GE Logiq E9 User manual

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GE Healthcare

LOGIQ E9

Service Manual

11/19/12 GEHC_FRNT_CVR.FM

Part Number: 5180263-100

Revision: Rev 5

GE HEALTHCARE

WARNING

(EN)

AVERTISSEMENT

(FR)

WARNUNG

(DE)

DIRECTION 5180263-100, REV 5 LOGIQ E9 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 BENÖTIGT, IST ES AUFGABE DES KUNDEN FÜR EINE ENTSPRECHENDE ÜBERSETZUNG ZU SORGEN.

• VERSUCHEN SIE NICHT, DAS GERÄT ZU REPARIEREN, BEVOR DIESES KUNDENDIENST-HANDBUCH NICHT ZU RATE GEZOGEN UND VERSTANDEN WURDE.

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

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AVISO

(ES)

ATENÇÃO

(PT-Br)

(PT-pt)

AVISO

AVVERTENZA

(IT)

DIRECTION 5180263-100, REV 5 LOGIQ E9 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)

DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

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 KÄÄNNÖKSEN HANKKIMINEN ON ASIAKKAAN VASTUULLA.

• ÄLÄ YRITÄ KORJATA LAITTEISTOA ENNEN KUIN OLET VARMASTI LUKENUT JA YMMÄRTÄNYT TÄMÄN HUOLTO-OHJEEN.

• MIKÄLI TÄTÄ VAROITUSTA EI NOUDATETA, SEURAUKSENA VOI OLLA 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 ΣΥΜΒΟΥΛΕΥΤΕΙ ΚΑΙ ΕΧΕΤΕ ΚΑΤΑΝΟΗΣΕΙ ΤΟ ΠΑΡΟΝ ΕΓΧΕΙΡΙΔΙΟ ΣΕΡΒΙΣ

• ΕΑΝ ΔΕ ΛΑΒΕΤΕ ΥΠΟΨΗ ΤΗΝ ΠΡΟΕΙΔΟΠΟΙΗΣΗ ΑΥΤΗ, ΕΝΔΕΧΕΤΑΙ ΝΑ

ΠΡΟΚΛΗΘΕΙ ΤΡΑΥΜΑΤΙΣΜΟΣ ΣΤΟ ΑΤΟΜΟ ΠΑΡΟΧΗΣ ΣΕΡΒΙΣ, ΣΤΟ ΧΕΙΡΙΣΤΗ Ή ΣΤΟΝ ΑΣΘΕΝΗ ΑΠΟ ΗΛΕΚΤΡΟΠΛΗΞΙΑ, ΜΗΧΑΝΙΚΟΥΣ Ή ΑΛΛΟΥΣ ΚΙΝΔΥΝΟΥΣ.

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.

GE HEALTHCARE

VIÐVÖRUN

(IS)

VÝSTRAHA

(CS)

ADVARSEL

(DA)

WAARSCHUWING

(NL)

DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

ÞESSI ÞJÓNUSTUHANDBÓK ER EINGÖNGU FÁANLEG Á ENSKU.

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

• 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.

•VPŘÍPADĚ, ŽE POSKYTOVATEL SLUŽEB ZÁKAZNÍKŮM POTŘEBUJE NÁVOD V JINÉM JAZYCE, JE ZAJIŠTĚNÍ PŘEKLADU DO ODPOVÍDAJÍCÍHO JAZYKA ÚKOLEM ZÁKAZNÍKA.

• NEPROVÁDĚJTE ÚDRŽBU TOHOTO ZAŘÍZENÍ, ANIŽ BYSTE SI PŘEČETLI TENTO SERVISNÍ NÁVOD A POCHOPILI JEHO OBSAH.

•VPŘÍPADĚ NEDODRŽOVÁNÍ TÉTO VÝSTRAHY MŮŽE DOJÍT ÚRAZU ELEKTRICKÁM PROUDEM PRACOVNÍKA POSKYTOVATELE SLUŽEB, OBSLUŽNÉHO PERSONÁLU NEBO PACIENTŮ VLIVEM ELEKTRICKÉHOP PROUDU, RESPEKTIVE VLIVEM K RIZIKU MECHANICKÉHO POŠKOZENÍ NEBO JINÉMU RIZIKU.

DENNE SERVICEMANUAL FINDES KUN PÅ ENGELSK.

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

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

• MANGLENDE OVERHOLDELSE AF DENNE ADVARSEL KAN MEDFØRE SKADE PÅ GRUND AF ELEKTRISK, MEKANISK ELLER ANDEN FARE FOR TEKNIKEREN, OPERATØREN ELLER PATIENTEN.

DEZE ONDERHOUDSHANDLEIDING IS ENKEL IN HET ENGELS VERKRIJGBAAR.

• ALS HET ONDERHOUDSPERSONEEL EEN ANDERE TAAL VEREIST, DAN IS DE KLANT VERANTWOORDELIJK VOOR DE VERTALING ERVAN.

• PROBEER DE APPARATUUR NIET TE ONDERHOUDEN VOORDAT DEZE ONDERHOUDSHANDLEIDING WERD GERAADPLEEGD EN BEGREPEN IS.

• INDIEN DEZE WAARSCHUWING NIET WORDT OPGEVOLGD, ZOU HET ONDERHOUDSPERSONEEL, DE OPERATOR OF EEN PATIËNT GEWOND KUNNEN RAKEN ALS GEVOLG VAN EEN ELEKTRISCHE SCHOK, MECHANISCHE OF ANDERE GEVAREN.

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BRĪDINĀJUMS

(LV)

ĮSPĖJIMAS

(LT)

ADVARSEL

(NO)

OSTRZEŻENIE

(PL)

DIRECTION 5180263-100, REV 5 LOGIQ E9 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, MECHANINIŲ AR KITŲ PAVOJŲ.

DENNE SERVICEHÅNDBOKEN FIN

NES 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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ATENŢIE

(RO)

ОСТОРОЖНО!

(RU) (BG)

ПРЕДУПРЕЖДЕНИЕ

UPOZORENJE

(SR)

DIRECTION 5180263-100, REV 5 LOGIQ E9 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 РУКОВОДСТВО ПО ОБСЛУЖИВАНИЮ ПРЕДОСТАВЛЯЕТСЯ ТОЛЬКО НА АНГЛИЙСКОМ ЯЗЫКЕ.

• ЕСЛИ СЕРВИСНОМУ ПЕРСОНАЛУ КЛИЕНТА НЕОБХОДИМО РУКОВОДСТВО НЕ НА АНГЛИЙСКОМ ЯЗЫКЕ, КЛИЕНТУ СЛЕДУЕТ САМОСТОЯТЕЛЬНО ОБЕСПЕЧИТЬ ПЕРЕВОД.

• ПЕРЕД ОБСЛУЖИВАНИЕМ ОБОРУДОВАНИЯ ОБЯЗАТЕЛЬНО ОБРАТИТЕСЬ К ДАНН

• НЕСОБ

ОМУ РУКОВОДСТВУ И ПОЙМИТЕ ИЗЛОЖЕННЫЕ В НЕМ СВЕДЕНИЯ.

ЛЮДЕНИЕ 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, РАЗЛИЧЕН

ОТ АНГЛИЙСКИ, ЗАДЪЛЖЕНИЕ НА КЛИЕНТА Е ДА

ПРЕДОСТАВИ ПРЕВОДАЧЕСКА УСЛУГА.

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

• НЕСПАЗВАНЕТО НА ТОВА ПРЕДУПРЕЖДЕНИЕ МОЖЕ ДА ДОВЕДЕ ДО НАРАНЯВАНЕ НА ДОСТАВЧИКА НА СЕРВИЗНИ УСЛУГИ, НА ОПЕРАТОРА ИЛИ ПАЦИЕНТА ВСЛЕДСТВИЕНА ТОКОВ УДАР, МЕХ

АНИЧНИ 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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UPOZORENJE

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UPOZORNENIE

(SK)

VARNING

(SV)

DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

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 NEBEZPEČENSTVA.

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.

GE HEALTHCARE

DİKKAT

(TR)

(JA)

Traditional

Chinese

DIRECTION 5180263-100, REV 5 LOGIQ E9 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)

(KO)

DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

GE HEALTHCARE

DANGER

WARNINGWARNING

DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

DAMAGE IN TRANSPORTATION

All packages should be closely examined at time of delivery. If damage is apparent write “Damage In Shipment” on ALL copies of the freight or express bill BEFORE delivery is accepted or “signed for” by a GE representative or hospital receiving agent. Whether noted or concealed, damage MUST be reported to the carrier immediately upon discovery, or in any event, within 14 days after receipt, and the contents and containers held for inspection by the carrier. A transportation company will not pay a claim for damage if an inspection is not requested within this 14 day period.

CERTIFIED ELECTRICAL CONTRACTOR STATEMENT - FOR USA ONLY

All electrical Installations that are preliminary to position ing of the equipment at the site prepar ed for the equipment shall be performed by licensed electrical contractors. Othe r co nnections b etween pieces o f electrical equipment, calibrations and testing shall be performed by q ualified GE Healthcare personne l. In performing all electrical work on these products, GE will use its own specially trained field engineers. All of GE’s electrical work on these products will comply with the requirements of the applicable electrical codes.

The purchaser of GE equipment shall only utilize qualified personnel (i.e., GE’s field engineers, personnel of third-party service companies with equivalent training, or licensed electricians) to perform electrical servicing on the equipment.

OMISSIONS & ERRORS

If there are any omissions, errors or suggestions for improving this documentation, please contact the GE Healthcare Global Documentation Group with specific information listing the system type, manual title, part number, revision number, page number and suggestion details.

Mail the information to: Service Documentation 9900 Innovation Drive (RP-2123) Wauwatosa, WI 53226, USA.

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

SERVICE SAFETY CONSIDERATIONS

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: Section 1-4 "Safety considerations" on page 1-

16. of the latest version of LOGIQ E9 Service Manual.

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GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 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.

PROPRIETARY TO GE HEALTHCARE

Permission to use this Advanced Service Software and related documentation (herein called the Material) by persons other than GE Healthcare employe es is provided only under an Advanced Service Package License relating specifically to this Proprietary Material. This is a different agreement from the one under which operating and basic service software is licensed. A license to use operating or basic service software does not extend to or cover this software or related documentation.

If you are a GE Healthcare employee or a customer who has entered into such a license agreement with GE Healthcare to use this proprietary software, you are authorized to use this Material according to the conditions stated in your license agreement.

However, you do not have the permission of GE Healthcare to alter, decompose or reverse-assemble the software, and unless you are a GE employee, you may not copy the Material. The Material is protected by Copyright and Trade Secret laws; the violation of which can result in civil damages and criminal prosecution.

If you are not party to such a license agreement or a GE Healthcare Employee, you must exit this Material now.

TRADEMARKS

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

COPYRIGHTS

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GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

Revision History

Date

Revision

Rev 1 2008/09/16 Initial R1.0.3 Release Rev 2 2008/12/01 R1.0.4 Release Rev 3 2009/10/01 R2.0.0 Release Rev 4 2011/01/14 R3.1.0 Release Rev 5 2012/11/06 R4 Release

YYYY/MM/DD

Reason for change

List of Effected Pages (LOEP)

Pages Revision Pages Revision Pages Revision

Title Page Rev 5 4-1 to 4-52 Rev 5 10-1 to 10-28 Rev 5

Warnings Rev 5 5-1 to 5-24 Rev 5 Index Rev 5

TOC Rev 5 6-1 to 8-226 Rev 5 Back Cover N/A 1-1 to 1-26 Rev 5 7-1 to 7-120 Rev 5 2-1 to 2-12 Rev 5 8-1 to 8-226 Rev 5 3-1 to 3-78 Rev 5 9-1 to 9-98 Rev 5

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GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 SERVICE MANUAL

Table of Contents

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 SERVICE MANUAL

CHAPTER 1

Introduction

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

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

Service manual overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 2

Contents in this service manual . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 3

Typical users of the “Basic” Service Manual . . . . . . . . . . . . . . . . . . . . . . . .1 - 4

LOGIQ E9 models covered by this manual . . . . . . . . . . . . . . . . . . . . . . . . .1 - 4

Product description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 5

Overview of the LOGIQ E9 ultrasound scanner . . . . . . . . . . . . . . . .1 - 6

Important conventions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 7

Conventions used in book . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 7

Standard hazard icons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 8

Product icons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 10

Safety considerations. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 16

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 16

Human safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 16

Mechanical safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 18

Electrical safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 20

Label locations. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 20

Dangerous procedure warnings. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 21

Lockout/Tagout (LOTO) requirements. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 22

Returning/Shipping Probes and Repair Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 22

Electromagnetic compatibility (EMC). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 23

What is EMC? . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 23

Compliance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 23

Electrostatic discharge (ESD) prevention . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 23

Customer assistance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 24

Contact information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 24

System manufacturer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 25

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GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 SERVICE MANUAL

CHAPTER 2

Site preparations

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

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

General console requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2

Console environmental requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2

Electrical requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 3

Site circuit breaker . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 4

EMI limitations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 5

Probes environmental requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 6

Time and manpower requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 6

Facility needs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 7

Purchaser responsibilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 7

Required facility needs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 8

Desirable features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 9

Minimal floor plan suggestions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 9

Networking setup requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 11

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 SERVICE MANUAL

CHAPTER 3

LOGIQ E9 Setup

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

Purpose of this chapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 1

Setup reminders. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 2

Average setup time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 2

Setup warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 2

Receiving and unpacking the equipment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 4

Purpose of this section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 4

Receiving and unpacking warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 4

Receiving the LOGIQ E9 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 5

The Tilt and Shock indicators . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 6

LOGIQ E9 Transportation Box Label . . . . . . . . . . . . . . . . . . . . . . . .3 - 7

Unpacking the LOGIQ E9 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 8

Packing materials - recycling information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 12

Preparing for setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 13

Verify Customer Order . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 13

Physical inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 13

Volume Navigation Stand . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 13

Back Cover Label and ETL testing laboratories

safety rating label (ETL may not be present) . . . . . . . . . . . . . . . .3 - 14

EMI protection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 15

Completing the setup. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 16

Purpose of this section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 16

LOGIQ E9 specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 16

Electrical specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 17

Connections on the I/O Rear Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 18

Connections on the Patient I/O panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 20

Connecting Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 20

Connect a probe . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 21

Power On/Boot Up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 22

Connect AC (mains) Power to the LOGIQ E9 . . . . .

Switch ON the AC Power to LOGIQ E9 . . . . . . . . . . . . . . . . . . . . . .3 - 24

Power shut down . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 26

Complete power down . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 28

. . . . . . . . . . . . .3 - 23

Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 31

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GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 SERVICE MANUAL

Purpose of this section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 31

LOGIQ E9 configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 31

Optional Peripherals/Peripheral Connection . . . . . . . . . . . . . . . . . . . . . . . . 3 - 32

Printer/DVR Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 33

Available Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 33

Software Options Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 33

Installing a Software Option . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 34

Connectivity overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 36

Physical connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 36

Connectivity Setup and Tips. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 36

Setup the LOGIQ E9 for DICOM Communications for R2.x.x Software (some features

only apply to R3.x.x) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 37

Devices, Services, Dataflows and Print Buttons . . . . . . . . . . . . . . . . . . . . . 3 - 39

How to Get the LOGIQ E9 to Recognize another Device on the Network . 3 - 40

How to Setup and Use a DICOM Image Storage Service . . . . . . . . . . . . . 3 - 41

Properties . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 44

Sending Images and Data to a DICOM Image Storage Service . . . 3 - 48

How to Setup and Use a DICOM Print Service . . . . . . . . . . . . . . . . 3 - 54

How to Setup and Use a DICOM Worklist Service . . . . . . . . . . . . . 3 - 57

How to Setup and Use a DICOM

MPPS (Modality Performed Procedure Step) Service . . . . . . . . 3 - 62

How to Setup and Use a DICOM Storage Commitment Service . . . 3 - 64

Structured Reporting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 66

How to Setup and Use a DICOM Query/Retrieve (Q/R) Service . . . 3 - 68

Spooler . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 72

Network “Sniffer” . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 74

Setup paperwork . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 78

User Manual(s) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 78

Product Locator Card . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 78

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 SERVICE MANUAL

CHAPTER 4

Functional Checks

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

Purpose of this chapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 1

Special Equipment required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 1

General procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 2

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 2

Power ON/Boot Up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 3

Connect AC (mains) Power to the LOGIQ E9 . . . . . . . . . . . . . . . . . .4 - 4

Turn Unit ON . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 5

Power shut down . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 7

Complete Power Down . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 9

Top Console position adjustment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 10

LCD Monitor Positions and Lock . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 11

To unlock the LCD Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 12

Removable Media . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 13

Archiving and Loading Presets . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 13

Space Management . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 13

Backup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 13

Moving and Transporting the LOGIQ E9 . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 14

To ensure safety while moving the LOGIQ E9 . . . . . . . . . . . . . . . . .4 - 15

Recording important settings and parameters . . . . . . . . . . . . . . . . . . . . . . .4 - 16

Connectivity — Recording the TCP/IP settings . . . . . . . . . . . . . . . . .4 - 17

Connectivity — WLAN . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 18

Connectivity — Recording the AE Title and Port settings . . . . . . . . .4 - 19

Connectivity — Recording Device Destination settings . . . . . . . . . .4 - 20

Connectivity — Recording Dataflow settings . . . . . . . . . . . . . . . . . .4 - 21

Connectivity — Recording the Print Key Assignments . . . . . . . . . . .4 - 22

Connectivity — Recording Miscellaneous settings . . . . . . . . . . . . . .4 - 23

Admin — Recording the Software Option Keys . . . . . . . . . . . . . . . .4 - 25

Admin — Users . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 26

System — Data Store Management . . . . . . . . . . . . . . . . . . . . . . . . .4 - 27

System — Recording Peripheral settings . . . . . . . . . . . . . . . . . . . . .4 - 28

System — Recording software and hardware versions . . . . . . . . . .4 - 29

Functional checks

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 30

Preparation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 30

Basic Controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 30

Performance Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 31

B-Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 32

6 -

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 30

Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 33

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 SERVICE MANUAL

M-Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 34

System CFM and PWD Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 35

PW/CW Doppler Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 36

Tissue Velocity Imaging (TVI) Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 37

Contrast checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 38

Basic Measurements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 38

Check Circumference/Area (Ellipse) Measurement . . . . . . . . . . . . . 4 - 39

Multi Image Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 40

Backup and Restore Database, Preset Configurations and Images . . . . . 4 - 40

Software Configuration Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 40

Probe/Connectors Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 41

Peripherals Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 42

Cineloop Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 43

Back End Processor checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 44

Mechanical Function Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 45

Operator I/O Movement - LCD . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 46

Application Turnover Check List. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 47

Software Configuration Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 47

Power supply test and adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 47

Power Supply Test Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 47

3D/4D and Volume Navigation Functional Check . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 47

Site Log . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 48

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 SERVICE MANUAL

CHAPTER 5

Components and Functions (Theory)

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

Purpose of this chapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 1

LOGIQ E9 description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 2

Purpose of this section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 2

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 2

LOGIQ E9 general description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 3

LOGIQ E9 Overall block diagram . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 3

Signal flow overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 7

LOGIQ E9’s Operating Modes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 9

Top Console with LCD monitor and Operator Panel . . . . . . . . . . . . . . . . . . . . . . . .5 - 12

Purpose of this section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 12

Transporting LOGIQ E9 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 12

Top Console description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 13

Operator Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 14

Operator Panel Block Diagram . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 15

Main Console. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 16

Main Console description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 16

Air Flow control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 17

General description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 17

Location in the LOGIQ E9 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 17

Casters and Brakes description. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 17

Power distribution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 18

Purpose of this section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 18

Main Power Supply . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 18

Power Up Sequence Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 21

Power Down Sequence description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 22

Cables for LOGIQ E9. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 23

Probes description. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 23

Product manuals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 24

User documentation

Service documentation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 24

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 24

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GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 SERVICE MANUAL

CHAPTER 6

Service Adjustments

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

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

LCD Monitor adjustments. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 2

Purpose of this section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 2

Cautions and Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 2

Access to Adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 3

LCD Adjustment Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 4

Advanced LCD Adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 5

for R3.x.x, procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 8

DC Offset Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 9

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 9

When to do a DC Offset Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 9

Operator Panel movement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 10

Purpose of this section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 10

Adjusting the XY Locking Mechanism . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 10

Adjusting the Z Mechanism . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 11

XY Manual Release for Lock and Brake Mechanism and Adjustment . . . . 6 - 11

XY Lock Adjustment for Lock and Brake Mechanism . . . . . . . . . . . 6 - 13

Using the Park Lock Properly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 16

Operator Panel XY movement - principle of operation . . . . . . . . . . . . . . . . 6 - 16

Direction Lock and Brake adjustments. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 17

Adjust time-out for DICOM servers. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 17

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 SERVICE MANUAL

CHAPTER 7

Diagnostics/Troubleshooting

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

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

Service Safety Considerations. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 2

Gathering Troubleshooting Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 3

Purpose of this Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 3

Collecting Vital System Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 4

Collecting a Screen Capture with Logs . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 5

Capturing Service Logs with ALT+D . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 7

Capturing Network Logs with Network Sniffer (Software R1.x.x) . . . . . . . . .7 - 8

Capturing Network Logs with Network Sniffer (Software R2.x.x or later) . . .7 - 14

Screen Captures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 20

Purpose of this Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 20

Ctrl+PrintScreen Shortcut . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 20

To Capture a Screen Image Using the Shortcut . . . . . . . . . . . . . . . . . . . . .7 - 20

Common Service Desktop . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 21

Purpose of this Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 21

Error Logs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 22

Diagnostics Window Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 24

Diagnostic Utility Freezes Up/Times Out . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 28

Diagnostic Symptom Guide . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 28

OP Panel Utilities - Op Panel Interface . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 30

Launching the Op Panel Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 31

Trackball Tab . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 35

Keyboard Tab . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 36

Slidepots Tab . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 37

Encoders Tab . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 38

Pushbuttons Tab . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 39

LEDs Tab . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 40

Touchscreen Tab . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 41

Ending th

Diagnostics - Common Diagnostics . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 42

Diagnostics for Service Diagnostics . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 43

e Program . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 41

Memory . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 47

GFI . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 50

System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 53

Noise . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 55

10 -

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 SERVICE MANUAL

Transmit/Receive . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 57

Analog Receive . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 58

Analog CW . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 61

I/O Board Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 67

Tx Power Supply Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 71

EPS (Extended Power Shutdown) or

CB (ChargeBoard used in BEP6) Tests . . . . . . . . . . . . . . . . . . . 7 - 73

bayBIRD Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 75

DVR Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 80

Essential Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 82

System Board . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 83

Hard Disk Drive Surface Scan . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 84

Hard Disk Drive Quick Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 85

Video Card . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 86

Network Adapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 87

Network Adapter Diagnostic Changes for R4 . . . . . . . . . . . . . . . . . 7 - 88

Memory . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 89

Diagnostics - BEP Interactive Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 90

Diagnostics - BEP Interactive Tests - R4.x and later . . . . . . . . . . . . . . . . . 7 - 91

Keyboard . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 92

Mouse (Trackball) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 94

Audio (Sound) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 95

Touch Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 96

Calibration Verification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 97

4D Motor Controller . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 98

Patient I/O Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 100

Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 101

InSite ExC Agent Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 102

Utilities - Common Utilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 103

Disruptive Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 104

IP Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 105

Windows Services . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 106

User Accounts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 107

System Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 108

Disk Defragmenter

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 109

Gather Logs Utility . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 110

Image Compress & Delete Utility . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 111

Scanner Documentation Interface . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 112

Distinct Network Monitor R1.x.x . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 113

Virtual Console Observation (VCO) . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 114

Telnet Server Control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 115

Utilities - Scanner Utilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 116

Replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 117

PM . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 118

Noise . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 119

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 SERVICE MANUAL

CHAPTER 8

Replacement procedures

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

Purpose of this chapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 1

Warnings and important information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 2

Purpose of this section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 2

Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 2

Returning/Shipping Probes and Repair Parts . . . . . . . . . . . . . . . . . . . . . . .8 - 4

Manpower - When two persons are needed . . . . . . . . . . . . . . . . . . . . . . . .8 - 4

Tools needed for servicing LOGIQ E9 . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 5

Definitions of Left, Rear / Back, Right and Front . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 6

Loading / Reloading / Upgrading the Software . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 7

Purpose of this section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 7

LOGIQ E9 models versus software requirement . . . . . . . . . . . . . . . . . . . . .8 - 8

Tools provided with the LOGIQ E9 or as part of an upgrade . . . . . . . . . . . .8 - 8

Space management - moving all images . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 9

Backing up the Patient Archive and System Configurations . . . . . . . . . . . .8 - 10

Loading the Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 10

Loading the System Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 11

Loading the Application Software . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 16

Functional Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 21

Loading the Application Software Only . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 21

Verify and Update Vital Product Data . . . . . . . . . . . . . . . . . . . . . . . .8 - 25

Replacing Covers and Bumpers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 26

Purpose of this section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 26

Side Covers replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 27

Side Covers removal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 28

Side Covers installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 29

Calibration and adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 30

Top Cover replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 31

Top Cover installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 32

Foot Rest Bumper replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 33

Foot Rest Bumper installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8

Front Cover replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 35

Front Cover removal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 36

Filter Cover replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 37

Rear Cover replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 38

Rear Cover removal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 39

Rear Cover installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 40

12 -

- 34

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 SERVICE MANUAL

Calibration and adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 41

Door, I/O Panel replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 42

Door, I/O Panel removal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 43

Rear Bumper replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 44

LCD Monitor V2 Arm Assembly Covers replacement . . . . . . . . . . . . . . . . . 8 - 45

Calibration and adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 46

Rear Handle replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 47

Rear Handle installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 48

Bulkhead Cover replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 49

Bulkhead Cover installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 51

Replacing Top Console Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 52

Purpose of this section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 52

LCD Monitor assembly replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 53

LCD Monitor installation - R3.x and earlier . . . . . . . . . . . . . . . . . . . 8 - 56

LCD Monitor V2 removal (used in R4.x and later production) . . . . . 8 - 58

LCD Monitor V2 installation (used in R4.x and later production) . . . 8 - 60

Calibration and adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 62

WLAN replacement - R2.x and R3.x only . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 63

WLAN removal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 64

Functional Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 67

Probe Holder Insert replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 68

Probe Holder Insert removal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 69

OP Panel Knobs replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 70

Upper Operator Panel / Touch Panel Assembly replacement . . . . . . . . . . 8 - 71

Upper OP Panel/Touch Panel Assembly removal . . . . . . . . . . . . . . 8 - 72

Upper OP Panel/Touch Panel Assembly installation . . . . . . . . . . . . 8 - 75

Calibration and adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 79

Alphanumeric (A/N) Keyboard replacement . . . . . . . . . . . . . . . . . . . . . . . . 8 - 80

Alphanumeric Keyboard assembly removal . . . . . . . . . . . . . . . . . . . 8 - 81

Alphanumeric Keyboard assembly installation . . . . . . . . . . . . . . . . 8 - 83

Calibration and adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 84

Lower Operator Panel (OP) replacement . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 85

Lower Operator Panel (OP) removal . . . . . . . . . . . . . . . . . . . . . . . . 8 - 86

Lower Op Panel Board replacement . . . . . . . . . . . . . . . . . . . . . . . . 8 - 88

Lower Operator Panel installation . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 98

Calibration and adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

8 - 99

Options Holder / Left or Right Support replacement . . . . . . . . . . . . . . . . . . 8 - 100

Options Holder removal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 101

Options Holder installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 102

Calibration and adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 103

Gel Warmer replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 104

Gel Warmer removal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 105

Gel Warmer installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 106

Calibration and adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 107

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 SERVICE MANUAL

Storage Tray / Transvaginal Probe Holder replacement . . . . . . . . . . . . . . .8 - 108

Storage Tray / Transvaginal Probe Holder installation . . . . . . . . . . .8 - 109

Replacing the Gel Warmer with a Storage Tray or TV/TR Probe Holder . . .8 - 110

Probe Cable Hooks replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 111

Probe Cable Hooks Functional Checks . . . . . . . . . . . . . . . . . . . . . . .8 - 112

Main Console parts replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 113

Purpose of this section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 113

Rear Filter and “handle type“ Bottom Filter replacement / cleaning . . . . . . .8 - 114

Bottom Filter installation (looped type strap) . . . . . . . . . . . . . . . . . . . . . . . .8 - 118

Removal Process with Non-loop Type Strap . . . . . . . . . . . . . . . . . . .8 - 120

Casters and Brakes replacement. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 123

Rear Casters replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 123

Rear Casters removal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 124

Rear Casters installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 125

Front Casters replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 126

Front Casters removal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 127

Front Casters installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 128

BEP (Back End Processor) parts replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 129

Purpose of this section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 129

BEP replacement - R3.x and earlier . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 130

BEP replacement - R4.x and later . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 138

BEP removal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 140

Calibration and adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 146

BEP PB installationBEP I/O Board Assembly

replacement - R3.x and earlier . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 147

BEP I/O Board removal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 149

BEP Side I/O Board Assembly replacement - R4.x and later . . . . . . . . . . .8 - 152

BEP Side I/O Board removal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 153

Calibration and adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 156

BEP HDD (Hard Disk Drive) replacement - R3.x and earlier . . . . . . . . . . . .8 - 157

HDD removal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 158

BEP HDD replacement - R4.x and later . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 161

HDD removal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 162

HDD installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 164

Calibration and adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 165

BEP Battery Pack replacement - R3.x and earlier . . . . . . . . . . . . . . . . . . . .8 - 166

BEP Battery Pack removal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 168

BEP Battery Pack installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 169

BEP Battery Pack replacement - R4.x and later . . . . . . . . . . . . . . . . . . . . .8 - 170

Battery Pack replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 172

BEP Battery Pack installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 173

Calibration and adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 174

14 -

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 SERVICE MANUAL

Main Power Supply parts replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 175

Purpose of this section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 175

Main Power Supply replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 176

Main Power Supply removal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 177

Main PS installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 179

Main Power Supply Fan Assembly replacement . . . . . . . . . . . . . . . . . . . . 8 - 181

Main Power Supply Fan Assembly removal . . . . . . . . . . . . . . . . . . 8 - 182

4D Motor Controller (4D MC) replacement . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 186

4D Motor Controller removal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 187

Peripherals replacement. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 196

Purpose of this section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 196

Internal Peripherals overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 197

DVD R/W drive replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 197

Calibration and adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 199

Digital Video Recorder (DVR) replacement . . . . . . . . . . . . . . . . . . . . . . . . 8 - 199

DVD Storage Tray replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 200

DVD Storage Tray removal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 201

Calibration and adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 202

Digital Graphic Printer replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 203

Calibration and adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 204

Printer Bracket replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 205

Printer Bracket removal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 206

Calibration and adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 207

V Nav Roll Stand and/or On-Board Stand Installation and/or Replacement . . . . . 8 - 208

Parts Reference - Roll Stand . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 209

Assembling or replacing the Roll Stand . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 211

Parts Reference - On-board V Nav Stand . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 217

On-Board V Nav Stand Option Contents, location and placement of parts 8 - 220

Assembling or replacing the On-Board V Nav Stand . . . . . . . . . . . . . . . . . 8 - 221

Adjusting Tension on Sliding Mechanism . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 224

Calibration and adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 225

Verification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 225

Functional Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 225

Routine Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 226

Cleaning the Mounting Assembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 226

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 SERVICE MANUAL

CHAPTER 9

Renewal Parts

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

Purpose of this chapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 1

Definitions of Left, Rear / Back, Right and Front . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 2

List of Abbreviations. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 3

Parts list groups. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 4

LOGIQ E9 Models and hardware/software compatibility. . . . . . . . . . . . . . . . . . . . .9 - 5

Software. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 6

Covers and Bumpers. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 9

Top Console parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 16

XYZ Mechanism parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 32

Main Console parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 35

Casters (Wheels) parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 37

Card Rack parts. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 39

DRX Boards Compatible Configurations . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 47

Front End Boards Compatible Configurations . . . . . . . . . . . . . . . . . . . . . . .9 - 48

GTX Boards Compatible Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 51

Back End Processor (BEP) parts. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 52

Back End Boards Compatible Configurations . . . . . . . . . . . . . . . . . . . . . . .9 - 59

Main Power Supply parts. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 60

Peripherals. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 63

Printers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 64

Digital Video Disc (DVD) Drive . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 66

Peripherals Compatible Configurations . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 67

Mains Power Cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 68

Internal Cables. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 70

Top Console Cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 70

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GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 SERVICE MANUAL

XYZ Controller cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 73

Main Power Supply cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 74

Card Rack cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 76

Back End Processor (BEP) cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 78

Peripherals Cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 84

Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 86

Options. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 90

Options Compatible Configurations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 93

Hardware Kit. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 94

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 SERVICE MANUAL

CHAPTER 10

Care & Maintenance

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

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

Periodic maintenance inspections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .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

System maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 3

Preliminary checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 3

“Standard” GE Tool Kit in the USA . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 4

Functional checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 6

System checks. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 6

Peripheral/option checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 7

Mains cable inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 7

Optional diagnostic checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 7

View the logs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 7

Physical inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 8

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

Air filter cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 9

Probe maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 9

Using a Phantom . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 9

Electrical Safety Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 9

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 9

Safety test overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 10

Leakage Current Limits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 11

Grounding continuity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 13

Chassis leakage current test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 14

Generic Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 15

Data sheet for enclosure/chassis leakage current . . . . . . . . . . . . . . . . . . . .10 - 16

Isolated patient lead (source) leakage-lead to ground . . . . . . . . . . . . . . . . .10 - 17

Generic Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 18

Isolated patient lead (source) leakage–lead to lead . . . . . . . . . . . . . . . . . . .10 - 19

Lead to lead leakage test record . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 20

Isolated patient lead (sink) leakage-isolation test . . . . . . . . . . . . . . . . . . . .10 - 20

18 -

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 SERVICE MANUAL

Isolated lead (sink) leakage test record . . . . . . . . . . . . . . . . . . . . . . 10 - 21

Probe leakage current test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 22

Mains on applied part . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 25

When There’s Too Much Leakage Current... . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 26

Chassis Fails . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 26

Probe Fails . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 26

Peripheral Fails . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 26

Still Fails . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 26

New Unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 27

ECG Fails . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 27

Ultrasound Equipment Quality Check (EQC and IQC) . . . . . . . . . . . . . . . . 10 - 27

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

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GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

Chapter 1 Introduction

Section 1-1 Overview

1-1-1 Purpose of this chapter

This chapter describes important issues related to safely servicing LOGIQ E9. The service provider must read and understand all the information presented here before installing or servicing a unit.

Chapter 1 Introduction 1 - 1

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

Section 1-2 Service manual overview

Attention

This manual contains necessary and sufficient information for the Field Service Engineer or Biotech Engineer to maintain and service the system safely. Advanced equipment training may be pr ovided by factory trained Field Service trainers for the agreed-upon time period.

This service manual provides installation and service information for the LOGIQ E9 ultrasound scanning unit. It is divided in 10 chapters as shown below, in Table 1-1 "Contents in this se rvice manual" on page

1-3.

Indications for Use

The LOGIQ E9 is intended for use by a qualified physician for ultrasound evaluation. Specific clinical applications and exam types include:

• Fetal/Obstetrics

• Abdominal (includes renal, GYN/Pelvic)

• Pediatric

• Small Organ (breast, testes, thyroid)

• Neonatal Cephalic

• Adult Cephalic

• Cardiac (adult and pediatric)

• Peripheral Vascular

• Musculo-skeletal Conventional and Superficial

• Urology (including prostate)

• Transrectal

• Transvaginal

• Transesophageal

• Intraoperative (abdominal, thoracic, vascular and neurosurgical)

Contraindication

The LOGIQ E9 ultrasound system is not intended for ophthalmic use or any use causing the acoustic beam to pass through the eye.

1 - 2 Section 1-2 - Service manual overview

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

1-2-1 Contents in this service manual

The service manual is divided into ten chapters. In the beginning of the manual, before chapter 1, you will find the language policy for GE Healthcare’s

service documentation, legal information, a revision overview, and the Table of Contents (TOC). An Index has been included after chapter 10.

Table 1-1 Contents in this service manual

CHAPTER

NUMBER CHAPTER TITLE DESCRIPTION

1 2 Site preparations Contains pre-setup requirements for the LOGIQ E9.

3 System Setup Contains setup procedure with procedure checklist. 4 Functional Checks Contains functional checks that must be performed as part of the

5 Components and Functions (Theory) Contains block diagrams and functional explanations of the

6 Service Adjustments Contains instructions on how to make any available adjustments to

7 Diagnostics/Troubleshooting Provides procedures for running diagnostic or related routines for the

8 Replacement procedures Provides disassembly procedures and reassembly procedures for all

9 Renewal Parts Contains a complete list of replacement parts for the LOGIQ E9.

10 Care & Maintenance Provides periodic maintenance procedures for LOGIQ E9.

N/A

Introduction Contains a content summary and warnings.

installation, or as required during servicing and periodic maintenance.

electronics.

the LOGIQ E9.

LOGIQ E9.

changeable FRUs, available option installation instructions, and upgrade installation instructions.

Index A quick way to the topic you’re looking for.

Chapter 1 Introduction 1 - 3

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

1-2-2 Typical users of the “Basic” Service Manual

• Service Personnel (setup, maintenance, etc.)

• Hospital’s Service Personnel

• Architectural Planners/Installation Planners (some parts of Chapter 2 - Site preparations)

1-2-3 LOGIQ E9 models covered by this manual

Table 1-2 LOGIQ E9 Software Configurations and Hardware/Software Compatibility -

Upgrade Options

CONSOLE

MODEL

NUMBER

5205000 LOGIQ E9, 100-240 VAC Y Y Y Y U U U U U U U 5205000-2 LOGIQ E9, 220-240 VAC Y Y Y Y U U U U U U U 5205000-3 LOGIQ E9, 100-240 VAC N N N N Y Y Y U U U U

DESCRIPTION SOFTWARE VERSION

Phase I BT2010 BT2011 BT2013

1.0.3 1.0.4 1.0.5 1.0.6 2.0.3 2.0.4 2.0.5 3.1.0 3.1.1 3.1.2

4 Rev. x.x

5205000-4 LOGIQ E9, 220-240 VAC N N N N Y Y Y U U U U 5205000-5 LOGIQ E9, 100-240 VAC N N N N N N N N Y Y U 5205000-6 LOGIQ E9, 220-240 VAC N N N N N N N N Y Y U 5205000-7 LOGIQ E9, 100-240 VAC N N N N N N N N N N Y

LOGIQ E9 Software Configurations and Hardware/Software Compatibility - Upgrade Options

LOGIQ E9 Software Configurations and Hardware/Software

Compatibility - Upgrade Options

Y Original U Upgrade available N Not supported

Front End Processor - see: 9-12-2 "Front End Boards Compatible Configurations" on page 9-48. Back End Processor - see: 9-13-1 "Back End Boards Compatible Configurations" on page 9-59.

NOTE: When not otherwise specified, the contents of this manual applies to all LOGIQ E9 models.

1 - 4 Section 1-2 - Service manual overview

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

1-2-4 Product description

Chapter 1 Introduction 1 - 5

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

1-2-4-1 Overview of the LOGIQ E9 ultrasound scanner

The LOGIQ E9 ultrasound unit is a high performance digital ultrasound imaging system with tota l data management.

The system provides image generation in B-Mode, Color Doppler, Power Doppler, M-Mode, Color M-Mode, PW and 4D, Tissue Velocity imaging, Volume-Guided Ultrasound and Contrast applications. The fully digital architecture of the LOGIQ E9 unit allows optimal usage of all scanning modes and probe types throughout the full spectrum of operating frequencies.

Signal flows from the Probe Connector Panel to the Front End, and then over to the Back End Proc essor and finally to the monitor and peripherals.

System configuration is stored on the hard drive in the Back End Processor. All necessary software is loaded from the hard drive on power up.

1-2-4-2 Purpose of the operator manual(s)

The operator manuals should be fully read and understood before operating the LOGIQ E9. The online versions of the operator manuals are availabl e via the Help function on LOGIQ E9’s operator

panel.

1 - 6 Section 1-2 - Service manual overview

GE HEALTHCARE

DANGER

WARNINGWARNING

CAUTION

NOTICE

DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

Section 1-3 Important conventions

1-3-1 Conventions used in book

1-3-1-1 Model designations

This manual covers the LOGIQ E9 scanners listed in 1-2-3 "LOGIQ E9 models covered by this manual"

on page 1-4.

1-3-1-2 Icons

Pictures, or icons, are used wherever they will reinforce the printed message. The icons, labels, and conventions used on the product and in the service information are described in this chapter.

1-3-1-3 Safety precaution messages

Various levels of safety precaution messages may be found on the equipment and in the service information. The different levels of concern are identified by a flag word that precedes the precautionar y message. Known or potential hazards to personnel are labeled in one of three ways:

•DANGER

• WARNING

•CAUTION When a hazard is present that can cause property damage, but has absolutely no personal injury risk,

a NOTICE is used.

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 abs olutely no personal injury risk.

Notice Example: Disk drive may crash.

NOTE: Notes are used to provide important information about an item or a procedure. NOTE: Be sure to read the notes; the information contained in a note can often save you time or effort.

Chapter 1 Introduction 1 - 7

GE HEALTHCARE

LASER

LIGHT

DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

1-3-2 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 grap hical icons (symbols) may be used to make you aware of specific types of hazards that could possibly cause harm. Even if a symbol isn’t used in this manual, it may be included for your reference.

Table 1-3 Standard hazard icons

DANGER WARNING CAUTION

BIOLOGICAL ELECTRICAL MOVING

ACOUSTIC OUTPUT EXPLOSION SMOKE / FIRE

LASER HEAT PINCH

1 - 8 Section 1-3 - Important conven ti o ns

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

1-3-2Standard hazard icons (cont’d)

Table 1-4 Standard hazard icons (cont’d)

RADIATION “ “

““

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

Table 1-5 Standard Icons that indicate that a special procedure is to be used

AVOID STATIC ELECTRICITY TAG AND LOCK OUT WEAR EYE PROTECTION

TAG

LOCKOUT

Date

Signed

HAND PROTECTION FOOT PROTECTION “

“

Chapter 1 Introduction 1 - 9

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

1-3-3 Product icons

The following table describes the purpose and location of safety labe ls and other important inform ation provided on the equipment.

Table 1-6 Product icons 1 of 6

LABEL/SYMBOL PURPOSE/MEANING LOCATION

Identification and Rating Plate

Type/Class Label

Manufacturer’s name and address

Date of manufacture

Serial Number

Catalog Number

Used to indicate the degree of safety or protection.

United States only Prescription Requirement label

Rear panel

Rating Plate

Rear panel

Authorized European Representative address

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

Equipment Type BF Applied Part (man in the box with paddle) symbol is in accordance with IEC 60417-5334.

1 - 10 Section 1-3 - Important conventio ns

Rear panel

Probe connectors including Doppler

probe connector

Probe

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

Table 1-6 Product icons (Continued) 2 of 6

LABEL/SYMBOL PURPOSE/MEANING LOCATION

Device Listing/Certification Labels

Equipment Type CF (heart in the box symbol) IEC 878-02-05 indicates equipment having a floating applied part having a degree of protection suitable for direct cardiac contact.

DEFIBRILLATOR-PROOF TYPE CF EQUIPMENT.

Laboratory logo or labels denoting conformance with industry safety standards such as UL or IEC.

This precaution is intended to prevent injury that may result if one person attempt to move the unit considerable distances or on an incline due to the weight of the unit.

DO NOT push the system. Use the handle to push/pull the system, e.g., DO NOT use the LCD. Failure to do so may cause serious injury or system damage.

Probe connectors and ECG connector.

On newer systems also on the rear of

the system.

At the ECG connector on front of

system.

Rear of console

Rear cover label

Rear of LCD Monitor

Rear of On-Board V Nav Stand

“DANGER - Risk of explosion used in...”

Follow Instructions for Use. “ATTENTION” - Consult accompanying documents is intended to alert the user to refer to the operator manual or other instructions when complete information cannot be provided on the label.

The system is not designed for use with flammable anesthetic gases.

Rear of particular Main Power Supply

Rear Cover,

Rear of LCD Monitor,

Miscellaneous Probe Labels

Rear cover console

Rear of console

Chapter 1 Introduction 1 - 11

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

Table 1-6 Product icons (Continued) 3 of 6

LABEL/SYMBOL PURPOSE/MEANING LOCATION

C-UL Mark Parts Indicates that the product has been

tested and approved in UL Laboratories, based on UL and CSA standards, through mutual approval activities.

This unit carries the CE mark. The LOGIQ E9 unit complies with

regulatory requirements of the European Directive 93/ 42/EEC concerning medical devices.

It also complies with emission limits for a Group 1, Class B Medical Device as stated in EN 60601-1-2 (IEC 60601-1-2).

Rear of LCD Monitor (inside)

Footswitch

Rear of console

“CAUTION” The equilateral triangle is usually used in combination with other symbols to advise or warn the user.

“ATTENTION - Consult accompanying documents”

is intended to alert the user to refer to the operator manual or other instructions when complete information cannot be provided on the label.

General Warning

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

“Mains OFF” Indicates the power off position of the mains power switch.

Various

Various, Rear Cover, Probe Label

Various

Rear of system adjacent to

MAINS Switch

“PINCH POINT” Indicates moving parts that may cause injury (such as LCD arm or XYZ Mech)

1 - 12 Section 1-3 - Important conventio ns

Various

GE HEALTHCARE

DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

Table 1-6 Product icons (Continued) 4 of 6

LABEL/SYMBOL PURPOSE/MEANING LOCATION

“Mains ON”

Indicates the Power ON position of the mains power switch.

“ON” Indicates the power on position of the power switch.

CAUTION

Rear of console

THE ON/OFF BUTTON ON THE OPERATOR PANEL DOES NOT ISOLATE MAINS SUPPLY

ON/OFF button

CAUTION SYSTEM SHUTDOWN USING THE ON/OFF BUTTON DOES NOT DISCONNECT LOGIQ E9 FROM MAINS VOLTAGE.

For disconnecting LOGIQ E9 from mains voltage after system shutdown, please set the circuit breaker close to the mains inlet to OFF as described in

4-2-4 "Power shut down" on page 4-7.

Operating Panel

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

“Equipotential” Indicates the terminal to be used for connecting equipotential conductors when interconnecting (grounding) with other equipment as described in IEC60601-1.

Alternating Current symbol is in accordance with IEC 60878-01-14.

This symbol indicates that waste electrical and electronic equipment must not be disposed of as unsorted municipal waste and must be collected separately. Please contact an authorized representative of the manufacturer for information concerning the decommissioning of your equipment.

Used several places inside the system.

Rear of console

Rear Panel, Rating Plate, Circuit

breaker label of console and Front

Panel (if applicable).

Rear of console

Rear of LCD Monitor (inside)

Chapter 1 Introduction 1 - 13

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

Table 1-6 Product icons (Continued) 5 of 6

LABEL/SYMBOL PURPOSE/MEANING LOCATION

This product consists of devices that may contain mercury, which must be

recycled or disposed of in accordance with local, state, or country laws. (Within this system, the backlight lamps in the monitor display, contain mercury.)

Rear of LCD Monitor (inside)

Rear Panel

ETL Listing Mark Monogram

GOST Symbol. Russia Regulatory Country Clearance.

ISO 7010 - P007 Volume Navigation Pacemaker Warning

Indicates the presence of hazardous substance(s) above the maximum concentration value. Maximum concentration values for electronic information products, as set by the People’s Republic of China Electronic Industry Standard SJ/T11364-2006, include the hazardous substances of lead, mercury, hexavalent chromium, cadmium, polybrominated biphenyl (PBB), and polybrominated diphenyl ether (PBDE). “10” indicates the number of years during which the hazardous substance(s) will not leak or mutate so that the use of this product will not result in any severe environmental pollution, bodily injury, or damage to any assets.

Rear Panel

V Nav Transmitter

Probe

1 - 14 Section 1-3 - Important conventio ns

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

Table 1-6 Product icons (Continued) 6 of 6

LABEL/SYMBOL PURPOSE/MEANING LOCATION

Indicates the presence of hazardous substance(s) above the maximum concentration value. Maximum concentration values for electronic information products, as set by the People’s Republic of China Electronic Industry Standard SJ/T11364-2006, include the hazardous substances of lead, mercury, hexavalent chromium, cadmium, polybrominated biphenyl (PBB), and polybrominated diphenyl ether (PBDE). “20” indicates the number of years during which the hazardous substance(s) will not leak or mutate so that the use of this product will not result in any severe environmental pollution, bodily injury, or damage to any assets.

China Rating Plate

How to lower LCD prior to transport

How to lock Operator Panel prior to transport

DO NOT place a finger, hand or any object on the joint of the monitor or monitor arm to avoid injury when moving the monitor and monitor arm.

Non-ionizing Electromagnetic Radiation Label

Rear of the LCD monitor.

Rear Panel

Chapter 1 Introduction 1 - 15

GE HEALTHCARE

DANGER

WARNINGWARNING

DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

Section 1-4 Safety considerations

1-4-1 Introduction

The following safety precautions must be observed during all phases of operation, service and repair of this equipment. Failure to comply with these precautions or with specific warnings elsewhere in this manual, violates safety standards of design, manufacture and intended use of the equipment.

1-4-2 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 E9 Training Seminar are authorized to service the

equipment.

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

IF THE COVERS ARE REMOVED FROM AN OPERATING LOGIQ E9, SOME METAL SURFACES MAY BE WARM ENOUGH TO POSE A POTENTIAL HEAT HAZARD IF TOUCHED, EVEN WHILE IN SHUTDOWN MODE.

BECAUSE OF THE LIMITED ACCESS TO CABINETS AND EQUIPMENT IN THE FIELD, PLACING PEOPLE IN AWKWARD POSITIONS, GE HAS LIMITED THE LIFTING WEIGHT FOR ONE PERSON IN THE FIELD TO 16 KG (35 LBS). ANYTHING OVER 16 KG (35 LBS) REQUIRES 2 PEOPLE.

USE ALL PERSONAL PROTECTION EQUIPMENT (PPE) SUCH AS GLOVES, SAFETY SHOES, SAFETY GLASSES, AND KNEELING PAD, TO REDUCE THE RISK OF INJUR Y.

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.

1 - 16 Section 1-4 - Safety considerations

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

1-4-2Human safety (cont’d)

WARNINGWARNING

When the top console is in its locked position, the gas shock is compressed and stores mechanical energy. During normal operation the top console, the weight of the monitor and the mechanical force of the gas shock are in balance. Take care if/ when you activate this gas shock. Personal injury can occur after the panel is removed and the shock pressure is released. Take care when you repair the elevation assembly.

Ensure that the system is turned off and unplugged.

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.

Beware that the Main Power Supply, Extended Power Shutdown and Back End Processor may be energized even if the power is turned off when the cord is still plugged into the AC Outlet

Risk of electrical shock, system must be turned off and disconnected from power source. Cord must be controlled at all times.

discharge as there are no test points to verify isolation. The Amber light on the Op Panel On/Off button will turn off.

Beware that the Main Power Supply, Extended Power Shutdown and Back End Processor may be energized even if the power is turned off when the cord is still plugged into the AC Outlet

Wait for at least 20 seconds for capacitors to

Use extreme caution as long as THE LOGIQ E9 is un-stable, not resting on all four Casters.

WARNINGWARNING

Tilting the console requires two people in order to avoid injury to service personnel and damage to the equipment.

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

Beware of possible sharp edges on all mechanical parts. If sharp edges are encountered, the appropriate PPE should be used to reduce the risk of injury.

Wear all PPE including gloves as indicated in the chemical MSDS.

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WARNINGWARNING

CAUTION

DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

1-4-3 Mechanical safety

While the software install procedure is designed to preserve data, you should save any patient data, images, system setups to a DVD or hardcopy before doing a software upgrade.

PRIOR TO ELEVATING THE SCANNER, VERIFY THAT THE KEYBOARD IS LOCKED IN ITS LOWEST POSITION. VERIFY THAT THE FRONT BRAKE IS LOCKED AND THE SCANNER IS UNABLE TO SWIVEL. VERIFY THAT THE REAR BRAKES ARE IN THE LOCKED POSITION.

WHEN THE UNIT IS RAISED FOR A REPAIR OR MOVED ALONG ANY INCLINE, USE EXTREME CAUTION SINCE IT MAY BECOME UNSTABLE AND TIP OVER.

ULTRASOUND PROBES ARE HIGHLY SENSITIVE MEDICAL INSTRUMENTS THAT CAN EASILY BE DAMAGED BY IMPROPER HANDLING. USE CARE WHEN HANDLING AND PROTECT FROM DAMAGE WHEN NOT IN USE. DO NOT USE A DAMAGED OR DEFECTIVE PROBE. FAILURE TO FOLLOW THESE PRECAUTIONS CAN RESULT IN SERIOUS INJURY AND EQUIPMENT DAMAGE.

REMEMBER: If the front caster swivel lock is engaged for transportation, pressing the release pedal once disengages the swivel lock. You must depress the release pedal a second time to engage the brake.

The system should NOT be moved with the Operator I/O Panel extended. Move the Operator I/O Panel to its centered and locked position. Lower the Operator I/O Panel as much as possible before moving the system.

BEFORE YOU MOVE OR TRANSPORT THE SYSTEM, MAKE SURE TO LOCK THE LCD MONITOR ARM FIRMLY AND FLIP DOWN THE MONITOR TO PREVENT DAMAGE TO THE SYSTEM.

Always lock the Top/Upper Console in its parking (locked) position before moving the scanner around.

TO AVOID INJURY WHEN YOU MOVE THE LCD MONITOR AND THE MONITOR ARM, DO NOT PUT YOUR FINGER, HAND, OR OBJECT ON THE JOINT OF THE MONITOR OR THE MONITOR ARM.

1 - 18 Section 1-4 - Safety considerations

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

1-4-3Mechanical safety (cont’d)

CAUTION

LOGIQ E9 WEIGHS 135 KG (298 LB), R3.X AND EARLIER, 140 KG (309 LB), R4.X AND LATER, OR MORE, DEPENDING ON INSTALLED PERIPHERALS, WHEN READY FOR USE. CARE MUST BE USED WHEN MOVING IT OR REPLACING ITS PARTS. FAILURE TO FOLLOW THE PRECAUTIONS LISTED BELOW COULD RESULT IN INJURY, UNCONTROLLED MOTION AND COSTLY DAMAGE. ALWAYS:

- BE SURE THE PATHWAY IS CLEAR.

- USE SLOW, CAREFUL MOTIONS.

- USE TWO PEOPLE WHEN MOVING ON INCLINES OR LIFTING MORE THAN 16 KG (35 LBS).

TO AVOID INJURY OR DAMAGE TO THE MONITOR, MAKE SURE THERE IS NOTHING WITHIN RANGE OF THE LCD BEFORE MOVING THE MONITOR AND MONITOR ARM. THIS INCLUDES PEOPLE AS WELL AS THINGS.

Ensure that nobody touches the console arm/frogleg when moving the Operator Panel.

Use Protective Glasses during drilling, filing and during all other work where eyes need protection.

CAUTION

NOTICE

Use Safety Shoes when doing work where there is any chance of foot damage.

Use Protective Gloves when drilling and cutting.

Be careful not to pinch any of the cables.

NOTE: Special care should be taken when transporting the unit in a vehicle, see 4-2-14-4 "T ransporting

the unit by vehicle" on page 4-18.

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WARNINGWARNING

DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

1-4-4 Electrical safety

1-4-4-1 Safe practices

Follow these guidelines to minimize shock hazards whenever you are using the scanner:

• The equipment chassis must be connected to an electrical ground.

• The unit is equipped with a three-conductor AC power cable. This must b e plugged into an approved electrical outlet with safety ground. A separate po we r outle t w ith a 20 am p circuit breaker for 120 VAC for 120V area, 7.5 amp circuit breaker for 220-240 VAC for 220/240V area or 15 amp circuit breaker for 100 VAC for Japan.

• The power outlet used for this equipment should not be shared with other types of equipment.

• Both the system power cable and the power co nnector must meet international electrical standard s.

Connecting a LOGIQ E9 scanner to the wrong voltage level will most likely destroy it.

1-4-4-2 Probes

Follow these guidelines before connecting a probe to the scanner:

• Inspect the probe prior to each use for damage or degr adation to the:

- housing

- cable strain relief

-lens

- seal

- connector pins

- locking mechanism

• Do not use a damaged or defective probe.

• Never immerse the probe connector or adapter into any liquid.

• The system has more than one type of probe port. Use the appropriate probe port designed for the probe you are connecting.

Section 1-5 Label locations

Refer to the current revision of the LOGIQ E9 Basic User Manual, 5180374-100, Chapter 2.

1 - 20 Section 1-5 - Label locations

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DANGER

WARNINGWARNING

DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

Section 1-6 Dangerous procedure warnings

Warnings, such as the example 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.

IF THE COVERS ARE REMOVED FROM AN OPERATING LOGIQ E9, SOME METAL SURFACES MAY BE WARM ENOUGH TO POSE A POTENTIAL HEAT HAZARD IF TOUCHED, EVEN WHILE IN SHUT DOWN MODE.

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.

Chapter 1 Introduction 1 - 21

GE HEALTHCARE

NOTICE

Signed

Date

TAG

LOCKOUT

DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

Section 1-7 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.) Disconnect the Extended Power Shutdown battery at J3 when working in the BEP.

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 E9 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 iso lation. The Amber light on the Op Panel On/Off button will turn off.

5. Disconnect the eps battery at j3 WHEN WORKING IN THE BEP. Beware that the Main Power Supply, Extended Power Shutdown and Back End Processor may be

energized even if the power is turned off when the cord is still plugged into the AC Outlet.

Section 1-8 Returning/Shipping Probes and Repair Parts

Equipment being returned must be clean and free of blood and other in fectious substances. GE Healthcare policy states that body fluids must be properly removed from any part or equipment prior

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

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

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

dripping with human blood that are now caked with dried blood; or which were used or intended for use in patient care” are “regulated medical waste” for tran sporta tion pu rposes and must be transported as a hazardous material.

1 - 22 Section 1-7 - Lockout/Tagout (LOTO) requirements

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WARNINGWARNING

DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

Section 1-9 Electromagnetic compatibility (EMC)

1-9-1 What is 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 inte nded due interfer ence from its enviro nment or when the device produces unacceptable levels of emission to its environmen t. This interference is often referred to as radio–frequency or electromagnetic interference (RFI/EMI) and can be radiated through space or conducted over interconnecting power of signal cables. In addition to ele ctromagnetic energy, EMC also includes possible effects from electrical fields, magnetic fields, electrostatic discharge and disturbances in the electrical power supply.

1-9-2 Compliance

LOGIQ E9 conforms to all applicable conducted and radiated emission limits and to immunity from electrostatic discharge, radiated and conducted RF fields, magnetic fields and power line transient requirements.

Applicable standards are: 47CFR Part 18, IEC60601–1–2:2001.

NOTE: For CE Compliance, it is critical that all covers, screws, shielding, gaskets, mesh, clamps, are

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

1-9-3 Electrostatic discharge (ESD) prevention

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

1. ALWAYS CONNECT YOURSELF, VIA AN ARM-WRIST STRAP, TO THE ADVISED ESD CONNECTION POINT LOCATED ON THE REAR OF THE SCANNER (TO THE RIGHT OF THE POWER CONNECTOR).

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

Risk of electrical shock, system must be turned off. Avoid all contact with electrical contacts, conductors and components. Always use non-conductive handles designed for the removal and replacement of ESD sensitive parts. All parts that have the potential for storing energy must be discharged or isolated before making contact.

Chapter 1 Introduction 1 - 23

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

Section 1-10 Customer assistance

1-10-1 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.

Before you call, identify the following information, and acquire image (Alt+D) to send to the Customer Care team:

1.) System ID serial number.

2.) Software version.

3.) Date and time of occurrence.

4.) Sequence of events leading to issue.

5.) Is the issue repeatable?

6.) Imaging mode, probe, preset/application.

7.) Media brand, speed, capacity, type.

8.) Save secondary image capture, cine loop, 4D multi-volume loop.

NOTE: Restart the application before resuming clinical scanning.

Table 1-7 Phone numbers for Customer Assistance

LOCATION PHONE NUMBER

USA GE Healthcare - GE Medical Systems

Ultrasound & Primary Care Diagnostics, LLC 9900 Innovation Drive Wauwatosa, WI 53226

Canada 1-800-668-0732

Latin America

Europe GE Ultraschall Deutschland Gmbh & Co. KG Beethovenstrasse 239 Postfach 11 05 60, D-42655 Solingen Germany

Asia (Singapore) GE Ultrasound Asia Service Department - Ultrasound 298 Tiong Bahru Road #15-01/06 Central Placa Singapore 168730

Service: On-site

Service Parts

Application Support

Service Application Support

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

+49 (0) 212-2802-652

Fax: +49 (0) 2122-8024-31

Tel: +65 6291-8528

Fax: +65 6291-7006

1-800-437-1171

1-800-558-2040

1-800-682-5327 or 1-262-524-5698

1-262-524-5300 1-262-524-5698

Japan Support Center

Phone: 81-426-48-2940 Fax: 81-426-48-2905

1 - 24 Section 1-10 - Customer assistance

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

1-10-2 System manufacturer

Table 1-8 System manufacturer

MANUFACTURER FAX NUMBER

GE Healthcare - GE Medical Systems Ultrasound and Primary Care Diagnostics, LLC 9900 Innovation Drive Wauwatosa, WI 53226 USA

Table 1-9 Authorized Representative

AUTHORIZED REPRESENTATIVE TELEPHONE / FAX NUMBER

The location of the CE marking is shown in the Safety chapter of this manual.

414-721-3865

+49 761 45 43 -0 /

+49 761 45 43 -233

Authorized EU Representative European registered place of business: GE Medical Systems Information Technologies GmbH(GEMS IT GmbH) Munzinger Strasse 3, D-79111 Freiburg, GERMANY

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1 - 26 Section 1-10 - Customer assistance

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Chapter 2 Site preparations

Section 2-1 Overview

2-1-1 Purpose of this chapter

This chapter provides the information re qu ir ed to plan and prepare for the setup of a LOGIQ E9. Included are descriptions of the facility and electrical needs to be met by the purchaser of the LOGIQ E9.

Chapter 2 Site preparations 2 - 1

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

Section 2-2 General console requirements

2-2-1 Console environmental requirements

2-2-1-1 If the LOGIQ E9 is very cold or hot

When unpacking the device, allow the temperature of the device to stabilize before powering up. The following table describes guidelines for reaching operational temperatures from storage or transport temperatures. See: Table 2-1’

Table 2-1 LOGIQ E9 Acclimate Time

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

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

Hrs 864200000002468101214161820

2-2-1-2 Environmental specifications

Table 2-2 Environmental Specifications for LOGIQ E9 Scanners

Temperature

Humidity

Pressure 70 - 106 kPa 70 - 106 kPa 70 - 106 kPa

Heat Dissipation

2-2-1-3 Cooling

The cooling requirement for the LOGIQ E9 scanner with LCD and onboard peripherals, is up to 4712 Btu/hr. This figure does not include cooling needed for lights, people, or other equipment in the room. Each person in the room places an additional 300 Btu/hr demand on the cooling system.

2-2-1-4 Lighting

Bright light is needed for LOGIQ E9 installation, updates and repairs. However, operator and patient comfort may be optimized if the room light is subdued and indirect. Therefore a combination lighting system (dim/bright) is recommended. Keep in mind that lighting controls and dimmers can be a source of EMI which could degrade image quality. These con tr ols should be selected to minimize possible interference.

Operational Storage Transport (< 16 hrs.)

10º - 35º C

(50º - 96º F)

30% - 80%

non-condensing

4712 Btu/hour “ “

-10º - 50º C

(-14º - 122º F)

30% - 80%

non-condensing

-10º - 50º C

(-14º - 122º F)

30% - 80%

non-condensing

2 - 2 Section 2-2 - General console requirements

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

2-2-2 Electrical requirements

2-2-2-1 General requirements

NOTE: GE Healthcare requires a dedicated power and ground for the proper operation of its Ultrasound

equipment. This dedicated power shall originate at the last distribution panel before the LOGIQ E9. The LOGIQ E9 will function on Voltages from 100-240 Volts and 50 or 60 Hz. However, if using 220 volt

power, then a center tapped power source is required. 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 LOGIQ E9 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 circui t, and a full size ground wire from the distribution panel to the LOGIQ E9 outlet.

NOTE: 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.

2-2-2-2 Electrical requirements for LOGIQ E9

In the table below, the electrical specifications for LOGIQ E9 include LCD and on board peripherals.

Table 2-3 Electrical specifications for the LOGIQ E9

POWER

PART NUMBER DESCRIPTION VOLTAGE TOLERANCES

5205000-x

LOGIQ E9, 100-240 VAC 100-240 VAC +/-10% 1100 W 50/60 Hz

CONSUMPTION FREQUENCY

The current drain varies, depending on the mains voltage.

• At 230 VAC, the current may be up to 7.5 A.

• At 100 VAC, the current may be up to 12 A.

2-2-2-3 Inrush current

During power on, an inrush circuit prevents the current from increasing above the stated values.

Table 2-4 Inrush current at different mains voltages

VOLTAGE 50 Hz 60 Hz

90 VAC 13 A 12 A 110 VAC 9 A 11 A 220 VAC 5.5 A 6 A 264 VAC 6 A 5 A

Chapter 2 Site preparations 2 - 3

GE HEALTHCARE

CAUTION

DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

2-2-2-4 Site circuit breaker

POWER OUTAGE MAY OCCUR. THE LOGIQ E9 SCANNER REQUIRES A DEDICATED SINGLE BRANCH CIRCUIT. TO AVOID CIRCUIT OVERLOAD AND POSSIBLE LOSS OF CRITICAL CARE EQUIPMENT, MAKE SURE YOU DO NOT HAVE ANY OTHER EQUIPMENT OPERATING ON THE SAME CIRCUIT.

It is recommended that the branch circuit breaker for the LOGIQ E9 be readily accessible.

2-2-2-5 Site power outlets

A dedicated AC power outlet must be within reach of the LOGIQ E9 without extension cords. Other outlets adequate for the external peripherals, medical and test equipment needed to support this LOGIQ E9 must also be present within 1 m (3.2 ft.) of the LOGIQ E9. Electrical installation must meet all current local, state, and national electrical codes.

2-2-2-6 LOGIQ E9 power plug

If the LOGIQ E9 arrives without a power plug, or wit h the wron g plug, you must conta ct your GE dealer or the installation engineer must supply what is locally required.

2-2-2-7 Power stability requirements

Voltage drop-out

Max 10 ms. Power transients (all applications) Less than 25% of nominal peak voltage for less than 1 millisecond for any type of transient, including

line frequency, synchronous, asynchronous, or aperiodic transients.

2 - 4 Section 2-2 - General console requirements

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

2-2-3 EMI limitations

Ultrasound machines are susceptible to Electromagnetic Interference (EMI) from radio frequencies, magnetic fields, and transients in the air or wiri ng. Ultrasound machines also generate EMI. The L OGIQ E9 complies with limits as stated on the EMC label. However there is no guarantee that interference will not occur in a particular installation.

Possible EMI sources should be identified before the LOGIQ E9 is installed. Electrical and electronic equipment may produce EMI unintentionally as the result of a 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 on page 2-5 for EMI Prevention tips.

Table 2-5 EMI prevention/abatement

EMI RULE DETAILS

Be aware of RF sources

Ground the LOGIQ E9

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

Keep the LOGIQ E9 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 LOGIQ E9 will have noisy images. Check grounding of the power cord and power outlet.

After you finish repairing or updating the LOGIQ E9, replace all covers and tighten all screws. Any cable with an external connection requires a magnet wrap at each end. Install the Card Rack cover over the Card Rack. 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 LOGIQ E9 until any loose metallic part is removed.

Never place a label where RF gaskets meet the LOGIQ E9. 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.

Cellular phones may transmit a 5 V/m signal; that could cause image artifacts.

Properly dress peripheral

cables

Do not allow cables to lie across the top of the Card Rack or hang out of the peripheral bays. Loop the excess length for peripheral cables inside the peripheral bays. Attach the LCD cables to the frame.

Chapter 2 Site preparations 2 - 5

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NOTICE

CAUTION

DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

2-2-4 Probes environmental requirements

Table 2-6 Environmental Requirements - Probes

Standard Probes 4D Probes

Operation:

Storage:

Temperatures in degrees Celsius (

SYSTEMS AND ELECTRONIC PROBES ARE DESIGNED FOR STORAGE TEMPERATURES OF

-10 TO +50 degrees C. or +60 degrees C, DEPENDING ON THE TYPE OF PROBE. WHEN EXPOSED TO LARGE TEMPERATURE VARIATIONS, THE PRODUCT SHOULD BE KEPT IN ROOM TEMPERATURE FOR 10 HOURS BEFORE USE.

Refer to the Table in section 2-2-1-1 on page 2-2 to determine the needed settlement time.

to 40o C (50 to 104 ºF) 18o to 40o C (64.4 to 104 ºF)

-10° to 60° C (14 to 140 ºF)

C) conversion to degrees F: (oF) = (oC * 9/5) + 32

to 50 o C (14 to 122 ºF)

-10

2-2-5 Time and manpower requirements

Site preparation takes time. Begin Pre-installation checks as soon as possible, if possible, six weeks before delivery, to allow enough time to make any changes.

HAVE TWO PEOPLE AVAILABLE TO DELIVER AND UNPACK THE LOGIQ E9. ATTEMPTS TO MOVE THE LOGIQ E9 CONSIDERABLE DISTANCES OR ON AN INCLINE BY ONE PERSON COULD RESULT IN INJURY OR DAMAGE OR BOTH.

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GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

Section 2-3 Facility needs

2-3-1 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- installatio n work before delivery. Purchaser responsibility includes:

• Procuring the materials required.

• Completing the preparations before de liver y of th e LO GI Q E9.

• Paying the costs for any alterations and modifications not specifically provided in the sales contract.

NOTE: All electrical installations 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, calibrations, and testing must also be performed by qualified personnel. The products involved (and the accompanying electrical installations) are highly sophisticated and special engineering competence is required. All electrical work on these products 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 LOGIQ E9 than the interface kit allows, presents challeng es to the installa tion team. To avoid delays during installation, such variances should be m ade known to the individ uals or group performing the installation at the earliest possible date (preferably prior to the 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 LOGIQ E9 reliability.

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GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

2-3-2 Required facility needs

NOTE: GE Healthcare requires a dedicated power and ground for the proper operation of its Ultrasound

equipment. This dedicated power shall originate at the last distribution panel before the system. The LOGIQ E9 will function on Voltages from 100-240 Volts and 50 or 60 Hz. However, if using 220 volt

power, then a center tapped power source is required. 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.

• Dedicated single branch power outlet of adequate amperage (see: Table 2-5 on page 2-5) meeting all local and national codes which is located less than 2.5 m (8 ft.) from the LOGIQ E9’s proposed location

• Door opening is at least 76 cm (30 in) wide.

• Proposed location for LOGIQ E9 is at least 0.46 m (18 inches) from the wall or objects 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 (3.2 ft.) of the LOGIQ E9 to connect cables.

• Power outlets for other medical equipment and gel warmer.

• Power outlets for test equipment within 1 m (3.2 ft.) of LOGIQ E9.

• 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 - 8 Section 2-3 - Facility needs

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

2-3-3 Desirable features

In addition to the Floor Plan Suggestions shown in Figure 2-1 and Figure 2-2, a nearby waiting room and a Receptacle for Bio–hazardous Waste, like used probe sheaths is suggested. Grid represents 305 x 305 mm (1 x 1 foot).

2-3-4 Minimal floor plan suggestions

Figure 2-1 Floor Plan Suggestion 4.27 x 5.18 m (14 x 17 foot)

121

Elasto

PWPW

CFCF

Body Pattern

ZoomZoom Ellipse

Ellipse

3D/4D

CommentComment

AutoAut o

ClearClear

Floor Plan Suggestion 4.27 x 5.18 m (14 x 17 foot) Key

Item Description Item Description

Secretaries or Doctors Desk

Film Viewer

Counter Top and Sink with hot and cold water

Emergency Oxygen

LOGIQ E9

11.

Network Interface

13.

Stool

15.

Storage for Linens and Equipment

17.

Lavatory and Dressing Room

File Cabinet

Counter Top Overhead Lights Dimmer - Dual Level Lighting (bright

and dim)

Suction Line Dedicated Power Outlet - Circuit Breaker protected and

10.

easily accessible 457 mm (18 inches) distance of LOGIQ E9 from wall or

12.

objects

14.

Footswitch

16.

Examination Table – 1930 x 610 mm (76 x 24 inches)

18.

Door – at least 762 mm (30 inches)

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GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

2-3-4Minimal floor plan suggestions (cont’d)

Figure 2-2 Floor Plan Suggestion 2.44 x 3.05 m (8 x 10 foot)

Elasto

121

CommentComment

ClearClear

Body Pattern

Ellipse

PWPW

ZoomZoom

3D/4D

CFCF

AutoAut o

Floor Plan Suggestion 2.44 x 3.05 m (8 x 10 foot) Key

Item Description Item Description

Door – at least 762 mm (30 inches) Counter Top, Sink with hot and cold water and Supplies

Storage

Probes/Supplies

Film Viewer

Linen Supply

Examination Table – 1930 x 610 mm (76 x 24 inches)

Footswitch

LOGIQ E9 Dedicated Power Outlet - Circuit Breaker protected and

11.

easily accessible 457 mm (18 inches) distance of LOGIQ E9 from wall or

13.

objects

Stool

10.

External Peripherals

12.

Network Interface

14.

GE Cabinet for Software and Manuals

2 - 10 Section 2-3 - Facility needs

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

2-3-5 Networking setup requirements

2-3-5-1 Stand alone scanner (without network connection)

None.

2-3-5-2 Scanner connected to hospital’s network

Supported networks:

• 10/100/1000 Mbps Ethernet network connection

• Up to 300 Mbps WLAN (option)

2-3-5-3 InSite Requirements

Need internet access available to be able to connect to Insite ExC.

2-3-5-4 Purpose of the 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 LCD and peripherals, enabling viewing to be done while scanning continues. With DICOM, images can be archived, stor ed , and r etrie ve d faster, easie r, a nd at a lower cost.

2-3-5-5 DICOM option setup requirements

To configure the LOGIQ E9 to work with other network connections, the site’s network administrator must provide information to complete the form in Figure 2-3 "Worksheet for DICOM Network

Information" on page 2-12. Ensure that there ar e no spa ces in any field of the form.

Entries must include:

• A host name, local port number, AE Title, IP address and Net Mask for the LOGIQ E9.

• 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 E9 revision of the device, is also included. This information may be useful for troubleshooting.

For connectivity setup information, refer to the current revision of the LOGIQ E9 Basic User Manual.

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

Chapter 2 Site preparations 2 - 11

GE HEALTHCARE

LOGIQ E9

Host Name

AE Title

Local Port

IP Address

Net Mask

...

Default Gateway

DICOM APPLICATION

NAME

Store 2

Store 3

Store 1

MAKE/ IP PORTAE TITLE

DICOM Print

Storage Commit

DICOM

MPPS

Worklist

...

Network Speed

Associated Storage AE _____________

__Raw Data __Allow Multiframe __Structured Reporting Compression_______

Vendor: ___________ Print Size: _________ Medium: ___________ Copies: ___________ Orientation: ________ Color ______________

OTHER CONFIGURATION

DHCP

DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

2-3-5-5 DICOM option setup requirements (cont’d)

Figure 2-3 Worksheet for DICOM Network Information

2 - 12 Section 2-3 - Facility needs

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

Chapter 3 LOGIQ E9 Setup

Section 3-1 Overview

3-1-1 Purpose of this chapter

This chapter contains information needed to set up the LOGIQ E9. Included is 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 setup, and how to check and test the unit, probes, and external peripherals for electrical safety are included in this procedure.

Chapter 3 LOGIQ E9 Setup 3 - 1

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DANGER

CAUTION

DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

Section 3-2 Setup reminders

3-2-1 Average setup time

Table 3-1 Average setup time

DESCRIPTION

UNPACKING THE LOGIQ E9 0.5 HOUR

SET UP LOGIQ E9 WO/OPTIONS 4 HOURS DEPENDENT ON THE CONFIGURATION

DICOM NETWORK CONFIGURATION 2 HOURS OR MORE DEPENDENT ON THE CONFIGURATION

INSTALL INSITE / ILINK 0.5 HOUR

3-2-2 Setup warnings

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!

TO PREVENT ELECTRICAL SHOCK, CONNECT THE UNIT TO A PROPERLY GROUNDED POWER OUTLET. DO NOT USE A THREE TO TWO PRONG ADAPTER. THIS DEFEATS SAFETY GROUNDING.

DO NOT WEAR THE ESD WRIST STRAP WHEN YOU WORK ON LIVE CIRCUITS AND MORE THAN 30 V PEAK IS PRESENT.

AVERAGE SETUP

TIME

COMMENTS

DO NOT OPERATE THIS UNIT UNLESS ALL BOARD COVERS AND FRAME PANELS ARE SECURELY IN PLACE. LOGIQ E9 PERFORMANCE AND COOLING REQUIRE THIS.

If the unit is very cold or hot, allow the temperature of the device to stabilize before powering up. The following table describes guidelines for reaching operational temperatures from storage or transport temperatures. See: 2-2-2 "Console environmental requirements" on page 2-2.

3 - 2 Section 3-2 - Setup reminders

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

3-2-2Setup warnings (cont’d)

CAUTION

OPERATOR MANUAL(S) THE USER MANUAL(S) SHOULD BE FULLY READ AND UNDERSTOOD BEFORE OPERATING

THE LOGIQ E9 AND KEPT NEAR THE UNIT FOR QUICK REFERENCE.

ACOUSTIC OUTPUT HAZARD ALTHOUGH THE ULTRASOUND ENERGY TRANSMITTED FROM THE LOGIQ E9 PROBE IS

WITHIN AIUM/NEMA STANDARDS, AVOID UNNECESSARY EXPOSURE. ULTRASOUND ENERGY CAN PRODUCE HEAT AND MECHANICAL DAMAGE.

Chapter 3 LOGIQ E9 Setup 3 - 3

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CAUTION

DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

Section 3-3 Receiving and unpacking the equipment

3-3-1 Purpose of this section

This section describes how to receive and unpack LOGIQ E9.

3-3-2 Receiving and unpacking warnings

TWO PEOPLE ARE NEEDED TO UNPACK THE UNIT BECAUSE OF ITS WEIGHT. ATTEMPTS TO MOVE THE UNIT CONSIDERABLE DISTANCES OR ON AN INCLINE BY ONE PERSON COULD RESULT IN INJURY OR DAMAGE OR BOTH.

TWO PEOPLE ARE REQUIRED WHENEVER A PART WEIGHING 16 KG (35 LBS) OR MORE MUST BE LIFTED.

REMEMBER TO USE RELEVANT PERSONAL PROTECTING EQUIPMENT (PPE) DURING PACKING/UNPACKING. CHECK WITH YOUR LOCAL EHS REPRESENTATIVE.

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GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

3-3-3 Receiving the LOGIQ E9

3-3-3-1 Overview

Improper handling during transportation may harm the equipment inside the package even if the package itself is undamaged.

3-3-3-2 Examine package

Examine package closely at time of delivery.

3-3-3-3 Damage in transportation

Follow this procedure if damage is apparent:

Table 3-2 Damage in transportation

STEP TASK

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.

Report the damage to the carrier.

• Whether noted or concealed, damage MUST be repor ted 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 w ill not pay a claim for damage if an inspection is not requested within this 14 day period.

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GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

3-3-4 The Tilt and Shock indicators

3-3-4-1 Overview

Improper handling during transportation may harm the equipment inside the package even if the package itself is undamaged.

To make it easier to detect if the handling during transportation has bee n improper, a Tilt or TIPNTELL indicator and a Shock indicator have been attached to the transportation box.

3-3-4-2 Position of the Tilt or TipNTell and Shock indicat ors

The Tilt and Shock indicators have been attached to the side of the transportation box.

Figure 3-1 Tilt and Shock indicators

Figure 3-2 TIPNTELL indicator and Label

NOTE: Before cutting the straps, check the Tilt or TIPNTELL and Shock indicators to make sure they

have not been triggered. If triggered, report it to the carrier. If not, then cut the straps around the crate.

3 - 6 Section 3-3 - Receiving and unpacking the equipment

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

3-3-4-3 LOGIQ E9 Transportation Box Label

The LOGIQ E9 Transportation Box Label is located on the transportation box.

Figure 3-3 LOGIQ E9 Transportation Box Labeling

SYMBOL DEFINITION/COMMENTS SYMBOL DEFINITION/COMMENTS

RECYCLING

Recyclable Wood

RECYCLING

China Specific

TOP,. UPRIGHT - Transportation

and Storage

KEEP DRY

(protect from moisture)

FRAGILE, Handle with Care

DO NOT STACK

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DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

3-3-5 Unpacking the LOGIQ E9

The instruction manual describes the best method for unpacking the LOGIQ E9 ultrasound scanning unit.

Table 3-3 Uncrating Instructions

Steps Corresponding Graphic

Before cutting the straps, check Shock and Tilt Tags to make sure they have not been triggered. If damaged, report it to the carrier. If not, then cut the straps around the crate.

Remove the top cover.

3 - 8 Section 3-3 - Receiving and unpacking the equipment

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DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

Table 3-3 Uncrating Instructions (Continued)

Steps Corresponding Graphic

Remove the outside shipping box.

Note: Two people are recommended for performing this step.

Remove the LCD foam.

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DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

Table 3-3 Uncrating Instructions (Continued)

Steps Corresponding Graphic

Remove the a) Probes and b) accessory boxes.

Remove the L-shaped Cardboard divider.

Note: Use special care when removing the divider.

3 - 10 Section 3-3 - Receiving and unpacking the equipment

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DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

Table 3-3 Uncrating Instructions (Continued)

Steps Corresponding Graphic

Remove the OP panel foam placed between the monitor and probe holder s.

Remove the lower OP panel brace placed between the lower OP panel and the wooden ramp, by moving upward and back. Remove the wooden ramp.

Attach the wooden ramp to the Pallet Base with Velcro on the rear side of the LOGIQ E9.

10.

Loosen the tie-down strap at the front of the LOGIQ E9. Push the brass piece to pull back handle, then push brass piece to loosen strap.

Chapter 3 LOGIQ E9 Setup 3 - 11

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

Table 3-3 Uncrating Instructions (Continued)

Steps Corresponding Graphic

11.

Disconnect the tie-down strap at the rear of the LOGIQ E9.

12.

Pull the LOGIQ E9 down the Pallet Base ramp.

Note: Remember to pull in the LOGIQ E9 from the back for safer transportation.

13.

Remove the clear plastic (wrapped around the LOGIQ E9) from the unit.

14.

Place all of the filling inside the Transportation Box. Close the box, and store the filling for possible future use.

Section 3-4 Packing materials - recycling information

The packing materials for LOGIQ E9 are recyclable:

• The Transportation Box is made of cardboard.

• Lever lockings (hinges) are made of zinc plated steel.

• The inner reinforcements are made of Ethafoam (Polyethylene foam).

• The plastic foil is made of LDPE (Low Density Polyethylene).

3 - 12 Section 3-4 - Packing materials - recycling information

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

Section 3-5 Preparing for setup

3-5-1 Verify Customer Order

Compare items received by the customer to that which is listed on the delivery order. Report any item s that are missing, back ordered, or damaged.

3-5-2 Physical inspection

Verify that the LOGIQ E9 arrived intact (visual inspection). If the LOGIQ E9 has been damaged, please refer to “Damage in Transportation “on page x in the beginning of this manual.

3-5-2-1 LOGIQ E9 voltage settings

See: 3-6-3-1 "Verification of the LOGIQ E9’s voltage setting" on page 3-17.

3-5-3 Volume Navigation Stand

To assemble the Volume Navigation Stand, See: 8-15-2 "Assembling or replacing the Roll Stand" on

page 8-550 or 8-15-4 "On-Board V Nav Stand Option Contents, location and placement of parts" on page 8-559.

Chapter 3 LOGIQ E9 Setup 3 - 13

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

3-5-3-1 Back Cover Label and ETL testing laboratories sa fety rating label (ETL may not be present)

Figure 3-4 Back Cover Label with ETL Label

LOGIQ E9

MEDICAL

EQUIPMENT

5197104 revX

135

Figure 3-5 Rating Plate Label - R3.x and earlier 100-120V shown

3 - 14 Section 3-5 - Preparing for setup

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

3-5-3-1 Back Cover Label and ETL testing laboratories safety rating label (ETL may not be present)

(cont’d)

Figure 3-6 Rating Plate Label - R4.x.x

3-5-4 EMI protection

This unit has been designed to minimize the effects of Electro-Ma gnetic Interference (EMI). Many of the covers, shields, and screws are provided primarily to protect the LOGIQ E9 from image artifacts caused by this interference. For this reason, it is imperative that all covers and hardware are installed and secured before the unit is put into operation.

See: 2-2-4 "EMI limitations" on page 2-5 for more information about EMI protection.

Chapter 3 LOGIQ E9 Setup 3 - 15

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

Section 3-6 Completing the setup

3-6-1 Purpose of this section

This section describes how to complete the set up of LOGIQ E9.

3-6-2 LOGIQ E9 specifications

3-6-2-1 LOGIQ E9 requirements verification

• Verify that the site meets the requirements listed in (see: Section 2-3 "Facility needs" on p age 2-7).

• Verify that the specifications below don’t conflict with any on-site conditions.

3-6-2-2 Physical dimensions

The physical dimensions of the LOGIQ E9 unit are summarized in Table 3-4.

Table 3-4 Physical dimensions of LOGIQ E9 with monitor and peripherals

PART NUMBER HEIGHT* WIDTH DEPTH UNIT

5205000,

-2, -3, -4, -5, -6

5205000-7

1130 585 830 mm

44.5 23.03 32.67 Inches

1300 585 830 mm

51.2 21.9 32.7 Inches

* Dimensions given with floating keyboard stowed for transport and the LCD Monitor down.

3-6-2-3 Weight with monitor and peripherals

Table 3-5 Weight of LOGIQ E9 with monitor and peripherals

PART NUMBER WEIGHT [KG] WEIGHT [LBS]

5205000,

-2, -3, -4, -5, -6 5205000-7 140 390

135 298

3-6-2-4 Acoustic noise output

Less than 48 dB(A) at 20 degrees Celsius, measured in the operators head position, 20 cm in front of the keyboard’s right corner, at 1.30 m above the floor, and in a distance of 1 meter at all four sides, 1 meter above the floor.

3 - 16 Section 3-6 - Completing the setup

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WARNINGWARNING

DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

3-6-3 Electrical specifications

CONNECTING A LOGIQ E9 UNIT TO THE WRONG VOLTAGE LEVEL WILL MOST LIKELY DESTROY THE UNIT.

3-6-3-1 Verification of the LOGIQ E9’s voltage setting

Verify that the mains voltage specified for the unit is available on-site. The voltage setting for the unit is found on a label on the back of the LOGIQ E9 on lower rear frame of

the LOGIQ E9.

3-6-3-2 Electrical specifications for LOGIQ E9

See: Table 2-3 on page 2-3 for the electrical specifications for LOGIQ E9 include LCD and on board peripherals.

Chapter 3 LOGIQ E9 Setup 3 - 17

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

3-6-4 Connections on the I/O Rear Panel

NOTE: Accessory equipment connected to the analog and digi tal interfaces must be certified according

to the respective IEC standards (e.g. IEC60950 for data processing equipmen t an d IEC606011 for medical equipment). Furthermore, all complete configurations shall comply with the valid version of the system standard IEC60601-1-1. Everybody who connects additional equipment to the signal input part or signal output part of LOGIQ E9, configures a medical system, and is therefore responsible that the system complies with the requirements of the valid version of IEC60601-1-1. If in doubt, consult the te chnical service department or your local represen tative for GE Healthcare.

3-6-4-1 Connect Ethernet

Connect the Ethernet cable to the Ethernet connector (3) on the External I/O (rear side of LOGIQ E9).

Figure 3-7 Ethernet, Audio (1) and DVI-I (2) connection for External Monitor on rear side of LOGIQ E9 - R3.x and earlier

3 - 18 Section 3-6 - Completing the setup

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CAUTION

DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

3-6-4-1 Connect Ethernet (cont’d)

Figure 3-8 Audio (1), Ethernet (2) and DVI-I (3) connection for External Monitor on rear side of LOGIQ E9 - R4.x

To avoid breaking the back cover while opening it in order to connec t up the network cable, use a flat blade screw driver or plastic card and pull hard to open up the back cover door.

3-6-4-2 Connect USB Flash Drive

Refer to the current revision of the LOGIQ E9 Basic User Manual, Chapter 3, Section 7.

Chapter 3 LOGIQ E9 Setup 3 - 19

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

3-6-5 Connections on the Patient I/O panel

3-6-5-1 Connect ECG

Refer to Chapter 10 in the Basic User Manual for more information.

3-6-6 Connecting Probes

3-6-6-1 Introduction to Connecting Probes

Probes can be connected at any time, whether the unit is on or off. R3.x and earlier LOGIQ E9s have two types of probe ports: one non-DLP probe port and three DLP

probe ports (Figure 3-10). R4.x LOGIQ E9s have one type of probe ports: four DLP probe ports (Figur e 3-9).

The non-DLP probe port is compatible with the S1-5, S4-10, 6Tc (TEE probe), and 3CRF probe connectors. The three DLP probe ports are specific to the LOGIQ E9 probe connectors.

Figure 3-9 Probe connectors - (1) Non-DLP and (2) DLP Probe Port - R3.x and earlier

R4.x and later LOGIQ E9s have one type of probe ports: four DLP probe ports (Figure 3-10).

Figure 3-10 Probe connectors, four DLP Probe Ports - R4.x

3 - 20 Section 3-6 - Completing the setup

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CAUTION

DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

3-6-6-2 Connect a probe

NOTE: It is not necessary to turn OFF power to connect or disconn e ct a pr ob e.

DO NOT ALLOW THE PROBE HEAD TO HANG FREELY. EXCESSIVE IMPACT TO THE PROBE WILL RESULT IN IRREPARABLE DAMAGE.

TO PREVENT PROBE CONNECTOR PINS DAMAGE, OR PCB BOARD DAMAGE, DO NOT USE EXCESSIVE FORCE WHEN CONNECTING THE PROBES.

1.) Before connecting the probe: a.) Perform a visual check of the probe pins and LOGIQ E9 sockets.

b.) Remove any dust or foam rests from the probe pins. c.) Verify the probe and the probe cable for any visual damage.

2.) Hold the probe connector vertically with the cable pointing upward.

3.) Turn the connector locking handle counter-clockwise to the horizontal position.

4.) Align the connector with the probe port and carefully push into place.

5.) Turn the locking handle clockwise to the full vertical position to lock in place.

6.) Position the probe cable so that it is not resting on the floor.

KEEP THE PROBE CABLES AWAY FROM THE WHEELS. DO NOT BEND THE PROBE CABLES. DO NOT CROSS CABLES BETWEEN PROBES.

3-6-6-3 Disconnect a probe

1.) Rotate the lock handle counter-clockwise to the horizontal position to unlock the connector.

2.) Remove the connector from the port.

3.) Ensure that the probe head is clean before placing the probe in its storage case, see: 10-6-4

"Cleaning" on page 10-11 for cleaning instructions.

REFER TO THE TEE PROBE MANUAL FOR FURTHER INSTRUCTIONS (DIRECTION KZ192871).

Chapter 3 LOGIQ E9 Setup 3 - 21

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DANGER

CAUTION

NOTICE

DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

3-6-7 Power On/Boot Up

3-6-7-1 Warnings

ALWAYS CONNECT THE UNIT TO A FIXED POWER SOCKET WHICH HAS THE PROTECTIVE GROUNDING CONNECTOR.

NEVER USE A THREE-TO-TWO PRONG ADAPTER; THIS DEFEATS THE SAFETY GROUND.

ENSURE THAT THE POWER CORD AND PLUG ARE INTACT AND THAT THE POWER PLUG IS THE PROPER HOSPITAL-GRADE TYPE (WHERE REQUIRED).

LOGIQ E9 REQUIRES ALL COVERS OPERATE THIS UNIT ONLY WHEN ALL BOARD COVERS AND FRAME PANELS ARE

SECURELY IN PLACE. THE COVERS ARE REQUIRED FOR SAFE OPERATION, GOOD LOGIQ E9 PERFORMANCE AND COOLING PURPOSES.

Use only power supply cords, cables and plugs provided by or designated by GE Healthcare.

NOTE: Do not cycle the Circuit Breaker ON-OFF-ON in less than five seconds. When turning OFF th e

Circuit Breaker, WAIT until the ON/OFF button is no longer lit. The LOGIQ E9 should deenergize completely before turning the circuit breaker ON.

3-6-7-2 Detailed Procedure

For a detailed procedure, see: 4-2-3 "Power ON/Boot Up" on page 4-3.

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GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

3-6-7-3 Connect AC (mains) Power to the LOGIQ E9

Connecting AC Power to the LOGIQ E9 ultrasound unit involves preliminary checks of the power cord, voltage level and compliance with electrical safety requirements.

NOTE: The LOGIQ E9 will function on Voltages from 100-240 Volts and 50 or 60 Hz. However, if using

220 volt power, then a center tapped power source is required (North America Only).

1.) Ensure that the wall outlet is of appropriate type, and that the Circuit Breaker is turned off.

2.) Uncoil the power cable, allowing sufficient slack so that the unit can be moved slightly.

3.) Verify that the power cable is without any visible scratches or any sign of damage.

4.) Verify that the on-site mains voltage is within the limits indicated on the rating label ne ar the Circuit

Breaker on the rear of the unit.

5.) Connect the Power Cable’s female plug to the Power Inlet at the rear of the unit.

6.) Lock the plug in position with the Retaining Clamp (ACC Clamp).

7.) Verify that the Mains Power Circuit Breaker is in OFF position, if not, switch it OFF.

Figure 3-11 The Circuit Breaker and ON/OFF button

8.) Connect the Power Cable’s other end (male plug) to a hospital grade mains power outlet with the

proper rated voltage, and the unit is ready for Power ON/Boot Up.

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GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

3-6-7-4 Switch ON the AC Power to LOGIQ E9

1.) Switch ON the Mains Power Circuit Breaker at the r ear of the unit. The ON/OFF button will become amber.

Figure 3-12 The Circuit breaker and ON/OFF button

You should hear a “click” from the relays in the AC Power and the unit is ready to boot. The ON/OFF button will turn amber. This indicates that there is power to the PS, but the system is OFF.

2.) Press once on the ON/OFF button on the Operator Panel to boot the unit. The ON/OFF button will

turn green when it is pressed. During a normal boot, you may observe that:

a.) The unit’s ventilation fan starts on full speed, but slows down after a few seconds (liste n to the

fan sound).

b.) Power is distributed to the peripherals, Operator Panel (Console), Monitor, Front End

Processor and Back End Processor. c.) Back End Processor and rest of the LOGIQ E9 starts with the sequence listed in the next steps: d.) Back End Processor is turned ON and starts to load the software. e.) The Start Screen is displayed on the monitor. f.) A start-up bar indicating the time used for software loading, is displayed on the monitor. g.) The software initiates and sets up the Front End electronics and the rest of the instrument. h.) The backlight in the keyboard is lit. i.) As soon as the software has been loaded, either a 2D screen is displayed on the screen,

indicating that a probe has been connected, or a No Mode screen is displayed, indicating that

no probe has been connected.

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GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

3-6-7-4 Switch ON the AC Power to LOGIQ E9 (cont’d)

Figure 3-13 2D Screen on the display

NOTE: Total time used for start-up is typically less than 170 seconds. When using the sleep mode

(R2.x.x or later), start-up time is less then 120 seconds. If starting after a power loss or a lockup, the start-up time may be up to four minutes.

Chapter 3 LOGIQ E9 Setup 3 - 25

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

3-6-8 Power shut down

When you switch off the unit, the system performs an automatic shutdown sequence.

Figure 3-14 System - Exit menu - R1.x.x

The SYSTEM - EXIT menu, used when switching off the unit, gives you these choices:

• Logoff

Use this button to log off the current user. The system remains ON and ready for a new user to log on. If the Logoff button is dimmed, it indicates that no user is logged on to the unit at the moment.

• Shutdown

Use this button to shut down the system. The entire system will shut down. It is recommended to perform a full shutdown at least once a week.

If the Shutdown button is dimmed, press the ON/OFF button or Alt F10 to shut down the unit.

•Cancel

Use this button to exit from the Syst em-Exit menu and return to the previous operation.

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GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

3-6-8Power shut down (cont’d)

Sleep mode (only available in LOGIQ E9 running R2.x.x and R3.x.x software).

Figure 3-15 System - Exit menu

The SYSTEM - EXIT menu, used when switching off the unit, gives you these choices:

• Logoff

• Shutdown

Use this button to shut down the system. The entire system will shut down. It is recommended to perform a full shutdown at least once a week.

If the Shutdown button is dimmed, press the ON/OFF button or Alt F10 to shut down the unit.

•Cancel

Use this button to exit from the Syst em-Exit menu and return to the previous operation.

Chapter 3 LOGIQ E9 Setup 3 - 27

GE HEALTHCARE DIRECTION 5180263-100, REV 5 LOGIQ E9 Service Manual

3-6-9 Complete power down

1.) Press once on the ON/OFF button on the Operator Panel to display the System - Exit menu.

Figure 3-16 Press once on the ON/OFF button

3 - 28 Section 3-6 - Completing the setup

GE Logiq E9 User manual

Specifications and Main Features

Frequently Asked Questions

User Manual