General Electric Venue 40 Basic Service Manual_SM_5314293-100_19 Venue 40 Basic Service Manual Part Number: 5314293-100 Revision: 19

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GE Healthcare

Venue 40

Basic Service Manual

Part Number: 5314293-100

Revision: 19

GE HEALTHCARE D

IRECTION 5314293-100, REVISION 19 VENUE 40 BASIC 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 BENö TIGT, IST ES AUFGABE DES KUNDEN FüR EINE ENTSPRECHENDE ÜBERSETZUNG ZU SORGEN.

• VERSUCHEN SIE NICHT, DAS GERä T 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 SCHLä GE, MECHANISCHE ODER SONSTIGE GEFAHREN KOMMEN.

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

ESTE MANUAL DE SERVICIO Só LO 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 TRADUCCIó N.

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, MECá NICAS O DE OTRA NATURALEZA.

ESTE MANUAL DE ASSISTêNCIA TéCNICA Só SE ENCONTRA DISPONíVEL EM INGLêS.

• SE QUALQUER OUTRO SERVIç O DE ASSISTê NCIA TéCNICA, QUE NãO A GEHC, SOLICITAR ESTES MANUAIS NOUTRO IDIOMA, é DA

ATENÇÃO

(PT-Br)

RESPONSABILIDADE DO CLIENTE FORNECER OS SERVIç OS DE TRADUçã O.

• Nã O TENTE REPARAR O EQUIPAMENTO SEM TER CONSULTADO E COMPREENDIDO ESTE MANUAL DE ASSISTêNCIA TéCNICA.

• O Nã O CUMPRIMENTO DESTE AVISO PODE POR EM PERIGO A SEGURANçA DO TéCNICO, OPERADOR OU PACIENTE DEVIDO A‘ CHOQUES ELé TRICOS, MECâ NICOS OU OUTROS.

AVISO

(PT-pt)

AVVERTENZA

(IT)

ESTE MANUAL DE ASSISTÊNCIA ESTÁ DISPONÍVEL APENAS EM INGLÊS.

• SE QUALQUER OUTRO SERVIÇO DE ASSISTÊNCIA TÉCNICA, QUE NÃO A GEHC, SOLICITAR ESTES MANUAIS NOUTRO IDIOMA, É DA RESPONSABILIDADE DO CLIENTE FORNECER OS SERVIÇOS DE TRADUÇÃO.

• NÃO TENTE EFECTUAR REPARAÇÕES NO EQUIPAMENTO SEM TER CONSULTADO E COMPREENDIDO PREVIAMENTE ESTE MANUAL.

• A INOBSERVÂNCIA DESTE AVISO PODE RESULTAR EM FERIMENTOS NO TÉCNICO DE ASSISTÊNCIA, OPERADOR OU PACIENTE EM CONSEQUÊNCIA DE CHOQUE ELÉCTRICO, PERIGOS DE ORIGEM MECÂNICA, BEM COMO DE OUTROS TIPOS.

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.

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IRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

KÄESOLEV TEENINDUSJUHEND ON SAADAVAL AINULT INGLISE KEELES.

• KUI KLIENDITEENINDUSE OSUTAJA Nõ UAB JUHENDIT INGLISE KEELEST ERINEVAS KEELES, VASTUTAB KLIENT Tõ LKETEENUSE OSUTAMISE EEST.

HOIATUS

(ET)

• ä RGE üRITAGE SEADMEID TEENINDADA ENNE EELNEVALT KäESOLEVA TEENINDUSJUHENDIGA TUTVUMIST JA SELLEST ARU SAAMIST.

• Kä ESOLEVA HOIATUSE EIRAMINE Võ IB PõHJUSTADA TEENUSEOSUTAJA, OPERAATORI Võ I PATSIENDI VIGASTAMIST ELEKTRILöö GI, MEHAANILISE Võ I MUU OHU TAGAJäRJEL.

TÄMÄ HUOLTO-OHJE ON SAATAVILLA VAIN ENGLANNIKSI.

• JOS ASIAKKAAN PALVELUNTARJOAJA VAATII MUUTA KUIN ENGLANNINKIELISTä MATERIAALIA, TARVITTAVAN Kä ä NNö KSEN HANKKIMINEN ON ASIAKKAAN VASTUULLA.

VAROITUS

(FI)

• ä Lä YRITä KORJATA LAITTEISTOA ENNEN KUIN OLET VARMASTI LUKENUT JA YMMä RTä NYT TäMä N HUOLTO-OHJEEN.

• MIKä LI Tä Tä VAROITUSTA EI NOUDATETA, SEURAUKSENA VOI OLLA PALVELUNTARJOAJAN, LAITTEISTON Kä YTTä Jä N TAI POTILAAN VAHINGOITTUMINEN Sä HKöISKUN, MEKAANISEN VIAN TAI MUUN VAARATILANTEEN VUOKSI.

ΠΡΟΕΙ∆ΟΠΟΙΗΣΗ

(EL)

FIGYELMEZTETÉS

(HU)

ΤΟ ΠΑΡΟΝ ΕΓΧΕΙΡΙ∆ΙΟ ΣΕΡΒΙΣ ∆ΙΑΤΙΘΕΤΑΙ ΣΤΑ ΑΓΓΛΙΚΑ ΜΟΝΟ.

• ΕΑΝ ΤΟ ΑΤΟΜΟ ΠΑΡΟΧΗΣ ΣΕΡΒΙΣ ΕΝΟΣ ΠΕΛΑΤΗ ΑΠΑΙΤΕΙ ΤΟ ΠΑΡΟΝ

ΕΓΧΕΙΡΙ∆ΙΟ ΣΕ ΓΛΩΣΣΑ ΕΚΤΟΣ ΤΩΝ ΑΓΓΛΙΚΩΝ, ΑΠΟΤΕΛΕΙ ΕΥΘΥΝΗ ΤΟΥ ΠΕΛΑΤΗ ΝΑ ΠΑΡΕΧΕΙ ΥΠΗΡΕΣΙΕΣ ΜΕΤΑΦΡΑΣΗΣ.

• ΜΗΝ ΕΠΙΧΕΙΡΗΣΕΤΕ ΤΗΝ ΕΚΤΕΛΕΣΗ ΕΡΓΑΣΙΩΝ ΣΕΡΒΙΣ ΣΤΟΝ ΕΞΟΠΛΙΣΜΟ ΕΚΤΟΣ ΕΑΝ

ΕΧΕΤΕ ΣΥΜΒΟΥΛΕΥΤΕΙ ΚΑΙ ΕΧΕΤΕ ΚΑΤΑΝΟΗΣΕΙ ΤΟ ΠΑΡΟΝ

ΕΓΧΕΙΡΙ∆ΙΟ ΣΕΡΒΙΣ.

• ΕΑΝ ∆Ε ΛΑΒΕΤΕ ΥΠΟΨΗ ΤΗΝ ΠΡΟΕΙ∆ΟΠΟΙΗΣΗ ΑΥΤΗ, ΕΝ∆ΕΧΕΤΑΙ ΝΑ ΠΡΟΚΛΗΘΕΙ ΤΡΑΥΜΑΤΙΣΜΟΣ ΣΤΟ ΑΤΟΜΟ ΠΑΡΟΧΗΣ ΣΕΡΒΙΣ, ΣΤΟ ΧΕΙΡΙΣΤΗ Ή ΣΤΟΝ ΑΣΘΕΝΗ ΑΠΟ ΗΛΕΚΤΡΟΠΛΗΞΙΑ, ΜΗΧΑΝΙΚΟΥΣ Ή ΑΛΛΟΥΣ ΚΙΝ∆ΥΝΟΥΣ.

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.

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GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

ÞESSI ÞJÓNUSTUHANDBÓK ER EINGÖNGU FÁANLEG Á ENSKU.

• EF ÞJÓNUSTUAÐILI VIÐSKIPTAMANNS ÞARFNAST ANNARS TUNGUMÁLS EN ENSKU, ER ÞAÐ Á ÁBYRGÐ VIÐSKIPTAMANNS AÐ ÚTVEGA ÞÝÐINGU.

VIÐVÖRUN

(IS)

• 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.

TENTO SERVISNÍ NÁVOD EXISTUJE POUZE V ANGLICKé M JAZYCE.

•VPř íPADě, ŽE POSKYTOVATEL SLUŽEB ZÁKAZNÍKŮM POTř EBUJE Ná VOD V JINéM JAZYCE, JE ZAJIšTěNí Př EKLADU DO ODPOVíDAJíCíHO JAZYKA úKOLEM Zá KAZNíKA.

• NEPROVÁDĚJTE úDRŽBU TOHOTO ZAř íZENí, ANIŽ BYSTE SI Př Eč ETLI

VÝSTRAHA

(CS)

TENTO SERVISNÍ NÁVOD A POCHOPILI JEHO OBSAH.

•VPř íPADě NEDODRŽOVá Ní TéTO VýSTRAHY MůŽE DOJíT ÚRAZU ELEKTRICKÁM PROUDEM PRACOVNíKA POSKYTOVATELE SLUŽEB, OBSLUŽNéHO PERSONá LU NEBO PACIENTů VLIVEM ELEKTRICKéHOP PROUDU, RESPEKTIVE VLIVEM K RIZIKU MECHANICKÉHO POŠKOZENÍ NEBO JINÉMU RIZIKU.

ADVARSEL

(DA)

WAARSCHUWING

(NL)

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 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.

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.

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IRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

šĪ APKALPES ROKASGRĀMATA IR PIEEJAMA TIKAI ANGĻU VALODĀ.

• JA KLIENTA APKALPES SNIEDZĒJAM NEPIECIEŠAMA INFORMĀCIJA CITĀ VALODĀ, NEVIS ANGĻU, KLIENTA PIENĀKUMS IR NODROŠINĀT TULKOŠANU.

BRĪDINĀJUMS

(LV)

• NEVEICIET APRĪKOJUMA APKALPI BEZ APKALPES ROKASGRĀMATAS IZLASĪŠANAS UN SAPRAŠANAS.

•ŠĪ BRĪDINĀJUMA NEIEVĒROŠANA VAR RADĪT ELEKTRISKĀS STRĀVAS TRIECIENA, MEHĀNISKU VAI CITU RISKU IZRAISĪTU TRAUMU APKALPES SNIEDZĒJAM, OPERATORAM VAI PACIENTAM.

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 SM

ŪGIO, MECHANINIŲ AR

KITŲ PAVOJŲ.

ADVARSEL

(NO)

OSTRZEŻENIE

(PL)

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 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.

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 PRó BOWAć 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.

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

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.

ATE NŢIE

(RO)

• 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.

Данное руко в о дс т в о по обслуживанию ПРЕДОСТАВЛЯЕТСЯ только на английском Языке.

• Ес ли сервисноМУ ПЕРСОНАЛУ клиента необходимо руко в о дст в о не на английском ЯЗЫКЕ, клиенту следует самостоЯтельно ОБЕСПЕЧИТЬ перевод.

ОСТОРОЖНО!

(RU)

• 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.

ПРЕДУПРЕЖДЕНИЕ

(BG)

UPOZORENJE

(SR)

ТОВА СЕРВИЗНО РЪКОВОДСТВО Е НАЛИЧНО САМО НА АНГЛИЙСКИ ЕЗИК.

• АКО ДОСТАВЧИКЪТ НА СЕРВИЗНИ УСЛУГИ НА КЛИЕНТ

СЕ НУЖДАЕ ОТ ЕЗИК, РАЗЛИЧЕН ОТ АНГЛИЙСКИ, ЗАДЪЛЖЕНИЕ НА КЛИЕНТА Е ДА ПРЕДОСТАВИ ПРЕВОДАЧЕСКА УСЛУГА.

• НЕ СЕ ОПИТВАЙТЕ ДА ИЗВЪРШВАТЕ СЕРВИЗНО ОБСЛУЖВАНЕ НА ТОВА ОБОРУДВАНЕ, ОСВЕН ВСЛУЧАЙ, ЧЕ СЕРВИЗНОТО РЪКОВОДСТВО Е ПРОЧЕТЕНО И СЕ РАЗБИРА.

• НЕСПАЗВАНЕТО НА ТОВА ПРЕДУПРЕЖДЕНИЕ МОЖЕ ДА ДОВЕДЕ ДО НАРАНЯВАНЕ НА ДОСТАВЧИКА НА СЕРВИЗНИ УСЛУГИ, НА

ОПЕРАТОРА ИЛИ ПАЦИЕНТА ВСЛЕДСТВИЕНА ТОКОВ УДАР, МЕХАНИЧНИ ИЛИ ДРУГИ РИСКОВЕ.

OVAJ PRIRUČNIK ZA SERVISIRANJE DOSTUPAN JE SAMO NA ENGLESKOM JEZIKU.

• AKO KLIJENTOV SERVISER ZAHTEVA JEZIK KOJI NIJE ENGLESKI,

ODGOVORNOST JE NA KLIJENTU DA PRUŽI USLUGE PREVOĐENJA.

• NEMOJTE POKUŠAVATI DA SERVISIRATE OPREMU AKO NISTE PROČITALI I RAZUMELI PRIRUČNIK ZA SERVISIRANJE.

• AKO NE POŠTUJETE OVO UPOZORENJE, MOŽE DOĆI DO POVREĐIVANJA SERVISERA, OPERATERA ILI PACIJENTA UZROKOVANOG ELEKTRIČNIM UDAROM, MEHANIČKIM I DRUGIM OPASNOSTIMA.

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TA SERVISNI PRIROČNIK JE NA VOLJO SAMO V ANGLEŠČINI.

• ČE PONUDNIK SERVISNIH STORITEV ZA STRANKO POTREBUJE NAVODILA V

DRUGEM JEZIKU, JE ZA PREVOD ODGOVORNA STRANKA SAMA.

OPOZORILO

(SL)

• NE POSKUŠAJTE SERVISIRATI OPREME, NE DA BI PREJ PREBRALI IN

RAZUMELI SERVISNI PRIROČNIK.

• ČE TEGA OPOZORILA NE UPOŠTEVATE, OBSTAJA NEVARNOST ELEKTRIČNEGA UDARA, MEHANSKIH ALI DRUGIH NEVARNOSTI IN POSLEDIČNIH POŠKODB PONUDNIKA SERVISNIH STORITEV, UPORABNIKA OPREME ALI PACIENTA.

OVAJ SERVISNI PRIRUČNIK DOSTUPAN JE SAMO NA ENGLESKOM JEZIKU.

• AKO KLIJENTOV SERVISER ZAHTIJEVA JEZIK KOJI NIJE ENGLESKI, ODGOVORNOST KLIJENTA JE PRUŽITI USLUGE PREVOĐENJA.

UPOZORENJE

(HR)

• NEMOJTE POKUŠAVATI SERVISIRATI OPREMU AKO NISTE PROČITALI I RAZUMJELI SERVISNI PRIRUČNIK.

• AKO NE POŠTUJETE OVO UPOZORENJE, MOŽE DOĆI DO OZLJEDE SERVISERA, OPERATERA ILI PACIJENTA PROUZROČENE STRUJNIM UDAROM, MEHANIČKIM I DRUGIM OPASNOSTIMA.

UPOZORNENIE

(SK)

VARNING

(SV)

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 NEPREČÍTATE SERVISNÚ PRÍRUČKU A NEPOROZUMIETE JEJ.

• ZANEDBANIE TOHTO UPOZORNENIA Mô ŽE VYÚSTIŤ DO ZRANENIA POSKYTOVATEĽA SLUŽIEB, OBSLUHUJúCEJ OSOBY ALEBO PACIENTA ELEKTRICKýM PRúDOM, PRÍPADNE DO MECHANICKéHO ALEBO INéHO NEBEZPEč ENSTVA.

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.

vii

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

BU SERVİS KILAVUZU YALNIZCA İNGİLİZCE OLARAK SAĞLANMIŞTIR.

•EĞER MÜŞTERİ TEKNİSYENİ KILAVUZUN İNGİLİZCE DIŞINDAKİ BİR DİLDE OLMASINI İSTERSE, KILAVUZU TERCÜME ETTİRMEK MÜŞTERİNİN SORUMLULUĞUNDADIR.

DİKKAT

(TR)

•SERVİS KILAVUZUNU OKUYUP ANLAMADAN EKİPMANLARA MÜDAHALE ETMEYİNİZ.

• BU UYARININ GÖZ ARDI EDİLMESİ, ELEKTRİK ÇARPMASI YA DA MEKANİK VEYA DİĞER TÜRDEN KAZALAR SONUCUNDA TEKNİSYENİN, OPERATÖRÜN YA DA HASTANIN YARALANMASINA YOL AÇABİLİR.

(JA)

Traditional

Chinese

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GE HEALTHCARE D

IRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

(ZH-CN)

(KO)

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC 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 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,

No.19, Changjiang Road, Wuxi National Hi-Tech Dev. Zone, Jiangsu, P.R.China 214028

GE Healthcare employees should use TrackWise to report service documentation issues. These issues will then be in the internal problem reporting tool and communicated to the writer.

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 D

IRECTION 5314293-100, REVISION 19 VENUE 40 BASIC 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.

GE may revise this publication from time to time without written notice.

TRADEMARKS

All products and their name brands are trademarks of their respective holders.

COPYRIGHTS

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

Revision History

Revision Date Reason for change

1 Sep 17th, 2008 Initial Release

2 Feb 26th, 2009 Add FRU replacement procedures, update repair parts list.

3 May 14th, 2009 Update UIs, diagnostics and FRU description

4 Jun 1st, 2009 Update renewal parts list

5 July 27th, 2009 Update renewal parts list

6 Nov 16th, 2009 Update as software updates to R1.0.4

7 Nov 23th, 2009 Update as software updates to R1.0.4, add 4C-SC

8 Jun 24th, 2010 Update as software updates to R2.x.x, add L8-18i-SC

9 Aug 12th, 2010 Update renewal parts list

10 Nov 12th, 2010 Update for software R2.0.3, update renewal parts list.

11 Dec 16th, 2010 Update renewal parts list and unpacking procedure.

12 Jun 10th, 2011 Update as software update, add E8CS-SC

13 Aug 01st, 2011 Update FRU list

14 Jan 12th, 2012 Update Chapter 9 about spare parts

15 Apr 11th, 2012 Update for Venue40 OB software R3.1.x

16 Dec 17, 2012 Update package label and add new spare parts

17 Apr. 08, 2013 Add two notes

18 Sep. 10, 2013 Update as 3-probe Port Box released

19 May. 28, 2014 Update the spare part list

List of Effected Pages(LOEP)

Pages Revision Pages Revision Pages Revision

Chapter 3 -

Title Page 19

Important

Precautions

pages i to x

Table of Contents

pages xi to xxviii

Chapter 1 -

Introduction

pages 1-1 to 1-14

Chapter 2 - Pre-

Installation

pages 2-1 to 2-10

Installation

pages 3-1 to 3-19

Chapter 4 - Functional

Checks

pages 4-1 to 4-18

Chapter 5 - Theory

pages 5-1 to 5-7

Chapter 6 - Service

Adjustments

pages 6-1 to 6-6

Chapter 7 -

Diagnostics/

Troubleshooting

pages 7-1 to 7-20

19 Back Cover 19

Chapter 8 -

Replacement

Procedures

pages8-1 to 8-28

Chapter 9 -

Replacement Parts

pages 9-1 to 9-17

Chapter 10 - Periodic

Maintenance

pages 10-1 to 10-22

Index

pages I to II

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GE HEALTHCARE D

IRECTION 5314293-100, REVISION 19 VENUE 40 PROPRIETARY SERVICE MANUAL

Table of Contents

CHAPTER 1

Introduction

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 1

Purpose of Chapter 1 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 1

Chapter Contents . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 1

Purpose of Service Manual . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 1

Typical Users of the Service Manual . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 2

Venue 40 Models Covered by this Manual . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 2

Purpose of Operator Manual(s) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 2

Important Conventions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 3

Conventions Used in Book . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 3

Standard Hazard Icons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 4

Product Icons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 5

Safety Considerations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 8

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 8

Human Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 8

Mechanical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 8

Electrical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 8

Labels Locations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 8

Battery Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 9

Dangerous Procedure Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 10

Lockout/Tagout (LOTO) requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 11

Returning/Shipping Probes and Repair Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 11

EMC, EMI, and ESD . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 12

Electromagnetic Compatibility (EMC) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 12

CE Compliance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 12

Electrostatic Discharge (ESD) Prevention . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 12

Customer Assistance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 13

Contact Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 13

System Manufacturer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 14

1 Table of Contents

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 PROPRIETARY SERVICE MANUAL

CHAPTER 2

Site Preparation

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 1

Purpose of this chapter 2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 1

Chapter Contents . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 1

General Console Requirements. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2

Console Environmental Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2

Electrical Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2

EMI Limitations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 4

Scan Probe Environmental Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 5

Facility Needs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 6

Recommended Ultrasound Room Layout . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 6

Required Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 7

Desirable Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 7

Networking Pre-installation Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 9

2 Table of Contents

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

CHAPTER 3

System Setup

Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 1

Purpose of Chapter 3 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 1

Average Setup Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 2

Installation Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 3

Safety Reminders . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 3

Receiving and Unpacking the Equipment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 4

Unpacking Venue 40 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 4

Unpacking Docking Station . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 9

Unpacking Docking Cart . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 12

Unpacking 3-probe Port Box . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 15

Moving into Position . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 17

Packing the Equipment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 17

Preparing for Installation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 18

Verify Customer Order . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 18

Physical Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 18

EMI Protection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 18

Completing the Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 19

Power On / Boot Up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 19

Power Off/ Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 25

Transducer Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 26

System Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 28

System Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 28

Electrical Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 29

Approved on-board peripherals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 29

Connecting Cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 30

Peripherals/Accessories Connector Panel . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 31

Available Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 40

Software/Option Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 40

Loading Base Image Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 41

Software version check-out . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 41

Paperwork . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 42

Product Locator Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 42

User Manual(s) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 42

Table of Contents 3

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 PROPRIETARY SERVICE MANUAL

CHAPTER 4

Functional Checks

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 1

Purpose for Chapter 4 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 1

Required Equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 1

General Procedure. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 2

Power On/Boot Up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 2

Power Off/ Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 2

Adjusting the Display Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 2

System Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 3

B Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 5

Color Flow Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 7

Power Doppler Imaging (PDI) Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . 4 - 9

M Mode Checks (R2.x.x, R3.x.x only) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 11

Basic Measurements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 13

Probe/Connectors Usage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 16

Using Cine . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 17

Software Configuration Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 18

Peripheral Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 18

High capacity SD Card checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 18

USB Memory Stick checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 18

B/W Printer checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 19

Slave USB Port checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 19

Wireless Network Card checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 19

Footswitch checks (only for R3.x.x) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 19

4 Table of Contents

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

CHAPTER 5

Components and Functions (Theory)

Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 1

Block Diagrams and Theory . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 2

Block Diagram of Venue 40 and Docking Station/Cart . . . . . . . . . . . . . . . . 5 - 2

Block Diagram of Venue 40 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 3

Block Diagram of Docking Station . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 5

Power Diagrams . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 7

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 7

AC Power . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 7

Battery charging . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 7

Table of Contents 5

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 PROPRIETARY SERVICE MANUAL

CHAPTER 6

Service Adjustments

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 1

Purpose of this chapter 6 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 1

Monitor Adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 2

Adjust brightness . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 2

Adjust volume . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 2

Adjust monitor on Docking Station/Docking Cart . . . . . . . . . . . . . . . . . . . . . 6 - 3

Stylus . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 5

6 Table of Contents

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

CHAPTER 7

Diagnostics/Troubleshooting

Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 1

Purpose of Chapter 7 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 1

Diagnostics . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 2

Diagnostic Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 2

Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 3

Console Troubleshooting Trees . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 3

Peripheral Troubleshooting Trees . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 17

Table of Contents 7

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 PROPRIETARY SERVICE MANUAL

CHAPTER 8

Replacement Procedures

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 1

Purpose of Chapter 8 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 1

Disassembly/Re-assemblyof Venue 40 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 2

Warning and Caution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 2

Returning/Shipping for repairs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 2

Standard tools list for Venue 40 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 3

Docking Station Desk Support Assy (FRU No. 405) . . . . . . . . . . . . . . . . . . 8 - 4

Docking Cart Plastic Shelf (FRU No. 510) . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 5

Docking Cart Printer Shelf (FRU No. 511) . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 6

Loading Base Image Software. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 7

Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 7

8 Table of Contents

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

CHAPTER 9

Renewal Parts

Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 1

Purpose of Chapter 9 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 1

List of Abbreviations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 1

Renewal Parts Lists . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 2

Power cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 2

Operator Console Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 5

Top Assy. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 6

Middle Cover Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 7

Bottom Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 8

Docking Station Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 10

Docking Cart Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 11

Accessories and Kits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 12

Manuals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 14

Probe . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 16

Table of Contents 9

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 PROPRIETARY SERVICE MANUAL

CHAPTER 10

Care & Maintenance

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 1

Periodic Maintenance Inspections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 1

Purpose of Chapter 10 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 1

Why do Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 2

Keeping Records . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 2

Quality Assurance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 2

Maintenance Task Schedule . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 2

How often should care & maintenance tasks be performed? . . . . . . . . . . . . 10 - 2

Tools Required. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 4

Standard GE Tool Kit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 4

Special Tools, Supplies and Equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 6

System Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 7

Preliminary Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 7

Functional Checks (See Also Chapter 4) . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 8

Input Power . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 9

Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 9

Physical Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 10

Optional Diagnostic Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 11

Probe Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 11

Battery Performance Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 12

Electrical Safety Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 13

Safety Test Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 13

GEMS Leakage Current Limits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 14

Outlet Test - Wiring Arrangement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 15

Chassis Leakage Current Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 16

Probe Leakage Current Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 18

When There's Too Much Leakage Current... . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 20

10 Table of Contents

GE HEALTHCARE D

IRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

Chapter 1 Introduction

Section 1-1 Overview

1-1-1 Purpose 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.

1-1-2 Chapter Contents

Table 1-1 Contents in Chapter 1

Section Description Page Number

1-1

1-2

1-3

1-6

1-7

Overview

Important Conventions

Safety Considerations

EMC, EMI, and ESD

Customer Assistance

1-1-3 Purpose of Service Manual

This Service Manual provides service information for the Venue 40 Ultrasound Scanning System. It

contains the following chapters:

1.) Chapter 1 - Introduction: Contains a content summary and warnings.

2.) Chapter 2 - Site Preparation: Contains pre-installation requirements for the Venue 40.

3.) Chapter 3 - System Setup: Contains installation procedures.

4.) Chapter 4 - Functional Checks: Contains functional checks that are recommended as part of the

installation, or as required during servicing and periodic maintenance.

5.) Chapter 5 - Components and Functions (Theory): Contains block diagrams and functional

explanations of the electronics.

6.) Chapter 6 - Service Adjustments: Contains instructions on how to make available adjustments to

the Venue 40.

7.) Chapter 7 - Diagnostics/Troubleshooting: Provides procedures for running diagnostic or related

routines for the Venue 40.

8.) Chapter 8 - Replacement Procedures: Provides disassembly procedures and reassembly

procedures for all changeable Field Replaceable Units (FRU).

9.) Chapter 9 - Renewal Parts: Contains a complete list of field replaceable parts for the Venue 40.

10.)Chapter 10 - Care & Maintenance: Provides periodic maintenance procedures for the Venue 40.

1-1

1-3

1-8

1-12

1-13

Chapter 1 Introduction 1-1

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

1-1-4 Typical Users of the Service Manual

• Repair Center Personnel (installation, maintenance, etc.).

• Online Center Personnel

1-1-5 Venue 40 Models Covered by this Manual

Table 1-2 Venue 40 Model Designations (R1.x.x)

Part Number Description

5324338 Venue 40 Console

5352135 Venue 40 Console light version

5365959 Venue 40 Console light version with film

5454161 Venue 40 Console China

Table 1-3 Venue 40 Model Designations (R2.0.x)

Part Number Description

5391353 Venue 40 Console

5392880 Venue 40 Console with film

5416098 Venue 40 Console for Korea

Table 1-4 Venue 40 Model Designations (R2.1.x)

Part Number Description

5418925 Venue 40 Console

Table 1-5 Venue 40 Model Designations (R3.0.x)

Part Number Description

5418778 Venue 40 Console

5418779 Venue 40 Console with film

5477730 Venue 40 Console China

5436436 Venue 40 Console Korea

Table 1-6 Venue 40 Model Designations (R3.1.x)

Part Number Description

5461896 Venue 40 Console

Table 1-7 Venue 40 Model Designations (R3.2.x)

Part Number Description

5487523 Venue 40 Console

1-1-6 Purpose of Operator Manual(s)

The Operator Manual(s) should be fully read and understood before operating the Venue 40 and also kept near the unit for quick reference.

1-2 Section 1-1 - Overview

GE HEALTHCARE D

IRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

Section 1-2 Important Conventions

1-2-1 Conventions 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.

Chapter 1 Introduction 1-3

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

1-2-2 Standard 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 1-8 Standard Hazard Icons

ELECTRICAL MECHANICAL RADIATION

LASER HEAT PINCH

LASER

LIGHT

Other hazard icons make you aware of specific procedures that should be followed.

Table 1-9 Standard Icons Indicating a Special Procedure Be Used

AVOID STATIC ELECTRICITY TAG AND LOCK OUT WEAR EYE PROTECTION

TAG

LOCKOUT

Date

Signed

EYE

PROTECTION

1-4 Section 1-2 - Important Conventions

GE HEALTHCARE D

IRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

1-2-3 Product Icons

The following table describes the purpose and location of safety labels and other important information

provided on the equipment.

Table 1-10 Warnings

LABEL/SYMBOL PURPOSE/MEANING LOCATION

Identification and Rating Plate

• Manufacture’s name and address

• Date of manufacture

• Model and serial numbers

• Electrical ratings (Volts, Amps, phase, and frequency)

Bottom panel of the console

Type/Class Label Used to indicate the degree of safety or

protection.

IP Code (IPX8) IPX8: MKF 2 1S/1S-MED HID GP26

Indicates the degree of protection provided by the enclosure per IEC60

529.

IPX8 can be used in an operating room environment.

Authorized European Representative address

United States only Prescription Requirement label

Equipment Type BF (man in the box symbol) IEC 878-02-03 indicates B Type equipment having a floating applied part.

General Warning Various

“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.

Bottom panel of the console

Probe connectors

Various

“CAUTION - Dangerous voltage” (the lightning flash with arrowhead in equilateral triangle) is used to indicate electric shock hazards.

“ON” indicates the power on position of the power switch. CAUTION This Power Switch DOES NOT ISOLATE Mains Supply

Various

Stick to Power Switch

Chapter 1 Introduction 1-5

GE HEALTHCARE

REF

DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

Table 1-10 Warnings

LABEL/SYMBOL PURPOSE/MEANING LOCATION

“Protective Earth” indicates the protective earth (grounding) terminal.

“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 is assessed and a control number.

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.

Inside of AC adapter with docking station

Bottom panel of the console

Rating Plate

REF

Catalog or model number. Rating Plate

Serial number Rating Plate

Direct Current.

For products to be powered from a DC supply.

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)

Rating Plate

Bottom

1-6 Section 1-2 - Important Conventions

GE HEALTHCARE D

IRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

Table 1-10 Warnings

LABEL/SYMBOL PURPOSE/MEANING LOCATION

Indicates the product contains hazardous materials in excess of the limits established by 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.

GOST symbol: Russia Regulatory Country Clearance.

Rear panel, rating plate

Rating Plate

This symbol is affixed to a battery to advise the user or owner that it must be recycled or disposed of in accordance with local, state, or country laws. The letter below indicates the toxic element (Pb=Lead, Cd=Cadimium, Hg=Mercury) that is contained in the battery that may require special recycling or disposal methods. Please contact a GEHC representative to facilitate servicing, removal and disposal options.

Utilize additional care and personnel when moving on steep inclines (>5 degrees) or loading into vehicle for transport.

Do not put anything weighed over 5kg on the shelf.

Do not push the system. Back of Docking Cart

Rating Plate of Docking Cart

Printer shelf of Docking Cart

Do not step on the system Base chassis covers of Docking Cart

Chapter 1 Introduction 1-7

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

Section 1-3 Safety Considerations

1-3-1 Introduction

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.

1-3-2 Human Safety

Operating personnel must not remove the system covers. Servicing should be performed by authorized personnel only. Only personnel who have participated in a Venue 40 Training are authorized to service the equipment.

1-3-3 Mechanical 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

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.

• 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.

1-3-4 Electrical 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.

1-3-5 Labels Locations

See Basic User Manual 5265930-1xx or 5419428-1xx for detail information.

1-8 Section 1-3 - Safety Considerations

GE HEALTHCARE D

IRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

1-3-6 Battery Safety

To avoid the risk of injury, follow the warning and cautions to make sure that the battery does not burst, ignite, or generate heat of fumes.

WARNINGWARNING

CAUTION

• The battery has a safety device. Do not disassemble or alter the battery.

• Charge the batteries only when the ambient temperature is between 0° and 40° C (32° and

104° F) and discharge the batteries between 0° and 40° C (32° and 104° F).

• Do not short-circuit the battery by directly connecting the negative terminals with metal

objects.

• Do not heat the battery or discard it in a fire.

• Do not expose the battery to temperature over 50° C (122° F). Keep it away from fire and other

heat sources.

• Do not charge the battery near a heat source, such as a fire or heater.

• Do not leave the battery in direct sunlight.

• Do not drop packs from height to prevent them from possible malfunction damage.

• Do not pierce the battery with a sharp object, hit it, or step on it.

• Do not use a damaged battery.

• Do not solder a battery.

• Do not connect the battery to an electrical power outlet.

• In the case of the Venue 40 will not be used for a long time, remove the battery.

To avoid the battery bursting, igniting, or fumes from the battery causing equipment damage, observe the following precautions:

• Do not immerse the battery in water or allow it to get wet.

• Do not put the battery into a microwave oven or pressurized container.

• If the battery leaks or emits an odor, remove it from all possible flammable sources.

• If the battery emits an odor or heat, is deformed or discolored, or in a way appears abnormal

during use, recharging or storage, immediately remove it and stop using it. If you have any questions about the battery, consult GE or your local representative.

• Short term (less than one month) storage of battery pack:

• Store the battery in a temperature range between 0° C (32° F) and 50° C (122°F).

• Use only GE recognized batteries.

• In case of the long term (3 months or more) storage:

• Store the battery in a temperature range of -20° C (-4° F) and 45° C (113°F).

• When charging for the first time after long-term storage. Recover such packs to original performance through repeating several cycles of full charging and discharging.

• When store packs for more than 6 months, charge at lease once charging require per 6 months to prevent leakage and deterioration in performance due to selfdischarging.

• When the system isn't powered on continuously more than 6 months, in order to prevent leakage and deterioration in performance of CMOS battery, power on the system at least once per 6 months for more than 10 hours to have CMOS battery fully charged. Time and date need to be re-setup.

Chapter 1 Introduction 1-9

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

1-3-7 Dangerous Procedure Warnings

Warnings, such as the examples below, precede potentially dangerous procedures throughout this manual. Instructions contained in the warnings must be followed.

DANGER

WARNINGWARNING

DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH, ARE PRESENT IN THIS EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING AND ADJUSTING.

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.

SYSTEM FILE DAMAGE MAY RESULT FROM FORCED SHUT DOWN OR REMOVING THE ACDC PLUG.

1-10 Section 1-3 - Safety Considerations

GE HEALTHCARE D

IRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

Section 1-4 Lockout/Tagout (LOTO) requirements

Follow OSHA Lockout/Tagout requirements (USA) or local Lockout/Tagout requirements by ensuring you are in total control of the AC power plug at all times during the service process.

To apply Lockout/Tagout:

1.) Plan and prepare for shutdown.

2.) Shutdown the equipment.

3.) Isolate the equipment.

4.) Apply Lockout/Tagout Devices.

5.) Remove battery.

6.) Control all stored and residual energy.

7.) Verify isolation.

All potentially hazardous stored or residual energy is relieved.

NOTICE

Energy Control and Power Lockout for Venue 40

WHEN SERVICING PARTS OF THE SYSTEM WHERE THERE IS EXPOSURE TO VOLTAGE GREATER THAN 30 VOLTS:

1. TURN OFF THE SCANNER.

2. UNPLUG THE SYSTEM.

3. MAINTAIN CONTROL OF THE SYSTEM POWER PLUG.

TAG

LOCKOUT

Date

Signed

4. WAIT FOR AT LEAST 20 SECONDS FOR CAPACITORS TO DISCHARGE AS THERE ARE NO

TEST POINTS TO VERIFY ISOLATION. THE AMBER LIGHT ON THE OP PANEL ON/OFF BUTTON WILL TURN OFF.

5. REMOVE THE SYSTEM BATTERY.

Section 1-5 Returning/Shipping Probes and Repair Parts

Equipment being returned must be clean and free of blood and other infectious substances.

GE Healthcare policy states that body fluids must be properly removed from any part or equipment prior to shipment. GE Healthcare 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.

Chapter 1 Introduction 1-11

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

Section 1-6 EMC, EMI, and ESD

1-6-1 Electromagnetic 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.

1-6-2 CE Compliance

The Venue 40 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.

1-6-3 Electrostatic Discharge (ESD) Prevention

WARNINGWARNING

DO NOT TOUCH ANY BOARDS WITH INTEGRATED CIRCUITS PRIOR TO TAKING THE NECESSARY ESD PRECAUTIONS:

FOLLOW GENERAL GUIDELINES FOR HANDLING OF ELECTROSTATIC SENSITIVE

EQUIPMENT.

1-12 Section 1-6 - EMC, EMI, and ESD

GE HEALTHCARE D

IRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

Section 1-7 Customer Assistance

1-7-1 Contact 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.

- Date and time of occurrence

- Sequence of events leading to issue

- Is the issue reproducible?

- Imaging mode, probe, application

- Media brand, speed, capacity, type

- Save image capture, cine loop

Table 1-11 Phone Numbers for Customer Assistance

Location Phone Number

USA

GE Medical Systems

Ultrasound Service Engineering

9900 Innovation Drive

Wauwatosa, WI 53226

Canada 1-800-668-0732

Latin America

Europe (OLC EMEA)

GE Ultraschall Deutschland GmbH& Co. KG

Beethovenstrasse 239

Postfach 11 05 60, D-42665 Solingen

Germany

Online Services Ultrasound Asia

Australia

China

India

Japan

Korea

Singapore

Service: On-site

Service: Parts

Applications support

Service

Applications support

Phone: +49 (0)212 2802 - 652 (English/German)

+33 1 3083 1300 (English/German all segments incl. training)

+43 (0) 7682-3800-26 (Volunson-Logiqbook)

Fax: +49 (0)212-2802-431

Phone: +(61) 1-8---647-855

+(86) 800-810-8188

+(91) 1-800-11-4567

+(81) 42-648-2924

+(82) 2620 13585

+(95) 6277-3444

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

Chapter 1 Introduction 1-13

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

1-7-2 System Manufacturer

Table 1-12 System Manufacturer

Manufacturer Phone Number

GE Medical Systems (China) Co., Ltd.

No.19, Changjiang Road, Wuxi National Hi-Tech Dev. Zone, Jiangsu, P.R.China 214028

TEL: +86 510-85225888

FAX: +86 510-85226688

1-14 Section 1-7 - Customer Assistance

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

Chapter 2 Site Preparation

Section 2-1 Overview

2-1-1 Purpose of this chapter 2

This chapter provides the information required to plan and prepare for the installation of a Venue 40. Included are descriptions of the facility and electrical needs to be met by the purchaser of the unit.

2-1-2 Chapter Contents

Table 2-1 Contents in Chapter 2

Section Description Page Number

2-1

2-2

Overview

General Console Requirements

2-1

2-2

Chapter 2 Site Preparation 2-1

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

Section 2-2 General Console Requirements

2-2-1 Console Environmental Requirements

Table 2-2 Environmental Requirements for Venue 40 Scanners

Operational Storage Transport

Temperature

Humidity

Pressure

Temperatures in degree C, conversion to degree F =(degree C*(9/5) + 32)

10 - 40 degree C -5 - 50 degree C -5 - 50 degree C

30 - 75% non-condensing

700 - 1060hPa 700 - 1060hPa 700 - 1060hPa

10 - 90% non-condensing

2-2-1-1 Lighting

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.

2-2-2 Electrical Requirements

NOTE: GE Medical 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.

2-2-2-1 Venue 40 Power Requirements

Table 2-3 Electrical Specifications for Venue 40

Voltage Power Current Frequency

100-240 V 180VA max. 1.3 A (max.) 50/ 60HZ

Table 2-4 Electrical Specification for Docking Cart

Voltage Power Current Frequency

100-240 V 380VA max. 2.7 A (max.) 50/ 60HZ

2-2 Section 2-2 - General Console Requirements

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

2-2-2-2 Inrush Current

Table 2-5 Inrush Current

Voltage Inrush Current

100V 75A(max)

240V 120A(max)

2-2-2-3 Site Circuit Breaker

It is recommended that the branch circuit breaker for the machine be readily accessible.

2-2-2-4 Site 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 within 1 m (3.2 ft.) of the unit. Electrical installation must meet all current local, state, and national electrical codes.

2-2-2-5 Unit 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.

Chapter 2 Site Preparation 2-3

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

2-2-3 EMI 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 Venue 40 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.

The presence of a broadcast station or broadcast van may also cause interference.

See Ta bl e 2 -6 for EMI Prevention tips.

Table 2-6 EMI Prevention/abatement

EMI Rule Details

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.

Keep the unit at least 5 meters or 15 feet away from other EMI sources. Special shielding 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.

2-4 Section 2-2 - General Console Requirements

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

2-2-4 Scan Probe Environmental Requirements

Operation:10° to 40° C

Storage:-10° to 60° 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

-10 TO + 60 degrees C. WHEN EXPOSED TO LARGE TEMPERATURE VARIATIONS, THE

PRODUCT SHOULD BE KEPT IN ROOM TEMPERATURE FOR 10 HOURS BEFORE USE.

Chapter 2 Site Preparation 2-5

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

Section 2-3 Facility Needs

2-3-1 Recommended Ultrasound Room Layout

2-3-1-1 Purchaser 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. Use 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.

2-6 Section 2-3 - Facility Needs

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

2-3-2 Required Features

NOTE: GE Medical 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 0.2m (0.67 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)

2-3-3 Desirable Features

• 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.

Chapter 2 Site Preparation 2-7

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

2-3-3-1 Recommended and Alternate Ultrasound Room Layout

Recommended standard floor plan and a minimal floor plan for ultrasound equipment:

FILM

FILE

C AB INET

SE CR ETA R YS O R DOCTO R’S D ES K

DEDICATED

PO W ER

R OOM ,

PR O C ESSIN G

FILM VIEW ER

CO UN TER TO P

RECEPTACLE

CO UN TER

TO P

SIN K

C O NS O LE

FOOT

SU C TIO N LINE

EM ERG ECY OX Y G EN

OVERHEAD LIG H TS D IMM E R

DOO R 42 IN.

(107 CM)

A 14 by 17 foot R ecommended Floor Plan

S cale : Each square equals one square foot

(46 CM)

S TOO L

76 IN.

(193 CM)

18 IN.

LINEN SUPPLY

EXAM INAT IO N

TAB LE

24 IN.

(61 CM)

PAT IENT

TO ILET

FA C ILITY

FILM VIEW ER

FILM SUPPLIES

SINK

LINEN SUPPLY

PR OB ES /SUPPLIES

EXTERNAL

PERIPHERALS

DEDICAT ED POW ER OUTLETS

G E C AB INET FOT SO FTW A RE AND MA NU A LS

DOO R 30 IN.

(76 CM)

24 IN. (61 CM)

FOOT

S TOO L

EXAM INAR IO N

TAB LE

LOGIQ Book XP

C O NS O LE

76 IN. (193 CM)

An 8 by 10 foot M inimal F loor Plan

Figure 2-1 RECOMMENDED ULTRASOUND ROOM LAYOUT

2-8 Section 2-3 - Facility Needs

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

2-3-4 Networking Pre-installation Requirements

2-3-4-1 Stand Alone Scanner (without Network Connection)

None.

2-3-4-2 Scanner Connected to Hospital’s Network

Supported networks:

Wireless LAN

2-3-4-3 Purpose of DICOM Network Function

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.

2-3-4-4 DICOM Option Pre-installation Requirements

To configure the Venue 40 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 Venue 40.

• 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

Venue 40 for DICOM APPLICATION INFORMATION. A field for the make (manufacturer) and the

revision of the device, is also included. This information may be useful for solving errors.

Chapter 2 Site Preparation 2-9

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

2-3-4-4 DICOM Option Pre-installation Requirements (cont’d)

Venue 40

Host Name

AE Title

ROUTING INFORMATION

ROUTER1 ROUTER2 ROUTER3

DICOM APPLICATION INFORMATION

NAME

Store 1

Store 2

Store 3

Local Port

Destination IP Addresses

...

MAKE/REVISION IP ADDRESSES PORTAE TITLE

IP Address

Net Mask

Default

...

GATEWAY IP Addresses

...

Store 4

Store 5

Store 6

Worklist

Storage Commit

MPPS

...

Figure 2-2 Worksheet for DICOM Network Information

2-10 Section 2-3 - Facility Needs

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

Chapter 3 System Setup

Section 3-1 Overview

3-1-1 Purpose 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 3-7 Contents in Chapter 3

Section Description Page Number

3-1

3-2

3-3

3-4

3-5

3-6

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

Loading Base Image Software

Software version check-out

Paperwork

3-1

3-4

3-17

3-18

3-19

3-28

3-40

3-41

3-42

Chapter 3 System Setup 3-1

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-1-2 Average Setup Time

Table 3-8 Average Installation Time

Description Average Installation Time Comments

Unpacking the scanner

Scanner wo/options

20 minutes

30 minutes

Dependent on the configuration that is required

The Venue 40 installation and functional checkout will take approximately one hour. Venue 40 consoles with optional equipment may take slightly longer.

3-2 Section 3-1 - Overview

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-1-3 Installation Warnings

8.) 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.

9.) 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 degrees C increment it's temperature is below 10 degrees C or above 40 degrees C.

DANGER

Equipment damage possibility. Turning the system on without acclimation after arriving at site may cause the system to be damaged.

Table 3-9 Time for Settlement

60 55 50 45 40 35 30 25 20 15 10 5 0 -5 -10 -15 -20 -25 -30 -35 -40

°C

140 131 122 113 104 95 86 77 68 59 50 41 32 23 14 5 -4 -13 -22 -31 -40

°F

864200000002468101214161820

hrs

3-1-4 Safety Reminders

DANGER

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

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 are securely in place.

DANGER

OPERATOR MANUAL(S) The User Manual(s) should be fully read and understood before operating the Venue 40 and kept near the unit for quick reference.

ACOUSTIC OUTPUT HAZARD Although the ultrasound energy transmitted from the Venue 40 probe is within FDA limits, avoid unnecessary exposure. Ultrasound energy can produce heat and mechanical damage

Chapter 3 System Setup 3-3

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

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.

3-2-1 Unpacking Venue 40

1.) Cut the four PLASTIC BANDs.

2.) Cut the adhesive tape and open top covers of paper carton.

Figure 3-3 Open top covers of paper carton.

3-4 Section 3-2 - Receiving and Unpacking the Equipment

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-2-1 Unpacking Venue 40 (cont’d)

3.) Take out the paper pad on the side. Refer to Figure 3-4 on page 3-5

4.) Take out the Accessories Package and Console Package. Refer to Figure 3-4 on page 3-5

Figure 3-4 Unpacking Venue 40

Item Description

1 Accessories Package

2 Console Package

3 Paper pad

Chapter 3 System Setup 3-5

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-2-1 Unpacking Venue 40 (cont’d)

5.) Open the Console Package, remove the pad. Take out stylus and battery package. Take out the console. Take off the protective bag and the PE bag. Refer to Figure 3-5 on page 3-6

Figure 3-5 Taking out the system

3-6 Section 3-2 - Receiving and Unpacking the Equipment

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-2-1 Unpacking Venue 40 (cont’d)

Item Description

1 Paper pad

2 Battery

3 Stylus Package

4 Battery Bag

5 Foam

6 Venue 40 Protective bag

7 PE bag

Chapter 3 System Setup 3-7

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-2-1 Unpacking Venue 40 (cont’d)

6.) Open the Accessories Package,

Figure 3-6 Opening Accessories box

Item Description

1 Cover pad

2 Biopsy kit (option)

3 USB cable with miniB

4 Probe bracket for needle guide (option)

5 Manuals (option)

6 SD Card Reader

7 Aquasonic gel

8 SD Card for data storage

9 Software SD Card - for re-loading software as needed

10 Power Cable (option)

NOTE: Make sure all the items in the checklist are in the Accessories box, contact GE Service if any

problem.

3-8 Section 3-2 - Receiving and Unpacking the Equipment

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-2-2 Unpacking Docking Station

1.) Cut the four PLASTIC BANDs.

2.) Cut the adhesive tape and open top covers of paper carton

Figure 3-7 Open top covers of paper carton.

Chapter 3 System Setup 3-9

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-2-2 Unpacking Docking Station (cont’d)

3.) Remove top foam, take out the Docking Station Module and probe holders.

4.) Take out the Base support module.

Figure 3-8 Unpacking the Docking Station

Item Description

1 Probe holder bag

2Foam

3 Docking Station bag

4 Probe holders

5 Docking Station module

6 Docking Station desk support module

7Carton

Power cord

3-10 Section 3-2 - Receiving and Unpacking the Equipment

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-2-2 Unpacking Docking Station (cont’d)

5.) Place the Docking Station Module on track of Base Support Module starting from the left, and

slowly move it to the right till it clicks:

Figure 3-9 Install the Docking Station

Chapter 3 System Setup 3-11

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-2-3 Unpacking Docking Cart

If the package of the Docking Cart is a wooden box,

1.) Cut the tape and take off the tool attached to the box.

2.) Insert the ending head of the tool to the hole of the tongue.

3.) Pull the tongue to the limit.

4.) Insert the plain head of the tool to the hole of the tongue.

5.) Pull the tongue until it ends up

6.) After all the tongues end up, separate the profile from tongue to open the whole box.

Figure 3-10 Open the box of Docking Cart (wooden box)

3-12 Section 3-2 - Receiving and Unpacking the Equipment

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-2-3 Unpacking Docking Cart (cont’d)

7.) Open the box, remove all the foam, cut the wire ties on the chassis. Take out the Docking Cart.

Figure 3-11 Unpacking Docking Cart (wooden box)

Item Description

1 Power cord bag

2 Probe holder bag and power cord

3 Printer Shelf kit (option)

Chapter 3 System Setup 3-13

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-2-3 Unpacking Docking Cart (cont’d)

If the package of the Docking Cart is paper carton,

1.) Cut the adhesive tape

2.) Open the top cover of paper carton

3.) Rotate the plastic locker counter clockwise and pull it out. Unlock all the four plastic lockers.

4.) Remove the carton frames on both sides.

5.) Remove all the foam and the ESD bag, cut the wire ties on the chassis. Take out the Docking Cart.

Figure 3-12 Unpack the Docking Cart (paper carton)

3-14 Section 3-2 - Receiving and Unpacking the Equipment

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-2-4 Unpacking 3-probe Port Box

NOTE: 3-probe Port Box is not available in China, Japan or Korea.

1.) Cut the four PLASTIC BANDs.

2.) Cut the adhesive tape and open top covers of paper carton.

Figure 3-13 Open top covers of paper carton

Chapter 3 System Setup 3-15

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-2-4 Unpacking 3-probe Port Box (cont’d)

3.) Remove the top foam, and take out the 3-probe Port Box, multi-probe holders, E8CS-SC probe holder and gel holder.

4.) Continue to remove the foam, and take out the printer shelf and the drawer.

Figure 3-14 Unpacking the 3-probe Port Box

Item Description

13-probe Port Box

2 Installation Instructions

3 Multi-probe Holder

4 E8CS-SC Probe Holder

5 Gel Holder

6 Gel Holder

7 Printer Shelf with Drawer ASSY

8 On Shelf Basket ASSY

9 Venue 40 3-probe Port Box User Instructions

10 Rating Plate Label for 3-probe Port Box Option

11 Rating Plate Label for 3-probe Port Box

3-16 Section 3-2 - Receiving and Unpacking the Equipment

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

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.

CAUTION

Please carefully unpack the system, and do not dispose the package of Venue 40, so that it can be reused for service.

Please keep the protective bag of Venue 40 in box, so that it can be used for shipping or transportation.

3-2-5 Moving into Position

CAUTION

Equipment Damage Possibility. Do not lift the unit by stylus.

In general, a single adult can move the Venue 40. Before moving, store all loose parts in original accessory box or in back pack. Return probes to original box.

Section 3-3 Packing the Equipment

Please pack Venue 40 in the reverse order of unpacking.

Figure 3-15 Labels on Package

Chapter 3 System Setup 3-17

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

Section 3-4 Preparing for Installation

3-4-1 Verify 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.

3-4-2 Physical Inspection

3-4-2-1 System Voltage Settings

• Verify that the Docking Station/Docking Cart is set to the correct voltage. The Voltage settings for the system is found on the rating plate.

• 220-240VAC(China); 100-120VAC(USA/Japan); 220-240VAC(Europe, Latin America).

NOTE: Check your local grid and confirm the voltage.

WARNINGWARNING

Connecting Docking Station/Cart to the wrong voltage level may destroy the system.

3-4-3 EMI 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.

3-18 Section 3-4 - Preparing for Installation

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

Section 3-5 Completing the Installation

3-5-1 Power On / Boot Up

3-5-1-1 Mount the system to Docking Station/Docking Cart

To Mount the system to Docking Station or Docking Cart:

1.) Place the Docking Station and system on a stable surface.

2.) Carefully pickup the system. Align the port on the box with the docking port and carefully push into place.

Figure 3-16 Mount system onto Docking Station/Docking Cart

Chapter 3 System Setup 3-19

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-5-1-1 Mount the system to Docking Station/Docking Cart (cont’d)

3.) Press the locking lever down to the right position

Figure 3-17 Press the locking lever

3-20 Section 3-5 - Completing the Installation

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-5-1-2 System Power on

1.) If the Docking Cart is like the following figure A, connect the power cord between Docking module and Cart.

If the Docking Cart is like the following figure B, go to step 2.

Figure 3-18 Connect power cord between Docking module and Cart

Chapter 3 System Setup 3-21

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-5-1-2 System Power on (cont’d)

2.) Plug the AC output connector into the rear panel of Docking Cart. Plug the AC power cord into a grounded, protective earth outlet.

Figure 3-19 Connect AC power cord

For Docking Station, plug the AC output connector into the AC power input socket, plug the other end into a grounded, protective earth outlet.

3-5-1-3 Turn on the system

Press the Power On/Off switch on top of the system once.

Figure 3-20 Power On/Off Switch

NOTE: The system can be used immediately after mounting to Docking Station/Cart.

NOTE: Docking Station/Cart charges battery if it is plugged into power source.

NOTE: It’s better to disconnect all the peripherals before the system is powered on, including SD card

and USB memory stick.

NOTE: Once the system is failed to boot up with SD card inserted, please remove the SD card from

the system, back up the data, format the SD card and restore the data to it.

3-22 Section 3-5 - Completing the Installation

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-5-1-4 Attach the stylus to system

There is a stylus for touch panel operation. To attach the stylus to system:

1.) Thread the looped end of the stylus strap through the stylus strap post on side of the Venue 40.

Figure 3-21 Connect stylus to Venue 40

Chapter 3 System Setup 3-23

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-5-1-4 Attach the stylus to system (cont’d)

2.) Thread the stylus through the loop.

Figure 3-22 Thread the loop

3.) Place the stylus on the top of the system or in the hole of probe holder.

Figure 3-23 Stylus attached to Venue 40

3-24 Section 3-5 - Completing the Installation

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-5-2 Power 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.

3-5-2-1 Back-end Processor Power Down

To power down the system:

1.) Press the Power On/Off switch on top of the system once.

2.) The System-Exit window is displayed.

Figure 3-24 System Exit Window

3.) The system will shut down in 30 seconds automatically. Use the stylus to select Shutdown to shut down the system or Cancel to cancel the process.

4.) The shutdown process takes a few seconds and is complete when the power status LED is turned off.

5.) Disconnect the probes.Clean or disinfect all probes as necessary. Store them in their shipping cases to avoid damage.

Chapter 3 System Setup 3-25

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-5-3 Transducer Connection

To connect the probe:

1.) Place the probe's carrying case on a stable surface and open the case.

2.) Carefully remove the probe and unwrap the probe cable.

3.) DO NOT allow the probe head to hang free. Impact to the probe head could result in irreparable damage.

4.) Plug the probe connector into the probe port on right side of Venue 40 with the label facing the front.

Figure 3-25 Connect the probe

5.) Carefully position the probe cord so it is free to move and is not resting on the floor.

NOTE: It is not necessary to turn OFF power

3-26 Section 3-5 - Completing the Installation

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-5-3 Transducer Connection (cont’d)

To disconnect the probe:

1.) Press the locking lever with blue mark to pop up the connector.

Figure 3-26 Pop up the locking lever

2.) Pull the probe and connector straight out of the probe port.

Figure 3-27 Disconnect the probe

NOTE: Please do not drag the probe cable in order to avoid cable damage.

Chapter 3 System Setup 3-27

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

Section 3-6 System Configuration

3-6-1 System Specifications

3-6-1-1 Physical Dimensions

The physical dimensions of the Venue 40 console are summarized in Figure 3-28 on page 3-28 .

Table 3-10 Physical Dimensions of Venue 40

Height Width Depth Unit

282 274 56 mm

11.1 10.8 2.2 inches

NOTE: Length is in mm

Figure 3-28 Overall Dimensions

3-28 Section 3-6 - System Configuration

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-6-2 Electrical Specifications

Table 3-11 Electrical Specifications for Venue 40

Voltage Tolerances Current Frequency

100-240 VAC +/-10% 1.6A (max) 50/60Hz

3-6-3 Approved on-board peripherals

Table 3-12 Approved on-board peripherals

Device Manufacturer Model Interface

B/W Printer SONY UP-D897 USB

USB Memory SanDisk SanDisk 4G USB

High Capacity SD Card KINGSTON KINGSTON 4G/8G

SD Card Transcend Transcend Class 6 SD Card 8G

SD Card Reader Transcend Transcend P5 USB

Wireless Network Card Edimax Edimax USB

Footswitch Steute MKF 2 1S/1S -MED HID GP26 USB

Note: Wireless Network Card is not available on software version R1.x.x. Note: Footswitch is not available on software version R1.x.x and R2.x.x.

Chapter 3 System Setup 3-29

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-6-4 Connecting Cables

WARNINGWARNING

Equipment damage possibility. Be sure to use the following recommended connecting cables to connect recording devices and a network with Venue 40 console.

Table 3-13 List of Connecting Cables

Name Part No. Figure NOTE

Printer USB Cable 5317527 For USB Printer

Docking USB Cable 5329083 For miniB USB port

3-30 Section 3-6 - System Configuration

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-6-5 Peripherals/Accessories Connector Panel

Venue 40 peripherals and accessories can be properly connected using the side connector panel.

3-6-5-1 Docking Station/Docking Cart Connector Panel

Located on the two sides of Docking Station/Docking Cart are input and output connectors.

Figure 3-29 Docking Station/Docking Cart Connector Panel

1.) Probe holder

2.) LED indicator: indicating AC Power, when there is AC Power, it is lit. Color: Green.

3.) LED indicator: indicating battery charging, when the battery is being charged, it is lit. Color: Green.

4.) AC power input socket

5.) MiniB USB port

6.) USB 2.0 port

7.) DVI port

8.) LAN port (not available for R1.x.x)

NOTE: Each outer (case) ground line of peripheral/accessory connectors are protectively grounded.

Signal ground lines are not isolated.

Chapter 3 System Setup 3-31

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-6-5-2 This section indicates the pin assignment for each connector.

1. Pin Assignment of AC input

Table 3-14 Pin Assignments of AC input

Pin No. Signal Pin No. Signal

1+20V3GND

2+20V4GND

2. Pin Assignment of USB

Table 3-15 Pin assignment of USB1-A

Pin No. Signal Pin No. Signal

1 +5VDC 3 DATA+

2 DATA- 4 GND

Table 3-16 Pin assignment of USBminiB

Pin No. Signal Pin No. Signal

1 +5VDC 3 DATA+

2 DATA- 4 GND

3. Pin assignment of DVI port

Table 3-17 Pin Assignments of DVI

Pin No. Signal Pin No. Signal

1 DATA2- 13 DATA3+

2DATA2+14+5VDC

3GND15GND

4 DATA4- 16 DETECT

5 DATA4+ 17 DATA0_

6 DDC_CLOCK 18 DATA0+

7 DDC_DATA 19 GND

8 NC 20 DATA5-

9 DATA1- 21 DATA5+

10 DATA1+ 22 GND

11 GND 23 CLOCK+

12 DATA3- 24 CLOCK_

3-32 Section 3-6 - System Configuration

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-6-5-3 Connect peripherals

1.) Insert SD Card to system.

Pull the SD Socket cover towards the back of the Venue 40 to make it easy to open. Open the SD Card Socket cover.

Figure 3-30 Open SD Card Socket cover

Insert the SD Card into the SD Card Socket on top of the system with the labeled side facing the front of the Venue 40

Figure 3-31 Insert SD Card to system

Chapter 3 System Setup 3-33

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-6-5-3 Connect peripherals (cont’d)

2.) Connect B/W printer to the system.

B/W Printer can be properly connected to the USB port of the Docking Station/Cart.

Figure 3-32 Connect B/W printer

3.) Connect USB Memory to the system. USB Memory stick can be properly connected using USB Port on the Docking Station/Cart.

Figure 3-33 Connect USB Memory Stick

3-34 Section 3-6 - System Configuration

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-6-5-3 Connect peripherals (cont’d)

4.) Connect external LCD to the DVI port of Docking Station/Docking Cart.

Figure 3-34 Connect external LCD

5.) Connect the Wireless Network Card to the USB port of the Docking Station/Cart.

Figure 3-35 Connect the Wireless Network Card

Chapter 3 System Setup 3-35

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-6-5-3 Connect peripherals (cont’d)

6.) Connect the footswitch to the USB port of the Docking Station/Cart.

Figure 3-1. Connect the footswitch

7.) Connect the 3-probe port box to the Docking Cart.

NOTE: 3-probe Port Box is not available in China, Japan or Korea.

a.) Remove any storage trays from the front of the Docking Cart. Mount the 3 probe port box on

the Docking Cart.

NOTE: Be sure to fully inset the grooves into the top side slides.

NOTE: The 3-probe Port Box shall be mounted to the front of the docking cart.

3-36 Section 3-6 - System Configuration

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-6-5-3 Connect peripherals (cont’d)

b.) Connect the 3-probe Port Box to the Venue 40

c.) Press the Cable Hook and Put the Cable into the Hook

NOTE: Pull the cable hook if it does not pop out completely.

d.) Connect the Probe Holders to the Docking Cart

Chapter 3 System Setup 3-37

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-6-5-3 Connect peripherals (cont’d)

e.) Connect the E8CS-SC Probe Holder and Gel Holder to the Probe Holders

f.) Connect the Probes to the 3-probe Port Box

g.) Mount the Printer Shelf to the Docking Cart

Attach the basket to the printer shelf and mount the printer shelf to the docking cart.

NOTE: Be sure to fully inset the grooves into the second side slides.

NOTE: The printer shelf shall be mounted to the back of the docking cart.

3-38 Section 3-6 - System Configuration

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-6-5-3 Connect peripherals (cont’d)

h.) Choose Probes

Power on the system and choose the appropriate probe from the pull-down menu.

NOTE: The order of the probes shown on the screen is the same as that of the probes connected to

the 3-probe Port Box.

If “No Probe” is shown in the pull-down menu, the following may have happened.

1.) No probe is connected to the relevant 3-probe box port.

2.) The probe may not be fully inserted into the slot. Recheck the connection to insure proper connection.

3.) The probe is connected to the 3-probe box port, but the software option key for this probe hasn’t been activated. If this is the case, the operator may need to contact the local GE representative and place an order for the additional software option. See “Add new software

option keys” in Basic User Manual for more information.

NOTE: 3-probe Port Box is only available for Venue 40 software R3.2.0 and above.

Chapter 3 System Setup 3-39

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

3-6-6 Available Probes

For different software versions, please see in specification in the Venue 40 Basic User Manual for Probes and intended use.

Table 3-18 List of Probes for Venue 40

Probe Name Material of Headshell Area of Using TYPE Catalog Number Part Number

ABDOMINAL, FETAL/OB, ADULT

CEPHALIC, CARDIAC, THORACIC/

3S-SC VALOX

12L-SC NORYL

4C-SC* NORYL

L8-18i-SC* VALOX

E8CS-SC* VALOX

PLEURAL, INTRAOPERATIVE, TISSUE

BIOPSY/FLUID DRAINAGE,

TRANSCRANIAL

ABDOMINAL, PERIPHERAL VASCULAR,

PEDIATRIC, SMALL ORGAN, NEONATAL

CEPHALIC, CONVENTIONAL

MUSCULOSKELETAL, SUPERFICIAL

MUSCULOSKELETAL, THORACIC/

PLEURAL, INTRAOPERATIVE, TISSUE

BIOPSY/FLUID DRAINAGE, VASCULAR

ACCESS, NONVASCULAR

ABDOMINAL, FETAL/OB, CONVENTIONAL

MUSCULOSKELETAL, THORACIC/

PLEURAL, INTROPERATIVE, TISSUE

BIOPSY/FLUID DRAINAGE

PERIPHERAL VASCULAR, SMALL

ORGAN, CONVENTIONAL

MUSCULOSKELETAL, SUPERFICIAL

SKELETAL, NONVASCULAR

FETAL/OB, GYN, UROLOGY,

TRANSVAGINAL

SECTOR H40452LD 5309652

LINEAR H40452LB 5304023

CONVEX H40452LM 5337604

LINEAR H40452LZ 5384872

CONVEX H40462LL 5413888

*Note: 4C-SC is not available on software version R1.0.x. *Note: L8-18i-SC is not available on software version R1.x.x.

*Note: E8CS-SC is not available on software version R1.x.x and R2.x.x.

Section 3-7 Software/Option Configuration

Refer to the Venue 40 Basic User Manual, Chapter 4, Customizing Your System for information on configuring items like Hospital, Department, Language, Date and Time

For information on configuring Software Options, Refer to the Venue 40 Basic User Manual, Chapter 4, Customizing Your System.

3-40 Section 3-7 - Software/Option Configuration

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

Section 3-8 Loading Base Image Software

This information has been moved, please refer to:

Section 8-3 "Loading Base Image Software" on page 8-7

Section 3-9 Software version check-out

1.) Power on Venue 40 scanner and wait until system booting to main screen.

2.) Click Patient using the stylus, press Utility.

3.) Select About in the left column.

4.) Check whether "Software version" is the right version for use.

Figure 3-36 Software version

Chapter 3 System Setup 3-41

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

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.

3-10-1 Product Locator Installation

NOTE: The Product Locator Installation Card shown may not be same as the provided Product Locator

card.

Figure 3-37 Product Locator Installation Card

3-10-2 User Manual(s)

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.

3-42 Section 3-10 - Paperwork

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IRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

Chapter 4 Functional Checks

Section 4-1 Overview

4-1-1 Purpose for Chapter 4

This chapter provides procedures for quickly checking major functions of the Venue 40 console, diagnostics by using the built-in service software, and power supply adjustments.

Section Description Page Number

4-1

4-2

4-3

4-4

4-5

Table 4-19 Contents in chapter 4

Section 4-2 Required Equipment

To perform these tests, you'll need any of the sector or linear transducers.

(normally you should check all the transducers used on the system)

Overview

Required Equipment

General Procedure

Software Configuration Checks

Peripheral Checks

4-1

4-2

4-18

Chapter 4 Functional Checks 4-1

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

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.

4-3-1 Power On/Boot Up

Press Power On/Off key once, the System starts.

4-3-2 Power 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.

To power down the system:

1.) Slightly press the Power On/Off switch once.

2.) The System-Exit window is displayed.

Figure 4-1 System Exit Window

3.) Select OK using the stylus.

4.) The shutdown process takes 15 seconds and the power off sequence is complete when the power status LED is turned off.

5.) Disconnect the probes. Clean or disinfect all probes as necessary. Store them in their shipping

cases to avoid damage.

CAUTION

DO NOT transport the unit until after the power off sequence has been completed. Failure to do so may result in corrupted patient files.

4-3-3 Adjusting the Display Monitor

Please refer to Section 6-2 "Monitor Adjustments" on page 6-2.

4-2 Section 4-3 - General Procedure

GE HEALTHCARE D

IRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

4-3-4 System Features

4-3-4-1 Control Panel

Figure 4-2 Control Panel Tour

1. Freeze

2. Save

3. Gain

4. Depth

5. Function keys located at the bottom of the system, vary according to different operation modes.

NOTE: There is only one depth key on R1.x.x system, except R1.1.1 (Global (CHN)).

Chapter 4 Functional Checks 4-3

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

4-3-4-2 Monitor Display

Figure 4-3 Monitor Display Tour

Table 4-20 Monitor Display Features

1. Hospital/Institute Name 12. Gain

2. Date and Time 13. Acoustic output readout

3. Function selection icons 14. Network status (R2.x.x, R3.x.x only)

4. Gray/Color bar 15. Battery/AC power status

5. Image 16. Storage device status

6. Measurements result window 17. Probe and application

7. Package name 18. Patient ID

8. Controls 19. Patient Name

9. Depth scale 20. Gestational age (R2.1.x, R3.x.x only)

10. Annotation 21. Center line mark (R3.x.x only)

11. Measurement calliper

4-4 Section 4-3 - General Procedure

GE HEALTHCARE D

IRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

4-3-5 B Mode Checks

4-3-5-1 Preparations

1.) Connect one of the probes listed in 3-6-6 "Available Probes" on page 3-40 to the System.

2.) Turn ON the scanner (if it isn’t turned on already)

Figure 4-4 B Mode Screen Picture Example

Chapter 4 Functional Checks 4-5

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

4-3-5-2 B Mode Control Panel Controls

Table 4-21 B Mode Control Panel Controls (on the right side of the Venue 40)

Step Task Expected Result(s)

Switch to B mode B Mode Starts

Adjust the field of view. Increasing the depth

Adjust Depth

may view larger/deeper structures rates, and decreasing the depth may view near the skin line. Press Depth to adjust Depth. Depth displays on the monitor in cm.

Adjust Gain

4-3-5-3 B Mode Function Controls

Table 4-22 B Mode Function Controls

Item Task Expected Result(s)

Press Patient Go into patient screen

Press PDI (only for R1.x.x and R2.x.x) Switch to PDI mode

Press Auto Auto tissue optimization

Press Guide Show needle guides

Press Mode (only for R3.x.x) Switch to mode selection menu

Press B-Steer+ (only for linear probes on

software version R3.x.x)

Controls the amount of echo information displayed in an image. Press Gain to adjust.

Press to slant the B-Mode linear image left or right to get more information without moving the probe.

4-6 Section 4-3 - General Procedure

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IRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

4-3-6 Color Flow Mode Checks

4-3-6-1 Preparations

1.) Connect one of the probes listed in 3-6-6 "Available Probes" on page 3-40 to the System.

2.) Turn ON the scanner (if it isn’t turned on already).

Figure 4-5 CFM Mode Screen Picture Example

Chapter 4 Functional Checks 4-7

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

4-3-6-2 Color Flow Mode Control Panel Controls

Table 4-23 Color Flow Mode Control Panel Controls (on the right side of the Venue 40)

Step Task Expected Result(s)

Switch to PDI mode PDI Mode Starts

Amplifies the overall strength of the echoes

Adjust Gain

processed in the Color Flow window. Turn the Gain dial (CFM Mode key) to the left/right to increase/decrease Gain.

4-3-6-3 Color Flow Mode Function Controls

Table 4-24 Color Flow Mode Function Controls

Item Task Expected Result(s)

Press B Switch to B mode

Press ROI Pos Adjust ROI position

Press Steer

Press PRF H/M/L

Slant the image to left/center/right

Increases/decreases the PRF on the color bar

Press Invert

NOTE: ROI Pos is not available on software version R1.x.x, except R1.1.1 (Global (CHN)).

Lets you view blood flow from a different perspective

4-8 Section 4-3 - General Procedure

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IRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

4-3-7 Power Doppler Imaging (PDI) Mode Checks

4-3-7-1 Preparations

1.) Connect one of the probes listed in 3-6-6 "Available Probes" on page 3-40 to the System.

2.) Turn ON the scanner (if it isn’t turned on already).

Figure 4-6 Power Doppler Mode Screen Picture Example

Chapter 4 Functional Checks 4-9

GE HEALTHCARE DIRECTION 5314293-100, REVISION 19 VENUE 40 BASIC SERVICE MANUAL

4-3-7-2 PDI Control Panel Controls

Table 4-25 PDI Mode Control Panel Controls (on the right side of the Venue 40)

Step Task Expected Result(s)

Switch to CF mode CF Mode Starts

Amplifies the overall strength of the echoes

Adjust Gain

processed in the Color Flow window. Turn the Gain dial (PW Mode key) to the left/right to increase/decrease Gain.

4-3-7-3 PDI Mode Function Controls

Table 4-26 PDI Mode Function Controls

Item Task Expected Result(s)

Press B Switch to B mode

Press ROI Pos Adjust ROI position

Press Steer

Press PRF H

Slant the image to left/center/right

Increases/decreases the PRF on the color bar

4-10 Section 4-3 - General Procedure

General Electric Venue 40 Basic Service Manual_SM_5314293-100_19 Venue 40 Basic Service Manual Part Number: 5314293-100 Revision: 19

Specifications and Main Features

Frequently Asked Questions

User Manual

Important Precautions

Section 1-1 Overview

1-1-1 Purpose of Chapter 1

1-1-2 Chapter Contents

1-1-3 Purpose of Service Manual

1-1-4 Typical Users of the Service Manual

1-1-5 Venue 40 Models Covered by this Manual

1-1-6 Purpose of Operator Manual(s)

Section 1-2 Important Conventions

1-2-1 Conventions Used in Book

1-2-2 Standard Hazard Icons

1-2-3 Product Icons

Section 1-3 Safety Considerations

1-3-1 Introduction

1-3-2 Human Safety

1-3-3 Mechanical Safety

1-3-4 Electrical Safety

1-3-5 Labels Locations

1-3-6 Battery Safety

1-3-7 Dangerous Procedure Warnings

Section 1-4 Lockout/Tagout (LOTO) requirements

Section 1-5 Returning/Shipping Probes and Repair Parts

Section 1-6 EMC, EMI, and ESD

1-6-1 Electromagnetic Compatibility (EMC)

1-6-2 CE Compliance

1-6-3 Electrostatic Discharge (ESD) Prevention

Section 1-7 Customer Assistance

1-7-1 Contact Information

1-7-2 System Manufacturer

Section 2-1 Overview

2-1-1 Purpose of this chapter 2

2-1-2 Chapter Contents

Section 2-2 General Console Requirements

2-2-1 Console Environmental Requirements

2-2-1-1 Lighting

2-2-2 Electrical Requirements

2-2-2-1 Venue 40 Power Requirements

2-2-2-2 Inrush Current

2-2-2-3 Site Circuit Breaker

2-2-2-4 Site Power Outlets

2-2-2-5 Unit Power Plug

2-2-3 EMI Limitations

2-2-4 Scan Probe Environmental Requirements

Section 2-3 Facility Needs

2-3-1 Recommended Ultrasound Room Layout

2-3-1-1 Purchaser Responsibilities

2-3-2 Required Features

2-3-3 Desirable Features

2-3-3-1 Recommended and Alternate Ultrasound Room Layout

2-3-4 Networking Pre-installation Requirements

2-3-4-1 Stand Alone Scanner (without Network Connection)

2-3-4-2 Scanner Connected to Hospital’s Network

2-3-4-3 Purpose of DICOM Network Function

2-3-4-4 DICOM Option Pre-installation Requirements

Section 3-1 Overview

3-1-1 Purpose of Chapter 3

3-1-2 Average Setup Time

3-1-3 Installation Warnings

3-1-4 Safety Reminders

Section 3-2 Receiving and Unpacking the Equipment

3-2-1 Unpacking Venue 40

3-2-2 Unpacking Docking Station

3-2-3 Unpacking Docking Cart

3-2-4 Unpacking 3-probe Port Box

3-2-5 Moving into Position

Section 3-3 Packing the Equipment

Section 3-4 Preparing for Installation

3-4-1 Verify Customer Order

3-4-2 Physical Inspection

3-4-2-1 System Voltage Settings

3-4-3 EMI Protection

Section 3-5 Completing the Installation

3-5-1 Power On / Boot Up

3-5-1-1 Mount the system to Docking Station/Docking Cart

3-5-1-2 System Power on

3-5-1-3 Turn on the system