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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
AVERTISSEMENT
• 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 PRESTATAIRE DE SERVICES DU CLIENT A BESOIN DE CE MANUEL DANS
UNE AUTRE LANGUE QUE L’ANGLAIS, IL INCOMBE AU CLIENT DE LE FAIRE
TRADUIRE.
• NE PAS TENTER D’INTERVENTION SUR LES ÉQUIPEMENTS TANT QUE LE
MANUEL DE MAINTENANCE 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
• 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.
• WARTEN SIE DIESES GERÄT NUR, WENN SIE DIE ENTSPRECHENDEN
ANWEISUNGEN IM KUNDENDIENST-HANDBUCH GELESEN HABEN UND
NACHVOLLZIEHEN KÖNNEN.
• 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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• ESTE MANUAL DE SERVICIO SÓLO ESTÁ DISPONIBLE EN INGLÉS.
• SI ALGÚN PROVEEDOR DE SERVICIOS AJENO A GEMS SOLICITA UN IDIOMA
QUE NO SEA EL INGLÉS, LA TRADUCCIÓN ES RESPONSABILIDAD DEL
CLIENTE.
• NO SE DEBERÁ DAR SERVICIO TÉCNICO AL EQUIPO SIN HABER
AV I S O
CONSULTADO Y COMPRENDIDO ESTE MANUAL DE SERVICIO.
• LA NO OBSERVANCIA DEL PRESENTE AVISO PUEDE DAR LUGAR A QUE EL
PROVEEDOR DE SERVICIOS, EL USUARIO O EL PACIENTE SUFRAN LESIONES
PROVOCADAS POR DESCARGAS ELÉCTRICAS, PROBLEMAS MECÁNICOS O
PELIGROS DE OTRA NATURALEZA.
• ESTE MANUAL DE ASSISTÊNCIA TÉCNICA SÓ SE ENCONTRA DISPONÍVEL EM
INGLÊS.
• 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.
ATENÇÃO
• NÃO TENTE REPARAR O EQUIPAMENTO SEM TER CONSULTADO E
COMPREENDIDO ESTE MANUAL DE ASSISTÊNCIA TÉCNICA.
• O NÃO CUMPRIMENTO DESTE AVISO PODE PÔR EM PERIGO A SEGURANÇA
DO TÉCNICO, OPERADOR OU PACIENTE DEVIDO A CHOQUES ELÉTRICOS,
MECÂNICOS OU OUTROS.
AVVERTENZA
HOIATUS
• IL PRESENTE MANUALE DI MANUTENZIONE È DISPONIBILE SOLTANTO IN
INGLESE.
• 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.
• 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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• TÄMÄ HUOLTO-OHJE ON SAATAVILLA VAIN ENGLANNIKSI.
• JOS ASIAKKAAN PALVELUNTARJOAJA VAATII MUUTA KUIN
ENGLANNINKIELISTÄ MATERIAALIA, TARVITTAVAN KÄÄNNÖKSEN
HANKKIMINEN ON ASIAKKAAN VASTUULLA.
• ÄLÄ YRITÄ KORJATA LAITTEISTOA ENNEN KUIN OLET VARMASTI LUKENUT
VAROITUS
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.
• ΤΟ ΠΑΡΟΝ ΕΓΧΕΙΡΙ∆ΙΟ ΣΕΡΒΙΣ ∆ΙΑΤΙΘΕΤΑΙ ΣΤΑ ΑΓΓΛΙΚΑ ΜΟΝΟ.
• ΕΑΝ ΤΟ ΑΤΟΜΟ ΠΑΡΟΧΗΣ ΣΕΡΒΙΣ ΕΝΟΣ ΠΕΛΑΤΗΑΠΑΙΤΕΙ ΤΟ ΠΑΡΟΝ
ΕΓΧΕΙΡΙ∆ΙΟ ΣΕ ΓΛΩΣΣΑ ΕΚΤΟΣ ΤΩΝ ΑΓΓΛΙΚΩΝ, ΑΠΟΤΕΛΕΙ ΕΥΘΥΝΗ ΤΟΥ
ΠΕΛΑΤΗ ΝΑ ΠΑΡΕΧΕΙ ΥΠΗΡΕΣΙΕΣ ΜΕΤΑΦΡΑΣΗΣ.
• ΜΗΝ ΕΠΙΧΕΙΡΗΣΕΤΕ ΤΗΝ ΕΚΤΕΛΕΣΗ ΕΡΓΑΣΙΩΝ ΣΕΡΒΙΣ ΣΤΟΝ ΕΞΟΠΛΙΣΜΟ
ΠΡΟΕΙ∆ΟΠΟΙΗΣΗ
ΕΚΤΟΣ ΕΑΝ ΕΧΕΤΕ ΣΥΜΒΟΥΛΕΥΤΕΙ
ΚΑΙ ΕΧΕΤΕ ΚΑΤΑΝΟΗΣΕΙ ΤΟ ΠΑΡΟΝ
ΕΓΧΕΙΡΙ∆ΙΟ ΣΕΡΒΙΣ.
• ΕΑΝ ∆Ε ΛΑΒΕΤΕ ΥΠΟΨΗ ΤΗΝ ΠΡΟΕΙ∆ΟΠΟΙΗΣΗ ΑΥΤΗ, ΕΝ∆ΕΧΕΤΑΙ ΝΑ
ΠΡΟΚΛΗΘΕΙ ΤΡΑΥΜΑΤΙΣΜΟΣ ΣΤΟ ΑΤΟΜΟ ΠΑΡΟΧΗΣ ΣΕΡΒΙΣ, ΣΤΟ ΧΕΙΡΙΣΤΗ Ή
ΣΤΟΝ ΑΣΘΕΝΗ ΑΠΟ ΗΛΕΚΤΡΟΠΛΗΞΙΑ, ΜΗΧΑΝΙΚΟΥΣ Ή ΑΛΛΟΥΣ ΚΙΝ∆ΥΝΟΥΣ.
FIGYELMEZTETÉS
VIÐVÖRUN
• 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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• TENTO SERVISNÍ NÁVOD EXISTUJE POUZE V ANGLICKÉM JAZYCE.
• V PŘÍPADĚ, 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
TENTO SERVISNÍ NÁVOD A POCHOPILI JEHO OBSAH.
• V PŘÍPADĚ 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.
• FORSØG IKKE AT SERVICERE UDSTYRET MEDMINDRE
ADVARSEL
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
BRĪDINĀJUMS
• 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 ELEKTRISKĀ
S STRĀVAS
TRIECIENA, MEHĀNISKU VAI CITU RISKU IZRAISĪTU TRAUMU APKALPES
SNIEDZĒJAM, OPERATORAM VAI PACIENTAM.
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• ŠIS EKSPLOATAVIMO VADOVAS YRA IŠLEISTAS TIK ANGLŲ KALBA.
• JEI KLIENTO PASLAUGŲ TEIKĖJUI REIKIA VADOVO KITA KALBA – NE ANGLŲ,
VERTIMU PASIRŪPINTI TURI KLIENTAS.
• NEMĖGINKITE ATLIKTI ĮRANGOS TECHNINĖS PRIEŽIŪROS DARBŲ, NEBENT
ĮSPĖJIMAS
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.
• IKKE FORSØK Å REPARERE UTSTYRET UTEN AT DENNE
ADVARSEL
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
ATE NŢIE
• 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 SIĘ 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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• ДАННОЕ РУКОВОДСТВО ПО ОБСЛУЖИВАНИЮ ПРЕДОСТАВЛЯЕТСЯТОЛЬКОНААНГЛИЙСКОМЯЗЫКЕ.
• ЕСЛИ СЕРВИСНОМУ ПЕРСОНАЛУ КЛИЕНТА НЕОБХОДИМО РУКОВОДСТВО
НЕ НА АНГЛИЙСКОМ ЯЗЫКЕ, КЛИЕНТУ СЛЕДУЕТ САМОСТОЯТЕЛЬНО
ОБЕСПЕЧИТЬ ПЕРЕВОД.
ОСТОРОЖНО!
• ПЕРЕД ОБСЛУЖИВАНИЕМ ОБОРУДОВАНИЯ ОБЯЗАТЕЛЬНО ОБРАТИТЕСЬ
К ДАННОМУ РУКОВОДСТВУ И ПОЙМИТЕ ИЗЛОЖЕННЫЕ В НЕМ СВЕДЕНИЯ.
• НЕСОБЛЮДЕНИЕ УКАЗАННЫХ ТРЕБОВАНИЙ МОЖЕТ ПРИВЕСТИ К ТОМУ,
ЧТО СПЕЦИАЛИСТ ПО ТЕХОБСЛУЖИВАНИЮ
, ОПЕРАТОР ИЛИ ПАЦИЕНТ
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.
• NEPOKÚŠAJTE SA VYKONÁVAŤ SERVIS ZARIADENIA SKÔR, AKO SI
UPOZORNENIE
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.
VAR NING
DİKKAT
• 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.
• EĞER MÜŞTERİ TEKNİSYENİ KILAVUZUN İNGİLİZCE DIŞINDAK
İ BİR DİLDE
OLMASINI İSTERSE, KILAVUZU TERCÜME ETTİRMEK MÜŞTERİNİN
SORUMLULUĞUNDADIR.
• 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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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 positioning of the equipment at the site prepared for the
equipment 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.
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.
GE Healthcare employees should use the iTrak System to report all documentation errors or omissions.
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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.
IRECTION 5344303-100, REVISION 3 VIVID P3 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.
1-1-2Chapter Contents
Table 1-1 Contents in Chapter 1
SectionDescriptionPage Number
1-1
1-2
1-3
1-4
1-5
Overview
Important Conventions
Safety Considerations
EMC, EMI, and ESD
Customer Assistance
1-1-3Purpose of Service Manual
This Service Manual provides service information for the Vivid P3 Ultrasound Scanning System. It
contains the following chapters:
1.) Chapter 1 - Introduction: Contains a content summary and warnings.
2.) Chapter 2 - Pre Installation: Contains pre-installation requirements for the Vivid P3.
•Contractors (Some parts of Chapter 2 - Pre-Installation)
1-1-5Vivid P3 Models Covered by this Manual
Table 1-2 Vivid P3 Model Designations
Part NumberDescription
5350375Vivid P3 System INDIA 230V
5350378Vivid P3 System CHINA 230V
5350379Vivid P3 System CHILE/KOREA 230V
5350380Vivid P3 System EUROPE 230V
5350381Vivid P3 System AMERICAS 110V
1-1-6Purpose of Operator Manual(s)
The Operator Manual(s) should be fully read and understood before operating the Vivid P3 and also
kept near the unit for quick reference.
1-2Section 1-1 - Overview
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Section 1-2
Important Conventions
1-2-1Conventions Used in Book
Icons
Pictures, or icons, are used wherever they reinforce the printed message. The icons, labels and
conventions used on the product and in the service information are described in this chapter.
Safety 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 precautionary
message. Known or potential hazards are labeled in one of 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.
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1-2-2Standard Hazard Icons
Important information will always be preceded by the exclamation point contained within a triangle, as
seen throughout this chapter. In addition to text, several different graphical icons (symbols) may be
used to make you aware of specific types of hazards that could cause harm.
Table 1-3 Standard Hazard Icons
ELECTRICALMECHANICALRADIATION
LASERHEAT
LASER
LIGHT
Other hazard icons make you aware of specific procedures that should be followed.
Table 1-4 Standard Icons Indicating a Special Procedure to be Used
AVOID STATIC ELECTRICITYTAG AND LOCK OUTWEAR EYE PROTECTION
TAG
&
LOCKOUT
Date
Signed
EYE
PROTECTION
1-4Section 1-2 - Important Conventions
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1-2-3Product Icons
The following table describes the purpose and location of safety labels and other important information
provided on the equipment.
Table 1-5 Warnings
LABEL/SYMBOLPURPOSE/MEANINGLOCATION
Identification and Rating Plate• Manufacture’s name
Type/Class LabelUsed to indicate the degree of safety or
IP Code (IPX1 or IPX8)Indicates the degree of protection
• Date of manufacture
• Model and serial numbers
• Electrical ratings (Volts, Amps, phase,
and frequency)
protection.
provided by the enclosure per IEC60
529. IPX1 cannot be used in operating
room environment; IPX8 can be used in
operating room environment.
Equipment Type BF (man in the box
symbol) IEC 878-02-03 indicates B
Type equipment having a floating
applied part.
See ‘Identification and Rating Plate’ on
<Italic>page 1-5 for more information.
Bottom of Footswitch
Probe and PCG marked Type BF
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.
“CAUTION - Dangerous voltage” (the
lightning flash with arrowhead in
equilateral triangle) is used to indicate
electric shock hazards.
“Mains OFF” indicates the power off
position of the mains power breaker.
“Mains ON” indicates the power on
position of the mains power breaker.
“ON” indicates the power on position of
the power switch.
CAUTION: This Power Switch DOES
NOT ISOLATE Mains Supply.
“Standby” indicates the power standby
position of the power switch.
CAUTION: This Power Switch DOES
NOT ISOLATE Mains Supply.
“Protective Earth” indicates the
protective earth (grounding) terminal.
Various
Rear panel and inside of console
See the Console Overview section for
location information.
See the Console Overview section for
location information.
See the Console Overview section for
location information.
Internal
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Table 1-5 Warnings
LABEL/SYMBOLPURPOSE/MEANINGLOCATION
“Equipotentiality” indicates the terminal
to be used for connecting equipotential
conductors when interconnecting
(grounding) with other equipment.
Connection of additional protective
earth conductors or potential
equalization conductors is not
necessary in most cases and is only
recommended for situations involving
multiple equipment in a high-risk patient
environment to provide assurance that
all equipment is at the same potential
and operates within acceptable leakage
current limits. An example of a highrisk patient would be a special
procedure where the patient has an
accessible conductive path to the heart
such as exposed cardiac pacing leads.
Alternating Current symbol is in
accordance with IEC 60878-01-14.
Rear of console
Rear Panel, Rating Plate, Circuit
breaker label of console and front panel
(if applicable).
Date of manufacture.
The date could be a year, year and
month, or year, month and day, as
appropriate. See ISO 8601 for date
formates.
Catalog or model number.Rating Plate
Serial numberRating Plate
Direct Current.
For products to be powered from a DC
supply.
Type CF Defib-Proof Applied Part (heart
in the box with paddle) symbolis in
accordance with IEC 60878-02-06.
Rating Plate
Rating Plate
ECG Module
1-6Section 1-2 - Important Conventions
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Table 1-5 Warnings
LABEL/SYMBOLPURPOSE/MEANINGLOCATION
This symbol indicates that the waste of
electrical and electronic equipment
must not be disposed 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.
No hazardous substance, above the
maximum concentration value, is
present. Maximum concentration
values for electronic information
products, as set by the People’s
Republic of China Electronic Industry
Standard SJ/T11364-2006, include the
hazardous substances of lead, mercury,
hexavalent chromium, cadmium,
polybrominated biphenyl (PBB), and
polybrominated diphenyl ether (PBDE).
Indicates the presence of hazardous
substance(s) above the maximum
concentration value. Maximum
concentration values for electronic
information products, as set by the
People’s Republic of China Electronic
Industry Standard SJ/T11364-2006,
include the hazardous substances of
lead, mercury, hexavalent chromium,
cadmium, polybrominated biphenyl
(PBB), and polybrominated diphenyl
ether (PBDE). “20” indicates the
number of years during which the
hazardous substance(s) will not leak or
mutate so that the use of this product
will not result in any severe
environmental pollution, bodily injury, or
damage to any assets.
DO NOT place a finger, hand or any
object on the joint of the monitor or
monitor arm to avoid injury when
moving the monitor and monitor arm.
Rating Plate
Rear Panel
Rear of the LCD monitor
Do not use the following devices near
this equipment: cellular phone, radio
receiver, mobile radio transmitter, radio
controlled toy, broadband power lines,
etc. Use of these devices near this
equipment could cause this equipment
to perform outside the published
specifications. Keep power to these
devices turned off when near this
equipment.
Rear Panel
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Table 1-5 Warnings
LABEL/SYMBOLPURPOSE/MEANINGLOCATION
“CAUTION
This unit weighs 80 kgs.
Special care must be taken to avoid
injury."
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.
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 sytem, the backlight lamps
in the monitor display, contain mercury.)
“Consult accompanying document” is
intended to alert the user to refer to the
operator manual or other instructions
when complete information cannot be
provided on the label.
On the console where easily seen
during transport
1-8Section 1-2 - Important Conventions
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Section 1-3
Safety Considerations
1-3-1Introduction
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.
1-3-2Human Safety
Operating personnel must not remove the system covers.
Servicing should be performed by authorized personnel only.
Only personnel who have participated in a Vivid P3 Training are authorized to service the equipment.
1-3-3Mechanical Safety
WARNINGWARNING
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.
WARNINGWARNING
CAUTION
NOTE:Special care should be taken when transporting the unit in a vehicle:
Never use a probe that has fallen to the floor. Even if it looks ok, it may be damaged.
The Vivid P3 weights 80kg or more, depending on installed peripherals, when ready for use. To
avoid possible injury and equipment damage:
ALWAYS:
•Use the handle to move the system.
•Do not let the system strike walls or door frame.
•Limit movement to a slow careful walk.
•Before transporting, place the system in its special storage case.
•Ensure that the system is firmly secured while inside the vehicle.
•Secure system with straps or as directed otherwise to prevent motion during transport.
•Prevent vibration damage by driving cautiously. Avoid unpaved roads, excessive speeds, and
erratic stops or starts.
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1-3-4Electrical Safety
To minimize shock hazard, the equipment chassis must be connected to an electrical ground. The
system is equipped with a three-conductor AC power cable. This must be plugged into an approved
electrical outlet with protective 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 connector meet international electrical standards.
1-10Section 1-3 - Safety Considerations
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1-3-5Labels Locations
Figure 1-1 Label Location for Vivid P3
Chapter 1 Introduction1-11
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1-3-5Labels Locations (cont’d)
Figure 1-2 Label Location for Vivid P3
1-12Section 1-3 - Safety Considerations
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1-3-5Labels Locations (cont’d)
Figure 1-3 Label Location for Vivid P3
Chapter 1 Introduction1-13
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1-3-5Labels Locations (cont’d)
Figure 1-4
1-14Section 1-3 - Safety Considerations
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1-3-5Labels Locations (cont’d)
Figure 1-5
Chapter 1 Introduction1-15
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1-3-6Warning labels location Tables
L1 (Figure 1-1)
D1: Standard LCD monitor may rotate while
transporting. Bind the system securely to prevent
damage in transportation.
D2: To avoid injury by tipping over, DO NOT PUSH
THIS UNIT FROM THE SIDES.
D3: DO NOT place a finger, hand or any object on
the joint of the monitor or monitor arm to avoid injury
when moving the monitor and monitor arm.Placing
objects on top of the monitor may cause the monitor
to tilt with the falling objects resulting in injury to the
operator.Do not place any objects on the monitor.
L2 (Figure 1-2)
D4: This machine should be used in compliance
with law. Some jurisdictions restrict certain uses,
such as gender determination.
L3 (
Figure 1-3)
D5: Identification and Rating Plate.
L4 (
Figure 1-4)
D6: “Consult accompanying document” is intended
to alert the user to refer to the operator manual or
other instructions when complete information
cannot be provided on the label.
D7: Do not use the following devices near this
equipment: cellular phone, radio receiver, mobile
radio transmitter, radio controlled toy, etc. Use of
these devices near this equipment could cause this
equipment to perform outside the published
specifications. Keep power to these devices turned
off when near this equipment.
D8: Caution: Federal Law restricts this device to
sale by or on the order of a physician.
D9: The CE Mark of Conformity indicates this
equipment conforms with the Council Directive 93/
42/EEC
D10: CISPR CAUTION: The Vivid P3 conforms to
the CISPR11, Group 1, Class A of the international
standard for Electromagnetic disturbance
characteristics.
D11: WEEE Label: This symbol indicates that the
waste of electrical and electronic equipment must
not be disposed 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.
D12: The equipment weighs approximately 80 kg
(176 lbs). To avoid possible injury and equipment
damage when transporting from one area of use to
another:
• Be sure the pathway is clear.• Limit movement to a
slow careful walk.• Use two or more persons to
move the equipment on inclines or long distance.
L6 (
Figure 1-4)
D14: Gost Label (Russia Only).
L7 (
Figure 1-5)
D15: TUV Label: TUV Listing and Certification Mark
is used to designate conformance to nationally
recognized product safety standards. The Mark
bears the name and/or logo of the testing laboratory,
product category, safety standard to which
conformity is assessed, and a control number
L8 (
Figure 1-5)
D16: Circuit breaker Label
L9 (
Figure 1-5)
D17: Line Input voltage Label.
L10 (
Figure 1-5)
D18: Signal ground point label CAUTION: This is
only for “FUNCTIONAL GROUNDING”, NOT
“PROTECTIVE EARTH”.
L11 (
Figure 1-5)
Lamp contains Mercury Dispose According to Stete/
Local Law.
1-16Section 1-3 - Safety Considerations
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1-3-7Dangerous Procedure Warnings
Warnings, such as the examples below, precede potentially dangerous procedures throughout this
manual. Instructions contained in the warnings must be followed.
DANGER
DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH, ARE PRESENT
IN THIS EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING
AND ADJUSTING.
WARNINGWARNING
WARNINGWARNING
WARNINGWARNING
EXPLOSION WARNING
DO NOT OPERATE THE EQUIPMENT IN AN EXPLOSIVE ATMOSPHERE.
OPERATION OF ANY ELECTRICAL EQUIPMENT IN SUCH AN ENVIRONMENT
CONSTITUTES A DEFINITE SAFETY HAZARD.
DO NOT SUBSTITUTE PARTS OR MODIFY EQUIPMENT
BECAUSE OF THE DANGER OF INTRODUCING ADDITIONAL HAZARDS, DO NOT
INSTALL SUBSTITUTE PARTS OR PERFORM ANY UNAUTHORIZED MODIFICATION
OF THE EQUIPMENT.
SHUT DOWN FORCEDLY OR PLUG IN/OUT ACDC INVALID MAY CAUSE THE
DAMAGE OF SYSTEM FILES.
1-3-8Lockout/Tagout Requirements (For USA Only)
Follow OSHA Lockout/Tagout requirements by ensuring you are in total control of the electrical Mains
plug.
1-3-9Returning/Shipping Probes and Repair Parts
Equipment being returned must be clean and free of blood and other infectious substances.
GEMS policy states that body fluids must be properly removed from any part or equipment prior to
shipment. GEMS employees, as well as customers, are responsible for ensuring that parts/equipment
have been properly decontaminated prior to shipment. Under no circumstance should a part or
equipment with visible body fluids be taken or shipped from a clinic or site (for example, body coils or
an ultrasound probe).
The purpose of the regulation is to protect employees in the transportation industry, as well as the
people who will receive or open this package.
NOTE:The US Department of Transportation (DOT) has ruled that “items that were saturated and/or
dripping with human blood that are now caked with dried blood; or which were used or intended
for use in patient care” are “regulated medical waste” for transportation purposes and must be
transported as a hazardous material.
NOTE:The USER/SERVICE staff should dispose all the waste properly as per federal, state, and local
waste disposal regulation.
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Section 1-4
EMC, EMI, and ESD
1-4-1Electromagnetic Compatibility (EMC)
Electromagnetic compatibility describes a level of performance of a device within its electromagnetic
environment. This environment consists of the device itself and its surroundings including other
equipment, power sources and persons with which the device must interface. Inadequate compatibility
results when a susceptible device fails to perform as intended due interference from its environment or
when the device produces unacceptable levels of emission to its environment. This interference is often
referred to as radio–frequency or electromagnetic interference (RFI/EMI) and can be radiated through
space or conducted over interconnecting power of signal cables. In addition to electromagnetic energy,
EMC also includes possible effects from electrical fields, magnetic fields, electrostatic discharge and
disturbances in the electrical power supply.
1-4-2CE Compliance
The Vivid P3 unit conforms to all applicable conducted and radiated emission limits and to immunity
from electrostatic discharge, radiated and conducted RF fields, magnetic fields and power line transient
requirements.
For applicable standards refer to the Safety Chapter in the Basic User Manual.
NOTE:For CE Compliance, it is critical that all covers, screws, shielding, gaskets, mesh, clamps, are in
good condition, installed tightly without skew or stress. Proper installation following all
comments noted in this service manual is required in order to achieve full EMC performance.
1-4-3Electrostatic Discharge (ESD) Prevention
WARNINGWARNING
DO NOT TOUCH ANY BOARDS WITH INTEGRATED CIRCUITS PRIOR TO TAKING
THE NECESSARY ESD PRECAUTIONS:
1.FOLLOW GENERAL GUIDELINES FOR HANDLING OF ELECTROSTATIC
SENSITIVE EQUIPMENT.
1-18Section 1-4 - EMC, EMI, and ESD
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Section 1-5
Customer Assistance
1-5-1Contact Information
If this equipment does not work as indicated in this service manual or in the User Manual, or if you
require additional assistance, please contact the local distributor or appropriate support resource, as
listed below.
Prepare the following information before you call:
-System ID serial number.
-Software version.
Table 1-6 Phone Numbers for Customer Assistance
LocationPhone Number
USA
GE Healthcare
Ultrasound Service Engineering
9900 Innovation Drive
Wauwatosa, WI 53226
Canada1-800-668-0732
Latin America
Europe
GE Ultraschall Deutschland GmbH& Co. KG
BeethovenstraBe 239
Postfach 11 05 60, D-42665 Solingen
Germany
Asia (Singapore)
GE Ultrasound Asia
Service Department - Ultrasound
298 Tiong Bahru Road #15-01/06
Central Plaza
Singapore 169730
Service: On-site
Service: Parts
Applications support
Service
Applications support
Phone: +33 (0)130-831-300 (General Imaging and Cardiac)
Fax: +49 (0)212-2802-431
Asia ultrasound tech support
ANZ+(61)1800647855
China+(86)8008108188
India+(91)1800114567
Korea+(82)262013585
SEA+(65)6277344
1-800–437–1171
1-800-558-2040
1-800-682-5327 or 1-262-524-5698
1-800-321-7937
1-262-524-5698
Japan Support Center
Phone: 81-42-648-2944
Fax: 81-42-648-2905
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1-5-2System Manufacturer
Table 1-7 System Manufacturer
Manufacturer
Wipro GE Healthcare Pvt Ltd
No:4, Kadugodi Industrial Area,
Bangalore,
Karnataka,
INDIA - 560067.
TEL: 91-80-41801000
FAX: 91-80-28452924
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Chapter 2
Pre Installation
Section 2-1
Overview
2-1-1Purpose of this chapter 2
This chapter provides the information required to plan and prepare for the installation of a Vivid P3.
Included are descriptions of the facility and electrical needs to be met by the purchaser of the unit.
2-1-2Chapter Contents
Table 2-1 Contents in Chapter 2
SectionDescriptionPage Number
2-1
2-2
2-3
Overview
General Console Requirements
Facility Needs
2-1
2-2
2-7
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Section 2-2
General Console Requirements
2-2-1Console Environmental Requirements
Table 2-2 Environmental Requirements for Vivid P3 Scanners
OperationalStorageTransport
Temperature
Humidity
Pressure
Temperatures in degree C, conversion to degree F =(degree C*(9/5) + 32)
10 - 40 degree C
50 - 104 degree F
30 - 75%
non-condensing
700 - 1060hPa700 - 1060hPa700 - 1060hPa
10 - 70 degree C
14- 158 degree F
30 - 90%
non-condensing
-40 - 60 degree C
-40 - 140 degree F
30 - 90%
non-condensing
Table 2-3 Environmental Requirements for an Ultrasound Room
ItemValues
Power Source
Radiation Shielding
Temperature
Humidity
Heat Dissipation
Floor Landing
Floor Condition
Weight
Refer to Table on page 2-3.
NONE REQUIRED for ULTRASOUND ENERGY
20-26 DEG. C (68-79 DEG F) for PATIENT COMFORT
50% to 70% for PATIENT COMFORT
1366 BTU/Hr.
Approximately 680 - 800 kg/m2 without Accessories
Gradient: WITHIN 5 degrees
80 kg (176lbs) without Accessories
2-2-1-1Cooling
The cooling requirement for the Vivid P3 is 1366 BTU/hr. This figure does not include cooling needed
for lights, people, or other equipment in the room. Each person in the room places an additional 300
BTU/hr. demand on the cooling system.
2-2-1-2Lighting
Bright light is needed for system installation, updates and repairs. However, operator and patient
comfort may be optimized if the room light is subdued and indirect. Therefore a combination lighting
system (dim/bright) is recommended. Keep in mind that lighting controls and diameters can be a source
of EMI which could degrade image quality. These controls should be selected to minimize possible
interface.
2-2Section 2-2 - General Console Requirements
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2-2-2Electrical Requirements
NOTE:GE Healthcare requires a dedicated power and ground for the proper operation of its
Ultrasound equipment. This dedicated power shall originate at the last distribution panel before
the system.
Sites with a mains power system with defined Neutral and Live:
The dedicated line shall consist of one phase, a neutral (not shared with any other circuit), and a full
size ground wire from the distribution panel to the Ultrasound outlet.
Sites with a mains power system without a defined Neutral:
The dedicated line shall consist of one phase (two lines), not shared with any other circuit, and a full
size ground wire from the distribution panel to the Ultrasound outlet.
Please note that image artifacts can occur, if at any time within the facility, the ground from the main
facility's incoming power source to the Ultrasound unit is only a conduit.
2-2-2-1Vivid P3 Power Requirements
Table 2-4 Electrical Specifications for Vivid P3
PARAMETERAREALIMITS
Voltage Range
100-120V
220-240V230 VAC ±10% (207-253 VAC)
PowerAll applicationsMAX. 425VA
Line FrequencyAll applications50/60Hz (±2Hz)
Power TransientsAll applications
Decaying OscillationAll applications
100 VAC
Less than 25% of nominal peak voltage
for less than 1 millisecond for any type of
transient, including line frequency,
synchronous, asynchronous, or
aperiodic transients.
Less than 15% of peak voltage for less
than 1 millisecond.
± 10% (90-110 VAC)
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2-2-2-2Inrush Current
Inrush current is not a factor to consider due to the inrush current limiting properties of the power
supplies.
2-2-2-3Site Circuit Breaker
It is recommended that the branch circuit breaker for the machine be readily accessible.
2-2-2-4Site Power Outlets
A dedicated AC power outlet must be within reach of the unit without extension cords. Other adequate
outlets for the external peripherals, medical and test equipment needed to support this unit must also
be present within1 m (3.2 ft.)of the unit. Electrical installation must meet all current local, state, and
national electrical codes.
2-2-2-5Unit Power Plug
If the unit arrives without a power plug, or with the wrong plug, you must contact your GE dealer or the
installation engineer must supply what is locally required.
2-2-2-6Power Stability Requirements
Voltage drop-out
Max 10 ms.
Power Transients
(All applications)
Less than 25% of nominal peak voltage for less than 1 millisecond for any type of transient, including
line frequency, synchronous, asynchronous, or aperiodic transients.
2-4Section 2-2 - General Console Requirements
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2-2-3EMI Limitations
Ultrasound machines are susceptible to Electromagnetic Interference (EMI) from radio frequencies,
magnetic fields, and transient in the air wiring. They also generate EMI. The Vivid P3 complies with
limits as stated on the EMC label. However there is no guarantee that interface will not occur in a
particular installation.
Possible EMI sources should be identified before the unit is installed.
Electrical and electronic equipment may produce EMI unintentionally as the result of defect.
These sources include:
•medical lasers
•scanners
•cauterizing guns
•computers
•monitors
•fans
•gel warmers
•microwave ovens
•light dimmers
•portable phones
•Lift
The presence of a broadcast station or broadcast van may also cause interference.
See Table 2-5 for EMI Prevention tips.
Table 2-5 EMI Prevention/abatement
EMI RuleDetails
Keep the unit at least 5 meters or 15 feet away from other EMI sources. Special shielding
Be aware of RF sources
Ground the unit
Replace all screws, RF
gaskets, covers, cores
Replace broken RF gaskets
Do not place labels where RF
gaskets touch metal
Use GE specified harnesses
and peripherals
Take care with cellular phones Cellular phones may transmit a 5 V/m signal; that could cause image artifacts.
may be required to eliminate interference problems caused by high frequency, high
powered radio or video broadcast signals.
Poor grounding is the most likely reason a unit will have noisy images. Check grounding of
the power cord and power outlet.
After you finish repairing or updating the system, replace all covers and tighten all screws.
Any cable with an external connection requires a magnet wrap at each end. Install the
shield over the front of card cage. Loose or missing covers or RF gaskets allow radio
frequencies to interfere with the ultrasound signals.
If more than 20% or a pair of the fingers on an RF gasket are broken, replace the gasket.
Do not turn on the unit until any loose metallic part is removed.
Never place a label where RF gaskets meet the unit. Otherwise, the gap created will permit
RF leakage. Or, if a label has been found in such a position, move the label.
The interconnect cables are grounded and require ferrite beads and other shielding. Also,
cable length, material, and routing are all important; do not change from what is specified.
Properly dress peripheral
cables
Do not allow cables to lie across the top of the card cage or hang out of the peripheral bays.
Loop the excess length for peripheral cables inside the peripheral bays. Attach the monitor
cables to the frame.
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2-2-4Scan Probe Environmental Requirements
Operation:10° to 40° C
Storage: 10° to 70° C
NOTE:Temperature in degrees C. Conversion to Degrees F = (Degrees C * (9/5) + 32).
NOTICE
SYSTEMS AND ELECTRONIC PROBES ARE DESIGNED FOR STORAGE TEMPERATURES OF
-20 TO + 50 degrees C. WHEN EXPOSED TO LARGE TEMPERATURE VARIATIONS, THE
PRODUCT SHOULD BE KEPT IN ROOM TEMPERATURE FOR 10 HOURS BEFORE USE.
2-2-5Time and Manpower Requirements
Site preparation takes time. Begin Pre-installation checks as soon as possible. If possible, allow six
weeks before delivery, for enough time to make necessary changes.
CAUTION
Have two people available to deliver and unpack the Vivid P3.
Attempts to move the unit considerable distances or on an incline by one person could result
in injury or damage or both.
2-6Section 2-2 - General Console Requirements
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Section 2-3
Facility Needs
2-3-1Recommended Ultrasound Room Layout
2-3-1-1Purchaser Responsibilities
The work and materials needed to prepare the site is the responsibility of the purchaser. Delay,
confusion, and waste of manpower can be avoided by completing pre installation work before delivery.
User the Pre Installation checklist to verify that all needed steps have been taken,
Purchaser reasonability includes:
•Procuring the materials required.
•Completing the preparations before delivery of the ultrasound system.
•Paying the costs for any alternations and modifications not specifically provided in the sales
contract.
NOTE:All electrical installation that are preliminary to the positioning of the equipment at the site
prepared for the equipment must be performed by licensed electrical contractors. Other
connections between pieces of electrical equipment, products involved (and the accompanying
electrical installations) are highly sophisticated and special engineering competence is
required. All electrical work on these product must comply with the requirements of applicable
electrical codes. The purchaser of GE equipment must only utilize qualified personnel to
perform electrical servicing on the equipment.
The desire to use a non-listed or customer provided product or to place an approved product further
from the system than the interface kit allows presents challenges to the installation team. To avoid
delays during installation, such variances should be made known to the individuals or group performing
the installation at the earliest possible date (preferable prior to purchase).
The ultrasound suite must be clean prior to delivery of the machine. Carpet is not recommended
because it collects dust and creates static. Potential sources of EMI (electromagnetic interference)
should also be investigated before delivery. Dirt, static, and EMI can negatively impact system.
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2-3-2Required Features
NOTE:GE Health Care Systems requires a dedicated power and ground for the proper operation of its
Ultrasound equipment. This dedicated power shall originate at the last distribution panel before
the system.
Sites with a mains power system with defined Neutral and Live:
The dedicated line shall consist of one phase, a neutral (not shared with any other circuit), and a full
size ground wire from the distribution panel to the Ultrasound outlet.
Sites with a mains power system without a defined Neutral:
The dedicated line shall consist of one phase (two lines), not shared with any other circuit, and a full
size ground wire from the distribution panel to the Ultrasound outlet.
Please note that image artifacts can occur, if at any time within the facility, the ground from the main
facility's incoming power source to the Ultrasound unit is only a conduit.
•Dedicated single branch power outlet of adequate amperage meeting all local and national codes
which is located less than 2.5 m (8 ft.) from the unit’s proposed location
•Door opening is at least 76 cm (30 in) wide
•Proposed location for unit is at least 0.3m (1 ft.) from the wall for cooling
•Power outlet and place for any external peripheral are within 2 m (6.5 ft.) of each other with
peripheral within 1 m of the unit to connect cables.
•Power outlets for other medical equipment and gel warmer
•Power outlets for test equipment and modem within 1 m (3.2 ft.) of unit
•Clean and protected space to store transducers (in their cases or on a rack)
•Material to safely clean probes (done with a plastic container, never metal)
2-3-3Desirable Features
•Door is at least 92 cm (3 ft.) wide
•Circuit breaker for dedicated power outlet is easily accessible
•Sink with hot and cold water
•Receptacle for bio–hazardous waste, like used probe sheaths
•Emergency oxygen supply
•Storage for linens and equipment
•Nearby waiting room, lavatory, and dressing room
•Dual level lighting (bright and dim)
•Lockable cabinet ordered by GE for its software and proprietary manuals.
2-8Section 2-3 - Facility Needs
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2-3-3-1Recommended and Alternate Ultrasound Room Layout
Recommended standard floor plan and a minimal floor plan for ultrasound equipment:
Figure 2-6 RECOMMENDED ULTRASOUND ROOM LAYOUT
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DICOM services provide the operator with clinically useful features for moving images and patient
information over a hospital network. Examples of DICOM services include the transfer of images to
workstations for viewing or transferring images to remote printers. As an added benefit, transferring
images in this manner frees up the on-board monitor and peripherals, enabling viewing to be done while
scanning continues. With DICOM, images can be archived, stored, and retrieved faster, easier, and at
a lower cost.
2-3-4-4DICOM Option Pre-installation Requirements
To configure the Vivid P3 to work with other network connections, the site’s network administrator must
provide some necessary information.
Information must include:
•A host name, local port number, AE Title, IP address and Net Mask for the Vivid P3.
•The IP addresses for the default gateway and other routers at the site for ROUTING
INFORMATION.
•The host name, IP address, port and AE Title for each device the site wants connected to the
for DICOM APPLICATION INFORMATION. A field for the make (manufacturer) and the revision
P3
of the device, is also included. This information may be useful for solving errors.
Vivid
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Figure 2-7 Worksheet for DICOM Network Information
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Chapter 3
Installation
Section 3-1
Overview
3-1-1Purpose of Chapter 3
This chapter contains information needed to install the unit. Included are references to a procedure that
describes how to receive and unpack the equipment and how to file a damage or loss claim.
How to prepare the facility and unit of the actual installation, and how to check and test the unit, probes,
and external peripherals for electrical safety are included in this procedure. Also included in this section
are guidelines for transporting the unit to a new site.
Table 3-1 Contents in Chapter 3
SectionDescriptionPage Number
3-1
3-2
3-3
3-4
3-5
3-6
3-6-6
3-7
3-8
3-9
3-10
Overview
Receiving and Unpacking the Equipment
Packing the Equipment
Preparing for Installation
Completing the Installation
System Configuration
Software/Option Configuration
Connectivity Installation Worksheet
Loading Base Image Software
Software Version check out
Paperwork
3-1-2Average Installation Time
DescriptionAverage Installation TimeComments
3-1
3-3
3-8
3-9
3-10
3-14
3-25
3-26
3-27
3-28
3-29
Table 3-2 Average Installation Time
Unpacking the scanner
Scanner /options
DICOM Option
Approximately 0.5 hour
Approximately 0.5 hour
30 minutes
Dependent on the configuration that is required
Dependent on the amount of configuration
The VIVID P3 installation and functional checkout will take approximately Four hour. VIVID P3 consoles
with optional equipment may take slightly longer.
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3-1-3Installation Warnings
11.)Since the VIVID P3 weighs approximately 80 kg (176 lbs) without options, preferably two people
should unpack it. Two people are also preferable for installing any additional bulky items.
12.)There are no operator serviceable components. To prevent shock, do not remove any covers or
panels. Should problems or malfunctions occur, unplug the power cord. Only qualified service
personnel should carry out servicing.
NOTE:For information regarding packing labels, refer to LABELS ON PACKAGE.
13.)After being transported, the unit may be very cold or hot. If this is the case, allow the unit to
acclimate before you turn it on. It requires one hour for each 2.5×C increment it's temperature is
below 10×C or above 40×C.
DANGER
Equipment damage possibility. Turning the system on without acclimation after arriving at site
may cause the system to be damaged.
WHEN USING ANY TEST INSTRUMENT THAT IS CAPABLE OF OPENING THE
AC GROUND LINE (I.E., METER’S GROUND SWITCH IS OPEN), DON’T TOUCH
THE UNIT!
CAUTION
DANGER
DANGER
If the unit is very cold or hot, do not turn on its power until it has had a chance to acclimate to
its operating environment.
To prevent electrical shock, connect the unit to a properly grounded power outlet. Do not use a
three to two prong adapter. This defeats safety grounding.
Do not operate this unit unless all board covers and frame panels are securely in place. System
performance and cooling require this.
DANGER
OPERATOR MANUAL(S)
The User Manual(s) should be fully read and understood before operating the VIVID P3 and kept
near the unit for quick reference.
DANGER
ACOUSTIC OUTPUT HAZARD
Although the ultrasound energy transmitted from the VIVID P3 probe is within FDA limits, avoid
unnecessary exposure. Ultrasound energy can produce heat and mechanical damage
3-2Section 3-1 - Overview
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Section 3-2
Receiving and Unpacking the Equipment
When a new system arrives, check that any components are not damaged and are not in short supply.
If shipping damage or shortage occurs, contact the address shown in Chapter 1.
The Packaging/Unpacking Procedure.
Topics discussed in the Packaging/Unpacking Procedure:
1.) Check the Shipment,
2.) Unpack the Unit,
3.) Handling Incomplete or Damaged Shipment
Please read these procedures before packing/unpacking the VIVID P3.
We strongly advice you to store the VIVID P3 packing material in undamaged condition in case of future
transportation.
Do not lift the unit by the Keyboard. This may cause equipment damage.
CAUTION
The crate with the VIVID P3 weighs approximately 80 kg. Be prepared for a sudden shift of weight
as the unit is removed from its base (pallet).
CAUTION
CAUTION
Inspect the Shcik watch and Tilt watch. Ensure that they are not fused. (Refer to the instructions
attached on the packing Box on howto check the Shcik watch and Tiltwatch)
1.) Cut the two Metal Bands.
Figure 3-1 Cutting the two metal bands
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Section 3-2 Receiving and Unpacking the Equipment (cont’d)
2.) Lift the TOP Cover up and off.
Figure 3-2 Remove the top cover
3.) Remove the Monitor Cap up and off...
Monitor Cap
Figure 3-3 Removing the Monitor Cap
3-4Section 3-2 - Receiving and Unpacking the Equipment
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Section 3-2 Receiving and Unpacking the Equipment (cont’d)
4.) Remove the three Plastic Joints from the Outer Sleeve.(Refer to the Labels on the Packing Box for
more detailed instructions)
5.) Remove the Outer Sleeve.
6.) Remove the Inner Sleeve.
Inner Sleeve
Plastic Joint
Palette Assy
Figure 3-4 Removing Plastic Joints and Sleeves
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Section 3-2 Receiving and Unpacking the Equipment (cont’d)
TM
7.) Remove the Plastic Wrapping around the VIVID
8.) Remove the Monitor Support and Monitor Packing.
9.) Remove the adhesive tapes attached at the four corners of the Top Cover.
10.)Put the Ramp Board on floor and prepare the slope to put the console down.
11.)Unlock the brakes on the front castors, then carefully put the console off the Palette.
P3.
Figure 3-5 Removing System from the Pallete
3-6Section 3-2 - Receiving and Unpacking the Equipment
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Section 3-2 Receiving and Unpacking the Equipment (cont’d)
NOTE:Check the shipping container for special instructions. Verify that the container is intact. In some
cases a secondary container may be used. If so, ask the carrier for unpacking instructions.
Figure 3-8 Labels on Package
CAUTION
Please carefully unpack the system, and do not dispose the package of VIVID P3, so that it can
be reused for service.
3-2-1Moving into Position
CAUTION
CAUTION
In general, a single adult can move the VIVID P3 along an even surface with no steep grades. At least two people should
move the machine when large humps, grooves, or grades are encountered. (It is better to pull from the rear rather than
push from the front of the unit). Before moving, store all loose parts in the unit. Wrap transducers in soft cloth or foam
to prevent damage.
Do not lift the unit by the keyboard. Use handle to move system.Do not tilt the unit more than 5
degrees to avoid tipping it over.
Equipment Damage Possibility. Lifting the console by holding covers may damage the covers.
Do not lift the console by holding any covers.
Although VIVID P3 is a compact and mobile machine, two people should move it over rough surfaces
or up and down grades.
3-2-2Adjusting System Clock
Set the system clock for the VIVID P3 to the local time. For procedure of adjusting the system clock,
refer to 4-5 Software Configuration Checks, in Chapter 4, FUNCTIONAL CHECKS.
3-2-3Product Locator Installation Card
Fill out proper customer Information on the Product Locator Installation Card. Mail this Installation Card
“Product Locator” to the address corresponding to your pole.
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NOTE:The Product Locator Installation Card shown may not be same as the provided Product Locator
card.
PRODUCT LOCATOR INSTALLATION CARD
Section 3-3
Packing the Equipment
Please pack VIVID P3 in the reverse order of unpacking.
3-8Section 3-3 - Packing the Equipment
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Section 3-4
Preparing for Installation
3-4-1Verify Customer Order
Compare items received by the customer to that which is listed on the delivery order. Report any items
that are missing, back ordered or damaged.
3-4-2Physical Inspection
3-4-2-1System Voltage Settings
•Verify that the scanner is set to the correct voltage. The Voltage ratings for the VIVID P3 Scanner
is found on Rating label near the Circuit Breaker at the rear of the system
WARNINGWARNING
Connecting a VIVID P3 scanner to the wrong voltage level will most likely destroy the
scanner.
3-4-3EMI Protection
This Unit has been designed to minimize the effects of Electro Magnetic Interference (EMI). Many of the
covers, shields, and screws are provided primarily to protect the system from image artifacts caused by
this interference. For this reason, it is imperative that all covers and hardware are installed and secured
before the unit is put into operation.
3-4-4Checking the Components
When a new system arrives, check that none of the components are damaged or in short supply. If
shipping damage or shortage occurs, contact the address shown in Chapter 1.
CAUTION
CAUTION
If the Power Plug is Modified or replaced to Suit the local Conditions and regulations, Ground
continuity check should be performed between Ground Pin on the Plug and the Metal Part on
the VIVID P3. Refer Section Chapter 10 for more details.
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Section 3-5
Completing the Installation
3-5-1Power On / Boot Up
NOTE:After turning off a system, wait at least ten seconds before turning it on again. The system may not be
able to boot if power is recycled too quickly.
3-5-1-1Scanner Power On
1.) Connect the Power Cable to the back of the system.
2.) Ensure the Cable Clip slips securely over the shoulders on the molded plug.
3.) Connect the Main Power Cable to a hospital grade power receptacle with the proper rated voltage.
Never use an adapter that would defeat the safety ground.
4.) Switch ON the Circuit Breaker at the rear of the system.
a. Circuit Breaker
b. Power Cable
When power is applied to the scanner and the rear Circuit Breaker is turned ON, power is distributed to
the Transformer Assembly and to the TMST.
3-10Section 3-5 - Completing the Installation
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3-5-1-2Turn on the system
Press the Power On/Off switch at the front of the system once.
Power On/Off switch
Figure 3-6 Power On/Off Switch
When the Power On/Off switch on the Control Panel is pressed once, the
TMST starts and the software code is distributed to initiate the scanner.
No status messages are displayed during this process.
3-5-2Power Off/ Shutdown
NOTE:After turning off a system, wait at least ten seconds before turning it on again. The system may not be
able to boot if power is recycled too quickly.
3-5-2-1TMST Power Down
To power down the system:
1.) Press the Power On/Off switch at the front of the system.
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2.) The System-Exit window is displayed.
Figure 3-7 System Exit Window
3.) Using the Trackball or Select key, select Shutdown.
4.) The shutdown process takes a few seconds and is complete when the power status LED is turned
Amber color.
5.) Disconnect the probes.Clean or disinfect all probes as necessary. Store them in their shipping
cases to avoid damage.
3-5-2-2Scanner Shutdown
1.) Switch OFF the Circuit Breaker at the back of the system.
2.) Disconnect the Mains Power Cable if necessary. For example: Relocating the scanner.
3-12Section 3-5 - Completing the Installation
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3-5-3Transducer Connection
1.) Connect a transducer to the upper transducer receptancle as follows:
A.) Ensure that the transducer twist lock lever points towards the 9 o’clock position.
B.) Insert the transducer connector on the receptacle guide pin until it touches the receptacle mating
surface.
C.) Twist the transducer lock lever vertically to lock it in place. Twist the lever to the horizontal position
to disconnect the transducer.
NOTE:Please ensure that the probe latch is in unlocked position before you connect the probe to the system.
Fig (A) Connecting the Probe Fig (B) Locking the Probe Lever
Figure 3-8 Connect the probe
NOTE:It is not necessary to turn OFF power to connect or disconnect a probe.
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Section 3-6
System Configuration
3-6-1System Specifications
3-6-1-1Physical Dimensions
The physical dimensions of the VIVID P3 console are summarized in Figure 3-9 on page 3-14 .
Table 3-4 Physical Dimensions of VIVID P3
HeightWidthDepthUnit
1347445595mm
53.017.523.4inches
Figure 3-9 Overall Dimensions
3-14Section 3-6 - System Configuration
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3-6-2Approved peripherals
Table 3-5 Approved peripherals
DeviceManufacturerModelInterface
B/W PrinterSONYUP-D897USB
B/W PrinterMitsubishiP93DUSB
Digital Color PrinterSONYUP-D23MDUSB
HPHP Officejet Pro K550USB
HPHP Laser Jet P2015dnUSB
HP Color Printer
3-pedal footswitchSteuteMKF 2-MED GP26USB
USB Memory SanDiskSanDisk 1GBUSB
ECGECG ModuleECG-USB1USB
USB HDD IomegaUSB HDD 160GBUSB
HPHP Officejet Pro K5400USB
HPHP Officejet 6000USB
HPHP Deskjet 460USB
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3-6-3Connecting Cables
WARNINGWARNING
Equipment damage possibility. Be sure to use the following recommended connecting cables to
connect recording devices and a network with VIVID P3 console.
Table 3-6 List of Connecting Cables
NameFigureNOTE
USB Cable
USB CableFor USB Printer
3-6-4Peripherals/Accessories Connector Panel
VIVID P3 peripherals and accessories can be properly connected using the Rear panel.
3-6-4-1Rear Panel Connector
Located on the Rear panel are USB Ports, VGA, S-Video, Composite Out, Ethernet port & Power outlet.
For USB ECG
Figure 3-10 Rear Panel
A.) USB ports for printers & ECG (B/W, Color and USB), Memory Stick, Footswitch, DVD-
RW, USB HDD.
B.) Ethernet port
C.) VGA Output
D.) S-Video Out
E.) Composite video out
F.) Power outlet
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3-6-4-2TOP Panel Connector
Located on the Top Right side panel are one USB Port for control connections for printer, USB Thumb
Drive and service tools.)
Figure 3-11 Left Side Panel
NOTICE
The USB devices should be connected to VIVID P3 first, power on USB devices before turning VIVID
P3 to work.
NOTE:Each outer (case) ground line of peripheral/accessory connectors are protectively grounded.
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3-6-4-3This section indicates the pin assignment for each connector.
1. S- Video Connector: 4 Pin, mini-Din
Table 3-7
Pin NoOutput SignalDescriptionPicture
1SVIDEO OUT/IN YGY (Luma) GND
2SVIDEO OUT/IN CGC (Chroma) GND
3SVIDEO OUT/IN YY (Luma) SIGNAL
4SVIDEO OUT/IN CC (Chroma) SIGNAL
S-Video Connector, 4 Pin
2. Pin Assignment of USB
Table 3-8 Pin assignment of USB1
Pin No.SignalPin No.Signal
1+5VDC3DATA+
2DATA-4GND
Table 3-9 Pin assignment of USB2
Pin No.SignalPin No.Signal
1+5VDC3DATA+
2DATA-4GND
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3-6-4-4Connect peripherals
A.) Connecting B/W printer UP-D897, Mitsubishi P93D or Color printer UP-D23MD to the system.
Only B/W Printer UP-D897 can be mounted in Front Utility area tray as shown in the figure below.
Fig (A)
VGP Tray Bottom
Fig (B)
VGP Tray top
Using two Captive fastener mount
VGP Tray bottom to the Sytem Utility
box.
Figure 3-12 Connect B/W printer Tray to the system
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B.) Mount the Sony UP-D897 printer to the VGP-UP-D 897-Mounting-Bracket using Four M3 x 8 scews
as indicated below.
A- Indicates the location of the mounting holes onthe VGP-UP-D897-Mounting-Bracket
A
A
Rear
Side of
B
B
the
printer.
Front side
of the
AA
Printer
BB
VGP-UP897-Mounting-Bracket(5314101)
B-Indicates the location of the mounting holes on the
Printer.
Rear Side of the Printer
Front Side Of
the Printer
Mounting the bracket to the printer by using M3X8 Screws
Figure 3-13 Mounting of VGP Tray to Printer
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C.) Insert or Slide the Sony UP-D897 B/W Printer with Bracket (Outcome of Step A) in to the Tray fixed
on the System and then connect USB & Power cables in the rear side of the printer and push back
fully and tighten the front captive fastener as indicated in the figure below.
Figure 3-14 Mounting the Sony UPD 897 on Vivid P3.
D.) Mounting procedure for Color printer UP-D23MD connect the USB Cable to any of the USB ports
available on rear panel and connect the power cable to the rear panel Power port.
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3-6-4-4Connect peripherals (cont’d)
E.) Connect Foot Switch to the system.
Foot Switch can be properly connected to any USB Ports in the Rear panel.
USB Ports
Foot switch
Figure 3-15 Connect Foot Switch to the system
F.) Connecting S-Video cable to the system.
S-Video O/P is available on rear panel.
G.) Connecting the CRT to the system.
SVGA connector available on Rear panel.
H.) Connect the USB Memory stick to the system. The USB Memory stick can be properly connected
in top panel USB port or in any of the Rear panel USB Ports.
Figure 3-16 USB Memory Connection
I.) Connect the USB HDD to the system. The USB Harddisk can be properly connected to Rear Panel
USB ports.
NOTE:Please scan the devices (USB Pen Drive, HDD etc...) for virus - before using it with the
system.
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J.) Connect the Color printer HP Laser jet P2015/ HP Officejet Pro K550/K5400/460, HP Officejet 6000
to the system. The USB Cable & power cable can be properly connected to the USB Ports & Power
Port in the Rear panel. Configure the printer, Config>Connectivity>Service>Standard print and
select the respective printer.
Power CableUSB CableUSB Cable
Figure 3-17 Color Printer Connection on the rear panel
K.) Connect the external monitor to the system. The monitor can be properly connected using the VGA
port in the Rear panel.
Press Ctrl+Alt+V
on the keyboard, a dialog box appears.
Figure 3-18 Graphics Controller Properties
Select Intel(R) Dual Display Clone
select OK
.
; check the Same display configuration driver on both display box and
Power cable
NOTE:Please refer to the operation manual for each peripheral information needed by the user to
operate the system safely.
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3-6-5Available Probes
See in specification in the VIVID P3 User Reference Manual for Probes and intended use.
Table 3-10 List of Probes for Vivid P3
Probe NameArea of UsingTYPECatalog Number
4CGENERAL PURPOSECONVEX H4904PC
E8CS
8CAbdomen, OB/GYN, UrologyMICRO-CONVEXH40412LJ
TRANSVAGINAL
TRANSRECTAL
MICRO-CONVEXH44801HR
11L
8L
3SCardiac, TranscranialSECTORH4701SZ
5csAbdomen, OB/GYN, UrologyCONVEXH4001DC
6SCardiac, PediatricSECTOR
t739INTRAOPERATIVELINEARH40212LM
Vascular, Small Parts,
SMALL PARTS
PERIPHERAL VASCULAR
LINEARH40412LY
LINEARH4001DB
H47082LR
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3-6-6Software/Option Configuration
Refer to the VIVID P3 Basic User Manual, Chapter 16, Customizing Your System for information on
configuring items like Hospital, Department, Language, Units (of measure), Date, Time and Date
Format.
For information on configuring Software Options, refer to the VIVID P3 Basic User Manual, Chapter 16,
Customizing Your System.
For information on configuring DICOM Connectivity, refer to the VIVID P3 Basic User Manual, Chapter
16, Customizing Your System.
NOTE:After Enabling the Software Option, you need to Reboot the system.
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Section 3-8
Loading Base Image Software
This information has been moved, please refer to:
Section 8-13 "Loading Base Image Software" on page 8-86
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Section 3-9Software Version check out
3-9-1Functional Check-out
1.) Power on VIVID P3 scanner and wait until system booting to main screen.
2.) Press Config
3.) Choose the About
key on control panel.
button on the right.
Figure 3-19 About
4.) Check whether "Software version" is the right version for use.
Figure 3-20 Software version
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Section 3-10
Paperwork
NOTE:During and after installation, the documentation (i.e. User Manuals, Installation Manuals...) for the
peripheral units must be kept as part of the original system documentation. This will ensure that all
relevant safety and user information is available during the operation and service of the complete
system.
3-10-1Product Locator Installation
NOTE:The Product Locator Installation Card shown may not be same as the provided Product Locator
card.
3-10-2User Manual(s)
User Check that the correct User Manual(s) for the system and software revision, is included with the
installation. Specific language versions of the User Manual may also be available. Check with your GE
Sales Representative for availability.
Figure 3-21 Product Locator Installation Card
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Chapter 4
Functional Checks
Section 4-1
Overview
4-1-1Purpose for Chapter 4
This chapter provides procedures for quickly checking major functions of the Vivid P3 console,
diagnostics by using the built-in service software, and power supply adjustments.
SectionDescriptionPage Number
4-1
4-2
4-3
4-4
4-5
Section 4-2
Required Equipment
To perform these tests, you'll need any of the sector, linear, or convex transducers.
(normally you should check all the transducers used on the system)
Overview
Required Equipment
General Procedure
Software Configuration Checks
Peripheral Checks
Table 4-1 Contents in chapter 4
4-1
4-1
4-2
4-43
4-43
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Section 4-3
General Procedure
CAUTION
SYSTEM REQUIRES ALL COVERS
Operate this unit only when all board covers and frame panels are securely in place. The covers
are required for safe operation, good system performance and cooling purposes.
NOTICE
Lockout/Tagout Requirements (For USA only)
Follow OSHA Lockout/Tagout requirements by ensuring you are in total control of the Power Cable on
the system.
TAG
&
LOCKOUT
Date
Signed
4-3-1Power On/Boot Up
After AC power cable is connected correctly to the transformer & Circiut breaker is switched on, the
power is applied to the scanner & the system is in Stand By mode. In the Control panel Power On/Off
key will be Amber color.
4-3-1-1
Boot Up
In the control Panel press the power On/Off key the led color will turn in Green color & the system will
boot.
A.Circiut breaker
B.Power cable
Figure 4-1 Connect AC adapter
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4-3-1-1Boot Up (cont’d)
When power is applied to the scanner, power is distributed to the Cooling Unit, Control Panel, LCD,
Peripherals and the Back-end Processor.
4-3-1-2Turn on the system
Press the Power On/Off switch at the front of the system once.
Power On/Off switch
Figure 4-2 Power On/Off Switch
When the Power On/Off switch on the Control Panel is pressed once, the Back-end Processor starts
and the software code is distributed to initiate the scanner.
No status messages are displayed during this process.
4-3-2Power Off/ Shutdown
NOTE:After turning off a system, wait at least ten seconds before turning it on again. The system may not be
able to boot if power is recycled too quickly.
4-3-2-1TMST Power Down
To power down the system:
1.) Press the Power On/Off switch at the front of the system once.
2.) The System-Exit window is displayed.
Figure 4-3 System Exit Window
3.) Using the Trackball or Select key, select Shutdown.
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4-3-2-1TMST Power Down (cont’d)
4.) The shutdown process takes 15 seconds and the power off sequence is complete when the power
status LED is turned Amber.
5.) Disconnect the probes. Clean or disinfect all probes as necessary. Store them in their shipping
cases to avoid damage.
4-3-2-2Scanner Shutdown
Disconnect the Mains Power Cable is necessary. For example: Relocating the scanner.
CAUTION
DO NOT unplug and/or transport the unit until after the power off sequence has been completed.
Failure to do so may result in corrupted patient files.
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4-3-3Archiving and Loading Presets
NOTE:Always save presets before any software reload. This ensures the presets loaded after the software
reload are as up–to–date as possible.
All user presets except changes to Summary, Anatomy, and Biometry pages, can be saved on an DVDR disk (or USB memory device) for reloading on the system.
NOTICE
Presets should NOT be saved on the same DVD-R disk (or USB memory device) as images. The
Archive Menu lists the images but does NOT list the presets stored on a DVD-R disk (or USB memory
device).
4-3-3-1Archiving Presets to an DVD-R Disk (or USB memory device)
1.) Insert an empty (blank) DVD-R disk into the DVD-RW.
2.) Access the Config Menu, and select System. The Backup sheet will be shown on the LCD display.
Figure 4-4 Backup Sheet
3.) Select the item to back up from the Backup section.
4.) Enter backup destination or browse through the disk to locate the destination.
5.) Select Backup now. The backup status for each item is displayed on the Result column.
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4-3-3-2Loading Presets from an DVD-R disk (or USB memory device)
1.) Insert the DVD-R disk with the archived Presets into the DVD-RW.
2.) Access to the Config Menu, and select System. The Restore sheet will be shown on the LCD
display. (see Figure 4-4)
3.) Select the item to restore from the Backup section.
4.) Enter restore destination or browse through the disk to locate the destination.
5.) Select Restore. The restore status for each item is displayed on the Result column.
4-3-4Adjusting the Display Monitor
Please refer to Section 6-2 "Monitor Adjustments" on page 6-2.
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