LC-Series-Service-Manual-5273008-4-00

Service manualGE Logiq Series178 pages10.6 MB

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[Page 1] GE Healthcare LOGIQ C Series Service Manual Part Number: 5273008-100 Revision: 4

[Page 2]

[Page 3] Important Precautions • THIS SERVICE MANUAL IS AVAILABLE IN ENGLISH ONLY. • IF A CUSTOMER’S SERVICE PROVIDER REQUIRES A LANGUAGE OTHER THAN ENGLISH, IT IS THE CUSTOMER’S RESPONSIBILITY TO PROVIDE TRANSLATION SERVICES. WARNING • DO NOT ATTEMPT TO SERVICE THE EQUIPMENT UNLESS THIS SERVICE (EN) 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. AVERTISSEMENT • NE PAS TENTER D’INTERVENTION SUR LES é QUIPEMENTS TANT QUE LE (FR) MANUEL SERVICE N’A PAS é Té CONSULTé ET COMPRIS. • LE NON-RESPECT DE CET AVERTISSEMENT PEUT ENTRAîNER CHEZ LE TECHNICIEN, L’OPé RATEUR OU LE PATIENT DES BLESSURES DUES à DES DANGERS é LECTRIQUES, 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 Fü R EINE ENTSPRECHENDE ÜBERSETZUNG ZU SORGEN. • VERSUCHEN SIE NICHT, DAS GERä T ZU REPARIEREN, BEVOR DIESES WARNUNG KUNDENDIENST-HANDBUCH NICHT ZU RATE GEZOGEN UND VERSTANDEN (DE) 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.

[Page 4] • ESTE MANUAL DE SERVICIO Só LO EXISTE EN INGLé S. • SI ALGú N PROVEEDOR DE SERVICIOS AJENO A GEHC SOLICITA UN IDIOMA QUE NO SEA EL INGLé S, ES RESPONSABILIDAD DEL CLIENTE OFRECER UN SERVICIO DE TRADUCCIó N. AVISO • NO SE DEBERá DAR SERVICIO Té CNICO AL EQUIPO, SIN HABER (ES) 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 ELé CTRICAS, MECá NICAS O DE OTRA NATURALEZA. • ESTE MANUAL DE ASSISTê NCIA Té CNICA Só SE ENCONTRA DISPONíVEL EM INGLê S. • SE QUALQUER OUTRO SERVIç O DE ASSISTê NCIA 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. ATENÇÃO (PT) • Nã O TENTE REPARAR O EQUIPAMENTO SEM TER CONSULTADO E COMPREENDIDO ESTE MANUAL DE ASSISTê NCIA Té CNICA. • O Nã O CUMPRIMENTO DESTE AVISO PODE POR EM PERIGO A SEGURANç A DO Té CNICO, OPERADOR OU PACIENTE DEVIDO A‘ CHOQUES ELé TRICOS, MECâ NICOS OU OUTROS. • 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. AVVERTENZA • SI PROCEDA ALLA MANUTENZIONE DELL’APPARECCHIATURA SOLO DOPO (IT) AVER CONSULTATO IL PRESENTE MANUALE ED AVERNE COMPRESO IL CONTENUTO. • NON TENERE CONTO DELLA PRESENTE AVVERTENZA POTREBBE FAR COMPIERE OPERAZIONI DA CUI DERIVINO LESIONI ALL’ADDETTO ALLA MANUTENZIONE, ALL’UTILIZZATORE ED AL PAZIENTE PER FOLGORAZIONE ELETTRICA, PER URTI MECCANICI OD ALTRI RISCHI. • KÄESOLEV TEENINDUSJUHEND ON SAADAVAL AINULT INGLISE KEELES. • KUI KLIENDITEENINDUSE OSUTAJA Nõ UAB JUHENDIT INGLISE KEELEST ERINEVAS KEELES, VASTUTAB KLIENT Tõ LKETEENUSE OSUTAMISE EEST. HOIATUS • ä RGE ü RITAGE SEADMEID TEENINDADA ENNE EELNEVALT Kä ESOLEVA (ET) 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. ii -

[Page 5] • TÄMÄ HUOLTO-OHJE ON SAATAVILLA VAIN ENGLANNIKSI. • JOS ASIAKKAAN PALVELUNTARJOAJA VAATII MUUTA KUIN ENGLANNINKIELISTä MATERIAALIA, TARVITTAVAN Kä ä NNö KSEN HANKKIMINEN ON ASIAKKAAN VASTUULLA. VAROITUS • ä Lä YRITä KORJATA LAITTEISTOA ENNEN KUIN OLET VARMASTI LUKENUT (FI) 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 ΕΓΧΕΙΡΙΔΙΟ ΣΕΡΒΙΣ ΔΙΑΤΙΘΕΤΑΙ ΣΤΑ ΑΓΓΛΙΚΑ ΜΟΝΟ . • ΕΑΝ ΤΟ ΑΤΟΜΟ ΠΑΡΟΧΗΣ ΣΕΡΒΙΣ ΕΝΟΣ ΠΕΛΑΤΗ ΑΠΑΙΤΕΙ ΤΟ ΠΑΡΟΝ ΕΓΧΕΙΡΙΔΙΟ ΣΕ ΓΛΩΣΣΑ ΕΚΤΟΣ ΤΩΝ ΑΓΓΛΙΚΩΝ , ΑΠΟΤΕΛΕΙ ΕΥΘΥΝΗ ΤΟΥ ΠΕΛΑΤΗ ΝΑ ΠΑΡΕΧΕΙ ΥΠΗΡΕΣΙΕΣ ΜΕΤΑΦΡΑΣΗΣ . • ΜΗΝ ΕΠΙΧΕΙΡΗΣΕΤΕ ΤΗΝ ΕΚΤΕΛΕΣΗ ΕΡΓΑΣΙΩΝ ΣΕΡΒΙΣ ΣΤΟΝ ΕΞΟΠΛΙΣΜΟ ΠΡΟΕΙΔΟΠΟΙΗΣΗ (EL) ΕΚΤΟΣ ΕΑΝ ΕΧΕΤΕ ΣΥΜΒΟΥΛΕΥΤΕΙ ΚΑΙ ΕΧΕΤΕ ΚΑΤΑΝΟΗΣΕΙ ΤΟ ΠΑΡΟΝ ΕΓΧΕΙΡΙΔΙΟ ΣΕΡΒΙΣ . • ΕΑΝ ΔΕ ΛΑΒΕΤΕ ΥΠΟΨΗ ΤΗΝ ΠΡΟΕΙΔΟΠΟΙΗΣΗ ΑΥΤΗ , ΕΝΔΕΧΕΤΑΙ ΝΑ ΠΡΟΚΛΗΘΕΙ ΤΡΑΥΜΑΤΙΣΜΟΣ ΣΤΟ ΑΤΟΜΟ ΠΑΡΟΧΗΣ ΣΕΡΒΙΣ , ΣΤΟ ΧΕΙΡΙΣΤΗ Ή ΣΤΟΝ ΑΣΘΕΝΗ ΑΠΟ ΗΛΕΚΤΡΟΠΛΗΞΙΑ , ΜΗΧΑΝΙΚΟΥΣ Ή ΑΛΛΟΥΣ ΚΙΝΔΥΝΟΥΣ . • EZEN KARBANTARTÁSI KÉZIKÖNYV KIZÁRÓLAG ANGOL NYELVEN ÉRHET Ő EL. • HA A VEV Ő SZOLGÁLTATÓJA ANGOLTÓL ELTÉR Ő NYELVRE TART IGÉNYT, AKKOR A VEV Ő FELEL Ő SSÉGE A FORDÍTÁS ELKÉSZÍTTETÉSE. FIGYELMEZTETÉS • NE PRÓBÁLJA ELKEZDENI HASZNÁLNI A BERENDEZÉST, AMÍG A (HU) KARBANTARTÁSI KÉZIKÖNYVBEN LEÍRTAKAT NEM ÉRTELMEZTÉK. • EZEN FIGYELMEZTETÉS FIGYELMEN KÍVÜL HAGYÁSA A SZOLGÁLTATÓ, M Ű KÖDTET Ő VAGY A BETEG ÁRAMÜTÉS, MECHANIKAI VAGY EGYÉB VESZÉLYHELYZET MIATTI SÉRÜLÉSÉT EREDMÉNYEZHETI. • ÞESSI ÞJÓNUSTUHANDBÓK ER EINGÖNGU FÁANLEG Á ENSKU. • EF ÞJÓNUSTUAÐILI VIÐSKIPTAMANNS ÞARFNAST ANNARS TUNGUMÁLS EN ENSKU, ER ÞAÐ Á ÁBYRGÐ VIÐSKIPTAMANNS AÐ ÚTVEGA ÞÝÐINGU. VIÐVÖRUN • REYNIÐ EKKI AÐ ÞJÓNUSTA TÆKIÐ NEMA EFTIR AÐ HAFA SKOÐAÐ OG (IS) SKILIÐ ÞESSA ÞJÓNUSTUHANDBÓK. • EF EKKI ER FARIÐ AÐ ÞESSARI VIÐVÖRUN GETUR ÞAÐ VALDIÐ MEIÐSLUM ÞJÓNUSTUVEITANDA, STJÓRNANDA EÐA SJÚKLINGS VEGNA RAFLOSTS, VÉLRÆNNAR EÐA ANNARRAR HÆTTU. iii

[Page 6] • TENTO SERVISNÍ NÁVOD EXISTUJE POUZE V ANGLICKé M JAZYCE. • V P ř íPAD ě , ŽE POSKYTOVATEL SLUŽEB ZÁKAZNÍK Ů M POT ř EBUJE Ná VOD V JINé M JAZYCE, JE ZAJIšT ě Ní P ř EKLADU DO ODPOVíDAJíCíHO JAZYKA ú KOLEM Zá KAZNíKA. • NEPROVÁD Ě JTE ú DRŽBU TOHOTO ZA ř íZENí, ANIŽ BYSTE SI P ř E č ETLI VÝSTRAHA TENTO SERVISNÍ NÁVOD A POCHOPILI JEHO OBSAH. (CS) • V P ř íPAD ě NEDODRŽOVá Ní Té TO VýSTRAHY M ů ŽE DOJíT ÚRAZU ELEKTRICKÁM PROUDEM PRACOVNíKA POSKYTOVATELE SLUŽEB, OBSLUŽNé HO PERSONá LU NEBO PACIENT ů VLIVEM ELEKTRICKé HOP 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. ADVARSEL • FORSØG IKKE AT SERVICERE UDSTYRET MEDMINDRE (DA) DENNE SERVICEMANUAL ER BLEVET LÆST OG FORSTÅET. • MANGLENDE OVERHOLDELSE AF DENNE ADVARSEL KAN MEDFØRE SKADE PÅ GRUND AF ELEKTRISK, MEKANISK ELLER ANDEN FARE FOR TEKNIKEREN, OPERATØREN ELLER PATIENTEN. • DEZE ONDERHOUDSHANDLEIDING IS ENKEL IN HET ENGELS VERKRIJGBAAR. • ALS HET ONDERHOUDSPERSONEEL EEN ANDERE TAAL VEREIST, DAN IS DE KLANT VERANTWOORDELIJK VOOR DE VERTALING ERVAN. • PROBEER DE APPARATUUR NIET TE ONDERHOUDEN VOORDAT DEZE WAARSCHUWING (NL) 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. • š Ī APKALPES ROKASGR Ā MATA IR PIEEJAMA TIKAI ANG Ļ U VALOD Ā . • JA KLIENTA APKALPES SNIEDZ Ē JAM NEPIECIEŠAMA INFORM Ā CIJA CIT Ā VALOD Ā , NEVIS ANG Ļ U, KLIENTA PIEN Ā KUMS IR NODROŠIN Ā T TULKOŠANU. BR Ī DIN Ā JUMS • NEVEICIET APR Ī KOJUMA APKALPI BEZ APKALPES ROKASGR Ā MATAS (LV) IZLAS Ī ŠANAS UN SAPRAŠANAS. • Š Ī BR Ī DIN Ā JUMA NEIEV Ē ROŠANA VAR RAD Ī T ELEKTRISK Ā S STR Ā VAS TRIECIENA, MEH Ā NISKU VAI CITU RISKU IZRAIS Ī TU TRAUMU APKALPES SNIEDZ Ē JAM, OPERATORAM VAI PACIENTAM. iv -

[Page 7] • ŠIS EKSPLOATAVIMO VADOVAS YRA IŠLEISTAS TIK ANGL Ų KALBA. • JEI KLIENTO PASLAUG Ų TEIK Ė JUI REIKIA VADOVO KITA KALBA – NE ANGL Ų , VERTIMU PASIR Ū PINTI TURI KLIENTAS. Į SP Ė JIMAS • NEM Ė GINKITE ATLIKTI Į RANGOS TECHNIN Ė S PRIEŽI Ū ROS DARB Ų , NEBENT (LT) VADOVAUTUM Ė T Ė S ŠIUO EKSPLOATAVIMO VADOVU IR J Į SUPRASTUM Ė TE • NEPAISANT ŠIO PERSP Ė JIMO, PASLAUG Ų TEIK Ė JAS, OPERATORIUS AR PACIENTAS GALI B Ū TI SUŽEISTAS D Ė L ELEKTROS SM Ū GIO, MECHANINI Ų AR KIT Ų PAVOJ Ų . • DENNE SERVICEHÅNDBOKEN FINNES BARE PÅ ENGELSK. • HVIS KUNDENS SERVICELEVERANDØR TRENGER ET ANNET SPRÅK, ER DET KUNDENS ANSVAR Å SØRGE FOR OVERSETTELSE. ADVARSEL • IKKE FORSØK Å REPARERE UTSTYRET UTEN AT DENNE (NO) 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 PODR Ę CZNIK SERWISOWY DOST Ę PNY JEST JEDYNIE W J Ę ZYKU ANGIELSKIM. • JE ś LI FIRMA ś WIADCZ Ą CA KLIENTOWI US ł UGI SERWISOWE WYMAGA UDOST ę PNIENIA PODR ę CZNIKA W J ę ZYKU INNYM NI Ż ANGIELSKI, OBOWI Ą ZEK ZAPEWNIENIA STOSOWNEGO T ł UMACZENIA SPOCZYWA NA KLIENCIE. OSTRZE Ż ENIE • NIE PRó BOWA ć SERWISOWA ć NINIEJSZEGO SPRZ ę TU BEZ UPRZEDNIEGO (PL) ZAPOZNANIA SI ę Z PODR ę CZNIKIEM SERWISOWYM. • NIEZASTOSOWANIE SI ę DO TEGO OSTRZE Ż ENIA MO ż E GROZI ć OBRA Ż ENIAMI CIA ł A SERWISANTA, OPERATORA LUB PACJENTA W WYNIKU PORA Ż ENIA PR Ą DEM, URAZU MECHANICZNEGO LUB INNEGO RODZAJU ZAGRO Ż E ń . • ACEST MANUAL DE SERVICE ESTE DISPONIBIL NUMAI ÎN LIMBA ENGLEZ Ă . • DAC Ă UN FURNIZOR DE SERVICII PENTRU CLIEN Ţ I NECESIT Ă O ALT Ă LIMB Ă DECÂT CEA ENGLEZ Ă , ESTE DE DATORIA CLIENTULUI S Ă FURNIZEZE O TRADUCERE. ATEN Ţ IE • NU ÎNCERCA Ţ I S Ă REPARA Ţ I ECHIPAMENTUL DECÂT ULTERIOR (RO) CONSULT Ă RII Ş I ÎN Ţ ELEGERII ACESTUI MANUAL DE SERVICE. • IGNORAREA ACESTUI AVERTISMENT AR PUTEA DUCE LA R Ă NIREA DEPANATORULUI, OPERATORULUI SAU PACIENTULUI ÎN URMA PERICOLELOR DE ELECTROCUTARE, MECANICE SAU DE ALT Ă NATUR Ă .

[Page 8] • Да н н о е рук о в о дс т в о п о о б с луж и в а н и ю ПРЕДОСТАВЛЯЕТСЯ т о ль к о н а а н г ли й с к о м Яз ы к е . • Ес ли с е рв и с н о МУ ПЕРСОНАЛУ к ли е н т а н е о б х о димо рук о в о дс т в о н е н а а н г ли йс к о м ЯЗЫКЕ , к ли е н т у с ле дуе т с а мо с т о Ят е ль н о ОБЕСПЕЧИТЬ п е ре в о д . ОСТОРОЖНО ! • ПЕРЕД ОБСЛУЖИВАНИЕМ ОБОРУДОВАНИЯ ОБЯЗАТЕЛЬНО ОБРАТИТЕСЬ (RU) К ДАННОМУ РУКОВОДСТВУ И ПОЙМИТЕ ИЗЛОЖЕННЫЕ В НЕМ СВЕДЕНИЯ . • НЕСОБЛЮДЕНИЕ УКАЗАННЫХ ТРЕБОВАНИЙ МОЖЕТ ПРИВЕСТИ К ТОМУ , ЧТО СПЕЦИАЛИСТ ПО ТЕХОБСЛУЖИВАНИЮ , ОПЕРАТОР ИЛИ ПАЦИЕНТ ПОЛУЧАТ УДАР ЗЛЕКТРИЧЕСКИМ ТОКОМ , МЕХАНИЧЕСКУЮ ТРАВМУ ИЛИ ДРУГОЕ ПОВРЕЖДЕНИЕ . • TÁTO SERVISNÁ PRÍRU Č KA JE K DISPOZíCII LEN V ANGLI Č TINE. • AK ZÁKAZNÍKOV POSKYTOVATE Ľ SLUŽIEB VYŽADUJE INÝ JAZYK AKO ANGLI Č TINU, POSKYTNUTIE PREKLADATE Ľ SKÝCH SLUŽIEB JE ZODPOVEDNOS Ť OU ZÁKAZNÍKA. UPOZORNENIE • NEPOKÚŠAJTE SA VYKONÁVA Ť SERVIS ZARIADENIA SKÔR, AKO SI (SK) NEPRE Č ÍTATE SERVISNÚ PRÍRU Č KU A NEPOROZUMIETE JEJ. • ZANEDBANIE TOHTO UPOZORNENIA Mô ŽE VYÚSTI Ť DO ZRANENIA POSKYTOVATE Ľ A SLUŽIEB, OBSLUHUJú CEJ OSOBY ALEBO PACIENTA ELEKTRICKýM PRú DOM, PRÍPADNE DO MECHANICKé HO ALEBO INé HO NEBEZPE č 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. VARNING • FÖRSÖK INTE UTFÖRA SERVICE PÅ UTRUSTNINGEN OM DU INTE HAR LÄST (SV) OCH FÖRSTÅR DEN HÄR SERVICEHANDBOKEN. • OM DU INTE TAR HÄNSYN TILL DEN HÄR VARNINGEN KAN DET RESULTERA I SKADOR PÅ SERVICETEKNIKERN, OPERATÖREN ELLER PATIENTEN TILL FÖLJD AV ELEKTRISKA STÖTAR, MEKANISKA FAROR ELLER ANDRA FAROR. • BU SERV İ S KILAVUZU YALNIZCA İ NG İ L İ ZCE OLARAK SA Ğ LANMI Ş TIR. • E Ğ ER MÜ Ş TER İ TEKN İ SYEN İ KILAVUZUN İ NG İ L İ ZCE DI Ş INDAK İ B İ R D İ LDE OLMASINI İ STERSE, KILAVUZU TERCÜME ETT İ RMEK MÜ Ş TER İ N İ N SORUMLULU Ğ UNDADIR. D İ KKAT • SERV İ S KILAVUZUNU OKUYUP ANLAMADAN EK İ PMANLARA MÜDAHALE (TR) ETMEY İ N İ Z. • BU UYARININ GÖZ ARDI ED İ LMES İ , ELEKTR İ K ÇARPMASI YA DA MEKAN İ K VEYA D İĞ ER TÜRDEN KAZALAR SONUCUNDA TEKN İ SYEN İ N, OPERATÖRÜN YA DA HASTANIN YARALANMASINA YOL AÇAB İ L İ R. vi -

[Page 9] (JA) (ZH-CN) (KO) vii

[Page 10] DAMAGE IN TRANSPORTATION All packages should be closely examined at time of delivery. If damage is apparent write “Damage In Shipment” on ALL copies of the freight or express bill BEFORE delivery is accepted or “signed for” by a GE representative or hospital receiving agent. Whether noted or concealed, damage MUST be reported to the carrier immediately upon discovery, or in any event, within 14 days after receipt, and the contents and containers held for inspection by the carrier. A transportation company will not pay a claim for damage if an inspection is not requested within this 14 day period. CERTIFIED ELECTRICAL CONTRACTOR STATEMENT - FOR USA ONLY All electrical Installations that are preliminary to positioning of the equipment at the site prepared for the equipment shall be performed by licensed electrical contractors. Other connections between pieces of electrical equipment, calibrations and testing shall be performed by qualified GE Healthcare personnel. In performing all electrical work on these products, GE will use its own specially trained field engineers. All of GE’s electrical work on these products will comply with the requirements of the applicable electrical codes. The purchaser of GE equipment shall only utilize qualified personnel (i.e., GE’s field engineers, personnel of third-party service companies with equivalent training, or licensed electricians) to perform electrical servicing on the equipment. OMISSIONS & ERRORS If there are any omissions, errors or suggestions for improving this documentation, please contact the GE Healthcare Global Documentation Group with specific information listing the system type, manual title, part number, revision number, page number and suggestion details. Mail the information to: Service Documentation, 9900 Innovation Drive (RP-2123), Wauwatosa, WI 53226, USA. GE Healthcare employees should use the iTrak System to report all documentation errors or omissions. SERVICE SAFETY CONSIDERATIONS DANGER DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH, ARE PRESENT IN THIS EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING AND ADJUSTING. WARNING WARNING 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. viii -

[Page 11] LEGAL NOTES The contents of this publication may not be copied or duplicated in any form, in whole or in part, without prior written permission of GE Healthcare. GE Healthcare may revise this publication from time to time without written notice. TRADEMARKS All products and their name brands are trademarks of their respective holders. COPYRIGHTS All Material Copyright© 2008 - 2009 by General Electric Company Inc. All Rights Reserved. ix

[Page 12] 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 May 22,2009 Update Korean Rating Plate List of Effected Pages(LOEP) Pages Revision Pages Revision Pages Revision Chapter 8 - Replacement Chapter 3 - Installation Title Page 4 4 Procedures 4 pages 3-1 to 3-24 pages 8-1 to 8-6 Chapter 4 - Functional Important Precautions Chapter 9 - Replacement Parts 4 Checks 4 4 pages i to x pages 9-1 to 9-8 pages 4-1 to 4-36 Table of Contents Chapter 5 - Theory Chapter 10 - Periodic Maintenance 4 4 4 pages i to x pages 5-1 to 5-4 pages 10-1 to 10-22 Chapter 6 - Service Chapter 1 - Introduction Index 4 Adjustments 4 4 pages 1-1 to 1-26 pages I to II pages 6-1 to 6-2 Chapter 7 - Diagnostics/ Chapter 2 - Pre-Installation 4 Troubleshooting 4 Back Cover 4 pages 2-1 to 2-10 pages 7-1 to 7-14 x -

[Page 13] 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 Important Conventions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 3 Conventions Used in Book . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 3 Standard Hazard Icons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 4 Product Icons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 5 Safety Considerations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 8 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 8 Human Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 8 Mechanical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 8 Electrical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 9 Label Locations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 9 Dangerous Procedure Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 22 Returning/Shipping Probes and Repair Parts . . . . . . . . . . . . . . . . . . . . . . . 1 - 22 EMC, EMI, and ESD. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 23 Electromagnetic Compatibility (EMC) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 23 CE Compliance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 23 Electrostatic Discharge (ESD) Prevention . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 23 Customer Assistance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 24 Contact Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 24 System Manufacturer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 25 Factory Site . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 25 Table of Contents i

[Page 14] 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 ii Table of Contents

[Page 15] 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 - 8 Product Locator Installation Card . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 8 Preparing for Installation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 9 Verify Customer Order . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 9 Physical Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 9 EMI Protection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 9 Completing the Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 10 Power On / Boot Up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 10 Power Off/ Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 10 Transducer Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 11 System Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 12 System Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 12 Electrical Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 12 On-Board Optional Peripherals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 12 Connecting Cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 13 Peripherals/Accessories Connector Panel . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 13 Available Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 19 Software/Option Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 19 Connectivity Installation Worksheet . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 20 Loading Base Image Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 21 Software Version check out . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 22 Functional Check-out . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 22 Paperwork . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 23 Product Locator Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 23 User Manual(s) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 23 Table of Contents iii

[Page 16] 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 iv Table of Contents

[Page 17] 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 Table of Contents v

[Page 18] CHAPTER 6 Service Adjustments Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 1 Purpose of this chapter 6 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 1 Monitor Adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 2 Adjustments Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 2 vi Table of Contents

[Page 19] 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 Table of Contents vii

[Page 20] 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 - 3 Loading Base Image Software. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 4 viii Table of Contents

[Page 21] 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 - 4 Accessories and kits. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 5 Manuals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 6 Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 7 Table of Contents ix

[Page 22] 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 x Table of Contents

[Page 23] 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 "Overview" 1-1 1-2 "Important Conventions" 1-3 1-3 "Safety Considerations" 1-8 1-4 "EMC, EMI, and ESD" 1-23 1-5 "Customer Assistance" 1-24 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.) Chapter 8 - Replacement Procedures: Provides disassembly procedures and reassembly procedures for all changeable Field Replaceable Units (FRU). 9.) Chapter 9 - Renewal Parts: Contains a complete list of field replaceable parts for the LOGIQ C Series. 10.) - Care & Maintenance: Provides periodic maintenance procedures for the LOGIQ C Series. Section 1-1 - Overview 1 - 1

[Page 24] 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 - Pre-Installation) 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 - 2 Section 1-1 - Overview

[Page 25] Section 1-2 Important Conventions 1-2-1 Conventions Used in Book Icons Pictures, or icons, are used wherever they reinforce the printed message. The icons, labels and conventions used on the product and in the service information are described in this chapter. Safety Precaution Messages Various levels of safety precaution messages may be found on the equipment and in the service information. The different levels of concern are identified by a flag word that precedes the precautionary message. Known or potential hazards are labeled in one of following ways: DANGER DANGER IS USED TO INDICATE THE PRESENCE OF A HAZARD THAT WILL CAUSE SEVERE PERSONAL INJURY OR DEATH IF THE INSTRUCTIONS ARE IGNORED. WARNING WARNING WARNING IS USED TO INDICATE THE PRESENCE OF A HAZARD THAT CAN CAUSE SEVERE PERSONAL INJURY AND PROPERTY DAMAGE IF INSTRUCTIONS ARE IGNORED. CAUTION 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. NOTICE 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. Section 1-2 - Important Conventions 1 - 3

[Page 26] 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 1-2 Standard Hazard Icons ELECTRICAL MECHANICAL RADIATION LASER HEAT PINCH LASER LIGHT Other hazard icons make you aware of specific procedures that should be followed. Table 1-3 Standard Icons Indicating a Special Procedure Be Used AVOID STATIC ELECTRICITY TAG AND LOCK OUT WEAR EYE PROTECTION TAG LOCKOUT EYE PROTECTION Signed Date 1 - 4 Section 1-2 - Important Conventions

[Page 27] 1-2-3 Product Icons The following table describes the purpose and location of safety labels and other important information provided on the equipment. Manufacturer's name and address Date of manufacture Rear of console Identification and Rating Plate Model and serial numbers On each probe Electrical ratings Type/Class Label Used to indicate the degree of safety or protection. Indicates the degree of protection provided by the IP Code (IPX1) enclosure per IEC 60529. Footswitch IPX1 cannot be used in an operating room environment. Type BF Applied Part (man in the box) symbol is in Beside the probe connectors accordance with IEC 60878-02-03. ATTENTION - Consult accompanying documents “is intended to alert the user to refer to the operator manual Various or other instructions when complete information cannot be provided on the label. “CAUTION - Dangerous voltage” (the lightning flash with arrowhead in equilateral triangle) is used to indicate Various electric shock hazards. Indicates the power on and power off position of the power switch. CAUTION Adjacent to On Switch This Power Switch DOES NOT ISOLATE Mains Supply “Protective Earth” Indicates the protective earth Inside PowerBox and Console (grounding) terminal. Section 1-2 - Important Conventions 1 - 5

[Page 28] Product schematics Indicates an earth GROUND potential Peripherals Indicates the product contains hazardous materials in excess of the limits established by Chinese standard SJ/T11363-2006 Requirements for Concentration Limits for Certain Hazardous Substances in Electronic Information Products. The number in the symbol is the Environment-friendly Use Period (EFUP), which indicates the period during which the toxic or hazardous Rear panel, rating plate substances or elements contained in electronic information products will not leak or mutate under normal operating conditions so that the use of such electronic information products will not result in any severe environmental pollution, any bodily injury or damage to any assets. This symbol indicates that waste electrical and elec- tronic equipment must not be disposed of as unsorted municipal waste and must be collected separately. Please contact an authorized representative of the Bottom manufacturer for information concerning the decommis- sioning of your equipment. Type CF Defib-Proof Applied Part (heart in the box with paddle) symbol is in accordance with IEC 60878-02-06. ECG Module Utilize additional care and personnel when moving on steep incline (>5 degrees) or loading into vehicle for transport. On the back of LCD Do not place any objects on the monitor. On the back of LCD 1 - 6 Section 1-2 - Important Conventions

[Page 29] Do not force the LCD monitor with your hands. On the back of LCD There is a pinch point on the LCD monitor. Take care to avoid injuring hands of fingers when flipping down the LCD monitor. On the back of LCD Use the rear handle for horizontal movement only. On the back of LCD Section 1-2 - Important Conventions 1 - 7

[Page 30] 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 WARNING WARNING WHEN THE UNIT IS RAISED FOR A REPAIR OR MOVED ALONG ANY INCLINE, USE EXTREME CAUTION SINCE IT MAY BECOME UNSTABLE AND TIP OVER. WARNING WARNING 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. WARNING WARNING NEVER USE A PROBE THAT HAS FALLEN TO THE FLOOR. EVEN IF IT LOOKS OK, IT MAY BE DAMAGED. CAUTION 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). WARNING WARNING AFTER UNPLUG POWER CORD, WAIT FOR AT LEAST 20 SECONDS FOR CAPACITORS TO DISCHARGE AS THERE ARE NO TEST POINTS TO VERIFY ISOLATION. 1 - 8 Section 1-3 - Safety Considerations

[Page 31] 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. WARNING WARNING DO NOT SERVICE OR DISASSEMBLE PARTS UNDER FRU UNIT LEVEL AT ANY CIRCUMSTANCES. 1-3-5 Label Locations Figure 1-1 Label Location of LOGIQ C2 (For 110V-120V) Section 1-3 - Safety Considerations 1 - 9

[Page 32] Figure 1-2 Label Location of LOGIQ C2 (For 220V-240V) 1 - 10 Section 1-3 - Safety Considerations

[Page 33] Figure 1-3 Label Location of LOGIQ C2 (China) Section 1-3 - Safety Considerations 1 - 11

[Page 34] Figure 1-4 Label Location of LOGIQ C2 (CKD Version, India only) 1 - 12 Section 1-3 - Safety Considerations

[Page 35] Figure 1-5 Label Location of LOGIQ C3 (For 110V-120V) Section 1-3 - Safety Considerations 1 - 13

[Page 36] Figure 1-6 Label Location of LOGIQ C3 (For 220V-240V) 1 - 14 Section 1-3 - Safety Considerations

[Page 37] Figure 1-7 Label Location of LOGIQ C3 (China) Section 1-3 - Safety Considerations 1 - 15

[Page 38] Figure 1-8 Label Location of LOGIQ C3 (Korea) 1 - 16 Section 1-3 - Safety Considerations

[Page 39] Figure 1-9 Label Location of LOGIQ C3 (CKD Version, India only) Section 1-3 - Safety Considerations 1 - 17

[Page 40] Figure 1-10 Label Location of LOGIQ C5 (For 110V-120V) 1 - 18 Section 1-3 - Safety Considerations

[Page 41] Figure 1-11 Label Location of LOGIQ C5 (For 220V-240V) Section 1-3 - Safety Considerations 1 - 19

[Page 42] Figure 1-12 Label Location of LOGIQ C5/C5 PRO (China) 1 - 20 Section 1-3 - Safety Considerations

[Page 43] Figure 1-13 Label Location of LOGIQ C5/C5 PRO (Korea) Section 1-3 - Safety Considerations 1 - 21

[Page 44] 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. DANGER DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH, ARE PRESENT IN THIS EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING AND ADJUSTING. WARNING WARNING 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. WARNING WARNING 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. WARNING WARNING SHUT DOWN FORCEDLY OR PLUG IN/OUT ACDC INVALID MAY CAUSE THE DAMAGE OF SYSTEM FILES. WARNING WARNING 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 - 22 Section 1-3 - Safety Considerations

[Page 45] 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 WARNING WARNING 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. Section 1-4 - EMC, EMI, and ESD 1 - 23

[Page 46] 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 1-5 Phone Numbers for Customer Assistance Location Phone Number USA Service: On-site 1-800-437-1171 GE Vingmed Ultrasound Ultrasound Service Engineering Service Parts 1-800-558-2040 9900 Innovation Drive Wauwatosa, WI 53226 Application Support 1-800-682-5327 or 1-262-524-5698 Canada 1-800-668-0732 Service 1-800-321-7937 Latin America Application Support 1-262-524-5698 Europe (OLC- EMEA) OLC - EMEA GE Ultraschall Deutschland GmbH Phone: +49 (0)212 2802 - 652 Beethovenstraße 239 +33 1 3083 1300 Postfach 11 05 60, D-42655 Solingen Fax: +49 (0) 212 2802 - 431 Germany Online Services Ultrasound Asia Australia Phone: +(61) 1-800-647-855 China +(86) 800-810-8188 India +(91) 1-800-11-4567 Japan +(81) 42-648-2924 Korea +(82) 2620 13585 Singapore +(95) 6277-3444 1 - 24 Section 1-5 - Customer Assistance

[Page 47] 1-5-2 System Manufacturer Table 1-6 System Manufacturer Manufacturer FAX Number GE Medical Systems (China) Co., Ltd. TEL: +86 510-85225888 No.19, Changjiang Road, Wuxi National Hi-Tech Development Zone, FAX: +86 510-85226688 Jiangsu, P.R. China 214028 1-5-3 Factory Site Table 1-7 Factory Site Factory Site FAX Number GE Medical Systems (China) Co., Ltd. TEL: +86 510-85225888 No.19, Changjiang Road, Wuxi National Hi-Tech Development Zone, FAX: +86 510-85226688 Jiangsu, P.R. China 214028 Wirpo GE Healthcare Pvt. Ltd., TEL: +91-80-41801000 No. 4, Kadugodi Industrial Area, Bangalore. 560067 Karnataka. India. FAX: +91-80-28452924 Section 1-5 - Customer Assistance 1 - 25

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[Page 49] 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 "Overview" 2-1 2-2 "General Console Requirements" 2-2 2-3 "Facility Needs" 2-6 Section 2-1 - Overview 2 - 1

[Page 50] 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 o o o 10 - 40 C -5 - 50 C -5 - 50 C Temperature o o o 50 - 104 F 23 - 122 F 23 - 122 F 30 - 75% 10 - 90% 10 - 90% Humidity non-condensing non-condensing non-condensing Pressure 700 - 1060hPa 700 - 1060hPa 700 - 1060hPa 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

[Page 51] 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 100-120V~ 500VA Voltage Range 220-240V~ 500VA Power All applications MAX. 750 VA Line Frequency All applications 50/60Hz ( ± 2Hz) Less than 25% of nominal peak voltage for less than 1 millisecond for any type of Power Transients All applications transient, including line frequency, synchronous, asynchronous, or aperiodic transients. Less than 15% of peak voltage for less Decaying Oscillation All applications than 1 millisecond. 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. CAUTION 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. 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

[Page 52] 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 Table 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 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 Ground the unit the power cord and power outlet. After you finish repairing or updating the system, replace all covers and tighten all screws. Replace all screws, RF Any cable with an external connection requires a magnet wrap at each end. Install the gaskets, covers, cores 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. Replace broken RF gaskets Do not turn on the unit until any loose metallic part is removed. Do not place labels where RF Never place a label where RF gaskets meet the unit. Otherwise, the gap created will permit gaskets touch metal RF leakage. Or, if a label has been found in such a position, move the label. Use GE specified harnesses The interconnect cables are grounded and require ferrite beads and other shielding. Also, and peripherals cable length, material, and routing are all important; do not change from what is specified. Take care with cellular phones Cellular phones may transmit a 5 V/m signal; that could cause image artifacts. Do not allow cables to lie across the top of the card cage or hang out of the peripheral bays. Properly dress peripheral Loop the excess length for peripheral cables inside the peripheral bays. Attach the monitor cables cables to the frame. 2 - 4 Section 2-2 - General Console Requirements

[Page 53] 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). NOTICE SYSTEMS AND ELECTRONIC PROBES ARE DESIGNED FOR STORAGE TEMPERATURES OF -10 TO + 60 degrees C. WHEN EXPOSED TO LARGE TEMPERATURE VARIATIONS, THE PRODUCT SHOULD BE KEPT IN ROOM TEMPERATURE FOR 10 HOURS BEFORE USE. Section 2-2 - General Console Requirements 2 - 5

[Page 54] 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

[Page 55] 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

[Page 56] 2-3-3 Recommended and Alternate Ultrasound Room Layout Recommended standard floor plan and a minimal floor plan for ultrasound equipment: DEDICATED ALALOG TELEPHONE LINE FOR CONNECTION TO INSITE 18 IN. (46 CM) LINEN SUPPLY DEDICATED POWER RECEPTACLE CONSOLE FILM PROCESSING ROOM, FILM VIEWER FOOT SW FILE COUNTER TOP COUNTER TOP STOOL CABINET EXAMINATION TABLE SINK 76 IN. (193 CM) SUCTION LINE 24 IN. EMERGECY (61 CM) OXYGEN SECRETARYS OR DOCTOR’S DESK OVERHEAD PATIENT LIGHTS DIMMER TOILET FACILITY DOOR 42 IN. (107 CM) A 14 by 17 foot Recommended Floor Plan Scale : Each square equals one square foot FILM VIEWER LINEN SUPPLY SINK FILM SUPPLIES PROBES/SUPPLIES EXTERNAL PERIPHERALS DEDICATED POWER OUTLETS FOOT LOGIQ 5 SW STOOL CONSOLE DEDICATED ANALOG TELEPHONE LINE FOR CONNECTION TO INSITE EXAMINARION GE CABINET 24 IN. TABLE FOT SOFTWARE (61 CM) 76 IN. AND MANUALS (193 CM) DOOR 30 IN. (76 CM) An 8 by 10 foot Minimal Floor Plan Figure 2-1 RECOMMENDED ULTRASOUND ROOM LAYOUT 2 - 8 Section 2-3 - Facility Needs

[Page 57] 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

[Page 58] 2-3-4-4 DICOM Option Pre-installation Requirements (cont’d) LOGIQ C Host Name Local Port IP Address . . . AE Title Net Mask . . . ROUTING INFORMATION GATEWAY IP Addresses Destination IP Addresses Default . . . ROUTER1 . . . . . . ROUTER2 . . . . . . ROUTER3 . . . . . . DICOM APPLICATION INFORMATION NAME MAKE/REVISION AE TITLE IP ADDRESSES PORT Store 1 . . . Store 2 . . . Store 3 . . . Store 4 . . . Store 5 . . . Store 6 . . . Worklist . . . Storage . . . Commit MPPS . . . Figure 2-2 Worksheet for DICOM Network Information 2 - 10 Section 2-3 - Facility Needs

[Page 59] 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

[Page 60] Section 3-2Setup Reminders 3-2-1 Average Installation Time Table 3-2 Average Installation Time Description Average Installation Time Comments Unpacking the scanner 0.5 hour Scanner wo/options 0.5 hour Dependant on the configuration that is required DICOM Option 0.5 hour 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

[Page 61] 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. CAUTION 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 ° C 60 55 50 45 40 35 30 25 20 15 10 5 0 -5 -10 -15 -20 -25 -30 -35 -40 ° F 140 131 122 113 104 95 86 77 68 59 50 41 32 23 14 5 -4 -13 -22 -31 -40 hrs 8 6 4 2 0 0 0 0 0 0 0 2 4 6 8 10 12 14 16 18 20 Chapter 3 System Setup 3 - 3

[Page 62] 3-2-3 Safety Reminders DANGER WHEN USING ANY TEST INSTRUMENT THAT IS CAPABLE OF OPENING THE AC GROUND LINE (I.E., METER’S GROUND SWITCH IS OPEN), DON’T TOUCH THE UNIT! CAUTION 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. CAUTION 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. CAUTION 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. CAUTION Do NOT wear the ESD wrist strap when you work on live circuits and more than 30 V peak is present. CAUTION 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. CAUTION Do not operate this unit unless all board covers and frame panels are securely in place. System performance and cooling require this. CAUTION 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

[Page 63] 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. CAUTION Do not lift the unit by the Keyboard. Equipment damage may result. CAUTION 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 Carte 1.) Disassemble the tape in the crate to get the bending head of tool. 2.) Insert benging head of tool into the hole on tongue. 3.) Pull the tongue to a certain degree. 4.) Insert the pain head into the hole of tongue to take place the bending head. 5.) Go on pull the tongue unless it ends up. 6.) After all the tongues ends up. separate the profile from tongue to open the whole box. 2) 3) 1) 4) Figure 3-2 Open the box Chapter 3 System Setup 3 - 5

[Page 64] Section 3-3 Receiving and Unpacking the Equipment (cont’d) Take out the system 1.) Remove all Laterals from the system. 2.) Remove the forks clip from the system. 3.) Remove the PE bag and plastic film from the system. 4.) Remove all the foam from the system 5.) Remove Accessories Carton from the system. 6.) Put forks in front of the platform. 7.) Put one of lateral plate on the 2 to make a bevel. 8.) Unlock the wheels of system and pull the system through the bevel. 1 1 Figure 3-3 Remove foam 1. Lateral 5. Top Foam 2. Forks Clip 6. Bottom Foam 3. Accessories Carton 7. Platform 4. ESD PE Bag 3 - 6 Section 3-3 - Receiving and Unpacking the Equipment

[Page 65] Section 3-3 Receiving and Unpacking the Equipment (cont’d) 5) 6) 7) Figure 3-4 Pull the System NOTE: When pulling system from the bevel, fix the bevel with one foot. Chapter 3 System Setup 3 - 7

[Page 66] 3-3-1 Moving into Position CAUTION 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 3-5 Product Locator Installation Card 3 - 8 Section 3-3 - Receiving and Unpacking the Equipment

[Page 67] 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. WARNING WARNING 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 - 9

[Page 68] 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 3-6 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 - 10 Section 3-5 - Completing the Installation

[Page 69] 3-5-2-1 Back-end Processor Power Down (cont’d) 2.) The System-Exit window is displayed. Figure 3-7 System Exit Window 3.) Using the Trackball or Select key, select Shutdown. 4.) The shutdown process takes a few seconds and is complete when the power status LED is turned amber. 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 - 11

[Page 70] 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 3-12 . 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 1 110 - 120 V AC 500VA 50/60Hz 2 220 - 240 V AC 500VA 50/60Hz 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 HP Printer HP HP 470b Officejet USB USB Memory SanDisk SanDisk 2G USB FSU2001 Footswitch Whanam USB FSU 1000 USB Hard Disk Seagate USBHDD 80G 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). 3 - 12 Section 3-6 - System Configuration

[Page 71] 3-6-4 Connecting Cables WARNING WARNING 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 For USB Printer 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. Figure 3-8 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. Chapter 3 System Setup 3 - 13

[Page 72] 3-6-5-2 Left Panel Connector 1 USB port is Located on the left panel. Figure 3-9 Left Connector Panel 1.) 1 USB Ports (Printers, Footswitch, etc) 3-6-5-3 Printer Box Rear Panel connector Figure 3-10 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. 3 - 14 Section 3-6 - System Configuration

[Page 73] 3-6-5-4 Pin assignment for each connector Table 3-9 Pin Assignments of External VGA Pin No. Signal Pin No. Signal 1 RED 9 NC 2 GREEN 10 NC 3 BLUE 11 NC 4 NC 12 NC 5 NC 13 HSY 6 GND 14 VSY 7 GND 15 NC 8 GND Table 3-10 Pin Assignments of USB Pin No. Signal Pin No. Signal 1 +5 VDC 5 +5 VDC 2 DATA 6 DATA 3 DATA 7 DATA 4 GND 8 GND Table 3-11 Pin Assignments of Audio Pin No. Signal Pin No. Signal 1 GND 4 NC 2 L+ 5 R+ 3 Speaker L 6 Speaker R Table 3-12 Pin Assignment of S-Video Pin No. Output Signal Pin No. Output Signal 1 GND 3 Y 2 GND 4 C Table 3-13 Pin Assignment of Composite Video Out Pin No. Output Signal Pin No. Output Signal 1 Composite Out 2 GND Chapter 3 System Setup 3 - 15

[Page 74] 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 3-11 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 3-12 Connect color printer to the system 3 - 16 Section 3-6 - System Configuration

[Page 75] C.) Connect Foot Switch to the system. Foot Switch can be properly connected using USB Ports. FSU 2001 FSU 1000 Figure 3-13 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 3-14 USB Memory Connection Chapter 3 System Setup 3 - 17

[Page 76] E.) ECG can be properly connected using USB ports. (ECG only supported by LOGIQ C5/C5 PRO) Figure 3-15 ECG F.) Connect the USB HDD to the system. The USB Harddisk can be properly connected using USB ports. Figure 3-16 USB Hard Disk Connection 3 - 18 Section 3-6 - System Configuration

[Page 77] G.) Connect HP 470b Officejet printer to the system. HP 470b Officejet Printer can be properly connected using USB Ports Figure 3-17 HP 470b Officejet printer Connection Chapter 3 System Setup 3 - 19

[Page 78] 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 Part Number 4C-RC NORYL GENERAL PURPOSE CONVEX H48102LE 5315581 3.8C-RC NORYL GENERAL PURPOSE CONVEX H48102LD 5315682 VETERINARY 6.5C-RC VALOX PEDIATRIC MICRO-CONVEX H48102LF 5315685 NEONATAL TRANSVAGINAL E6C-RC VALOX MICRO-CONVEX H48102LH 5315687 TRANSRECTAL TRANSVAGINAL E7C-RC VALOX MICRO-CONVEX H48102LG 5315686 TRANSRECTAL SMALL PARTS 7.5L-RC VALOX LINEAR H48102LJ 5315683 PERIPHERAL VASCULAR SMALL PARTS 7L-RC VALOX LINEAR H48102LK 5315684 PERIPHERAL VASCULAR 3S-RC VALOX CARDIAC SECTOR H40452LA 5315689 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 - 20 Section 3-7 - Software/Option Configuration

[Page 79] Section 3-8 Connectivity Installation Worksheet Site System Information Floor: Comments: Site: Dept: Room: LOGIQ SN: Type: REV: CONTACT INFORMATION Name Title Phone E-Mail Address TCP/IP Settings Name - AE Title: IP Settings Remote Archive Setup IP Address: Remote Archive IP: Subnet Mask: Remote Archive Name: Default Gateway: Services (Destination Devices) Device Type Manufacturer Name IP Address Port AE Title Chapter 3 System Setup 3 - 21

[Page 80] Section 3-9 Loading Base Image Software Refer to Section 8-3 "Loading Base Image Software" on page 8-4. 3 - 22 Section 3-9 - Loading Base Image Software

[Page 81] 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 key on control panel. 3.) Choose the About button on the right. Figure 3-18 About and Software version 4.) Check whether “Software version” is the right version for use. Chapter 3 System Setup 3 - 23

[Page 82] 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 3-19 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 - 24 Section 3-11 - Paperwork

[Page 83] 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

[Page 84] Section 4-3 General Procedure CAUTION SYSTEM REQUIRES ALL COVERS Operate this unit only when all board covers and frame panels are securely in place. The covers are required for safe operation, good system performance and cooling purposes. 4-3-1 Power On/Boot Up 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 4-20 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

[Page 85] 4-3-2-1 Back-end Processor Power Down (cont’d) 2.) The System-Exit window is displayed. Figure 4-21 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. CAUTION DO NOT unplug and/or transport the unit until after the power off sequence has been completed. Failure to do so may result in corrupted patient files. Chapter 4 Functional Checks 4 - 3

[Page 86] 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 CD- R disk (or USB memory device) for reloading on the system. NOTICE 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 4-22 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. 4 - 4 Section 4-3 - General Procedure

[Page 87] 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

[Page 88] 4-3-5 System Features 4-3-5-1 Control Panel Figure 4-23 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

[Page 89] 4-3-5-2 LOGIQ C Series SoftMenu Key Tour 1.) Top Menu Controls op Menu Controls Figure 4-24 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 4-25 Sub Menu Controls Chapter 4 Functional Checks 4 - 7

[Page 90] 4-3-5-3 Monitor Display Figure 4-26 Monitor Display Tour Table 4-2 Monitor Display Features 1. Institution/Hospital Name, Date, Time, Operator 12. Probe Identifier. Exam Study. 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 15. Trackball Functionality Status: Scroll, M&A (Measurement probe orientation marking on the probe. and Analysis), Position, Size, Scan Area Width and Tilt. 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. 4 - 8 Section 4-3 - General Procedure

[Page 91] 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 3-20, in Chapter 3 Installation to the System probe connector. 2.) Turn ON the scanner (if it isn’t turned on already). Secondary Menu SoftMenu Key Biopsy Kit Frequency Frame Average Virtual Convex Line Density Edge Enhance Focus Width Colorize B softener Dynamic Range Power Output Gray Map Suppression Rotation Range Focus Rejection Focus Position TGC Focus Number Depth B Mode Scan Area Freeze Zoom Figure 4-27 Controls available in B Mode Figure 4-28 B Mode Screen Picture Example Chapter 4 Functional Checks 4 - 9

[Page 92] 4-3-6-2 B Mode OP Panel Controls Table 4-3 B Mode Control Panel Controls 1 Press B Mode key B Mode Starts Adjust the field of view. Increasing the depth may view larger/deeper structures rates, and decreasing the depth may view near the skin 2 Adjust Depth 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 3 Adjust Gain 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 4 Adjust Focus 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 region of interest or anatomy. Press the 5 Activate Auto Optimize 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 7 Adjust Time Gain Compensation (TGC) 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 8 Adjust Scan Area (ROI). Press Scan Area and move the Trackball to narrow/widen the angle. Changes the location of the focal point(s). A 9 Adjust Zoom triangular focus marker indicates the depth of the focal point. 10 Zoom Clear Clear Zoom to normal condition. Toggles the left/right orientation of the scan 11 Reverse image. 4 - 10 Section 4-3 - General Procedure

[Page 93] 4-3-6-3 B Mode Softmenu Table 4-4 B Mode Softmenu Enables gray scale image colorization. To 1 Activate Colorize deactivate, reselect a Gray Map. Edge Enhance brings out subtle tissue differences and boundaries by enhancing the 2 Adjust Edge Enhance 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 3 Activate Grey Map received are presented as shades of gray. Multi Frequency mode lets you downshift to 4 Adjust Frequency the probe's next lower frequency or shift up to a higher frequency. Temporal filter that averages frames together. 5 Adjust Frame Average This has the effect of presenting a smoother, softer image. Rotates the image by selecting the value from 6 Adjust Rotation the pop-up menu. Optimizes image quality and allows user to reduce beam intensity. 10% increments 7 Power output between 0-100%. Values greater than 0.1 are displayed. Dynamic Range controls how echo intensities are converted to shades of gray, 8 Dynamic Range thereby increasing the adjustable range of contrast. Increases the number of transmit focal zones or moves the focal zone(s) so that you can tighten up the beam for a specific area. A 9 Focus Number and Position 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 10 Adjust Rejection minimum amplitude before it will be processed). Chapter 4 Functional Checks 4 - 11

[Page 94] 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 3-20, in Chapter 3 Installation to the System probe connector. 2.) Turn ON the scanner (if it isn’t turned on already). Secondary Menu Primary Menu Power Output Anatomical M Dynamic Range Colorize Rejection Full Timeline Sweep Speed TGC Display Format M Cursor M-Mode Gain Figure 4-29 Controls available in M Mode Figure 4-30 M Mode Screen Picture Example 4 - 12 Section 4-3 - General Procedure

[Page 95] 4-3-7-2 M Mode OP Panel Controls Table 4-5 M Mode OP Panel Controls 1 Press M Mode key M Mode Starts Controls the amount of echo information displayed in an image. Turn B Mode dial to 2 Adjust Gain the left/right to increase/decrease Gain. Gain displays on the monitor in G (dB). Displays the M-Mode cursor on the B-Mode 3 Display M-Mode Cursor image. Press Cursor and Trackball to position M-Mode Cursor. Chapter 4 Functional Checks 4 - 13

[Page 96] 4-3-7-3 M Mode Softmenu Table 4-6 M Mode Softmenu Changes the speed at which the time line is 1 Adjust Sweep Speed 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 2 Adjust Edge Enhance 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 3 Activate Grey Map received are presented as shades of gray. Enables gray scale image colorization. To 4 Activate Colorize deactivate, reselect a Gray Map. Displays only timeline screen. Press the Full 5 Activate Full Timeline Timescreen to activate. Select the format to display B image and M 6 Select Display Format 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, 7 Adjust Dynamic Range thereby increasing the adjustable range of contrast. Optimizes image quality and allows user to reduce beam intensity. 10% increments 8 Power output between 0-100%. Values greater than 0.1 are displayed. 9 Anatomical M Enter into AMM Mode (Option). Selects a level below which echoes will not be amplified (an echo must have a certain 10 Adjust Rejection minimum amplitude before it will be processed). 4 - 14 Section 4-3 - General Procedure

[Page 97] 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 3-20, in Chapter 3 Installation to the System probe connector. 2.) Turn ON the scanner (if it isn’t turned on already). Secondary Menu Primary Menu Rejection Frequency Dynamic Range SV Length Display Format Sweep Speed Full Timeline Trace Method Angle Steer Trace Sensitivity Angle Correct Trace direction Quick Angle Modify, Auto Calcs Baseline PW/CF Ratio Invert TGC Duplex PRF Time Resolution Wall Filter Colorize Gray Map Power Output Auto Calcs Spectral Average PW-Mode Cycles, to Average Gain M/D Cursor B Pause Cursor Figure 4-31 Controls available in Doppler Mode Figure 4-32 Doppler Mode Screen Picture Example Chapter 4 Functional Checks 4 - 15

[Page 98] 4-3-8-2 Doppler Mode OP Panel Controls Table 4-7 Doppler Mode OP Panel Controls 1 Press PW Mode key PW Mode Starts Amplifies the overall strength of the echoes processed in the Color Flow window. Turn the 2 Adjust Gain 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 3 Display M/D-Mode Cursor sample volume graphic. Click SV gate to adjust sample volume gate size. Toggle between simultaneous and update presentation while viewing Spectral Doppler. 4 B-Pause Press B Pause to toggle between simultaneous and update. 4 - 16 Section 4-3 - General Procedure

[Page 99] 4-3-8-3 Doppler Mode OP Panel Controls Table 4-8 Doppler Mode Touch Panel Controls Selects a level below which echoes will not be amplified (an echo must have a certain 1 Adjust Rejection minimum amplitude before it will be processed). Changes the speed at which timeline is 2 Adjust Sweep Speed swept. Press Sweep Speed up/down to increase/decrease the value. Displays only timeline screen. Press the Full 3 Activate Full Timeline Timescreen to activate. Display layout can be preset to have B-Mode 4 Select Display Format and Time-motion side-by-side or over-under. Enables the adjustment of the probe’s operating frequency. Press Frequency and 5 Adjust Frequency select desired value. The selected frequency is displayed in the status window. 6 Trace Direction Allows to select different trace direction. Vertically inverts the spectral trace without affecting the baseline position. Press invert to 7 Invert invert the spectral trace. The Plus and Minus signs on the velocity scale reverse when the spectrum is inverted. 8 Auto Calculation Enables or disables auto calculation. Activates the window to modify the auto 9 Modify Calcs calculation items. 10 Trace Method Allows to select different trace method. Colorize the gray scale image to enhance the eyes’ discrimination capability. Press the 11 Activate Colorize Cololize, Trackball to cycle through available maps and press Set to select. Displays a map window adjacent to the image. Move the trackball to select the map. 12 Activate Gray Map The image reflects the map as scrolled through the selections. Press Set to select. Controls how echo intensities are converted 13 Dynamic Range 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 14 Adjust Angle Correct 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 15 Adjust Angle Steer probes. Click Angle Steer to the left to slant the linear image. Adjusts the baseline to accommodate faster 16 Move Baseline or slower blood flows to eliminate aliasing. Chapter 4 Functional Checks 4 - 17

[Page 100] Table 4-8 Doppler Mode Touch Panel Controls Velocity scale determines pulse repetition frequency. If the sample volume gate range Change PRF (Pulse Repetition Frequencies) exceeds single gate PRF capability, the - (Wall Filter) system automatically switches to high PRF mode. Multiple gates appear, and HPRF is indicated on the display. Adjusts the sensitivity to get more accurate 18 Trace Sensitivity envelope trace. 19 Time Resolution Adjusts the resolution in frequency domain. Optimizes the smoothness of the spectrum. 20 Spectral Average Different levels can be selected. Optimizes image quality and allows user to reduce beam intensity. 10% increments 21 Power output between 0-100%. Values greater than 0.1 are displayed. 22 SV Length Sizes the sample volume gate. Wall Filter insulates the Doppler signal from 23 Wall Filter excessive noise caused from vessel movement. 4 - 18 Section 4-3 - General Procedure

[Page 101] 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 3-20, in Chapter 3 Installation to the System probe connector. 2.) Turn ON the scanner (if it isn’t turned on already). Primary Menu Secondary Menu Frequency Baseline Spatial Filter Line Density Angle Steer Flash Suppression Packet Size Transparency Map PRF Focus Position Map Frame Average Threshold Power Output Invert Wall Filter Virtual Convex TGC CF Mode Gain Figure 4-33 Controls available in Color Flow Mode Figure 4-34 CFM Mode Screen Picture Example Chapter 4 Functional Checks 4 - 19

[Page 102] 4-3-9-2 Color Flow Mode OP Panel Controls Table 4-9 Color Flow Mode OP Panel Controls 1 Press CFM-Mode key CFM Mode Starts Amplifies the overall strength of the echoes processed in the Color Flow window. Turn the 2 Adjust Gain Gain dial (CFM Mode key) to the left/right to increase/decrease Gain. 4 - 20 Section 4-3 - General Procedure

[Page 103] 4-3-9-3 Color Flow Mode Softmenu Key Table 4-10 Color Flow Mode Softmenu Key Threshold assigns the gray scale level at 1 Threshold which color information stops. Controls the number of samples gathered for 2 Packet Size a single color flow vector. Allows a specific color map to be selected. 3 Select Color maps 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 4 Adjust Frequency select desired value. The selected frequency is displayed in the status window. Averages color frames. Press Frame 5 Set Frame Average Average up/down to smooth temporal averaging. Views blood flow from a different perspective. 6 Color Invert Press Invert to reverse the color map. Trades frame rate for sensitivity and spatial resolution. If the frame rate is too slow, 7 Adjust LIne Density reduce the size of the region of interest, select a different line density setting, or reduce the packet size. 8 Activate Spatial Filter Dynamic Range controls how echo intensities are converted to shades of gray, 9 Adjust Dynamic Range thereby increasing the adjustable range of contrast. Eliminates the motion artifacts. Press Ace to 10 Activate ACE activate. Slants the Color Flow region of interest or the 11 Adjust Angle Steer Doppler line to obtain a better Doppler angle. Adjusts the baseline to accommodate faster 12 Move Baseline or slower blood flows to eliminate aliasing. Velocity scale determines pulse repetition frequency. If the sample volume gate range Change PRF exceeds single gate PRF capability, the (Pulse Repetition Frequency) system automatically switches to high PRF mode. Multiple gates appear, and HPRF is indicated on the display. 14 Transparency Map Allows to select specific transparency map 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 15 Focus Position graphic caret corresponding to the focal zone position(s) appears on the right edge of the image. 16 Capture Chapter 4 Functional Checks 4 - 21

[Page 104] Table 4-10 Color Flow Mode Softmenu Key Optimizes image quality and allows user to reduce beam intensity. 10% increments 17 Power output between 0-100%. Values greater than 0.1 are displayed. Wall Filter insulates the Doppler signal from 18 Wall Filter excessive noise caused from vessel movement. 4 - 22 Section 4-3 - General Procedure

[Page 105] 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 once; an active caliper displays. 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 . The system displays the distance or tissue depth 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 once. 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 once; an active caliper displays. 2.) To position the active caliper, 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 caliper, move the TRACKBALL . 5.) Adjust the ELLIPSE ; 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 upward button. To decrease the size, adjust the ELLIPSE downward button. 8.) To toggle between active calipers, press MEASURE . 9.) To complete the measurement, press SET . The system displays the circumference and area in the measurement results window. Before you complete a measurement: - To erase the ellipse and the current data measured, press CLEAR once. The original caliper is displayed to restart the measurement. - To exit the measurement function without completing the measurement, press CLEAR a second time. Chapter 4 Functional Checks 4 - 23

[Page 106] 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. WARNING WARNING 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. 4 - 24 Section 4-3 - General Procedure

[Page 107] 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 NOTICE Clipboard* function is not available on LOGIQ C2 PRO. Chapter 4 Functional Checks 4 - 25

[Page 108] 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 button on the Keyboard. 2.) Select CONNECTIVITY , then REMOVABLE MEDIA . Properly label and Insert the backup media. 3.) Select the media type from the drop down menu. 4.) Enter the label for the media as shown in Figure 4-35. It is best to use all capital letters with no spaces or punctuation marks. Press Format . Figure 4-35 Format and Verify Media 5.) The Ultrasound system displays a pop-up menu, as shown in Figure 4-36. When the formatting has been completed, press OK to continue. 6.) If desired, verify that the format was successful by returning to Utility->Connectivity- >Removable Media and selecting VERIFY as shown in Figure 4-35. Figure 4-36 Format Successful Pop-up Menu 4 - 26 Section 4-3 - General Procedure

[Page 109] 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. Check here to backup presets and configurations Figure 4-37 Backup/Restore Menu Chapter 4 Functional Checks 4 - 27

[Page 110] 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 CAUTION 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. Check here to restore presets and configurations. Figure 4-38 Backup/Restore Menu 4 - 28 Section 4-3 - General Procedure

[Page 111] 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 4-39 Format CD Screen 5.) Select Backup/Restore, then EZBackup/Move. 6.) Select “Backup File Older Than in Days”. Choose the days which want to older than current exam date. Figure 4-40 EZBackup/Move Chapter 4 Functional Checks 4 - 29

[Page 112] 4-3-14-4 Archiving Images (cont’d) 7.) Press PATIENT and set the Dataflow to store images directly to CD-ROM. 8.) From the image screen, press EZBACKUP/MOVE . The Move Images pop-up appears. Figure 4-41 Image Archive Move Pop-up Menu 9.) Press Next on pop-up message. 10.)A media check message appears. Press OK to continue. Figure 4-42 Media check message 4 - 30 Section 4-3 - General Procedure

[Page 113] 4-3-14-4 Archiving Images (cont’d) 11.)Press Finish after Backup/Move complete. Figure 4-43 EZBackup/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”. Reminder Dialog Interval Days Figure 4-44 Emergency Repair Disk Chapter 4 Functional Checks 4 - 31

[Page 114] 4.) Return to scan mode. Press Ctrl + B, the Emergency Disk Making window pop-up appears. Figure 4-45 Emergency Disk Making Pop-up Menu 5.) Press Next on pop-up message. 6.) A storage information message appears. Press Next to continue. Figure 4-46 Storage Information message 4 - 32 Section 4-3 - General Procedure

[Page 115] 7.) Press Finish after Emergency Disk Making complete. Figure 4-47 Emergency Disk Making Complete All databases, presets and images should now be saved to Emergency Disk. 8.) Press Ctrl + R, Emergency Disk Recovery window pop-up appear. Figure 4-48 Emergency Disk Recovery 9.) Press Next on pop-up message. Chapter 4 Functional Checks 4 - 33

[Page 116] 10.)A recovery information message appears. Press Next to continue. Figure 4-49 Recovery Information message 11.)Press Finish after Emergency Disk Recovery complete. Figure 4-50 Emergency Disk Recovery Complete 1.) 4 - 34 Section 4-3 - General Procedure

[Page 117] Section 4-4 Software Configuration Checks Table 4-11 Software Configuration Checks Step Task to do Expected Result(s) 1. Check Date and Time setting Date and Time are correct 2. Check that Location (Hospital Name) is correct Location Name is correct 3. Check Language settings Desired Language is displayed 4. The default function for Store and Print Keys are Store Check assignment of Printer Keys (store image), Print (print). Store and Print Keys can also be assigned as desired by the customer 5. Check that all of the customer’s options are set up correct All authorized functions are enabled Section 4-5 Peripheral Checks Check that peripherals work as described below: Table 4-12 Peripheral Checks Step Task to do Expected Result(s) 1. Press ( FREEZE ) Stop image acquisition. 2. Press ( PRINT ) on the Control Panel The image displayed on the screen is printed on B&W printer. Connect with Foot Switch on USB port and 3. To start image acquisition (the same function as ( FREEZE ) key). press once. Chapter 4 Functional Checks 4 - 35

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[Page 119] Chapter 5 Components and Functions (Theory) Section 5-1 Overview 5-1-1 Purpose of Chapter 5 This chapter explains LOGIQ C Series' system concepts, component arrangement, and subsystem function. Table 5-1 Contents in Chapter 5 Section Description Page Number 5-1 "Overview" 5-1 5-2 "Block Diagram" 5-2 5-3 "Common Service Platform" 5-4 Chapter 5 Components and Functions (Theory) 5 - 1

[Page 120] Section 5-2Block Diagram 5-2-1 System Diagram Figure 5-51 LOGIQ C Series System Diagram 5 - 2 Chapter 5 Components and Functions (Theory)

[Page 121] 5-2-2 Software Diagram Figure 5-52 LOGIQ C Series Software Diagram Chapter 5 Components and Functions (Theory) 5 - 3

[Page 122] Section 5-3 Common Service Platform 5-3-1 Introduction The Service Platform contains a set of software modules that are common to all PC backend ultrasound and cardiology systems. The Common Service Platform will increase service productivity and reduce training and service costs. 5 - 4 Chapter 5 Components and Functions (Theory)

[Page 123] Chapter 6 Service Adjustments Section 6-1 Overview 6-1-1 Purpose of this chapter 6 This section describes how to test and adjust the scanner. These tests are optional. You may use them to check the system for errors. Table 6-2 Contents in chapter Section Description Page Number 6-1 "Overview" 6-1 6-2 "Monitor Adjustments" 6-2 Chapter 6 Service Adjustments 6 - 1

[Page 124] Section 6-2 Monitor Adjustments 6-2-1 Adjustments Procedures To adjust the brightness: For LOGIQ C2/C2 PRO: Adjust the LCD monitor’s button, located the right side of the LCD Monitor. For LOGIQ C3/C3 PRO: Adjust the LCD monitor’s button, located the bottom of the LCD Monitor. LOGIQ C2/C2 PRO LOGIQ C3/C3 PRO/C5/C5 PRO Figure 6-53 LCD Monitor 6 - 2 Section 6-2 - Monitor Adjustments

[Page 125] Chapter 7 Diagnostics/Troubleshooting Section 7-1 Overview 7-1-1 Purpose of Chapter 7 This section describes how to setup and run the tools and software that help maintain image quality and system operation. Very basic host, system and board level diagnostics are run whenever power is applied. Some Service Tools may be run at the application level. However most software tests are required. Table 7-3 Contents in Chapter 7 Section Description Page Number 7-1 "Overview" 7-1 7-2 "Gathering Trouble Data" 7-2 7-3 "USB Quick Save" 7-4 7-4 "Screen Captures" 7-6 7-5 "Common Diagnostics" 7-9 7-6 "Network Configuration" 7-12 Section 7-1 - Overview 7 - 1

[Page 126] Section 7-2 Gathering Trouble Data 7-2-1 Overview There may be a time when it would be advantageous to capture trouble images and system data (logs) for acquisition to be sent back to the manufacturer for analysis. There are different options to acquire this data that would give different results. 7-2-2 Collect Vital System Information The following information is necessary in order to properly analyze data or images being reported as a malfunction or being returned to the manufacturer: - Product Name = LOGIQ C Series From the Utility>System>General>About screen: Applications Software - Software Version - Software Part Number System Image Software - Image Revision - Image Part Number 7 - 2 Section 7-2 - Gathering Trouble Data

[Page 127] 7-2-3 Collect a Trouble Image with Logs If the system should malfunction, press the Alt-D keys simultaneously. This will collect a screen capture of the image monitor, system presets and the following logs: - Keyboard Shadow Log - Error Logs - Crash Log - Power Supply - Temperature NOTE: Power Supply and Temperature logs are not currently being updated by the LOGIQ C Series. This Alt-D function is available at all times. Figure 7-54 ALT-D Dialog Box When Alt-D is pressed, a menu box appears that allows for: - A place to enter a description of the problem - A choice to store to a pre-formatted CD-R, RD (Removable Disk) or to the Export directory D: drive. The subsequent file is compressed and time stamped. The screen capture is a bitmap which eliminates the possibility of artifacts from compression. Section 7-2 - Gathering Trouble Data 7 - 3

[Page 128] Section 7-3 USB Quick Save NOTE: USB Quick Save function not support by LOGIQ C2/C2 PRO. 7-3-1 Overview There may be times when the customer or field engineer will want to directly save images into USB memory. This is accomplished by saving individual Cine clips (moving images- avi format) or still images (jpg format) directly to a USB memory disk by pressing Print or Store Key. There’s no factory default print key to accomplish USB Quick Save. However, customer may have customize Print and Store Key function. When performing a USB Quick Save, you can only define one USB Quick Save operation with either Print or Store keys. NOTE: The print key that has been assigned to the USB Quick Save function should not have any other service functions assigned to it. 7-3-2 Check and Record the Print or Store Key Function Check the function of the Print or Store Key in the event that the customer may have made some custom settings. 4.) In the Physical Print Buttons field, select Print or Store. The Connectivity/Buttons Screen will be displayed like the one shown below. Figure 7-55 Defining Print or Store Key Operation If Print or Store key is not set to Image Area, proceed to step 5 to record the customer’s customized settings. 5.) In the Destinations section, record the service that is displayed. 6.) In the Physical Print Buttons section, record the parameters related to the service. 7 - 4 Section 7-3 - USB Quick Save

[Page 129] 7-3-3 Setting the Print or Store Key to USB Quick Save If the Print or Store Key is not set to screen capture: 1.) While on the Connect screen, with the Buttons tab displayed, go to the Destinations list. 2.) From the list select USB Quick Save . Press [>>] to add the selection to the Printflow View section. 3.) Ensure that the Physical Print Buttons section for capture Area is set to Image Area and No Image Compression. 4.) The Print and Store Key should now be set up for USB Quick Save, sending the images directly to the USB memory. NOTICE It is unable to get full screen using USB Quick Save, just Image Area is available. Section 7-3 - USB Quick Save 7 - 5

[Page 130] Section 7-4 Screen Captures NOTE: Screen Capture not support by LOGIQ C2 PRO/C3 PRO/C5 PRO. There may be times when the customer or field engineer will want to capture a presentation on the screen. This is accomplished by first saving the image(s) to the clipboard using a Print or Store Key. The Store key is the factory default print key to accomplish a secondary Screen Capture. However, the customer may have customized the Store Key function. 7-4-1 Check and Record the Store Key Function Check the function of the Store Key in the event that the customer may have made some custom settings. 4.) In the Physical Print Buttons field, select Store. The Connectivity/Buttons Screen will be displayed like the one shown in Figure 7-55 on page 7-4 . If Store key is not set to Whole Screen, as shown in Figure 7-55, proceed to step 5 to record the customer’s customized settings. 5.) In the Destinations section, record the service that is displayed. 6.) In the Physical Print Buttons section, record the parameters related to the service. 7-4-2 Setting the Store Key to Screen Capture If the Store Key is not set to screen capture: 1.) While on the Connect screen, with the Buttons tab displayed, go to the Destinations list. 2.) From the list select Copy To Dataflow . Press [>>] to add the selection to the Printflow View section. 3.) Ensure that the Physical Print Buttons section for capture Area is set to Whole Screen, secondary Capture and No Image Compression. 4.) The Store Key should now be set up for whole screen capture, sending the screens to the image buffer (clipboard). 7-4-3 Capturing a Screen The following is a generic process to capture any screen from the scanner: 1.) Navigate to and display the image/screen to be captured. 2.) Press STORE . This will place a snapshot of the screen on the “clipboard” displayed at the bottom of the scan image display. 7 - 6 Section 7-4 - Screen Captures

[Page 131] 7-4-3 Capturing a Screen (cont’d) Clipboard Thumbnai ls Menu Figure 7-56 Select Image to Capture 3.) Click FREEZE to unfreeze the image to view the image screen and the snapshots displayed on the bottom. 4.) Highlight the snapshot to be stored to RD (Removable Disk) or CD-R. 5.) Select Menu on the right side of the image screen, then highlight and select SAVE AS. Save As Figure 7-57 Menu > Save As Section 7-4 - Screen Captures 7 - 7

[Page 132] 7-4-3 Capturing a Screen (cont’d) Figure 7-58 Save Dialog Box 6.) A Save dialog box will be opened. Choose d:\export folder as the archive location to save the image on the hard disk or CD-R. NOTICE After capture the snapshot of the screen to the “clipboard” and save it to the hard disk or other media, it is not full screen image on the hard disk or media. 7-4-4 Reset the Store Key to Customer’s Functionality If the customer had programmed the Store Key to a function other than screen capture, restore that functionality recorded in section 7-3-2 on page 7-4. Refer to Figure 7-55. 4.) In the Physical Print Button field, select Store. 5.) In the Destinations list, select the service(s) recorded in step 5, Section 7-3-2. 6.) In the Physical Print Buttons section, select the parameters related to the service recorded in step 6, Section 7-3-2. 7 - 8 Section 7-4 - Screen Captures

[Page 133] Section 7-5 Common Diagnostics 7-5-1 Utilities Provides two selections: 7-5-1-1 Disruptive Mode Allows you to enable or disable disruptive mode troubleshooting. 7-5-1-2 System Shutdown Allows for system shutdown from the diagnostic menu. Select to Restart System or Shutdown System. Also, select to retain Disruptive Mode or Not. After submitting to restart or shutdown a confirmation screen gives one last chance to confirm or cancel the request. Section 7-5 - Common Diagnostics 7 - 9

[Page 134] 7-5-2 PC Diagnostics (Non-Interactive Tests) 7-5-2-1 Essential Tests 7-5-2-2 System Board 7-5-2-3 Hard Disk Surface Scan 7-5-2-4 Hard Disk Quick Test 7-5-2-5 PCIBus 7-5-2-6 Video Card 7-5-2-7 Network Interface 7-5-2-8 CMOS 7-5-2-9 DRAM Memory 7-5-2-10 Parallel Port 7 - 10 Section 7-5 - Common Diagnostics

[Page 135] 7-5-3 PC Diagnostics (Interactive Tests) 7-5-3-1 Keyboard Test 7-5-3-2 Mouse Test 7-5-4 Restart LOGIQ C Series After Diagnostics Always shutdown the system and reboot after a diagnostics session. Section 7-5 - Common Diagnostics 7 - 11

[Page 136] Section 7-6 Network Configuration 7-6-1 Network Configuration 7-6-1-1 Wire-LAN Network 1.) Connect system with network. 2.) Press Utility -> Connectivity -> TCPIP, in IP Settings window check the Enable DHCP box. In Network Speed box, choose the proper speed available. Figure 7-59 Enable DHCP 7 - 12 Section 7-6 - Network Configuration

[Page 137] 7-6-1-1 Wire-LAN Network (cont’d) NOTE: If user want to setup static IP address, uncheck Enable DHCP option, input static address in IP- Address box, Subnet Mask and Default Gateway box. In Network Speed box, choose the proper speed available. Figure 7-60 Input static address 3.) Click Save, in popped-up dialog choose Shutdown. Figure 7-61 Save and reboot inquiry dialog 4.) After the system shutdown, reboot the system. 5.) After reboot, the network icon at the left bottom of screen turns green. Figure 7-62 Network icon Section 7-6 - Network Configuration 7 - 13

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[Page 139] Chapter 8 Replacement Procedures Section 8-1 Overview 8-1-1 Purpose of Chapter 8 This chapter describes replacement procedures for the following modules and subsystems. Table 8-1 Contents in Chapter 8 Section Description Page Number 8-1 "Overview" 8-1 8-2 "DISASSEMBLY/RE-ASSEMBLY" 8-2 8-2-1 "Warning and Caution" 8-2 8-2-2 "Air filter and Knob Screw (FRU No. 5030)" 8-3 8-3 "Loading Base Image Software" 8-4 Section 8-1 - Overview 8 - 1

[Page 140] Section 8-2 DISASSEMBLY/RE-ASSEMBLY 8-2-1 Warning and Caution WARNING WARNING ONLY QUALIFIED SERVICE PERSONNEL SHOULD REMOVE ANY COVERS OR PANELS. ELECTRICAL HAZARDS EXISTS AT SEVERAL POINTS INSIDE. BECOME THOROUGHLY FAMILIAR WITH ALL HAZARDOUS VOLTAGES AND HIGH CURRENT LEVELS TO AVOID ACCIDENTAL CONTACT CAUTION Do not wear the ESD wrist strap when you remove a part of power supply unit. Turn OFF power and unplug the power cord before removing a part of power supply unit. However be sure to turn off power and wear the strap before you remove a circuit boards. WARNING WARNING DO NOT SERVICE OR DISASSEMBLE PARTS UNDER FRU UNIT LEVEL AT ANY CIRCUMSTANCES. 8 - 2 Section 8-2 - DISASSEMBLY/RE-ASSEMBLY

[Page 141] 8-2-2 Air filter and Knob Screw (FRU No. 5030) 8-2-2-1 Tools • Common phillips screwdrivers 8-2-2-2 Preparations • Shut Down the System and disconnect the power cord. 8-2-2-3 Removal Procedure 1.) Unscrew the knob screw which fix air filter on the edge of power box. 2.) Pull out the air filter. 8-2-2-4 Mounting procedure Install the new parts in the reverse order of removal. 1) 2) Figure 8-63 Air filter and Knob Screw Disassembly Section 8-2 - DISASSEMBLY/RE-ASSEMBLY 8 - 3

[Page 142] Section 8-3Loading Base Image Software NOTE: While it is believed to be unnecessary, It would not hurt to disconnect the system from the network and remove all transducers. NOTE: Please ensure power cable is connected during system upgrade! 1.) Insert the disk labeled “System & Application Software” into the DVD ROM drive. 2.) Properly turn off the scanner by momentarily pressing the Power On/Off Switch. Select “Shut Down” from the System Exit menu. 3.) If the system will not shutdown normally, hold down the Power On/Off Switch until the light turns from green to amber. 4.) Turn on the system. System will detect the DVD-RW automatically. 5.) Press any key to continue when below message display as shown below. Figure 8-64 Upgrade message 8 - 4 Section 8-3 - Loading Base Image Software

[Page 143] Section 8-3 Loading Base Image Software (cont’d) 6.) Select one of the options for loading the system. Select choice 1] to load the complete disk. Figure 8-65 Selection for loading the system WARNING WARNING While the software install procedure is designed to preserve data, you should select choice [2] to format disk C only. WARNING WARNING If software upgrades to R1.1.5 in China, you should select choice [1] to load or upgrade complete disk. 7.) Press any key to continue when below message display as shown below. Figure 8-66 Upgrade continue message Section 8-3 - Loading Base Image Software 8 - 5

[Page 144] Section 8-3 Loading Base Image Software (cont’d) 8.) System CD will be loaded as shown in the screen below. Figure 8-67 Upgrading message 9.) System updating finished, refer to Figure 8-68 on page 8-6 . Figure 8-68 System upgrade complete 10.)Press power key to reboot system, then remove the CDROM from the drive immediately. When system first time boot up after upgrading complete, type Serial Number and Option Key before starting up. 8 - 6 Section 8-3 - Loading Base Image Software

[Page 145] Chapter 9 Renewal Parts Section 9-1 Overview 9-1-1 Purpose of Chapter 9 This chapter gives you an overview of Renewal Parts for LOGIQ C Series. Table 9-1 Contents in Chapter 9 Section Description Page Number 9-1 "Overview" 9-1 9-2 "List of Abbreviations" 9-1 9-3 "Renewal Parts Lists" 9-2 9-4 "Operator Console Assy" 9-3 9-5 "Keyboard Assy" 9-4 9-6 "Accessories and kits" 9-5 9-7 "Manuals" 9-6 9-8 "Probes" 9-7 Section 9-2 List of Abbreviations • Assy - Assembly • Ctrl - Control • FRU 1 - Replacement part available in part hub • FRU 2 - Replacement part available from the manufacturer (lead time involved) • Int - Internal • I/O - Input/Output • LCD - Liquid Crystal Display • MON - Monitor • PAT. - Patient • PC - Personal Computer (Back End Processor) Chapter 9 Renewal Parts 9 - 1

[Page 146] Section 9-3Renewal Parts Lists 9-3-1 Equipment Models Covered in this Chapter Table 9-2 ACDC Power Pack & ACDC Power Cable list Part Name Part Number Description Quantity FRU AC Power Cord 5316943 Power cord Europe Class 1 1 AC Power Cord 5316948 Power cord China Class 1 1 AC Power Cord 5316949 Power cord India Class 1 1 AC Power Cord 5316950 Power cord Argentina Class 1 1 AC Power Cord 5316951 Power cord UK Class 1 1 AC Power Cord 5316952 Power cord Denmark Class 1 1 AC Power Cord 5316954 Power cord Switzerland Class 1 1 AC Power Cord 5316955 Power cord Australia Class 1 1 AC Power Cord 5316956 Power cord USA Class 1 1 9 - 2 Section 9-3 - Renewal Parts Lists

[Page 147] Section 9-4Operator Console Assy LCD Assy Keyboard Assy Body Assy Base Assy LOGIQ C2/C2 PRO LOGIQ C3/C3 PRO LOGIQ C5/C5 PRO Figure 9-69 Operator Console Assy Chapter 9 Renewal Parts 9 - 3

[Page 148] Section 9-5 Keyboard Assy Table 9-3 Keyboard Assy 5322545 LOGIQ C2/C2 PRO KBD Top Assy 1 1 5322547 LOGIQ C3/C3 PRO KBD Top Assy 1 1 5322548 LOGIQ C5/C5 PRO KBD Top Assy 1 1 2000 5315718 LOGIQ C2/C2 PRO KBD Top Assy For Russian 1 1 5315719 LOGIQ C3/C3 PRO KBD Top Assy For Russian 1 1 5315720 LOGIQ C5/C5 PRO KBD Top Assy For Russian 1 1 9 - 4 Section 9-5 - Keyboard Assy

[Page 149] Section 9-6Accessories and kits Table 9-4 Accessories and Kits 5245387 LOGIQ C2/C2 PRO Cable Kits 1 2 5248887 LOGIQ C3/C3 PRO/C5/C5 PRO Cable Kits 1 2 6020 5315735-2 Cable Kits_LOGIQC3,C5 for One Box units 1 2 5315692-2 Cable KITS_LOGIQC2 for One Box units 1 2 7010 5315707 Collector UPD897 kits 1 2 7021 5315282-3 LOGIQ C Series system and application DVD R112 1 2 7021A 5315282-4 LOGIQ C Series system and application DVD R113 1 2 7021B 5315282-5 LOGIQ C Series system and application DVD R114 1 2 7021C 5315282-6 LOGIQ C Series system and application DVD R115 1 2 7022 LOGIQ C PRO Series system and application DVD 5315283-3 1 2 R112 LOGIQ C PRO Series system and application DVD 7022A 5315283-4 1 2 R113 LOGIQ C PRO Series system and application DVD 7022B 5315282-5 1 2 R114 LOGIQ C PRO Series system and application DVD 7022C 5315283-6 1 2 R115 LOGIQ C Series system and application DVD R115 7023 5336393 1 2 for China Chapter 9 Renewal Parts 9 - 5

[Page 150] Section 9-7Manuals 5273008-100 LOGIQ C Series Service Manual 1 N System User Manuals 5265060 -100 User Manual, LOGIQ C2/C2 PRO, English 1 N 5265060 -101 User Manual, LOGIQ C2/C2 PRO, French 1 N 5265060 -106 User Manual, LOGIQ C2/C2 PRO, Spanish 1 N 5265060 -108 User Manual, LOGIQ C2/C2 PRO, German 1 N 5265060 -111 User Manual, LOGIQ C2/C2 PRO, Italian 1 N 5265060 -127 User Manual, LOGIQ C2/C2 PRO, portuguese 1 N 5265060 -141 User Manual, LOGIQ C2/C2 PRO, Chinese 1 N 5268001 -100 User Manual, LOGIQ C3/C3 PRO, English 1 N 5268001 -101 User Manual, LOGIQ C3/C3 PRO, French 1 N 5268001 -106 User Manual, LOGIQ C3/C3 PRO, Spanish 1 N 5268001 -108 User Manual, LOGIQ C3/C3 PRO, German 1 N 5265060 -111 User Manual, LOGIQ C3/C3 PRO, Italian 1 N 5268001 -127 User Manual, LOGIQ C3/C3 PRO, portuguese 1 N 5268001 -141 User Manual, LOGIQ C3/C3 PRO, Chinese 1 N 5268596 -100 User Manual, LOGIQ C5/C5 PRO, English 1 N 5268596 -101 User Manual, LOGIQ C5/C5 PRO, French 1 N 5268596 -106 User Manual, LOGIQ C5/C5 PRO, Spanish 1 N 5268596 -108 User Manual, LOGIQ C5/C5 PRO, German 1 N 5268596 -111 User Manual, LOGIQ C5/C5 PRO, Italian 1 N 5268596 -127 User Manual, LOGIQ C5/C5 PRO, portuguese 1 N 5268596 -141 User Manual, LOGIQ C5/C5 PRO, Chinese 1 N System Quick Start Guide 5271093 -100 Quick Start Guide, LOGIQ C2/C2 PRO 1 N 5262559 -100 Quick Start Guide, LOGIQ C3/C3 PRO 1 N 5272220 -100 Quick Start Guide, LOGIQ C5/C5 PRO 1 N 9 - 6 Section 9-7 - Manuals

[Page 151] Section 9-8Probes Table 9-5 Probes on LOGIQ C Series Item Part Name Part Number Description Quantity FRU 8801 4C-RC 5315581 Probe (Center Frequency: 3.75MHz) 1 1 8802 3.8C-RC 5315682 Probe (Center Frequency: 3.75MHz) 1 1 8803 7L-RC 5315684 Probe (Center Frequency: 7.5MHz) 1 1 8804 7.5C-RC 5315683 Probe (Center Frequency: 7.5MHz) 1 1 8805 6.5C-RC 5315685 Probe (Center Frequency: 6.5MHz) 1 1 8806 E6C-RC 5315687 Probe (Center Frequency: 6.5MHz) 1 1 8807 E7C-RC 5315686 Probe (Center Frequency: 6.5MHz) 1 1 8808 3S-RC 5315689 Probe (Center Frequency: 2.0MHz) 1 1 NOTICE 3S-RC* is not available on LOGIQ C2/C2 PRO. NOTICE All the spare parts should be disposed according to local laws. Chapter 9 Renewal Parts 9 - 7

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[Page 153] Chapter 10 Care & Maintenance Section 10-1 Overview 10-1-1 Periodic Maintenance Inspections It has been determined by engineering that your system does not have any high wear components that fail with use, therefore no Periodic Maintenance Inspections are mandatory. Some Customers Quality Assurance Programs may require additional tasks and or inspections at a different frequency than listed in this manual. 10-1-2 Purpose of Chapter 10 This chapter describes Care & Maintenance on the scanner and peripherals. These procedures are intended to maintain the quality of the ultrasound systems performance . Read this chapter completely and familiarize yourself with the procedures before performing a task. Table 10-1 Contents in Chapter 10 Section Description Page Number 10-1 "Overview" 10-1 10-2 "Why do Maintenance" 10-2 10-3 "Maintenance Task Schedule" 10-2 10-4 "Tools Required" 10-4 10-5 "When There's Too Much Leakage Current..." 10-20 CAUTION Practice good ESD prevention. Wear an anti–static strap when handling electronic parts and even when disconnecting/connecting cables. DANGER THERE ARE SEVERAL PLACES ON THE BACKPLANE, THE AC DISTRIBUTION, AND DC DISTRIBUTION THAT ARE DANGEROUS. BE SURE TO DISCONNECT THE SYSTEM POWER PLUG AND OPEN THE MAIN CIRCUIT BREAKER BEFORE YOU REMOVE ANY PARTS. BE CAUTIOUS WHENEVER POWER IS STILL ON AND COVERS ARE REMOVED. CAUTION Do not pull out or insert circuit boards while power is ON. CAUTION Do not operate this unit unless all board covers and frame panels are securely in place. System performance and cooling require this. Section 10-1 - Overview 10 - 1

[Page 154] Section 10-2 Why do Maintenance 10-2-1 Keeping Records It is good business practice that ultrasound facilities maintain records of quality checks and corrective maintenance. The Ultrasound Inspection Certificate (provided on page 10-21) provides the customer with documentation that the ultrasound scanner is maintained on a periodic basis. A copy of the Ultrasound Periodic Maintenance Inspection Certificate should be kept in the same room or near the scanner. 10-2-2 Quality Assurance In order to gain accreditation from organizations such as the American College of Radiology (USA), it is the customer’s responsibility to have a quality assurance program in place for each scanner. The program must be directed by a medical physicists, the supervising radiologist/physician or appropriate designee. Routine quality control testing must occur regularly. The same tests are performed during each period so that changes can be monitored over time and effective corrective action can be taken. Testing results, corrective action and the effects of corrective action must be documented and maintained on the site. Your GE service representative can help you with establishing, performing and maintaining records for a quality assurance program. Please contact us for coverage information and/or price for service. Section 10-3 Maintenance Task Schedule 10-3-1 How often should care & maintenance tasks be performed? The Care & Maintenance Task Schedule (provided on page 10-3) specifies how often your LOGIQ C Series should be serviced and outlines items requiring special attention. NOTE: It is the customer’s responsibility to ensure the LOGIQ C Series care & maintenance is performed as scheduled in order to retain its high level of safety, dependability and performance. Your GE Service Representative has an in-depth knowledge of your LOGIQ C Series ultrasound scanning system and can best provide competent, efficient service. Please contact us for coverage information and/or price for service. The service procedures and recommended intervals shown in the Care & Maintenance Task Schedule assumes that you use your LOGIQ C Series for an average patient load (10-12 per day) and not use it as a primary mobile unit which is transported between diagnostic facilities. NOTE: If conditions exist which exceed typical usage and patient load, then it is recommended to increase the maintenance frequencies. 10 - 2 Section 10-2 - Why do Maintenance

[Page 155] Section 10-3 Maintenance Task Schedule (cont’d) Table 10-2 Customer Care Schedule Per Facilities Service at Indicated Time Daily Weekly Monthly QA Program Notes Clean Probe Holders • more frequently depending on Clean Air Filter • your environment Inspect AC Mains Cable • Mobile Unit Check Weekly Inspect Cables and Connectors • Clean Console • Inspect Wheels, Casters, brakes and • Mobile Unit Check Daily Swivel Locks Check Control Panel Movement • Mobile Unit Check Daily also after corrective Console Leakage Current Checks • maintenance also after corrective Peripheral Leakage Current Checks • maintenance also after corrective Surface Probe Leakage Current Checks • maintenance Endocavity Probe Leakage also after corrective Current Checks maintenance Transesphongeal Probe Leakage also after corrective Current Checks maintenance Surgical Probe Leakage also after corrective Current Checks maintenance also after corrective Measurement Accuracy Checks • maintenance also after corrective Functional Checks • maintenance Section 10-3 - Maintenance Task Schedule 10 - 3

[Page 156] Section 10-4 Tools Required 10-4-1 Standard GE Tool Kit The following is a description of the “Standard” GE tool kit in the USA. Not all tools are required for PMs. Table 10-3 Overview of GE-1 Tool Kit Contents Tool ID Description Tool ID Description 9-45358 Pliers Retaining Ring 9-XL9971MM Xcelite-hex Blade 1.27mm 9-4078 Scribe 9-XL9972MM Xcelite-hex Blade 1.5mm 9-44572 Wrench Open End 3/8 - 7/16 9-XL9973MM Xcelite-hex Blade 2 mm 9-44579 Wrench Open End 1/2 - 9/16 9-XL9974MM Xcelite-hex Blade 2.5mm 9-44579 Wrench Open End 1/2 - 9/16 9-XL9975MM Xcelite-hex Blade 3mm 9-45385 Pliers, Arc Joint 7 inch 9-XL9976MM Xcelite-hex Blade 4mm 9-45378 Pliers, Slip Joint 9-XL9977MM Xcelite-hex Blade 5mm 9-4518 Pliers, Long Nose, Miniature 9-XL991CM Handle 9-4518 Pliers, Long Nose, Miniature C2356E Screw starter - Kedman Quick Wedge 9-44776 Ignition Wrench Set, 10 pc. BLBO Box - 18 Compartment 9-44601 Wrench, Adj., 4 inch DWL4283T Box - 5 Compartment 9-4151 Screwdriver, Blade, Stubby 9-41322 Pickup Tool, Claw type 9-41421 Screwdriver, Blade, Pocket clip 9-6757 6 pc Needle File Set 9-41594 Screwdriver, Blade 1/8 in. x 4 in. 9-9487 Utility Knife 9-41581 Screwdriver, Blade 3/16 in. x 4 in. 9-45341 Pliers Vice Grip 10 inch 9-39451 20' Steel Tape, locking Spring load 9-3001 Xacto Pen Knife 9-GH807 Ratchet, Offset, Slotted 9-HT62002 Solder Aid, Fork and Hook 68-412 Ratchet, Offset, Phillips 9-4099 Mirror, Round, Telescoping 9-GH130 Tapered Reamer 9-GH3001 Steel Rule Decimal 6 inch 9-41584 Screwdriver, slotted 1/4 in.X 6 in. 9-GH300ME Steel Rule Metric 6 inch 9-4118 Screwdriver, Phillips #2, Stubby 9-XL9920 Xcelite-hex Blade.050 inch 9-41293 Screwdriver, Phillips #0 9-XL9921 Xcelite-hex Blade 1/16 inch 9-41294 Screwdriver, Phillips #1 9-XL9922 Xcelite-hex Blade 5/16 inch 9-41295 Screwdriver, Phillips #2 9-XL9923 Xcelite-hex Blade 3/32 inch 9-46677 Hex Keys, 20 pc., Metric 9-XL9924 Xcelite-hex Blade 1/8 inch 9-34701 1/4 in. Standard.Socket set (19 pc) 9-XL9925 Xcelite-hex Blade 5/32 inch 9-43499 1/2 inch Socket 1/4 inch drive 9-XL9926 Xcelite-hex Blade 3/16 inch 9-4355 Flex Spinner 9-XL99764 Xcelite-hex Blade 7/64 9-43523 Breaker 9-XL99964 Xcelite-hex Blade 9/64 9-43531 6 inch Ext. 9-XLM60 Mini-screwdriver kit 10 - 4 Section 10-4 - Tools Required

[Page 157] Table 10-3 Overview of GE-1 Tool Kit Contents (Continued) Tool ID Description Tool ID Description 9-65283 Case 8.5 in. x 4.5 in. x 2 in. Deep 9-45072 Pliers 6 inch Diagonal 9-46696 Hex Keys 9-XL100X Wire Stripper/Cutter 5 inch - 100X 9-39829 Torpedo Level, Magnetic 9-XL87CG Pliers - very fine needle nose-87CG 9-38461 Hammer, Ball Peen, 4 oz 9-WEWDT-07 Weller-Soldering-Replacement Tip(1) 9-4280 Universal Joint 1/4 inch 9-WS175-E Wiss - Surgical Scissors 9-WEW60P3 Weller - Soldering Iron, 3 wire KH174 Hemostat 5 inch Straight 9-WECT5B6 Weller - Soldering Iron Tip KH175 Hemostat 5 inch curved 9-WEWDP12 Weller - Desoldering Pump 9-Z9480121 Alignment tool (red) 93383 Flashlight Mini-Mag Lite (AAA Bat.) 9-GH408 Tweezers 21576 Brush - Bristle 9-4516 Pliers 4 1/4 inch Diagonal Table 10-4 Overview of GE-2 Tool Kit Contents(Continued) GE-2 Sears Kit (#99034) Tool ID Description Tool ID Description 9-45381 Pliers, Arc Joint 9 1/2 inch 9-44067 Socket 1 1/16 in. for 1/2 in. drive 9-45092 Pliers, Linesman 8 1/2 inch 9-42679 Socket 10MM Hex for 1/2 in. drive (2273333) 9-42882 Punch, Pin 3/32 inch 9-44262 Extension 10 inch for 1/2 in. drive (2273405) 9-42884 Punch, Pin 5/32 inch 9-4258 3/8 inch to 1/2 inch Adapter 9-42886 Punch, Pin 1/4 inch 9-34374 3/8 inch Metric Socket Set - 12 PT 9-42973 Cold Chisel 1/2 inch 9-44311 16mm Socket 12 pt. 9-GH77 Center Punch Automatic 9-33485 Metal Socket Tray 9-GH890 File Handle, Adj. 9-33484 Metal Socket Tray 9-31276 File, Round, Bastard 8 inch 9-33484 Metal Socket Tray 9-31277 File, Half Round, Bastard 8 inch 9-52068 Tap and Drill Set 9-31263 File, Flat Mill 8 inch 9-52722 #6 Tap 21045C Close Quarter Saw 9-52723 #8 Tap 9-44604 Wrench, Adj 10 inch High Speed Drill Set 9-41587 Screwdriver 5/16 inch x 8 inch #36 Drill 9-41586 Screwdriver, Stubby 5/16 inch #29 Drill 9-GH19512 Countersink 1/2 inch 9-44046 3/8 inch Socket Set 9-44741 12 PC Combination Wrench Set Section 10-4 - Tools Required 10 - 5

[Page 158] 10-4-2 Special Tools, Supplies and Equipment 10-4-2-1 Specific Requirements for Care & Maintenance Table 10-5 Overview of Requirements for Care & Maintenance Tool Part Number Comments Digital Volt Meter (DVM) Electric Safety Analyzer DALE 600 46-285652G1 For 120V Unit Electric Safety Analyzer DALE 46-328406G2 For 220V Units 600E Leakage Current Ultrasound Kit 2113015 For 120V and 220V Units 46–194427P231 Kit includes anti–static mat, wrist strap and cables for 200 to 240 46–194427P279 V system Anti Static Kit 46–194427P369 3M #2204 Large adjustable wrist strap 46–194427P373 3M #2214 Small adjustable wrist strap 46–194427P370 3M #3051 conductive ground cord 46–194427P278 120V Anti Static Vacuum Cleaner 46–194427P279 230V Air Filter air intake Safety Analyzer 46–285652G1 DALE 600 KIT (or equivalent) for electrical tests E7010GG 60 minute SVHS VCR Cassette E7010GF 120 minute SVHS VCR Head Cleaner See VCR user manual for requirements E8381AA blank 128 M disk E8381AB blank 230 M disk 3.5” MOD MEDIA 5.25” MOD Media 3.5” MOD Media Cleaner 2117811 cleans the diskettes 5.25” MOD Media Cleaner cleans the diskettes 3.5” MOD Head Cleaner Kit 2148392 cleans the drive heads 5.25” MOD Head Cleaner Kit cleans the drive heads QIQ Phantom E8370RB RMI Grayscale Target Model 403GS CD-RW Media For LOGIQ C Series B/W Printer Cleaning Sheet See printer user manual for requirements Color Printer Cleaning Sheet See printer user manual for requirements Disposable Gloves 10 - 6 Section 10-4 - Tools Required

[Page 159] 10-4-3 Input Power 10-4-3-1 Mains Cable Inspection Table 10-6 Mains Cable Inspection Step Item Description 1 Unplug Cord Disconnect the mains cable from the wall and system. 2 Inspect Inspect it and its connectors for damage of any kind. Verify that the LINE, NEUTRAL and GROUND wires are properly attached to the terminals, and that no 3 Verify strands may cause a short circuit. 4 Verify Inlet connector retainer is functional. 10-4-4 Cleaning 10-4-4-1 General Cleaning Table 10-7 General Cleaning Step Item Description Use a fluid detergent in warm water on a soft, damp cloth to carefully wipe the entire system. Be careful 1 Console not to get the cloth too wet so that moisture does not enter the console. 2 Probe Holder Clean probe holders (they may need to be soaked to remove excess gel). NOTE: For your convenience or of the air filter is too dirty, replacement filters are available. refer to Chapter 9 for the air filter replacement part number. 10-4-5 Physical Inspection Table 10-8 Physical Checks Step Item Description Verify that all system labeling is present and in readable condition. refer to the LOGIQ C Series User 1 Labeling Manual for details. 2 Scratches & Dents Inspect the console for dents, scratches or cracks. Check all wheels and casters for wear and verify operation of foot brake, to stop the unit from moving, 3 Wheels & Brakes and release mechanism. Check all caster locks and caster swivel locks for proper operation. Cables & Check all internal cable harnesses and connectors for wear and secure connector seating. Pay Connectors special attention to footswitch assembly and probe strain or bend reliefs. Shielding & Check to ensure that all EMI shielding, internal covers, air flow panels and screws are in place. Covers Missing covers and hardware could cause EMI/RFI problems while scanning. 6 External I/O Check all connectors for damage and verify that the labeling is good. 7 Op Panel Lights Check for proper operation of all operator panel and TGC lights. 8 Monitor Light Check for proper operation of any monitor lights if available. External 9 Check for proper operation of any external microphones by recording an audio test. Microphone Section 10-4 - Tools Required 10 - 7

[Page 160] 10-4-6 Outlet Test - Wiring Arrangement - USA & Canada Test all outlets in the area for proper grounding and wiring arrangement by plugging in the neon outlet tester and noting the combination of lights that are illuminated. Any problems found should be reported to the hospital immediately and the receptacle should not be used. Figure 10-1 Typical Outlet Tester The Dale 600 has self-contained lamps designed for testing the outlet wiring arrangement. Plug the Dale 600 into each outlet to be tested comparing the lamp status. Combination of Lights REVERSE OPEN Condition CORRECT OPEN HOT/GROUND WIRING POLARITY GROUND HOT REVERSED Figure 10-2 Dale 600 Outlet Test NOTE: No outlet tester can detect the condition where the Neutral (grounded supply) conductor and the Grounding (protective earth) conductor are reversed. If later tests indicate high leakage currents, this should be suspected as a possible cause and the outlet wiring should be visually inspected. 10 - 8 Section 10-4 - Tools Required

[Page 161] 10-4-7 Grounding Continuity CAUTION Electric Shock Hazard. The patient must not be contacted to the equipment during this test Measure the resistance from the third pin of the attachment plug to the exposed metal parts of the case. The ground wire resistance should be less than 0.2 ohms. reference the procedure in the IEC 601-1.1. Figure 10-3 Ground Continuity Test 10-4-7-1 Meter Procedure Follow these steps to test the ground wire resistance. 1.) Turn the LOGIQ C Series unit OFF. 2.) Plug the unit into the meter, and the meter into the tested AC wall outlet. 3.) Plug the black chassis cable into the meter's “CHASSIS” connector and attach the black chassis cable clamp to an exposed metal part of the LOGIQ C Series unit. 4.) Set the meter's “FUNCTION” switch to the RESISTANCE position. 5.) Set the meter's “POLARITY” switch to the OFF (center) position. 6.) Measure and record the ground wire resistance. Section 10-4 - Tools Required 10 - 9

[Page 162] 10-4-7-2 Dale 600 - Ground Continuity The Dale 600 measures line cord resistance from the third pin of the attachment plug to the meter’s Chassis Cable clamp. Test the grounding continuity of the system to all exposed metal parts in accordance with the IEC 601-1.1 procedure as above. refer to the Dale 600 Instruction Manual for meter self tests and operation. Record measured resistance of the grounding continuity. The ground wire resistance should be less than 0.2 (Use any safety analyzer.) 10 - 10 Section 10-4 - Tools Required

[Page 163] 10-4-8 Chassis Leakage Current Test 10-4-8-1 Definition This test measures the current that would flow in a grounded person who touched accessible metal parts of the bedside station if the ground wire should break. The test verifies the isolation of the power line from the chassis. The meter is connected from accessible metal parts of the case to ground. Measurements should be made with the unit On and Off, with the power line polarity Normal and Reversed. Record the highest reading. CAUTION Electric Shock Hazard. When the meter's ground switch is OPEN, don't touch the unit! CAUTION Equipment damage possibility. Never switch the Polarity and the status of Neutral when the unit is powered ON. Be sure to turn the unit power OFF before switching them using the POLARITY switch and/or the NEUTRAL switch. Otherwise, the unit may be damaged. 10-4-8-2 Generic Procedure The test verifies the isolation of the power line from the chassis. The testing meter is connected from accessible metal parts of the case to ground. Measurements should be made with the unit ON and OFF, with the power line polarity Normal and Reversed. Record the highest reading of current. Figure 10-4 Set Up for Chassis Source Leakage Current, IEC 601-1 Clause 19 - Continuos Leakage Currents and Patient, Auxiliary Currents When using the Microguard or a similar test instrument, its power plug may be inserted into the wall outlet and the equipment under test is plugged into the receptacle on the panel of the meter. This places the meter in the grounding conductor and the current flowing from the case to ground will be indicated in any of the current ranges. The maximum allowable limit for chassis source leakage is shown in Table 10-14. Section 10-4 - Tools Required 10 - 11

[Page 164] 10-4-8-3 Dale 600 Meter Procedure When measuring system chassis currents with the Dale 600, always use the CHASSIS selection of the external/chassis function switch. This requires the ground clip lead and changing the meters switches in accordance with the IEC 601-1.1. refer to the Dale 600 Instruction Manual for meter self-test and operation. Record the highest leakage current measured. Follow these steps to test the unit for leakage current. 1.) Turn the LOGIQ C Series unit OFF. 2.) Plug the unit into the meter, and the meter into the tested AC wall outlet 3.) Plug the black chassis cable into the meter's “CHASSIS” connector and attach the black chassis cable clamp to an exposed metal part of the LOGIQ C Series. 4.) Set the tester's “FUNCTION” switch to CHASSIS position. 5.) Follow the test conditions described for respective test points shown in Table 10-9. Table 10-9 Chassis Leakage Current Test Condition TEST CONDITION 1 Mounting screw for probe receptacle 2 caster support 3 Mounting screw for CRT housing 4 Mounting screw for peripheral plugged into unit 5 Mounting screw for other peripheral powered by unit 6.) Keep a record of the results with other hard copies of PM data kept on site. 10-4-8-4 Dale 600 Meter Procedure The Dale 600 provides five snap type ECG buttons for testing patient leads. Snap on all patient leads to the meter and assure that the ground clip is connected to the system’s ground terminal. Select the meter’s LEAD-GND function. Select and test each ECG lead positions (except “ALL”) of the LEAD selector, testing each to the power condition combinations found in “PATIENT LEAD LEAKAGE” table in the “PM CHECKLIST”. Record the highest leakage current measured for each Power selection. Line voltage is applied to the ECG leads during this test. To avoid possible electric shock CAUTION hazard, the system being tested must not be touched by patients, users or anyone while the ISO TEST switch is depressed. When the meter's ground switch is OPEN, don't touch the unit! Follow these steps to test the ECG module for leakage current. 1.) Turn the LOGIQ C Series unit OFF. 2.) Plug the unit into the meter, and the meter into the tested AC wall outlet. 3.) Plug the black chassis cable into the meter's “CHASSIS” connector and attach the black chassis cable clamp to an exposed metal part of the LOGIQ C Series unit. 4.) Connect the patient leads to the corresponding snaps located at the upper front of the Dale 600/ 600E. Lead nomenclature for this test is not important. 10 - 12 Section 10-4 - Tools Required

[Page 165] 10-4-8-4 Dale 600 Meter Procedure (cont’d) 5.) Set the meter's “FUNCTION” switch to LEAD TO GROUND position to measure the patient lead to ground leakage current. 6.) Select and test each ECG lead positions (except ALL) of the LEAD selector, testing each to the power condition combinations. Table 10-10 Testing Power Conditions ECG Power Meter’s Polarity Switch Meter’s Neutral Switch ON NORM CLOSED ON NORM OPEN ON REVERSE CLOSED ON REVERSE OPEN OFF NORM CLOSED OFF NORM OPEN OFF REVERSE CLOSED OFF REVERSE OPEN Section 10-4 - Tools Required 10 - 13

[Page 166] 10-4-8-4 Dale 600 Meter Procedure (cont’d) 7.) Record the patient lead to ground leakage current measured on the data sheet. 8.) Set the meter's “FUNCTION” switch to LEAD TO LEAD position to measure the lead to lead leakage current. 9.) Select and test each ECG lead positions (except ALL) of the LEAD selector, testing each to the power condition combinations. 10.)Record the lead to lead leakage current measured on the data sheet. 11.)Set the meter's “FUNCTION” switch to LEAD ISO position to measure the patient lead isolation current. 12.)Select and test each ECG lead positions (except ALL) of the LEAD selector, testing each to the power condition combinations. 13.)Depress the rocker switch to ISO TEST and read the isolation current. To apply the voltage to the lead safely, the voltage is only applied when the rocker switch is depressed to ISO TEST. 14.)Record the patient lead isolation current measured on the data sheet. 10-4-9 Isolated Patient Lead (Source) Leakage–Lead to Lead reference the procedure in the IEC 60601-1. When using the Dale 600, switch the meter’s function selector to the LEAD-LEAD position. Select and test each of the five ECG lead positions (except ALL) on the LEAD selector, testing each to the power condition combinations found in the table. Record the highest leakage current measured. 10-4-9-1 Dale 600 Patient Lead Tests NEUTRAL POLARITY 1.) Closed Normal 2.) Open Normal 3.) Closed Reversed 4.) Open Reversed 10-4-10 Isolated Patient Lead (Sink) Leakage-Isolation Test reference the procedure in the IEC 60601-1. When using the Dale 600, switch the meter’s function selector to the LEAD-ISO. Select the ALL position on the lead selector. Depress the rocker switch to ISO TEST to test lead isolation. CAUTION Line voltage is applied to the ECG leads during this test. To avoid possible electric shock hazard, the system being tested must not be touched by patients, users or anyone while the ISO TEST switch is depressed. NOTE: It is not necessary to test each lead individually or power condition combinations as required in previous tests. 10 - 14 Section 10-4 - Tools Required

[Page 167] 10-4-10-1 Data Sheet for ECG Leakage Current The test passes when all readings measure less than the value shown in the table below. Record all data on the PM Inspection Certificate. Table 10-11 Maximum Allowance Limit for ECG Leakage Current Maximum Allowance Limit AC Power GROUND Source GROUND OPEN CLOSED Patient Lead to Ground Leakage Current Test 115V 10uA 10uA and 220/240V 500uA 10uA Patient Lead to Lead Leakage Current Test Table 10-12 Maximum Allowance Limit for ECG Leakage Current AC Power Maximum Source Allowance Limit 115V 20uA Patient Lead Isolation Current Test 220/240V 5mA Table 10-13 Typical Data Sheet for ECG Leakage Current Tester Tester Tester Lead Selector ECG Polarity Ground Power Switch Switch RL RA LA LL C ON NORM CLOSED ON REVERSE CLOSED ON NORM OPEN ON REVERSE OPEN OFF NORM CLOSED OFF REVERSE CLOSED OFF NORM OPEN OFF REVERSE OPEN Section 10-4 - Tools Required 10 - 15

[Page 168] 10-4-11 Probe Leakage Current Test 10-4-11-1 Definition This test measures the current that would flow to ground from any of the probes through a patient who is being scanned and becomes grounded by touching some other grounded surface. 10-4-11-2 Generic Procedure Measurements should be made with the ground open and closed, with power line polarity normal and reversed, and with the unit Off and On. For each combination, the probe must be active to find the worst case condition. POLARITY REVERSING SWITCH H (BLACK) PROBE CONSOLE N (WHITE) POWER OUTLET G (GREEN) MOMENTARY SWITCH LEAKAGE TEST METER Figure 10-5 Set Up for Probe Leakage Current NOTE: Each probe will have some amount of leakage current, dependent on its design. Small variations in probe leakage currents are normal from probe to probe. Other variations will result from differences in line voltage and test lead placement. 10-4-11-3 Meter Procedure Using Probe Adapter The Dale 600/600E provides a method for testing probes independently from the system. The meter utilizes a probe adapter to apply a test potential commonly to all connector pins. The probe's imaging area is immersed in a saline solution along with a grounding probe from the meter to complete the current path. Saline solution is a mixture of water and salt. The salt adds a free ion to the water, making it conductive. Normal saline solution is 0.9% salt or 1/2 gram salt per 1 liter of water. If saline is not available, a mixture of 1 quart water with one or more grams of table salt, mixed thoroughly, will substitute. To avoid probe damage and possible electric shock, do not immerse probes into any liquid CAUTION beyond the level indicated in the probe users manual. Do not touch the probe, conductive liquid or any part of the unit under test while the ISO TEST switch is depressed. Follow these steps to test each transducer for leakage current. 1.) Turn the LOGIQ C Series unit OFF. 2.) Plug the unit into the test meter, and the meter into the tested AC wall outlet. 3.) Connect the probe for test with the meter's appropriate adapter. 4.) Plug the saline probe into the meter's “CHASSIS” connector. 5.) Plug the probe adapter into the meter's connector marked “EXTERNAL”. 10 - 16 Section 10-4 - Tools Required

[Page 169] 10-4-11-3 Meter Procedure Using Probe Adapter (cont’d) Figure 10-6 Transducer Source Leakage Current Test 6.) Set the meter's “FUNCTION” switch to EXTERNAL position. 7.) Add the saline probe and the imaging area of the probe into the saline bath. 8.) Have unit power ON for the first part; turn it OFF for the second half. 9.) Depress the ISO TEST rocker switch and record the highest current reading. 10.)Follow the test conditions described in Table 10-14 for every transducer. 11.)Keep a record of the results with other hand copies of PM data. Section 10-4 - Tools Required 10 - 17

[Page 170] 10-4-11-4 No Meter Probe Adapter Procedure Figure 10-7 Check Without Probe Adapter Follow these steps to test each transducer for leakage current. 1.) Turn the LOGIQ C Series unit OFF. 2.) Plug the unit into the test meter, and the meter into the tested AC wall outlet. 3.) Plug the external probe into the meter's (Dale 600) “EXTERNAL” connector. 4.) Set the meter's “FUNCTION” switch to EXTERNAL position. 5.) Connect the probe for test with the connector of the console. 6.) Add the saline probe and the imaging area of the probe into the saline bath. 7.) Have unit power ON for the first part; turn it OFF for the second half. 8.) Depress the ISO TEST rocker switch and record the highest current reading. 9.) Follow the test conditions described in Table 10-14 for every transducer. 10.)Keep a record of the results with other hand copies of PM data. 10 - 18 Section 10-4 - Tools Required

[Page 171] 10-4-11-5 Data Sheet for Transducer Source Leakage Current The test passes when all readings measure less than the values. Record all data on the PM Inspection Certificate. Equipment damage possibility. Never switch the Polarity and the status of Neutral when the unit CAUTION is powered ON. Be sure to turn the unit power OFF before switching them using the POLARITY switch and/or the NEUTRAL switch. Otherwise, the unit may be damaged Table 10-14 Typical Data Sheet For Transducer Source Leakage Current Transducer Tested: Tester Power Polarity Tester GROUND or Unit Power Switch NEUTRAL Switch Measurement ON NORM OPEN ON NORM CLOSED ON REV OPEN ON REV CLOSED OFF NORM OPEN OFF NORM CLOSED OFF REV OPEN OFF REV CLOSED Section 10-4 - Tools Required 10 - 19

[Page 172] Section 10-5 When There's Too Much Leakage Current... CHASSIS FAILS Check the ground on the power cord and plug for continuity. Ensure the ground is not broken, frayed, or intermittent. Replace any defective part. Tighten all grounds. Ensure star washers are under all ground studs. Inspect wiring for bad crimps, poor connections, or damage. Test the wall outlet; verify it is grounded and is free of other wiring abnormalities. Notify the user or owner to correct any deviations. As a work around, check the other outlets to see if they could be used instead. NOTE: No outlet tester can detect the condition where the white neutral wire and the green grounding wire are reversed. If later tests indicate high leakage currents, this should be suspected as a possible cause and the outlet wiring should be visually inspected. PROBE FAILS Test the probe in another connector to isolate if the fault lies with the probe or the scanner. NOTE: Each probe will have some amount of leakage, dependent on its design. Small variations in probe leakage currents are normal from probe to probe. Other variations will result from differences in line voltage and test lead placement. The maximum allowable leakage current for body surface contact probe differs from inter-cavity probe. Be sure to enter the correct probe type in the appropriate space on the check list. If excessive leakage current is slot dependent, inspect the system connector for bent pins, poor connections, and ground continuity. If the problem remains with the probe, replace the probe. PERIPHERAL FAILS Tighten all grounds. Ensure star washers are under all ground studs. Inspect wiring for bad crimps, poor connections, or damage. STILL FAILS If all else fails, begin isolation by removing the probes, external peripherals, then the on board ones, one at a time while monitoring the leakage current measurement. NEW UNIT If the leakage current measurement tests fail on a new unit and if situation can not be corrected, submit a Safety Failure Report to document the system problem. Remove unit from operation. ECG FAILS Inspect cables for damage or poor connections. 10 - 20 Section 10-5 - When There's Too Much Leakage Current...

[Page 173] ULTRASOUND INSPECTION CERTIFICATE Customer Name: System ID: Dispatch Number / Date Performed: Warranty/Contract/HBS System Type Model Number: Serial Number: Manufacture Date: Probe 1: Frequency: Scan Format*: Model Number: Serial Number: Probe 2: Frequency: Scan Format*: Model Number: Serial Number: Probe 3: Frequency: Scan Format*: Model Number: Serial Number: Probe 4: Frequency: Scan Format*: Model Number: Serial Number: Probe 5: Frequency: Scan Format*: Model Number: Serial Number: Probe 6: Frequency: Scan Format*: Model Number: Serial Number: Probe 7: Frequency: Scan Format*: Model Number: Serial Number: Probe 8: Frequency: Scan Format*: Model Number: Serial Number: Probe 9: Frequency: Scan Format*: Model Number: Serial Number: * Scan Format: Phased Array, Linear Array, Curved Array, Mechanical Array or Other FUNCTIONAL CHECKS PHYSICAL INSPECTION AND CLEANING OK? or Physical Inspection and Cleaning Functional Check (if applicable) N/A (if applicable) Inspect Clean B-Mode Function Console Doppler Modes Function Monitor CF-Mode Function Touch Panel M-Mode Function Air Filter Applicable Software Options Probe Holders Applicable Hardware Options External I/O Control Panel Wheels, Brakes & Swivel Locks Monitor Cables and Connectors GE Approved Peripherals (VCR, CD-RW, MOD, Touch Panel Printers) Measurement Accuracy GE Approved Peripherals COMMENTS: ______________________________________________________________________________ ______________________________________________________________________________ ______________________________________________________________________________ ______________________________________________________________________________ Section 10-5 - When There's Too Much Leakage Current... 10 - 21

[Page 174] ELECTRICAL SAFETY Max Value Value Electrical Test Performed Allowed Measured OK? Comments Outlet (correct ground &wiring config.) System Ground Continuity Chassis Source Leakage Current - Probe Chassis Source Leakage Current - Caster Chassis Source Leakage Current - CRT Patient Lead Source Leakage (Lead to Ground) Patient Lead Source Leakage (Lead to Lead) Patient Lead Source Leakage (Isolation) Peripheral 1 Leakage Current Peripheral 1Ground Continuity Peripheral 2 Leakage Current Peripheral 2Ground Continuity Peripheral 3 Leakage Current Peripheral 3Ground Continuity PROBES Probe Number Max Value Max Value (from previous page) Allowed Measured OK? Comments Probe 1: Probe 2: Probe 3: Probe 4: Probe 5: Probe 6: Probe 7: Probe 8: Probe 9: Final Check. All system covers are in place. System scans with all probes as expected. Accepted by: ______________________________________________________________________ 10 - 22 Section 10-5 - When There's Too Much Leakage Current...

[Page 175] GE VINGMED ULTRASOUND INDEX A,B Functional Checks, 4-1 Abbreviations, 9-1 Basic Measurements, 4-23 Archiving Images Control Panel, 4-6 Move, 4-29 Image Management, 4-25 Backup Monitor Display, 4-8 Patient Database, 4-26 Peripherals, 4-35 Preset Configurations, 4-26 Probes/Connector Usage, 4-24 Basic Measurements Functional Checks, 4-23 Body pattern G display location, 4-8 Gathering Trouble Data, 7-2 Boot Up, 3-10 General Cleaning, 10-7 Gray/color bar display location, 4-8 Caps lock display location, 4-8 H CE Compliance, 1-23 Hazard Icons, 1-4 Cine gauge Hospital name display location, 4-8 display location, 4-8 Color Mode Human Safety, 1-8 Overview, 4-15 Connectivity Worksheet, 3-20 Contact Information, 1-24 Image Management Control Panel, 4-6 Functional Checks, 4-25 Customer Assistance, 1-24 Image preview display location, 4-8 Imaging parameters D display location, 4-8 Dangerous Procedure Warnings, 1-22 Institution name Date/Time display location, 4-8 display location, 4-8 Depth scale display location, 4-8 DICOM Network Function, 2-9 Measurement summary window display location, 4-8 Mechanical Safety, 1-8 E Media Electrical Safety, 1-9 Formatting, 4-26 Electrostatic Discharge Warning, 1-23 Monitor Display EMI, 1-23 Functioanl Checks, 4-8 ESD, 1-23 Monitor display Exam study location, 4-8 display location, 4-8 Move Archiving Images, 4-29 Focal zone O display location, 4-8 Index I

[Page 176] Operator identification Vital System Information, 7-2 display location, 4-8 P Ultrasound Room Layout, 2-8 P4 Key Function, 7-4, , 7-6 Patient identification display location, 4-8 V Patient name Voltage Settings, 3-9 display location, 4-8 PC Diagnostics, 7-10 Hard Drive Tests, 7-10 Keyboard Test, 7-11 Warnings and Cautions, 1-8 Memory Tests, 7-10 PC Diagnostics (Interactive Tests), 7-11 Peripherals Functional Checks, 4-35 Power On, 3-10 Power-up Procedures Voltage Settings, 3-9 Probe identifier display location, 4-8 Probe orientation marker display location, 4-8 Probes/Connector Usage Functional Checks, 4-24 Product Icons, 1-5 Required Features, 2-7 Restore Patient Database, 4-28 Preset Configurations, 4-28 Safety Considerations, 1-8 Screen Captures, 7-6 Service Manual Purpose of, 1-1 System Manufacturer, 1-25 TGC display location, 4-8 Touch Panel Functional Checks, 4-6 Trouble Image with Logs, 7-3 Troubleshooting Gathering Trouble Data, 7-2 Screen Captures, 7-6 Trouble Image with Logs, 7-3 II Index

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