General Electric LOGIQ 7 SERVICE MANUAL_SM_2286865_14 BENCH FUME HOOD with Auto-return Sash LV05 Style Installation Instructions

Download

Technical Publication

Direction 2286865 REVISION 14

GE Healthcare

LOGIQ™ 7 Service Manual

EALTHCARE

GE H D

IRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

Important Precautions

• THIS SERVICE MANUAL IS AVAILABLE IN ENGLISH ONLY.

• IF A CUSTOMER’S SERVICE PROVIDER REQUIRES A LANGUAGE OTHER THAN ENGLISH, IT IS THE CUSTOMER’S RESPONSIBILITY TO PROVIDE TRANSLATION SERVICES.

WARNING

AVERTISSEMENT

• DO NOT ATTEMPT TO SERVICE THE EQUIPMENT UNLESS THIS SERVICE MANUAL HAS BEEN CONSULTED AND IS UNDERSTOOD.

• FAILURE TO HEED THIS WARNING MAY RESULT IN INJURY TO THE SERVICE PROVIDER, OPERATOR OR PATIENT FROM ELECTRIC SHOCK, MECHANICAL OR OTHER HAZARDS.

• CE MANUEL DE MAINTENANCE N’EST DISPONIBLE QU’EN ANGLAIS.

• SI LE PRESTATAIRE DE SERVICES DU CLIENT A BESOIN DE CE MANUEL DANS UNE AUTRE LANGUE QUE L’ANGLAIS, IL INCOMBE AU CLIENT DE LE FAIRE TRADUIRE.

• NE PAS TENTER D’INTERVENTION SUR LES é QUIPEMENTS TANT QUE LE MANUEL DE MAINTENANCE N’A PAS éTé CONSULTé ET COMPRIS.

• LE NON-RESPECT DE CET AVERTISSEMENT PEUT ENTRAîNER CHEZ LE TECHNICIEN, L’OPéRATEUR OU LE PATIENT DES BLESSURES DUES à DES DANGERS éLECTRIQUES, Mé CANIQUES OU AUTRES.

WARNUNG

• DIESES KUNDENDIENST-HANDBUCH EXISTIERT NUR IN ENGLISCHER SPRACHE.

• FALLS EIN FREMDER KUNDENDIENST EINE ANDERE SPRACHE BENö TIGT, IST ES AUFGABE DES KUNDEN, FüR EINE ENTSPRECHENDE ÜBERSETZUNG ZU SORGEN.

• WARTEN SIE DIESES GERÄT NUR, WENN SIE DIE ENTSPRECHENDEN ANWEISUNGEN IM KUNDENDIENST-HANDBUCH GELESEN HABEN UND NACHVOLLZIEHEN KÖNNEN.

• 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.

- i

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

• ESTE MANUAL DE SERVICIO Só LO ESTÁ DISPONIBLE EN INGLéS.

• SI ALGúN PROVEEDOR DE SERVICIOS AJENO A GEMS SOLICITA UN IDIOMA QUE NO SEA EL INGLéS, LA TRADUCCIÓN ES RESPONSABILIDAD DEL CLIENTE.

• NO SE DEBERá DAR SERVICIO Té CNICO AL EQUIPO SIN HABER

AV I S O

CONSULTADO Y COMPRENDIDO ESTE MANUAL DE SERVICIO.

• LA NO OBSERVANCIA DEL PRESENTE AVISO PUEDE DAR LUGAR A QUE EL PROVEEDOR DE SERVICIOS, EL USUARIO O EL PACIENTE SUFRAN LESIONES PROVOCADAS POR DESCARGAS ELéCTRICAS, PROBLEMAS MECÁNICOS O PELIGROS DE OTRA NATURALEZA.

• ESTE MANUAL DE ASSISTê NCIA TéCNICA Só SE ENCONTRA DISPONíVEL EM INGLê S.

• SE QUALQUER OUTRO SERVIç O DE ASSISTê NCIA TéCNICA, QUE Nã O A GEMS, SOLICITAR ESTES MANUAIS NOUTRO IDIOMA, é DA RESPONSABILIDADE DO CLIENTE FORNECER OS SERVIç OS DE TRADUç ã O.

ATENÇÃO

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

• O Nã O CUMPRIMENTO DESTE AVISO PODE PÔR EM PERIGO A SEGURANç A DO TéCNICO, OPERADOR OU PACIENTE DEVIDO A CHOQUES ELéTRICOS, MECâ NICOS OU OUTROS.

AVVERTENZA

HOIATUS

• IL PRESENTE MANUALE DI MANUTENZIONE è DISPONIBILE SOLTANTO IN INGLESE.

• SE UN ADDETTO ALLA MANUTENZIONE ESTERNO ALLA GEMS RICHIEDE IL MANUALE IN UNA LINGUA DIVERSA, IL CLIENTE è TENUTO A PROVVEDERE DIRETTAMENTE ALLA TRADUZIONE.

• SI PROCEDA ALLA MANUTENZIONE DELL’APPARECCHIATURA SOLO DOPO AVER CONSULTATO IL PRESENTE MANUALE ED AVERNE COMPRESO IL CONTENUTO.

• NON TENERE CONTO DELLA PRESENTE AVVERTENZA POTREBBE FAR COMPIERE OPERAZIONI DA CUI DERIVINO LESIONI ALL’ADDETTO ALLA MANUTENZIONE, ALL’UTILIZZATORE ED AL PAZIENTE PER FOLGORAZIONE ELETTRICA, PER URTI MECCANICI OD ALTRI RISCHI.

• KÄESOLEV TEENINDUSJUHEND ON SAADAVAL AINULT INGLISE KEELES.

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

• ä RGE ü RITAGE SEADMEID TEENINDADA ENNE EELNEVALT Kä ESOLEVA TEENINDUSJUHENDIGA TUTVUMIST JA SELLEST ARU SAAMIST.

• Kä ESOLEVA HOIATUSE EIRAMINE Võ IB Põ HJUSTADA TEENUSEOSUTAJA, OPERAATORI Võ I PATSIENDI VIGASTAMIST ELEKTRILö ö GI, MEHAANILISE Võ I MUU OHU TAGAJä RJEL.

ii -

EALTHCARE

GE H D

IRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

• TÄMÄ HUOLTO-OHJE ON SAATAVILLA VAIN ENGLANNIKSI.

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

• ä Lä YRITä KORJATA LAITTEISTOA ENNEN KUIN OLET VARMASTI LUKENUT

VAROITUS

JA YMMä RTä NYT Tä Mä N HUOLTO-OHJEEN.

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

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

• ΕΑΝ ΤΟ ΑΤΟΜΟ ΠΑΡΟΧΗΣ ΣΕΡΒΙΣ ΕΝΟΣ ΠΕΛΑΤΗ ΑΠΑΙΤΕΙ ΤΟ ΠΑΡΟΝ

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

• ΜΗΝ ΕΠΙΧΕΙΡΗΣΕΤΕ ΤΗΝ ΕΚΤΕΛΕΣΗ ΕΡΓΑΣΙΩΝ ΣΕΡΒΙΣ ΣΤΟΝ ΕΞΟΠΛΙΣΜΟ

ΠΡΟΕΙ∆ΟΠΟΙΗΣΗ

ΕΚΤΟΣ ΕΑΝ ΕΧΕΤΕ ΣΥΜΒΟΥΛΕΥΤΕΙ ΚΑΙ ΕΧΕΤΕ ΚΑΤΑΝΟΗΣΕΙ ΤΟ ΠΑΡΟΝ ΕΓΧΕΙΡΙ∆ΙΟ ΣΕΡΒΙΣ.

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

FIGYELMEZTETÉS

VIÐVÖRUN

• EZEN KARBANTARTÁSI KÉZIKÖNYV KIZÁRÓLAG ANGOL NYELVEN ÉRHETŐ EL.

• HA A VEVŐ SZOLGÁLTATÓJA ANGOLTÓL ELTÉRŐ NYELVRE TART IGÉNYT, AKKOR A VEVŐ FELELŐSSÉGE A FORDÍTÁS ELKÉSZÍTTETÉSE.

• NE PRÓBÁLJA ELKEZDENI HASZNÁLNI A BERENDEZÉST, AMÍG A KARBANTARTÁSI KÉZIKÖNYVBEN LEÍRTAKAT NEM ÉRTELMEZTÉK.

• EZEN FIGYELMEZTETÉS FIGYELMEN KÍVÜL HAGYÁSA A SZOLGÁLTATÓ, MŰKÖDTETŐ VAGY A BETEG ÁRAMÜTÉS, MECHANIKAI VAGY EGYÉB VESZÉLYHELYZET MIATTI SÉRÜLÉSÉT EREDMÉNYEZHETI.

• ÞESSI ÞJÓNUSTUHANDBÓK ER EINGÖNGU FÁANLEG Á ENSKU.

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

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

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

- iii

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

• TENTO SERVISNÍ NÁVOD EXISTUJE POUZE V ANGLICKé M JAZYCE.

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

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

VÝSTRAHA

TENTO SERVISNÍ NÁVOD A POCHOPILI JEHO OBSAH.

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

• DENNE SERVICEMANUAL FINDES KUN PÅ ENGELSK.

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

• FORSØG IKKE AT SERVICERE UDSTYRET MEDMINDRE

ADVARSEL

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.

WAARSCHUWING

BRÎDINÂJUMS

• DEZE ONDERHOUDSHANDLEIDING IS ENKEL IN HET ENGELS VERKRIJGBAAR.

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

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

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

• ðÎ APKALPES ROKASGRÂMATA IR PIEEJAMA TIKAI ANGÏU VALODÂ.

• JA KLIENTA APKALPES SNIEDZÇJAM NEPIECIEÐAMA INFORMÂCIJA CITÂ VALODÂ, NEVIS ANGÏU, KLIENTA PIENÂKUMS IR NODROÐINÂT TULKOÐANU.

• NEVEICIET APRÎKOJUMA APKALPI BEZ APKALPES ROKASGRÂMATAS IZLASÎÐANAS UN SAPRAÐANAS.

• ÐÎ BRÎDINÂJUMA NEIEVÇROÐANA VAR RADÎT ELEKTRISKÂS STRÂVAS TRIECIENA, MEHÂNISKU VAI CITU RISKU IZRAISÎTU TRAUMU APKALPES SNIEDZÇJAM, OPERATORAM VAI PACIENTAM.

iv -

EALTHCARE

GE H D

IRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

• ÐIS EKSPLOATAVIMO VADOVAS YRA IÐLEISTAS TIK ANGLØ KALBA.

• JEI KLIENTO PASLAUGØ TEIKËJUI REIKIA VADOVO KITA KALBA – NE ANGLØ, VERTIMU PASIRÛPINTI TURI KLIENTAS.

• NEMËGINKITE ATLIKTI ÁRANGOS TECHNINËS PRIEÞIÛROS DARBØ, NEBENT

ÁSPËJIMAS

VADOVAUTUMËTËS ÐIUO EKSPLOATAVIMO VADOVU IR JÁ SUPRASTUMËTE

• NEPAISANT ÐIO PERSPËJIMO, PASLAUGØ TEIKËJAS, OPERATORIUS AR PACIENTAS GALI BÛTI SUÞEISTAS DËL ELEKTROS SMÛGIO, MECHANINIØ AR KITØ PAVOJØ.

• DENNE SERVICEHÅNDBOKEN FINNES BARE PÅ ENGELSK.

• HVIS KUNDENS SERVICELEVERANDØR TRENGER ET ANNET SPRÅK, ER DET KUNDENS ANSVAR Å SØRGE FOR OVERSETTELSE.

• IKKE FORSØK Å REPARERE UTSTYRET UTEN AT DENNE

ADVARSEL

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.

OSTRZEŻENIE

ATE NŢIE

• NINIEJSZY PODRĘCZNIK SERWISOWY DOSTĘPNY JEST JEDYNIE W JĘZYKU ANGIELSKIM.

• JEśLI FIRMA śWIADCZĄCA KLIENTOWI USłUGI SERWISOWE WYMAGA UDOSTęPNIENIA PODRę CZNIKA W JęZYKU INNYM NIŻ ANGIELSKI, OBOWIĄZEK ZAPEWNIENIA STOSOWNEGO TłUMACZENIA SPOCZYWA NA KLIENCIE.

• NIE PRó BOWAć SERWISOWAć NINIEJSZEGO SPRZęTU BEZ UPRZEDNIEGO ZAPOZNANIA SIę Z PODRęCZNIKIEM SERWISOWYM.

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

• ACEST MANUAL DE SERVICE ESTE DISPONIBIL NUMAI ÎN LIMBA ENGLEZĂ.

• DACĂ UN FURNIZOR DE SERVICII PENTRU CLIENŢI NECESITĂ O ALTĂ LIMBĂ DECÂT CEA ENGLEZĂ, ESTE DE DATORIA CLIENTULUI SĂ FURNIZEZE O TRADUCERE.

• NU ÎNCERCAŢI SĂ REPARAŢI ECHIPAMENTUL DECÂT ULTERIOR CONSULTĂRII I ÎNŢELEGERII ACESTUI MANUAL DE SERVICE.

• IGNORAREA ACESTUI AVERTISMENT AR PUTEA DUCE LA RĂNIREA DEPANATORULUI, OPERATORULUI SAU PACIENTULUI ÎN URMA PERICOLELOR DE ELECTROCUTARE, MECANICE SAU DE ALTĂ NATURĂ.

- v

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

• Данное рук о во дс тв о по обслуживанию ПРЕДОСТАВЛЯЕТСЯ только на английском Язы ке .

• Ес ли сервисноМУ ПЕРСОНАЛУ клиента необходимо рук о во дс тво

не на английском ЯЗЫКЕ, клиенту следует самостоЯтельно ОБЕСПЕЧИТЬ перевод.

ОСТОРОЖНО!

• ПЕРЕД ОБСЛУЖИВАНИЕМ ОБОРУДОВАНИЯ ОБЯЗАТЕЛЬНО ОБРАТИТЕСЬ К ДАННОМУ РУКОВОДСТВУ И ПОЙМИТЕ ИЗЛОЖЕННЫЕ В НЕМ СВЕДЕНИЯ.

• НЕСОБЛЮДЕНИЕ УКАЗАННЫХ ТРЕБОВАНИЙ МОЖЕТ ПРИВЕСТИ К ТОМУ, ЧТО СПЕЦИАЛИСТ ПО ТЕХОБСЛУЖИВАНИЮ, ОПЕРАТОР ИЛИ ПАЦИЕНТ ПОЛУЧАТ УДАР ЗЛЕКТРИЧЕСКИМ ТОКОМ, МЕХАНИЧЕСКУЮ ТРАВМУ ИЛИ ДРУГОЕ ПОВРЕЖДЕНИЕ.

• TÁTO SERVISNÁ PRÍRUČKA JE K DISPOZíCII LEN V ANGLIČTINE.

• AK ZÁKAZNÍKOV POSKYTOVATEĽ SLUŽIEB VYŽADUJE INÝ JAZYK AKO ANGLIČTINU, POSKYTNUTIE PREKLADATEĽSKÝCH SLUŽIEB JE ZODPOVEDNOSŤOU ZÁKAZNÍKA.

• NEPOKÚŠAJTE SA VYKONÁVAŤ SERVIS ZARIADENIA SKÔR, AKO SI

UPOZORNENIE

NEPREČÍTATE SERVISNÚ PRÍRUČKU A NEPOROZUMIETE JEJ.

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

VARNING

DKKAT

• DEN HÄR SERVICEHANDBOKEN FINNS BARA TILLGÄNGLIG PÅ ENGELSKA.

• OM EN KUNDS SERVICETEKNIKER HAR BEHOV AV ETT ANNAT SPRÅK ÄN ENGELSKA ANSVARAR KUNDEN FÖR ATT TILLHANDAHÅLLA ÖVERSÄTTNINGSTJÄNSTER.

• FÖRSÖK INTE UTFÖRA SERVICE PÅ UTRUSTNINGEN OM DU INTE HAR LÄST OCH FÖRSTÅR DEN HÄR SERVICEHANDBOKEN.

• OM DU INTE TAR HÄNSYN TILL DEN HÄR VARNINGEN KAN DET RESULTERA I SKADOR PÅ SERVICETEKNIKERN, OPERATÖREN ELLER PATIENTEN TILL FÖLJD AV ELEKTRISKA STÖTAR, MEKANISKA FAROR ELLER ANDRA FAROR.

• BU SERVS KILAVUZU YALNIZCA NGLZCE OLARAK SAĞLANMITIR.

• EĞER MÜTER TEKNSYEN KILAVUZUN NGLZCE DIINDAK BR DLDE OLMASINI STERSE, KILAVUZU TERCÜME ETTRMEK MÜTERNN SORUMLULUĞUNDADIR.

• SERVS KILAVUZUNU OKUYUP ANLAMADAN EKPMANLARA MÜDAHALE ETMEYNZ.

• BU UYARININ GÖZ ARDI EDLMES, ELEKTRK ÇARPMASI YA DA MEKANK VEYA DĞER TÜRDEN KAZALAR SONUCUNDA TEKNSYENN, OPERATÖRÜN YA DA HASTANIN YARALANMASINA YOL AÇABLR.

vi -

EALTHCARE

GE H D

IRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

- vii

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

DAMAGE IN TRANSPORTATION

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

CERTIFIED ELECTRICAL CONTRACTOR STATEMENT

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 Medical Systems 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 Medical Systems 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 Medical Systems employees should use the iTrak System to report all documentation errors or omissions.

viii -

EALTHCARE

GE H D

IRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

LEGAL NOTES

The contents of this publication may not be copied or duplicated in any form, in whole or in part, without prior written permission of GE Medical Systems.

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

PROPRIETARY TO GE MEDICAL SYSTEMS

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

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

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

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

TRADEMARKS

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

COPYRIGHTS

- ix

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

x -

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

Revision History

Revision Date Reason for change

0 September 1, 2001 Initial Release

1 November 20, 2001 Revision 1

Electrical Requirements (sec2), STCW and TXCW theory, Monitor video

2 February 22, 2002

3 November 11, 2002

specification (sec5), TRAP2 Dip SW, QCON Dip SW, LV2 unit released,Trackball cleaning (sec 6), New diagnostics (sec 7), New LFC procedure added (sec8), New part number (sec9)

Probe precaution (sec1), Optional peripherals (sec3), Dongles (sec5), Trackball cleaning, Jumper and Dip switch setting (sec6), Diagnostics (sec7), PC box replacement, software loading for R2 (sec8), New part number (sec9),

4 April 2, 2003

5 October 22, 2003

6 September 17, 2004 BT04

7 March 3, 2005 For L7Pro: Renewal Parts (sec9), Component Replacement (sec8)

8 September 30, 2005 BT06

9 June 26, 2006 BT06-2 released

10 September 22, 2006 Minor correction (sec 8), V65x (Sec1, Sec3, Sec5, Sec8, Sec9)

11 March 5, 2007 BT07 Supported

12 May 28, 2007 Setting Report Printer added (sec 8)

13 Oct.1, 2007 R7.5.x supported, other modifications (all sections)

14 July 16, 2008 BT09 newly released

Monitor and LCD Adjustment, DDBF and Trap settings (sec6), Keyboard FRU replacement (sec8), Renewal Parts (sec9)

Added: New Printer and probe (Sec. 3), HDD Jumper setting (sec 6), New PC box and DGVIC replacement, MOD setting, Service dongle notice at Ghost, R3 software, DVD, TxCW connection notice (sec 8), New spare parts (Sec. 9)

- xi

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

List of Effected Pages

PAGES REVISION PAGES REVISION PAGES REVISION

Title Page 14 1-1 to 1-23 14 Back Cover N/A

Warnings

i to v

Rev Hist/LOEP

vii to viii

Table of Contents

ix to xxiv

14 2-1 to 2-11 14

14 3-1 to 3-25 14

14 4-1 to 4-31 14

5-1 to 5-45 14

6-1 to 6-41 14

7-1 to 7-2 14

8-1 to 8-60 14

9-1 to 9-91 14

10-1 to 10-33 14

xii -

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

Table of Contents

CHAPTER 1

Introduction

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

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

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

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

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

LOGIQ™ 7 Models Covered by this Manual . . . . . . . . . . . . . . . . . . . . . . . .1 - 2

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

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

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

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

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 10

Human Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 10

Mechanical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 10

Electrical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 11

Label Locations (For BT07 or later, including R7.5.x) . . . . . . . . . . . . . . . . .1 - 12

Label Locations (For BT04, BT06, and V65x) . . . . . . . . . . . . . . . . . . . . . . .1 - 14

Lockout/Tagout Requirements (For USA Only) . . . . . . . . . . . . . . . . . . . . . .1 - 18

Returning/Shipping Probes and Repair Parts . . . . . . . . . . . . . . . . . . . . . . .1 - 18

How to remove the Ghost CD-ROM . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 19

Electromagnetic Compatibility . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 21

Electrostatic Discharge (ESD) Prevention . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 21

CE Compliance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 21

Customer Assistance. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 22

System Manufacture . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 22

Contact Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 22

CHAPTER 2

Pre Installation

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

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

Table of Contents xiii

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

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

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

Electrical Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 3

EMI Limitations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 5

Probes Environmental Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 6

Facility Needs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 7

Purchaser Responsibilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 7

Required Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 8

Desirable Ultrasound Room Facilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 8

Recommended and Alternate Ultrasound Room Layout . . . . . . . . . . . . . . .2 - 9

CHAPTER 3

Installation

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

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

Average Installation Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 1

Installation Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 2

Safety Reminders . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 5

Moving into Position . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 6

LCD Monitor Tilt Caution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 7

LCD Monitor Swing CautionLCD Monitor Tilt Caution . . . . . . . . . . . . . . . . .3 - 8

LCD Monitor Removal Caution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 9

Shipping Delivery Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 9

Preparing for Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 10

Verify Customer Order . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 10

Physical Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 10

EMI Protection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 10

Completing the Installation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 11

Probe (Transducer) Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 11

Optional Peripherals/Peripheral Connection . . . . . . . . . . . . . . . . . . . . . . . .3 - 12

Available Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 15

Video Specification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 17

Software Option Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 17

Installation Paperwork . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 18

Peripherals/Accessories Connector Panel . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 18

xiv -

EALTHCARE

GE H DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

CHAPTER 4

Functional Checks

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

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

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

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

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

Lockout/Tagout Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 2

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

Power Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 7

System Stand-by . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 7

Using CD-R/MOD/DVD Drive . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 9

Archiving and Loading Presets for BT07 (Including R7.5.x) . . . . . . . . . . . . 4 - 11

Archiving and Loading Presets for BT06/V65x or lower . . . . . . . . . . . . . . . 4 - 16

Basic Controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 20

Performance Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 20

Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 21

Basic Measurements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 21

ECG Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 22

Cineloop Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 22

Backend Processor Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 22

Probe/Connectors Usage (QG) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 22

Peripheral Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 23

Mechanical Functions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 24

Application Turnover Check List. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 27

Software Configuration Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 27

Diagnostics . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 28

Service Software Menu . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 28

Diagnostics Test Menu . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 28

Utility Menu . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 28

Power Supply . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 29

Power Supply Test Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 29

Power Supply Adjustment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 29

Site Log . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 30

- xv

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

CHAPTER 5

Components and Functions (Theory)

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

Hardware Compatibility Matrix. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 2

Hardware Compatibility BT09 or later . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 2

Hardware Identification Tip . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 8

Peripheral Compatibility . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 11

Block Diagrams and Theory. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 12

Block Diagram (R7.5.x or later, 19 inch LCD model) . . . . . . . . . . . . . . . . . .5 - 12

General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 13

CPU/Back End Processor (For BEP4 for BT09 or later) . . . . . . . . . . . . . . .5 - 14

CPU/Back End Processor (For BT06-2 or later) . . . . . . . . . . . . . . . . . . . . .5 - 21

Patient I/O (Option) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 23

External I/O (Rear Panel) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 23

Peripherals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 23

Interconnect Cabling (BT09 or later) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 24

Difference points between BT07 (or later) and BT06 (or earlier) Systems for R7.5.x 17"

to 19" LCD Monitor Upgrade . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 26

Common Service Platform. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 27

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 27

Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 36

Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 36

Replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 37

Remote Software/Option Installation and Updates . . . . . . . . . . . . . . . . . . .5 - 38

InSite II Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 39

Password . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 40

For Operator Login Window . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 40

For Service Login Window . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 40

For Maintenance Access Window . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 41

Air Flow Control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 42

Air Flow Distribution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 42

Filters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 42

Fans . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 43

Monitor Video Specification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 44

Input . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 44

xvi -

EALTHCARE

GE H DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

Outputs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 44

SVHS and Composite Video . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 45

CHAPTER 6

Service Adjustments

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

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

LV Unit Adjustments (For BT03 or lower) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 2

Access to Adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 2

Adjustments Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 3

Caster Brake/Swivel Function Adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 4

Brake Function Adjustment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 4

Swivel Function Adjustment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 8

Reloading the Probe Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 9

Monitor and LCD Adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 10

CRT Monitor Contrast and Brightness Adjustment . . . . . . . . . . . . . . . . . . . 6 - 10

19 inch LCD Monitor Brightness Adjustment . . . . . . . . . . . . . . . . . . . . . . . 6 - 12

17 inch LCD Monitor Contrast and Brightness Adjustment . . . . . . . . . . . . 6 - 13

LCD Monitor Resolution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 14

LCD Touch Panel Adjustment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 14

BW Printer Setting / Adjustment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 27

Parameters for UP-D897 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 27

Parameters for UP-D895 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 29

Service Tips - Print Quality . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 30

Service Tips - Print Speed . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 31

Cleaning the Trackball . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 33

Jumper and Dip Switch Setting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 37

Dip Switch Setting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 37

Jumper Setting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 39

Printer Dip Switch Setting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 39

- xvii

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

CHAPTER 7

Diagnostics/Troubleshooting

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

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

Diagnostic Procedure Summary . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 2

CHAPTER 8

Replacement Procedures

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

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

Returning/Shipping Probes and Repair Parts . . . . . . . . . . . . . . . . . . . . . . .8 - 1

Software Loading Procedures for BT09 (R8.x.x or later). . . . . . . . . . . . . . . . . . . . .8 - 3

CHAPTER 9

Renewal Parts

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

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

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

Renewal Parts List For BT09. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 2

BT09, 19inch LCD: Equipment Models Covered in this Chapter (LOGIQ 7) 9 - 2

BT09 Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 3

Renewal Parts List For R7.5.x . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 5

R7.5.x, 19inch LCD: Equipment Models Covered in this Chapter (LOGIQ 7) 9 - 5

R7.5.x Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 6

Renewal Parts List For BT07. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 8

BT07, CRT: Equipment Models Covered in this Chapter (LOGIQ 7) . . . . . .9 - 8

BT07, LCD: Equipment Models Covered in this Chapter (LOGIQ 7) . . . . . .9 - 9

BT07 PRO: Equipment Models Covered in this Chapter (LOGIQ 7 PRO) . .9 - 10

BT07 Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 11

Renewal Parts List For V65x . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 13

xviii -

EALTHCARE

GE H DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

V65x, CRT: Equipment Models Covered in this Chapter (LOGIQ 7) . . . . . 9 - 13

V65x, LCD: Equipment Models Covered in this Chapter (LOGIQ 7) . . . . . 9 - 14

V65x PRO: Equipment Models Covered in this Chapter (LOGIQ 7 PRO) . 9 - 15

V65x Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 16

Renewal Parts List For BT06-2 or later . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 17

BT06-2, CRT: Equipment Models Covered in this Chapter (LOGIQ 7) . . . 9 - 17 BT06-2, LCD: Equipment Models Covered in this Chapter (LOGIQ 7) . . . 9 - 18 BT06-2 PRO: Equipment Models Covered in this Chapter (LOGIQ 7 PRO) 9 - 19

BT06-2 Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 20

Renewal Parts List For BT06-2 CONSIP (SOI) . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 23

BT06-2 CONSIP: Equipment Models Covered in this Chapter (LOGIQ 7) . 9 - 23

BT06-2 CONSIP Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 24

Renewal Parts List For BT04 and BT06. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 25

BT06, CRT: Equipment Models Covered in this Chapter (LOGIQ 7) . . . . . 9 - 25

BT06, LCD: Equipment Models Covered in this Chapter (LOGIQ 7) . . . . . 9 - 26

BT06: Equipment Models Covered in this Chapter (LOGIQ 7 PRO) . . . . . 9 - 27

BT04: Equipment Models Covered in this Chapter (LOGIQ 7) . . . . . . . . . . 9 - 28

BT04: Equipment Models Covered in this Chapter (LOGIQ 7 PRO) . . . . . 9 - 29

Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 30

Casters and Pedals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 32

Plastic Covers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 34

Recording Devices . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 36

Probe Holder . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 37

OP Panel and Keys . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 38

Circuit Board Assemblies . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 40

HDD and Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 42

Power Units . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 44

Options, Peripherals and Cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 47

Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 52

LCD Option . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 54

Renewal Parts List for BT03 or lower . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 57

Equipment Models Covered in this Chapter . . . . . . . . . . . . . . . . . . . . . . . . 9 - 57

Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 60

Casters and Pedals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 62

Plastic Covers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 65

Recording Devices . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 67

Probe Holder . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 69

OP Panel and Keys . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 70

Circuit Board Assemblies . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 73

- xix

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

HDD and Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 75

Power Units . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 78

Options, Peripherals and Cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 80

Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 90

CHAPTER 10

Periodic Maintenance

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

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

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

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

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

Periodic Maintenance Schedule . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 2

How often should PMs be performed? . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 2

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

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

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

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

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

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

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

Using a Phantom . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 11

Electrical Safety Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 12

Safety Test Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 12

Grounding Continuity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 15

Isolated Patient Lead (Source) Leakage–Lead to Ground . . . . . . . . . . . . . .10 - 19

Isolated Patient Lead (Source) Leakage–Lead to Lead . . . . . . . . . . . . . . . .10 - 22

Isolated Patient Lead (Sink) Leakage-Isolation Test . . . . . . . . . . . . . . . . . .10 - 22

Probe Leakage Current Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 24

xx -

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

Chapter 1 Introduction

Section 1-1 Overview

1-1-1 Purpose of Chapter 1

This Chapter describes important issues related to safety servicing this ultrasound machine. The service provider must read and understand all the information presented here before installing or servicing a unit.

1-1-2 Chapter Contents

Table 1-1 Contents in Chapter 1

Section Description Page Number

1-1

1-2

1-3

1-4

1-5

Overview

Important Conventions

Safety Considerations

EMC, EMI, and ESD

Customer Assistance

1-1-3 Purpose of Service Manual

This manual provides service information on the LOGIQ™ 7 Ultrasound Scanning System. It contains the following chapters:

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

2.) Chapter 2, Pre-Installation: Contains any pre-installation requirements for the LOGIQ™ 7.

3.) Chapter 3, Installation: Contains the LOGIQ™ 7 installation procedure with installation

checklist.

4.) Chapter 4, Functional Checks: Contains functional checks that must be performed as part of

the installation, or as required during servicing and periodic maintenance.

5.) Chapter 5 Theory: Contains block diagrams and functional explanations of the LOGIQ™ 7

electronics.

6.) Chapter 6, Service Adjustments: Contains instructions on how to make any available

adjustments to the LOGIQ™ 7.

7.) Chapter 7, Diagnostics/Trouble Shooting: Provides procedures for running and diagnostic

or related routines for the LOGIQ™ 7.

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

procedures for all changeable FRU.

9.) Chapter 9, Renewal Parts: Contains a complete list of replacement parts for the LOGIQ™ 7.

10.)Chapter 10, Periodic Maintenance: Provides periodic maintenance procedures for the

LOGIQ™ 7.

1-1

1-5

1-10

1-21

1-22

Section 1-1 - Overview 1-1

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

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

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

• Hospital’s Service Personnel

• Architects (Some parts of Chapter 2 - Pre-Installation)

1-1-5 LOGIQ™ 7 Models Covered by this Manual

Table 1-2 LOGIQ™ 7 Model Designations

Part Number Description Reference Remarks

2287317 LOGIQ™ 7 100V / NTSC Console and Peripherals BT01

2304806 LOGIQ™ 7 120V / NTSC Console and Peripherals BT01

2304807 LOGIQ™ 7 220V / PAL Console and Peripherals BT01

2304808 LOGIQ™ 7 220V / NTSC Console and Peripherals BT01

2354857 LOGIQ™ 7 100V / NTSC Console and Peripherals (Style B/Ver2) BT02

2354858 LOGIQ™ 7 120V / NTSC Console and Peripherals (Style B/Ver2) BT02

2354859 LOGIQ™ 7 220V / PAL Console and Peripherals (Style B/Ver2) BT02

2354860 LOGIQ™ 7 220V / NTSC Console and Peripherals (Style B/Ver2) BT02

2355589 LOGIQ™ 7 100V / NTSC Console and Peripherals (Style B/Ver2) BT02

2389221 LOGIQ™ 7 100V / NTSC Console and Peripherals (Style C/Ver3) BT03

2389220 LOGIQ™ 7 120V / NTSC Console and Peripherals (Style C/Ver3) BT03

2389219 LOGIQ™ 7 220V / PAL Console and Peripherals (Style C/Ver3) BT03

2389218 LOGIQ™ 7 220V / NTSC Console and Peripherals (Style C/Ver3) BT03

2389217 LOGIQ™ 7 100V / NTSC Console and Peripherals (Style C/Ver3) BT03

5118055 LOGIQ™ 7 100V / NTSC Console and Peripherals (Style D/Ver4) BT04

5118056 LOGIQ™ 7 120V / NTSC Console and Peripherals (Style D/Ver4) BT04

5118057 LOGIQ™ 7 220V / PAL Console and Peripherals (Style D/Ver4) BT04

5118058 LOGIQ™ 7 220V / NTSC Console and Peripherals (Style D/Ver4) BT04

5118059 LOGIQ™ 7 100V / NTSC Console and Peripherals (Style D/Ver4) BT04

5148047 LOGIQ™ 7 100V / NTSC Console and Peripherals, CRT monitor (Style E) BT06 CRT

5148048 LOGIQ™ 7 120V / NTSC Console and Peripherals, CRT monitor (Style E) BT06 CRT

5148049 LOGIQ™ 7 220V / PAL Console and Peripherals, CRT monitor (Style E) BT06 CRT

5148050 LOGIQ™ 7 220V / NTSC Console and Peripherals, CRT monitor (Style E) BT06 CRT

5148052 LOGIQ™ 7 100V / NTSC Console and Peripherals, LCD monitor (Style E) BT06 LCD

5148053 LOGIQ™ 7 120V / NTSC Console and Peripherals, LCD monitor (Style E) BT06 LCD

5148054 LOGIQ™ 7 220V / PAL Console and Peripherals, LCD monitor (Style E) BT06 LCD

5148055 LOGIQ™ 7 220V / NTSC Console and Peripherals, LCD monitor (Style E) BT06 LCD

5148057 LOGIQ™ 7PRO 100V / NTSC Console and Peripherals (Style E) BT06 PRO

1-2 Section 1-1 - Overview

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

Table 1-2 LOGIQ™ 7 Model Designations

Part Number Description Reference Remarks

5148058 LOGIQ™ 7PRO 120V / NTSC Console and Peripherals (Style E) BT06 PRO

5148059 LOGIQ™ 7PRO 220V / PAL Console and Peripherals (Style E) BT06 PRO

5148060 LOGIQ™ 7 220V / NTSC Console and Peripherals (Style E) BT06 PRO

5176232 LOGIQ™ 7 100V / NTSC Console and Peripherals, CRT monitor BT06-2 CRT

5176567 LOGIQ™ 7 120V / NTSC Console and Peripherals, CRT monitor BT06-2 CRT

5176948 LOGIQ™ 7 220V / PAL Console and Peripherals, CRT monitor BT06-2 CRT

5176508 LOGIQ™ 7 220V / NTSC Console and Peripherals, CRT monitor BT06-2 CRT

5176713 LOGIQ™ 7 100V / NTSC Console and Peripherals, LCD monitor BT06-2 LCD

5176888 LOGIQ™ 7 120V / NTSC Console and Peripherals, LCD monitor BT06-2 LCD

5176300 LOGIQ™ 7 220V / PAL Console and Peripherals, LCD monitor BT06-2 LCD

5176380 LOGIQ™ 7 220V / NTSC Console and Peripherals, LCD monitor BT06-2 LCD

5176619 LOGIQ™ 7PRO 100V / NTSC Console and Peripherals BT06-2 PRO

5176454 LOGIQ™ 7PRO 120V / NTSC Console and Peripherals BT06-2 PRO

5176439 LOGIQ™ 7PRO 220V / PAL Console and Peripherals BT06-2 PRO

5176774 LOGIQ™ 7 220V / NTSC Console and Peripherals BT06-2 PRO

5179605 LOGIQ™ 7PRO 220V / PAL Console and Peripherals, LCD monitor BT06-2 CONSIP

5183269 LOGIQ™ 7 100V / NTSC Console and Peripherals, CRT monitor V65x CRT

5183237 LOGIQ™ 7 120V / NTSC Console and Peripherals, CRT monitor V65x CRT

5183396 LOGIQ™ 7 220V / PAL Console and Peripherals, CRT monitor V65x CRT

5183304 LOGIQ™ 7 220V / NTSC Console and Peripherals, CRT monitor V65x CRT

5183330 LOGIQ™ 7 100V / NTSC Console and Peripherals, LCD monitor V65x LCD

5183410 LOGIQ™ 7 120V / NTSC Console and Peripherals, LCD monitor V65x LCD

5183412 LOGIQ™ 7 220V / PAL Console and Peripherals, LCD monitor V65x LCD

BT06 New

Hardware -

requires

software R6.2.x

or later

SOI (BT06-2

PRO with LCD)

5183190 LOGIQ™ 7 220V / NTSC Console and Peripherals, LCD monitor V65x LCD

5183352 LOGIQ™ 7PRO 100V / NTSC Console and Peripherals V65x PRO

5183136 LOGIQ™ 7PRO 120V / NTSC Console and Peripherals V65x PRO

5183125 LOGIQ™ 7PRO 220V / PAL Console and Peripherals V65x PRO

5183515 LOGIQ™ 7PRO 220V / NTSC Console and Peripherals V65x PRO

5191090 LOGIQ™ 7 100V / NTSC Console and Peripherals, CRT monitor (Style H) BT07 CRT

5191824 LOGIQ™ 7 120V / NTSC Console and Peripherals, CRT monitor (Style H) BT07 CRT

5191341 LOGIQ™ 7 220V / PAL Console and Peripherals, CRT monitor (Style H) BT07 CRT

5191701 LOGIQ™ 7 220V / NTSC Console and Peripherals, CRT monitor (Style H) BT07 CRT

5191499 LOGIQ™ 7 100V / NTSC Console and Peripherals, LCD monitor (Style H) BT07 LCD

5191946 LOGIQ™ 7 120V / NTSC Console and Peripherals, LCD monitor (Style H) BT07 LCD

Section 1-1 - Overview 1-3

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

Table 1-2 LOGIQ™ 7 Model Designations

Part Number Description Reference Remarks

5191853 LOGIQ™ 7 220V / PAL Console and Peripherals, LCD monitor (Style H) BT07 LCD

5191441 LOGIQ™ 7 220V / NTSC Console and Peripherals, LCD monitor (Style H) BT07 LCD

5191006 LOGIQ™ 7 100V / NTSC Console and Peripherals (Style H) BT07 PRO

5191258 LOGIQ™ 7 120V / NTSC Console and Peripherals (Style H) BT07 PRO

5191436 LOGIQ™ 7 220V / PAL Console and Peripherals (Style H) BT07 PRO

5191259 LOGIQ™ 7 220V / NTSC Console and Peripherals (Style H) BT07 PRO

5244924 LOGIQ™ 7 100V / NTSC Console and Peripherals, LCD monitor (Style I) R7.5.x LCD

5244925 LOGIQ™ 7 120V / NTSC Console and Peripherals, LCD monitor (Style I) R7.5.x LCD

5244926 LOGIQ™ 7 220V / PAL Console and Peripherals, LCD monitor (Style I) R7.5.x LCD

5244927 LOGIQ™ 7 220V / NTSC Console and Peripherals, LCD monitor (Style I) R7.5.x LCD

5309921 LOGIQ™ 7 LCD, 100V, 60Hz, NTSC, Japan BT09 BEP4 Intro

5309922 LOGIQ™ 7 LCD, 120V, 60Hz, NTSC BT09 BEP4 Intro

5309923 LOGIQ™ 7 LCD, 220V, 50Hz, PAL BT09 BEP4 Intro

5309924 LOGIQ™ 7 LCD, 220V, 60Hz, NTSC, Asia BT09 BEP4 Intro

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

The Operator Manual(s) should be fully read and understood before operating the LOGIQ™ 7 and also kept near the unit for quick reference.

1-4 Section 1-1 - Overview

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

Section 1-2 Important Conventions

1-2-1 Conventions Used in Book

Model Designations.

This manual covers the LOGIQ™ 7scanners.

Icons.

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

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 three ways:

DANGER

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

WARNINGWARNING

CAUTION

NOTICE

NOTE: Notes are used to provide important information about an item or a procedure. Be sure to read

WARNING IS USED TO INDICATE THE PRESENCE OF A HAZARD THAT CAN CAUSE SEVERE PERSONAL INJURY OR PROPERTY DAMAGE IF INSTRUCTIONS ARE IGNORED.

Caution is used to indicate the presence of a hazard that will or can cause minor personal injury and property damage if instructions are ignored.

Equipment Damage Possible Notice is used when a hazard is present that can cause property damage but has absolutely no personal injury risk. Example: Disk Drive will crash.

the notes; the information contained in a note can often save you time or effort.

Section 1-2 - Important Conventions 1-5

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

1-2-2 Standard Hazard Icons

Important Information will always be preceded by the exclamation point contained within a triangle, as seen throughout this chapter. In addition to text, several different graphical icons (symbols) may be used to make you aware of specific types of hazards that could possibly cause harm.

Some others make you aware of specific procedures that should be followed.

Table 1-3 Standard Hazard Icons

ELECTRICAL MECHANICAL RADIATION

LASER HEAT PINCH

LASER

LIGHT

Some others make you aware of specific procedures that should be followed.

Table 1-4 Standard Icons that indicates that a special procedure is to be used

AVOID STATIC ELECTRICITY TAG AND LOCK OUT WEAR EYE PROTECTION

TAG

LOCKOUT

Date

Signed

EYE

PROTECTION

1-6 Section 1-2 - Important Conventions

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

1-2-3 Product Icons

The following table describes the purpose and location of safety labels and other important information provided on the equipment.

Table 1-5 Warnings

Label/Symbol Purpose/Meaning Location Note

Manufacturer's name and address

Identification and Rating Plate

Date of manufacture Model and serial numbers Electrical ratings

Rear of console near power inlet

Type/Class Label

IP Code (IPX8)

Device Listing/Certification Labels

CAUTION - This unit weighs...Special

care must be used to avoid...”

Used to indicate the degree of safety or protection.

Indicates the degree of protection provided by the enclosure per IEC60

529. IPX8 indicates can be used in operating room environment.

Equipment Type BF (man in the box symbol) IEC 60878-02-03 indicates B Type equipment having a floating applied part.

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

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

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

Footswitch

Probe connectors and PCG connector

ECG connector and Probes marked Type CF

Rear of console

On the console where easily seen during transport

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

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

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

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

Rear of console

Various

Section 1-2 - Important Conventions 1-7

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

Table 1-5 Warnings

Label/Symbol Purpose/Meaning Location Note

“General Warning Sign” Rear panel and UPS battery BT07 or later

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

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

“Mains ON” indicates the power on position of the mains power switch.

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

Rear panel and inside of console BT07 or later

Rear of system adjacent to mains switch

Rear of system adjustment to mains switch

Adjacent to On/Standby Switch

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

“Equipotentiality” Indicates the terminal to be used for connecting equipotential conductors when interconnecting (grounding) with other equipment.

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

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

Various

Rear of console

Rear Panel, Rating Plate, Circuit breaker label of console and front panel (if applicable).

Rear Panel BT07 or later

1-8 Section 1-2 - Important Conventions

BT07 or later

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

Table 1-5 Warnings

Label/Symbol Purpose/Meaning Location Note

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

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

Probe BT07 or later

Rear Panel, China Rating Plate BT07 or later

Do not use the following devices near this equipment: cellular phone, radio receiver, mobile radio transmitter, radio controlled toy, broadband power lines, etc. Use of these devices near this equipment could cause this equipment to perform outside the published specifications. Keep power to these devices turned off when near this equipment.

Rear Panel BT07 or later

Section 1-2 - Important Conventions 1-9

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

Section 1-3 Safety Considerations

1-3-1 Introduction

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

1-3-2 Human Safety

Operating personnel must not remove the system covers.

Servicing should be performed by authorized personnel only.

Only personnel who have participated in a LOGIQ™ 7Training Seminar are authorized to service the equipment.

1-3-3 Mechanical Safety

WARNINGWARNING

CAUTION

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

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

NEVER USE A PROBE THAT HAS FALLEN TO THE FLOOR. EVEN IF IT LOOKS OK, IT MAY BE DAMAGED.

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

Disconnect all probes before moving the scanner around.

The LOGIQ™ 7 weights 225 kg or more, depending on installed peripherals, (496 lbs, or more) when ready for use. Care must be used when moving it or replacing its parts. Failure to follow the precautions listed below could result in injury, uncontrolled motion and costly damage.

ALWAYS:

• Be sure the path way is clear.

• Use slow, careful motions.

• Use two people when moving on inclines or lifting more than 23 kg (50 lb).

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

• Secure the unit in an upright position.

• Lock the wheels (brake).

• DO NOT use the Control Panel as an anchor point.

• Place the probes in the carrying case.

• Eject any Magnet Optical disk from the MO Drive (if installed).

1-10 Section 1-2 - Important Conventions

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

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. If an extension cord is used with the system, make sure that the total current rating of the system does not exceed the extension cord rating.

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.

Section 1-2 - Important Conventions 1-11

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

1-3-5 Label Locations (For BT07 or later, including R7.5.x)

NOTE: For the symbols shown in the illustration below, refer to previous pages in this chapter.

(1)

(14)

(21)

(17)

(10)

100-120V

220-240V

〜

(15)

GE Yokogawa Medical Systems

(12)

ETL LISTED

CONFORMS TO UL STD. 2601-1

CERTIFIED TO

46477

CAN/CSA C22.2 NO. 601.1

ETL TESTING LABORATORIES INC.

CORTLAND, NEW YORK 13043

(2)

(3)

(4)

(5)

(6)

(7)

(9)

(8)

Japan/USA/Asia Console(100V)

(11)

Except for R7.5.x

(13)

(2)

(5)

(16)

Label for China

(1)

(3)

(6)

(7)

LCD model ONLY

(18)

CAUTION

Figure 1-1 OUTSIDE MARKINGS OF LOGIQ™ 7 For BT07

or later, including R7.5.x (Back Side)

1-12 Section 1-2 - Important Conventions

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

1-3-5 Label Locations (For BT07 or later, including R7.5.x) (cont’d)

1.) Possible Shock Hazard

2.) Caution for devices near by the equipment

3.) Caution for Transportation

4.) Prescription Devices (For USA Only)

5.) CE Marking of conformity

6.) WEEE mark

7.) CISPR

8.) Voltage Range

9.) Signal Ground Point Label

10.)Power Indication Label

11.)Caution for Grounding Reliability (For USA, Canada and Japan)

12.)ETL Label

13.)Identification and Rating Plate (USA/Asia 120V console)

14.)Identification and Rating Plate (Europe/Asia/USA 220V console)

15.)Identification and Rating Plate (Jpan 100V console)

16.)Identification and Rating Plate (China)

17.)Label that indicates the presence of hazardous substance(s) above the maximum concentration value.

18.)Identification and Rating Plate (Korean)

19.)Caution label on the monitor

20.)Caution label for the range of motion

21.)This machine should be used in compliance with law. Some jurisdictions restrict certain uses, such as gender determination. - Korea Console

Section 1-2 - Important Conventions 1-13

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

1-3-6 Label Locations (For BT04, BT06, and V65x)

NOTE: For the symbols shown in the illustration below, refer to previous pages in this chapter.

3.2.

10.

Figure 1-2 OUTSIDE MARKINGS OF LOGIQ™ 7 For BT04

or later (Back Side)

1.) Possible Shock Hazard

2.) Caution for devices near by the equipment

3.) Caution for Transportation

4.) Prescription Devices (For USA Only)

5.) CE Marking of conformity and WEEE mark

6.) CISPR

7.) Voltage Range

8.) Signal Ground Point Label

9.) Power Indication Label

10.)Caution for Grounding Reliability (For USA, Canada and Japan)

1-14 Section 1-2 - Important Conventions

GE HEALTHCARE

DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

1-3-6 Label Locations (For BT04, BT06, and V65x) (cont’d)

China220VCo (RightSide)

Figure 1-3 OUTSIDE MARKINGS OF LOGIQ™ 7 For BT04

or later

1.) ETL Label

2.) Identification and Rating Plate

3.) SFDA or SDA Label (For China ONLY)

Section 1-2 - Important Conventions 1-15

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

1-3-7 Label Locations (For BT03 or lower)

NOTE: For the symbols shown in the illustration below, refer to previous pages in this chapter.

3.2.

Figure 1-4 OUTSIDE MARKINGS OF LOGIQ™ 7 For BT03

or lower (Back Side)

1.) Possible Shock Hazard

2.) Caution for devices near by the equipment

3.) Caution for Transportation

4.) Prescription Devices (For USA Only)

5.) CE Marking of conformity

6.) CISPR

7.) Voltage Range

8.) Signal Ground Point Label

9.) Power Indication Label

10.)Caution for Grounding Reliability (For USA, Canada and Japan)

10.

1-16 Section 1-2 - Important Conventions

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

1-3-7 Label Locations (For BT03 or lower) (cont’d)

China220VConsole (RightSide)

Figure 1-5 OUTSIDE MARKINGS OF LOGIQ™ 7 For BT03

or lower (Left Side)

1.) ETL Label

2.) Identification and Rating Plate

3.) SDA Label (For China ONLY)

Section 1-2 - Important Conventions 1-17

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

1-3-8 Dangerous Procedure Warnings

Warnings, such as the example below, precede potentially dangerous procedures through our 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.

WARNINGWARNING

EXPLOSION WARNING: DO NOT OPERATE THE EQUIPMENT IN AN EXPLOSIVE ATMOSPHERE. OPERATION OF ANY ELECTRICAL EQUIPMENT IN SUCH AN ENVIRONMENT CONSTITUTES A DEFINITE SAFETY HAZARD.

DO NOT SUBSTITUTE PARTS OR MODIFY EQUIPMENT: BECAUSE OF THE DANGER OF INTERDICTING ADDITIONAL HAZARDS, DO NOT INSTALL SUBSTITUTE PARTS OR PERFORM ANY UNAUTHORIZED MODIFICATION OF THE EQUIPMENT.

1-3-9 Lockout/Tagout Requirements (For USA Only)

Follow OSHA Lockout/Tagout requirements by ensuring you are in total control of the electrical Mains plug.

NOTICE

Energy Control and Power Lockout for LOGIQ™ 7 When servicing parts of the system where there is exposure to voltage greater than 30 Volts:

Unplug the system Maintain control of the system power plug There are no test points to verify isolation, discharge

Beware that the AC Control Box, Front End Processor and Back End Processor may be energized even if the power is turned off when the cord is still plugged into the AC Outlet.

you must wait for at least 20 seconds for capacitors to

1-3-10 Returning/Shipping Probes and Repair Parts

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

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

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

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

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

1-18 Section 1-2 - Important Conventions

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

1-3-11 How to remove the Ghost CD-ROM

The Ghost CD-ROM (Base System Software Load Image CD-ROM) is mounted on the PC-BOX inside the scanner using velcro tapes. The upper side of the PC-BOX cover contains sharp edge causing a FE to have possibility of cutting his hand if he removes the CD-ROM with the PC-BOX cover closed.

PC-BOX Cover

For BT04 or later

Ghost CD-ROM

Sharp Edge

CD-ROMs

NG: WITH PC BOX COVER CLOSED

Do NOT remove the Ghost CD-ROM when the PC-Box cover is closed.

PC-BOX Cover

OK: WITH PC BOX COVER OPEN

Figure 1-6 How to Remove Ghost CD-ROM

Section 1-2 - Important Conventions 1-19

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

1-3-11 How to remove the Ghost CD-ROM (cont’d)

The sharp edge of the PC Box Cover are chamfered before shipment. However, the Ghost CD-ROM must be removed with the PC-Box cover open according to the following steps.

1.) Disconnect the DVI-D connector, then remove the four mounting bolts (three hex bolts and one phillips screw).

Hex bolt

PC Box Cover

Figure 1-7 Removing Bolts

2.) Open the PC box cover and remove the Ghost CD-ROM from the PC box.

PC Box Cover

Hex bolts

Phillips screw

DVI-D connector

Open

Figure 1-8 Removing Ghost CD-ROM

1-20 Section 1-2 - Important Conventions

Ghost CD-ROM

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

Section 1-4 EMC, EMI, and ESD

1-4-1 Electromagnetic Compatibility

Electro Magnetic 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 interface from its environment or when the device produces unacceptable levels of mission to its environment. This interface is often referred to as radio-frequency or electromagnetic interface (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 Electrostatic Discharge (ESD) Prevention

WARNINGWARNING

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

1.) Always connect yourself, via an arm-wrist strap, to the dedicated ground point located on the rear of the scanner (to the left of the power connector) or a proper frame ground.

2.) Follow general guide lined for handling of electrostatic sensitive equipment.

1-4-3 CE Compliance

The LOGIQ™ 7 unit conforms to all applicable conducted and radiated emission limits and immunity from electrostatic discharge, radiated and conducted RF fields, magnetic fields and power line transient requirements.

Applicable standards are: 47CFR Part18, IEC60601-1-2, and 806-13.

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.

Section 1-2 - Important Conventions 1-21

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

Section 1-5 Customer Assistance

This system is not repairable by the customer. If this equipment does not work as indicated in the Operator Manual, please contact your service support center. If the service engineer needs additional information to repair this equipment, please contact the following address (The necessary information will be provided to the Service Engineer as needed).

1-5-1 System Manufacture

Table 1-6 System Manufacture

GE YOKOGAWA MEDICAL SYSTEMS

4-7-127 Asahigaoka, Hino-shi, Tokyo, 191-8503 JAPAN

1-5-2 Contact Information

For GE Service:

Table 1-7 Phone Numbers for Customer Assistance

Location Phone Number

USA/ Canada GE Medical Systems Ultrasound Service Engineering 4855 W. Electric Avenue Milwaukee, WI 53219

Customer Answer Center

Latin America GE Medical Systems Ultrasound Service Engineering 4855 W. Electric Avenue Milwaukee, WI 53219

Customer Answer Center

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

Tel: 1-800-321-7937

1-800-682-5327 1-262-524-5698 Fax: +1-414-647-4125

Tel: 1-262-524-5300

1-262-524-5698 Fax: +1-414-647-4125

Tel: +33 0 130 831 300 - CARDIAC +33 0 130 831 300 - GENERAL IMAGING Fax: +49 212 2802 431

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

ASIA (Japan) +65-277-3512

Tel: +65-6277-3512

Fax: +65 6272-3997

1-22 Section 1-5 - Customer Assistance

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

1-5-2 Contact Information (cont’d)

NOTE: If this equipment does not work as indicated in the Operator Manual(s), contact your support

center. Have the system ID number available when you call.

Section 1-5 - Customer Assistance 1-23

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

This page was intentionally left blank.

1-24 Section 1-5 - Customer Assistance

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

Chapter 2 Pre Installation

Section 2-1 Overview

2-1-1 Purpose of this chapter 2

This chapter provides the information required to plan and prepare for the installation of a LOGIQ™ 7. Included are descriptions of the facility and electrical needs to be met by the purchaser of the unit. A checklist is also provided at the end of this section to help determine whether the proper planning and preparation is accomplished before the actual equipment installation is scheduled.

Table 2-1 Contents in Chapter 2

Section Description Page Number

2-1

2-2

2-3

Overview

General Console Requirements

Facility Needs

2-1

2-2

2-7

Section 2-1 - Overview 2-1

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

Section 2-2 General Console Requirements

2-2-1 Console Environmental Requirements

Table 2-2 Environmental Requirements for LOGIQ™ 7 Scanners

Operational Storage Transport

Temperature

Humidity

Pressure

10 - 35 oC

50 - 95

30 - 80% non-condensing

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

-10 - 50 14 - 122

30 - 80% non-condensing

-10 - 50 14 - 122

30 - 80% non-condensing

Table 2-3 Environmental Requirements for an Ultrasound Room

Item Values

Power Source

Current Rating

Radiation Shielding

Temperature

Humidity

Heat Dissipation

Floor Landing

Floor Condition

Refer to Table 2-4 on page 2-3.

20A (120V, 100V); 7.5A (220-240V) CIRCUIT BREAKER

NONE REQUIRED for ULTRASOUND ENERGY

20-26 DEG. C (68-79 DEG F) for PATIENT COMFORT

50% to 70% for PATIENT COMFORT

3500 BTU/Hr.

Approximately 680 - 800 kg/m2 without Accessories

Gradient: WITHIN 5 degrees

Weight

Approximately 225 kg (496lbs) without Accessories

2-2-1-1 Cooling

The cooling requirement for the LOGIQ™ 7 is 3500 BTU/hr. This figure does not include cooling needed for lights, people, or other equipment in the room. Each person in the room places an additional 300 BTU/hr. demand on the cooling system.

2-2-1-2 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 Section 2-2 - General Console Requirements

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

2-2-2 Electrical Requirements

2-2-2-1 Electrical Requirements

NOTE: GE Medical Systems requires a dedicated power and ground for the proper operation of its

Ultrasound equipment. This dedicated power shall originate at the last distribution panel before the system.

Sites with a mains power system 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 The dedicated line shall consist of one phase (two lines), not shared with any other circuit, and a full size ground wire from the distribution panel to the Ultrasound outlet.

Please note that image artifacts can occur, if at any time within the facility, the ground from the main facility's incoming power source to the Ultrasound unit is only a conduit.

2-2-2-2 LOGIQ™ 7 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 2-4 Electrical Specifications for LOGIQ™ 7

PARAMETER AREA LIMITS

Voltage Range

Power All applications MAX. 1200 VA

with defined Neutral and Line:

without a defined Neutral:

100V 100 VAC ±10% (90-110 VAC)

220V 220-240 VAC ±10% (198-264 VAC)

120V 120 VAC ±10% (108-132 VAC)

Line Frequency All applications 50/60Hz (±2Hz)

Power Transients All applications

Decaying Oscillation All applications

2-2-2-3 Inrush Current

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

2-2-2-4 Site Circuit Breaker

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

CAUTION

POWER OUTAGE MAY OCCURE. The LOGIQ™ 7 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.

Section 2-2 - General Console Requirements 2-3

Less than 25% of nominal peak voltage for less than 1 millisecond for any type of transient, including line frequency, synchronous, asynchronous, or aperiodic transients.

Less than 15% of peak voltage for less than 1 millisecond.

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

2-2-2-5 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.

2-2-2-6 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.

2-2-2-7 Power Stability Requirements

Voltage drop-out

Max 10 ms.

Power Transients

Refer Table

2-4 Section 2-2 - General Console Requirements

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

2-2-3 EMI Limitations

Ultrasound machines are susceptible to Electromagnetic Interference (EMI) from radio frequencies, magnetic fields, and transient in the air wiring. They also generate EMI. The LOGIQ™ 7 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.

Table 2-5 EMI Prevention/abatement

EMI Rule Details

Be aware of RF sources

Ground the unit

Replace all screws, RF gaskets, covers, cores

Replace broken RF gaskets

Do not place labels where RF gaskets touch metal

Use GE specified harnesses and peripherals

Take care with cellular phones

Keep the unit at least 5 meters or 15 feet away from other EMI sources. Special shielding may be required to eliminate interference problems caused by high frequency, high powered radio or video broadcast signals.

Poor grounding is the most likely reason a unit will have noisy images. Check grounding of the power cord and power outlet.

After you finish repairing or updating the system, replace all covers and tighten all screws. Any cable with an external connection requires a magnet wrap at each end. Install the shield over the front of card cage. Loose or missing covers or RF gaskets allow radio frequencies to interface with the ultrasound signals.

If more than 20% or a pair of fingers on the RF gaskets are broken, replace the gaskets. Do not turn on the unit until any loose metallic part is removed.

Never place a label where RF gaskets meet the unit. Otherwise, the gap created will permit RF leakage. Or, if a label has been found in such a position, move the label.

The interconnect cables are grounded and require ferrite beads and other shielding. Also, cable length, material, and routing are all important; do not change from what is specified.

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

Properly dress peripheral cables

Section 2-2 - General Console Requirements 2-5

Do not allow cables to lie across the top of the card cage or hang out of the peripheral bays. Loop the excess length for peripheral cables inside the peripheral bays. Attach the monitor cables to the frame.

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

2-2-4 Probes Environmental Requirements

Table 2-6 Operation and storage Temperatures for 2D Probes

Operational Storage Transport

Temperature

Humidity

Pressure

10 - 40 oC 50 - 104

30 - 85% non-condensing

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

-10 - 60 14 - 140

30 - 90% non-condensing

-40 - 60

-40 - 140

30 - 90% non-condensing

Table 2-7 Operation and storage Temperatures for 4D Probes

Operational Storage Transport

Temperature

Humidity

Pressure

18 - 30 oC

64- 86

Max. 70% non-condensing

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

-10 - 50 14 - 122

Max. 90% non-condensing

-10 - 50 14 - 122

Max. 90% non-condensing

2-6 Section 2-2 - General Console Requirements

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

Section 2-3 Facility Needs

2-3-1 Purchaser Responsibilities

The work and materials needed to prepare the site is the responsibility of the purchaser. Delay, confusion, and waste of manpower can be avoided by completing pre 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.

Section 2-3 - Facility Needs 2-7

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

2-3-2 Required Features

• Dedicated single branch power outlet of adequate amperage (see Table 2-3) 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.

NOTE: The LOGIQ™ 7 has four outlets inside the unit. One is for the monitor and three for on board peripherals.

• Power outlets for other medical equipment and gel warmer

• Power outlets for test equipment and modem within 1 m (3.2 ft.) of unit

• Clean and protected space to store transducers (in their cases or on a rack)

• Material to safely clean probes (done with a plastic container, never metal)

2-3-3 Desirable Ultrasound Room Facilities

• Door is at least 92 cm (3 ft.) wide

• Circuit breaker for dedicated power outlet is easily accessible

• Sink with hot and cold water

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

• Emergency oxygen supply

• Storage for linens and equipment

• Nearby waiting room, lavatory, and dressing room

• Dual level lighting (bright and dim)

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

2-8 Section 2-3 - Facility Needs

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

2-3-4 Recommended and Alternate Ultrasound Room Layout

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

LOGIQ

Figure 2-1 RECOMMENDED ULTRASOUND ROOM

LAYOUT

Section 2-3 - Facility Needs 2-9

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

2-3-5 Networking Pre-installation Requirements

2-3-5-1 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.

2-3-5-2 DICOM Option Pre-installation Requirements

To configure the LOGIQ™ 7 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™ 7.

• 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™ 7 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.

2-10 Section 2-3 - Facility Needs

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

2-3-5-2 DICOM Option Pre-installation Requirements (cont’d)

LOGIQ™ 7

Host Name

Local Port

IP Address

AE Title

ROUTING INFORMATION

ROUTER1 ROUTER2 ROUTER3

DICOM APPLICATION INFORMATION

NAME

Store 1

Store 2

Store 3

Store 4

Destination IP Addresses

...

MAKE/REVISION IP ADDRESSES PORTAE TITLE

Net Mask

Default

...

GATEWAY IP Addresses

...

Store 5

Store 6

Worklist

Storage Commit

MPPS

...

Figure 2-2 Worksheet for DICOM Network Information

Section 2-3 - Facility Needs 2-11

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

This page was intentionally left blank.

2-12 Section 2-3 - Facility Needs

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

Chapter 3 Installation

Section 3-1 Overview

3-1-1 Purpose of Chapter 3

This chapter contains information needed to install the unit. Included are references to a procedure that describes how to receive and unpack the equipment and how to file a damage or loss claim. How to prepare the facility and unit of the actual installation, and how to check and test the unit, probes, and external peripherals for electrical safety are included in this procedure. Also included in this section are guidelines for transporting the unit to a new site.

Table 3-1 Contents in Chapter 3

Section Description Page Number

3-1

3-2

3-3

3-4

3-5

Overview

Receiving and Unpacking the Equipment

Preparing for Installation

Completing the Installation

Installation Paperwork

3-1-2 Average Installation Time

Table 3-2 Average Installation Time

Description Average Installation Time Comments

Unpacking the scanner

Scanner wo/options

DICOM Option

InSite Option

0.5 hour

3-1

3-3

3-10

3-11

3-18

Dependant on the configuration that is required

Dependant on the amount of configuration

The LOGIQ™ 7 has been designed to be installed and checked out by an experienced service technician in approximately four hours. LOGIQ™ 7 consoles with optional equipment may take slightly longer.

Section 3-1 - Overview 3-1

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

3-1-3 Installation Warnings

1.) Since the LOGIQ™ 7 weighs approximately 225 kg. (496 lb) 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.

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 40×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 Time for Settlement

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

°C

140 131 122 113 104 96 86 77 68 59 50 41 32 23 14 5 -4 -13 -22 -31 -40

°F

864200000002468101214161820

hrs

3-1-3-1 Brake Pedal Operation

WARNINGWARNING

REMEMBER: IF THE FRONT CASTER SWIVEL LOCK IS ENGAGED FOR TRANSPORTATION, PRESSING THE RELEASE PEDAL ONCE EDISENGAGES THE SWICEL LOCK. YOU MUST DEPRESS THE RELEASE PEDAL A SECOND TIME TO ENGAGE THE BRAKE.

3-2 Section 3-1 - Overview

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

Section 3-2 Receiving and Unpacking the Equipment

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

Example shown: LOGIQ 7 system

Outer Sleeve

Monitor Sleeve For CRT

Box for Peripherals

Front Cushion

Slope

Cap

Plastic Joint

Monitor Sleeve For LCD

Rear Cushion

Plastic Band

Skid

Figure 3-1 Unpacking Procedures

Unpacking Procedures:

1.) Cut the two Metal Bands.

2.) Lift the Cap up and off.

3.) Remove the six (6) Plastic Joints from the Outer Sleeves.

4.) Remove the Outer Sleeves.

5.) Remove the Monitor Sleeve.

6.) Remove the Box for Peripherals.

7.) Remove the Front and Rear Cushions.

8.) Slide out and set up the Slope.

9.) Unlock the brakes by stepping down on the brake pedal in front, then carefully roll the LOGIQ™ 7 rear side first off the Skid.

Section 3-1 - Overview 3-3

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

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

NOTE: Check the shipping container for special instructions. Verify that the container is intact. In some

cases a secondary container may be used. If so, ask the carrier for unpacking instructions.

NOTICE

For the protection of LCD monitor, re-use the packing sleeve whenever possible, in case of shipment after unpacking.

Secure the LCD Sleeve with adhesive tape after placing it to the proper location.

Adhesive Tape (Each side)

Pull over the sleeve to the LCD arm.

Turn over the LCD monitor, and place the sleeve to the location above. Make sure LCD arm is locked.

Figure 3-2 Labels on Package

3-4 Section 3-1 - Overview

Make sure the LCD arm hinge is placed inside of the protective pad.

Note: These labels are attached onto the shipping box, defining environment at which consoles are to be transported or stored.

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

3-2-1 Safety Reminders

DANGER

CAUTION

WHEN USING ANY TEST INSTRUMENT THAT IS CAPABLE OF OPENING THE AC GROUND LINE (I.E., METER’S GROUND SWITCH IS OPEN), DO NOT TOUCH THE UNIT!

Two people should unpack the unit because of its weight. Two people are required whenever a part weighing 19kg (35 lb.) or more must be lifted.

If the unit is very cold or hot, do not turn on its power until it has had a chance to acclimate to its operating environment.

To prevent electrical shock, connect the unit to a properly grounded power outlet. Do not use a three to two prong adapter. This defeats safety grounding.

Do NOT wear the ESD wrist strap when you work on live circuit and more than 30 V peak is present.

Do not use a 20 Amp to 15 Amp adapter on the 120 Vac unit’s power cord. This unit requires a dedicated 20 A circuit and can have a 15 A plug if the on board peripherals do not cause the unit to draw more than 14.0 amps.

Do not operate this unit unless all board covers and frame panels are securely in place. System performance and cooling require this.

OPERATOR MANUAL(S) The User Manual(s) should be fully read and understood before operating the LOGIQ™ 7 and kept near the unit for quick reference.

CAUTION

ACOUSTIC OUTPUT HAZARD Although the ultrasound energy transmitted from the LOGIQ™ 7 probe is within FDA limits, avoid unnecessary exposure. Ultrasound energy can produce heat and mechanical damage.

Do not lift the unit by the Keyboard. Equipment damage may result.

The crate with the LOGIQ™ 7 weighs approximately 340 kg. (749.7 lb) Be prepared for a sudden shift of weight as the unit is removed from its base (pallet)

Section 3-1 - Overview 3-5

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

3-2-2 Moving into Position

CAUTION

Do not lift the unit by the Keyboard. 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.

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

In general, a single adult can move the LOGIQ™ 7 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™ 7 is a compact and mobile machine, two people should move it over rough surfaces or up and down grades.

For LCD Model ONLY: Always lock the LCD monitor arm before removing the LCD monitor. This prevents the monitor arm from being suddenly and unexpectedly extended when removing the LCD monitor. Failure to heed this warning may result in personal harm, harm to others or death..

Arm Lock (LCD Model ONLY)

3-6 Section 3-1 - Overview

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

3-2-3 LCD Monitor Tilt Caution

CAUTION

Do NOT put your hand here! Your fingers might be pinched when adjusting angle of the LCD monitor.

For R7.5.x 19inch LCD system

Figure 3-3 LCD Monitor Tilt Caution

Section 3-1 - Overview 3-7

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

3-2-4 LCD Monitor Swing CautionLCD Monitor Tilt Caution

CAUTION

Arm can be swung 180 degree left and right, and stick out from the side frame. Pay attention to the location from the wall in the room for room layout, and notice the attention to customer for Examination Table side.

LCD will hit the KBD in case of moving over the right/left side.

3-8 Section 3-1 - Overview

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

3-2-5 LCD Monitor Removal Caution

CAUTION

Always lock the LCD monitor arm before removing the LCD monitor. This prevents the monitor arm from being suddenly and fastly extended when removing the LCD monitor. Failure to heed this warning may result in personal harm, harm to others or death.

Arm Lock (LCD Model ONLY)

3-2-6 Shipping Delivery Requirements

Do NOT hold the scanner at the LCD monitor or rotaing arm using the belt as shown. Always hold it at the body part of the console.

CAUTION

Always hold the scanner at the body.

Figure 3-4 Shipping Delivery Requirements

Section 3-1 - Overview 3-9

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

Section 3-3 Preparing for Installation

3-3-1 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.

3-3-2 Physical Inspection

3-3-2-1 System Voltage Settings

• Verify that the scanner is set to the correct voltage. The Voltage settings for the LOGIQ™ 7 Scanner is found on the label onto the rear lower of the scanner.

WARNINGWARNING

CONNECTING A LOGIQ™ 7 SCANNER TO THE WRONG VOLTAGE LEVEL WILL MOST LIKELY DESTROY THE SCANNER.

WARNINGWARNING

PROTECTIVE EARTH MUST BE TAKEN WHEN CONNECTING AC POWER CABLE (200V) WITHOUT ITS PLUG TO WALL OUTLET.

3-3-3 EMI Protection

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

3-10 Section 3-3 - Preparing for Installation

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

Section 3-4 Completing the Installation

3-4-1 Probe (Transducer) Connection

1.) Connect a transducer to the upper transducer receptacle as follows:

NOTICE

NOTE: It is not necessary to turn OFF power to connect or disconnect a transducer.

To make effective use of the memory space:

1. When a scanner has one linear probe, it must be connected to the most left receptacle.

2. When a scanner has several linear probes, they must be connected from the left to the right.

a.) Ensure that the transducer twist lock lever to the horizontal position. b.) Insert the transducer connector on the receptacle guide pin until it touches the receptacle

mating surface.

c.) Twist the transducer twist lock lever to vertical position to lock it in place. Twist the lever to the

horizontal position to disconnect the transducer.

2.) Connect the main power cable to a hospital grade power receptacle with the proper rated voltage checked during pre installation. Never use a three-to-two prong adapter; this defeats the safety ground.

Section 3-4 - Completing the Installation 3-11

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

3-4-2 Optional Peripherals/Peripheral Connection

Depending on the customer order, the peripheral(s) already has been installed onto the scanner before shipment. If it does not, select the proper location to install the peripherals, following the table below.

Console Top

Device Room

Figure 3-5 Optional Peripherals/Peripheral Connection

Location for

peripheral

Consle Top Not used Not used VCR or DVD recorder

Device Room Used

One peripheral

(Color printer ONLY)

One peripheral (VCR

or DVD recorder)

Used Color Pinter

Two peripherals

3-12 Section 3-4 - Completing the Installation

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

3-4-2 Optional Peripherals/Peripheral Connection (cont’d)

Check if the fixing belts are loosen. If it is, tighten the belts again to secure the peripheral(s). If necessary, remove the peripheral from the device room to tighten the belts.

Connect the related cables between the peripheral and

Belts

LOGIQ 7 if they are NOT connected each other.

Belts

Figure 3-6 How to Hold Peripherals

3-4-2-1 Approved on-board peripherals

Refer to Section 5-3 Peripheral Compatibility.

Section 3-4 - Completing the Installation 3-13

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

3-4-2-1 Approved on-board peripherals (cont’d)

Connecting Cables

CAUTION

Equipment damage possibility. Be sure to use the following recommended connecting cables to connect recording devices and a network with LOGIQ™ 7 console.

Table 3-4 List of Connecting Cables

Name Part No. Figure NOTE

Power Supply Cable P9509EE

USB Serial Bridge

Cable

AV Cable 2119874

Mini-Plug Cable P9509BE

RS232C Cable

Cross

RS232C Cable

Straight

2304621

The followings are the cables for BT04 ore lower system ONLY.

2305550

2305549

Connected to power

For converting the signal of RS232C cable to USB cable: connected to VCR1 on the Rear Panel

Connected to Video-In/Out on the Rear Panel

Shutter control signals: connected to B/W Printer

For control signals: connected to Serial Bridge Cable

BNC Cable 2297053

USB Cable 2324360

SCSI cables

(UP-D50 ONLY)

2375479

3-4-2-2 Reference off-board peripherals and options

None.

For control signal: connected to Composite B/W

Connected to USB port.

Connected toSCSI port and SCSI Cable Connector.

3-14 Section 3-4 - Completing the Installation

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

3-4-3 Available Probes

See in specification in the LOGIQ™ 7 Reference Manual for Probes and intended use. See Chapter 9 - Renewal Parts for Part Numbers to be used when ordering new or replacement probes.

Table 3-5 List of Transducers supported (All models)

Material of

Probe Name

Headshell

Area of Using TYPE Catalog Number Part Number

3C PES ABDOMINAL CONVEX

5C PES ABDOMINAL CONVEX

8C PBT

E8C

M7C PBT ABDOMINAL CONVEX

M12L PBT SMALL PARTS LINEAR

7L NORYL

10L NORYL SUPERFICIAL LINEAR

10S ABS PEDIATRIC SECTOR

3.5C NORYL ABDOMINAL CONVEX

3.5CS NORYL ABDOMINAL CONVEX

NORYL

PBT

NEONATAL

PEDIATRICS

TRANSVAGINAL MICRO-CONVEX

ABDOMINAL

SUPERFICIAL

MICRO-CONVEX

LINEAR

H79802P

H40412LB

H79822P

H40412LA

H79792P

H40412LJ

H79852P

H40412LE

H79832P

H40412LC

H79842P

H40412LD

H79862P

H40412LF

H79872P

H40412LG

H79922P

H4901PC

H79812P H4901PE

H78042P

H40412LK

2286353 2286354

2294515 2294516

2348093 2348094

2294640 2294641

2294513 2294514

2294510 2294511

2294520 2294521

2294522 2294523

2309478 2298589

2303215 2050357

2380854 2051858

3S NORYL CARDIOLOGY SECTOR

i12L ABS INTRAOPERATIVE LINEAR

M3S PBT CARDIOLOGY SECTOR

TRASOPHAGEAL FOR

6T-OR-TEE PU: PolyUrethane

7S PBT CARDIOLOGY SECTOR

BE9C PBT TRANSRECTAL MICRO-CONVEX

T739 NORYL INTRAOPERATIVE LINEAR

4D3C_L PBT ABDOMINAL CONVEX Volume H44801G

ADULT

CARDIOLOGY

SECTOR

H79632P H4701SZ

H79322P

H4012L

H79892P

H45011SZ

H79932P

H45521DX

H78082P

H40422LB

H40412LW

H76572SR H40212LM

Section 3-4 - Completing the Installation 3-15

2348878 2323337

2270556 2264883

2293726 2378099

5131947

KN100068

2355698 2347471

2389381 2389382

2259245 2259246

5121652

KTZ195893

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

Table 3-5 List of Transducers supported (All models)

Material of

Probe Name

Headshell

Area of Using TYPE Catalog Number Part Number

4D10L PBD SUPERFICIAL LINEAR Volume H44801GB

4C PBT ABDOMINAL CONVEX H4904PC

12L Noryl SUPERFICIAL LINEAR H40412LH

P2D ABS CARDIOLOGY CWD H4830JE TE100024

P6D --- SUPERFICIAL CWD H4830JG TQ100002

NOTE: PES: Polyethersulfone NORYL: Modified Polyphenylene Oxide PU: Polyurethane

PBT: Polybutylene Terephthalate ABS: Acrylonitrile Butadiene Styrene

NOTE: Some probes indicated on the table above have two different part numbers. The upper row

shows the part numbers of probes for Japan. The lower row shows the part numbers of probes for regions other than Japan. Probes which have only one part number are not available in Japan.

The following transducers, additional to ones listed in Table 3-6, are supported by V65x and later LOGIQ 7 models.

Table 3-6 List of Transducers supported by V65x and later

Material of

Probe Name

Headshell

Area of Using TYPE Catalog Number Part Number

5121651

KTZ156836

5131944 5123455

2295375 2295377

9L PBT

4DE7C PBT OB Gyn Urology CONVEX Volume H44801GA 5121650

VASCULAR SMALL

PARTS

LINEAR H40412LT 5131433

The following transducers, additional to ones listed in Table 3-7, are supported by R7.5.x and later LOGIQ 7 models.

Table 3-7 List of Transducers supported by R7.5.x and later

Material of

Probe Name

3CRF PU: PolyUrethane ABDOMINAL MICRO-CONVEX H40442LP

Headshell

Area of Using TYPE Catalog Number Part Number

The following transducers, additional to ones listed in Table 3-8, are supported by BT09 and later LOGIQ 7 models.

Table 3-8 List of Transducers supported by BT09 and later

Material of

Probe Name

11L PBT SUPERFICIAL LINEAR

Headshell

Area of Using TYPE Catalog Number Part Number

H78842P

H40412LY

5214820 5196216

5251881 5171885

3-16 Section 3-4 - Completing the Installation

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

3-4-4 Video Specification

Table 3-9 Video Specifications

CRT LCD

800x600

Timing Parameter

Horizontal Rate [kHz] 46.88 Horizontal Rate [kHz] 64

Horizontal Period [µs] 21.33 Horizontal Period [µs] 15.625

Pixel Clock [MHz] 49.50 Pixel Clock [MHz] 108

H Blank Width [µs] 5.17 H Blank Width [µs] 3.778 (408dots)

H Sync Width [µs] 1.62 H Sync Width [µs] 1.037 (112dots)

H Front Porch [µs] 0.32 H Sync Front Porch [µs] 0.444 (48dots)

Active Horizontal Period [µs] 16.16 Active Horizontal Period [µs]

Vertical Rate [Hz] 75.00 Vertical Rate [Hz] 60.0

Vertical Period [ms] 13.33 Vertical Period [ms]

V Sync Width [lines=ms] 25=0.53 V Sync Front Porch [ms] 0.016 (1 line) V Front Porch [lines=µs] 3=64.00 Equalization Porch None

Equalization Gate [lines=µs] 1=21.3 Lines: Field/Frame 1066

Lines: Field/Frame 625 Active Lines/Frame 1024

Active Lines/Frame 600

75Hz

Timing Parameter

1280 x 1024

60Hz

11.852

(1280dots)

16.67

(1066lines)

3-4-5 Software Option Configuration

3-4-5-1 Onsite check and configuration

Select Utility > Admin > System Admin and check the option software to be installed.

Section 3-4 - Completing the Installation 3-17

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

Section 3-5 Installation Paperwork

NOTE: During and after installation, the documentation (i.e. Users Manual, 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 informations are available during the operation and service of the complete system.

3-5-1 Peripherals/Accessories Connector Panel

LOGIQ™ 7 peripherals and accessories can be properly connected using the rear connector panel located behind the rear door, front connector panel located next to the video printer, and Footswitch connector located bottom of the OP panel.

3-18 Section 3-5 - Installation Paperwork

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

3-5-1-1 Rear Panel Connector

Located on the rear panel are video input and output connectors, audio input and output, camera expose connectors, footswitch connector power connector and control connections for VCR, printer, and service tools.

This section indicates the pin assignment for each connector.

Rear Pannel Connector for BT04 and later models

S-Video

Video In

Audio

Out

Cmpst

S-Video

Video Out

Out

B/WColor

Circuit

Breaker

Circuit

Breaker

Power

VGA

Camera

Expose

c/ Re

Ethernet

Insite

B/WColor

VCR2 VCR1 Service

100-120V 350VA Max

AC Line Input

1200VA

240V

120V

220

100

50/ 60Hz

Figure 3-7 Rear Pannel Connector (BT04 or later)

Section 3-5 - Installation Paperwork 3-19

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

3-5-1-1 Rear Panel Connector (cont’d)

Rear Pannel Connector for BT03 or lower

USB1.1 (USB compatible) or (USB + USB Serial Bridge + RS232C)

USB1.1 (USB compatible) or (USB + USB Serial Bridge



+ RS232C)

(Reserved for future use)



Figure 3-8 Rear Panel Connector (BT03 or lower)

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. The specified peripherals/accessories only can be connected to the USB ports.

3-20 Section 3-5 - Installation Paperwork

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

3-5-1-1 Rear Panel Connector (cont’d)

Pin Assignment of S-Video Connector

Connector: S-Terminal, 4-pin

Pin Assignment of VGA Connector

Table 3-10 Pin Assignment of S-Video Connector

Pin No Output/Input Signal Description

1 SVIDEO OUT/IN YG Y (Luma) GND

2 SVIDEO OUT/IN CG C (Chroma) GND

3 SVIDEO OUT/IN Y Y (Luma) SIGNAL

4 SVIDEO OUT/IN C C (Chroma) SIGNAL

Connector: Shrank D-Sub, 15-pin

Table 3-11 Pin Assignment of VGA Connector

Pin No Output Signal Description

1 IO VGA OUT1 R Red

2 IO VGA OUT1 G Green

3 IO VGA OUT1 B Blue

6 IO VGA OUT1 RG Reg GND

7 IO VGA OUT1 GG Green GND

8 IO VGA OUT1 BG Blue GND

13 IO VGA OUT1 HS H Sync

14 IO VGA OUT1 VS V Sync

Others GND GND

Pin Assignment of Service/VCR 1/VCR 2 Connector, USB1.1

Connector: 4 pin

1 2 3 4

Table 3-12 Pin Assignment of Service/VCR 1/VCR 2 Connector

Pin No Output Signal Description

1 VBUSn Power Supply

2 Dn Data (-)

3 Dn Data (+)

4 GNDn Power Ground

Section 3-5 - Installation Paperwork 3-21

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

3-5-1-1 Rear Panel Connector (cont’d)

Pin Assignment of Digital Int. Connector

2 4 6

Connector: 6-pin

Table 3-13 Pin Assignment of IEEE-1394 Connector)

1 3 5

Pin Assignment of Ethernet

Connector: RJ-45 Modular, 8-pin

Table 3-14 Pin Assignment of Ethernet Connector

8 1

Pin No Output Signal Description

1 VP 1394 Power Supply

2 VG 1394 Power Ground

3 TPB 1394 Data B (-)

4 TPB 1394 Data B (+)

5 TPA 1394 Data A (-)

6 TPA 1394 Data A (+)

Pin No Output Signal Description

1 ETHER TD Ethernet TD+

Pin Assignment of Insite

Connector: RJ-11 Modular, 6-pin

Table 3-15 Pin Assignment of Insite Connector

8 1

2 ETHER TD Ethernet TD-

3 ETHER RD Ethernet RD+

6 ETHER RD Ethernet RD-

Others NC Non-connection

Pin No Output Signal Description

2 TEL L4 Telephone L4

3 TEL L2 Telephone L2

4 TEL L1 Telephone L1

5 TEL L3 Telephone L3

Others NC Non-connection

3-22 Section 3-5 - Installation Paperwork

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

3-5-1-1 Rear Panel Connector (cont’d)

Pin Assignment for Camera B/W

Table 3-16 Pin Assignment of Mini-Jack for Controlling B/W Camera

Pin No Output Signal

1PRINT

2 Signal GND

NOTE: Output level of control signals indicated in the above tables are TTL level.

Pin Assignment of Insite

Table 3-17 Pin Assignment of Mini-Jack for Controlling Color Camera

Pin No Output Signal

3-5-1-2 Front Connector Panel

Located on the front panel are Microphone, LED, and Reset.

For BT03 or lower

Microphone

LED (HD access)

Figure 3-9 Front Connector Panel

1 SHUTTER

2 Signal GND

Note:USB1.1. Some systems do NOT have this port. If your system has this port, do NOT use this

port! Instead, use the

USB port located at the rear connector panel.

Reset

For BT04 or later

USB2.0 You can use the serial port.

Serial

Section 3-5 - Installation Paperwork 3-23

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

3-5-1-3 B/W Printer Connector Panel

Table 3-18 Pin Assignment of Mini-Jack for Controlling B/W Printer

Pin No Output Signal

1PRINT

2 Signal GND

3-5-1-4 Footswitch Connector Panel

Round 5 pin connector.

Table 3-19 Pin Assignment of Mini-Jack for Footswitch

Pin No Output Signal

1SW1-WH

2SW2-RD

3SW3-GN

4 SW1-BK, SW2-BK, SW3-BK

5Frame GND

NOTE: Output level of control signals indicated in the above tables are TTL level.

3-24 Section 3-5 - Installation Paperwork

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

This page was intentionally left blank.

Section 3-5 - Installation Paperwork 3-25

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

3-26 Section 3-5 - Installation Paperwork

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

Chapter 4 Functional Checks

Section 4-1 Overview

4-1-1 Purpose for Chapter 4

This chapter provides procedures for quickly checking major functions of the LOGIQ™ 7 console, diagnostics by using the built-in service software, and power supply adjustments.

Table 4-1 Contents in chapter 4

Section Description Page Number

NOTICE

4-1

4-2

4-3

4-4

4-5

4-6

4-7

Most of the information pertaining to this Functional Checks chapter is found in the LOGIQ™ 7 Quick

Overview

General Procedure

Functional Checks

Application Turnover Check List

Diagnostics

Power Supply

Site Log

Guide (Direction Number 2291859-100). Look for the letters (QG) after a section in the Table of Contents to determine if the information is in this chapter or in the Quick Guide.

4-1-2 Special Equipment Required

• An empty (blank) MO Disk.

• At least one transducer. (normally you should check all the transducers used on the system.)

4-1

4-2

4-20

4-27

4-28

4-29

4-30

Section 4-1 - Overview 4-1

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

Section 4-2 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.

4-2-1 Lockout/Tagout Requirements

Follow OSHA Lockout/Tagout requirements by ensuring you are in total control of the plug.

4-2-2 Power On/Boot Up

NOTE: After turning off the 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.

4-2-2-1 Power Up

1.) Connect the Main Power Cable at the rear of the System.

WARNINGWARNING

PROTECTIVE EARTH MUST BE TAKEN WHEN CONNECTING AC POWER CABLE (200V) WITHOUT ITS PLUG TO WALL OUTLET.

2.) Connect the Main Power cable to an appropriate mains power outlet.

3.) Switch ON the Main Circuit Breaker at the rear of the System.

Main Circuit Breaker

Main Power Cable

Figure 4-1 Circuit Breaker

When power is applied to the Scanner, and the Rear Circuit breaker is turned ON, Power is distributed to the Fans, Control panel, Monitor, Internal and External I/O’s, Cage Boards, Peripherals and the Backend Processor. When the Power ON/OFF key is pressed once, the Backend Processor starts and its software code is distributed to initiate the scanner.

4-2 Section 4-2 - General Procedure

For BT04 or lator

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

4-2-2-1 Power Up (cont’d)

4.) Press the ON/OFF

key at the front of the System once.

Figure 4-2 Power On/Off Standby Switch Location

4-2-2-2 Power Up Sequence

NOTE: For consoles with BEP4 (BT09), power switch lamp is darker compared to existing BT04-BT07

consoles with BEP3. This is NOT abnormality and system will function normally regardless of the brightness of the power button.

1.) The Start Up Screen will be shown on the Monitor display when the system is turned ON.

Figure 4-3 Start Up Screen

Section 4-2 - General Procedure 4-3

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

2.) After initialization is complete, all lighted buttons on the Control Panel light and the default B-Mode screen or Patient screen (no probes are connected) is displayed on the monitor display.

4-2-2-3 Entering Maintenance Mode

4-2-2-3-1 R6.2.x or later

1.) Insert the service dongle into any USB port.

2.) Wait for scanner boot-up.

3.) Tap ON/OFF the power switch.

4.) Click on Exit.

Figure 4-4 Clicking on Exit

5.) Enter the proper password to enter the maintenance mode.

6.) Click on OK.

Figure 4-5 Clicking on OK

4-4 Section 4-2 - General Procedure

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

4-2-2-3 Entering Maintenance Mode (cont’d)

7.) Click on maintenance.

Figure 4-6 Clicking on Maintetance

8.) Click on Exit to window.

Figure 4-7 Clicking on Exit to Window

Section 4-2 - General Procedure 4-5

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

4-2-2-3 Entering Maintenance Mode (cont’d)

4-2-2-3-2 R 4.x.x to R6.0.x

1.) The Start Up Screen will be shown on the Monitor display when the system is turned ON.

2.) The “Probing for maintenance access” dialog appears. Enter Password, then click on OK.

3.) Then Start Loader display will be shown on the Monitor display.Click on Maintenance.

Figure 4-8 Clicking on Mainttenance

4.) Click on Exit to Windows in maintenace diaglog window.Then the scanner is booted up automatically.

4-2-2-3-3 R2.x.x to R4.x.x

1.) Insert the service dongle in the Service port located at the rear panel.

2.) The Start Up Screen will be shown on the Monitor display when the system is turned ON.

3.) Then Start Loader display will be shown on the Monitor display. Then the scanner is booted up automatically.

NOTE: To enter the Maintenance Mode, select Maintenance button.

Figure 4-9 Start Application Window

NOTE: Start is selected automatically when it time out.

4-6 Section 4-2 - General Procedure

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

4-2-3 Power Shutdown

Purpose: This is a description on how to Shutdown the system.

4-2-3-1 Complete Power Down

1.) Press the ON/OFF

2.) Switch OFF the Main Circuit Breaker at the rear of the system Refer to Figure 4-1.

3.) Disconnect the Main Power Cable if needed. Refer to Figure 4-1.

key at the front of the System for about two (2) seconds. Refer to Figure 4-2.

4-2-4 System Stand-by

LOGIQ 7 is available with Stand-by option. The option is effective in reducing the scanner power up time, when used as portable device.

Users must follow the procedures in order to use the option.

NOTE: Do not use more than 20 Stand-by mode continuously without shutting down the system. The

scanner must be powered off daily.

1.) Press the POWER switch once.

2.) Select Standby.At this point, both the touch panel and the main monitor will go blank. Keyboard

lights also turns dark. Power switch button will be illuminated.

NOTICE

Standby

Figure 4-10 Selecting Standby

3.) Wait more than 20seconds.

Do not disconnect the power cable immediately.

4.) Plug off the power cord from wall outlet.

Do not press the Power button without connecting the power cable.

5.) Transport the scanner as required, but re-connect to power outlet within 20 minutes. If not powered

system may shut down due to loss of sustained battery power.

6.) Connect the scanner to a wall electrical outlet.

Section 4-2 - General Procedure 4-7

GE HEALTHCARE

DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

4-2-4 System Stand-by (cont’d)

7.) To power up the scanner, tap POWER button momentary, and wait for power up. It will approximately 45seconds for the scanner to power up.

NOTICE

Do not press the Power button long time, as it will cause the system to power down.

Stand-by Sequence

Stand-by

uence

Wait

Press POWER button

Select "Standby"

Che ck Monitor

OFF

Check Touch

Panel OFF

OFF

Connect to electrical outlet

(Power Cord)

Stan dby may be

faile d

Note1 : BT09 Release with BEP4 Hardware have "Blinking Power Button" capability to indicate the console in Stand-by condition. For BEP3 and earlier, Power button must be "OFF" before disconnecting the power cord.

Che ck POWER

button

(Note 1)

OFF or Blinking

Wait more than 20 seconds

Disconnect Power Cord

Figure 4-11 Stand-by Sequence

4-8 Section 4-2 - General Procedure

Press POWER button

Wait 5 se conds

Scanner Start up completion

in 45 seconds

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

4-2-5 Using CD-R/MOD/DVD Drive

4-2-5-1 Using CD-R or DVD Drive

NOTICE

CD-R Drive

Never move the unit with a disk in the CD-R or DVD because the drive actuator will not be locked and the CD-R or DVD could break.

1.) Push the EJECT

2.) Put the disk onto the disk tray.

3.) Press the EJECT

4.) There are a number of methods to eject a disk from the CD-R or DVD. Ejection is automatic in some cases. Manual ejection methods, listed in preferred order of use, are:

a.) Press EJECT b.) Press and hold EJECT

c.) Mechanical ejection. Insert the end of a paper clip into the hole while system power is OFF.

Avoid mechanical ejection whenever possible. Mechanical ejection leaves the actuator unlocked and the MOD susceptible to damage if moved. If forced to use this method, reboot the system, then insert and eject a known good disk using one of the other methods.

button, the disk tray will appear.

button to insert the disk into the CD-R or DVD device.

button on the CD-R or DVD while system is ON.

button while the system is booting.

Eject Button

Mechanical

Eject Hole

DVD Drive

Figure 4-12 CD-R or DVD drive

NOTE: Be careful not to scratch the disk when wiping it off for cleaning.

NOTE: Keeping your CD-R or DVD disc in an original CD-R or DVD case or caddy all the time will

prevent it from becoming dirty or damaged.

NOTE: Media Requirement:

Please be aware of the following regarding saving data to DVD-R on R6.0.x.:

Use x8 or x16 speed compatible DVD-R. When it is the upgraded R6.0.x system from R4.x.x. or prior version, some systems have a number "4" or "5" printed on the disc tray of the media drive and others don't. If there is no number printed on the disc tray, use x4 or x16 speed compatible DVD-R.

Section 4-2 - General Procedure 4-9

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

4-2-5-2 Using MOD Drive

1.) Before installing an MO disk in the MOD, check the MO disk for loose hardware or damaged labels which could jam inside the MO Drive. Also ensure that the slide switch in one corner of the disk is set so that the disk is write enabled (disk hole closed).

2.) Insert the disk into the MOD with the label facing up.

NOTICE

MO Drive

Never move the unit with a disk in the MOD because the drive actuator will not be locked and the MOD could break.

3.) The are a number of methods to eject a disk from the MOD. Ejection is automatic in some cases. Manual ejection methods, listed in preferred order of use, are:

a.) Press EJECT b.) Press and hold EJECT

button on the MOD while system is ON.

button while the system is booting.

c.) Mechanical eject. Insert the end of a paper clip into the hole while system power is OFF.

Eject Button

Mechanical

Eject Hole

Figure 4-13 MOD drive

4-10 Section 4-2 - General Procedure

MO Drive

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

4-2-6 Archiving and Loading Presets for BT07 (Including R7.5.x)

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

reload are as up–to–date as possible.

All user presets except changes to Summary, Anatomy, and Biometry pages, can be saved on an CDR/MO/DVD-R disk for reloading on the system.

NOTICE

Presets should NOT be saved on the same CD-R/MO/DVD-R disk as images. The Archive Menu lists the images but does NOT list the presets stored on a CD-R/MO/DVD-R disk.

4-2-6-1 Regional Preset - General (Supported from BT07)

NOTICE

Do not attempt to change/use Regional Preset buttons for Upgraded BT07. For Upgrade BT07 always use Factory Default in order to avoid preset conflict. Contact application specialist for details.

This feature has the capability to have factory default preset defined by the following regions; Americas, Europe, Asia, or Japan.

Table 4-2

Presets Unique to Regions Presets NOT unique to Regions

System Imaging (System>System Imaging page) System Measure (System->System Measure page) Imaging Settings (Imaging page) Comments (Comments page) Body Patterns (Body Patterns page) Application (Application page) 3D/4D (3D/4D page) Measure (Measure page) : Utility/Measure Advanced and Doppler preset

System General (System>General page) Connectivity (Connectivity page) Reports (Report page) Measure (Measure page) : Utility/Measure M&A and OB Table preset

Section 4-2 - General Procedure 4-11

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

4-2-6-2 Using Regional Preset

Regional Preset is selected during Application Load (Refer to 8-8-13 - Installing R7.x.x Application Software for details).

Current Regional Preset is displayed under Utility > System > About .

NOTICE

Figure 4-14 Current Regional Preset

For Upgraded BT07, this field always shows "None" as Region Preset is feature available for pure BT07 and onward.

Factory Default Regional Preset can be re-loaded from Utility > Systme > About > Additional About.

Figure 4-15 Factory Default Regional Preset

4-12 Section 4-2 - General Procedure

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

4-2-6-3 Cautions Using Regional Preset

• Do not attempt to modify Regional Preset on Upgraded BT07.

• Backup/Restore function should be used between the same region systems. Unexpected setting

may result if you restore the preset files to another region setting system.

CAUTION

When software is upgraded (from BT07 and on) re-loaded or upgraded (from BT07and on), make sure to select the factory default. Because the preset region information in globalconfig.res file shall not be upgraded, if different region presets are loaded, then it may cause conflict between system setting and region presets.

4-2-6-4 Formatting CD-R/DVD-R Disk

1.) Insert an empty (blank) CD-R/DVD-R disk into the CD-R/DVD-R device.

2.) Access to the Utility Menu on the Touch Panel, and select Connectivity>Removable Media.

3.) Select the removable media from media list.

4.) Type a name for the removable media in Label field.

5.) Select Format button.

Figure 4-16 Selecting Format Button

Section 4-2 - General Procedure 4-13

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

4-2-6-5 Archiving Presets to an CD-R/DVD-R Disk

1.) Insert an empty (blank) formatted CD-R/DVD-R disk into the CD-R/DVD-R device.

2.) Access to the Utility Menu on the Touch Panel, and select System>Backup/Restore. The Backup

screen will be shown on the monitor.

3.) Select the item to back up either from Resource Files.

4.) Select the media to locate the items.

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

Figure 4-17 Clicking on Backup

6.) Make sure “Finished OK” is displayed on the Result column.

4-14 Section 4-2 - General Procedure

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

4-2-6-6 Loading Presets from an CD-R/DVD-R disk

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

2.) Access to the Utility Menu on the Touch Panel, and select System>Backup/Restore. The Restore

sheet will be shown on the monitor.

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

4.) Click on Restore. A message to make sure the restore process is displayed on the monitor. Click

OK. The restore status for each item is displayed on the Result column.

Figure 4-18 Clicking on Restore

5.) Make sure “Finished OK” is displayed on the Result column.

4-2-6-7 Regional Preset - Files

Service Tip: The system shall have each region preset files into:

• Americas : C:/Pegasus/target/resources/Pegasus/ Americas/userdefs/

• Europe: C:/Pegasus/target/resources/Pegasus/Europe/userdefs/

• Asia: C:/Pegasus/target/resources/Pegasus/ Asia/userdefs/

• Japan: C:/Pegasus/target/resources/Pegasus/Japan/userdefs/

When region is selected, Region preset files are copied to:

• C:/Pegasus/target/resources/idunn/userdefs/

Section 4-2 - General Procedure 4-15

GE HEALTHCARE DIRECTION 2286865, REVISION 14 LOGIQ™ 7 SERVICE MANUAL

4-2-7 Archiving and Loading Presets for BT06/V65x or lower

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

reload are as up–to–date as possible.

All user presets except changes to Summary, Anatomy, and Biometry pages, can be saved on an CDR/MO/DVD-R disk for reloading on the system.

NOTICE

4-2-7-1 Formatting CD-R/MO/DVD-R Disk

Presets should NOT be saved on the same CD-R/MO/DVD-R disk as images. The Archive Menu lists the images but does NOT list the presets stored on a CD-R/MO/DVD-R disk.

1.) Insert an empty (blank) CD-R/MO/DVD-R disk into the CD-R/MO/DVD-R device.

2.) Access to the Utility Menu on the Touch Panel, and select Connectivity>Removable Media or

Tools.

Figure 4-19 Formatting Removable Media1

4-16 Section 4-2 - General Procedure

General Electric LOGIQ 7 SERVICE MANUAL_SM_2286865_14 BENCH FUME HOOD with Auto-return Sash LV05 Style Installation Instructions

Specifications and Main Features

Frequently Asked Questions

User Manual

Section 1-1 Overview

1-1-1 Purpose of Chapter 1

1-1-2 Chapter Contents

1-1-3 Purpose of Service Manual

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

1-1-5 LOGIQ™ 7 Models Covered by this Manual

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

Section 1-2 Important Conventions

1-2-1 Conventions Used in Book

1-2-2 Standard Hazard Icons

1-2-3 Product Icons

Section 1-3 Safety Considerations

1-3-1 Introduction

1-3-2 Human Safety

1-3-3 Mechanical Safety

1-3-4 Electrical Safety

1-3-5 Label Locations (For BT07 or later, including R7.5.x)

1-3-6 Label Locations (For BT04, BT06, and V65x)

1-3-7 Label Locations (For BT03 or lower)

1-3-8 Dangerous Procedure Warnings

1-3-9 Lockout/Tagout Requirements (For USA Only)

1-3-10 Returning/Shipping Probes and Repair Parts

1-3-11 How to remove the Ghost CD-ROM

Section 1-4 EMC, EMI, and ESD

1-4-1 Electromagnetic Compatibility

1-4-2 Electrostatic Discharge (ESD) Prevention

1-4-3 CE Compliance

Section 1-5 Customer Assistance

1-5-1 System Manufacture

1-5-2 Contact Information

Section 2-1 Overview

2-1-1 Purpose of this chapter 2

Section 2-2 General Console Requirements

2-2-1 Console Environmental Requirements

2-2-2 Electrical Requirements

2-2-3 EMI Limitations

2-2-4 Probes Environmental Requirements

Section 2-3 Facility Needs

2-3-1 Purchaser Responsibilities

2-3-2 Required Features

2-3-3 Desirable Ultrasound Room Facilities

2-3-4 Recommended and Alternate Ultrasound Room Layout

2-3-5 Networking Pre-installation Requirements

Section 3-1 Overview

3-1-1 Purpose of Chapter 3

3-1-2 Average Installation Time

3-1-3 Installation Warnings

Section 3-2 Receiving and Unpacking the Equipment

3-2-1 Safety Reminders

3-2-2 Moving into Position

3-2-3 LCD Monitor Tilt Caution

3-2-4 LCD Monitor Swing CautionLCD Monitor Tilt Caution

3-2-5 LCD Monitor Removal Caution

3-2-6 Shipping Delivery Requirements

Section 3-3 Preparing for Installation

3-3-1 Verify Customer Order

3-3-2 Physical Inspection

3-3-3 EMI Protection

Section 3-4 Completing the Installation

3-4-1 Probe (Transducer) Connection

3-4-2 Optional Peripherals/Peripheral Connection

3-4-3 Available Probes

3-4-4 Video Specification

3-4-5 Software Option Configuration

Section 3-5 Installation Paperwork

3-5-1 Peripherals/Accessories Connector Panel

Section 4-1 Overview

4-1-1 Purpose for Chapter 4

Functional Checks

4-1-2 Special Equipment Required

Section 4-2 General Procedure

4-2-1 Lockout/Tagout Requirements

4-2-2 Power On/Boot Up

4-2-3 Power Shutdown

4-2-4 System Stand-by

4-2-5 Using CD-R/MOD/DVD Drive