Labels Locations
Page 87
GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
Table 1-23 Label on Rear Cover - Vivid 7, Details Descriptions (cont’d) sheet 2 of 2
DESCRIPTIONILLUSTRATION
Vivid 7 SCANNERS PRODUCED
AFTER SEPTEMBER 2004:
“TESTED AND PRODUCTION
MONITORED BY TUV PRODUCT
SERVICE NRTL WITH RESPECT TO
ELECTRICAL SHOCK, FIRE AND
MECHANICAL HAZARDS ONLY IN
ACCORDANCE WITH UL2601-1 AND
CAN/CSA C22.2 NO.601.1”
Products produced before September
2004 will bear the c-UL-us Classification
mark, shown below.
Vivid 7 SCANNERS PRODUCED
BEFORE SEPTEMBER 2004:
“CLASSIFIED BY UNDERWRITERS
LABORATARIES INC WITH RESPECT
TO ELECTRICAL SHOCK, FIRE AND
MECHANICAL HAZARDS ONLY IN
ACCORDANCE WITH UL2601-1 AND
CAN/CSA C22.2 NO.601.1”
Vivid 7 SCANNERS PRODUCED AFTER SEPTEMBER 2004:
This unit carries the CE mark.
The Vivid 7 unit complies with regulatory
requirements of the European Directive
93/ 42/EEC concerning medical devices.
It also complies with emission limits for a
Group 1, Class B Medical Device as
stated in EN 60601-1-2 (IEC 60601-1-2).
(Units produced before 2 May 2002
have the CE0301 label.)
The sign indicates that Non Ionizing
Radiation is/may be emitted from the
unit.
Chapter 1 - Introduction1 - 49
Page 88
GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
1-5-17Labels on Internal I/O (Inside Scanner)
Label on Front-End Card Cage Side of Internal I/O
Figure 1-2 Labels on Internal I/O (Inside Scanner), Front-End Card Cage Side of Internal I/O
1 - 50Section 1-5 - Labels Locations
Page 89
GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
1-5-18Labels on Internal I/O (Inside Scanner)
Label on Back-End Processor Side of Internal I/O
Figure 1-3 Labels on Internal I/O (Inside Scanner), Back-End Processor Side of Internal I/O
Chapter 1 - Introduction1 - 51
Page 90
GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
1-5-18 Labels on Internal I/O (Inside Scanner) (cont’d)
i
F
610
51
1511
A1
5
1
M
A2
5
69
1
M
A3
69
159
81
F
A4
915
18
M
A5
Connectors to/from Back End
Bac
nt
k
e
En
r
na
d
l
I
O
m
o
P
r
oc
d
ul
e
e
s
s
e
s
o
r(
e
BEP
n
f
r
o
m
)
s
i
d
e
A6
A8
+3.3V
A1BW printer video, printer remote control
A2VCR remote control (RS232)
A3Spare RS232
A4Signals & power to/from top console
A5Signals to/from top console
A6Audio left out to VCR
A7Audio right out to VCR
A8Audio left reply from VCR
A9Audio right reply from VCR
A10SVideo out to VCR
A11SVideo in from VCR
A7
A9
+5V
+6V
+10V
+15V
+5V
+12V
From
Back
-5V
End
-15V
A10
F
1
5
B4
B8
5
69
1
M
69
B3
69
A11
F
125
6
9
B5
B1USB#1 (top console conection)
B2USB#2 (external i/o connection)
B310/100 Base-TX Ethernet
B4Audio in to BEP, Audio out from BEP, Microphone in to BEP
B5PC2IO board signals
B6PC2IO board signals and power
B7COM (external i/o connection) NOT USED
B8COM (modem - setup as COM2)
B9BEP Power Supply control (UPS)
26
50
B1B2
F
1
1425
13
B6
B7
5
1
M
5
1
M
B9
P31
Connector to motherboard
P32
Figure 1-4 Label on Internal I/O on units with BEP2
1 - 52Section 1-5 - Labels Locations
Page 91
GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
1-5-18 Labels on Internal I/O (Inside Scanner) (cont’d)
NOTE:On units with RFI ONLY: A11 has been moved from the Internal I/O module to the BEP.
Figure 1-5 Label on Internal I/O on units with BEP2.2, BEP3 and BEP3.2
Chapter 1 - Introduction1 - 53
Page 92
GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
1-5-19Label, Internal Connections (Int.Conn.)
Located on the outside of the Front-End Card Rack (FEP1) Cover (inside Vivid 7). Different versions of
the label have been used since production start.
AC
Cable and Connector numbering and naming system used:
IIO= Internal IO module
EIO= External IO module
BEP= Backend Processor
FEP= Frontend Processor
ACP= AC controller module
ACD= AC distribution box
ACT= AC isolation transformer module
BEPIO= IO module on the BEP
Axx : connectors on IIO with other connections than the BEP
Bxx : connectors on IIO that are connected to BEP
Cxx : connectors on BEP, except for the BEPIO
Dxx : connectors on BEPIO
Exx : connector on the BEP power supply
Fxx : connectors on ACP
Gxx : connectors on FEP
Hxx : external accesable connectors (Doppler probe)
Kxx : connectors on MODEM
Mxx : connectors on ACT
Nxx : connectors on ACD
Lxx : connectors on EIO
F
connector
to EIO
A
P30
P31
A13
A12
F
F
81
81
159
159
Connector to
motherboard
14
25
P32
A12 Spare power (future option)
A13 Power to 3D box (future option)
A14 AC power control
A15 Signals to rotation adapter (future option)
A16 Signals to 3D box (future option)
M
M
1
18
915
M
1
69
13
5
A15
A14
A16
25
1
n
e
e
s
O
I
I
L4: Audio out (right)
L5: Audio out (left)
L6: Trig out
L7: Foot switch
L8: Serial port
L9: Remote expose #1
L10: Remote expose #2
L11: Analog modem
L12: Composite video output
L13: B&W video output
L14: S-Video output
L15: SVGA output
L16: USB
L17: Ethernet
e
d
i
s
P
E
F
m
o
r
f
Distribution
box
N5
N4
N3
N2
N1
External IO module
L1L2
69
M
5
1
Service
use ONLY
(remote
power on/off
control)
Monitor
F1
115V
H1
TX-128
RX-128
Relay board
G1
Board location in Front End Processor (FEP)
L3
69
4
M
5
1
1
Analogue
RS-232
phone
Connect
Connect
to InSite
to InSite
MODEM
MODEM
Peripherals
Modem
F3
F2
115V
230V
or
230V
F6
From Isolation
transformer
BF-64
BF-64
RFT-1
FEC-2
SDP-2
L4
L5
L11L12 L13 L14
Back End
Processor
Front End
F4
F5
230V
230V
DC-power
IMP
Not used
G3
G2
supply
TX-power
G4
L6
L7
External IO module
(Front view)
supply
Rack
RESET
115V or 230V inlet
voltage selection
115V
Cable to
C15
Isolation
transformer
module
M
L8
F
L15
WARNING !
Live Voltage inside,
do not open.
AC power control module
230V
F7
To Isolation
transformer
M1
L9
L10
L16
L17
n
l
a
o
r
F
t
n
o
c
F9
230V
115V
Voltage Selection
V
0
2
1
on Peripherals
-
0
V
0
0
1
4
=
2
-
t
V
0
e
5
2
l
1
2
n
i
1
=
s
e
V
0
m
i
3
t
2
2
)
r
e
o
g
a
t
l
½
(
o
v
K4
69
15
M
F8
Cutout in the label
Modem
power
supply
60,0
Modem
MT5634ZBA
K3
K1
K2
Part no. : FB314746
Rev. : 05
Figure 1-6 Label on FEP1, Internal Connections
1 - 54Section 1-5 - Labels Locations
Page 93
GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL
1-5-20Label, Internal Connections (Int.Conn.)
Located on the outside of the Front-End Card Rack’s cover (inside unit). Different versions of the label
have been used since production start.
AC
Cable and Connector numbering and naming system used:
IIO= Internal IO module
EIO= External IO module
BEP= Backend Processor
FEP= Frontend Processor
ACP= AC controller module
ACD= AC distribution box
ACT= AC isolation transformer module
BEPIO= IO module on the BEP
Axx : connectors on IIO with other connections than the BEP
Bxx : connectors on IIO that are connected to BEP
Cxx : connectors on BEP, except for the BEPIO
Dxx : connectors on BEPI O
Exx : connector on the BEP power supply
Fxx : connectors on ACP
Gxx : connectors on FE P
Hxx : external accesable connectors (Doppler probe)
Kxx : connectors on MODE M
Mxx : connectors on ACT
Nxx : connectors on ACD
Lxx : connectors on EIO
F
connector
to EIO
P30
IIO seen from F
A
1
L4: Audio out (right)
L5: Audio out (left)
L6: Trig out
L7: Foot switch
L8: Serial port
L9: Remote expose #1
L10: Remote expose #2
L11: Analog modem
L12: Composite video output
L13: B&W video output
L14: S-Video output
L15: SVGA output
L16: USB
L17: Ethernet
25
P31
A13
A12
F
F
81
81
159
159
A12 Spare power (future option)
Connector to
motherboard
1425
P32
A13 Power to 3D box (future option)
A14 AC power control
A15 Signals to rotation adapter (future optio n)
A16 Signals to 3D box (future optio n)
M
M
113
18
915
M
15
69
A15
A14
A16
EP side
Distribution
box
N5
N4
N3
N2
N1
External IO module
L1L2
69
M
15
Service
use ONLY
(remote
power on/of f
control)
Monitor
F1F2F3F4
115V
H1
TX-128
RX-128
Relay board
G1
Board location in Front End Processor (FEP)
L3
69
M
14
15
Analogue
RS-232
phone
Connect
Connect
to InSit e
to InSit e
M ODEM
M ODEM
Peripherals
Modem
115V
230V
or
230V
F6
From Isolation
transformer
BF-64
BF-64
TX128 (optional)
L4 L5
L11L12 L13 L14
Back End
Processor
230V
230V
DC-power
RFI
G2
TX-powe r
L6
L7
External IO module
(Front view)
Front End
F5
supply
G3
suppl y
G4
Rack
RESET
115V or 230V inlet
voltage selection
115V
Cable to
C15
Isolation
transformer
modul e
M
L8
F
L15
WARNING !
Live Voltage inside,
do not open.
AC power control modul e
230V
F7
To Isolation
transformer
M1
L9
L10
L16
L17
115V = 100-1
230V = 220-2
(½ or 2 times i
an
ol
F
contr
F9
230V
115V
Voltage Selection
20V
on Peripherals
40V
nlet
e)
voltag
15
M
F8
69
60,0
Modem
K3
MT5634ZBA
K1K2
Part no. : FC314311
Rev. : 01
Modem
power
K4
supply
Figure 1-7 Label on FEP2 (w/RFI)
Chapter 1 - Introduction1 - 55
Page 94
GE HEALTHCARE
DIRECTION FC091194, REVISION 12 VIVID 7 SERVICE MANUAL