GE LOGIQ e, LOGIQ e Vet, LOGIQ i, Vivid e Service Manual

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GE Healthcare

LOGIQ e/LOGIQ e Vet/LOGIQ i/ Vivid e

Basic Service Manual

Part Number: 5370626-100

Revision: 7

GE HEALTHCARE

WARNING

(EN)

AVERTISSEMENT

(FR)

WARNUNG

(DE)

DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E 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.

• 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.

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 GERäT ZU REPARIEREN, BEVOR DIESES KUNDENDIENST-HANDBUCH NICHT ZU RATE GEZOGEN UND VERSTANDEN WURDE.

• WIRD DIESE WARNUNG NICHT BEACHTET, SO KANN ES ZU VERLETZUNGEN DES KUNDENDIENSTTECHNIKERS, DES BEDIENERS ODER DES PATIENTEN DURCH ELEKTRISCHE SCHLäGE, MECHANISCHE ODER SONSTIGE GEFAHREN KOMMEN.

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AVISO

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ATENÇÃO

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(PT-pt)

AVISO

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DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

ESTE MANUAL DE SERVICIO SóLO EXISTE EN INGLéS.

• SI ALGúN PROVEEDOR DE SERVICIOS AJENO A GEHC SOLICITA UN IDIOMA QUE NO SEA EL INGLéS, ES RESPONSABILIDAD DEL CLIENTE OFRECER UN SERVICIO DE TRADUCCIóN.

• NO SE DEBERá DAR SERVICIO TéCNICO AL EQUIPO, SIN HABER CONSULTADO Y COMPRENDIDO ESTE MANUAL DE SERVICIO.

• LA NO OBSERVANCIA DEL PRESENTE AVISO PUEDE DAR LUGAR A QUE EL PROVEEDOR DE SERVICIOS, EL OPERADOR O EL PACIENTE SUFRAN LESIONES PROVOCADAS POR CAUSAS ELéCTRICAS, MECáNICAS O DE OTRA NATURALEZA.

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

• SE QUALQUER OUTRO SERVIçO DE ASSISTêNCIA TéCNICA, QUE NãO A GEHC, SOLICITAR ESTES MANUAIS NOUTRO IDIOMA, é DA RESPONSABILIDADE DO CLIENTE FORNECER OS SERVIçOS DE TRADUçãO.

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

• O NãO CUMPRIMENTO DESTE AVISO PODE POR EM PERIGO A SEGURANçA DO TéCNICO, OPERADOR OU PACIENTE DEVIDO A‘ CHOQUES ELéTRICOS, MECâNICOS OU OUTROS.

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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HOIATUS

(ET)

VAROITUS

(FI)

ΠΡΟΕΙΔΟΠΟΙΗΣΗ

(EL)

FIGYELMEZTETÉS

(HU)

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KÄESOLEV TEENINDUSJUHEND ON SAADAVAL AINULT INGLISE KEELES.

• KUI KLIENDITEENINDUSE OSUTAJA NõUAB JUHENDIT INGLISE KEELEST ERINEVAS KEELES, VASTUTAB KLIENT TõLKETEENUSE OSUTAMISE EEST.

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

• KäESOLEVA HOIATUSE EIRAMINE VõIB PõHJUSTADA TEENUSEOSUTAJA, OPERAATORI VõI PATSIENDI VIGASTAMIST ELEKTRILööGI, MEHAANILISE VõI MUU OHU TAGAJäRJEL.

TÄMÄ HUOLTO-OHJE ON SAATAVILLA VAIN ENGLANNIKSI.

• JOS ASIAKKAAN PALVELUNTARJOAJA VAATII MUUTA KUIN ENGLANNINKIELISTä MATERIAALIA, TARVITTAVAN Kää NNöKSEN HANKKIMINEN ON ASIAKKAAN VASTUULLA.

• äLä YRITä KORJATA LAITTEISTOA ENNEN KUIN OLET VARMASTI LUKENUT JA YMMäRTäNYT TäMäN HUOLTO-OHJEEN.

• MIKäLI TäTä VAROITUSTA EI NOUDATETA, SEURAUKSENA VOI OLLA PALVELUNTARJOAJAN, LAITTEISTON KäYTTäJäN TAI POTILAAN VAHINGOITTUMINEN SäHKöISKUN, MEKAANISEN VIAN TAI MUUN VAARATILANTEEN VUOKSI.

ΤΟ ΠΑΡΟΝ ΕΓΧΕΙΡΙΔΙΟ ΣΕΡΒΙΣ ΔΙΑΤΙΘΕΤΑΙ ΣΤΑ ΑΓΓΛΙΚΑ ΜΟΝΟ.

• ΕΑΝ ΤΟ ΑΤΟΜΟ ΠΑΡΟΧΗΣ ΣΕΡΒΙΣ ΕΝΟΣ ΠΕΛΑΤΗ ΑΠΑΙΤΕΙ ΤΟ ΠΑΡΟΝ

ΕΓΧΕΙΡΙΔΙΟ ΣΕ ΓΛΩΣΣΑ ΕΚΤΟΣ ΤΩΝ ΑΓΓΛΙΚΩΝ, ΑΠΟΤΕΛΕΙ ΕΥΘΥΝΗ ΤΟΥ ΠΕΛΑΤΗ ΝΑ ΠΑΡΕΧΕΙ ΥΠΗΡΕΣΙΕΣ ΜΕΤΑΦΡΑΣΗΣ.

• ΜΗΝ ΕΠΙΧΕΙΡΗΣΕΤΕ ΤΗΝ ΕΚΤΕΛΕΣΗ ΕΡΓΑΣΙΩΝ ΣΕΡΒΙΣ ΣΤΟΝ ΕΞΟΠΛΙΣΜΟ ΕΚΤΟΣ ΕΑΝ ΕΧΕΤΕ ΣΥΜΒΟΥΛΕΥΤΕ

Ι ΚΑΙ ΕΧΕΤΕ ΚΑΤΑΝΟΗΣΕΙ ΤΟ ΠΑΡΟΝ

ΕΓΧΕΙΡΙΔΙΟ ΣΕΡΒΙΣ.

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

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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ADVARSEL

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ÞESSI ÞJÓNUSTUHANDBÓK ER EINGÖNGU FÁANLEG Á ENSKU.

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

• REYNIÐ EKKI AÐ ÞJÓNUSTA TÆKIÐ NEMA EFTIR AÐ HAFA SKOÐAÐ OG SKILIÐ ÞESSA ÞJÓNUSTUHANDBÓK.

• EF EKKI ER FARIÐ AÐ ÞESSARI VIÐVÖRUN GETUR ÞAÐ VALDIÐ MEIÐSLUM ÞJÓNUSTUVEITANDA, STJÓRNANDA EÐA SJÚKLINGS VEGNA RAFLOSTS, VÉLRÆNNAR EÐA ANNARRAR HÆTTU.

TENTO SERVISNÍ NÁVOD EXISTUJE POUZE V ANGLICKéM JAZYCE.

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

• NEPROVÁDĚJTE úDRŽBU TOHOTO ZAř íZENí, ANIŽ BYSTE SI Př Eč ETLI TENTO SERVISNÍ NÁVOD A POCHOPILI JEHO OBSAH.

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

DENNE SERVICEMANUAL FINDES KUN PÅ ENGELSK.

• HVIS EN KUNDES TEKNIKER HAR BRUG FOR ET ANDET SPROG END ENGELSK, ER DET KUNDENS ANSVAR AT SØRGE FOR OVERSÆTTELSE.

• FORSØG IKKE AT SERVICERE UDSTYRET MEDMINDRE DENNE SERVICEMANUAL ER BLEVET LÆST OG FORSTÅET.

• MANGLENDE OVERHOLDELSE AF DENNE ADVARSEL KAN MEDFŘRE SKADE PĹ GRUND AF ELEKTRISK, MEKANISK ELLER ANDEN FARE FOR TEKNIKEREN, OPERATŘREN 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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ĮSPĖJIMAS

(LT)

ADVARSEL

(NO)

OSTRZEŻENIE

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DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E 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.

• 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.

•NEMĖGINKITE ATLIKTI ĮRANGOS TECHNINĖS PRIEŽIŪROS DARBŲ, NEBENT VADOVAUTUMĖTĖS ŠIUO EKSPLOATAVIMO VADOVU IR JĮ SUPRASTUMĖTE

• NEPAISANT ŠIO PERSPĖJIMO, PASLAUGŲ TEIKĖJAS, OPERATORIUS AR PACIENTAS GALI BŪTI SUŽEISTAS DĖL ELEKTROS SMŪGIO, MEC

HANINIŲ AR

KITŲ PAVOJŲ.

DEN

NE 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 PRóBOWAć SERWISOWAć NINIEJSZEGO SPRZęTU BEZ UPRZEDNIEGO ZAPOZNANIA SIę Z PODRęCZNIKIEM SERWISOWYM.

• NIEZASTOSOWANIE SIę DO TEGO OSTRZEŻENIA MOżE GROZIć OBRAŻENIAMI CIAłA SERWISANTA, OPERATORA LUB PACJENTA W WYNIKU PORAŻENIA PRĄDEM, URAZU MECHANICZNEGO LUB INNEGO RODZAJU ZAGROŻEń.

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ОСТОРОЖНО!

(RU) (BG)

ПРЕДУПРЕЖДЕНИЕ

UPOZORENJE

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DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E 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.

• 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 рук о во дс тво по обслуживанию ПРЕДОСТАВЛЯЕТСЯ только на английском Яз ыке.

• Ес ли сервисноМУ ПЕРСОНАЛУ клиента необходимо руко во дс тво не на английском ЯЗЫКЕ, клиенту следует самостоЯтельно ОБЕСПЕЧИТЬ перевод.

• ПЕРЕД ОБСЛУЖИВАНИЕМ ОБОРУДОВАНИЯ ОБЯЗАТЕЛЬНО ОБРАТИТЕСЬ К ДАННОМУ РУКОВОДСТВУ И П

ОЙМИТЕ 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.

ТОВА СЕРВИЗНО РЪКОВОДСТВО Е НАЛИЧНО САМО НА АНГЛИЙСКИ ЕЗИК.

• АКО ДОСТАВЧИКЪТ НА СЕРВИЗНИ УСЛУГИ НА КЛИЕНТ СЕ НУЖДАЕ ОТ ЕЗ

ИК, РА

ЗЛИЧЕН 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 ВСЛЕДСТВ

ИЕНА 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.

• 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.

• 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.

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 MôŽE 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.

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GE HEALTHCARE

DİKKAT

(TR)

(JA)

Traditional

Chinese

DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E 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.

•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.

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GE HEALTHCARE

(ZH-CN)

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DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

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GE HEALTHCARE

DANGER

WARNINGWARNING

DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E 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 co nnectio ns b etween p ieces o f electrical equipment, calibrations and testing shall be perfor med 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,

GE Medical Systems (China) Co., Ltd. No.19 Changjiang Road WuXi National Hi-Tech Development Zone Jiangsu, P.R China 214028 TEL: +86 510 85225888; FAX: +86 510 85226688

GE Healthcare employees should contact the product's Lead Service Integrator (LSI) to rep or t se rvice documentation issues. DO NOT use TrackWise for this purpose. The LSI will then use the internal problem reporting tool to communicate these issues to the writer.

SERVICE SAFETY CONSIDERATIONS

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

Use all Personal Protection Equipment (PPE) such as gloves, safety shoes, safety glasses, and kneeling pad, to reduce the risk of injury.

For a complete review of all safety requirements, see the Chapter 1, Safety Considerations section in the Service Manual.

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GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E 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 Healthcare.

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

TRADEMARKS

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

COPYRIGHTS

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GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

Revision History

Revision Date Reason for change

1 23, Qct. 2009 Initial Release 2 13, May 2010 Update for Software update and adding new probes 3 29, June 2010 Update to add Isolation Cart enhanced Version 4 30, November 2010 Update LOGIQ e Spare Parts and add USA CKD address 5 25, April 2011 Add Vivid e R6.x.x 6 25, Sep 2011 Update for LOGIQ e Vet R6.x.x 7 5, Oct 2011 Update for LOGIQ e R7.x.x

List of Effected Pages (LOEP)

Pages Revision Pages Revision Pages Revision

Title Page 7 3-1 to 3-32 7 8-1 to 8-10 7

Warnings i to -xii 7 4-1 to 4-38 7 9-1 to 9-32 7

TOC 7 5-1 to 5-20 7 10-1 to 10-21 7 1-1 to 1-20 7 6-1 to 6-2 7 Index 7 2-1 to 2-10 7 7-1 to 7-28 7 Back Cover N/A

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GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC 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 Basic Service Manual . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 2

LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e Models Covered by this Manual . . 1 - 3

Purpose of Operator Manual(s) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 5

Important Conventions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 5

Conventions Used in Book . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 5

Standard Hazard Icons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 6

Product Icons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 7

Safety Considerations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 11

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 11

Human Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 11

Mechanical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 11

Electrical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 12

Label Location . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 13

Battery Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 14

Dangerous Procedure Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 16

Lockout/Tagout (LOTO) requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 16

Returning/Shipping Probes and Repair Parts . . . . . . . . . . . . . . . . . . . . . . . 1 - 17

EMC, EMI, and ESD . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 18

Electromagnetic Compatibility (EMC) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 18

CE Compliance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 18

Electrostatic Discharge (ESD) Prevention . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 18

Customer Assistance. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 19

Contact Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 19

System Manufacturer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 20

Factory Sites . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 20

1 Table of Contents

GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

CHAPTER 2

Site preparations

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

Table of Contents 2

GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

CHAPTER 3

System Setup

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

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

Average Installation Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 2

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

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

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

Moving into Position . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 7

Packing the Equipment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 7

Preparing for Installation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 8

Verify Customer Order . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 8

Physical Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 8

EMI Protection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 8

Completing the Installation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 9

Power On / Boot Up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 9

Power Off/ Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 10

Transducer Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 11

System Configuration. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 12

System Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 12

Electrical Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 12

Approved peripherals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 13

Connecting Cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 14

Peripherals/Accessories Connector Panel . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 14

Available Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 25

Software/Option Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 27

Connectivity Installation Worksheet . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 28

Loading Base Image Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 29

Software Version check out . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 30

Functional Check-out . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 30

Paperwork . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 31

Product Locator Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 31

User Manual(s) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 31

Table of Contents 3

GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC 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 - 3

Archiving and Loading Presets . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 5

Adjusting the Display Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 6

Lockout/Tagout (LOTO) requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 6

System Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 7

B Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 10

M Mode Controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 13

Color Flow Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 16

Doppler Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 20

CWD Functional Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 24

Basic Measurements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 25

Probe/Connectors Usage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 25

Using Cine . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 26

Image Management (QG) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 27

Backup and Restore Database, Preset Configurations and Images . . . . . 4 - 28

Software Configuration Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 37

Peripheral Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 37

Table of Contents 4

GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

CHAPTER 5

Components and Functions (Theory)

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

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

Block Diagram . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 2

General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 3

External I/O . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 4

Peripherals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 4

Wiring . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 5

Power Diagrams. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 6

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 6

AC Power . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 6

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

Air Flow Distribution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 8

Fans . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 9

Common Service Platform . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 10

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 10

Global Service User Interface (GSUI) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 10

Service Home Page . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 12

Error Logs Tab . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 13

Diagnostics . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 17

Image Quality . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 18

Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 18

Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 19

Utilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 19

Replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 20

PM . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 20

Table of Contents 5

GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

CHAPTER 6

Service Adjustments

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

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

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

Adjustments Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 2

Table of Contents 6

GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

CHAPTER 7

Diagnostics/Troubleshooting

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

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

Gathering Trouble Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 2

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 2

Collect Vital System Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 2

Collect a Trouble Image with Logs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 3

USB Quick Save. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 4

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 4

Check and Record the P3 Key Function . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 4

Setting the P3 Key to USB Quick Save . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 5

Screen Captures. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 6

Check and Record the P1 Key Function . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 6

Setting the P1 Key to Screen Capture . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 6

Capturing a Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 6

Reset the P1 Key to Customer’s Functionality . . . . . . . . . . . . . . . . . . . . . . 7 - 8

Global Service User Interface (GSUI) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 9

Enter global service user interface . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 9

Active Diagnostic Function . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 10

Control Frame . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 10

Common Diagnostics . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 12

Utilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 12

PC Diagnostics (Non-Interactive Tests) . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 13

PC Diagnostics (Interactive Tests) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 14

Restart the system after diagnostics . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 14

Network and Insite II Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 15

Network Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 15

Insite II Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 19

Insite II Configuration (For LOGIQ e R6.x.x) . . . . . . . . . . . . . . . . . . . . . . . 7 - 24

Table of Contents 7

GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

CHAPTER 8

Replacement Procedures

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

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

Disassembly/Re-assembly of LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e . . . . . . . . . 8 - 1

Warning and Caution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 1

Handle Assy (FRU No. 313) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 2

Loading Base Image Software. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 4

Checks after FRU replacement (Debrief Guidelines). . . . . . . . . . . . . . . . . . . . . . . . 8 - 9

8 Table of Contents

GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E 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

Equipment Models Covered in this Chapter . . . . . . . . . . . . . . . . . . . . . . . . 9 - 2

Operator Console Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 3

LCD Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 4

Keyboard Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 6

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

Cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 14

Isolation Cart Components. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 15

Isolation Cart Enhanced Version Components. . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 17

Accessories and Kits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 19

Manuals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 24

Probe . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 29

Table of Contents 9

GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC 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

Special Tools, Supplies and Equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 4

System Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 5

Preliminary Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 5

Functional Checks (See Also Chapter 4) . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 6

Input Power . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 7

Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 7

Physical Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 8

Optional Diagnostic Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 9

Probe Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 9

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

Electrical Safety Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 11

Safety Test Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 11

GEMS Leakage Current Limits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 12

Outlet Test - Wiring Arrangement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 13

Chassis Leakage Current Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 14

Probe Leakage Current Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 16

When There's Too Much Leakage Current.... . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 19

10 Table of Contents

GE HEALTHCARE

IRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E 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

1-4

1-5

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 LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e

Ultrasound Scanning System. It contains the following chapters:

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

2.) Chapter 2 - Site preparations: Contains pre-installation requirements for the LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e .

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 availa ble adjustments to the LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e .

7.) Chapter 7 - Diagnostics/Troubleshooting: Provides procedure s for running diagnostic or related routines for the LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e .

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 LOGIQ e/ LOGIQ e Vet/LOGIQ i/Vivid e .

10.)Chapter 10 - Care & Maintenance: Provides periodic maintenance procedures for the LOGIQ e/ LOGIQ e Vet/LOGIQ i/Vivid e .

1-1

1-6

1-12

1-16

1-17

Chapter 1 Introduction 1-1

GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

1-1-4 Typical Users of the Basic Service Manual

• Service Personnel (installation, maintenance, etc.).

• Hospital’s Service Personnel

• Contractors (Some parts of Chapter 2 - Site Preparations)

1-2 Section 1-1 - Overview

GE HEALTHCARE

IRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

1-1-5 LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e Models Covered by this Manual

Table 1-2 LOGIQ e R4.x.x Model Designations

Part Number Description

5151219 LOGIQ e R4.x.x Console for USA 5151220 LOGIQ e R4.x.x Console for Argentina 5151243 LOGIQ e R4.x.x Console for Europe 5151247 LOGIQ e R4.x.x Console for China 5151252 LOGIQ e R4.x.x Console for Japanese 5151253 LOGIQ e R4.x.x Console for Australia 5151251 LOGIQ e R4.x.x Console for India

Table 1-3 LOGIQ e R5.0.x / LOGIQ e Vet Model Designations

Part Number Description

5199260 LOGIQ e / LOGIQ e Vet R5.0.x Console for USA 5198329 LOGIQ e / LOGIQ e Vet R5.0.x Console for Argentina 5199670 LOGIQ e / LOGIQ e Vet R5.0.x Console for Europe 5198793 LOGIQ e / LOGIQ e Vet R5.0.x Console for China 5198161 LOGIQ e / LOGIQ e Vet R5.0.x Console for Japanese 5199693 LOGIQ e / LOGIQ e Vet R5.0.x Console for Australia 5212841 LOGIQ e / LOGIQ e Vet R5.0.x Console for India

Table 1-4 LOGIQ e R5.2.x Model Designations

Part Number Description

5323370 LOGIQ e R5.2.x Console for USA 5323375 LOGIQ e R5.2.xConsole for Argentina 5323371 LOGIQ e R5.2.xConsole for Europe 5323380 LOGIQ e R5.2.xConsole for Japanese 5323378 LOGIQ e R5.2.xConsole for Australia 5323377 LOGIQ e R5.2.x Console for India

Table 1-5 LOGIQ e R6.x.x Model Designations

Part Number Description

5389028 LOGIQ e R6.x.x Console for USA 5389808 LOGIQ e R6.x.x Console for Argentina 5389810 LOGIQ e R6.x.x Console for Europe 5389811 LOGIQ e R6.x.x Console for Chinese 5389812 LOGIQ e R6.x.x Console for Japanese 5389813 LOGIQ e R6.x.x Console for Australia 5389814 LOGIQ e R6.x.x Console for India 5410642 LOGIQ e R6.x.x Console for CKD USA 5410642 LOGIQ e R6.x.x Console for CKD Taiwan

Chapter 1 Introduction 1-3

GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

Table 1-6 LOGIQ e R6.x.x Model Designations

Part Number Description

5432745 LOGIQ e R7.x.x Console for USA 5432746 LOGIQ e R7.x.x Console for Europe 5432747 LOGIQ e R7.x.x Console for Japan

Table 1-7 LOGIQ i R4.x.x Model Designations

Part Number Description

5176830 LOGIQ i R4.1.x Console for USA 5179969 LOGIQ i R4.1.x Console for Argentina 5179685 LOGIQ i R4.1.x Console for Europe 5179209 LOGIQ i R4.1.x Console for China 5179748 LOGIQ i R4.1.x Console for Japanese 5179191 LOGIQ i R4.1.x Console for Australia 5179176 LOGIQ i R4.1.x Console for India

Table 1-8 LOGIQ i R5.x.x Model Designations

Part Number Description

5245475 LOGIQ i R5.x.x Console for USA 5245476 LOGIQ i R5.x.x Console for Argentina 5245477 LOGIQ i R5.x.x Console for Europe 5245478 LOGIQ i R5.x.x Console for China 5245480 LOGIQ i R5.x.x Console for Australia 5245481 LOGIQ i R5.x.x Console for India

Table 1-9 Vivid e R4.x.x Model Designations

Part Number Description

5171613 Vivid e R4.x.x Console for USA 5172528 Vivid e R4.x.x Console for Argentina 5171633 Vivid e R4.x.x Console for Europe 5171603 Vivid e R4.x.xConsole for China 5171755 Vivid e R4.x.x Console for Japanese 5172272 Vivid e R4.x.x Console for Australia 5172286 Vivid e R4.x.x Console for India/South Africa 5183318 Vivid e R4.x.x Console with SKD ECG

Table 1-10 Vivid e R5.x.x Model Designations

Part Number Description

5198601 Vivid e R5.x.x Console for USA 5212203 Vivid e R5.x.x Console for Argentina 5212894 Vivid e R5.x.x Console for Asia

1-4 Section 1-1 - Overview

GE HEALTHCARE

IRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

Table 1-10 Vivid e R5.x.x Model Designations

Part Number Description

5199815 Vivid e R5.x.x Console for China 5213329 Vivid e R5.x.x Console for Japan 5212851 Vivid e R5.x.x Console for Australia 5199644 Vivid e R5.x.x Console for India/South Africa 5183318 Vivid e R5.x.x Console with SKD ECG for Europe

Table 1-11 Vivid e R6.x.x Model Designations

Part Number Description

5411312 Vivid e R6.x.x Console for EU 5411381 Vivid e R6.x.x Console for USA 5411382 Vivid e R6.x.x Console for China 5411383 Vivid e R6.x.x Console for Argentina 5411384 Vivid e R6.x.x Console for Japan 5411385 Vivid e R6.x.x Console for Australia 5411386 Vivid e R6.x.x Console for India 5411388 Vivid e R6.x.x Console for SKD ECG 5410641 Vivid e R6.x.x Console for CKD Taiwan

Table 1-12 LOGIQ e Vet R6.x.x Model Designations

Part Number Description

5198415-2 LOGIQ e Vet R6.x.x Console for EU 5199518-2 LOGIQ e Vet R6.x.x Console for USA

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

The Operator Manual(s) should be fully read and understood before operating the LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e and also kept near the unit for quick reference.

Chapter 1 Introduction 1-5

GE HEALTHCARE

DANGER

WARNINGWARNING

CAUTION

NOTICE

DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E 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 iden tified by a flag word that precedes the precautionary message. Known or potential hazards are labeled in one of following ways:

DANGER IS USED TO INDICATE THE PRESENCE OF A HAZARD THAT WILL CAUSE SEVERE PERSONAL INJURY OR DEATH IF THE INSTRUCTIONS ARE IGNORED.

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.

NOTE: Notes provide important information about an item or a procedure.

Information contained in a NOTE can often save you time or effort.

1-6 Section 1-2 - Important Conventions

GE HEALTHCARE

LASER

LIGHT

Signed

Date

TAG

LOCKOUT

EYE

PROTECTION

IRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E 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 1-13 Standard Hazard Icons

ELECTRICAL MECHANICAL RADIATION

LASER HEAT PINCH

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

Table 1-14 Standard Icons Indicating a Special Procedure Be Used

AVOID STATIC ELECTRICITY TAG AND LOCK OUT WEAR EYE PROTECTION

Chapter 1 Introduction 1-7

GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

1-2-3 Product Icons

The following table describes the purpose and locatio n of safety labels and other important in formation provided on the equipment.

Table 1-15 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 (IPX1 or IPX8) IPX1: FSU-2001 IPX8: MKF 2-MED GP26, FSU-1000

Indicates the degree of protection provided by the enclosure per IEC60

529. IPX1 cannot be used in operating

room environment; IPX8 can be used in 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.

Bottom panel of the adapter.

Bottom of Footswitch

Bottom panel

Probe connectors

General Warning. Various

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

1-8 Section 1-2 - Important Conventions

Various

GE HEALTHCARE

REFREF

SNSN

IRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

Table 1-15 Warnings

LABEL/SYMBOL PURPOSE/MEANING LOCATION

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

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

“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.

Catalog or model number. Rating Plate

Inside of AC adapter

Stick to Power Switch

Bottom panel of the console

Rating Plate

Serial number Rating Plate

Direct Current. For products to be powered from a DC

supply.

Input Rating Plate

For use with adapter model TWADP 100

Description Rating Plate

Type CF Defib-Proof Applied Part (heart in the box with paddle) symbolis in accordance with IEC 60878-02-06.

Rating Plate

ECG Module

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GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

Table 1-15 Warnings

LABEL/SYMBOL PURPOSE/MEANING LOCATION

“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.

Various

Do not push the system.

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.

When closing the LCD cover, use caution to avoid injuring hands or fingers as there is a closing mechanism which allows the LCD cover to automatically close.

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.

Rear of Docking Cart and rear of Isolation Cart.

Rating Plate

Rear panel, rating plate

This product consists of devices that may contain mercury, which must be recycled or disposed of in accordance with local, state, or country laws. (Within this system, the backlight lamps in the monitor display contain mercury.)

1-10 Section 1-2 - Important Conventions

Bottom panel of the console

GE HEALTHCARE

IRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

Table 1-15 Warnings

LABEL/SYMBOL PURPOSE/MEANING LOCATION

The separate collection symbol is affixed to a battery, or its packaging, to advise you that the battery must be recycled or disposed of in accordance with local or country laws. The letters below the separate collection symbol indicate whether certain elements (Pb=Lead, Cd=Cadmium, Hg=Mercury) are contained in the battery . T o minimize potential effects on the environment and human health, it is important that all marked batteries that you remove from the product are properly recycled or disposed. For information on how the battery may be safely removed from the device, please consult the service manual or equipment instructions. Information on the potential effects on the environment and human health of the substances used in batteries is available at this url: http:// www.gehealthcare.com/euen/weeerecycling/index.html

Battery Pack

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).

Do not connect the DVD-RW to the system while scanning.

GOST Symbol. Russia Regulatory Country Clearance.

DVD-RW

Bottom

Chapter 1 Introduction 1-11

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WARNINGWARNING

CAUTION

DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

Section 1-3 Safety Considerations

1-3-1 Introduction

The following safety precautions must be observed duri ng 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 LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e Training are authorized to service the equipment.

1-3-3 Mechanical Safety

Ultrasound probes are highly sensitive medical instruments that can ea sily be damaged by improper handling. Use care when handling and protect from damage when not in use. Do not use a damaged or defective probe. Failure to follow these precautions can result in serious injury and equipment damage.

Never use a probe that has fallen to the floor. Even if it looks ok, it may be damaged.

The LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e weights 4.6kg or more, depending on installed peripherals, when ready for use. To avoid possible injury and equipment damage:

ALWAYS:

• Use the handle to move the system.

• Do not let the system strike walls or door frame.

• Limit movement to a slow careful walk.

NOTE: Special care should be taken when transporting the unit in a vehicle:

• 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 Label Location

Please refer to Basic User Manual for label location information.

1-12 Section 1-3 - Safety Considerations

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WARNINGWARNING

CAUTION

NOTICE

IRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

1-3-6 Battery Safety

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

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

• Charge and discharge the batteries only when the ambient temperature is between 10 and

40 C (50 F and 122 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 5 0° 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 heat er.

• 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.

• Do not contact PCM ( Power Control and Monitor, it’s a small board in the battery) directly

to prevent packs from ESD damage.

• In case of longer non-use of the LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e , please make sure the

battery is removed.

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 containe r.

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

• If the battery emits an odor or heat, is defor med or discolored, or in a way appears ab normal

during use, recharging or storage, immediately remove it a nd s top using it . If you hav e a ny 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 mon ths, charge at lease once char ging 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.

The battery shall be shipped in about 30% charged state. Those packs have to be fully charged and discharged up to 3 times to utilize Li-lon smart packs before use.

Chapter 1 Introduction 1-13

GE HEALTHCARE

DANGER

WARNING

NOTICE

Signed

Date

TAG

LOCKOUT

DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E 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.

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.

SHUT DOWN FORCEDLY OR PLUG IN/OUT ACDC INVALID MAY CAUSE THE DAMAGE OF SYSTEM FILES.

1-3-8 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.

Energy Control and Power Lockout for LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e 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.

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.

1-14 Section 1-3 - Safety Considerations

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IRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

1-3-9 Returning/Shipping Probes and Repair Parts

Equipment being returned must be clean and free of blood and other infectious substances. GEMS policy states that body fluids must be properly removed from any part or equipment prior to

shipment. GEMS employees, as well as customers, are responsible for ensuring that parts/equipment have been properly decontaminated prior to shipment. Under no circumstance should a part or equipment with visible body fluids be taken or shipped from a clinic or site (for example, body coils or an ultrasound probe).

The purpose of the regulation is to protect employees in the transportation industry, as well as the people who will receive or open this package.

NOTE: The US Department of Transportation (DOT) has ruled that “items that were saturated an d/ or

dripping with human blood that are now caked with dried blood; or which were used or intended for use in patient care” are “regulate d medi cal waste” for transportatio n purposes an d 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.

The ultrasound system is not meant to be long term storage of patient data or images. The user us responsible for the date on the system and a regular backup is highly recommended.

If the system is sent for repair, please ensure that any patient information is backup and erased from the system before shipping. It is always possible during system failure and repair to lose patient data. GE is not responsible for the loss of this data.

If PHI (Patient Healthcare Information) data needs to be sent to GE employees for service purposes, GE will ascertain agreement from the customer. The patient information shall only be transferred by approved service processes, tools and devices restricting access, protecting o r encryptin g data where required, and providing traceability in the form of paper or electronic documents at each stage of the procedure while maintaining compliance with cross-border restrictions of patient information transfers.

Chapter 1 Introduction 1-15

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WARNING

DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

Section 1-4 EMC, EMI, and ESD

1-4-1 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/EM I) and can be r adi ated th ro ugh space or conducted over interconnecting power of signal cables. In ad dition to electromagnetic energy, EMC also includes possible effects from electrical fields, magnetic fields, electrostatic discharge and disturbances in the electrical power supply.

1-4-2 CE Compliance

The LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e unit conforms to all applicable conducted and radiated emission limits and to immunity from electrostatic discharge, radia ted an d co nd uc te d RF fiel ds , 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, shield ing, gaskets, mesh, clamps, are in

good condition, installed tightly without skew or stress. Proper installation following all comments noted in this service manual is required in order to achieve full EMC performance.

1-4-3 Electrostatic Discharge (ESD) Prevention

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

1.FOLLOW GENERAL GUIDELINES FOR HANDLING OF ELECTROSTATIC SENSITIVE EQUIPMENT.

1-16 Section 1-4 - EMC, EMI, and ESD

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IRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

Section 1-5 Customer Assistance

1-5-1 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 loca l distributor or appropriate support resource, as listed below.

Prepare the following information before you call:

- System ID serial number.

- Software version.

Table 1-16 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 GE Ultraschall Deutschland GmbH& Co. KG BeethovenstraBe 239 Postfach 11 05 60, D-42665 Solingen Germany

Asia (Singapore) GE Ultrasound Asia Service Department - Ultrasound 298 Tiong Bahru Road #15-01/06 Central Plaza Singapore 169730

Japan Support Center

Service: On-site

Service: Parts

Applications support

Service

Applications support

Phone: +33 (0)130-831-300 (General Imaging and Cardiac)

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

Tel: +65 291-8528

Fax: +65 6291-7006

Phone: 81-42-648-2944 Fax: 81-42-648-2905

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 1-17

GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

1-5-2 System Manufacturer

Table 1-17 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

1-5-3 Factory Sites

Table 1-18 Factory Sites

GE Medical Systems (China) Co., Ltd. No.19, Changjiang Road, Wuxi National Hi-Tech Dev. Zone, Jiangsu,

P.R.China 214028 GE Ultrasound Korea:

65-1, Sangdaewon-dong, Jungwon-gu, Seongnam-si, Gyeonggi-do, Korea 462-120

GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC DBA GE Healthcare

9900 Innovation Drive Wauwatosa, WI 53226

U.S.A

TEL: +86 510-85225888 FAX: +86 510-85226688

Manufacturer Phone Number

TEL: +86 510-85225888 FAX: +86 510-85226688

TEL: +82-31-740-6112 FAX: +82-31-740-6435

TEL: (1) 800-437-1171 FAX: (1) 414-721-3865

1-18 Section 1-5 - Customer Assistance

GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

Chapter 2 Site preparations

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 LOGIQ e/ LOGIQ e Vet/LOGIQ i/Vivid e . 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

2-3

Overview

General Console Requirements

Facility Needs

2-1

2-2

2-6

Chapter 2 Site preparations 2-1

GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

Section 2-2 General Console Requirements

2-2-1 Console Environmental Requirements

Table 2-2 Environmental Requirements for LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e 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 contr ols 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 LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e Power Requirements

Table 2-3 Electrical Specifications for LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e

Adapter Voltage Power Current Frequency

TWADP100 100-240 VAC 130VA max. 1.3 A (max.) 50/ 60HZ

2-2 Section 2-2 - General Console Requirements

GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

2-2-2-2 Inrush Current

Inrush current is not a factor to consider due to the inrush current limiting properties of the power supplies.

Table 2-4 Inrush Current

Inrush Current

Voltage

100V 0.38A 0.41A 240V 0.20A 0.21A

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 ins ta llatio n mus t 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.

2-2-2-6 Power Stability Requirements

Voltage drop-out

Max 10 ms.

Power Transients

Console Only Console with all peripherals

(All applications) Less than 25% of nominal peak voltage for less than 1 millisecond for any type of transient, including

line frequency, synchronous, asynchronous, or aperiodic transients.

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GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E 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 LOGIQ e/LOGIQ e Vet/ LOGIQ i/Vivid e 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 Table 2-5 for EMI Prevention tips.

Table 2-5 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

NOTICE

DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

2-2-4 Scan Probe Environmental Requirements

Operation:10° to 40° C Storage:-10° to 50° C

NOTE: The recommended storage temperature range of 6Tc-RS is between 0°C and 45°C. NOTE: Temperature in degrees C. Conversion to Degrees F = (Degrees C * (9/5) + 32).

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 preparations 2-5

GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E 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. User the Pre Installation checklist to verify that all needed steps have been taken, Purchaser reasonability includes:

• Procuring the materials required.

• Completing the preparations before de livery 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 accompan ying 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 pres ents challenges to the installation team. To avoid delays during installation, such variances should be made known to th e 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

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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

• Door is at least 92 cm (3 ft.) wide

• Circuit breaker for dedicated power outlet is easily accessible

• Sink with hot and cold water

• Receptacle for bio–hazardous waste, like used probe sheaths

• Emergency oxygen supply

• Storage for linens and equipment

• Nearby waiting room, lavatory, and dressing room

• Dual level lighting (bright and dim)

• Lockable cabinet ordered by GE for its software and proprietary manuals.

Chapter 2 Site preparations 2-7

GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E 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 RYS O R DOCTO R’S D ES K

DEDICATED

PO W ER

R OOM ,

PR O CESSIN G

FILM VIEW ER

CO UN TER TO P

RECEPTA CLE

CO UN TER

TO P

SINK

SU C TIO N LINE

EM ER G EC Y OX Y G EN

OVERHEAD LI G H TS DIMM ER

(107 CM)

DOO R 42 IN.

C O NS O LE

FOOT

A 14 by 17 foot R ecommended Floor Plan

Scale : Each square equals one square foot

(46 CM)

STOO 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

SINK

FILM SUPPLIES

LINEN SUPPLY

PR OB ES /SUPPLIES

EXTERNAL

PE RIPHERALS

DEDICATED POW ER OUTLETS

DOO R 30 IN.

(76 CM)

24 IN. (61 CM)

FOOT

STOO L

EXAM INA R IO N

TAB LE

LOGIQ Book XP

C O NS O LE

76 IN. (193 CM)

G E C AB INET FOT SO FTW ARE AND MA NU ALS

An 8 by 10 foot M inimal Floor Plan

Figure 2-1 RECOMMENDED ULTRASOUND ROOM LAYOUT

2-8 Section 2-3 - Facility Needs

GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E 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 prin ters. As an added benefit, transferring images in this manner frees up the on-board moni tor and peripherals, enabling viewing to be don e while scanning continues. With DICOM, images can be archived, stored, and retrieved faste r, easier , and at a lower cost.

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

To configure the LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e 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 LOGIQ e/LOGIQ e Vet/ LOGIQ i/Vivid e .

• 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

LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e 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 preparations 2-9

GE HEALTHCARE

LOGIQ e/

Host Name

AE Title

Local Port

IP Address

Net Mask

...

ROUTING INFORMATION

ROUTER2 ROUTER3

ROUTER1

...

... ... ...

Destination IP Addresses

GATEWAY IP Addresses

Default

DICOM APPLICATION INFORMATION

NAME

Store 2

Store 3

Store 1

MAKE/REVISION IP ADDRESSES PORTAE TITLE

Store 5

Store 6

Store 4

Storage Commit

MPPS

Worklist

...

DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

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

Figure 2-2 Worksheet for DICOM Network Information

2-10 Section 2-3 - Facility Needs

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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 3-1 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

3-11

Overview

Receiving and Unpacking the Equipment

Packing the Equipment

Preparing for Installation

Completing the Installation

System Configuration

Software/Option Configuration

Connectivity Installation Worksheet

Loading Base Image Software

Software Version check out

Paperwork

3-1

3-4

3-7

3-8

3-9

3-12

3-27

3-28

3-29

3-30

3-31

Chapter 3 System Setup 3-1

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3-1-2 Average Installation Time

Table 3-2 Average Installation Time

Description Average Installation Time Comments

Unpacking the scanner Scanner wo/options DICOM Option

20 minutes 30 minutes 30 minutes

Dependent on the configuration that is required Dependent on the amount of configuration

The LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e installation and functional checkout will take approximately one hour. LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e consoles with optional equipment may take slightly longer.

3-2 Section 3-1 - Overview

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DANGER

CAUTION

DANGER

DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E 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×C increment it's temperature is below 10×C or above 40×C.

Equipment damage possibility. Turning the system on without acc limat ion af t er arriving a t s ite may cause the system to be damaged.

Table 3-3 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

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!

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 t he unit to a prop erly grounded powe r 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.

OPERATOR MANUAL(S) The User Manual(s) should be fully read and under stood before operating th e LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e and kept near the unit for quick reference.

ACOUSTIC OUTPUT HAZARD Although the ultrasound energy transmitte d from the LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e probe is within FDA limits, avoid unnecessary exposure. Ultrasound energy can produce heat and mechanical damage

Chapter 3 System Setup 3-3

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Adhesive tape

Plastic Bands

DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

Section 3-2 Receiving and Unpacking the Equipment

When a new system arrives, check that any components are not damaged and ar e not in short supply. If shipping damage or shortage occurs, contact the address shown in Chapter 1.

1.) Cut the four PLASTIC BANDs.

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

Figure 3-1 Open top covers of paper carton.

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

GE HEALTHCARE

CAUTION

Paper Pad

Console and interleavers

Console Package

Accessories Package

DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

Section 3-2 Receiving and Unpacking the Equipment (cont’d)

3.) Take out the Paper pad.

4.) Take out console together with 2 interleavers from console package.

5.) Take out the interleavers beside Accessor ies Pa cka ge .

6.) Take out Accessories Package.

Figure 3-2 Unpacking the equipment

Do not lift the unit by the rubber band. Equipment damage may result.

Chapter 3 System Setup 3-5

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Console

Interleaver

DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

Section 3-2 Receiving and Unpacking the Equipment (cont’d)

7.) Remove 2 interleavers.

8.) Remove plastic bag.

Figure 3-3 Removing interleavers and plastic bag

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

GE HEALTHCARE

CAUTION

DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E 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.

Please carefully unpack the system, and do not dispose the package of LOGIQ e/LOGIQ e Vet/ LOGIQ i/Vivid e , so that it can be reused for service.

3-2-1 Moving into Position

Do not lift the unit by the rubber band. Use handle to move system.

Equipment Damage Possibility. Lifting the console by holding covers may damage the covers. Do not lift the console by holding any covers.

In general, a single adult can move the LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e . 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 LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e in the re ve rse orde r of un pa ck ing .

Figure 3-4 Labels on Package

Chapter 3 System Setup 3-7

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WARNINGWARNING

DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E 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 scanner is set to the corr ect voltage. The Voltag e settings for the LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e Scanner is found on a label located on the AC adapter.

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

Connecting a LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e scanner to the wrong voltage level will most likely destroy the scanner.

3-4-3 EMI Protection

This Unit has been designed to minimize the effects of Electro Magnetic Interference (EMI). Many of th e covers, shields, and screws are provided primarily to protect the system from image artifacts cau sed 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.

3-8 Section 3-4 - Preparing for Installation

GE HEALTHCARE

UPUP

DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

Section 3-5 Completing the Installation

3-5-1 Power On / Boot Up

NOTE: After turning off a system, wait at least ten seconds before turning it on again. The system may not be

able to boot if power is recycled too quickly.

3-5-1-1 Scanner Power On

Lower the handle. Plug the AC adapter output connector into the system DC input port ( located on the system’s rear panel) with the arrow side upward. Plug the AC adapter power cor d into a grounded, protective earth outlet.

Figure 3-5 Connect AC adapter

When power is applied to the scanner, power is distributed to the Cooling Unit, Control Panel, LCD, Peripherals and the Back-end Processor.

Chapter 3 System Setup 3-9

GE HEALTHCARE

Power On/Off switch

DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

3-5-1-2 Turn on the system

Press the Power On/Off switch at the front of the system once.

Figure 3-6 Power On/Off Switch

When the Power On/Off switch on the Control Panel is pressed once, the Back-end Processor sta rts and the software code is distributed to initiate the scanner.

No status messages are displayed during this process.

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 at the front of the system once.

2.) The System-Exit window is displayed.

Figure 3-7 System Exit Window

3.) Using the Trackball or Select key, select Shutdown.

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

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

6.) Close LCD cover.

3-10 Section 3-5 - Completing the Installation

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Probe Latch

DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

3-5-2-2 Scanner Shutdown

Disconnect the Mains Power Cable if necessary. For example: Relocating the scanner.

3-5-3 Transducer Connection

1.) Carefully open the system LCD display, plug the probe connector into the prob e port, then lock the probe latch upward.

NOTE: Please ensure that the probe latch is in an unlocked position before you connect the probe to the

system.

Figure 3-8 Connect the probe

NOTE: It is not necessary to turn OFF power to conne ct or disco nn e ct a pr ob e.

Chapter 3 System Setup 3-11

GE HEALTHCARE

WEIGHT: 4.6KG NOTE: Length is in mm

DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

Section 3-6 System Configuration

3-6-1 System Specifications

3-6-1-1 Physical Dimensions

The physical dimensions of the LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e console are summarized in

Figure 3-9 on page 3-12 .

Table 3-4 Physical Dimensions of LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e

Height Width Depth Unit

Console

Only

61 100 340 375 287 337 mm

2.4 3.9 13.4 14.8 11.3 13.3 inches

Console

with handle

Console

Only

Console

with handle

Console Only

Console with

handle

Unit

Figure 3-9 Overall Dimensions

3-6-2 Electrical Specifications

Table 3-5 Electrical Specifications for LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e

Adapter Voltage Tolerances Current Frequency

TWADP100 100-240 VAC +/-10% 1.3A (max) 50/60Hz

3-12 Section 3-6 - System Configuration

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3-6-3 Approved peripherals

Table 3-6 Approved on-board peripherals

Device Manufacturer Model Interface Remark

B/W Printer SONY UP-D897 USB

Digital Color Printer

HP Color Printer

DVD-RW

Wireless Lan Adapter

3-pedal footswitch Steute MKF 2-MED GP26 USB 1-pedal footswitch Whanam FSU2001 USB 1-pedal footswitch Whanam FSU-1000 USB

USB Memory

USB HUB

ECG NORAV ECG-USB1 USB

USB HDD

DVD-Recorder Panasonic

SONY UP-D23MD USB SONY UP-D25MD USB

HP HP Officejet Pro K5400 USB HP HP Officejet Pro K8600 USB

HP HP Deskjet 470 USB LITEON LITEON DX-20A4P USB LITEON LITEON Model eHAU 120 USB LITEON LITEON Model eHAU 324 USB

NetGear WN111V2 USB NetGear WG111V3 USB

Linksys Linksys WUSB54G USB

SanDisk CRUZER 2G USB SanDisk CRUZER 4G USB

SanDisk

Shenzhen Gaojian HE 702A USB Shenzhen Gaojian HE420GE USB

Seagate USB HDD 80G USB Seagate USB HDD 250G USB Seagate USB HDD 500G USB

CRUZER 4G with U3

Application

MD-800E MD-800U USB

USB

Only supported by LOGIQ e R6.x.x

and LOGIQ e R7.x.x.

Not supported by LOGIQ e R4.x.x,

LOGIQ e R6.x.x, Vivid e R4.x.x,

LOGIQ i R4.x.x

Video Transfer Pinnacle

BarCode Reader*

Handheld Handheld 3800G USB Handheld Handheld 4600G USB

Pinnacle Video Transfer -

8230-10022-11

USB

Not supported by LOGIQ e R5.0.x,

LOGIQ e Vet R5.0.x, Vivid e

R5.0.x, LOGIQ i R5.0.x

Only supported by LOGIQ e R5.2.x,

R6.x.x, R7.x.x, LOGIQ e Vet 6.x.x

NOTE: For detailed installation information and connection procedures, please refer to Peripheral

Installation manual.

NOTE: BarCode Reader* is supported by LOGIQ e Software version R5.2.x, R6.x.x only.

Chapter 3 System Setup 3-13

GE HEALTHCARE

WARNINGWARNING

DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

3-6-4 Connecting Cables

Equipment damage possibility. Be sure to use the following recommended connecting cables to connect recording devices and a network with LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e console.

Table 3-7 List of Connecting Cables

Name Part No. Figure NOTE

USB Cable 5122305

3-6-5 Peripherals/Accessories Connector Panel

LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e periphera ls and accessories can be properly connected u sing the side connector panel.

3-6-5-1 Rear Panel Connector

Located on the rear panel are video input and output connectors, power connector and ethernet port.

For USB Printer & USB DVD-RW

Figure 3-10 Rear Connector Panel

1.) Port for DC input (AC Adapter)

2.) Docking Connector

3.) SVGA Output

4.) Ethernet port

3-14 Section 3-6 - System Configuration

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DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

3-6-5-2 Left Panel Connector

Located on the left side panel are two USB Ports for control connections for printer, service tools and earphone port.

Figure 3-11 Left Side Panel

1.) Two interchangeable USB Port (Digital Printers, DVD-RW and/or FootSwitch, etc)

2.) Earphone Port.

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

Signal ground lines are not isolated.

Chapter 3 System Setup 3-15

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

1. Pin Assignment of DC input Connector: 4 Pin, Female

Table 3-8 Pin Assignments of DC input

Pin No. Signal Pin No. Signal

1+20V3GND

2+20V4GND

2. Pin Assignment of USB

Table 3-9 Pin assignment of USB1

Pin No. Signal Pin No. Signal

1 +5VDC 3 DATA+

2 DATA- 4 GND

Table 3-10 Pin assignment of USB2

Pin No. Signal Pin No. Signal

1 +5VDC 3 DATA+

2 DATA- 4 GND

3. Pin assignment of RS232C for external VGA Connector: D-SUB, 15Pin, Female

Table 3-11 Pin Assignments of RS232C for External VGA

Pin No. Signal Pin No. Signal

1RED9 N/A

2 GREEN 10 SGND

3BLUE11 N/A

4N/A12N/A

5 GND 13 HSYNC

6 RGND 14 VSYNC

7GGND15 N/A

8BGND16

3-16 Section 3-6 - System Configuration

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NOTICE

DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

3-6-5-4 Connect peripherals

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

B/W Printer can be properly connected using USB Port1 or USB Port 2 (Figure 3-12 on page 3-17 ).

Figure 3-12 Connect B/W printer to the system

B.) Connect UP-D23MD color printer to the system.

UP-D23MD Color Printer can be properly connected using USB Port1 or USB Por t 2 (Figure 3-13

on page 3-17 ).

Figure 3-13 Connect digital colo r printer to the system

HP Deskjet 470 /HP Officejet Pro K5400 Color Printer must connect with PIT (Printer Isolation Transformer) when being used.

Chapter 3 System Setup 3-17

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CAUTION

DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

3-6-5-4 Connect peripherals (cont’d)

C.) Connect DVD-RW to the system.

DVD-RW can be properly connected using USB Port1 or USB Port2 (Figure 3-14 on page 3-18 ).

Figure 3-14 Connect DVD-RW to the system

DO NOT connect DVD-RW to the system while scanning.

LITEON DVD-RW drive recommended media list

Media issues are common throughout the DVD-RW drive industry. Because DVD media vendors often change disc suppliers, quality levels may change due to manufacturing differences. This means that you may encounter DVD/CD creation problems with media that may have worked successfully before. Overall system configuration and other factors may also affect the success of creating a DVD/CD.

The following media types have been tested. LITEON highly recommends that you use the media types on this list when creating your DVDs/CDs.

Not all brands of media have been tested a nd, therefore, you may encounter success with other brands not listed. This list will be updated as other media is tested and approved.

Table 3-12 LITEON DVD-RW drive recommended media list

Brand Name Type

SONY DVD-R SONY CD-R

SONY DVD-RW Mitsubishi CD-R Mitsubishi CD-RW Mitsubishi DVD-R Mitsubishi DVD-RW

JVC DVD-R

MBI CD-R

MBI DVD-R Taiyo Yuden CD-R Taiyo Yuden DVD-R

3-18 Section 3-6 - System Configuration

GE HEALTHCARE

3-pedal footswitch

1-pedal footswitch

Wireless Lan Adapter

DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

3-6-5-4 Connect peripherals (cont’d)

D.) Connect FootSwitch to the system.

FootSwitch can be properly connected using USB Port1 or USB Port2.

Figure 3-15 Connect Foot Switch to the system

E.) Connect Wireless LAN Adapter to the system.

Wireless LAN Adapter can be properly connected using USB port.

Figure 3-16 Connect Wireless LAN Adapter to the system

F.) Connect the CRT to the system.

CRT can be properly connected using the SVGA output.

Chapter 3 System Setup 3-19

GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

3-6-5-4 Connect peripherals (cont’d)

G.) Connect the USB Memory to the system. The USB Memory can be properly connected using USB

port 1 or 2.

Figure 3-17 USB Memory Connection

H.) Connect the ECG to the system. ECG can be properly connected using USB port 1 or 2.

Figure 3-18 ECG

3-20 Section 3-6 - System Configuration

GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

3-6-5-4 Connect peripherals (cont’d)

I.) Connect the USB HDD to the system. The USB Harddisk can be properly connected using USB

port 1 and 2.

Figure 3-19 Emergency Disk Connection

J.) Connect the BarCode Reader to the system, the BarCode Reader can be properly connected via

USB port 1 or 2.

Figure 3-20 BarCode Reader Connection

Chapter 3 System Setup 3-21

GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

3-6-5-4 Connect peripherals (cont’d)

K.) Connect the Sandisk U3 USB Flash Drive to the system. The Sandisk U3 USB Flash Drive can be

properly connected using USB port 1 and 2.

Figure 3-21 Sandisk U3 USB Flash Drive Connection

NOTE: The Password of the Sandisk U3 USB Flash Drive is Predefined. NOTE: The Sandisk U3 USB Flash Drive is only available on LOGIQ e R6.x.x and LOGIQ e R7.x.x.

Connect the security enabled Sandisk U3 USB Flash Drive into the system, input the password in the pop-up dialog. Click OK to login, click Cancel to cancel.

Figure 3-22 Input the password

The Sandisk U3 USB Flash Drive can be used if the right password is entered. An error message will display if the wrong password is entered.

3-22 Section 3-6 - System Configuration

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3-6-5-4 Connect peripherals (cont’d)

Figure 3-23 Wrong password error

Click OK, input the password again. The Sandisk U3 USB Flash Drive will be locked if reaching the maximum number of failed password

attempts.

Figure 3-24 Sandisk U3 USB Flash Drive locked

NOTE: Please refer to the operation manual of each peripheral for information needed by the user to

operate the system safely.

For detailed installation information, pleas e re fe r to th e LO GI Q e/ LO GI Q e Vet/LOGIQ i/Vivid e Peripheral Installation Instruction manual.

Chapter 3 System Setup 3-23

GE HEALTHCARE

For LOGIQ e R5.x.x, R6.x.x, R7.x.x, LOGIQ i R5.x.x,

For LOGIQ e R4.x.x, LOGIQ i R4.x.x, Vivid e R4.x.x

Vivid e R5.x.x/R6.x.x

DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

3-6-5-4 Connect peripherals (cont’d)

L.) Connect the external monitor to the system. The monitor can be properly connected using the VGA

port.

Figure 3-25 VGA Connection

Press Ctrl+Alt+V

Select Intel(R) Dual Display Clone and select OK

on the keyboard, a dialog box appears.

Figure 3-26 Graphics Controller Properties

; check the Same display configuration driver on both display box

NOTE: Please refer to the operation manual of each peripheral for information needed by the user to

operate the system safely.

NOTE: For LOGIQ e R5.2.x, R6.x.x, R7.x.x, the default set is dual, it will not pop up Figure 3-26.

For detailed installation information, pleas e re fe r to th e LO GI Q e/ LO GI Q e Vet/LOGIQ i/Vivid e Peripheral Installation manual.

3-24 Section 3-6 - System Configuration

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3-6-6 Available Probes

See in specification in the LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e User Reference Manu al for Probe s and intended use.

For LOGIQ e R4.0.x, the system supports 4C-RS, E8C-RS, 8C-RS, i12L-RS, 8L-RS, 3S-RS, 12L-RS Probes.

For LOGIQ e R5.0.x, the system supports 4C-RS, E8C-RS, 8C-RS, i12L-RS, 8L-RS, 3S-RS, 12L-RS, i/t739-RS, 9L-RS Probes.

For LOGIQ e R5.2.x, the system supports 4C-RS, E8C-RS, 8C-RS, i12L-RS, 8L-RS, 3S-RS, 12L-RS, i/t739-RS, 9L-RS, 16L-RS Probes.

For LOGIQ e R6.x.x, the system supports 4C-RS, E8C-RS, 8C-RS, i12L-RS, 8L-RS, 3S-RS, 12L-RS, i/t739-RS, 9L-RS, 16L-RS, 6Tc-RS, 6S-RS Probes.

For LOGIQ e R7.x.x, the system supports 4C-RS, E8C-RS, 8C-RS, i12L-RS, 8L-RS, 3S-RS, 12L-RS, i/t739-RS, 9L-RS, 16L-RS, 6Tc-RS, 6S-RS, L8-18i-RS,P2D Probes.

For LOGIQ i R4.x.x, the system supports 4C-RS, E8C-RS, 8C-RS, i12L-RS, 8L-RS, 3S-RS, 12L-RS Probes.

For LOGIQ i R5.x.x, the system supports 4C-RS, E8C-RS, 8C-RS, i12L-RS, 8L-RS, 3S-RS, 6S-RS, 12L-RS, i/t739-RS, P2D, 9L-RS Probes.

For Vivid e R4.x.x, the system supports 4C-RS, i12L-RS, 8L-RS, 3S-RS Probes. For Vivid e R5.0.x, the system supports 4C-RS, i12L-RS, 8L-RS, 3S-RS, 8C-RS, 9L-RS, P2D Probes. For Vivid e R5.2.x, the system supports 4C-RS, 8C-RS, E8C-RS, 8L-RS, 9L-RS, 12L-RS, i12L-RS, 3S-

RS, 6S-RS, P2D Probes. For Vivid e R6.x.x, the system supports 4C-RS, 8C-RS, E8C-RS, 8L-RS, 9L-RS, 12L-RS, i12L-RS, 3S-

RS, 6S-RS, P2D, 6Tc-RS Probes. For LOGIQ e Vet R5.0.x, the system supports 4C-RS Vet, E8C-RS Vet, 8C-RS Vet, i12L-RS Vet, 8L-

RS Vet, 3S-RS Vet, 12L-RS Vet, 9L-RS Vet, i739-RS LC, 6S Vet-RS For LOGIQ e Vet R5.2.x, the system supports 4C-RS Vet, E8C-RS Vet, 8C-RS Vet, i12L-RS Vet, 8L-

RS Vet, 3S-RS Vet, 12L-RS Vet, 9L-RS Vet For LOGIQ e Vet R6.x.x, the system supports 4C-RS Vet, E8C-RS Vet, 8C-RS Vet, i12L-RS Vet, 8L-

RS Vet, 3S-RS Vet, 12L-RS Vet, 9L-RS Vet, 6S Vet-RS, i739-RS-LC, 6Tc-RS Vet

NOTE: 16L-RS is not available in China.

Chapter 3 System Setup 3-25

GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

3-6-6 Available Probes (cont’d)

Table 3-13 List of Probes for LOGIQ e/LOGIQ i/Vivid e

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

4C-RS NORYL GENERAL PURPOSE CONVEX H4000SR 5131629

E8C-RS VALOX TRANSVAGINAL TRANSRECTAL MICRO-CONVEX H40402LN 2290777

8C-RS VALOX

i12L-RS ABS (GE)

8L-RS VALOX

3S-RS VALOX

12L-RS NORYL

9L-RS VALOX SMALL PATS VASCULAR LINEAR H40442LL 5213143 i739-RS VALOX INTRAOPERATIVE LINEAR H40402LJ 2404995 t739-RS VALOX INTRAOPERATIVE LINEAR H40412LP 2404999

P2D CARDIOLOGY Non-Imaging CW H45551CA KE100003

6S-RS VALOX CARDIOLOGY PEDIATRICS SECTOR H45021RP 47236956

16L-RS VALOX

6Tc-RS VALOX TRANSESOPHAGEAL FOR ADULT SECTOR H45551ZE KN100104

INTRAOPERATIVE SMALL PARTS

VETERINARY

PEDIATRIC NEONATAL

VASCULAR PEDIATRICS

SMALL PARTS

PERIPHERAL VASCULAR

CARDIOLOGY

TRANSVAGINAL ABDOMEN

SMALL PARTS

PERIPHERAL VASCULAR

SMALL PARTS

PERIPHERAL VASCULAR

MICRO-CONVEX H40402LS 2354971

LINEAR H40402LW 2377942

LINEAR H40402LT 2376127

SECTOR H4000PD 2355686

LINEAR H40402LY 5154514

LINEAR H40452LJ 5317271

NOTE: 16L-RS is not available in China.

3-26 Section 3-6 - System Configuration

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3-6-6 Available Probes (cont’d)

Table 3-14 List of Probes for LOGIQ e Vet

Probe Name Material of Headshell Ar ea of Using TYPE Catalog Number Part Number

4C-RS Vet NORYL GENERAL PURPOSE CONVEX H40442LY 5198378

E8C-RS Vet VALOX

8C-RS Vet VALOX

TRANSVAGINAL

TRANSRECTAL

VETERINARY

PEDIATRIC NEONATAL

MICRO-CONVEX H41562LL 5134643

MICRO-CONVEX H41562LK 5134642

i12L-RS Vet ABS (GE)

8L-RS Vet VALOX

3S-RS Vet VALOX

12L-RS Vet NORYL

9L-RS Vet VALOX SMALL PARTS VASCULAR LINEAR H40442LW 5220453

i739-RS-LC VALOX INTRAOPERATIVE LINEAR H41482LS 5136420

6SVet-RS VALOX

6Tc-RS Vet VALOX

INTRAOPERATIVE SMALL

PARTS VASCULAR

PEDIATRICS

SMALL PARTS

PERIPHERAL VASCULAR

CARDIOLOGY

TRANSVAGINAL

ABDOMEN

SMALL PARTS

PERIPHERAL VASCULAR

CARDIOLOGY

PEDIATRICS

TRANSVAGINAL FOR

ADULT

LINEAR H41562LN 5134645

LINEAR H41562LM 5134644

SECTOR H41562LR 5134647

LINEAR H40442LZ 5212304

SECTOR H40452L 5198571

SECTOR H48922LB 5430790

NOTE: i739-RS-LC , 6SVet-RS and 6Tc-RS Vet probes are only availble for R6.x.x.

Section 3-7 Software/Option Configuration

Refer to the LOGIQ e/LOGIQ e Vet/L OGIQ i/Vivid e Basic User Manual, Chapter 16, Customizing Your System for information on configuring items like Hospital, Department, Lang uage, Units (of measure), Date, Time and Date Format.

For information on configuring Software Op tio ns , Refe r t o th e LO GI Q e/L OGI Q e Vet/ LOGI Q i/ Viv id e Basic User Manual, Chapter 16, Customizing Your System.

For information on configuring DICOM Connectivity, Refer to the LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e Basic User Manual, Chapter 16, Customizing Your System.

Chapter 3 System Setup 3-27

GE HEALTHCARE

Site System Information

Services (Destination Devices)

TCP/IP Settings

Device Type

Manufacturer

Name

IP Address

Port

AE Title

1 2 3 4 5 6 7 8 9 10 11 12

Name - AE Title:

Dept:

LOGIQ SN:

Type:

Floor:

Room:

REV:

Comments:

CONTACT INFORMATION

Name

Title

Phone

E-Mail Address

Site:

IP Settings

IP Address:

Subnet Mask:

Default Gateway:

Remote Archive Setup

Remote Archive IP:

Remote Archive Name:

DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

Section 3-8 Connectivity Installation Worksheet

3-28 Section 3-8 - Connectivity Installation Workshee t

GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

Section 3-9 Loading Base Image Software

This information has been moved, please refer to:

Section 8-3 "Loading Base Image Software" on page 8-4

Chapter 3 System Setup 3-29

GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

Section 3-10Software Version check out

3-10-1 Functional Check-out

1.) Power on LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e scanner and wait until system booting to main screen.

2.) Press Utility/Config

3.) Choose the About

key on control panel.

button on the right.

Figure 3-27 About

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

Figure 3-28 Software version

3-30 Section 3-10 - Software Version check out

GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

Section 3-11 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.

3-11-1 Product Locator Installation

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

card.

3-11-2 User Manual(s)

User Check that the correct User Manual(s) for the system and software revision, is included with the installation. Specific language versions of the User Manual may also be available. Check with your GE Sales Representative for availability.

Figure 3-29 Product Locator Installation Card

Chapter 3 System Setup 3-31

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This page was intentionally left blank.

3-32 Section 3-11 - Paperwork

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IRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E 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 LOGIQ e/LOGIQ e Vet/ LOGIQ i/Vivid e console, diagnostics by using the built-in service software, and power supply adjustments.

Table 4-1 Contents in chapter 4

Section Description Page Number

4-1

4-2

4-3

4-4

4-5

Section 4-2 Required Equipment

To perform these tests, you'll need any of the sector, linear, or convex transducers. (normally you should check all the transducers used on the system)

Overview

Required Equipment

General Procedure

Software Configuration Checks

Peripheral Checks

4-1

4-2

4-37

Chapter 4 Functional Checks 4-1

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CAUTION

NOTICE

Signed

Date

TAG

LOCKOUT

UPUP

DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

Section 4-3 General Procedure

SYSTEM REQUIRES ALL COVERS Operate this unit only when all board covers and fr ame panels are securely in place . The covers are required for safe operation, good system performance and cooling purposes.

Lockout/Tagout Requirements (For USA only) Follow OSHA Lockout/Tagout requirements by ensuring you are in total control of the Power Cable on

the system.

4-3-1 Power On/Boot Up

After AC/DC is connected correctly to the scanner, the power is applied to the scanner. When the Control panel Power On/Off key is pressed once, the System starts.

4-3-1-1 Scanner Power On

Lower the handle. Plug the AC adapter output connector into the system DC input po rt (located on the system’s rear panel) with the arrow side upward. Plug the AC adapter power cor d into a grounded, protective earth outlet.

Figure 4-30 connect AC adapter

4-2 Section 4-3 - General Procedure

GE HEALTHCARE

Power On/Off switch

IRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

4-3-1-1 Scanner Power On (cont’d)

When power is applied to the scanner, power is distributed to the Cooling Unit, Control Panel, LCD, Peripherals and the Back-end Processor.

4-3-1-2 Turn on the system

Press the Power On/Off switch at the front of the system once.

Figure 4-31 Power On/Off Switch

When the Power On/Off switch on the Control Panel is pressed once, the Back-end Processor starts and the software code is distributed to initiate the scanner.

No status messages are displayed during this process.

4-3-2 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.

4-3-2-1 Back-end Processor Power Down

To power down the system:

1.) Press the Power On/Off switch at the front of the system once.

2.) The System-Exit window is displayed.

3.) Using the Trackball or Select key, select Shutdown.

Figure 4-1 System Exit Window

Chapter 4 Functional Checks 4-3

GE HEALTHCARE

CAUTION

DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

4-3-2-1 Back-end Processor Power Down (cont’d)

4.) The shutdown process takes 15 seconds and the power off sequence is complete when the powe r

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.

6.) Close LCD cover.

4-3-2-2 Scanner Shutdown

Disconnect the Mains Power Cable is necessary. For example: Relocating the scanner.

DO NOT unplug and/or transport the unit until after the power off sequence has been comple ted. Failure to do so may result in corrupted patient files.

4-3-2-3 Full Maintenance Reboot

Full Maintenance Reboot will fully restart the whole system for performance improvement.

NOTE: It’s recommended to do Full Maintenance Reboot at least daily or when system starts to slow

down or lag in its reaction.

1.) Press the Power On/Off switch at the front of the system once.

2.) Click “Full Maintenance Reboot”.

3.) Full Maintenance Reboot dialog is display ed .

Figure 4-2 “Full Maintenance Reboot” dialog

4-3-2-4 Exit (only activated for LOGIQ e R6.0.2)

Exit will reboot application.

1.) Press the Power On/Off switch at the front of the system once.

2.) Click “Exit”.

3.) The application will reboot.

4-4 Section 4-3 - General Procedure

GE HEALTHCARE

NOTICE

IRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

4-3-3 Archiving and Loading Presets

NOTE: Always save presets before any software reload. This ensures the presets loaded after the software

reload are as up–to–date as possible.

All user presets except changes to Summary, Anatomy, and Biometry page s, can be saved on an DVDR disk (or USB memory device) for reloading on the system.

Presets should NOT be saved on the same DVD-R disk (or USB memory device) as images. The Archive Menu lists the images but does NOT list the presets stored on a DVD-R disk (or USB memory device).

4-3-3-1 Archiving Presets to an DVD-R Disk (or USB memory device)

1.) Insert an empty (blank) DVD-R disk into the DVD-RW.

2.) Access to the Utility/Config Menu, and select System. The Backup sheet will be shown on the LCD

display.

Figure 4-3 Backup Sheet

3.) Select the item to Backup/Restore.

4.) Enter backup destination or browse through the disk to locate the destination.

5.) Select Backup now. The backup status for each item is displayed on the Result column.

Chapter 4 Functional Checks 4-5

GE HEALTHCARE

NOTICE

Signed

Date

TAG

LOCKOUT

DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

4-3-3-2 Loading Presets from an DVD-R disk (or USB memory device)

1.) Insert the DVD-R disk with the archived Presets into the DVD-RW.

2.) Access to the Utility/Config Menu, and select System. The Restore sheet will be shown on th e LCD

display. (see Figure 4-3 on page 4-5 )

3.) Select the item to restore either from Resource Files.

4.) Enter restore destination or browse through the disk to locate the destination.

5.) Select Restore. The restore status for each item is displayed on the Result column.

4-3-4 Adjusting the Display Monitor

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

4-3-5 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.

Energy Control and Power Lockout for LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e 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.

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.

4-6 Section 4-3 - General Procedure

GE HEALTHCARE

IRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

4-3-6 System Features

4-3-6-1 Control Panel

Figure 4-4 Control Panel Tour

1.) TGC

2.) New Patient

3.) End Exam

4.) Mode/Gain/Auto Keys

5.) Preset Key

6.) Imaging/Measurement Keys

7.) Depth/Zoom/Ellipse

8.) Image Keys

9.) Print Keys

10.)Freeze

11.) Keyboard

Chapter 4 Functional Checks 4-7

GE HEALTHCARE

DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

4-3-6-2 LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e SoftMenu Key Tour

In general, there are two types of softMenu keys: Paddle Switch and adjustable knobs.

Figure 4-5 SoftMenu Key Tour

1.) The Paddle Switch is used to access and adjust the Sub SoftMenu.

2.) Press the adjustable knobs to toggle option menu between line one and line two.

3.) Rotate the adjustable knobs to adjust the correspondi ng paramete rs.

4-8 Section 4-3 - General Procedure

GE HEALTHCARE

5 6

21 22

12 3

IRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

4-3-6-3 Monitor Display

Figure 4-6 Monitor Display Tour

Table 4-2 Monitor Display Features

1. Institution/Hospital Name, Date, Time, Operator Identification, system status (real-time of frozen).

2. Patient Name, Patient Identification. 14. Focal Zone.

3. Acoustic Output Readout, 15. TGC (not shown on the image).

4. GE Symbol: Probe Orientation Marker. Coincides with a probe orientation marking on the probe.

5. Image Preview. 17. Depth Scale.

6. Gray/Color Bar. 18. SoftMenu

7. Cine Gauge. 19. Caps Lock: On/Off.

8. Measurement Summary Window. 20. Start menu icon.

9. Image. 21. Battery icon.

10. Measurement. 22. Network icon.

11. Results Window. 23. Trackball Functionality Status: Scroll, M&A (Measurement

12. Probe Identifier. Exam Study. 24. Active key for Depth/Zoom/Ellipse

13. Imaging Parameters by Mode (current mode highlighted).

16. Body Pattern.

and Analysis), Position, Size, Scan Area Width and Tilt.

Chapter 4 Functional Checks 4-9

GE HEALTHCARE

SoftMenu Key Primary Menu

Scan Area

B Mode

Zoom/Depth

Freeze

Secondary Menu

DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

4-3-7 B Mode Checks

4-3-7-1 Preparations

1.) Connect one of the probes listed in 3-6-6 "Available Probes" on pa ge 3-25, in Chapter 3 Installation to the System probe connector.

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

NOTE: The keyboard layout varies from each Product, the following figures show LOGIQ e R5.x.x as

an example.

Figure 4-7 Controls available in B Mode

Figure 4-8 B Mode Screen Picture Example

4-10 Section 4-3 - General Procedure

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IRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

4-3-7-2 B Mode OP Panel Controls

Table 4-3 B Mode Control Panel Controls

Step Task Expected Result(s) Comments

Press B Mode key B Mode Starts

Adjust the field of view. Increasing the depth may view larger/deeper structures rates, and

Adjust Depth

Adjust Gain

Adjust Focus

decreasing the depth may view near the skin line.Press Up/Down Button to increase/ decrease. Depth displays on the monitor in cm.

Controls the amount of echo information displayed in an image. Turn B Mode dial to the left/right to increase/decrease Gain. Gain displays on the monitor in Gn (dB).

Increases the number of focal zones or moves the focal zone(s) to tighten up the beam for specific area. Press the control to toggle between Focus Position and Focus Number. Press Up/Down Button to move or adjust the focal numbers.

Activate Auto Optimize

Adjust Time Gain Compensation (TGC)

Adjust Scan Area

Adjust Zoom

Reverse

Optimize the image based upon a specified region of interest or anatomy. Press the Center Button in the Gain Dial to toggle the ATO/ACE On and Off.

Amplifies the returning signals to correct for the attenuation caused by tissues at increasing depth. TGC slide pots spaced proportional to the depth. Move the slide pots to the left/right to decrease/increase TGC. A TGC curve appears on the display.

Widen or narrow the size of the sector angle to maximize the image’s region of interest (ROI). Press Scan Area and move the Trackball to narrow/widen the angle.

Changes the location of the focal point(s). A triangular focus marker indicates the depth of the focal point.

Toggles the left/right orientation of the scan image.

Chapter 4 Functional Checks 4-11

GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

4-3-7-3 B Mode Softmenu Key

Table 4-4 B Mode Softmenu Key

Step Task Expected Result(s) comments

Adjust Rejection

Activate Colorize

Adjust Edge Enhance

Adjust Edge Enhance/Contour

Activate Gray Map

Adjust Frequency

Adjust Frame Average

Adjust DDP

Selects a level below which echoes will not be amplified (an echo must have a certain minimum amplitude before it will be processed).

Enables gray scale image colorization. To deactivate, reselect a Gray Map.

Edge Enhance brings out subtle tissue differences and boundaries by enhancing the gray scale differences corresponding to the edges of structures. Adjustments to M Mode's edge enhancement affects the M Mode only.

Determines how the echo intensity levels received are presented as shades of gray.

Multi Frequency mode lets you downshift to the probe's next lower frequency or shift up to a higher frequency.

Temporal filter that averages frames together. This has the effect of presenting a smoother, softer image.

For LOGIQ e, LOGIQ e Vet and LOGIQ i

For Vivid e

For LOGIQ e, LOGIQ e Vet and LOGIQ i

For Vivid e

Adjust Rotation

Adjust Line Density

Adjust Frame Rate

Power output

Dynamic Range

Focus Number and Position

Virtual Convex Virtual Convex for linear probe

Virtual Apex Virtual Convex for Sector probe

Rotates the image by selecting the value from the pop-up menu.

Optimizes B Mode frame rate or spatial resolution for the best possible image.

Optimizes image quality and allows user to reduce beam intensity. 2% increments between 0-100%. Values greater than 0.1 are displayed.

Dynamic Range controls how echo intensities are converted to shades of gray, thereby increasing the adjustable range of contrast.

Increases the number of transmit focal zones or moves the focal zone(s) so that you can tighten up the beam for a specific area. A graphic caret corresponding to the focal zone position(s) appears on the right edge of the image.

4-12 Section 4-3 - General Procedure

For LOGIQ e, LOGIQ e Vet and LOGIQ i

For Vivid e

Only for LOGIQ e R5.x.x/R6.x.x/ R7.x.x, LOGIQ e Vet, LOGIQ i R5.x.x, Vivid e R5.x.x, Vivid e R6.x.x

GE HEALTHCARE

Primary Menu Secondary Menu

M Mode

Gain

M/D Cursor

IRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

4-3-8 M Mode Controls

4-3-8-1 Preparations

1.) Connect one of the probes listed in 3-6-6 "Available Probes" on pa ge 3-25, in Chapter 3 Installation to the System probe connector.

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

Figure 4-9 Controls available in M Mode

Figure 4-10 M Mode Screen Picture Example

Chapter 4 Functional Checks 4-13

GE HEALTHCARE DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

4-3-8-2 M Mode OP Panel Controls

Table 4-5 M Mode OP Panel Controls

Step Task Expected Result(s) Comments

Press M Mode key M Mode Starts

Controls the amount of echo information

Adjust Gain

displayed in an image. Turn B Mode dial to the left/right to increase/decrease Gain. Gain displays on the monitor in Gn (dB).

Display M-Mode Cursor

Displays the M-Mode cursor on the B-Mode image. Press Cursor and Trackball to position M-Mode Cursor.

4-14 Section 4-3 - General Procedure

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IRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

4-3-8-3 M Mode Softmenu Key

Table 4-6 M Mode Softmenu Key

Step Task Expected Result(s) Comments

Selects a level below which echoes will not be

Adjust Rejection

amplified (an echo must have a certain minimum amplitude before it will be processed).

Adjust Sweep Speed

Adjust Edge Enhance

Adjust Edge Enhance/Contour

Activate Gray Map

Activate Colorize

Activate Full Timeline

Select Display Format

Select Layout

Adjust Dynamic Range

Changes the speed at which the time line is swept. The following speed values are available, 1, 2, 3, 4, 6, 8, 12, 16.

Determines how the echo intensity levels received are presented as shades of gray.

Enables gray scale image colorization. To deactivate, reselect a Gray Map.

Displays only timeline screen. Press the Full Timescreen to activate.

Select the format to display B image and M image on the LCD. Press Display Format, and select from the pop up menu.

Select the Layout to display B image and M image on the LCD. Press Display Format, and select from the pop up menu.

Dynamic Range controls how echo intensities are converted to shades of gray, thereby increasing the adjustable range of contrast.

For LOGIQ e, LOGIQ e Vet and LOGIQ i

For Vivid e

For LOGIQ e, LOGIQ e Vet and LOGIQ i

For Vivid e

Power output

Optimizes image quality and allows user to reduce beam intensity. 2% increments between 0-100%. Values greater than 0.1 are displayed.

Chapter 4 Functional Checks 4-15

GE HEALTHCARE

Primary Menu

CF Mode

Gain

Secondary Menu

DIRECTION 5370626-100, REVISION 7 LOGIQ E/LOGIQ E VET/LOGIQ I/VIVID E BASIC SERVICE MANUAL

4-3-9 Color Flow Mode Checks

4-3-9-1 Preparations

1.) Connect one of the probes listed in 3-6-6 "Available Probes" on pa ge 3-25, in Chapter 3 Installation to the System probe connector.

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

Figure 4-11 Contro ls available in Color Flow Mode

Figure 4-12 CFM Mode Screen Picture Example

4-16 Section 4-3 - General Procedure

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