General Electric LOGIQ C SERIES BASIC SERVICE MANUAL_SM_5273008-100_9 LOGIQ C Series Basic Service Manual

GE
LOGIQ C Series
Basic Service Manual
Part Number: 5273008-100
Revision: 9
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AVERTISSEMENT
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WARNUNG
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Important Precautions

THIS SERVICE MANUAL IS AVAILABLE IN ENGLISH ONLY.
• IF A CUSTOMER’S SERVICE PROVIDER REQUIRES A LANGUAGE OTHER THAN ENGLISH, IT IS THE CUSTOMER’S RESPONSIBILITY TO PROVIDE TRANSLATION SERVICES.
• 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, Mé CANIQUES OU AUTRES.
DIESES KUNDENDIENST-HANDBUCH EXISTIERT NUR IN ENGLISCHER SPRACHE.
• FALLS EIN FREMDER KUNDENDIENST EINE ANDERE SPRACHE BENö TIGT, IST ES AUFGABE DES KUNDEN FüR EINE ENTSPRECHENDE ÜBERSETZUNG ZU SORGEN.
• VERSUCHEN SIE NICHT, DAS GERä T ZU REPARIEREN, BEVOR DIESES KUNDENDIENST-HANDBUCH NICHT ZU RATE GEZOGEN UND VERSTANDEN WURDE.
• WIRD DIESE WARNUNG NICHT BEACHTET, SO KANN ES ZU VERLETZUNGEN DES KUNDENDIENSTTECHNIKERS, DES BEDIENERS ODER DES PATIENTEN DURCH ELEKTRISCHE SCHLä GE, MECHANISCHE ODER SONSTIGE GEFAHREN KOMMEN.
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ESTE MANUAL DE SERVICIO Só LO EXISTE EN INGLéS.
• SI ALGúN PROVEEDOR DE SERVICIOS AJENO A GEHC SOLICITA UN IDIOMA QUE NO SEA EL INGLéS, ES RESPONSABILIDAD DEL CLIENTE OFRECER UN SERVICIO DE TRADUCCIó N.
• NO SE DEBERá DAR SERVICIO TéCNICO AL EQUIPO, SIN HABER CONSULTADO Y COMPRENDIDO ESTE MANUAL DE SERVICIO.
• LA NO OBSERVANCIA DEL PRESENTE AVISO PUEDE DAR LUGAR A QUE EL PROVEEDOR DE SERVICIOS, EL OPERADOR O EL PACIENTE SUFRAN LESIONES PROVOCADAS POR CAUSAS ELéCTRICAS, MECá NICAS O DE OTRA NATURALEZA.
ESTE MANUAL DE ASSISTêNCIA TéCNICA Só SE ENCONTRA DISPONíVEL EM INGLêS.
• SE QUALQUER OUTRO SERVIç O DE ASSISTêNCIA Té CNICA, QUE Nã O A GEHC, SOLICITAR ESTES MANUAIS NOUTRO IDIOMA, é DA RESPONSABILIDADE DO CLIENTE FORNECER OS SERVIç OS DE TRADUç ã O.
• Nã O TENTE REPARAR O EQUIPAMENTO SEM TER CONSULTADO E COMPREENDIDO ESTE MANUAL DE ASSISTêNCIA TéCNICA.
• O Nã O CUMPRIMENTO DESTE AVISO PODE POR EM PERIGO A SEGURANç A DO TéCNICO, OPERADOR OU PACIENTE DEVIDO A‘ CHOQUES ELé TRICOS, MECâ NICOS 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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KÄESOLEV TEENINDUSJUHEND ON SAADAVAL AINULT INGLISE KEELES.
• KUI KLIENDITEENINDUSE OSUTAJA Nõ UAB JUHENDIT INGLISE KEELEST ERINEVAS KEELES, VASTUTAB KLIENT Tõ LKETEENUSE OSUTAMISE EEST.
• ä RGE üRITAGE SEADMEID TEENINDADA ENNE EELNEVALT Kä ESOLEVA TEENINDUSJUHENDIGA TUTVUMIST JA SELLEST ARU SAAMIST.
• Kä ESOLEVA HOIATUSE EIRAMINE Võ IB Põ HJUSTADA TEENUSEOSUTAJA, OPERAATORI Võ I PATSIENDI VIGASTAMIST ELEKTRILö ö GI, MEHAANILISE Võ I MUU OHU TAGAJä RJEL.
TÄMÄ HUOLTO-OHJE ON SAATAVILLA VAIN ENGLANNIKSI.
• JOS ASIAKKAAN PALVELUNTARJOAJA VAATII MUUTA KUIN ENGLANNINKIELISTä MATERIAALIA, TARVITTAVAN Kä ä NNö KSEN HANKKIMINEN ON ASIAKKAAN VASTUULLA.
• ä Lä YRITä KORJATA LAITTEISTOA ENNEN KUIN OLET VARMASTI LUKENUT JA YMMä RTä NYT Tä Mä N HUOLTO-OHJEEN.
• MIKä LI Tä Tä VAROITUSTA EI NOUDATETA, SEURAUKSENA VOI OLLA PALVELUNTARJOAJAN, LAITTEISTON Kä YTTä Jä N TAI POTILAAN VAHINGOITTUMINEN Sä HKö ISKUN, MEKAANISEN VIAN TAI MUUN VAARATILANTEEN VUOKSI.
ΤΟ ΠΑΡΟΝ ΕΓΧΕΙΡΙ∆ΙΟ ΣΕΡΒΙΣ ∆ΙΑΤΙΘΕΤΑΙ ΣΤΑ ΑΓΓΛΙΚΑ ΜΟΝΟ.
ΕΑΝ ΤΟ ΑΤΟΜΟ ΠΑΡΟΧΗΣ ΣΕΡΒΙΣ ΕΝΟΣ ΠΕΛΑΤΗ ΑΠΑΙΤΕΙ ΤΟ ΠΑΡΟΝ
ΕΓΧΕΙΡΙ∆ΙΟ ΣΕ ΓΛΩΣΣΑ ΕΚΤΟΣ ΤΩΝ ΑΓΓΛΙΚΩΝ, ΑΠΟΤΕΛΕΙ ΕΥΘΥΝΗ ΤΟΥ ΠΕΛΑΤΗ ΝΑ ΠΑΡΕΧΕΙ ΥΠΗΡΕΣΙΕΣ ΜΕΤΑΦΡΑΣΗΣ.
• ΜΗΝ ΕΠΙΧΕΙΡΗΣΕΤΕ ΤΗΝ ΕΚΤΕΛΕΣΗ ΕΡΓΑΣΙΩΝ ΣΕΡΒΙΣ ΣΤΟΝ ΕΞΟΠΛΙΣΜΟ ΕΚΤΟΣ
ΕΑΝ ΕΧΕΤΕ ΣΥΜΒΟΥΛΕΥΤΕΙ ΚΑΙ ΕΧΕΤΕ ΚΑΤΑΝΟΗΣΕΙ ΤΟ ΠΑΡΟΝ
ΕΓΧΕΙΡΙ∆ΙΟ ΣΕΡΒΙΣ.
• ΕΑΝ ∆Ε ΛΑΒΕΤΕ ΥΠΟΨΗ ΤΗΝ ΠΡΟΕΙ∆ΟΠΟΙΗΣΗ ΑΥΤΗ, ΕΝ∆ΕΧΕΤΑΙ ΝΑ ΠΡΟΚΛΗΘΕΙ ΤΡΑΥΜΑΤΙΣΜΟΣ ΣΤΟ ΑΤΟΜΟ ΠΑΡΟΧΗΣ ΣΕΡΒΙΣ, ΣΤΟ ΧΕΙΡΙΣΤΗ Ή ΣΤΟΝ ΑΣΘΕΝΗ ΑΠΟ ΗΛΕΚΤΡΟΠΛΗΞΙΑ, ΜΗΧΑΝΙΚΟΥΣ Ή ΑΛΛΟΥΣ ΚΙΝ∆ΥΝΟΥΣ.
EZEN KARBANTARTÁSI KÉZIKÖNYV KIZÁRÓLAG ANGOL NYELVEN ÉRHETŐ EL.
• HA A VEVŐ SZOLGÁLTATÓJA ANGOLTÓL ELTÉRŐ NYELVRE TART IGÉNYT, AKKOR A VEVŐ FELELŐSSÉGE A FORDÍTÁS ELKÉSZÍTTETÉSE.
• NE PRÓBÁLJA ELKEZDENI HASZNÁLNI A BERENDEZÉST, AMÍG A KARBANTARTÁSI KÉZIKÖNYVBEN LEÍRTAKAT NEM ÉRTELMEZTÉK.
• EZEN FIGYELMEZTETÉS FIGYELMEN KÍVÜL HAGYÁSA A SZOLGÁLTATÓ, MŰKÖDTETŐ VAGY A BETEG ÁRAMÜTÉS, MECHANIKAI VAGY EGYÉB VESZÉLYHELYZET MIATTI SÉRÜLÉSÉT EREDMÉNYEZHETI.
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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 ANGLICKé M JAZYCE.
•VPř íPADě, ŽE POSKYTOVATEL SLUŽEB ZÁKAZNÍKŮM POTř EBUJE Ná VOD V JINéM JAZYCE, JE ZAJIšTě Ní Př EKLADU DO ODPOVíDAJíCíHO JAZYKA úKOLEM Zá KAZNíKA.
• NEPROVÁDĚJTE úDRŽBU TOHOTO ZAř íZENí, ANIŽ BYSTE SI Př Eč ETLI TENTO SERVISNÍ NÁVOD A POCHOPILI JEHO OBSAH.
•VPř íPADě NEDODRŽOVá Ní TéTO VýSTRAHY MůŽE DOJíT ÚRAZU ELEKTRICKÁM PROUDEM PRACOVNíKA POSKYTOVATELE SLUŽEB, OBSLUŽNéHO PERSONá LU NEBO PACIENTů VLIVEM ELEKTRICKéHOP PROUDU, RESPEKTIVE VLIVEM K RIZIKU MECHANICKÉHO POŠKOZENÍ NEBO JINÉMU RIZIKU.
DENNE SERVICEMANUAL FINDES KUN PÅ ENGELSK.
• HVIS EN KUNDES TEKNIKER HAR BRUG FOR ET ANDET SPROG END ENGELSK, ER DET KUNDENS ANSVAR AT SØRGE FOR OVERSÆTTELSE.
• FORSØG IKKE AT SERVICERE UDSTYRET MEDMINDRE DENNE SERVICEMANUAL ER BLEVET LÆST OG FORSTÅET.
• MANGLENDE OVERHOLDELSE AF DENNE ADVARSEL KAN MEDFŘRE SKADE PĹ GRUND AF ELEKTRISK, MEKANISK ELLER ANDEN FARE FOR TEKNIKEREN, OPERATŘREN ELLER PATIENTEN.
DEZE ONDERHOUDSHANDLEIDING IS ENKEL IN HET ENGELS VERKRIJGBAAR.
• ALS HET ONDERHOUDSPERSONEEL EEN ANDERE TAAL VEREIST, DAN IS DE KLANT VERANTWOORDELIJK VOOR DE VERTALING ERVAN.
• PROBEER DE APPARATUUR NIET TE ONDERHOUDEN VOORDAT DEZE ONDERHOUDSHANDLEIDING WERD GERAADPLEEGD EN BEGREPEN IS.
• INDIEN DEZE WAARSCHUWING NIET WORDT OPGEVOLGD, ZOU HET ONDERHOUDSPERSONEEL, DE OPERATOR OF EEN PATIËNT GEWOND KUNNEN RAKEN ALS GEVOLG VAN EEN ELEKTRISCHE SCHOK, MECHANISCHE OF ANDERE GEVAREN.
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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 SM
ŪGIO, MECHANINIŲ AR
KITŲ PAVOJŲ.
DENNE SERVICEHÅNDBOKEN FINNES BARE PÅ ENGELSK.
• HVIS KUNDENS SERVICELEVERANDØR TRENGER ET ANNET SPRÅK, ER DET KUNDENS ANSVAR Å SØRGE FOR OVERSETTELSE.
• IKKE FORSØK Å REPARERE UTSTYRET UTEN AT DENNE 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 ś WIADCZĄCA KLIENTOWI USłUGI SERWISOWE WYMAGA UDOSTęPNIENIA PODRę CZNIKA W JęZYKU INNYM NIŻ ANGIELSKI, OBOWIĄZEK ZAPEWNIENIA STOSOWNEGO TłUMACZENIA SPOCZYWA NA KLIENCIE.
• NIE PRó BOWAć SERWISOWAć NINIEJSZEGO SPRZęTU BEZ UPRZEDNIEGO ZAPOZNANIA SIę Z PODRę CZNIKIEM 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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ACEST MANUAL DE SERVICE ESTE DISPONIBIL NUMAI ÎN LIMBA ENGLEZĂ.
• DACĂ UN FURNIZOR DE SERVICII PENTRU CLIENŢI NECESITĂ O ALTĂ LIMBĂ DECÂT CEA ENGLEZĂ, ESTE DE DATORIA CLIENTULUI SĂ FURNIZEZE O TRADUCERE.
• NU ÎNCERCAŢI SĂ REPARAŢI ECHIPAMENTUL DECÂT ULTERIOR CONSULTĂRII ŞI ÎNŢELEGERII ACESTUI MANUAL DE SERVICE.
• IGNORAREA ACESTUI AVERTISMENT AR PUTEA DUCE LA RĂNIREA DEPANATORULUI, OPERATORULUI SAU PACIENTULUI ÎN URMA PERICOLELOR DE ELECTROCUTARE, MECANICE SAU DE ALTĂ NATURĂ.
Данное рук о во дс тв о по обслуживанию ПРЕДОСТАВЛЯЕТСЯ только на английском Яз ыке.
• Ес ли сервисноМУ ПЕРСОНАЛУ клиента необходимо рук о во дс т во не на английском ЯЗЫКЕ, клиенту следует самостоЯтельно ОБЕСПЕЧИТЬ перевод.
ПЕРЕД ОБСЛУЖИВАНИЕМ ОБОРУДОВАНИЯ ОБЯЗАТЕЛЬНО
ОБРАТИТЕСЬ
К ДАННОМУ РУКОВОДСТВУ И ПОЙМИТЕ ИЗЛОЖЕННЫЕ В НЕМ СВЕДЕНИЯ.
НЕСОБЛЮДЕНИЕ УКАЗАННЫХ ТРЕБОВАНИЙ МОЖЕТ ПРИВЕСТИ К ТОМУ,
ЧТО СПЕЦИАЛИСТ ПО ТЕХОБСЛУЖИВАНИЮ, ОПЕРАТОР ИЛИ ПАЦИЕНТ ПОЛУЧАТ УДАР ЗЛЕКТРИЧЕСКИМ ТОКОМ, МЕХАНИЧЕСКУЮ ТРАВМУ ИЛИ ДРУГОЕ ПОВРЕЖДЕНИЕ.
ТОВА СЕРВИЗНО РЪКОВОДСТВО Е НАЛИЧНО САМО НА АНГЛИЙСКИ ЕЗИК.
• АКО ДОСТАВЧИКЪТ НА СЕРВИЗНИ УСЛУГИ НА КЛИЕНТ
СЕ НУЖДАЕ ОТ ЕЗИК, РАЗЛИЧЕН ОТ АНГЛИЙСКИ, ЗАДЪЛЖЕНИЕ НА КЛИЕНТА Е ДА ПРЕДОСТАВИ ПРЕВОДАЧЕСКА УСЛУГА.
• НЕ СЕ ОПИТВАЙТЕ ДА ИЗВЪРШВАТЕ СЕРВИЗНО ОБСЛУЖВАНЕ НА ТОВА ОБОРУДВАНЕ, ОСВЕН ВСЛУЧАЙ, ЧЕ СЕРВИЗНОТО РЪКОВОДСТВО Е ПРОЧЕТЕНО И СЕ РАЗБИРА.
• НЕСПАЗВАНЕТО НА ТОВА ПРЕДУПРЕЖДЕНИЕ МОЖЕ ДА ДОВЕДЕ ДО НАРАНЯВАНЕ НА ДОСТАВЧИКА НА СЕРВИЗНИ УСЛУГИ, НА
ОПЕРАТОРА ИЛИ ПАЦИЕНТА ВСЛЕДСТВИЕНА ТОКОВ УДАР, МЕХАНИЧНИ ИЛИ ДРУГИ РИСКОВЕ.
OVAJ PRIRUČNIK ZA SERVISIRANJE DOSTUPAN JE SAMO NA ENGLESKOM JEZIKU.
• AKO KLIJENTOV SERVISER ZAHTEVA JEZIK KOJI NIJE ENGLESKI,
ODGOVORNOST JE NA KLIJENTU DA PRUŽI USLUGE PREVOĐENJA.
• NEMOJTE POKUŠAVATI DA SERVISIRATE OPREMU AKO NISTE PROČITALI I RAZUMELI PRIRUČNIK ZA SERVISIRANJE.
• AKO NE POŠTUJETE OVO UPOZORENJE, MOŽE DOĆI DO POVREĐIVANJA SERVISERA, OPERATERA ILI PACIJENTA UZROKOVANOG ELEKTRIČNIM UDAROM, MEHANIČKIM I DRUGIM OPASNOSTIMA.
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TA SERVISNI PRIROČNIK JE NA VOLJO SAMO V ANGLEŠČINI.
ČE PONUDNIK SERVISNIH STORITEV ZA STRANKO POTREBUJE NAVODILA V
DRUGEM JEZIKU, JE ZA PREVOD ODGOVORNA STRANKA SAMA.
• 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 Mô ŽE VYÚSTIŤ DO ZRANENIA POSKYTOVATEĽA SLUŽIEB, OBSLUHUJúCEJ OSOBY ALEBO PACIENTA ELEKTRICKýM PRúDOM, PRÍPADNE DO MECHANICKéHO ALEBO INé HO NEBEZPEč ENSTVA.
DEN HÄR SERVICEHANDBOKEN FINNS BARA TILLGÄNGLIG PÅ ENGELSKA.
• OM EN KUNDS SERVICETEKNIKER HAR BEHOV AV ETT ANNAT SPRÅK ÄN ENGELSKA ANSVARAR KUNDEN FÖR ATT TILLHANDAHÅLLA ÖVERSÄTTNINGSTJÄNSTER.
• FÖRSÖK INTE UTFÖRA SERVICE PÅ UTRUSTNINGEN OM DU INTE HAR LÄST OCH FÖRSTÅR DEN HÄR SERVICEHANDBOKEN.
• OM DU INTE TAR HÄNSYN TILL DEN HÄR VARNINGEN KAN DET RESULTERA I SKADOR PÅ SERVICETEKNIKERN, OPERATÖREN ELLER PATIENTEN TILL FÖLJD AV ELEKTRISKA STÖTAR, MEKANISKA FAROR ELLER ANDRA FAROR.
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DİKKAT
(TR)
(JA)
Traditional
Chinese
IRECTION 5273008-100, REVISION 9 LOGIQ C SERIES BASIC SERVICE MANUAL
D
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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(ZH-CN)
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IRECTION 5273008-100, REVISION 9 LOGIQ C SERIES BASIC SERVICE MANUAL
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DANGER
WARNINGWARNING
IRECTION 5273008-100, REVISION 9 LOGIQ C SERIES BASIC SERVICE MANUAL
D
DAMAGE IN TRANSPORTATION
All packages should be closely examined at time of delivery. If damage is apparent write “Damage In Shipment” on ALL copies of the freight or express bill BEFORE delivery is accepted or “signed for” by a GE representative or hospital receiving agent. Whether noted or concealed, damage MUST be reported to the carrier immediately upon discovery, or in any event, within 14 days after receipt, and the contents and containers held for inspection by the carrier. A transportation company will not pay a claim for damage if an inspection is not requested within this 14 day period.
CERTIFIED ELECTRICAL CONTRACTOR STATEMENT - FOR USA ONLY
All electrical Installations that are preliminary to positioning of the equipment at the site prepared for the equipment shall be performed by licensed electrical contractors. Other connections between pieces of electrical equipment, calibrations and testing shall be performed by qualified GE personnel. In performing all electrical work on these products, GE will use its own specially trained field engineers. All of GE’s electrical work on these products will comply with the requirements of the applicable electrical codes.
The purchaser of GE equipment shall only utilize qualified personnel (i.e., GE’s field engineers, personnel of third-party service companies with equivalent training, or licensed electricians) to perform electrical servicing on the equipment.
OMISSIONS & ERRORS
If there are any omissions, errors or suggestions for improving this documentation, please contact the GE Global Documentation Group with specific information listing the system type, manual title, part number, revision number, page number and suggestion details.
Mail the information to:
Service Documentation, GE Medical Systems (China) Co., Ltd. No.19 Changjiang Road WuXi National Hi-Tech Development Zone Jiangsu, P.R China 214028 TEL: +86 510 85225888; FAX: +86 510 85226688
GE Healthcare employees should 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 the Chapter 1, Safety Considerations section in the Service Manual.
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LEGAL NOTES
The contents of this publication may not be copied or duplicated in any form, in whole or in part, without prior written permission of GE.
GE may revise this publication from time to time without written notice.
PROPRIETARY TO GE
Permission to use this Advanced Service Software and related documentation (herein called the material) by persons other than GE employees 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 employee or a customer who has entered into such a license agreement with GE 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 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 Employee, you must exit this Material now.
TRADEMARKS
All products and their name brands are trademarks of their respective holders.
COPYRIGHTS
All Material Copyright© 2008 - 2014 by General Electric Company Inc. All Rights Reserved.
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IRECTION 5273008-100, REVISION 9 LOGIQ C SERIES BASIC SERVICE MANUAL
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Revision History

Revision Date Reason for change
1 June 10,2008 Initial Release
2 October 20,2008 Add new spare parts in Chapter 9
3 January 21,2009 Add CKD information
4 February 02,2010 Update Korean Rating Plate
5 May 22,2010 Update the procedure for unpacking the equipment in Chapter 3
6 July 13,2010 Update Label Locations information in Chapter 1
7 June 14 ,2010 Add keyboard lamp usage infromation in chapter 6
8 December 05,2012 Update environmental labels and add new spare parts
9 Auguest 05,2014 Update the spare parts

List of Effected Pages(LOEP)

Pages Revision Pages Revision Pages Revision
Title Page 9
Important PrecautionsI
pages i to x
Table of Contents
pages i to x
Chapter 1 - Introduction
pages 1-1 to 1-12
Chapter 2 - Site Preparation
pages 2-1 to 2-10
Chapter 3 -System Setup
pages 3-1 to 3-22
Chapter 4 - Functional
9
9
9
9
Checks
pages 4-1 to 4-36
Chapter 5 - Theory
pages 5-1 to 5-4
Chapter 6 - Service
Adjustments
pages 6-1 to 6-2
Chapter 7 - Diagnostics/
Troubleshooting
pages 7-1 to 7-14
9
9
9
9
9 Back Cover 9
Chapter 8 - Replacement
Procedures
pages 8-1 to 8-6
Chapter 9 - Replacement Parts
pages 9-1 to 9-8
Chapter 10 - Periodic Maintenance
pages 10-1 to 10-22
Index
pages I to II
9
9
9
9
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IRECTION 5273008-100, REVISION 9 LOGIQ C SERIES BASIC SERVICE MANUAL
Table of Contents
CHAPTER 1
Introduction
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 1
Purpose of Chapter 1 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 1
Purpose of Service Manual . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 1
Typical Users of the Basic Service Manual . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 2
Purpose of Operator Manual(s) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 2
LOGIQ C2/C3/C5 Models covered by this manual . . . . . . . . . . . . . . . . . . . 1 - 2
Important Conventions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 4
Conventions Used in Book . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 4
Standard Hazard Icons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 5
Product Icons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 5
Safety Considerations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 6
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 6
Human Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 6
Mechanical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 6
Electrical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 7
Label Locations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 7
Dangerous Procedure Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 8
Returning/Shipping Probes and Repair Parts . . . . . . . . . . . . . . . . . . . . . . . 1 - 8
EMC, EMI, and ESD . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 9
Electromagnetic Compatibility (EMC) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 9
CE Compliance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 9
Electrostatic Discharge (ESD) Prevention . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 9
Customer Assistance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 10
Contact Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 10
System Manufacturer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 11
Factory Site . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 11
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CHAPTER 2
Site Preparations
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 1
Purpose of chapter 2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 1
General Console Requirements. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2
Console Environmental Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2
Electrical Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2
EMI Limitations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 4
Scan Probe Environmental Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 5
Facility Needs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 6
Purchaser Responsibilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 6
Required Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 7
Recommended and Alternate Ultrasound Room Layout . . . . . . . . . . . . . . . 2 - 8
Networking Pre-installation Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 9
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CHAPTER 3
System Setup
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 1
Purpose of Chapter 3 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 1
Setup Reminders . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 2
Average Installation Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 2
Installation Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 3
Safety Reminders . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 4
Receiving and Unpacking the Equipment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 5
Moving into Position . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 6
Product Locator Installation Card . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 6
Preparing for Installation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 7
Verify Customer Order . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 7
Physical Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 7
EMI Protection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 7
Completing the Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 8
Power On / Boot Up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 8
Power Off/ Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 8
Transducer Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 9
System Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 10
System Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 10
Electrical Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 10
On-Board Optional Peripherals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 11
Connecting Cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 12
Peripherals/Accessories Connector Panel . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 12
Available Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 18
Software/Option Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 18
Connectivity Installation Worksheet . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 19
Loading Base Image Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 20
Software Version check out . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 21
Functional Check-out . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 21
Paperwork . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 22
Product Locator Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 22
User Manual(s) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 22
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CHAPTER 4
Functional Checks
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 1
Purpose for Chapter 4 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 1
Required Equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 1
General Procedure. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 2
Power On/Boot Up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 2
Power Off/ Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 2
Archiving and Loading Presets . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 4
Adjusting the Display Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 5
System Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 6
B Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 9
M Mode Controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 12
Doppler Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 15
Color Flow Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 19
Basic Measurements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 23
Probe/Connectors Usage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 24
Using Cine . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 24
Image Management (QG) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 25
Backup and Restore Database, Preset Configurations and Images . . . . . . 4 - 26
Software Configuration Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 35
Peripheral Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 35
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CHAPTER 5
Components and Functions (Theory)
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 1
Purpose of Chapter 5 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 1
Block Diagram . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 2
System Diagram
5 - 2
Software Diagram . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 3
Common Service Platform . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 4
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 4
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CHAPTER 6
Service Adjustments
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 1
Purpose of this chapter 6 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 1
Monitor Adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 2
Adjustments Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 2
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CHAPTER 7
Diagnostics/Troubleshooting
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 1
Purpose of Chapter 7 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 1
Gathering Trouble Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 2
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 2
Collect Vital System Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 2
Collect a Trouble Image with Logs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 3
USB Quick Save. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 4
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 4
Check and Record the Print or Store Key Function . . . . . . . . . . . . . . . . . . 7 - 4
Setting the Print or Store Key to USB Quick Save . . . . . . . . . . . . . . . . . . . 7 - 5
Screen Captures. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 6
Check and Record the Store Key Function . . . . . . . . . . . . . . . . . . . . . . . . 7 - 6
Setting the Store Key to Screen Capture . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 6
Capturing a Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 6
Reset the Store Key to Customer’s Functionality . . . . . . . . . . . . . . . . . . . . 7 - 8
Common Diagnostics . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 9
Utilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 9
PC Diagnostics (Non-Interactive Tests) . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 10
PC Diagnostics (Interactive Tests) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 11
Restart LOGIQ C Series After Diagnostics . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 11
Network Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 12
Network Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 12
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CHAPTER 8
Replacement Procedures
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 1
Purpose of Chapter 8 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 1
DISASSEMBLY/RE-ASSEMBLY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 2
Warning and Caution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 2
Air filter and Knob Screw (FRU No. 5030) . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 2
Loading Base Image Software. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 3
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CHAPTER 9
Renewal Parts
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 1
Purpose of Chapter 9 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 1
List of Abbreviations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 1
Renewal Parts Lists . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 2
Equipment Models Covered in this Chapter . . . . . . . . . . . . . . . . . . . . . . . . 9 - 2
Operator Console Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 3
Keyboard Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 3
Accessories and kits. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 4
Manuals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 6
Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 7
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CHAPTER 10
Care & Maintenance
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 1
Periodic Maintenance Inspections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 1
Purpose of Chapter 10 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 1
Why do Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 2
Keeping Records . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 2
Quality Assurance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 2
Maintenance Task Schedule . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 2
How often should care & maintenance tasks be performed? . . . . . . . . . . . . 10 - 2
Tools Required. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 4
Standard GE Tool Kit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 4
Special Tools, Supplies and Equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 6
Input Power . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 7
Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 7
Physical Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 7
Outlet Test - Wiring Arrangement - USA & Canada . . . . . . . . . . . . . . . . . . . 10 - 8
Grounding Continuity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 9
Chassis Leakage Current Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 11
Isolated Patient Lead (Source) Leakage–Lead to Lead . . . . . . . . . . . . . . . . 10 - 14
Isolated Patient Lead (Sink) Leakage-Isolation Test . . . . . . . . . . . . . . . . . . 10 - 14
Probe Leakage Current Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 16
When There's Too Much Leakage Current... . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 20
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Chapter 1 Introduction

Section 1-1 Overview

1-1-1 Purpose of Chapter 1

This chapter describes important issues related to safely servicing the LOGIQ C Series. The service
provider must read and understand all the information presented in this manual before installing or
servicing a unit.
Table 1-1 Contents in Chapter 1
Section Description Page Number
1-1
1-2
1-3
1-4
1-5
"Overview"
"Important Conventions"
"Safety Considerations"
"EMC, EMI, and ESD"
"Customer Assistance"

1-1-2 Purpose of Service Manual

This Service Manual provides installation and service information for the LOGIQ C Series and contains
the following chapters:
1.) - Introduction: Contains a content summary and warnings.
2.) - Site Preparations: Contains pre-installation requirements for the LOGIQ C Series.
3.) - System Setup: Contains installation procedures.
4.) - Functional Checks: Contains functional checks that are recommended as part of the installation,
or as required during servicing and periodic maintenance.
5.) - Components and Functions (Theory): Contains block diagrams and functional explanations of
the electronics.
6.) - Service Adjustments: Contains instructions on how to make available adjustments to the LOGIQ
C Series.
7.) - Diagnostics/Troubleshooting: Provides procedures for running diagnostic or related routines
for the LOGIQ C Series.
8.) - Replacement Procedures: Provides disassembly procedures and reassembly procedures for all
changeable Field Replaceable Units (FRU).
9.) - Renewal Parts: Contains a complete list of field replaceable parts for the LOGIQ C Series.
10.) - Care & Maintenance: Provides periodic maintenance procedures for the LOGIQ C Series.
1-1
1-4
1-6
1-9
1-10
Chapter 1 Introduction 1-1
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1-1-3 Typical Users of the Basic Service Manual

Service Personnel (installation, maintenance, etc.).
Hospital’s Service Personnel
Contractors (Some parts of Chapter 2 - Site Preparation)

1-1-4 Purpose of Operator Manual(s)

The Operator Manual(s) should be fully read and understood before operating the LOGIQ C Series and also kept near the unit for quick reference.
NOTE: Probe information displayed on screen does not necessarily reflect the probes available on your
ultrasound system. Please refer to the probe list for available probes and features.

1-1-5 LOGIQ C2/C3/C5 Models covered by this manual

Table 1-2 LOGIQ C2 Model Designations
Part Number Description
5270586
5310386
5310387
5262932
5310757
LOGIQ C2 Console for Europe
LOGIQ C2 Console for China
LOGIQ C2 Pro Console for China
LOGIQ C2 Console for India
LOGIQ C2 Console for Argentina
Table 1-3 LOGIQ C3 Model Designations
Part Number Description
5268906
5310388
5310389
5265742
5315917
5316706
5310821
LOGIQ C3 Console for Europe
LOGIQ C3 Console for China
LOGIQ C3 Pro Console for China
LOGIQ C3 Console for India
LOGIQ C3 Console (110V)
LOGIQ C3 Console for Korea
LOGIQ C3 Console for Argentina
1-2 Section 1-1 - Overview
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1-1-5 LOGIQ C2/C3/C5 Models covered by this manual (cont’d)
Table 1-4 LOGIQ C3 Model Designations
Part Number Description
52711114
5310390
5310391
5269046
5316707
5315918
5310823
5391533
5391534
5391538
5391536
LOGIQ C5 Console for Europe
LOGIQ C5 Console for China
LOGIQ C5 Pro Console for China
LOGIQ C5 Console for India
LOGIQ C5 Console for Korea
LOGIQ C5 Console (110V)
LOGIQ C5 Console for Argentina
LOGIQ C5 3-Probe Console for China
LOGIQ C5 Pro 3-Probe Console for China
LOGIQ C5 3-Probe Console (110V)
LOGIQ C5 3-Probe Console for Argentina
Chapter 1 Introduction 1-3
GE
DANGER
WARNINGWARNING
CAUTION
NOTICE
IRECTION 5273008-100, REVISION 9 LOGIQ C SERIES BASIC SERVICE MANUAL
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Section 1-2 Important Conventions

1-2-1 Conventions Used in Book

Icons
Pictures, or icons, are used wherever they reinforce the printed message. The icons, labels and conventions used on the product and in the service information are described in this chapter.
Safety Precaution Messages
Various levels of safety precaution messages may be found on the equipment and in the service information. The different levels of concern are identified by a flag word that precedes the precautionary message. Known or potential hazards are labeled in one of following ways:
DANGER IS USED TO INDICATE THE PRESENCE OF A HAZARD THAT WILL CAUSE SEVERE PERSONAL INJURY OR DEATH IF THE INSTRUCTIONS ARE IGNORED.
WARNING IS USED TO INDICATE THE PRESENCE OF A HAZARD THAT CAN CAUSE SEVERE PERSONAL INJURY AND PROPERTY DAMAGE IF INSTRUCTIONS ARE IGNORED.
Caution is used to indicate the presence of a hazard that will or can cause minor personal injury and property damage if instructions are ignored.
Equipment Damage Possible Notice is used when a hazard is present that can cause property damage but has absolutely no
personal injury risk.
Example: Disk drive will crash.
NOTE: Notes provide important information about an item or a procedure.
Information contained in a NOTE can often save you time or effort.
1-4 Section 1-2 - Important Conventions
GE
LASER
LIGHT
Signed
Date
TAG
&
LOCKOUT
EYE
PROTECTION
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1-2-2 Standard Hazard Icons

Important information will always be preceded by the exclamation point contained within a triangle, as
seen throughout this chapter. In addition to text, several different graphical icons (symbols) may be
used to make you aware of specific types of hazards that could cause harm.
Table 1-5 Standard Hazard Icons
ELECTRICAL MECHANICAL RADIATION
LASER HEAT PINCH
Other hazard icons make you aware of specific procedures that should be followed.
Table 1-6 Standard Icons Indicating a Special Procedure Be Used
AVOID STATIC ELECTRICITY TAG AND LOCK OUT WEAR EYE PROTECTION

1-2-3 Product Icons

Please refer to User Manual (Basic user Manual/User Guide) for the detail Product Icons information.
Chapter 1 Introduction 1-5
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WARNING
WARNING
WARNING
WARNING
WARNING
WARNING
CAUTION
WARNING
WARNING
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Section 1-3 Safety Considerations

1-3-1 Introduction

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

1-3-2 Human Safety

Servicing should be performed by authorized personnel only. Only personnel who have participated in a LOGIQ C Series Training are authorized to service the equipment.

1-3-3 Mechanical Safety

WHEN THE UNIT IS RAISED FOR A REPAIR OR MOVED ALONG ANY INCLINE, USE EXTREME CAUTION SINCE IT MAY BECOME UNSTABLE AND TIP OVER.
ULTRASOUND PROBES ARE HIGHLY SENSITIVE MEDICAL INSTRUMENTS THAT CAN EASILY BE DAMAGED BY IMPROPER HANDLING. USE CARE WHEN HANDLING AND PROTECT FROM DAMAGE WHEN NOT IN USE. DO NOT USE A DAMAGED OR DEFECTIVE PROBE. FAILURE TO FOLLOW THESE PRECAUTIONS CAN RESULT IN SERIOUS INJURY AND EQUIPMENT DAMAGE.
NEVER USE A PROBE THAT HAS FALLEN TO THE FLOOR. EVEN IF IT LOOKS OK, IT MAY BE DAMAGED.
The LOGIQ C Series weighs 75 kg 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 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 75 kg (169 lbs).
AFTER UNPLUG POWER CORD, WAIT FOR AT LEAST 20 SECONDS FOR CAPACITORS TO DISCHARGE AS THERE ARE NO TEST POINTS TO VERIFY ISOLATION.
1-6 Section 1-3 - Safety Considerations
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WARNINGWARNING
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1-3-3 Mechanical Safety (cont’d)
NOTE: Special care should be taken when transporting the unit in a vehicle:
Secure the unit in an upright position.
Lock the wheels (brake)

1-3-4 Electrical Safety

To minimize shock hazard, the equipment chassis must be connected to an electrical ground. The
system is equipped with a three-conductor AC power cable. This must be plugged into an approved
electrical outlet with safety ground. The power outlet used for this equipment should not be shared with
other types of equipment.
Both the system power cable and the power connector meet international electrical standards.
DO NOT SERVICE OR DISASSEMBLE PARTS UNDER FRU UNIT LEVEL AT ANY CIRCUMSTANCES.

1-3-5 Label Locations

See LC2/C2 PRO, LC3/LC3 PRO, LC5/C5PRO Basic User Manual (5265060-100,5268001-
100,5268596-100) section “Warning Label Location” for more Information.
Chapter 1 Introduction 1-7
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DANGER
WARNING
WARNING
WARNING
WARNING
WARNING
WARNING
WARNING
WARNING
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1-3-6 Dangerous Procedure Warnings

Warnings, such as the examples below, precede potentially dangerous procedures throughout this manual. Instructions contained in the warnings must be followed.
DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH, ARE PRESENT IN THIS EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING AND ADJUSTING.
EXPLOSION WARNING
DO NOT OPERATE THE EQUIPMENT IN AN EXPLOSIVE ATMOSPHERE. OPERATION OF ANY ELECTRICAL EQUIPMENT IN SUCH AN ENVIRONMENT CONSTITUTES A DEFINITE SAFETY HAZARD.
DO NOT SUBSTITUTE PARTS OR MODIFY EQUIPMENT
BECAUSE OF THE DANGER OF INTRODUCING ADDITIONAL HAZARDS, DO NOT INSTALL SUBSTITUTE PARTS OR PERFORM ANY UNAUTHORIZED MODIFICATION OF THE EQUIPMENT.
SHUT DOWN FORCEDLY OR PLUG IN/OUT ACDC INVALID MAY CAUSE THE DAMAGE OF SYSTEM FILES.
AFTER UNPLUG POWER CORD, WAIT FOR AT LEAST 20 SECONDS FOR CAPACITORS TO DISCHARGE AS THERE ARE NO TEST POINTS TO VERIFY ISOLATION.

1-3-7 Returning/Shipping Probes and Repair Parts

Equipment being returned must be clean and free of blood and other infectious substances.
GEMS policy states that body fluids must be properly removed from any part or equipment prior to shipment. GEMS employees, as well as customers, are responsible for ensuring that parts/equipment have been properly decontaminated prior to shipment. Under no circumstance should a part or equipment with visible body fluids be taken or shipped from a clinic or site (for example, body coils or an ultrasound probe).
The purpose of the regulation is to protect employees in the transportation industry, as well as the people who will receive or open this package.
NOTE:The USER/SERVICE staff should dispose all the waste properly as per federal, state, and local
waste disposal regulation.
1-8 Section 1-3 - Safety Considerations
GE
WARNING
WARNING
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Section 1-4 EMC, EMI, and ESD

1-4-1 Electromagnetic Compatibility (EMC)

Electromagnetic compatibility describes a level of performance of a device within its electromagnetic
environment. This environment consists of the device itself and its surroundings including other
equipment, power sources and persons with which the device must interface. Inadequate compatibility
results when a susceptible device fails to perform as intended due interference from its environment or
when the device produces unacceptable levels of emission to its environment. This interference is often
referred to as radio–frequency or electromagnetic interference (RFI/EMI) and can be radiated through
space or conducted over interconnecting power of signal cables. In addition to electromagnetic energy,
EMC also includes possible effects from electrical fields, magnetic fields, electrostatic discharge and
disturbances in the electrical power supply.

1-4-2 CE Compliance

The LOGIQ C Series unit conforms to all applicable conducted and radiated emission limits and to
immunity from electrostatic discharge, radiated and conducted RF fields, magnetic fields and power line
transient requirements.
For applicable standards refer to the Safety Chapter in the Basic User Manual.
NOTE:For CE Compliance, it is critical that all covers, screws, shielding, gaskets, mesh, clamps, are in good
condition, installed tightly without skew or stress. Proper installation following all comments
noted in this service manual is required in order to achieve full EMC performance.

1-4-3 Electrostatic Discharge (ESD) Prevention

DO NOT TOUCH ANY BOARDS WITH INTEGRATED CIRCUITS PRIOR TO TAKING THE NECESSARY ESD PRECAUTIONS:
1.FOLLOW GENERAL GUIDELINES FOR HANDLING OF ELECTROSTATIC SENSITIVE EQUIPMENT.
Chapter 1 Introduction 1-9
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Section 1-5 Customer Assistance

1-5-1 Contact Information

If this equipment does not work as indicated in this service manual or in the User Manual, or if you require additional assistance, please contact the local distributor or appropriate support resource, as listed below.
Prepare the following information before you call:
- System ID serial number.
- Software version.
Table 1-7 Phone Numbers for Customer Assistance
Location Phone Number
USA
GE Vingmed Ultrasound
Ultrasound Service Engineering
9900 Innovation Drive
Wauwatosa, WI 53226
Canada 1-800-668-0732
Latin America
Europe (OLC- EMEA)
GE Ultraschall Deutschland GmbH
Beethovenstraße 239
Postfach 11 05 60, D-42655 Solingen
Germany
Online Services Ultrasound Asia
Australia
China
India
Japan
Korea
Singapore
Service: On-site
Service Parts
Application Support
Service
Application Support
OLC - EMEA
Phone: +49 (0)212 2802 - 652
+33 1 3083 1300
Fax: +49 (0) 212 2802 - 431
Phone: +(61) 1-800-647-855
+(86) 800-810-8188
+(91) 1-800-11-4567
+(81) 42-648-2924
+(82) 2620 13585
+(95) 6277-3444
1-800-437-1171
1-800-558-2040
1-800-682-5327 or 1-262-524-5698
1-800-321-7937
1-262-524-5698
1-10 Section 1-5 - Customer Assistance
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1-5-2 System Manufacturer

Table 1-8 System Manufacturer
Manufacturer FAX Number
GE Medical Systems (China) Co., Ltd.
No.19, Changjiang Road, Wuxi National Hi-Tech Development Zone, Jiangsu, P.R. China 214028

1-5-3 Factory Site

Table 1-9 Factory Site
GE Medical Systems (China) Co., Ltd.
No.19, Changjiang Road, Wuxi National Hi-Tech Development Zone, Jiangsu, P.R. China 214028
Wirpo GE Healthcare Pvt. Ltd.,
No. 4, Kadugodi Industrial Area, Bangalore. 560067 Karnataka. India.
TEL: +86 510-85225888
FAX: +86 510-85226688
Factory Site FAX Number
TEL: +86 510-85225888
FAX: +86 510-85226688
TEL: +91-80-41801000
FAX: +91-80-28452924
Chapter 1 Introduction 1-11
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1-12 Section 1-5 - Customer Assistance
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Chapter 2 Site Preparations

Section 2-1 Overview

2-1-1 Purpose of chapter 2

This chapter provides the information required to plan and prepare for the installation of LOGIQ C Series.Included are descriptions of the facility and electrical needs to be met by the purchaser of the unit.
Table 2-1 Contents in Chapter 2
Section Description Page Number
2-1
2-2
2-3
"Overview"
"General Console Requirements"
"Facility Needs"
2-1
2-2
2-6
Section 2-1 - Overview 2 - 1
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IRECTION 5273008-100, REVISION 9 LOGIQ C SERIES BASIC SERVICE MANUAL

Section 2-2 General Console Requirements

2-2-1 Console Environmental Requirements

Table 2-2 Environmental Requirements for LOGIQ C Series Scanners
Operational Storage Transport
Temperature
Humidity
Pressure
o
10 - 40oC
50 - 104
30 - 75% non-condensing
700 - 1060hPa 700 - 1060hPa 700 - 1060hPa
o
F
-5 - 50
C
o
23 - 122
10 - 90% non-condensing
F
o
-5 - 50
C
o
23 - 122
10 - 90% non-condensing
F
NOTE: Temperature in degrees C. Conversion to Degrees F = (Degrees C * 9/5) + 32.
2-2-1-1 Lighting
Bright light is needed for system installation, updates and repairs. However, operator and patient comfort may be optimized if the room light is subdued and indirect. Therefore a combination lighting system (dim/bright) is recommended. Keep in mind that lighting controls and diameters can be a source of EMI which could degrade image quality. These controls should be selected to minimize possible interface.

2-2-2 Electrical Requirements

NOTE: GE Healthcare requires a dedicated power and ground for the proper operation of its Ultrasound
equipment. This dedicated power shall originate at the last distribution panel before the system.
Sites with a mains power system with defined Neutral and Live:
The dedicated line shall consist of one phase, a neutral (not shared with any other circuit), and a full size ground wire from the distribution panel to the Ultrasound outlet.
Sites with a mains power system without a defined Neutral:
The dedicated line shall consist of one phase (two lines), not shared with any other circuit, and a full size ground wire from the distribution panel to the Ultrasound outlet.
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 Section 2-2 - General Console Requirements
GE
CAUTION
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IRECTION 5273008-100, REVISION 9 LOGIQ C SERIES BASIC SERVICE MANUAL
2-2-2 Electrical Requirements (cont’d)
2-2-2-1 LOGIQ C Series Power Requirements
The following power line parameters should be monitored for one week before installation. We recommend that you use an analyzer Dranetz Model 606-3 or Dranetz Model 626:
Table 2-3 Electrical Specifications for LOGIQ C Series
PARAMETER AREA LIMITS
Voltage Range
Power All applications MAX. 750 VA
Line Frequency All applications 50/60Hz (±2Hz)
Power Transients All applications
Decaying Oscillation All applications
2-2-2-2 Inrush Current
Inrush Current is not a factor to consider due to the inrush current limiting properties of the power supplies.
2-2-2-3 Site Circuit Breaker
It is recommended that the branch circuit breaker for the machine be ready accessible.
POWER OUTAGE MAY OCCURE. The LOGIQ C Series 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.
100-120V~ 500VA
220-240V~ 500VA
Less than 25% of nominal peak voltage for less than 1 millisecond for any type of transient, including line frequency, synchronous, asynchronous, or aperiodic transients.
Less than 15% of peak voltage for less than 1 millisecond.
2-2-2-4 Site Power Outlets
A desiccated AC power outlet must be within reach of the unit without extension cords. Other outlets adequate for the external peripherals, medical and test equipment needed to support this unit must also be present within 1 m (3.2 ft.) of the unit. Electrical installation must meet all current local, state, and national electrical codes.
2-2-2-5 Unit Power Plug
If the unit arrives without the power plug, or with the wrong plug, you must contact your GE dealer or the installation engineer must supply what is locally required.
2-2-2-6 Power Stability Requirements
Voltage drop-out
Max 10 ms.
Power Transients
(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.
Section 2-2 - General Console Requirements 2 - 3
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2-2-3 EMI Limitations

Ultrasound machines are susceptible to Electromagnetic Interference (EMI) from radio frequencies, magnetic fields, and transient in the air wiring. They also generate EMI. The LOGIQ C Series complies with limits as stated on the EMC label. However there is no guarantee that interface will not occur in a particular installation.
Possible EMI sources should be identified before the unit is installed.
Electrical and electronic equipment may produce EMI unintentionally as the result of defect.
These sources include:
medical lasers,
scanners,
cauterizing guns,
•computers,
•monitors,
fans,
gel warmers,
microwave ovens,
light dimmers,
portable phones.
The presence of broadcast station or broadcast van may also cause interference. See for EMI Prevention tips.
See Ta bl e 2 -4 for EMI Prevention tips.
Table 2-4 EMI Prevention/abatement
EMI Rule Details
Keep the unit at least 5 meters or 15 feet away from other EMI sources. Special shielding
Be aware of RF sources
Ground the unit
Replace all screws, RF gaskets, covers, cores
Replace broken RF gaskets
Do not place labels where RF gaskets touch metal
Use GE specified harnesses and peripherals
Take care with cellular phones Cellular phones may transmit a 5 V/m signal; that could cause image artifacts.
may be required to eliminate interference problems caused by high frequency, high powered radio or video broadcast signals.
Poor grounding is the most likely reason a unit will have noisy images. Check grounding of the power cord and power outlet.
After you finish repairing or updating the system, replace all covers and tighten all screws. Any cable with an external connection requires a magnet wrap at each end. Install the shield over the front of card cage. Loose or missing covers or RF gaskets allow radio frequencies to interface with the ultrasound signals.
If more than 20% or a pair of fingers on the RF gaskets are broken, replace the gaskets. Do not turn on the unit until any loose metallic part is removed.
Never place a label where RF gaskets meet the unit. Otherwise, the gap created will permit RF leakage. Or, if a label has been found in such a position, move the label.
The interconnect cables are grounded and require ferrite beads and other shielding. Also, cable length, material, and routing are all important; do not change from what is specified.
Properly dress peripheral cables
Do not allow cables to lie across the top of the card cage or hang out of the peripheral bays. Loop the excess length for peripheral cables inside the peripheral bays. Attach the monitor cables to the frame.
2 - 4 Section 2-2 - General Console Requirements
GE
NOTICE
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2-2-4 Scan Probe Environmental Requirements

Operation:10° to 40° C
Storage:-10° to 50° C
NOTE: Temperature in degrees C. Conversion to Degrees F = (Degrees C * (9/5) + 32).
SYSTEMS AND ELECTRONIC PROBES ARE DESIGNED FOR STORAGE TEMPERATURES OF
-10 TO + 60 degrees C. WHEN EXPOSED TO LARGE TEMPERATURE VARIATIONS, THE PRODUCT SHOULD BE KEPT IN ROOM TEMPERATURE FOR 10 HOURS BEFORE USE.
Section 2-2 - General Console Requirements 2 - 5
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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 installation work before delivery. User the Pre Installation checklist to verify that all needed steps have been taken, Purchaser reasonability includes:
Procuring the materials required.
Completing the preparations before delivery of the ultrasound system.
Paying the costs for any alternations and modifications not specifically provided in the sales contract.
NOTE: All electrical installation that are preliminary to the positioning of the equipment at the site
prepared for the equipment must be performed by licensed electrical contractors. Other connections between pieces of electrical equipment, products involved (and the accompanying electrical installations) are highly sophisticated and special engineering competence is required. All electrical work on these product must comply with the requirements of applicable electrical codes. The purchaser of GE equipment must only utilize qualified personnel to perform electrical servicing on the equipment.
The desire to use a non-listed or customer provided product or to place an approved product further from the system than the interface kit allows presents challenges to the installation team. To avoid delays during installation, such variances should be made known to the individuals or group performing the installation at the earliest possible date (preferable prior to purchase). The ultrasound suite must be clean proof to delivery of the machine. Carpet is not recommended because it collects dust and creates static. Potential sources of EMI (electromagnetic interference) should also be investigated before delivery. Dirt, static, and EMI can negatively impact system.
2 - 6 Section 2-3 - Facility Needs
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2-3-2 Required Features

NOTE: GE Medical Systems requires a dedicated power and ground for the proper operation of its
Ultrasound equipment. This dedicated power shall originate at the last distribution panel before the system.
Sites with a mains power system with defined Neutral and Live:
The dedicated line shall consist of one phase, a neutral (not shared with any other circuit), and a full size ground wire from the distribution panel to the Ultrasound outlet.
Sites with a mains power system without a defined Neutral:
The dedicated line shall consist of one phase (two lines), not shared with any other circuit, and a full size ground wire from the distribution panel to the Ultrasound outlet.
Please note that image artifacts can occur, if at any time within the facility, the ground from the main facility's incoming power source to the Ultrasound unit is only a conduit.
Dedicated single branch power outlet of adequate amperage meeting all local and national codes which is located less than 2.5 m (8 ft.) from the unit’s proposed location
Door opening is at least 76 cm (30 in) wide
Proposed location for unit is at least 0.3 m (1 ft.) from the wall for cooling
Power outlet and place for any external peripheral are within 2 m (6.5 ft.) of each other with peripheral within 1 m of the unit to connect cables.
Section 2-3 - Facility Needs 2 - 7
GE
LINEN SUPPLY
EXAMINATION
TABLE
FILM VIEWER
COUNTER TOP
FILE
CABINET
SECRETARYS OR DOCTOR’S DESK
FILM
PROCESSING
ROOM,
OVERHEAD LIGHTS DIMMER
DEDICATED
POWER
RECEPTACLE
EXTERNAL
PERIPHERALS
SINK
COUNTER
TOP
FILM VIEWER
FILM SUPPLIES
SINK
LINEN SUPPLY
PROBES/SUPPLIES
24 IN. (61 CM)
EXAMINARION
TABLE
76 IN. (193 CM)
DOOR
30 IN.
(76 CM)
An 8 by 10 foot Minimal Floor Plan
DEDICATED POWER OUTLETS
DEDICATED ANALOG TELEPHONE LINE FOR CONNECTION TO INSITE
A 14 by 17 foot Recommended Floor Plan
GE CABINET FOT SOFTWARE AND MANUALS
Scale : Each square equals one square foot
DOOR
42 IN.
(107 CM)
DEDICATED ALALOG TELEPHONE LINE FOR CONNECTION TO INSITE
SUCTION LINE
EMERGECY OXYGEN
24 IN.
(61 CM)
76 IN.
(193 CM)
PATIENT
TOILET
FACILITY
FOOT
SW
FOOT
SW
LOGIQ 5
CONSOLE
CONSOLE
18 IN.
(46 CM)
STOOL
STOOL
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2-3-3 Recommended and Alternate Ultrasound Room Layout

Recommended standard floor plan and a minimal floor plan for ultrasound equipment:
2 - 8 Section 2-3 - Facility Needs
Figure 2-1 RECOMMENDED ULTRASOUND ROOM LAYOUT
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2-3-4 Networking Pre-installation Requirements

2-3-4-1 Stand Alone Scanner (without Network Connection)
None.
2-3-4-2 Scanner Connected to Hospital’s Network
Supported networks:
Wire LAN
2-3-4-3 Purpose of DICOM Network Function
DICOM services provide the operator with clinically useful features for moving images and patient information over a hospital network. Examples of DICOM services include the transfer of images to workstations for viewing or transferring images to remote printers. As an added benefit, transferring images in this manner frees up the on-board monitor and peripherals, enabling viewing to be done while scanning continues. With DICOM, images can be archived, stored, and retrieved faster, easier, and at a lower cost.
2-3-4-4 DICOM Option Pre-installation Requirements
To configure the LOGIQ C Series to work with other network connections, the site’s network administrator must provide some necessary information.
Information must include:
A host name, local port number, AE Title, IP address and Net Mask for the LOGIQ C Series.
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 C Series for DICOM APPLICATION INFORMATION. A field for the make (manufacturer)
and the revision of the device, is also included. This information may be useful for solving errors.
Section 2-3 - Facility Needs 2 - 9
GE
LOGIQ C
Host Name
AE Title
Local Port
IP Address
Net Mask
...
...
ROUTING INFORMATION
ROUTER2 ROUTER3
ROUTER1
...
...
...
...
...
...
...
Destination IP Addresses
GATEWAY IP Addresses
Default
DICOM APPLICATION INFORMATION
NAME
Store 2
Store 3
Store 1
MAKE/REVISION IP ADDRESSES PORTAE TITLE
Store 5
Store 6
Store 4
Storage Commit
MPPS
Worklist
...
...
...
...
...
...
...
...
...
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2-3-4-4 DICOM Option Pre-installation Requirements (cont’d)
.
Figure 2-2 Worksheet for DICOM Network Information
2 - 10 Section 2-3 - Facility Needs
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IRECTION 5273008-100, REVISION 9 LOGIQ C BASIC SERIES SERVICE MANUAL
Chapter 3 System Setup

Section 3-1 Overview

3-1-1 Purpose of Chapter 3

This chapter contains information needed to install the unit. Included are references to a procedure that describes how to receive and unpack the equipment and how to file a damage or loss claim. How to prepare the facility and unit of the actual installation, and how to check and test the unit and external peripherals for electrical safety are included in this procedure. Also included LOGIQ C Series in this section are guidelines for transporting the unit to a new site.
Table 3-1 Contents in Chapter 3
Section Description Page Number
3-1 "Overview" 3-1
3-2 "Setup Reminders" 3-2
3-3 "Receiving and Unpacking the Equipment" 3-3
3-4 "Preparing for Installation" 3-4
3-5 "Completing the Installation" 3-5
3-6 "System Configuration" 3-6
3-7 "Software/Option Configuration" 3-7
3-8 "Connectivity Installation Worksheet" 3-8
3-9 "Loading Base Image Software" 3-9
3-10 "Software Version check out" 3-10
3-11 "Paperwork" 3-11
Chapter 3 System Setup 3 - 1
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Section 3-2Setup Reminders

3-2-1 Average Installation Time

Table 3-2 Average Installation Time
Description Average Installation Time Comments
Unpacking the scanner
Scanner wo/options
DICOM Option
0.5 hour
0.5 hour
0.5 hour
Dependant on the configuration that is required
Dependant on the amount of configuration
The LOGIQ C Series has been designed to be installed and checked out by an experienced service technician in approximately 1 hour. LOGIQ C Series consoles with optional equipment may take slightly longer.
3 - 2 Section 3-2 - Setup Reminders
GE
CAUTION
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3-2-2 Installation Warnings

1.) Since the LOGIQ C Series weighs approximately 75 kg without options, preferably two people should unpack it. Two people are also preferable for installing any additional bulky items.
2.) There are no operator serviceable components. To prevent shock, do not remove any covers or panels. Should problems or malfunctions occur, unplug the power cord. Only qualified service personnel should carry out servicing and troubleshooting.
NOTE: For information regarding packing labels, refer to LABELS ON PACKAGE.
3.) After being transported, the unit may be very cold or hot. If this is the case, allow the unit to acclimate before you turn it on. It requires one hour for each 2.5°C increment it's temperature is below 10°C or above 30°C.
Equipment damage possibility. Turning the system on without acclimation after arriving at site may cause the system to be damaged.
Table 3-3 Acclimation Time
60 55 50 45 40 35 30 25 20 15 10 5 0 -5 -10 -15 -20 -25 -30 -35 -40
°C
140 131 122 113 104 95 86 77 68 59 50 41 32 23 14 5 -4 -13 -22 -31 -40
°F
864200000002468101214161820
hrs
Chapter 3 System Setup 3 - 3
GE
DANGER
CAUTION
CAUTION
CAUTION
CAUTION
CAUTION
CAUTION
CAUTION
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3-2-3 Safety Reminders

WHEN USING ANY TEST INSTRUMENT THAT IS CAPABLE OF OPENING THE AC GROUND LINE (I.E., METER’S GROUND SWI TCH IS OPEN), DON’T TOUCH THE UNIT!
Two people should unpack the unit because of its weight. Two people are required whenever a part weighing 19kg (35 lb.) or more must be lifted.
If the unit is very cold or hot, do not turn on its power until it has had a chance to acclimate to its operating environment.
To prevent electrical shock, connect the unit to a properly grounded power outlet. Do not use a three to two prong adapter. This defeats safety grounding.
Do NOT wear the ESD wrist strap when you work on live circuits and more than 30 V peak is present.
Do not use a 20 Amp to 15 Amp adapter on the 120 Vac unit’s power cord. This unit requires a dedicated 20 A circuit and can have a 15A plug if the on board peripherals do not cause the unit to draw more than 14.0 amps.
Do not operate this unit unless all board covers and frame panels are securely in place. System performance and cooling require this.
OPERATOR MANUAL(S) The User Manual(s) should be fully read and understood before operating the LOGIQ C Series and kept near the unit for quick reference.
Figure 3-1 Environmental Labels
3 - 4 Section 3-2 - Setup Reminders
GE
CAUTION
CAUTION
2)
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Section 3-3 Receiving and Unpacking the Equipment

When a new system arrives, check that any components are not damaged and are not in short supply. If shipping damage or shortage occurs, contact the address shown in Chapter 1.
Do not lift the unit by the Keyboard. Equipment damage may result.
The crate with the LOGIQ C Series weighs approximately 75kg. Be prepared for a sudden shift of weight as the unit is removed from its base (pallet)
Unpacking the the equipment
1.) Remove all the strapping tapes from the packing box.
2.) Remove the upper cover of the packing box and then rotate the knob to the right to open the packing box.
3.) Remove the PE bag and plastic film from the system.
4.) Remove Accessories Carton from the system.
5.) Remove the PE bag and plastic film from the syste
6.) Lift down the system .
Figure 3-2 Open the box
Chapter 3 System Setup 3 - 5
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CAUTION
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3-3-1 Moving into Position

Do not tilt the unit more than 5 degrees to avoid tipping it over. To avoid injury by tipping over. Set the monitor to the lowest position before moving.
In general, a single adult can move the LOGIQ C Series along an even surface with no steep grades. At least two people should move the machine when large humps, grooves, or grades will be encountered. (It is better to pull from the rear rather than push from the front of the unit). Before moving, store all loose parts in the unit. Wrap transducers in soft cloth or foam to prevent damage.
Although LOGIQ C Series is a mobile machine, two people should move it over rough surfaces or up and down grades.

3-3-2 Product Locator Installation Card

NOTE: The Product Locator Installation Card shown may not be same as the provided Product Locator
card.
Figure 3-3 Product Locator Installation Card
3 - 6 Section 3-3 - Receiving and Unpacking the Equipment
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WARNINGWARNING
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Section 3-4 Preparing for Installation

3-4-1 Verify Customer Order

Compare items received by the customer to that which is listed on the delivery order. Report any items that are missing, back ordered or damaged.

3-4-2 Physical Inspection

3-4-2-1 System Voltage Settings
Verify that Docking Cart is set to the correct voltage. The Voltage settings for the LOGIQ C Series is found on a label to the right of the Power switch and External I/O, on the rear of the system.
Connecting a LOGIQ C Series to the wrong voltage level will most likely destroy it.
3-4-2-2 Video Formats
Check that the video format is set to the locally used video standard, NTSC or PAL.

3-4-3 EMI Protection

This Unit has been designed to minimize the effects of Electro Magnetic Interference (EMI). Many of the covers, shields, and screws are provided primarily to protect the system from image artifacts caused by this interference. For this reason, it is imperative that all covers and hardware are installed and secured before the unit is put into operation.
Chapter 3 System Setup 3 - 7
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Section 3-5 Completing the Installation

3-5-1 Power On / Boot Up

NOTE: After turning off a system, wait at least ten seconds before turning it on again. The system may not be
able to boot if power is recycled too quickly.
3-5-1-1 Scanner Power On
When power is applied to the scanner, power is distributed to the Cooling Unit, Control Panel, LCD, Peripherals and the Back-end Processor.
3-5-1-2 Turn on the system
Press the Power On/Off switch at the front of the system once.
Figure 3-4 Power On/Off Switch
When the Power On/Off switch on the Control Panel is pressed once, the Back-end Processor starts and the software code is distributed to initiate the scanner.
No status messages are displayed during this process.

3-5-2 Power Off/ Shutdown

NOTE: After turning off a system, wait at least ten seconds before turning it on again. The system may not be
able to boot if power is recycled too quickly.
3-5-2-1 Back-end Processor Power Down
To power down the system:
1.) Press the Power On/Off switch once.
3 - 8 Section 3-5 - Completing the Installation
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3-5-2-1 Back-end Processor Power Down (cont’d)
2.) The System-Exit window is displayed.
Figure 3-5 System Exit Window
3.) Using the Trackball or Select key, select Shutdown.
4.) The shutdown process takes a few seconds and is complete when the power status LED is turned amber.
5.) Disconnect the probes.Clean or disinfect all probes as necessary. Store them in their shipping cases to avoid damage.
3-5-2-2 Scanner Shutdown
Disconnect the Mains Power Cable if necessary. For example: Relocating the scanner.

3-5-3 Transducer Connection

1.) Plug the probe connector into the probe port, then lock the probe.
NOTE: Please ensure that the probe latch is in an unlocked position before you connect the probe to the
system.
NOTE: It is not necessary to turn OFF power to connect or disconnect a probe.
Chapter 3 System Setup 3 - 9
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Section 3-6 System Configuration

3-6-1 System Specifications

3-6-1-1 Physical Dimensions
The physical dimensions of the LOGIQ C Series unit are summarized in Table 3-4 on page 3-10 . The Size of LOGIQ C Series.
Table 3-4 Physical Dimensions of LOGIQ C Series
Height Width Depth Unit
1400 500 700 mm
55.16 19.70 27.58 inches
3-6-1-2 Weight
Table 3-5 Weight of LOGIQ C Series With Monitor and Without Other Peripherals
Model Weight [kg] Weight [lb]
LOGIQ C Series Approximately 75 Approximately 165

3-6-2 Electrical Specifications

Table 3-6 Electrical Specifications for LOGIQ C Series
System Voltage Current Frequency
1
2
110 -120 V AC
220- 240 V AC
500VA 50/60Hz
500VA 50/60Hz
3 - 10 Section 3-6 - System Configuration
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3-6-3 On-Board Optional Peripherals

Table 3-7 List of Optional Peripherals
Device Manufacturer Model Video Signal
B/W Printer SONY UP-D897MD USB
B/W Printer SONY UP-D257MD USB
HP Printer HP HP 470b Officejet USB
USB Memory SanDisk SanDisk 2G USB
USB Memory SanDisk SanDisk 4G USB
Footswitch Whanam FSU2001 USB
USB Hard Disk Seagate USBHDD 80G USB
USB Hard Disk Seagate USBHDD 250G USB
Color Printer SONY UP-D23MD USB
ECG NORAV ECG -USB1 USB
NOTE: Color Printer and ECG are only supported by LOGIQ C5/C5 PRO.
NOTE: For detailed installation information and connection procedures, please refer to Peripheral Installation
Instruction manual (5266280-100).
Chapter 3 System Setup 3 - 11
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3-6-4 Connecting Cables

Equipment damage possibility. Be sure to use the following recommended connecting cables to connect recording devices and a network with LOGIQ C Series console.
Table 3-8 List of Connecting Cables
Name Part No. Figure NOTE
USB Cable 5122305

3-6-5 Peripherals/Accessories Connector Panel

LOGIQ C Series peripherals and accessories can be properly connected using the side connector panel.
3-6-5-1 Rear Panel Connector
Located on the rear panel are Network port, 2 USB port, S-Video Out, VGA, Audio Out, Composite Out.
For USB Printer
Figure 3-6 Rear Connector Panel
1.) Network Port
2.) 2 USB Ports (Printers, Footswitch, etc)
3.) S-Video Out
4.) VGA
5.) Audio Out
6.) Composite Out
NOTE: Audio Out is not supported by LOGIQ C2/C2 PRO.
3 - 12 Section 3-6 - System Configuration
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3-6-5-2 Left Panel Connector
1 USB port is Located on the left panel.
Figure 3-7 Left Connector Panel
1.) 1 USB Ports (Printers, Footswitch, etc)
3-6-5-3 Printer Box Rear Panel connector
Figure 3-8 Printer Box Rear Connector Panel
1.) 1 USB Ports only for B/W Printer
NOTE: Each outer (case) ground line of peripheral/accessory connectors are protectively grounded.
Signal ground lines are not isolated, except the Service port (3). All of signal lines (include signal GND) of the Service port are isolated.
Chapter 3 System Setup 3 - 13
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3-6-5-4 Pin assignment for each connector
Table 3-9 Pin Assignments of External VGA
Pin No. Signal Pin No. Signal
1RED9 NC
2 GREEN 10 NC
3BLUE11 NC
4NC12NC
5NC13HSY
6 GND 14 VSY
7 GND 15 NC
8GND
Table 3-10 Pin Assignments of USB
Pin No. Signal Pin No. Signal
1 +5 VDC 5 +5 VDC
2DATA6DATA
3DATA7DATA
4GND8GND
Table 3-11 Pin Assignments of Audio
Pin No. Signal Pin No. Signal
1GND4 NC
2L+5R+
3 Speaker L 6 Speaker R
Table 3-12 Pin Assignment of S-Video
Pin No. Output Signal Pin No. Output Signal
1GND3 Y
2GND4 C
Table 3-13 Pin Assignment of Composite Video Out
Pin No. Output Signal Pin No. Output Signal
1 Composite Out 2 GND
3 - 14 Section 3-6 - System Configuration
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3-6-5-5 Connect Peripherals
A.) Connect B/W printer to the system.
B/W Printer can be properly connected using USB Ports.
Figure 3-9 Connect B/W printer to the system
B.) Connect UP-D23 color printer to the system. (Only supported by LOGIQ C5/C5 PRO)
UP-D23 Color Printer can be properly connected using USB Ports.
Figure 3-10 Connect color printer to the system
Chapter 3 System Setup 3 - 15
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3-6-5-5 Connect Peripherals (cont’d)
C.) Connect Foot Switch to the system.
Foot Switch can be properly connected using USB Ports.
Figure 3-11 Connect Foot Switch to the system
D.) Connect the USB Memory to the system. The USB Memory can be properly connected using USB
ports.
Figure 3-12 USB Memory Connection
E.) ECG can be properly connected using USB ports. (ECG only supported by LOGIQ C5/C5 PRO)
Figure 3-13 ECG
3 - 16 Section 3-6 - System Configuration
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3-6-5-5 Connect Peripherals (cont’d)
F.) Connect the USB HDD to the system. The USB Harddisk can be properly connected using USB
ports.
Figure 3-14 USB Hard Disk Connection
G.) Connect HP 470b Officejet printer to the system. HP 470b Officejet Printer can be properly
connected using USB Ports
Figure 3-15 HP 470b Officejet printer Connection
Chapter 3 System Setup 3 - 17
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3-6-6 Available Probes

See in specification in the LOGIQ C Series User Reference Manual for Probes and intended use.
Table 3-14 List of Probes on LOGIQ C Series
Probe Name Material of Headshell Area of Using TYPE Catalog Number
4C-RC
3.8C-RC
6.5C-RC
E6C-RC
E7C-RC
7.5L-RC
7L-RC
3S-RC
NORYL GENERAL PURPOSE CONVEX H48102LE
NORYL GENERAL PURPOSE CONVEX H48102LD
VETERINARY
VALOX
VALOX
VALOX
VALOX
VALOX
VALOX CARDIAC SECTOR H40452LA
PEDIATRIC
NEONATAL
TRANSVAGINAL
TRANSRECTAL
TRANSVAGINAL
TRANSRECTAL
SMALL PARTS
PERIPHERAL VASCULAR
SMALL PARTS
PERIPHERAL VASCULAR
MICRO-CONVEX H48102LF
MICRO-CONVEX H48102LH
MICRO-CONVEX H48102LG
LINEAR H48102LJ
LINEAR H48102LK

Section 3-7 Software/Option Configuration

Refer to the LOGIQ C Series Basic User Manual, Chapter 16, Customizing Your System for information on configuring items like Hospital, Department, Language, Units (of measure), Date, Time and Date Format.
For information on configuring Software Options, Refer to the LOGIQ C Series Basic User Manual, Chapter 16, Customizing Your System.
For information on configuring DICOM Connectivity, Refer to the LOGIQ C Series Basic User Manual, Chapter 16, Customizing Your System.
3 - 18 Section 3-7 - Software/Option Configuration
GE
Site System Information
Services (Destination Devices)
TCP/IP Settings
Device Type
Manufacturer
Name
IP Address
Port
AE Title
1 2 3 4 5 6 7 8 9 10 11 12
Name - AE Title:
Dept:
LOGIQ SN:
Type:
Floor:
Room:
REV:
Comments:
CONTACT INFORMATION
Name
Title
Phone
E-Mail Address
Site:
IP Settings
IP Address:
Subnet Mask:
Default Gateway:
Remote Archive Setup
Remote Archive IP:
Remote Archive Name:
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Section 3-8 Connectivity Installation Worksheet

Chapter 3 System Setup 3 - 19
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Section 3-9 Loading Base Image Software

Refer to
Section 8-3 "Loading Base Image Software" on page 8-3.
3 - 20 Section 3-9 - Loading Base Image Software
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Section 3-10Software Version check out

3-10-1 Functional Check-out

1.) Power on LOGIQ C Series scanner and wait until system booting to main screen.
2.) Press UTILITY
3.) Choose the About
key on control panel.
button on the right.
Figure 3-16 About and Software version
4.) Check whether “Software version” is the right version for use.
Chapter 3 System Setup 3 - 21
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Section 3-11 Paperwork

NOTE: During and after installation, the documentation (i.e. User Manuals, Installation Manuals...) for the
peripheral units must be kept as part of the original system documentation. This will ensure that all relevant safety and user information is available during the operation and service of the complete system.

3-11-1 Product Locator Installation

NOTE: The Product Locator Installation Card shown may not be same as the provided Product Locator
card.
Figure 3-17 Product Locator Installation Card

3-11-2 User Manual(s)

User Check that the correct User Manual(s) for the system and software revision, is included with the installation. Specific language versions of the User Manual may also be available. Check with your GE Sales Representative for availability.
3 - 22 Section 3-11 - Paperwork
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Chapter 4 Functional Checks

Section 4-1 Overview

4-1-1 Purpose for Chapter 4

This chapter provides procedures for quickly checking major functions of the LOGIQ C Series console,
diagnostics by using the built-in service software, and power supply.
Table 4-1 Contents in Chapter 4
Section Description Page Number
4-1 "Overview" 4-1
4-2 "Required Equipment" 4-1
4-3 "General Procedure" 4-2
4-4 "Software Configuration Checks" 4-35
4-5 "Peripheral Checks" 4-35

Section 4-2 Required Equipment

To perform these tests, you'll need any of the sector, linear, or convex transducers.
(normally you should check all the transducers used on the system)
Chapter 4 Functional Checks 4 - 1
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CAUTION
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Section 4-3 General Procedure

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

4-3-1 Power On/Boot Up

After connect the system to the electrical supply, the power is applied to the scanner. When the Control panel Power On/Off key is pressed once, the System starts.
4-3-1-1 Scanner Power On
When power is applied to the scanner, power is distributed to the Cooling Unit, Control Panel, LCD, Peripherals and the Back-end Processor.
4-3-1-2 Turn on the system
Press the Power On/Off switch at the front of the system once.
Figure 4-1 Power On/Off Switch
When the Power On/Off switch on the Control Panel is pressed once, the Back-end Processor starts and the software code is distributed to initiate the scanner.
No status messages are displayed during this process.

4-3-2 Power Off/ Shutdown

NOTE: After turning off a system, wait at least ten seconds before turning it on again. The system may not be
able to boot if power is recycled too quickly.
4-3-2-1 Back-end Processor Power Down
To power down the system:
1.) Press the Power On/Off switch at the front of the system once.
4 - 2 Section 4-3 - General Procedure
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CAUTION
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4-3-2-1 Back-end Processor Power Down (cont’d)
2.) The System-Exit window is displayed.
Figure 4-2 System Exit Window
3.) Using the Trackball or Select key, select Shutdown.
4.) The shutdown process takes a few seconds and the power off sequence is complete when the power status LED is turned amber.
5.) Disconnect the probes.Clean or disinfect all probes as necessary. Store them in their shipping cases to avoid damage.
4-3-2-2 Scanner Shutdown
Disconnect the Mains Power Cable is necessary. For example: Relocating the scanner.
DO NOT unplug and/or transport the unit until after the power off sequence has been completed. Failure to do so may result in corrupted patient files.
Chapter 4 Functional Checks 4 - 3
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NOTICE
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4-3-3 Archiving and Loading Presets

NOTE: Always save presets before any software reload. This ensures the presets loaded after the software
reload are as up–to–date as possible.
NOTE: The system may crash if use a DVD for Archive/Backup/EZBackup/Restore, so always use a
CD-R or USB HDD for Archive/Backup/EZBackup/Restore. DVD only can be used for upgrade.
All user presets except changes to Summary, Anatomy, and Biometry pages, can be saved on an CD­R disk (or USB memory device) for reloading on the system.
Presets should NOT be saved on the same CD-R disk (or USB memory device) as images. The Archive Menu lists the images but does NOT list the presets stored on a CD-R disk (or USB memory device).
4-3-3-1 Archiving Presets to an CD-R Disk (or USB memory device)
1.) Insert an empty (blank) CD-R disk into the DVD-RW.
2.) Access to the Utility Menu, and select System. The Backup sheet will be shown on the LCD display.
Figure 4-3 Backup Sheet
3.) Select the item to back up either from Resource Files.
4.) Enter backup destination or browse through the disk to locate the destination.
5.) Select Backup now. The backup status for each item is displayed on the Result column.
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4-3-3-2 Loading Presets from an CD-R disk (or USB memory device)
1.) Insert the CD-R disk with the archived Presets into the DVD-RW.
2.) Access to the Utility Menu, and select System. The Restore sheet will be shown on the LCD display.
3.) Select the item to restore either from Resource Files.
4.) Enter restore destination or browse through the disk to locate the destination.
5.) Select Restore. The restore status for each item is displayed on the Result column.

4-3-4 Adjusting the Display Monitor

Please refer to Section 6-2 "Monitor Adjustments" on page 6-2
Chapter 4 Functional Checks 4 - 5
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4-3-5 System Features

4-3-5-1 Control Panel
Figure 4-4 Control Panel Tour
1.) Power On/Off Switch
2.) Probe Key
3.) Top Menu Controls
4.) Keyboard
5.) Preset, Comment, Harmonics keys
6.) Patient key
7.) Mode keys: B-Mode, M-Mode, PW-Mode, CF Mode.
8.) Gain/Auto key
9.) Zoom key
10.)Ellipse key
11.)Depth key
12.)Reverse, Print, Store keys
13.)Left, Right key
14.)Freeze key
15.)Trackball
16.)Imaging/Measurement keys
17.)TGC
18.)Gel Holder
19.)Probe Holder
NOTE: LOGIQ C2/C2 PRO do not have Harmonics keys and press CTRL+H to active Harmonics mode
NOTE: LOGIQ C2/C2 PRO do not support PW Mode and CF Mode, and do not have PW and CF mode
key, LOGIQ C3/C3 PRO do not support CF Mode, and do not have CF mode key.
4 - 6 Section 4-3 - General Procedure
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4-3-5-2 LOGIQ C Series SoftMenu Key Tour
1.) Top Menu Controls op Menu Controls
Figure 4-5 SoftMenu Key Tour
2.) Sub menu Controls: Activates Sub Menu for Modes and toggles/changes functions
A.) Press F5 on the keyboard to activate Sub Menu,
B.) Use the Direction keys to toggle/change functions
Figure 4-6 Sub Menu Controls
Chapter 4 Functional Checks 4 - 7
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4-3-5-3 Monitor Display
Figure 4-7 Monitor Display Tour
Table 4-2 Monitor Display Features
1. Institution/Hospital Name, Date, Time, Operator Identification, system status (real-time of frozen).
2. Patient Name, Patient Identification. 13. Imaging Parameters by Mode (current mode highlighted).
3. Acoustic Output Readout, 14. Focal Zone.
4. GE Symbol: Probe Orientation Marker. Coincides with a probe orientation marking on the probe.
5. Image Preview. 16. Body Pattern.
6. Grey/Color Bar. 17. Depth Scale.
7. Cine Gauge. 18. SoftMenu
8. Measurement Summary Window. 19. Caps Lock: On/Off.
9. Image. 20. Start menu icon.
10. Measurement. 21. Card icon.
11. Results Window.
12. Probe Identifier. Exam Study.
15. Trackball Functionality Status: Scroll, M&A (Measurement and Analysis), Position, Size, Scan Area Width and Tilt.
4 - 8 Section 4-3 - General Procedure
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Secondary Menu
Biopsy Kit Frame Average Line Density Focus Width B softener Power Output Suppression Range Focus
Zoom
Depth
Scan Area
Freeze
TGC
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4-3-6 B Mode Checks

4-3-6-1 Preparations
1.) Connect one of the probes listed in 3-6-6 "Available Probes" on page 3-18, in Chapter 3 Installation to the System probe connector.
2.) Turn ON the scanner (if it isn’t turned on already).
SoftMenu Key
Frequency Virtual Convex Edge Enhance Colorize Dynamic Range Gray Map Rotation Rejection Focus Position Focus Number
B Mode
Figure 4-8 Controls available in B Mode
Figure 4-9 B Mode Screen Picture Example
Chapter 4 Functional Checks 4 - 9
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4-3-6-2 B Mode OP Panel Controls
Table 4-3 B Mode Control Panel Controls
Step Task Expected Result(s)
1
Press B Mode key B Mode Starts
Adjust the field of view. Increasing the depth may view larger/deeper structures rates, and
2
3
4
Adjust Depth
Adjust Gain
Adjust Focus
decreasing the depth may view near the skin line.Press Up/Down Button to increase/ decrease. Depth displays on the monitor in cm.
Controls the amount of echo information displayed in an image. Turn B Mode dial to the left/right to increase/decrease Gain. Gain displays on the monitor in G (dB).
Increases the number of focal zones or moves the focal zone(s) to tighten up the beam for specific area. Press the control to toggle between Focus Position and Focus Number. Press Up/Down Button to move or adjust the focal numbers.
Optimize the image based upon a specified
5
Activate Auto Optimize
7
Adjust Time Gain Compensation (TGC)
8
Adjust Scan Area
9
Adjust Zoom
10
Zoom Clear Clear Zoom to normal condition.
11
Reverse
region of interest or anatomy. Press the Center Button in the Gain Dial to toggle the ATO/ACE On and Off.
Amplifies the returning signals to correct for the attenuation caused by tissues at increasing depth. TGC slide pots spaced proportional to the depth. Move the slide pots to the left/right to decrease/increase TGC. A TGC curve appears on the display.
Widen or narrow the size of the sector angle to maximize the image’s region of interest (ROI). Press Scan Area and move the Trackball to narrow/widen the angle.
Changes the location of the focal point(s). A triangular focus marker indicates the depth of the focal point.
Toggles the left/right orientation of the scan image.
4 - 10 Section 4-3 - General Procedure
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4-3-6-3 B Mode Softmenu
Table 4-4 B Mode Softmenu
Step Task Expected Result(s)
1
Activate Colorize
2
Adjust Edge Enhance
3
Activate Grey Map
4
Adjust Frequency
5
Adjust Frame Average
6
Adjust Rotation
7
Power output
8
Dynamic Range
Enables gray scale image colorization. To deactivate, reselect a Gray Map.
Edge Enhance brings out subtle tissue differences and boundaries by enhancing the gray scale differences corresponding to the edges of structures. Adjustments to M Mode's edge enhancement affects the M Mode only.
Determines how the echo intensity levels received are presented as shades of gray.
Multi Frequency mode lets you downshift to the probe's next lower frequency or shift up to a higher frequency.
Temporal filter that averages frames together. This has the effect of presenting a smoother, softer image.
Rotates the image by selecting the value from the pop-up menu.
Optimizes image quality and allows user to reduce beam intensity. 10% increments between 0-100%. Values greater than 0.1 are displayed.
Dynamic Range controls how echo intensities are converted to shades of gray, thereby increasing the adjustable range of contrast.
9
Focus Number and Position
10
Adjust Rejection
Increases the number of transmit focal zones or moves the focal zone(s) so that you can tighten up the beam for a specific area. A graphic caret corresponding to the focal zone position(s) appears on the right edge of the image.
Selects a level below which echoes will not be amplified (an echo must have a certain minimum amplitude before it will be processed).
Chapter 4 Functional Checks 4 - 11
GE
Secondary Menu
Gain
M Cursor
Primary Menu
Power Output Anatomical M Dynamic Range Colorize Rejection Full Timeline Sweep Speed Display Format
M-Mode
TGC
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4-3-7 M Mode Controls

4-3-7-1 Preparations
1.) Connect one of the probes listed in 3-6-6 "Available Probes" on page 3-18, in Chapter 3 Installation to the System probe connector.
2.) Turn ON the scanner (if it isn’t turned on already).
Figure 4-10 Controls available in M Mode
4 - 12 Section 4-3 - General Procedure
Figure 4-11 M Mode Screen Picture Example
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4-3-7-2 M Mode OP Panel Controls
Table 4-5 M Mode OP Panel Controls
Step Task Expected Result(s)
1
Press M Mode key M Mode Starts
Controls the amount of echo information
2
Adjust Gain
displayed in an image. Turn B Mode dial to the left/right to increase/decrease Gain. Gain displays on the monitor in G (dB).
3
Display M-Mode Cursor
Displays the M-Mode cursor on the B-Mode image. Press Cursor and Trackball to position M-Mode Cursor.
Chapter 4 Functional Checks 4 - 13
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4-3-7-3 M Mode Softmenu
Table 4-6 M Mode Softmenu
Step Task Expected Result(s)
1
Adjust Sweep Speed
2
Adjust Edge Enhance
3
Activate Grey Map
4
Activate Colorize
5
Activate Full Timeline
6
Select Display Format
7
Adjust Dynamic Range
8
Power output
9
Anatomical M Enter into AMM Mode (Option).
Changes the speed at which the time line is swept. The following speed values are available, 1, 2, 3, 4, 6, 8, 12, 16.
Edge Enhance brings out subtle tissue differences and boundaries by enhancing the gray scale differences corresponding to the edges of structures. Adjustments to M Mode's edge enhancement affects the M Mode only.
Determines how the echo intensity levels received are presented as shades of gray.
Enables gray scale image colorization. To deactivate, reselect a Gray Map.
Displays only timeline screen. Press the Full Timescreen to activate.
Select the format to display B image and M image on the LCD. Press Display Format, and select from the pop up menu.
Dynamic Range controls how echo intensities are converted to shades of gray, thereby increasing the adjustable range of contrast.
Optimizes image quality and allows user to reduce beam intensity. 10% increments between 0-100%. Values greater than 0.1 are displayed.
Selects a level below which echoes will not be
10
Adjust Rejection
amplified (an echo must have a certain minimum amplitude before it will be processed).
4 - 14 Section 4-3 - General Procedure
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Secondary Menu
Gain
M/D Cursor
Primary Menu
Frequency SV Length Sweep Speed Angle Steer Angle Correct Quick Angle Baseline Invert PRF Wall Filter
PW-Mode
Rejection Dynamic Range Display Format Full Timeline Trace Method Trace Sensitivity Trace direction Modify, Auto Calcs PW/CF Ratio Duplex Time Resolution Colorize Gray Map Power Output Auto Calcs Spectral Average Cycles, to Average
B Pause Cursor
TGC
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4-3-8 Doppler Mode Checks

NOTE: Doppler Mode is not supported by LOGIQ C2/C2 PRO.
4-3-8-1 Preparations
1.) Connect one of the probes listed in 3-6-6 "Available Probes" on page 3-18, in Chapter 3 Installation to the System probe connector.
2.) Turn ON the scanner (if it isn’t turned on already).
Figure 4-12 Controls available in Doppler Mode
Figure 4-13 Doppler Mode Screen Picture Example
Chapter 4 Functional Checks 4 - 15
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4-3-8-2 Doppler Mode OP Panel Controls
Table 4-7 Doppler Mode OP Panel Controls
Step Task Expected Result(s)
1
Press PW Mode key PW Mode Starts
Amplifies the overall strength of the echoes
2
Adjust Gain
3
Display M/D-Mode Cursor
4
B-Pause
processed in the Color Flow window. Turn the Gain dial (PW Mode key) to the left/right to increase/decrease Gain.
Displays the M/D-Mode cursor on the B-Mode image. Press Cursor and Trackball to position sample volume graphic. Click SV gate to adjust sample volume gate size.
Toggle between simultaneous and update presentation while viewing Spectral Doppler. Press B Pause to toggle between simultaneous and update.
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4-3-8-3 Doppler Mode OP Panel Controls
Table 4-8 Doppler Mode Touch Panel Controls
Step Task Expected Result(s)
Selects a level below which echoes will not be
1
Adjust Rejection
amplified (an echo must have a certain minimum amplitude before it will be processed).
2
Adjust Sweep Speed
3
Activate Full Timeline
4
Select Display Format
5
Adjust Frequency
6
Trace Direction Allows to select different trace direction.
7
Invert
8
Auto Calculation Enables or disables auto calculation.
9
Modify Calcs
10
Trace Method Allows to select different trace method.
11
Activate Colorize
Changes the speed at which timeline is swept. Press Sweep Speed up/down to increase/decrease the value.
Displays only timeline screen. Press the Full Timescreen to activate.
Display layout can be preset to have B-Mode and Time-motion side-by-side or over-under.
Enables the adjustment of the probe’s operating frequency. Press Frequency and select desired value. The selected frequency is displayed in the status window.
Vertically inverts the spectral trace without affecting the baseline position. Press invert to invert the spectral trace. The Plus and Minus signs on the velocity scale reverse when the spectrum is inverted.
Activates the window to modify the auto calculation items.
Colorize the gray scale image to enhance the eyes’ discrimination capability. Press the Cololize, Trackball to cycle through available maps and press Set to select.
12
Activate Gray Map
13
Dynamic Range
14
Adjust Angle Correct
15
Adjust Angle Steer
16
Move Baseline
Displays a map window adjacent to the image. Move the trackball to select the map. The image reflects the map as scrolled through the selections. Press Set to select.
Controls how echo intensities are converted to shades of gray. Click Dynamic Range to increase/decrease the value.
Estimates the flow velocity in a direction at an angle to the Doppler vector by computing the angle between the Doppler vector and the flow to be measured.
Slant the Color Flow linear image left or right to get more information without moving probes. Click Angle Steer to the left to slant the linear image.
Adjusts the baseline to accommodate faster or slower blood flows to eliminate aliasing.
Chapter 4 Functional Checks 4 - 17
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Table 4-8 Doppler Mode Touch Panel Controls
Step Task Expected Result(s)
Velocity scale determines pulse repetition frequency. If the sample volume gate range
Change PRF (Pulse Repetition Frequencies)
17
- (Wall Filter)
exceeds single gate PRF capability, the system automatically switches to high PRF mode. Multiple gates appear, and HPRF is indicated on the display.
18
Trace Sensitivity
19
Time Resolution Adjusts the resolution in frequency domain.
20
Spectral Average
21
Power output
22
SV Length
23
Wall Filter
Adjusts the sensitivity to get more accurate envelope trace.
Optimizes the smoothness of the spectrum. Different levels can be selected.
Optimizes image quality and allows user to reduce beam intensity. 10% increments between 0-100%. Values greater than 0.1 are displayed.
Sizes the sample volume gate.
Wall Filter insulates the Doppler signal from excessive noise caused from vessel movement.
4 - 18 Section 4-3 - General Procedure
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Primary Menu
CF Mode
Gain
Frequency Spatial Filter Angle Steer Packet Size PRF Map Threshold Invert Wall Filter Virtual Convex
Baseline
Line Density Flash Suppression Transparency Map Focus Position Frame Average Power Output
Secondary Menu
TGC
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4-3-9 Color Flow Mode Checks

NOTE: Color Flow Mode only support by LOGIQ C5/C5 PRO
4-3-9-1 Preparations
1.) Connect one of the probes listed in 3-6-6 "Available Probes" on page 3-18, in Chapter 3 Installation to the System probe connector.
2.) Turn ON the scanner (if it isn’t turned on already).
Figure 4-14 Controls available in Color Flow Mode
Figure 4-15 CFM Mode Screen Picture Example
Chapter 4 Functional Checks 4 - 19
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4-3-9-2 Color Flow Mode OP Panel Controls
Table 4-9 Color Flow Mode OP Panel Controls
Step Task Expected Result(s)
1
Press CFM-Mode key CFM Mode Starts
Amplifies the overall strength of the echoes
2
Adjust Gain
processed in the Color Flow window. Turn the Gain dial (CFM Mode key) to the left/right to increase/decrease Gain.
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4-3-9-3 Color Flow Mode Softmenu Key
Table 4-10 Color Flow Mode Softmenu Key
Step Task Expected Result(s)
1
Threshold
2
Packet Size
3
Select Color maps
4
Adjust Frequency
5
Set Frame Average
6
Color Invert
7
Adjust LIne Density
8
Activate Spatial Filter
9
Adjust Dynamic Range
Threshold assigns the gray scale level at which color information stops.
Controls the number of samples gathered for a single color flow vector.
Allows a specific color map to be selected. After a selection has been made, the color bar displays the resultant map.
Enables the adjustment of the probe’s operating frequency. Press Frequency and select desired value. The selected frequency is displayed in the status window.
Averages color frames. Press Frame Average up/down to smooth temporal averaging.
Views blood flow from a different perspective. Press Invert to reverse the color map.
Trades frame rate for sensitivity and spatial resolution. If the frame rate is too slow, reduce the size of the region of interest, select a different line density setting, or reduce the packet size.
Dynamic Range controls how echo intensities are converted to shades of gray, thereby increasing the adjustable range of contrast.
10
Activate ACE
11
Adjust Angle Steer
12
Move Baseline
Change PRF
13
(Pulse Repetition Frequency)
14
Transparency Map Allows to select specific transparency map
15
Focus Position
16
Capture
Eliminates the motion artifacts. Press Ace to activate.
Slants the Color Flow region of interest or the Doppler line to obtain a better Doppler angle.
Adjusts the baseline to accommodate faster or slower blood flows to eliminate aliasing.
Velocity scale determines pulse repetition frequency. If the sample volume gate range exceeds single gate PRF capability, the system automatically switches to high PRF mode. Multiple gates appear, and HPRF is indicated on the display.
Increases the number of transmit focal zones or moves the focal zone(s) so that you can tighten up the beam for a specific area. A graphic caret corresponding to the focal zone position(s) appears on the right edge of the image.
Chapter 4 Functional Checks 4 - 21
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Table 4-10 Color Flow Mode Softmenu Key
Step Task Expected Result(s)
Optimizes image quality and allows user to
17
Power output
reduce beam intensity. 10% increments between 0-100%. Values greater than 0.1 are displayed.
18
Wall Filter
Wall Filter insulates the Doppler signal from excessive noise caused from vessel movement.
4 - 22 Section 4-3 - General Procedure
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4-3-10 Basic Measurements

NOTE: The following instructions assume that you first scan the patient and then press Freeze.
4-3-10-1 Distance and Tissue Depth Measurements
1.) Press MEASURE
2.) To position the active caliper at the start point (distance) or the most anterior point (tissue
depth), move the TRACKBALL
3.) To fix the start point, press Set. The system fixes the first caliper and displays a second active caliper.
4.) To position the second active caliper at the end point (distance) or the most posterior point (tissue depth), move the TRACKBALL
5.) To complete the measurement, press SET value in the measurement results window.
Before you complete a measurement:
To toggle between active calipers, press MEASURE
To erase the second caliper and the current data measured and start the measurement again, press
CLEAR
NOTE: To rotate through and activate previously fixed calipers, adjust CURSOR SELECT
NOTE: After you complete the measurement, to erase all data that has been measured to this point,
but not data entered onto worksheets, press CLEAR
4-3-10-2 Circumference/Area (Ellipse) Measurement
1.) Press MEASURE
2.) To position the active caliper, move the TRACKBALL
3.) To fix the start point, press SET
4.) To position the second caliper, move the TRACKBALL
5.) Adjust the ELLIPSE
once.
caliper.
once; an active caliper displays.
.
.
. The system displays the distance or tissue depth
.
.
.
once; an active caliper displays.
.
. The system fixes the first caliper and displays a second active
.
; an ellipse with an initial circle shape appears.
NOTE: Be careful not to press the Ellipse control as this activates the Body Pattern.
6.) To position the ellipse and to size the measured axes (move the calipers), move the
TRACKBALL
7.) To increase the size, adjust the ELLIPSE ELLIPSE
8.) To toggle between active calipers, press MEASURE
9.) To complete the measurement, press SET in the measurement results window.
Before you complete a measurement:
- To erase the ellipse and the current data measured, press CLEAR
is displayed to restart the measurement.
- To exit the measurement function without completing the measurement, press CLEAR
second time.
.
upward button. To decrease the size, adjust the
downward button.
.
. The system displays the circumference and area
Chapter 4 Functional Checks 4 - 23
once. The original caliper
a
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4-3-10-3 Worksheets
Measurement/Calculation worksheets are available to display and edit measurements and calculations. There are generic worksheets as well as Application specific worksheets. The worksheets are selected from the Measurement Touch Panel.
4-3-10-4 Report Pages
Measurements/Calculations that are included on the worksheet can also be displayed on Report Pages. Report Pages can be customized to meet the appropriate needs of the user.

4-3-11 Probe/Connectors Usage

4-3-11-1 Connecting a probe
1.) Place the probe's carrying case on a stable surface and open the case.
2.) Carefully remove the probe and unwrap the probe cable.
3.) DO NOT allow the probe head to hang free. Impact to the probe head could result in irreparable damage.
4.) Align the connector with the probe port and carefully push into place.
5.) Lock the probe.
6.) Carefully position the probe cord so it is free to move and is not resting on the floor.
4-3-11-2 Activating the probe
The probe activates in the currently-selected operating mode. The probe's default settings for the mode and selected exam are used automatically.
4-3-11-3 Deactivating the probe
1.) Press the Freeze key.
2.) Gently wipe the excess gel from the face of the probe. (Refer to the Basic User Manual for complete probe cleaning instructions.)
3.) Carefully slide the probe around the right side of the keyboard, toward the probe holder. Ensure that the probe is placed gently in the probe holder.
4-3-11-4 Disconnecting the probe
Probes can be disconnected at any time. However, the probe should not be selected as the active probe.
1.) Unlock the probe.
2.) Pull the probe and connector straight out of the probe port.
3.) Carefully slide the probe and connector away from the probe port and around the right side of the keyboard.
4.) Ensure the cable is free.
5.) Be sure that the probe head is clean before placing the probe in its storage box.
Take the following precautions with the probe cables: Do not bend, be sure to keep probe cables free from the wheels.

4-3-12 Using Cine

4-3-12-1 Activating CINE
Press Freeze, then roll the Trackball to activate CINE. To start CINE Loop playback, press Run/Stop. To stop CINE Loop playback. press Run/Stop.
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NOTICE
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4-3-12-2 Quickly Move to Start/End Frame
Press First to move to the first CINE frame; press Last to move to the last CINE frame.
4-3-12-3 Start Frame/End Frame
Press the Start Frame Two-Button Softkey to move to the beginning of the CINE Loop. Adjust the Start Frame up/down Two-Button Softkey upward to move forward through the CINE Loop. Adjust the
Softkey downward to move backward through the CINE Loop.
Press the End Frame Two-Button Softkey to move to the end of the CINE Loop. Adjust the End Frame up/down Two-Button Softkey upward to move forward through the CINE Loop. Adjust the Softkey downward to move backward through the CINE Loop.
4-3-12-4 Adjusting the CINE Loop Playback Speed
Adjust the Loop Speed up/down Two-Button Softkey to increase/decrease the CINE Loop playback speed.
4-3-12-5 Moving through a CINE Loop Frame By Frame
Adjust the Frame by Frame up/down Two-Button Softkey to move through CINE memory one frame at a time.

4-3-13 Image Management (QG)

For Image Management functionality refer to the LOGIQ C Series Quick Guide. It talks about several topics:
Clipboard*
Printing Images
Browsing and Managing an Exam’s Stored Image
Connectivity, and Dataflow Concept and Creation
Starting an Exam
Configuring Connectivity
•TCP/IP
Services (Destinations)
Buttons
Views
Verifying and Pinging a Device
Clipboard* function is not available on LOGIQ C2 PRO.
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4-3-14 Backup and Restore Database, Preset Configurations and Images

4-3-14-1 Formatting Media
NOTE: The system may crash if use a DVD for Archive/Backup/EZBackup/Restore, so always use a
CD-R or USB HDD for Archive/Backup/EZBackup/Restore. DVD only can be used for upgrade.
1.) To format the backup media, select the UTILITY
2.) Select CONNECTIVITY
media.
3.) Select the media type from the drop down menu.
4.) Enter the label for the media as shown in Figure 4-16. It is best to use all capital letters with no
spaces or punctuation marks. Press Format
Figure 4-16 Format and Verify Media
, then REMOVABLE MEDIA. Properly label and Insert the backup
button on the Keyboard.
.
5.) The Ultrasound system displays a pop-up menu, as shown in Figure 4-17. When the formatting
has been completed, press OK
6.) If desired, verify that the format was successful by returning to Utility >Removable Media
Figure 4-17 Format Successful Pop-up Menu
4 - 26 Section 4-3 - General Procedure
and selecting VERIFY as shown in Figure 4-16.
to continue.
->Connectivity-
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Check here to backup presets and configurations
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4-3-14-2 Backup System Presets and Configurations
NOTE: Always backup any preset configurations before a software reload. This ensures that if the presets need
to be reloaded, after the software update, they will be the same ones the customer was using prior to service.
1.) Insert a formatted CD into the drive.
2.) On the Keyboard, press UTILITY
3.) On the LCD display, press SYSTEM
4.) On the LCD display, select BACKUP/RESTORE
.
.
.
NOTE: If you are not logged in as GE Service or with administrator privileges, the Operator Login
window is displayed. Log on with administrator privileges.
5.) In the Backup list, select Patient Archive, Report Archive and User Defined Configuration.
6.) In the Media field, select CD/DVD (or USB memory device).
7.) Select BACKUP
.
The system performs the backup. As it proceeds, status information is displayed on the Backup/Restore screen.
Figure 4-18 Backup/Restore Menu
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CAUTION
Check here to restore presets and configurations.
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4-3-14-3 Restore System Presets and Configurations
The restore procedure overwrites the existing database on the local hard drive. Make sure to insert the correct CD (or USB memory device).
1.) Insert the Backup/Restore CD (or USB memory device) into the drive.
2.) On the Keyboard, press UTILITY
3.) On the LCD display, press SYSTEM
4.) On the LCD display, select BACKUP/RESTORE
.
.
.
NOTE: If you are not logged in with administrator privileges, the Operator Login window is displayed.
Log on with administrator privileges.
5.) In the Restore list, select Patient Archive, Report Archive and User Defined Configuration.
6.) In the Media field, select the Backup/Restore CD/DVD (or USB memory device).
7.) Select RESTORE
.
The system performs the restore. As it proceeds, status information is displayed on the Backup/Restore screen.
Figure 4-19 Backup/Restore Menu
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Choose the days which want to older than current exam date.
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4-3-14-4 Archiving Images
1.) Insert the archive media. To format the archive media, select the Utility button on the
Keyboard.
2.) Select Connectivity, then Removable Media.
3.) Format the CD. Verify the format if desired.
4.) Images will be moved from the hard drive by date. Therefore, the best way is to label media by
date.
NOTE: Images will be moved from the hard drive by date. Therefore, the best way to label media is by
date. When images are moved to the archive media, they will be deleted from the system hard drive. However, the patient database (backed up earlier) maintains pointers to the location of the images on the archive media.
Figure 4-20 Format CD Screen
5.) Select Backup/Restore, then EZBackup/Move.
6.) Select “Backup File Older Than in Days”.
Figure 4-21 EZBackup/Move
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4-3-14-4 Archiving Images (cont’d)
7.) Press PATIENT
8.) From the image screen, press EZBACKUP/MOVE
and set the Dataflow to store images directly to CD-ROM.
. The Move Images pop-up appears.
Figure 4-22 Image Archive Move Pop-up Menu
9.) Press Next
on pop-up message.
10.)A media check message appears. Press OK
to continue.
Figure 4-23 Media check message
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Reminder Dialog Interval Days
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4-3-14-4 Archiving Images (cont’d)
11.)Press Finish
after Backup/Move complete.
All databases, presets and images should now be saved to removable media.
4-3-14-5 Full Backup
1.) Connect the USB HDD to system.
2.) Select Backup/Restore, then Emergency Repair Disk.
3.) Select “Reminder Dialog Interval Days”.
Figure 4-24 EZBackup/Move complete
Figure 4-25 Emergency Repair Disk
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4-3-14-5 Full Backup (cont’d)
4.) Return to scan mode. Press Ctrl + B, the Emergency Disk Making window pop-up appears.
Figure 4-26 Emergency Disk Making Pop-up Menu
5.) Press Next
on pop-up message.
6.) A storage information message appears. Press Next
to continue.
Figure 4-27 Storage Information message
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