GE HEALTHCARE Logiq Book XP series Basic Service Manual

GE Healthcare

LOGIQ BOOK XP Series

Basic Service Manual

Part Number: 5194296-100

Revision: 10

GE H EALTHCARE

D IRECTION 5194296-100, R EVISION 10 LOGIQ BOOK XP S ERIES B ASIC S ERVICE M ANUAL

Important Precautions

WARNING

(EN)

THIS SERVICE MANUAL IS AVAILABLE IN ENGLISH ONLY.

• IF A CUSTOMER’S SERVICE PROVIDER REQUIRES A LANGUAGE OTHER

THAN ENGLISH, IT IS THE CUSTOMER’S RESPONSIBILITY TO PROVIDE

TRANSLATION SERVICES.

• DO NOT ATTEMPT TO SERVICE THE EQUIPMENT UNLESS THIS SERVICE

MANUAL HAS BEEN CONSULTED AND IS UNDERSTOOD.

• FAILURE TO HEED THIS WARNING MAY RESULT IN INJURY TO THE SERVICE

PROVIDER, OPERATOR OR PATIENT FROM ELECTRIC SHOCK, MECHANICAL

OR OTHER HAZARDS.

AVERTISSEMENT

(FR)

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

• SI LE TECHNICIEN DU CLIENT A BESOIN DE CE MANUEL DANS UNE AUTRE

LANGUE QUE L’ANGLAIS, C’EST AU CLIENT QU’IL INCOMBE DE LE FAIRE

TRADUIRE.

• NE PAS TENTER D’INTERVENTION SUR LES ÉQUIPEMENTS TANT QUE LE

MANUEL SERVICE N’A PAS ÉTÉ CONSULTÉ ET COMPRIS.

• LE NON-RESPECT DE CET AVERTISSEMENT PEUT ENTRAÎNER CHEZ LE

TECHNICIEN, L’OPÉRATEUR OU LE PATIENT DES BLESSURES DUES À DES

DANGERS ÉLECTRIQUES, MÉCANIQUES OU AUTRES.

WARNUNG

(DE)

DIESES KUNDENDIENST-HANDBUCH EXISTIERT NUR IN ENGLISCHER

SPRACHE.

• FALLS EIN FREMDER KUNDENDIENST EINE ANDERE SPRACHE BENÖTIGT,

IST ES AUFGABE DES KUNDEN FÜR EINE ENTSPRECHENDE ÜBERSETZUNG

ZU SORGEN.

• VERSUCHEN SIE NICHT, DAS GERÄT ZU REPARIEREN, BEVOR DIESES

KUNDENDIENST-HANDBUCH NICHT ZU RATE GEZOGEN UND VERSTANDEN

WURDE.

• WIRD DIESE WARNUNG NICHT BEACHTET, SO KANN ES ZU VERLETZUNGEN

DES KUNDENDIENSTTECHNIKERS, DES BEDIENERS ODER DES PATIENTEN

DURCH ELEKTRISCHE SCHLÄGE, MECHANISCHE ODER SONSTIGE

GEFAHREN KOMMEN.

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AVISO

(ES)

ESTE MANUAL DE SERVICIO SÓLO EXISTE EN INGLÉS.

• SI ALGÚN PROVEEDOR DE SERVICIOS AJENO A GEHC SOLICITA UN IDIOMA

QUE NO SEA EL INGLÉS, ES RESPONSABILIDAD DEL CLIENTE OFRECER UN

SERVICIO DE TRADUCCIÓN.

• NO SE DEBERÁ DAR SERVICIO TÉCNICO AL EQUIPO, SIN HABER

CONSULTADO Y COMPRENDIDO ESTE MANUAL DE SERVICIO.

• LA NO OBSERVANCIA DEL PRESENTE AVISO PUEDE DAR LUGAR A QUE EL

PROVEEDOR DE SERVICIOS, EL OPERADOR O EL PACIENTE SUFRAN

LESIONES PROVOCADAS POR CAUSAS ELÉCTRICAS, MECÁNICAS O DE

OTRA NATURALEZA.

ATENÇÃO

(PT-Br)

ESTE MANUAL DE ASSISTÊNCIA TÉCNICA SÓ SE ENCONTRA DISPONÍVEL EM

INGLÊS.

• SE QUALQUER OUTRO SERVIÇO DE ASSISTÊNCIA TÉCNICA, QUE NÃO A

GEHC, SOLICITAR ESTES MANUAIS NOUTRO IDIOMA, É DA

RESPONSABILIDADE DO CLIENTE FORNECER OS SERVIÇOS DE TRADUÇÃO.

• NÃO TENTE REPARAR O EQUIPAMENTO SEM TER CONSULTADO E

COMPREENDIDO ESTE MANUAL DE ASSISTÊNCIA TÉCNICA.

• O NÃO CUMPRIMENTO DESTE AVISO PODE POR EM PERIGO A SEGURANÇA

DO TÉCNICO, OPERADOR OU PACIENTE DEVIDO A‘ CHOQUES ELÉTRICOS,

MECÂNICOS OU OUTROS.

AVISO

(PT-pt)

ESTE MANUAL DE ASSISTÊNCIA ESTÁ DISPONÍVEL APENAS EM INGLÊS.

• SE QUALQUER OUTRO SERVIÇO DE ASSISTÊNCIA TÉCNICA, QUE NÃO A

GEHC, SOLICITAR ESTES MANUAIS NOUTRO IDIOMA, É DA

RESPONSABILIDADE DO CLIENTE FORNECER OS SERVIÇOS DE TRADUÇÃO.

• NÃO TENTE EFECTUAR REPARAÇÕES NO EQUIPAMENTO SEM TER

CONSULTADO E COMPREENDIDO PREVIAMENTE ESTE MANUAL.

• A INOBSERVÂNCIA DESTE AVISO PODE RESULTAR EM FERIMENTOS NO

TÉCNICO DE ASSISTÊNCIA, OPERADOR OU PACIENTE EM CONSEQUÊNCIA

DE CHOQUE ELÉCTRICO, PERIGOS DE ORIGEM MECÂNICA, BEM COMO DE

OUTROS TIPOS.

ii

AVVERTENZA

(IT)

IL PRESENTE MANUALE DI MANUTENZIONE È DISPONIBILE SOLTANTO IN

INGLESE.

• SE UN ADDETTO ALLA MANUTENZIONE ESTERNO ALLA GEHC RICHIEDE IL

MANUALE IN UNA LINGUA DIVERSA, IL CLIENTE È TENUTO A PROVVEDERE

DIRETTAMENTE ALLA TRADUZIONE.

• SI PROCEDA ALLA MANUTENZIONE DELL’APPARECCHIATURA SOLO DOPO

AVER CONSULTATO IL PRESENTE MANUALE ED AVERNE COMPRESO IL

CONTENUTO.

• NON TENERE CONTO DELLA PRESENTE AVVERTENZA POTREBBE FAR

COMPIERE OPERAZIONI DA CUI DERIVINO LESIONI ALL’ADDETTO ALLA

MANUTENZIONE, ALL’UTILIZZATORE ED AL PAZIENTE PER FOLGORAZIONE

ELETTRICA, PER URTI MECCANICI OD ALTRI RISCHI.

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HOIATUS

(ET)

KÄESOLEV TEENINDUSJUHEND ON SAADAVAL AINULT INGLISE KEELES.

• KUI KLIENDITEENINDUSE OSUTAJA NÕUAB JUHENDIT INGLISE KEELEST

ERINEVAS KEELES, VASTUTAB KLIENT TÕLKETEENUSE OSUTAMISE EEST.

• ÄRGE ÜRITAGE SEADMEID TEENINDADA ENNE EELNEVALT KÄESOLEVA

TEENINDUSJUHENDIGA TUTVUMIST JA SELLEST ARU SAAMIST.

• KÄESOLEVA HOIATUSE EIRAMINE VÕIB PÕHJUSTADA TEENUSEOSUTAJA,

OPERAATORI VÕI PATSIENDI VIGASTAMIST ELEKTRILÖÖGI, MEHAANILISE

VÕI MUU OHU TAGAJÄRJEL.

VAROITUS

(FI)

TÄMÄ HUOLTO-OHJE ON SAATAVILLA VAIN ENGLANNIKSI.

• JOS ASIAKKAAN PALVELUNTARJOAJA VAATII MUUTA KUIN

ENGLANNINKIELISTÄ MATERIAALIA, TARVITTAVAN KÄÄNNÖKSEN

HANKKIMINEN ON ASIAKKAAN VASTUULLA.

• ÄLÄ YRITÄ KORJATA LAITTEISTOA ENNEN KUIN OLET VARMASTI LUKENUT

JA YMMÄRTÄNYT TÄMÄN HUOLTO-OHJEEN.

• MIKÄLI TÄTÄ VAROITUSTA EI NOUDATETA, SEURAUKSENA VOI OLLA

PALVELUNTARJOAJAN, LAITTEISTON KÄYTTÄJÄN TAI POTILAAN

VAHINGOITTUMINEN SÄHKÖISKUN, MEKAANISEN VIAN TAI MUUN

VAARATILANTEEN VUOKSI.

ΠΡΟΕΙΔΟΠΟΙΗΣΗ

(EL)

ΤΟ ΠΑΡΟΝ ΕΓΧΕΙΡΙΔΙΟ ΣΕΡΒΙΣ ΔΙΑΤΙΘΕΤΑΙ ΣΤΑ ΑΓΓΛΙΚΑ ΜΟΝΟ.

• ΕΑΝ ΤΟ ΑΤΟΜΟ ΠΑΡΟΧΗΣ ΣΕΡΒΙΣ ΕΝΟΣ ΠΕΛΑΤΗ ΑΠΑΙΤΕΙ ΤΟ ΠΑΡΟΝ

ΕΓΧΕΙΡΙΔΙΟ ΣΕ ΓΛΩΣΣΑ ΕΚΤΟΣ ΤΩΝ ΑΓΓΛΙΚΩΝ, ΑΠΟΤΕΛΕΙ ΕΥΘΥΝΗ ΤΟΥ

ΠΕΛΑΤΗ ΝΑ ΠΑΡΕΧΕΙ ΥΠΗΡΕΣΙΕΣ ΜΕΤΑΦΡΑΣΗΣ.

• ΜΗΝ ΕΠΙΧΕΙΡΗΣΕΤΕ ΤΗΝ ΕΚΤΕΛΕΣΗ ΕΡΓΑΣΙΩΝ ΣΕΡΒΙΣ ΣΤΟΝ ΕΞΟΠΛΙΣΜΟ

ΕΚΤΟΣ ΕΑΝ ΕΧΕΤΕ ΣΥΜΒΟΥΛΕΥΤΕΙ ΚΑΙ ΕΧΕΤΕ ΚΑΤΑΝΟΗΣΕΙ ΤΟ ΠΑΡΟΝ

ΕΓΧΕΙΡΙΔΙΟ ΣΕΡΒΙΣ.

• ΕΑΝ ΔΕ ΛΑΒΕΤΕ ΥΠΟΨΗ ΤΗΝ ΠΡΟΕΙΔΟΠΟΙΗΣΗ ΑΥΤΗ, ΕΝΔΕΧΕΤΑΙ ΝΑ

ΠΡΟΚΛΗΘΕΙ ΤΡΑΥΜΑΤΙΣΜΟΣ ΣΤΟ ΑΤΟΜΟ ΠΑΡΟΧΗΣ ΣΕΡΒΙΣ, ΣΤΟ ΧΕΙΡΙΣΤΗ Ή

ΣΤΟΝ ΑΣΘΕΝΗ ΑΠΟ ΗΛΕΚΤΡΟΠΛΗΞΙΑ, ΜΗΧΑΝΙΚΟΥΣ Ή ΑΛΛΟΥΣ ΚΙΝΔΥΝΟΥΣ.

FIGYELMEZTETÉS

(HU)

EZEN KARBANTARTÁSI KÉZIKÖNYV KIZÁRÓLAG ANGOL NYELVEN ÉRHET Ő EL.

• HA A VEV Ő SZOLGÁLTATÓJA ANGOLTÓL ELTÉRŐ NYELVRE TART IGÉNYT,

AKKOR A VEV Ő FELELŐSSÉGE A FORDÍTÁS ELKÉSZÍTTETÉSE.

• NE PRÓBÁLJA ELKEZDENI HASZNÁLNI A BERENDEZÉST, AMÍG A

KARBANTARTÁSI KÉZIKÖNYVBEN LEÍRTAKAT NEM ÉRTELMEZTÉK.

• EZEN FIGYELMEZTETÉS FIGYELMEN KÍVÜL HAGYÁSA A SZOLGÁLTATÓ,

M ŰKÖDTETŐ VAGY A BETEG ÁRAMÜTÉS, MECHANIKAI VAGY EGYÉB

VESZÉLYHELYZET MIATTI SÉRÜLÉSÉT EREDMÉNYEZHETI.

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VIÐVÖRUN

(IS)

VÝSTRAHA

(CS)

ÞESSI ÞJÓNUSTUHANDBÓK ER EINGÖNGU FÁANLEG Á ENSKU.

• EF ÞJÓNUSTUAÐILI VIÐSKIPTAMANNS ÞARFNAST ANNARS TUNGUMÁLS EN

ENSKU, ER ÞAÐ Á ÁBYRGÐ VIÐSKIPTAMANNS AÐ ÚTVEGA ÞÝÐINGU.

• REYNIÐ EKKI AÐ ÞJÓNUSTA TÆKIÐ NEMA EFTIR AÐ HAFA SKOÐAÐ OG

SKILIÐ ÞESSA ÞJÓNUSTUHANDBÓK.

• EF EKKI ER FARIÐ AÐ ÞESSARI VIÐVÖRUN GETUR ÞAÐ VALDIÐ MEIÐSLUM

ÞJÓNUSTUVEITANDA, STJÓRNANDA EÐA SJÚKLINGS VEGNA RAFLOSTS,

VÉLRÆNNAR EÐA ANNARRAR HÆTTU.

TENTO SERVISNÍ NÁVOD EXISTUJE POUZE V ANGLICKÉM JAZYCE.

• V P ŘÍPADĚ, ŽE POSKYTOVATEL SLUŽEB ZÁKAZNÍKŮM POTŘEBUJE NÁVOD

V JINÉM JAZYCE, JE ZAJIŠT ĚNÍ PŘEKLADU DO ODPOVÍDAJÍCÍHO JAZYKA

ÚKOLEM ZÁKAZNÍKA.

• NEPROVÁD ĚJTE ÚDRŽBU TOHOTO ZAŘÍZENÍ, ANIŽ BYSTE SI PŘEČETLI

TENTO SERVISNÍ NÁVOD A POCHOPILI JEHO OBSAH.

• V P ŘÍPADĚ NEDODRŽOVÁNÍ TÉTO VÝSTRAHY MŮŽE DOJÍT ÚRAZU

ELEKTRICKÁM PROUDEM PRACOVNÍKA POSKYTOVATELE SLUŽEB,

OBSLUŽNÉHO PERSONÁLU NEBO PACIENT Ů VLIVEM ELEKTRICKÉHOP

PROUDU, RESPEKTIVE VLIVEM K RIZIKU MECHANICKÉHO POŠKOZENÍ NEBO

JINÉMU RIZIKU.

ADVARSEL

(DA)

DENNE SERVICEMANUAL FINDES KUN PÅ ENGELSK.

• HVIS EN KUNDES TEKNIKER HAR BRUG FOR ET ANDET SPROG END

ENGELSK, ER DET KUNDENS ANSVAR AT SØRGE FOR OVERSÆTTELSE.

• FORSØG IKKE AT SERVICERE UDSTYRET MEDMINDRE

DENNE SERVICEMANUAL ER BLEVET LÆST OG FORSTÅET.

• MANGLENDE OVERHOLDELSE AF DENNE ADVARSEL KAN MEDF ŘRE SKADE

P Ĺ GRUND AF ELEKTRISK, MEKANISK ELLER ANDEN FARE FOR

TEKNIKEREN, OPERAT ŘREN ELLER PATIENTEN.

WAARSCHUWING

(NL)

DEZE ONDERHOUDSHANDLEIDING IS ENKEL IN HET ENGELS VERKRIJGBAAR.

• ALS HET ONDERHOUDSPERSONEEL EEN ANDERE TAAL VEREIST, DAN IS DE

KLANT VERANTWOORDELIJK VOOR DE VERTALING ERVAN.

• PROBEER DE APPARATUUR NIET TE ONDERHOUDEN VOORDAT DEZE

ONDERHOUDSHANDLEIDING WERD GERAADPLEEGD EN BEGREPEN IS.

• INDIEN DEZE WAARSCHUWING NIET WORDT OPGEVOLGD, ZOU HET

ONDERHOUDSPERSONEEL, DE OPERATOR OF EEN PATIËNT GEWOND

KUNNEN RAKEN ALS GEVOLG VAN EEN ELEKTRISCHE SCHOK,

MECHANISCHE OF ANDERE GEVAREN.

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BR ĪDINĀJUMS

(LV)

Š Ī APKALPES ROKASGRĀMATA IR PIEEJAMA TIKAI ANGĻU VALODĀ.

• JA KLIENTA APKALPES SNIEDZ ĒJAM NEPIECIEŠAMA INFORMĀCIJA CITĀ

VALOD Ā, NEVIS ANGĻU, KLIENTA PIENĀKUMS IR NODROŠINĀT TULKOŠANU.

• NEVEICIET APR ĪKOJUMA APKALPI BEZ APKALPES ROKASGRĀMATAS

IZLAS ĪŠANAS UN SAPRAŠANAS.

• Š Ī BRĪDINĀJUMA NEIEVĒROŠANA VAR RADĪT ELEKTRISKĀS STRĀVAS

TRIECIENA, MEH ĀNISKU VAI CITU RISKU IZRAISĪTU TRAUMU APKALPES

SNIEDZ ĒJAM, OPERATORAM VAI PACIENTAM.

ĮSPĖJIMAS

(LT)

ŠIS EKSPLOATAVIMO VADOVAS YRA IŠLEISTAS TIK ANGL Ų KALBA.

• JEI KLIENTO PASLAUG Ų TEIKĖJUI REIKIA VADOVO KITA KALBA – NE ANGLŲ,

VERTIMU PASIR ŪPINTI TURI KLIENTAS.

• NEM ĖGINKITE ATLIKTI ĮRANGOS TECHNINĖS PRIEŽIŪROS DARBŲ, NEBENT

VADOVAUTUM ĖTĖS ŠIUO EKSPLOATAVIMO VADOVU IR JĮ SUPRASTUMĖTE

• NEPAISANT ŠIO PERSP ĖJIMO, PASLAUGŲ TEIKĖJAS, OPERATORIUS AR

PACIENTAS GALI B ŪTI SUŽEISTAS DĖL ELEKTROS SMŪGIO, MECHANINIŲ AR

KIT Ų PAVOJŲ.

ADVARSEL

(NO)

DENNE SERVICEHÅNDBOKEN FINNES BARE PÅ ENGELSK.

• HVIS KUNDENS SERVICELEVERANDØR TRENGER ET ANNET SPRÅK, ER DET

KUNDENS ANSVAR Å SØRGE FOR OVERSETTELSE.

• IKKE FORSØK Å REPARERE UTSTYRET UTEN AT DENNE

SERVICEHÅNDBOKEN ER LEST OG FORSTÅTT.

• MANGLENDE HENSYN TIL DENNE ADVARSELEN KAN FØRE TIL AT

SERVICELEVERANDØREN, OPERATØREN ELLER PASIENTEN SKADES PÅ

GRUNN AV ELEKTRISK STØT, MEKANISKE ELLER ANDRE FARER.

OSTRZE ŻENIE

(PL)

NINIEJSZY PODR ĘCZNIK SERWISOWY DOSTĘPNY JEST JEDYNIE W JĘZYKU

ANGIELSKIM.

• JE ŚLI FIRMA ŚWIADCZĄCA KLIENTOWI USłUGI SERWISOWE WYMAGA

UDOST ĘPNIENIA PODRĘCZNIKA W JĘZYKU INNYM NIŻ ANGIELSKI,

OBOWI ĄZEK ZAPEWNIENIA STOSOWNEGO TłUMACZENIA SPOCZYWA NA

KLIENCIE.

• NIE PRÓBOWA Ć SERWISOWAĆ NINIEJSZEGO SPRZĘTU BEZ UPRZEDNIEGO

ZAPOZNANIA SI Ę Z PODRĘCZNIKIEM SERWISOWYM.

• NIEZASTOSOWANIE SI Ę DO TEGO OSTRZEŻENIA MOżE GROZIĆ

OBRA ŻENIAMI CIAłA SERWISANTA, OPERATORA LUB PACJENTA W WYNIKU

PORA ŻENIA PRĄDEM, URAZU MECHANICZNEGO LUB INNEGO RODZAJU

ZAGRO ŻEŃ.

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ATEN ŢIE

(RO)

ACEST MANUAL DE SERVICE ESTE DISPONIBIL NUMAI ÎN LIMBA ENGLEZ Ă.

• DAC Ă UN FURNIZOR DE SERVICII PENTRU CLIENŢI NECESITĂ O ALTĂ LIMBĂ

DECÂT CEA ENGLEZ Ă, ESTE DE DATORIA CLIENTULUI SĂ FURNIZEZE O

TRADUCERE.

• NU ÎNCERCA ŢI SĂ REPARAŢI ECHIPAMENTUL DECÂT ULTERIOR

CONSULT ĂRII ŞI ÎNŢELEGERII ACESTUI MANUAL DE SERVICE.

• IGNORAREA ACESTUI AVERTISMENT AR PUTEA DUCE LA R ĂNIREA

DEPANATORULUI, OPERATORULUI SAU PACIENTULUI ÎN URMA

PERICOLELOR DE ELECTROCUTARE, MECANICE SAU DE ALT Ă NATURĂ.

ОСТОРОЖНО!

(RU)

ДАННОЕ РУКОВОДСТВО ПО ОБСЛУЖИВАНИЮ ПРЕДОСТАВЛЯЕТСЯ ТОЛЬКО

НА АНГЛИЙСКОМ ЯЗЫКЕ.

• ЕСЛИ СЕРВИСНОМУ ПЕРСОНАЛУ КЛИЕНТА НЕОБХОДИМО РУКОВОДСТВО

НЕ НА АНГЛИЙСКОМ ЯЗЫКЕ, КЛИЕНТУ СЛЕДУЕТ САМОСТОЯТЕЛЬНО

ОБЕСПЕЧИТЬ ПЕРЕВОД.

• ПЕРЕД ОБСЛУЖИВАНИЕМ ОБОРУДОВАНИЯ ОБЯЗАТЕЛЬНО ОБРАТИТЕСЬ

К 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.

ПРЕДУПРЕЖДЕНИЕ

(BG)

ТОВА СЕРВИЗНО РЪКОВОДСТВО Е НАЛИЧНО САМО НА АНГЛИЙСКИ ЕЗИК.

• АКО ДОСТАВЧИКЪТ НА СЕРВИЗНИ УСЛУГИ НА КЛИЕНТ СЕ НУЖДАЕ ОТ

ЕЗИК, РАЗЛИЧЕН ОТ АНГЛИЙСКИ, ЗАДЪЛЖЕНИЕ НА КЛИЕНТА Е ДА

ПРЕДОСТАВИ ПРЕВОДАЧЕСКА УСЛУГА.

• НЕ СЕ ОПИТВАЙТЕ ДА ИЗВЪРШВАТЕ СЕРВИЗНО ОБСЛУЖВАНЕ НА ТОВА

ОБОРУДВАНЕ, ОСВЕН ВСЛУЧАЙ, ЧЕ СЕРВИЗНОТО РЪКОВОДСТВО Е

ПРОЧЕТЕНО И СЕ РАЗБИРА.

• НЕСПАЗВАНЕТО НА ТОВА ПРЕДУПРЕЖДЕНИЕ МОЖЕ ДА ДОВЕДЕ ДО

НАРАНЯВАНЕ НА ДОСТАВЧИКА НА СЕРВИЗНИ УСЛУГИ, НА ОПЕРАТОРА

ИЛИ ПАЦИЕНТА ВСЛЕДСТВИЕНА ТОКОВ УДАР, МЕХАНИЧНИ ИЛИ ДРУГИ

РИСКОВЕ.

UPOZORENJE

(SR)

OVAJ PRIRU ČNIK ZA SERVISIRANJE DOSTUPAN JE SAMO NA ENGLESKOM

JEZIKU.

• AKO KLIJENTOV SERVISER ZAHTEVA JEZIK KOJI NIJE ENGLESKI,

ODGOVORNOST JE NA KLIJENTU DA PRUŽI USLUGE PREVO ĐENJA.

• NEMOJTE POKUŠAVATI DA SERVISIRATE OPREMU AKO NISTE PRO ČITALI I

RAZUMELI PRIRU ČNIK ZA SERVISIRANJE.

• AKO NE POŠTUJETE OVO UPOZORENJE, MOŽE DO ĆI DO POVREĐIVANJA

SERVISERA, OPERATERA ILI PACIJENTA UZROKOVANOG ELEKTRI ČNIM

UDAROM, MEHANI ČKIM I DRUGIM OPASNOSTIMA.

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OPOZORILO

(SL)

TA SERVISNI PRIRO ČNIK JE NA VOLJO SAMO V ANGLEŠČINI.

• ČE PONUDNIK SERVISNIH STORITEV ZA STRANKO POTREBUJE NAVODILA V

DRUGEM JEZIKU, JE ZA PREVOD ODGOVORNA STRANKA SAMA.

• NE POSKUŠAJTE SERVISIRATI OPREME, NE DA BI PREJ PREBRALI IN

RAZUMELI SERVISNI PRIRO ČNIK.

• ČE TEGA OPOZORILA NE UPOŠTEVATE, OBSTAJA NEVARNOST

ELEKTRI ČNEGA UDARA, MEHANSKIH ALI DRUGIH NEVARNOSTI IN

POSLEDI ČNIH POŠKODB PONUDNIKA SERVISNIH STORITEV, UPORABNIKA

OPREME ALI PACIENTA.

UPOZORENJE

(HR)

OVAJ SERVISNI PRIRU ČNIK DOSTUPAN JE SAMO NA ENGLESKOM JEZIKU.

• AKO KLIJENTOV SERVISER ZAHTIJEVA JEZIK KOJI NIJE ENGLESKI,

ODGOVORNOST KLIJENTA JE PRUŽITI USLUGE PREVO ĐENJA.

• NEMOJTE POKUŠAVATI SERVISIRATI OPREMU AKO NISTE PRO ČITALI I

RAZUMJELI SERVISNI PRIRU ČNIK.

• AKO NE POŠTUJETE OVO UPOZORENJE, MOŽE DO ĆI DO OZLJEDE

SERVISERA, OPERATERA ILI PACIJENTA PROUZRO ČENE STRUJNIM

UDAROM, MEHANI ČKIM I DRUGIM OPASNOSTIMA.

UPOZORNENIE

(SK)

TÁTO SERVISNÁ PRÍRU ČKA JE K DISPOZÍCII LEN V ANGLIČTINE.

• AK ZÁKAZNÍKOV POSKYTOVATE Ľ SLUŽIEB VYŽADUJE INÝ JAZYK AKO

ANGLI ČTINU, POSKYTNUTIE PREKLADATEĽSKÝCH SLUŽIEB JE

ZODPOVEDNOS ŤOU ZÁKAZNÍKA.

• NEPOKÚŠAJTE SA VYKONÁVA Ť SERVIS ZARIADENIA SKÔR, AKO SI

NEPRE ČÍTATE SERVISNÚ PRÍRUČKU A NEPOROZUMIETE JEJ.

• ZANEDBANIE TOHTO UPOZORNENIA MÔŽE VYÚSTI Ť DO ZRANENIA

POSKYTOVATE ĽA SLUŽIEB, OBSLUHUJÚCEJ OSOBY ALEBO PACIENTA

ELEKTRICKÝM PRÚDOM, PRÍPADNE DO MECHANICKÉHO ALEBO INÉHO

NEBEZPE ČENSTVA.

VARNING

(SV)

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.

vii

GE H EALTHCARE


D İKKAT

(TR)

BU SERV İS KILAVUZU YALNIZCA İNGİLİZCE OLARAK SAĞLANMIŞTIR.

• E ĞER MÜŞTERİ TEKNİSYENİ KILAVUZUN İNGİLİZCE DIŞINDAKİ BİR DİLDE

OLMASINI İSTERSE, KILAVUZU TERCÜME ETTİRMEK MÜŞTERİNİN

SORUMLULU ĞUNDADIR.

• SERV İS KILAVUZUNU OKUYUP ANLAMADAN EKİPMANLARA MÜDAHALE

ETMEY İNİZ.

• BU UYARININ GÖZ ARDI ED İLMESİ, ELEKTRİK ÇARPMASI YA DA MEKANİK

VEYA D İĞER TÜRDEN KAZALAR SONUCUNDA TEKNİSYENİN, OPERATÖRÜN

YA DA HASTANIN YARALANMASINA YOL AÇAB İLİR.

(JA)

Traditional

Chinese viii -

GE H EALTHCARE


(ZH-CN)

(KO)

ix

GE H EALTHCARE


DAMAGE IN TRANSPORTATION

All packages should be closely examined at time of delivery. If damage is apparent write “Damage In

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

CERTIFIED ELECTRICAL CONTRACTOR STATEMENT - FOR USA ONLY

All electrical Installations that are preliminary to positioning of the equipment at the site prepared for the equipment shall be performed by licensed electrical contractors. Other connections between pieces of electrical equipment, calibrations and testing shall be performed by qualified GE Healthcare personnel.

In performing all electrical work on these products, GE will use its own specially trained field engineers.

All of GE’s electrical work on these products will comply with the requirements of the applicable electrical codes.

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

OMISSIONS & ERRORS

If there are any omissions, errors or suggestions for improving this documentation, please contact the

GE Healthcare Global Documentation Group with specific information listing the system type, manual title, part number, revision number, page number and suggestion details.

Mail the information to:

Service Documentation,

GE Medical Systems (China) Co., Ltd.

No.19 Changjiang Road

WuXi National Hi-Tech Development Zone

Jiangsu, P.R China 214028

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

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

SERVICE SAFETY CONSIDERATIONS

DANGER

DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH, ARE PRESENT IN

THIS EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING AND

ADJUSTING.

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

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

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GE H EALTHCARE


LEGAL NOTES

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

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

TRADEMARKS

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

COPYRIGHTS

All Material Copyright© 2009-2012 by General Electric Company Inc. All Rights Reserved.

xi

GE H EALTHCARE


Revision History

Revision

9

10

7

8

5

6

3

4

1

2

Date

2007/06/25

2007/12/19

2008/09/18

2008/12/04

2010/09/15

2010/10/22

2011/12/25

2012/03/15

2012/05/29

2012/12/17

Reason for change

Initial Release.

Add one Caution for CMOS battery

Add one label for battery

Delete section “Using a Phantom”

Update the section “Important Precaution”

Update to add Isolation Cart Enhanced Version

Update for software R2.2.2 release

Update Application Software upgrade instruction and add new spare parts

Add instruction for loading system software with USB memory stick and add new spare parts

Update package label and add new spare parts

List of Effected Pages(LOEP)

Pages

Title Page

Important Precautions i to ix

Table of Contents pages i to xii

Chapter 1 - Introduction pages 1-1 to 1-18

Chapter 2 - Pre-Installation pages 2-1 to 2-10

Chapter 3 - Installation pages 3-1 to 3-50

Chapter 4 - Functional

Checks pages 4-1 to 4-30

Revision

N/A

10

10

10

10

10

10

Pages

Chapter 5 - Theory pages 5-1 to 5-18

Chapter 6 - Service

Adjustments pages 6-1 to 6-2

Chapter 7 - Diagnostics/

Troubleshooting pages 7-1 to 7-24

Chapter 8 - Replacement

Procedures pages 8-1 to 8-6

Chapter 9 - Replacement

Parts pages 9-1 to 9-16

Chapter 10 - Periodic

Maintenance pages 10-1 to 10-20

Index pages I to II

Revision

10

10

10

10

10

10

10 xii -

1

GE H EALTHCARE

D IRECTION 5194296-100, R EVISION 10 LOGIQ B OOK XP S ERIES B ASIC S ERVICE M ANUAL

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

Purpose of Operator Manual(s) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 2

Important Conventions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 3

Conventions Used in Book . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 3

Standard Hazard Icons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 4

Product Icons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 5

Safety Considerations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 9

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 9

Human Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 9

Mechanical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 9

Electrical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 10

Labels Locations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 10

Battery Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 11

Dangerous Procedure Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 13

Lockout/Tagout Requirements (For USA Only) . . . . . . . . . . . . . . . . . . . . . . 1 - 14

Returning/Shipping Probes and Repair Parts . . . . . . . . . . . . . . . . . . . . . . . 1 - 15

EMC, EMI, and ESD . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 16

Electromagnetic Compatibility (EMC) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 16

CE Compliance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 16

Electrostatic Discharge (ESD) Prevention . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 16

Customer Assistance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 17

Contact Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 17

System Manufacturer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 18

Table of Contents

2

GE H EALTHCARE

D IRECTION 5194296-100, R EVISION 10

CHAPTER 2

Pre Installation

LOGIQ B OOK XP S ERIES B ASIC S ERVICE M ANUAL

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

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

Chapter Contents . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 1

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

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

Lighting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2

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

LOGIQ Book XP Series Power Requirements . . . . . . . . . . . . . . . . 2 - 2

Inrush Current . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 3

Site Circuit Breaker . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 3

Site Power Outlets . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 3

Unit Power Plug . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 3

Power Stability Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 3

EMI Limitations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 4

Scan Probe Environmental Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 5

Facility Needs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 6

Recommended Ultrasound Room Layout . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 6

Purchaser Responsibilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 6

Required Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 7

Desirable Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 7

Recommended and Alternate Ultrasound Room Layout . . . . . . . . . . 2 - 8

Networking Pre-installation Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 9

Stand Alone System (without Network Connection) . . . . . . . . . . . . . 2 - 9

System Connected to Hospital’s Network . . . . . . . . . . . . . . . . . . . . . 2 - 9

Purpose of DICOM* Network Function . . . . . . . . . . . . . . . . . . . . . . . 2 - 9

DICOM* Option Pre-installation Requirements . . . . . . . . . . . . . . . . . 2 - 9

Table of Contents

GE H EALTHCARE


CHAPTER 3

Installation


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

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

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

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

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

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

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

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

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

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

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

System Voltage Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 8

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

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

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

System Power On . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 9

Turn on the system . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 10

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

Back-end Processor Power Down . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 10

System Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 11

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

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

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

Physical Dimensions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 12

Electrical Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 13

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

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

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

Rear Panel Connector . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 14

Connect peripherals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 18

Available Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 24

Software/Option Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 25

Connectivity Installation Worksheet . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 26

Table of Contents 3

GE H EALTHCARE


Loading the System Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 27

Loading the System Software with CD . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 28

Loading Base Image Software (For R2.2.1 or lower) . . . . . . . . . . . . 3 - 28

Upgrading Application Software (For R2.2.1 or lower) . . . . . . . . . . . 3 - 30

Loading the system software with DVD (For R2.2.2) . . . . . . . . . . . . . . . . . . 3 - 33

Loading the System Software with USB Memory Stick (For R2.2.2 or above) 3 - 38

Functional Check-out . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 43

Option Key Update . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 44

Probe Recognition Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 48

Peripheral Devices Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 48

Reinstall DICOM Devices . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 49

Paperwork . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 50

Product Locator Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 50

User Manual(s) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 50

4 Table of Contents

GE H EALTHCARE


CHAPTER 4

Functional Checks


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

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

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

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

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

System Power On . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 2

Turn on the system . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 3

Power Off/ Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 3

Back-end Processor Power Down . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 3

System Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 4

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

Archiving Presets to an CD-R disk . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 5

Loading Presets from an CD-R disk . . . . . . . . . . . . . . . . . . . . . . . . 4 - 5

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

Brightness . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 6

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

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

Control Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 7

LOGIQ Book XP Series SoftMenu Key Tour . . . . . . . . . . . . . . . . . 4 - 8

Monitor Display . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 9

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

Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 10

B Mode OP Panel Controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 11

B Mode Softmenu Key . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 12

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

Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 13

M Mode OP Panel Controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 14

M Mode Softmenu Key . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 15

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

Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 16

Color Flow Mode OP Panel Controls . . . . . . . . . . . . . . . . . . . . . . . . 4 - 17

Color Flow Mode Softemenu Key . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 18

Doppler Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 19

Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 19

Doppler Mode OP Panel Controls . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 20

Doppler Mode OP Panel Controls . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 21

Basic Measurements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 22

Distance and Tissue Depth Measurements . . . . . . . . . . . . . . . . . . . 4 - 22

Circumference/Area (Ellipse) Measurement . . . . . . . . . . . . . . . . . . 4 - 22

Worksheets . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 23


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Report* Pages . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 23

Probe/Connectors Usage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 23

Connecting a probe . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 23

Activating the probe . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 23

Deactivating the probe . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 23

Disconnecting the probe . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 23

Using Cine . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 24

Activating CINE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 24

Quickly Move to Start/End Frame . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 24

Start Frame/End Frame . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 24

Adjusting the CINE Loop Playback Speed . . . . . . . . . . . . . . . . . . . . 4 - 24

Moving through a CINE Loop Frame By Frame . . . . . . . . . . . . . . . . 4 - 24

Image Management (QG) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 24

Backup and Restore Database, Preset Configurations and Images . . . . . . 4 - 25

Formatting Media . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 25

Backup System Presets and Configurations . . . . . . . . . . . . . . . . . . . 4 - 26

Restore System Presets and Configurations . . . . . . . . . . . . . . . . . . 4 - 27

Archiving Images . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 28

Software Configuration Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 30

Peripheral Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 30


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CHAPTER 5

Components and Functions (Theory)

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

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

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

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

Power Diagrams . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 4

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 4

AC Power . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 4

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

Fans . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 6

Common Service Platform . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 7

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 7

Global Service User Interface (GSUI) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 7

Internationalization . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 7

Service Login . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 7

Access / Security . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 7

The usage for security cable . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 8

Service Home Page . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 9

Error Logs Tab (Not available on LOGIQ Book XP Series now) . . . . . . . 5 - 10

Logs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 11

Utilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 12

Search . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 12

Exit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 13

Diagnostics . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 14

Diagnostics Execution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 14

Diagnostic Reports . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 14

Image Quality . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 15

Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 15

Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 16

Utilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 16

Replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 16

PM . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 17


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CHAPTER 6

Service Adjustments


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

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

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

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


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CHAPTER 7

Diagnostics/Troubleshooting


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


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

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

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

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

Screen Captures. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 4

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

Setting the P3 Key to Screen Capture . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 5

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

Reset the P3 Key to Customer’s Functionality . . . . . . . . . . . . . . . . . . . . . . 7 - 7

Global Service User Interface (GSUI) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 8

Enter global service user interface . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 8

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

Reset Database . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 11

Clean Userdefs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 13

Update FPGA . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 15

Control Frame . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 15

Button . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 15

Loop Count . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 15

Progress Indicator . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 16

Short Text Message . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 16

Background Color . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 16

Common Diagnostics . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 17

Utilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 17

Disruptive Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 17

System Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 17

PC Diagnostics (Non-Interactive Tests) . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 18

CPU Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 18

Hard Drive Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 18

Memory Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 18

CD Drive Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 18

Video Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 18

USB Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 18

PC Diagnostics (Interactive Tests) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 18

Keyboard Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 18

LCD Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 18


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LOGIQ Book XP Series Diagnostic Descriptions . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 19

Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 19

FRU Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 20

MST . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 20

DFP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 21

DTX . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 22

DCNN . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 23

PC . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 24


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CHAPTER 8

Replacement Procedures


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


Disassembly/Re-assembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 1

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

Handle Assy (FRU No. 312) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 2

Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 2

Needed Manpower . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 2

Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 2

Removal Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 2

Mounting procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 2

Trackball Roller Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 4

Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 4

Needed Manpower . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 4

Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 4

Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 4

Loading the System Software. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 6


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CHAPTER 9

Renewal Parts


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

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

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

Renewal Parts Lists . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 2

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

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

Keyboard Assy. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 4

Bottom Assy. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 4

Isolation Cart Components . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 5

Isolation Cart Enhanced Version Components . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 7

Accessories and Kits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 10

Manuals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 14

Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 15


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CHAPTER 10

Care & Maintenance

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

Periodic Maintenance Inspections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 1

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

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

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

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

Maintenance Task Schedule . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 2

How often should care & maintenance tasks be performed? . . . . . . . . . . . 10 - 2

Tools Required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 4

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

Specific Requirements for Care & Maintenance . . . . . . . . . . . . . . . 10 - 4

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

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

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

System Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 6

Peripheral/Option Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 7

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

AC/DC Adapter Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 7

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

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

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

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

View the Logs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 9

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

Probe Related Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 9

Basic Probe Care . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 9

Basic Probe Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 9

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

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

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

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

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

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

Definition . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 14

Generic Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 14

Data Sheet for enclosure Source Leakage Current . . . . . . . . . . . . . 10 - 15


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

Definition . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 16

Generic Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 16

No Meter Probe Adapter Procedure . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 16

Data Sheet for Transducer Source Leakage Current . . . . . . . . . . . . 10 - 17

When There's Too Much Leakage Current... . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 18


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Chapter 1

Introduction


Section 1-1

Overview

1-1-1

1-1-2

Purpose of Chapter 1

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

Chapter Contents

Table 1-1 Contents in Chapter 1

Section

1-1

1-2

1-3

1-4

1-5

Overview

Important Conventions

Safety Considerations

EMC, EMI, and ESD

Customer Assistance

Description Page Number

1-1

1-3

1-9

1-15

1-16

1-1-3 Purpose of Service Manual

This Service Manual provides service information for the LOGIQ Book XP Series Ultrasound Scanning

System. It contains the following chapters:

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

2.) Chapter 2 - Pre Installation: Contains pre-installation requirements for the LOGIQ Book XP

Series.

3.) Chapter 3 - Installation: Contains installation procedures.

4.) Chapter 4 - Functional Checks: Contains functional checks that are recommended as part of the installation, or as required during servicing and periodic maintenance.

5.) Chapter 5 - Components and Functions (Theory): Contains block diagrams and functional explanations of the electronics.

6.) Chapter 6 - Service Adjustments: Contains instructions on how to make available adjustments to the LOGIQ Book XP Series.

7.) Chapter 7 - Diagnostics/Troubleshooting: Provides procedures for running diagnostic or related routines for the LOGIQ Book XP Series.

8.) Chapter 8 - Replacement Procedures: Provides disassembly procedures and reassembly procedures for all changeable Field Replaceable Units (FRU).

9.) Chapter 9 - Renewal Parts: Contains a complete list of field replaceable parts for the LOGIQ Book

XP Series.

10.)Chapter 10 - Care & Maintenance: Provides periodic maintenance procedures for the LOGIQ

Book XP Series.

Chapter 1 Introduction 1-1

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1-1-4


Typical Users of the Basic Service Manual

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

• Hospital’s Service Personnel

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

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

The Operator Manual(s) should be fully read and understood before operating the LOGIQ Book XP

Series and also kept near the unit for quick reference.

1-2 Section 1-1 - Overview

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Section 1-2

Important Conventions

1-2-1


Conventions Used in Book

Icons

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

Safety Precaution Messages

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

DANGER

DANGER IS USED TO INDICATE THE PRESENCE OF A HAZARD THAT WILL

CAUSE SEVERE PERSONAL INJURY OR DEATH IF THE INSTRUCTIONS ARE

IGNORED.

WARNING IS USED TO INDICATE THE PRESENCE OF A HAZARD THAT CAN CAUSE

SEVERE PERSONAL INJURY AND PROPERTY DAMAGE IF INSTRUCTIONS ARE

IGNORED.

CAUTION

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

NOTICE Equipment Damage Possible

Notice is used when a hazard is present that can cause property damage but has absolutely no personal injury risk.

Example: Disk drive will crash.

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

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


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1-2-2


Standard Hazard Icons

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

Table 1-2 Standard Hazard Icons

ELECTRICAL MECHANICAL RADIATION

LASER HEAT PINCH

LASER

LIGHT

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

Table 1-3 Standard Icons Indicating a Special Procedure Be Used

AVOID STATIC ELECTRICITY TAG AND LOCK OUT WEAR EYE PROTECTION

TAG

&

LOCKOUT

Signed Date

EYE

PROTECTION

1-4 Section 1-2 - Important Conventions

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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 1-4 Warnings

LABEL/SYMBOL

Identification and Rating Plate

PURPOSE/MEANING LOCATION

• Manufacture’s name and address

• Date of manufacture

• Model and serial numbers

• Electrical ratings (Volts, Amps, phase, and frequency)

Bottom panel of the console

Type/Class Label

IP Code (IPX1)

Used to indicate the degree of safety or protection.

Bottom panel of the adapter.

Indicates the degree of protection provided by the enclosure per IEC60

529. Can not be used in operating room environment.

Footswitch

Authorized European Representative address

Bottom panel

United States only Prescription

Requirement label

Bottom panel

Equipment Type BF (man in the box symbol) IEC 878-02-03 indicates B

Type equipment having a floating applied part.

Probe connectors

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

Various

General Warning Various

Do not push the system.

Rear of Isolation Cart


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LABEL/SYMBOL


PURPOSE/MEANING

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

Various

LOCATION

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

Various

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

“Off” indicates the power Off position of the power switch.

CAUTION

This Power Switch DOES NOT

ISOLATE Mains Supply

Power on/off switch

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

Inside of AC adapter

“TUV” Listing and Certification Mark is used to designate conformance to nationally recognized product safety standards. The Mark bears the name and /or logo of the testing laboratory, product category, safety standard is assessed and a control number.


Date of manufacture.

The date could be a year, year and month, or year, month and day, as appropriate. See ISO 8601 for date formates.

Rating Plate

Catalog or model number.

Rating Plate

1-6

Serial number Rating Plate

Equipment Class II.

For products not relying protective earth such as products having double or reinforced insulation.

Rating Plate

Direct Current.

For products to be powered from a DC supply.

Rating Plate

Section 1-2 - Important Conventions

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LABEL/SYMBOL


PURPOSE/MEANING

Input Rating Plate

For use with adapter model TWADP

100

Rating Plate

LOCATION

Description Rating Plate

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

ECG Module

Do not connect the CD-RW to system while scanning

CD-RW

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

Rating Plate

Indicates the product contains hazardous materials in excess of the limits established by Chinese standard

SJ/T11363-2006 Requirements for

Concentration Limits for Certain

Hazardous Substances in Electronic

Information Products. The number in the symbol is the Environment-friendly

Use Period (EFUP), which indicates the period during which the toxic or hazardous substances or elements contained in electronic information products will not leak or mutate under normal operating conditions so that the use of such electronic information products will not result in any severe environmental pollution, any bodily injury or damage to any assets.

Rear panel, rating plate

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



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LABEL/SYMBOL


PURPOSE/MEANING

The separate collection symbol is affixed to a battery, or its packaging, to advise you that the battery must be recycled or disposed of in accordance with local or country laws. The letters below the separate collection symbol indicate whether certain elements

(Pb=Lead, Cd=Cadmium, Hg=Mercury) are contained in the battery. To minimize potential effects on the environment and human health, it is important that all marked batteries that you remove from the product are properly recycled or disposed. For information on how the battery may be safely removed from the device, please consult the service manual or equipment instructions. Information on the potential effects on the environment and human health of the substances used in batteries is available at this url: http://www.gehealthcare.com/euen/ weee-recycling/index.html

Battery pack

LOCATION

GOST Symbol. Russia Regulatory

Country Clearance.

Bottom

1-8 Section 1-2 - Important Conventions

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Section 1-3

Safety Considerations

1-3-1

1-3-2

1-3-3


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.

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 Book XP Series Training are authorized to service the equipment.

Mechanical Safety

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.

CAUTION

The LOGIQ Book XP Series weights 4.3kg or more, depending on installed peripherals, when ready for use. To avoid possible injury and equipment damage:

ALWAYS:

• Use the handle to move the system.

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

• Limit movement to a slow careful walk.

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

• Before transporting, place the system in its special storage case.

• Ensure that the system is firmly secured while inside the vehicle.

• Secure system with straps or as directed otherwise to prevent motion during transport.

• Prevent vibration damage by driving cautiously. Avoid unpaved roads, excessive speeds, and erratic stops or starts.


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1-3-4


Electrical Safety

To minimize shock hazard, the equipment chassis must be connected to an electrical ground. The system is equipped with a three-conductor AC power cable. This must be plugged into an approved electrical outlet with protective ground.

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

Both the system power cable and the power connector meet international electrical standards.

1-3-5 Labels Locations

Please refer to Basic User Manual for label location information.

1-10 Section 1-3 - Safety Considerations

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1-3-6


Battery Safety

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

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

• Charge the batteries only when the ambient temperature is between 0

° and 40° C (32° and

104

° F).

• Do not short-circuit the battery by directly connecting the negative terminals with metal objects.

• Do not heat the battery or discard it in a fire.

• Do not expose the battery to temperature over 60

° C (140° F). Keep it away from fire and other heat sources.

• Do not charge the battery near a heat source, such as a fire or heater.

• Do not leave the battery in direct sunlight.

• Do not drop packs from height to prevent them from possible malfunction damage.

• Do not pierce the battery with a sharp object, hit it, or step on it.

• Do not use a damaged battery.

• Do not solder a battery.

• Do not connect the battery to an electrical power outlet.

• Do not contact PCM (Power Control and Monitor, it is a small board in the battery) directly to prevent packs from ESD damage.

• In the case of longer non-use of the LOGIQ Book XP Series, please make sure the battery is removed.

CAUTION

To avoid the battery bursting, igniting, or fumes from the battery causing equipment damage, observe the following precautions:

• Do not immerse the battery in water or allow it to get wet.

• Do not put the battery into a microwave oven or pressurized container.

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

• If the battery emits an odor or heat, is deformed or discolored, or in a way appears abnormal during use, recharging or storage, immediately remove it and stop using it. If you have any questions about the battery, consult GE or your local representative.

• Store the battery between -20

° C (-4° F) and 60° C (140°F).

• Use only GE recognized batteries.

• In case of the long term (3 months or more) storage:

• Store the battery in a temperature range of 10

° C (50° F) and 30° C (86°F).

• When charging for the first time after long-term storage. Recover such packs to original performance through repeating several cycles of full charging and discharging.

• When store packs for more than 6 months, charge at lease once charging require per 6 months to prevent leakage and deterioration in performance due to self-discharging.

• When the system isn't powered on continuously more than 6 months, in order to prevent leakage and deterioration in performance of CMOS battery, power on the system at least once per 6 months for more than 15 hours to have CMOS battery fully charged. Time and date need to be re-setup.

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


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1-3-7


Dangerous Procedure Warnings

Warnings, such as the examples below, precede potentially dangerous procedures throughout this manual. Instructions contained in the warnings must be followed.

DANGER

DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH, ARE PRESENT

IN THIS EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING

AND ADJUSTING.

EXPLOSION WARNING

DO NOT OPERATE THE EQUIPMENT IN AN EXPLOSIVE ATMOSPHERE.

OPERATION OF ANY ELECTRICAL EQUIPMENT IN SUCH AN ENVIRONMENT

CONSTITUTES A DEFINITE SAFETY HAZARD.

DO NOT SUBSTITUTE PARTS OR MODIFY EQUIPMENT

BECAUSE OF THE DANGER OF INTRODUCING ADDITIONAL HAZARDS, DO NOT

INSTALL SUBSTITUTE PARTS OR PERFORM ANY UNAUTHORIZED MODIFICATION

OF THE EQUIPMENT.

SHUT DOWN FORCEDLY OR PLUG IN/OUT ACDC INVALID MAY CAUSE THE

DAMAGE OF SYSTEM FILES.


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1-3-8


Lockout/Tagout Requirements (For USA Only)

Follow OSHA Lockout/Tagout requirements (USA) or local Lockout/Tagout requirements by ensuring you are in total control of the AC power plug at all times during the service process.

To apply Lockout/Tagout:

1.) Plan and prepare for shutdown.

2.) Shutdown the equipment.

3.) Isolate the equipment.

4.) Apply Lockout/Tagout Devices.

5.) Remove battery.

6.) Control all stored and residual energy.

7.) Verify isolation.

All potentially hazardous stored or residual energy is relieved.

Signed

NOTICE

TAG

&

LOCKOUT

Date

Energy Control and Power Lockout for LOGIQ Book XP Series

WHEN SERVICING PARTS OF THE SYSTEM WHERE THERE IS EXPOSURE TO VOLTAGE

GREATER THAN 30 VOLTS:

1. TURN OFF THE SCANNER.

2. UNPLUG THE SYSTEM.

3. MAINTAIN CONTROL OF THE SYSTEM POWER PLUG.

4. WAIT FOR AT LEAST 20 SECONDS FOR CAPACITORS TO DISCHARGE AS THERE ARE NO

TEST POINTS TO VERIFY ISOLATION. THE AMBER LIGHT ON THE OP PANEL ON/OFF BUTTON

WILL TURN OFF.

5. REMOVE THE SYSTEM BATTERY.


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1-3-9


Returning/Shipping Probes and Repair Parts

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

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

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

NOTE:

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.

The USER/SERVICE staff should dispose all the waste properly as per federal, state, and local waste disposal regulation.

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

If the system is sent for repair, please ensure that any patient information is backup and erased from the system before shipping. It is always possible during system failure and repair to lose patient data.

GE is not resposible for the loss of this data.

If PHI (Patient Healthcare Information) data needs to be sent to GE employees for service purposes,

GE will ascertain agreement from the customer. The patient information shall only be transferred by approved service processes, tools and devices restricting access, protecting or encrypting data where required, and providing traceability in the form of paper or electronic documents at each stage of the procedure while maintaining compliance with cross-border restrictions of patient information transfers.


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Section 1-4

EMC, EMI, and ESD

1-4-1

1-4-2

NOTE:

1-4-3


Electromagnetic Compatibility (EMC)

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

EMC also includes possible effects from electrical fields, magnetic fields, electrostatic discharge and disturbances in the electrical power supply.

CE Compliance

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

For applicable standards refer to the Safety Chapter in the Basic User Manual.

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.

Electrostatic Discharge (ESD) Prevention

DO NOT TOUCH ANY BOARDS WITH INTEGRATED CIRCUITS PRIOR TO TAKING

THE NECESSARY ESD PRECAUTIONS:

1.FOLLOW GENERAL GUIDELINES FOR HANDLING OF ELECTROSTATIC

SENSITIVE EQUIPMENT.


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Section 1-5

Customer Assistance

1-5-1


Contact Information

If this equipment does not work as indicated in this service manual or in the User Manual, or if you require additional assistance, please contact the local distributor or appropriate support resource, as listed below.

Prepare the following information before you call:

-

-

System ID serial number.

Software version.

Table 1-5 Phone Numbers for Customer Assistance

Location Phone Number

USA

GE Medical Systems

Ultrasound Service Engineering

9900 Innovation Drive

Wauwatosa, WI 53226

Service: On-site

Service: Parts

1-800–437–1171

1-800-558-2040

Canada

Latin America

Service

Applications Support

1-800-321-7937

1-262-524-5698

Europe

GE Ultraschall Deutschland GmbH& Co. KG Phone: +33 (0)130-831-300 (General Imaging and Cardiac)

BeethovenstraBe 239

Postfach 11 05 60, D-42665 Solingen

Germany

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

Asia (Singapore)

GE Ultrasound Asia

Service Department - Ultrasound

298 Tiong Bahru Road #15-01/06

Central Plaza

Singapore 169730

Applications support

Tel: +65 6291-8528

Fax: +65 272-3997

+81 426-482902

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

1-800-668-0732

Japan support Center

Phone: 81-42-648-2944

Fax: 81-42-648-2905

1-16 Section 1-5 - Customer Assistance

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1-5-2 System Manufacturer


Table 1-6 System Manufacturer

Manufacturer

GE Medical Systems (China) Co., Ltd.

No.19, Changjiang Road, Wuxi National Hi-Tech Dev. Zone, Jiangsu, P.R.

China 214028

GE Ultrasound Korea:

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

Korea 462-120

Phone Number

TEL: +86 510-85225888

FAX: +86 510-85226688

TEL: +82-31-740-6112

FAX: +82-31-740-6435


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This page was intentionally left blank.

1-18 Section 1-5 - Customer Assistance

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Chapter 2

Pre Installation


Section 2-1

Overview

2-1-1

2-1-2

Purpose of this chapter 2

This chapter provides the information required to plan and prepare for the installation of a LOGIQ Book

XP Series. Included are descriptions of the facility and electrical needs to be met by the purchaser of the unit.

Chapter Contents


Section

2-1

2-2

2-3

Description

Overview

General Console Requirements

Facility Needs

Page Number

2-1

2-2

2-6

Chapter 2 Pre Installation 2-1

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Section 2-2

General Console Requirements

2-2-1


Console Environmental Requirements

Table 2-2 Environmental Requirements for LOGIQ Book XP Series Systems

Operational Storage Transport

Temperature

Humidity

Pressure

10 - 40 degree C

30 - 75% non-condensing

700 - 1060hPa

-5 - 50 degree C


700 - 1060hPa

Temperatures in degree C, conversion to degree F = (degree C*(9/5) + 32)

-5 - 50 degree C


700 - 1060hPa

2-2-1-1

2-2-2

NOTE:

2-2-2-1

Lighting

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

Electrical Requirements

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

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

Sites with a mains power system with defined Neutral and Live:

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

Sites with a mains power system without a defined Neutral:

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

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

LOGIQ Book XP Series Power Requirements

Table 2-3 Electrical Specifications for LOGIQ Book XP Series

Adapter Name

ADM-9020M-GE

Voltage

100-240 VAC

Power

108VA

Tolerances

±10%

Current

1.08-0.45A

Frequency

50-60HZ

2-2 Section 2-2 - General Console Requirements

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2-2-2-2


Inrush Current

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

Table 2-4 Inrush Current

Voltage

100V

240V

Console Only

0.38A

0.20A

Inrush Current

Console with all peripherals

0.41A

0.21A

2-2-2-3

2-2-2-4

2-2-2-5

2-2-2-6

Site Circuit Breaker

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

Site Power Outlets

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

Unit Power Plug

If the unit arrives without a power plug, or with the wrong plug, you must contact your GE dealer or the installation engineer must supply what is locally required.

Power Stability Requirements

Voltage drop-out

Max 10 ms.

Power Transients

(All applications)

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


GE H EALTHCARE


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 Book XP Series complies with limits as stated on the EMC label. However there is no guarantee that interface will not occur in a particular installation.

Possible EMI sources should be identified before the unit is installed.

Electrical and electronic equipment may produce EMI unintentionally as the result of defect.

These sources include:

• medical lasers,

• scanners,

• cauterizing guns,

• computers,

• monitors,

• fans,

• gel warmers,

• microwave ovens,

• light dimmers,

• portable phones.

The presence of a broadcast station or broadcast van may also cause interference.

See Table 2-5 for EMI Prevention tips.

Table 2-5 EMI Prevention/abatement

EMI Rule Details

Be aware of RF sources

Ground the unit

Replace all screws, RF gaskets, covers, cores

Replace broken RF gaskets

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

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

After you finish repairing or updating the system, replace all covers and tighten all screws.

Any cable with an external connection requires a magnet wrap at each end. Install the shield over the front of card cage. Loose or missing covers or RF gaskets allow radio frequencies to interfere with the ultrasound signals.

If more than 20% or a pair of the fingers on an RF gasket are broken, replace the gasket.

Do not turn on the unit until any loose metallic part is removed.

Do not place labels where RF gaskets touch metal

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.

Use GE specified harnesses and peripherals

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.

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

Properly dress peripheral cables

Do not allow cables to lie across the top of the card cage or hang out of the peripheral bays.

Loop the excess length for peripheral cables inside the peripheral bays. Attach the monitor cables to the frame.

2-4 Section 2-2 - General Console Requirements

GE H EALTHCARE


2-2-4


Scan Probe Environmental Requirements

Operation:10° to 40° C

Storage:-10° to 50° C

NOTE: Temperature in degrees C. Conversion to Degrees F = (Degrees C * (9/5) + 32).

NOTICE SYSTEMS AND ELECTRONIC PROBES ARE DESIGNED FOR STORAGE TEMPERATURES OF

-10 TO + 50 degrees C. WHEN EXPOSED TO LARGE TEMPERATURE VARIATIONS, THE

PRODUCT SHOULD BE KEPT IN ROOM TEMPERATURE FOR 10 HOURS BEFORE USE.


GE H EALTHCARE


Section 2-3

Facility Needs

2-3-1

2-3-1-1

NOTE:


Recommended Ultrasound Room Layout

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.

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 prior to delivery of the machine. Carpet is not recommended because it collects dust and creates static. Potential sources of EMI (electromagnetic interference) should also be investigated before delivery. Dirt, static, and EMI can negatively impact system.

2-6 Section 2-3 - Facility Needs

GE H EALTHCARE


2-3-2 Required Features

NOTE:


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

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

Sites with a mains power system with defined Neutral and Live:

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

Sites with a mains power system without a defined Neutral:

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

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

• Dedicated single branch power outlet of adequate amperage meeting all local and national codes which is located less than 2.5 m (8 ft.) from the unit’s proposed location

• Door opening is at least 76 cm (30 in) wide

• Proposed location for unit is at least 0.2m (0.67 ft.) from the wall for cooling

• Power outlet and place for any external peripheral are within 2 m (6.5 ft.) of each other with peripheral within 1 m of the unit to connect cables.

• Power outlets for other medical equipment and gel warmer

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

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

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

2-3-3 Desirable Features

• Door is at least 92 cm (3 ft.) wide

• Circuit breaker for dedicated power outlet is easily accessible

• Sink with hot and cold water

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

• Emergency oxygen supply

• Storage for linens and equipment

• Nearby waiting room, lavatory, and dressing room

• Dual level lighting (bright and dim)

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


GE H EALTHCARE


2-3-3-1

LOGIQ B

Recommended and Alternate Ultrasound Room Layout

OOK XP S ERIES B ASIC S

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

ERVICE M ANUAL

D E D IC AT E D

P O W E R

R E C EP TA C LE

18 IN.

(46 C M ) LINEN SUPPLY

C O NS O LE

FILM V IEW E R

C O UN T E R TO P

FOOT

S W

S TOO L

SIN K

SU C T IO N LINE

E M E R G E C Y

OX Y G EN

76 IN.

(193 C M )

24 IN.

(61 C M )

SE CR E TA R YS O R

D O C TO R ’S D ES K

O V E R H E A D

LIG H T S D IMM E R

P AT IEN T

TO ILET

FILM V IEW E R

FILM SUPPLIES

SIN K

D OO R

42 IN.

(107 C M )

A 14 by 17 foot R ecommended Floor Plan

S cale : Each square equals one square foot

LINEN SUPPLY

P R OB ES /SUPPLIES

E XT E R N A L

PE R IPH E R A LS

S TOO L

FOOT

S W

LO G IQ B oo k X P

C O NS O LE

D E D IC AT E D PO W E R

O U T LE T S

24 IN.

(61 C M )

E XAM INA R IO N

TAB LE

76 IN.

(193 C M )

D OO R

30 IN.

(76 C M )

A n 8 by 10 foot M inimal Floor Plan

G E C AB INE T

FOT SO FT W A R E

A N D MA NU A LS

Figure 2-1 RECOMMENDED ULTRASOUND ROOM LAYOUT


GE H EALTHCARE


2-3-4


Networking Pre-installation Requirements

2-3-4-1

2-3-4-2

2-3-4-3

Stand Alone System (without Network Connection)

None.

System Connected to Hospital’s Network

Supported networks:

Wireless LAN

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 monitor and peripherals, enabling viewing to be done while scanning continues. With DICOM*, images can be archived, stored, and retrieved faster, easier, and at a lower cost.

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

To configure the LOGIQ Book XP Series to work with other network connections, the site’s network administrator must provide some necessary information.

Information must include:

• A host name, local port number, AE Title, IP address and Net Mask for the LOGIQ Book XP Series.

• The IP addresses for the default gateway and other routers at the site for ROUTING

INFORMATION.

• The host name, IP address, port and AE Title for each device the site wants connected to the

LOGIQ Book XP Series for DICOM* APPLICATION INFORMATION. A field for the make

(manufacturer) and the revision of the device, is also included. This information may be useful for solving errors.

NOTICE * DICOM is option on LOGIQ Book XP Series.


GE H EALTHCARE


2-3-4-4

.

LOGIQ B

DICOM* Option Pre-installation Requirements (cont’d)

OOK XP S ERIES B ASIC S ERVICE M ANUAL

.

LOGIQ Book

Host Name

AE Title

Local Port IP Address

Net Mask .

.

.

.

.

.

ROUTING INFORMATION

ROUTER1

ROUTER2

ROUTER3 .

.

.

Destination

IP Addresses

.

.

.

DICOM APPLICATION INFORMATION

NAME MAKE/REVISION

.

.

.

AE TITLE

Store 1

Default

GATEWAY IP Addresses

.

.

.

.

.

.

.

.

.

.

.

.

IP ADDRESSES

.

.

.

PORT

Store 2

Store 3 .

.

.

.

.

.

Store 4

Store 5

Store 6 .

.

.

.

.

.

.

.

.

Worklist

Storage

Commit

MPPS

.

.

.

Figure 2-2 Worksheet for DICOM Network Information

.

.

.

.

.

.


GE H EALTHCARE


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.


Section

3-1

3-6

3-7

3-8

3-9

3-2

3-3

3-4

3-5

Description

Overview

Receiving and Unpacking the Equipment

Packing the Equipment

Preparing for Installation

Completing the Installation

System Configuration

Software/Option Configuration

Connectivity Installation Worksheet

Loading the System Software

Page Number

3-1

3-12

3-25

3-26

3-27

3-4

3-7

3-8

3-9

3-1-2 Average Installation Time

Table 3-2 Average Installation Time

Description

Unpacking the system

Scanner wo/options

DICOM* Option

Average Installation Time

20 minutes

30 minutes

30 minutes

Comments

Dependent on the configuration that is required

Dependent on the amount of configuration

NOTICE * This function is option on LOGIQ Book XP Series.

The LOGIQ Book XP Series installation and functional checkout will take approximately one hour.

LOGIQ Book XP Series consoles with optional equipment may take slightly longer.

Chapter 3 Installation 3-1

GE H EALTHCARE


3-1-3


Installation Warnings

1.) There are no operator serviceable components. To prevent shock, do not remove any covers or panels. Should problems or malfunctions occur, unplug the power cord. Only qualified service personnel should carry out servicing.

NOTE: For information regarding packing labels, refer to LABELS ON PACKAGE.

2.) 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.

DANGER

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

°C

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

°F

140 131 122 113 104 95 86 77 68 59 50 41 32 23 14 5 -4 -13 -22 -31 -40 hrs 8 6 4 2 0 0 0 0 0 0 0 2 4 6 8 10 12 14 16 18 20

3-2 Section 3-1 - Overview

GE H EALTHCARE


3-1-4 Safety Reminders


DANGER

WHEN USING ANY TEST INSTRUMENT THAT IS CAPABLE OF OPENING THE

AC GROUND LINE (I.E., METER’S GROUND SWITCH IS OPEN), DON’T TOUCH

THE UNIT!

CAUTION

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.

DANGER

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.

DANGER

Do not operate this unit unless all board covers are securely in place.

DANGER

OPERATOR MANUAL(S)

The User Manual(s) should be fully read and understood before operating the LOGIQ Book XP

Series and kept near the unit for quick reference.

DANGER

ACOUSTIC OUTPUT HAZARD

Although the ultrasound energy transmitted from the LOGIQ Book XP Series probe is within FDA limits, avoid unnecessary exposure. Ultrasound energy can produce heat and mechanical damage


GE H EALTHCARE


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.

1.) Cut the four PLASTIC BANDs.

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

Adhesive tape

Plastic Bands

1

2

3-4

Figure 3-1 Open top covers of paper carton.

Section 3-2 - Receiving and Unpacking the Equipment

GE H EALTHCARE


Section 3-2 Receiving and Unpacking the Equipment

(cont’d)

3.) Take out the Paper pad.

4.) Take out console together with 2 interleavers.

5.) Take out the interleavers beside Accessories Package.

6.) Take out Accessories Package..

Paper pad

Console and interleavers interleaver

Figure 3-2 Unpacking the equipment

CAUTION

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


GE H EALTHCARE



(cont’d)

7.) Remove 2 interleavers.

8.) Remove plastic bag.

Interleaver

Plastic bag

Console

Figure 3-3 Removing interleavers and plastic bag

Interleaver

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

GE H EALTHCARE



(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.

Figure 3-4 Labels on Package

CAUTION

Please carefully unpack the system, and do not dispose the package of LOGIQ Book XP Series, so that it can be reused for service.

3-2-1 Moving into Position

CAUTION

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

CAUTION

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 Book XP Series. Before moving, store all loose parts in original accessory box or in back pack. Return probes to original box.

Section 3-3

Packing the Equipment

Please pack LOGIQ Book XP Series in the reverse order of unpacking.


GE H EALTHCARE


Section 3-4

Preparing for Installation

3-4-1

3-4-2

3-4-2-1

3-4-3


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.

Physical Inspection

System Voltage Settings

• Verify that the system is set to the correct voltage. The Voltage settings for the LOGIQ Book XP

Series System is found on a label located on the AC adapter.

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

Connecting a LOGIQ Book XP Series System to the wrong voltage level will most likely destroy the system.

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.

3-8 Section 3-4 - Preparing for Installation

GE H EALTHCARE


Section 3-5

Completing the Installation

3-5-1

NOTE:

3-5-1-1


Power On / Boot Up

After turning off a system, wait at least ten seconds before turning it on again. The system may not be able to boot if power is recycled too quickly.

System Power On

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

Figure 3-5 connect AC adapter

When power is applied to the system, power is distributed to the Cooling Unit, Control Panel, LCD,

Peripherals and the Back-end Processor.

CAUTION

The system should rest on the handle to allow an air gap to prevent overheating.


GE H EALTHCARE


3-5-1-2 Turn on the system

LOGIQ B OOK

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

XP S ERIES B ASIC S ERVICE M ANUAL

Power On/Off switch

3-5-2

NOTE:

3-5-2-1

Figure 3-6 Power On/Off Switch

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

No status messages are displayed during this process.

Power Off/ Shutdown


Back-end Processor Power Down

To power down the system:

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

2.) The System-Exit window is displayed.

3-10

Figure 3-7 System Exit Window

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

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

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

6.) Close LCD cover.

Section 3-5 - Completing the Installation

GE H EALTHCARE


3-5-2-2 System Shutdown

LOGIQ B OOK XP S ERIES B ASIC S

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

ERVICE M ANUAL

3-5-3

NOTE:

Transducer Connection

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

Please ensure that the probe latch is in an unlocked position before you connect the probe to the systsem.

NOTE:

Figure 3-8 Connect the probe

It is not necessary to turn OFF power to connect or disconnect a probe.


GE H EALTHCARE


Section 3-6

System Configuration

3-6-1

3-6-1-1


System Specifications

Physical Dimensions

The physical dimensions of the LOGIQ Book XP Series console are summarized in Figure 3-9 on page

3-12 .

Table 3-4 Physical Dimensions of LOGIQ Book XP Series

Height

78-99.5

3.07-3.92

Width

350

13.78

Depth

280-320

11-12.6

Unit mm inches

3-12

WEIGHT: 4.3KG (9.5 lb.)

NOTE: Length is in mm

350

Figure 3-9 Overall Dimensions

Section 3-6 - System Configuration

GE H EALTHCARE


3-6-2 Electrical Specifications


Table 3-5 Electrical Specifications for LOGIQ Book XP Series

Adapter

ADM-9020M-GE

Voltage

100-240 VAC

Tolerances

+/-10%

Current

1.08-0.45 A

Frequency

50/60Hz

3-6-3

NOTE:

Approved peripherals

Table 3-6 Approved peripherals

Device

B/W Printer

B/W Printer

Digital Color Printer

Digital Color Printer

Deskjet Color Printer

Officejet Color Printer



USB DVD-RW

USB DVD-RW

USB DVD-RW

USB DVD-RW

USB DVD-RW

USB DVD-RW

Wireless LAN Adapter



Network Adapter

Network Adapter

Network Adapter

Network Adapter

Footswitch

Footswitch

USB Memory

USB Memory

USB HUB

USB HUB

Manufacturer

LITEON

LITEON

Cisco

Cisco

Cisco

Netgear

TRENDNet

Netgear

TRENDNet

Whanam

Whanam

Sandisk

Sandisk

GAOJIAN

GAOJIAN

SONY

Mitsubishi

SONY

SONY

HP

HP

HP

HP

LITEON

LITEON

LITEON

Plextor

Model

UP-D897

P95D

UP-D23MD

UP-D25MD

HP470

HP K5400

HP K8600

HP 100 Mobile

LITEON DX-20A4P

LITEON Model eHAU 120

LITEON Model eHAU 324

PX-L890UE

LITEON eSAU108 DVDRW

LITEON eUAU108 DVDRW

LDK10250

AIR-CB2AG-A-K9

AIR-CB2AG-J-K9 (Only for Japan)

P/N:FA511

TE100-PCBUSR

ETX-PCM (Only for Japan)

TU2-ET100

FSU2001

FSU1000

Sandisk 2G

Sandisk 4G

HE702A

HE 420GE

See each option installation instructions for installation and connection procedures.

Interface

USB

USB

PCMCIA

PCMCIA

PCMCIA

PCMCIA

PCMCIA

PCMCIA

USB

USB

USB

USB

USB

USB

USB

USB

USB

USB

USB

USB

USB

USB

USB

USB

USB

USB

USB

Wire LAN card(FA511) must be worked with patient isolation box (P/N: EP200132), for details, please refer to option manual.


GE H EALTHCARE


3-6-4 Connecting Cables


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

Table 3-7 List of Connecting Cables

Name Part No.

Figure NOTE

USB Cable 5135661 For USB Printer & USB CD-RW

3-6-5

3-6-5-1

Peripherals/Accessories Connector Panel

LOGIQ Book XP Series peripherals and accessories can be properly connected using the rear connector panel.

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 printer, and service tools.

3-14 Section 3-6 - System Configuration

GE H EALTHCARE


3-6-5-1 Rear Panel Connector (cont’d)

LOGIQ B

This section indicates the pin assignment for each connector.


1

3

4

2

Figure 3-10 Rear Connector Panel

1.) PCMCIA Port for PC Card

2.) SVGA Output (CRT monitor option is not supported)

3.) Two interchangeable USB Port (Digital Printer, CD-RW and/or Footswitch, etc.)

4.) Port for DC input (AC Adapter)

NOTICE The USB devices should be connected to LOGIQ Book XP Series first, power on USB devices before turning LOGIQ Book XP Series to work.

NOTE:

NOTE:

After User insert the PC Card into the PCMCIA Port, a “Beep” of buzzer will be heard, which means the

Card works properly, otherwise, please pull out the Card and insert again.

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

Signal ground lines are not isolated.


GE H EALTHCARE



1. Pin Assignment of DC/DC input

Connector: 3 Pin, Female

Table 3-8 Pin Assignments of DC/DC input


Pin No.

1

2

Signal

+

NC

Pin No.

3

Signal

-

3-16

2. Pin Assignment of USB

Table 3-9 Pin assignment of USB1

Pin No.

1

2

Signal

+5VDC

DATA-

Table 3-10 Pin assignment of USB2

Pin No.

3

4

Pin No.

1

2

Signal

+5VDC

DATA-

Pin No.

3

4

Signal

DATA+

GND

Signal

DATA+

GND

3. Pin assignment of RS232C for external VGA

Connector: D-SUB, 15Pin, Female

Table 3-11 Pin Assignments of RS232C for External VGA

Pin No.

7

8

5

6

3

4

1

2

Signal

RED

GREEN

BLUE

N/A

GND

RGND

GGND

BGND

Pin No.

13

14

15

16

9

10

11

12

Signal

N/A

SGND

N/A

N/A

HSYNC

VSYNC

N/A


GE H EALTHCARE



4. Pin Assignment of PCMCIA

LOGIQ B

Table 3-12 Pin Assignments of PCMCIA

Pin No.

1

23

24

25

26

27

28

20

21

22

17

18

19

14

15

16

11

12

13

8

9

10

5

6

7

2

3

4

Signal

DGND

BCADR14

BWE_C#

BRDY_IREO#

PPCMVCCB

PPCMVPPB

BCADR15

BCADR16

BCADR12

BCADR7

BCADR6

BCADR5

BCADR4

BCADR3

BCADR2

BCADR1

BCDATA3

BCDATA4

BCDATA5

BCDATA6

BCDATA7

BCE1#

BCADR10

BOE#

BCADR11

BCADR9

BCADR8

BCADR13

Pin No.

35

57

58

59

60

61

62

54

55

56

51

52

53

48

49

50

45

46

47

42

43

44

39

40

41

36

37

38

Signal

DGND

BCADR19

BCADR20

BCADR21

PPCMVCCB

PPCMVPPB

BCADR22

BCADR23

BCADR24

BCADR25

BVC2#

BRESET

BWAIT#

BINPACK#

BREG#

BBCD2

BCD1#

BCDATA11

BCDATA12

BCDATA13

BCDATA14

BCDATA15

BCE2#

BVS1#

BIORD#

BIOWR#

BCADR17

BCADR18

Chapter 3 Installation


3-17

GE H EALTHCARE


Table 3-12 Pin Assignments of PCMCIA

3-6-5-2

Pin No.

29

30

31

32

33

34

Signal

BCADR0

BCDATA0

BCDATA1

BCDATA2

BIOCS16#

DGND

Pin No.

63

64

65

66

67

68

LOGIQ B

Signal

BBCD1

BCDATA8

BCDATA9

BCDATA10

BCD2#

DGND


Connect peripherals

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

B/W Printer can be properly connected using USB Port1 or USB Port 2( Figure 3-11 on page 3-18 ).

Figure 3-11 Connect B/W printer to the system


GE H EALTHCARE


3-6-5-2


Connect peripherals (cont’d)

B.) Connect color printer to the system.

Color Printer can be properly connected using USB Port1 or USB Port 2( Figure 3-12 on page 3-19 ).

Figure 3-12 Connect digital color printer to the system

NOTICE HP470 Deskjet Color Printer and HP K5400 Officejet Color Printer must connect with PIT (Printer

Isolation Transformer) when being used.


GE H EALTHCARE


3-6-5-2

LOGIQ B OOK XP S


C.) Connect CD-RW to the system.

CD-RW can be properly connected using USB Port1 or USB Port2.

ERIES B ASIC S ERVICE M ANUAL

3-20

Figure 3-13 Connect CD-RW to the system

Iomega CD-RW drive recommended media list

Media issues are common throughout the CD-RW drive industry. Because CD media vendors often change disc suppliers, quality levels may change due to manufacturing differences. This means that you may encounter CD creation problems with media that may have worked successfully before.

Overall system configuration and other factors may also affect the success of creating a CD.

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

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

Table 3-13 Iomega CD-RW drive recommended media list

Brand Name

Acer

Digital Research

Fuji Photo Film

Fuji Photo Film

Fuji Photo Film

Hi-Val

Imation

Iomega Verbatim

Kodak

Type

CDR80

CDR80

CDR74

CDR74

CDR80

CDR80

CDR80

CDR

CDR

Product Code

Acer Media

DRCDR3250

CD-R74C

CD-R650D

CD-R700D

CDR80 16x

CDR80 16x

CD-R74

CDR Ultima


Speed

40x-1x

32x-1x

24x-1x

24x-1x

24x-1x

24x-1x

24x-1x

32x-1x

16x-1x

GE H EALTHCARE


Table 3-13 Iomega CD-RW drive recommended media list

Brand Name

Kodak

Mitsui

Mitsui

Mitsubishi Chemical




Ricoh

Ricoh

Ricoh

Ricoh

Ricoh

Ricoh

Ricoh

Ricoh

Ricoh

CDRW

CDRW

Samsung CDR74

Sentinel CDR74

TDK

TDK

TDK

TDK

48x

CDR74

CDR74

CDR80

TDK

Verbatim

Verbatim

Verbatim

Yamaha

CDRW

CDR

CDR

CDRW

Type

CDR

CDR

CDR

Ultra CDRW

HS CDRW

CDRW

CDRW

CDR74

CDR74

CDR80

HS CDRW

CDRW

CDRW

CDRW

Product Code

CDR Gold Ultima

CDR74

CDR80

-

RW74EU1

RW74Q1

RW74U1P

Type 74R-SG

Type 74-SFSGH2

CD-R Type 80

CDRW 74 10x

74R-AZ2

74R-AZ2M3

74R-AZ2M4

74R-AZ

74R-AZAM

Premium CDR-74

-

CD-R74S

CD-R74A

CD-R80A

CD-RW74

DataLifePlus CD-R 700

DataLifePlus CD-R 650

DataLifePlus CD-RW 650

CD-RW74M4

2x

2x

32x-1x

16x-1x

48x-1x

24x-1x

24x-1x

24x-1x

4x/2x

48x-1x

24x-1x

4x/2x

4x/2x

Speed

16x-1x

32x-1x

32x-1x

24x

12x/10x/8x/4x

4x/2x

4x/2x

24x-1x

24x-1x

24x-1x

12x/10x/8x/4x

4x/2x

4x/2x

4x/2x


GE H EALTHCARE


3-6-5-2

LOGIQ B OOK XP S ERIES


D.) Connect Footswitch to the system.

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

B ASIC S ERVICE M ANUAL

Wireless

LAN Card

Footswitch FSU 1000

Footswitch FSU 2001

Figure 3-14 Connect Footswitch to the system

E.) Connect Wireless LAN Card to the system.

Wireless LAN Card can be properly connected using Signal Port for Card.

3-22

Figure 3-15 Connect Wireless LAN Card to the system

F.) Connect the CRT to the system.

CRT can be properly connected using the SVGA output.


GE H EALTHCARE


3-6-5-2



G.) Connect the USB Memory to the system. The USB Memory can be properly connected using USB port 1 or 2.

Figure 3-16 USB Memory Connection

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

NOTE:

Figure 3-17 ECG Connection

Please refer to the operation manual of each peripheral for information needed by the user to operate the system safely.

For detailed installation information, please refer to the LOGIQ Book XP Series Peripheral Installation

Instruction manual 5194298-100.


GE H EALTHCARE


3-6-6 Available Probes


See in specification in the LOGIQ Book XP Series User Reference Manual for Probes and intended use.

Table 3-14 List of Probes on LOGIQ Book XP/XP PRO

Probe Name Material of Headshell

3C-RS NORYL

E8C-RS

8C-RS i12L-RS

8L-RS

3S-RS i739-RS

T739-RS

VALOX

VALOX

ABS (GE)

VALOX

VALOX

NORYL

NORYL

Area of Using

GENERAL PURPOSE

TRANSVAGINAL

TRANSRECTAL

VETERINARY

PEDIATRIC

NEONATAL

INTRAOPERATIVE

SMALL PARTS

VASCULAR PEDIATRICS

SMALL PARTS

PERIPHERAL VASCULAR

CARDIOLOGY

TRANSVAGINAL

ABDOMEN

INTRAOPERATIVE

SMALL PARTS

PERIPHERAL VASCULAR

INTRAOPERATIVE

SMALL PARTS

PERIPHERAL VASCULAR

TYPE

CONVEX

MICRO-CONVEX

MICRO-CONVEX

LINEAR

LINEAR

SECTOR

LINEAR

LINEAR

Catalog Number Part Number

H40402LL 2290776

H40402LN

H40402LS

H40402LW

H40402LT

H4000PD

H40402LJ

H40412LP

2290777

2354971

2377942

2376127

2355686

2404995

2404999


GE H EALTHCARE


3-6-6 Available Probes

(cont’d)


Table 3-15 List of Probes on LOGIQ Book XP Vet

Probe Name Material of Headshell

3C-RS NORYL

E8C-RS

8C-RS i12L-RS

8L-RS

3S-RS i739-RS LC

T739-RS

VALOX

VALOX

ABS (GE)

VALOX

VALOX

NORYL

NORYL

Area of Using

GENERAL PURPOSE

TRANSVAGINAL

TRANSRECTAL

VETERINARY

PEDIATRIC

NEONATAL

INTRAOPERATIVE

SMALL PARTS

VASCULAR PEDIATRICS

SMALL PARTS

PERIPHERAL VASCULAR

CARDIOLOGY

TRANSVAGINAL

ABDOMEN

INTRAOPERATIVE

SMALL PARTS

PERIPHERAL VASCULAR

INTRAOPERATIVE

SMALL PARTS

PERIPHERAL VASCULAR

TYPE

CONVEX

MICRO-CONVEX

MICRO-CONVEX

LINEAR

LINEAR

SECTOR

LINEAR

LINEAR

Catalog Number Part Number

H41562LJ 5134641

H41562LL

H41562LK

H41562LN

H41562LM

H41562LR

H41482LS

H41562LP

5134643

5134642

5134645

5134644

5134647

5136420

5134646

Section 3-7

Software/Option Configuration

Refer to the LOGIQ Book XP Series Basic User Manual, Chapter 16, Customizing Your System for information on configuring items like Hospital, Department, Language, Units (of measure), Date, Time and Date Format.

For information on configuring Software Options, Refer to the LOGIQ Book XP Series Basic User

Manual, Chapter 16, Customizing Your System.

For information on configuring DICOM* Connectivity, Refer to the LOGIQ Book XP Series Basic User

Manual, Chapter 16, Customizing Your System.



GE H EALTHCARE


Section 3-8

Connectivity Installation Worksheet

Site System Information

Site:

Dept:

LOGIQ SN: Type:

Floor:

Room:

REV:


Comments:

CONTACT INFORMATION

Name Title Phone E-Mail Address

TCP/IP Settings

Name - AE Title:

IP Settings

IP Address:

Subnet Mask:

Default Gateway:

Remote Archive Setup

Remote Archive IP:

Remote Archive Name:

Services (Destination Devices)

Manufacturer

7

8

5

6

3

4

1

2

9

10

11

12

Device Type Name

3-26

IP Address Port

Section 3-8 - Connectivity Installation Worksheet

AE Title

GE H EALTHCARE


Section 3-9

Loading the System Software

NOTE:

NOTE:


System Software may also be referred to as the Base Image or Ghost.

While the software install procedure is designed to preserved data, you should save any patient data, images, system setups and customer presets to CD, DVD, USB Flash

Drive, or USB Hard Disk before doing a software upgrade.

Before loading the system software, please ensure that the power can be continuously supplied and there is no risk of power cut off during loading procedure.

There are three methods to load the system software:

• Load the system software with CD. Refer to section 3-9-1 "Loading the System Software with CD" from page 3-28 to page 3-32

• Load the system software with DVD. Refer to section 3-9-2 "Loading the system software with DVD

(For R2.2.2)" from page 3-33 to page 3-37

• Load the system software with USB memory stick. Refer to section 3-9-3 "Loading the System

Software with USB Memory Stick (For R2.2.2 or above)" from page 3-38 to page 3-42


GE H EALTHCARE


3-9-1 Loading the System Software with CD


3-9-1-1

NOTE:

Loading Base Image Software (For R2.2.1 or lower)

While it is believed to be unnecessary, It would not hurt to disconnect the system from the network and remove all transducers.

1.) Insert the disk labeled “Base System Software Load Image” into the CDROM drive.

2.) Properly turn off the system by momentarily pressing the Power On/Off Switch. Select

Shutdown from the System Exit menu. Wait for the Standby Switch to turn amber.

3.) If the system will not shutdown normally, hold down the Power On/Off Switch until the light turns from green to amber.

Figure 3-18 Shutdown Dialog Box

4.) Turn on the system. system will detect the CDRW automatically as shown in Figure 3-19 on page 3-28 .

3-28

Figure 3-19 System Update

Section 3-9 - Loading the System Software

GE H EALTHCARE


3-9-1-2 Upgrading Application Software (For R2.2.1 or lower) (cont’d)

5.) Press any key on the Keyboard to continue the steps.

6.) Press any key to continue when below message display as shown in Figure 3-19 on page 3-

28 .

Figure 3-20 Update message

7.) System CD will be loaded as shown in Figure 3-21 on page 3-29 .

Figure 3-21 System CD loading

8.) After finish updating system CD, take out “System Software CD” from CD-RW, prepare to upgrade “Application Software”.Refer to Figure 3-22 on page 3-29 .

9.) After finish updating system CD, take out “System Software CD” from CD-RW, prepare to upgrade “Application Software”.Refer to Figure 3-22 on page 3-29

Figure 3-22 Update Successful


GE H EALTHCARE

D IRECTION

3-9-1-2

5194296-100, R EVISION 10 LOGIQ B OOK XP S ERIES B ASIC S ERVICE M ANUAL

Upgrading Application Software (For R2.2.1 or lower)

While the software install procedure is designed to preserve data, you should save any patient data, images, system setups to a CD-RW or hardcopy.

1.) Disconnect the system from the network.

2.) Place the “Application Software” CD-ROM into the CD-ROM drive.

3.) Power off the system.

4.) Connect the CD-ROM drive to the system.

5.) Power on the system. Wait for a dialog box like the one in Figure 3-23 on page 3-30 .

Figure 3-23 Start Application Window

6.) Select INSTALL SW ....

7.) There will be two dialog boxes popping up warning you that you are about to install new software as shown in Figure 3-24 on page 3-30 . In both cases click OK.

3-30

Figure 3-24 Start Loader Dialog Boxes

8.) Now you just have to wait till the Software loads (Approximately for 10 minutes).

9.) When the process has completed, the window will turn dark and you will see the following message in Figure 3-25 on page 3-31 .


GE H EALTHCARE



Figure 3-25 Software Load Complete

10.)When it completes loading, the system will reboot.

11.)Remove the CD from the drive.

If possible, while the system is rebooting remove the CD from the drive. If you didn’t do that don’t worry you will get a dialog box like the one shown in Figure 3-26 on page 3-31 .

Figure 3-26 Start Software

12.)REMOVE the Applications CD

13.)From the Start Applications dialog box, select START.

14.)Select UPGRADE button to upgrade the FPGA while the following message box appears by pressing the unmarked key of the trackball.

Figure 3-27 Upgrade FPGA


GE H EALTHCARE



15.)Click on the SHUT DOWN button to shut down the system after FPGA upgrade completing.

Figure 3-28 FPGA Upgrade

3-32 Section 3-9 - Loading the System Software

GE H EALTHCARE


3-9-2


Loading the system software with DVD (For R2.2.2)

NOTE:

While the software install procedure is designed to preserve data, you should save any patient data, images, system setups to CD, DVD, USB Flash Drive, or USB Hard Disk.

Because any data may be lost or impacted during upgrade process, the preserved patient data on the system should be backed up before application software upgrade.



3.) Connect the DVD-ROM to the system and turn on the DVD-ROM.

4.) Place the “Application Software” DVD into the DVD-ROM drive.

5.) Power on the system. The system will operate automatically to start application software upgrading process.

Figure 3-29 Software Loading

6.) The system operates automatically to scan USB Devices as shown in

Figure 3-29 on page 3-33

Figure 3-30 Scanning USB Devices


GE H EALTHCARE


3-9-2 Loading the system software with DVD (For R2.2.2)

(cont’d)

7.) Press any key on the keyboard to continue the steps when message displays as shown in

Figure 3-31 on page 3-34

Figure 3-31 Software upgrade continuing


GE H EALTHCARE



(cont’d)

8.) The system provides three options [a], [b] and [c] as shown in Figure 3-32 on page 3-35 .

To select [a], the complete disk will be loaded. This option is recommended for application software upgrade.

NOTE: When to select [a] to load complete disk, please ensure that any patient data on the disk has been backed up.

-

-

To select [b], only the bootable C: partition is loaded. This option is intended for recovery of a system that will not boot up. It is not recommended for application software upgrade because during upgrade process, the data on the system would possibly be impacted.

To select [c] to quit system upgrade process.

9.) To continue upgrading application software process, select [a] and input “a“.

Figure 3-32 Loading selection


GE H EALTHCARE



(cont’d)

10.)When the message displays as shown in Figure 3-33 on page 3-36 , input “Yes“ and press on

“Enter“ key on the keyboard to continue the steps.

Figure 3-33 Upgrading selection

11.)The system DVD is being loaded as shown in Figure 3-34 on page 3-36 . The Progress

Indicator displays the loading progress status.

3-36

Figure 3-34 Upgrading progress status


GE H EALTHCARE



(cont’d)

12.)When the system DVD loading as shown in Figure 3-34 on page 3-36 is completed, the system upgrade process is completed successfully. Follow the instruction as shown in Figure

3-35 on page 3-37

Figure 3-35 Upgrade completed


GE H EALTHCARE


3-9-3


Loading the System Software with USB Memory Stick (For R2.2.2 or above)

NOTE: Because any data may be lost or impacted during upgrade process, the preserved patient data on the system should be backed up before application software upgrade.



3.) Insert USB memory stick labeled “System & Application Software” to the system.

4.) Turn on the system. System will detect the USB memory stick automatically.

5.) Press any key to continue when below message display as shown in Figure 3-36 on page 3-

38 .

Figure 3-36 System Software load message


GE H EALTHCARE


3-9-3 Loading the System Software with USB Memory Stick (For R2.2.2 or above)

(cont’d)

6.) The system software load instruction window displays. Select one of the options for loading the system. Select choice [a] to load the complete disk. Refer to Figure 3-37 on page 3-39

NOTICE If you select [a], ALL existing software and data will be erased. If backup has not been performed, all data like Patient Database, System Configuration and User Configurations

(Customer Presets) will be lost.

To select [a], the complete disk will be loaded. This option is recommended for application software upgrade.

NOTE: When to select [a] to load complete disk, please ensure that any patient data on the disk has been backed up.

-

-

To select [b], only the bootable C: partition is loaded. This option is intended for recovery of a system that will not boot up. It is not recommended for application software upgrade because during upgrade process, the data on the system would possibly be impacted.

To select [c] to quit system upgrade process.

Figure 3-37 System Software load instruction

While the software install procedure is designed to preserve data, you should select choice [b] to format disk C only.


GE H EALTHCARE



(cont’d)

7.) Input “Yes” or “No” and press Enter key to continue.

Figure 3-38 Confirmation on loading the system


GE H EALTHCARE



(cont’d)

8.) System USB memory stick will be loaded as shown in Figure 3-39 on page 3-41 . Wait for the software installation to complete. (Typical installation time: 5-10 minutes). Status bar on the screen indicates progress.

Do not interrupt the software loading at any time.

Figure 3-39 System USB memory stick loading

If the screen displays as show in Figure 3-40 on page 3-41 following step 7 , wait about 1 minute until

Figure 3-39 on page 3-41 displays.

Figure 3-40 System USB memory stick loading blank message


GE H EALTHCARE



(cont’d)

9.) After finish updating system, remove the USB memory stick and press any key to shut down the system. Refer to Figure 3-41 on page 3-42 .

NOTE: If you don not remove the USB memory stick, the software system loading process repeats when the system boots up.

Figure 3-41 System upgrade complete


GE H EALTHCARE


3-9-4


Functional Check-out

1.) Power on LOGIQ Book XP Series system and wait until system booting to main screen.

2.) Press UTILITY key on control panel

3.) Choose the About button on the right.

Figure 3-42 General Screen

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

NOTE:

Figure 3-43 About Screen

The software version information displayed in Figure 3-43 on page 3-43 does not necessarily reflect the software version you install on your ultrasound system. The real software version will display on your ultrasound system after you have completed loading the system software.


GE H EALTHCARE


3-9-5 Option Key Update

NOTE:

NOTE:


After the system software loading completion, please input option key and check the option strings to ensure that the options are activated and working.

Option key is required to be input when the system is powered on after software loading completion.

1.) Power on the system.

2.) Input series number of the system and select “OK“.

3.) Input option key according to SW Option Key label.

4.) Press “OK” and the system enters scanning mode.

5.) Refer to the process as below to verify if the options are activated and working.

Select Utility -> Advanced -> Admin -> System Admin , then check “option” list. If the option is enable or permanent, it means the option function is available; if the option is disabled, it means the function is invalid.

3-44

Figure 3-44 Option key screen


GE H EALTHCARE



(cont’d)

6.) Some of the options are in disabled status. That means the function of these options is not available. To activate these options, the user need to add new option key. Please select “New“.

Figure 3-45 Add new option key

7.) The system pops up a dialogue box for the user to input option key. Input option key according to

SW Option Key label. Select “OK“.

Figure 3-46 Input new option key


GE H EALTHCARE



(cont’d)

8.) The option key is displayed in the SW Option Key list. The status of the options become Valid. That means the function of these options is availabe.

Figure 3-47 Valid new option


GE H EALTHCARE



(cont’d)

The status of activated Options is described in two methods:

• Valid until: (date). This status means the option is working only until the displayed date. After the date, the function of this option becomes disabled. If the options need to be activated again, the user need to apply for the option key and input it to activate the options.

• Permanent. This status means the option is working without a date limitation.

Figure 3-48 Valid option status


GE H EALTHCARE


3-9-6 Probe Recognition Check

NOTE:


After the system software loading completion, please check to ensure that the system can recognize the probes.

Plug in the probe. In scanning mode, the probe information is displayed on the right top location of the screen. For the probe specification for intended use on LOGIQ Book XP Series, please refer to

3-6-6 on page 3-24 .

Plug in at least one of each type of probe and check if each of the probes is recognized and the probe information is displayed correctly.

3-9-7

Figure 3-49 Probe identification

Peripheral Devices Check

Please check to ensure that all the peripheral devices work properly.

For the instruction of peripheral devices check, please refer to Section 4-5 on page 3-30 .


GE H EALTHCARE


3-9-8


Reinstall DICOM Devices

Reinstall any DICOM devices used by the customers and check to ensure these DICOM devices work properly.

The instruction about installing DICOM devices is not incorporated in this manual. To access the instruction about installing DICOM devices please refer to another manual Basic User Manual. Please use the latest revision of this document.


GE H EALTHCARE


Section 3-10

Paperwork

NOTE:

3-10-1

NOTE:


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

Product Locator Installation

The Product Locator Installation Card shown may not be same as the provided Product Locator card.

3-10-2

Figure 3-50 Product Locator Installation Card

User Manual(s)

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

Sales Representative for availability.

3-50 Section 3-10 - Paperwork

GE H EALTHCARE


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 Book XP Series console, diagnostics by using the built-in service software, and power supply adjustments.

Table 4-1 Contents in chapter 4

Section

4-1

4-2

4-3

4-4

4-5

Overview

Required Equipment

General Procedure

Software Configuration Checks

Peripheral Checks


4-1

4-1

4-2

4-30

4-30

Section 4-2

Required Equipment

To perform these tests, you'll need any of the sector, linear, or convex transducers.

(normally you should check all the transducers used on the system)

Chapter 4 Functional Checks 4-1

GE H EALTHCARE


Section 4-3

General Procedure


CAUTION

SYSTEM REQUIRES ALL COVERS

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

NOTICE Lockout/Tagout Requirements (For USA only)

Follow OSHA Lockout/Tagout requirements by ensuring you are in total control of the Power Cable on the system.

TAG

&

LOCKOUT

Signed Date

4-3-1

4-3-1-1

Power On/Boot Up

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

System Power On

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

4-2

Figure 4-1 connect AC adapter

When power is applied to the system, power is distributed to the Cooling Unit, Control Panel, LCD,

Peripherals and the Back-end Processor.

Section 4-3 - General Procedure

GE H EALTHCARE


4-3-1-2 Turn on the system

LOGIQ B OOK

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

XP S ERIES B ASIC S ERVICE M ANUAL

Power On/Off switch

4-3-2

NOTE:

4-3-2-1

Figure 4-2 Power On/Off Switch

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

No status messages are displayed during this process.

Power Off/ Shutdown


Back-end Processor Power Down

To power down the system:

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

2.) The System-Exit window is displayed.

Figure 4-3 System Exit Window

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

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

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

6.) Close LCD cover.


GE H EALTHCARE


4-3-2-2 System Shutdown

LOGIQ B OOK XP S ERIES B ASIC S ERVICE

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

M ANUAL

CAUTION

DO NOT unplug and/or transport the unit until after the power off sequence has been completed.

Failure to do so may result in corrupted patient files.

4-4 Section 4-3 - General Procedure

GE H EALTHCARE


4-3-3 Archiving and Loading Presets

NOTE:


Always save presets before any software reload. This ensures the presets loaded after the software reload are as up–to–date as possible.

All user presets except changes to Summary, Anatomy, and Biometry pages, can be saved on an CD-

R disk for reloading on the system.

NOTICE Presets should NOT be saved on the same CD-R disk as images. The Archive Menu lists the images but does NOT list the presets stored on a CD-R disk.

4-3-3-1 Archiving Presets to an CD-R disk

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

2.) Access to the Utility Menu, and select Backup/Restore. The Backup sheet will be shown on the monitor.

4-3-3-2

Figure 4-4 Backup Sheet

3.) Select the item to back up either from Resource Files.

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

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

Loading Presets from an CD-R disk

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

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

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

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

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

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


GE H EALTHCARE


4-3-4 Adjusting the Display Monitor

4-3-4-1


Brightness

To adjust the brightness:

Adjust the Brightness Slide pots, located on the right of side of the LCD, see Figure 4-5 on page 4-6 .

4-3-5

Figure 4-5 Brightness Slide pots

Record the final brightness setting and leave this information with the system.

Lockout/Tagout (LOTO) requirements

Follow OSHA Lockout/Tagout requirements (USA) or local Lockout/Tagout requirements by ensuring you are in total control of the AC power plug at all times during the service process.

To apply Lockout/Tagout:

1.) Plan and prepare for shutdown.

2.) Shutdown the equipment.

3.) Isolate the equipment.

4.) Apply Lockout/Tagout Devices.

5.) Remove battery.

6.) Control all stored and residual energy.

7.) Verify isolation.

All potentially hazardous stored or residual energy is relieved.

Signed

NOTICE

TAG

&

LOCKOUT

Date

Energy Control and Power Lockout for LOGIQ Book XP Series

WHEN SERVICING PARTS OF THE SYSTEM WHERE THERE IS EXPOSURE TO VOLTAGE

GREATER THAN 30 VOLTS:

1. TURN OFF THE SCANNER.

2. UNPLUG THE SYSTEM.

3. MAINTAIN CONTROL OF THE SYSTEM POWER PLUG.

4. WAIT FOR AT LEAST 20 SECONDS FOR CAPACITORS TO DISCHARGE AS THERE ARE NO

TEST POINTS TO VERIFY ISOLATION. THE AMBER LIGHT ON THE OP PANEL ON/OFF BUTTON

WILL TURN OFF.

5. REMOVE THE SYSTEM BATTERY.


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4-3-6 System Features

4-3-6-1 Control Panel


Figure 4-6 Control Panel Tour

1.) TGC

2.) New Patient

3.) End Exam

4.) Mode/Gain/Auto Keys

5.) Preset Key

6.) Imaging/Measurement Keys

7.) Depth

8.) Reverse

9.) Image Keys

10.)Print Keys

11.)Freeze

12.)Keyboard


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4-3-6-2 LOGIQ Book XP Series SoftMenu Key Tour


In general, there are three types of softMenu keys: Paddle Switch, Push Button and two-button key.

1

2 3

Figure 4-7 SoftMenu Key Tour

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

2.) The Push Button Softkey is used to toggle between line one and line two.

3.) The up/down Two-button Softkeys are used to increase/decrease quantities.


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4-3-6-3 Monitor Display


Figure 4-8 Monitor Display Tour

Table 4-2 Monitor Display Features

1. Institution/Hospital Name, Date, Time, Operator

Identification, system status (real-time of frozen).

2. Patient Name, Patient Identification.

3. Acoustic Output Readout,

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

5. Image Preview.

6. Gray/Color Bar.

7. Cine Gauge.

8. Measurement Summary Window.

9. Image.

10. Measurement.

11. Results Window.

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

14. Focal Zone.

15. TGC (not shown on the image).

16. Body Pattern.

17. Depth Scale.

18. SoftMenu

19. Caps Lock: On/Off.

20. Start Menu icon.

21. Battery icon.

22. Card icon.

23. Trackball Functionality Status: Scroll, M&A (Measurement and Analysis), Position, Size, Scan Area Width and Tilt.

12. Probe Identifier. Exam Study.


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4-3-7 B Mode Checks

4-3-7-1


Preparations

1.) Connect one of the probes listed in 3-6-6 "Available Probes" on page 3-24 , in Chapter 3 Installation to the System probe connector.

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

Secondary Menu

Rejection

Frame Average

Biopsy

Line Density

Focus Width

B Softner

Suppression

Power Output

ECG OnOff

TGC

Zoom

B Mode

Scan Area

SoftMenu Key

Primary Menu

Frequency

Gray Map

Dynamic Range

Image Rotate

Focus Position

Colorize

Edge Enhance

Updown Invert

Focus Number

Virtual Convex

Depth

Reverse

Freeze

Figure 4-9 Controls available in B Mode

4-10

Figure 4-10 B Mode Screen Picture Example


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


Table 4-3 B Mode Control Panel Controls

Step

1

2

3

4

5

7

8

9

10

11

Task

Press B Mode key

Adjust Depth

Adjust Gain

Adjust Focus

Activate Auto Optimize

Adjust Time Gain

Compensation (TGC)

Adjust Scan Area

Adjust Zoom

Zoom Clear

Reverse

Expected Result(s)

B Mode Starts

Adjust the field of view. Increasing the depth may view larger/deeper structures rates, and decreasing the depth may view near the skin line.Press Up/Down Button to increase/ decrease. Depth displays on the monitor in cm.

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

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

Press Up/Down Button to move or adjust the focal numbers.

Optimize the image based upon a specified region of interest or anatomy. Press the

Center Button in the Gain Dial to toggle the ATO/ACE On and Off.

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

Widen or narrow the size of the sector angle to maximize the image’s region of interest

(ROI). Press Scan Area and move the Trackball to narrow/widen the angle.

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

Clear Zoom to normal condition.

Toggles the left/right orientation of the scan image.


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4-3-7-3 B Mode Softmenu Key


Table 4-4 B Mode Softmenu Key

Step

1

2

3

4

5

6

7

9

10

11

12

13

Task Expected Result(s)

Adjust Rejection

Activate Colorize

Adjust Edge Enhance

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

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

Edge Enhance brings out subtle tissue differences and boundaries by enhancing the gray scale differences corresponding to the edges of structures. Adjustments to M

Mode's edge enhancement affects the M Mode only.

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

Activate Gray Map

Adjust Frequency

Adjust Frame Average

Adjust Rotation

Adjust Line Density

Power output

Dynamic Range

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

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

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

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

Optimizes image quality and allows user to reduce beam intensity. 10% increments between 0-100%. Values greater than 0.1 are displayed.

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

Focus Number and Position

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

ECG OnOff On/Off ECG function


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4-3-8 M Mode Controls

4-3-8-1


Preparations


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

secondary Menu

Rejection

Power Output

Primary Menu

Gray Map

Dynamic Range

Sweep Speed

Display Format

Colorize

Edge Enhance

Full Timeline

M/D Cursor

Gain

M Mode

Figure 4-11 Controls available in M Mode

Figure 4-12 M Mode Screen Picture Example


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


Table 4-5 M Mode OP Panel Controls

Step

1

2

3


Press M Mode key

Adjust Gain

M Mode Starts

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

Display M-Mode Cursor

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


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4-3-8-3 M Mode Softmenu Key


Table 4-6 M Mode Softmenu Key

4

6

7

Step

1

2

3

8

9

10

Task

Adjust Rejection

Adjust Sweep Speed

Adjust Edge Enhance

Activate Gray Map

Activate Colorize

Activate Full Timeline

Select Display Format

Adjust Dynamic Range

Power output



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

Edge Enhance brings out subtle tissue differences and boundaries by enhancing the gray scale differences corresponding to the edges of structures. Adjustments to M

Mode's edge enhancement affects the M Mode only.

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

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

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

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

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



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4-3-9 Color Flow Mode Checks

4-3-9-1


Preparations



Secondary Menu

Baseline

Line Density

Focus Position

ACE

Capture

Spatial Filter

Power Output

Primary Menu

Frequency

Frame Average

Quick Angle

Color Invert

PRF

Color Map

Threshold

Packet Size

Wall Filter

CF Mode

Gain

Figure 4-13 Controls available in Color Flow Mode

4-16

Figure 4-14 CFM Mode Screen Picture Example


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4-3-9-2 Color Flow Mode OP Panel Controls


Table 4-7 Color Flow Mode OP Panel Controls

Step

1

Task

Press CFM-Mode key

2 Adjust Gain


CFM Mode Starts

Amplifies the overall strength of the echoes processed in the Color Flow window. Turn the Gain dial (CFM Mode key) to the left/right to increase/decrease Gain.


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4-3-9-3 Color Flow Mode Softemenu Key


Table 4-8 Color Flow Mode Softmenu Key

Step

1

2

Threshold

Packet Size

Task

3

4

5

6

7

Select Color maps

Adjust Frequency

Set Frame Average

Color Invert

Adjust LIne Density


Threshold assigns the gray scale level at which color information stops.

Controls the number of samples gathered for a single color flow vector.

Allows a specific color map to be selected. After a selection has been made, the color bar displays the resultant map.

Enables the adjustment of the probe’s operating frequency. Press Frequency and select desired value. The selected frequency is displayed in the status window.

Averages color frames. Press Frame Average up/down to smooth temporal averaging.

Views blood flow from a different perspective. Press Invert to reverse the color map.

Trades frame rate for sensitivity and spatial resolution. If the frame rate is too slow, reduce the size of the region of interest, select a different line density setting, or reduce the packet size.

8

9

Activate Spatial Filter

Activate ACE

10

11

12

13

Adjust Quick angle

Move Baseline

Change PRF

(Pulse Repetition

Frequency)

Focus Position

Eliminates the motion artifacts. Press Ace to activate.

Slants the Color Flow region of interest or the Doppler line to obtain a better

Doppler angle.

Adjusts the baseline to accommodate faster or slower blood flows to eliminate aliasing.

Velocity scale determines pulse repetition frequency. If the sample volume gate range exceeds single gate PRF capability, the system automatically switches to high PRF mode. Multiple gates appear, and HPRF is indicated on the display.

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

14 Capture

15

16

Power output

Wall Filter


Wall Filter insulates the Doppler signal from excessive noise caused from vessel movement.


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4-3-10 Doppler Mode Checks

4-3-10-1


Preparations



Secondary Menu

Rejection

Dynamic Range

Display Format

Full Timeline

Trace Direction

Auto Calculations

Modify Calcs

Trace Method

Trace Sensitivity

Time Resolution

Power Output

Spectral Average

Primary Menu

Frequency

Baseline

Quick Angle

Sweep Speed

PRF

SV Length

Colorize

Angle Correct

Spectral Invert

Wall Filter

PW Mode

Gain

M/D Cursor

B Pause

Figure 4-15 Controls available in Doppler Mode

Figure 4-16 Doppler Mode Screen Picture Example


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4-3-10-2 Doppler Mode OP Panel Controls


Table 4-9 Doppler Mode OP Panel Controls

Step

1

Task

Press PW Mode key

2

3

4

Adjust Gain

Display M/D-Mode Cursor

B Pause


PW Mode Starts

Amplifies the overall strength of the echoes processed in the Color Flow window.

Turn the Gain dial (PW Mode key) to the left/right to increase/decrease Gain.

Displays the M/D-Mode cursor on the B-Mode image. Press Cursor and Trackball to position sample volume graphic. Click SV gate to adjust sample volume gate size.

Toggle between simultaneous and update presentation while viewing Spectral

Doppler. Press B Pause to toggle between simultaneous and update.


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4-3-10-3 Doppler Mode OP Panel Controls


Table 4-10 Doppler Mode Softmenu Key

Step

1

2

3

4

5

6

7

18

19

20

8

9

10

11

12

13

14

15

16

17

21

22

23


Adjust Rejection

Adjust Sweep Speed

Activate Full Timeline

Select Display Format

Adjust Frequency


Changes the speed at which timeline is swept. Press Sweep Speed up/down to increase/decrease the value.

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

Display layout can be preset to have B-Mode and Time-motion side-by-side or overunder.

Enables the adjustment of the probe’s operating frequency. Press Frequency and select desired value. The selected frequency is displayed in the status window.

Trace Direction

Invert

Wall Filter

Vertically inverts the spectral trace without affecting the baseline position. Press invert to invert the spectral trace. The Plus and Minus signs on the velocity scale reverse when the spectrum is inverted.

Auto Calculation

Modify Calcs

Trace Method

Activate Colorize

Activate Gray Map

Dynamic Range

Adjust Angle Correct

Adjust Quick Angle

Move Baseline

Estimates the flow velocity in a direction at an angle to the Doppler vector by computing the angle between the Doppler vector and the flow to be measured.

Currently only support +/- 30, +/- 60 degree.

Adjusts the baseline to accommodate faster or slower blood flows to eliminate aliasing.

Change PRF (Pulse

Repetition Frequencies) -

(Wall Filter)

Velocity scale determines pulse repetition frequency. If the sample volume gate range exceeds single gate PRF capability, the system automatically switches to high

PRF mode. Multiple gates appear, and HPRF is indicated on the display.

Trace Sensitivity

Time Resolution

Spectral Average

Colorize the gray scale image to enhance the eyes’ discrimination capability. Press the Cololize, Trackball to cycle through available maps and press Set to select.

Displays a map window adjacent to the image. Move the trackball to select the map.

The image reflects the map as scrolled through the selections. Press Set to select.

Controls how echo intensities are converted to shades of gray. Click Dynamic Range to increase/decrease the value.

Estimates the flow velocity in a direction at an angle to the Doppler vector by computing the angle between the Doppler vector and the flow to be measured.

Power output

SV Length


Sizes the sample volume gate.

Wall Filter insulates the Doppler signal from excessive noise caused from vessel movement.


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4-3-11 Basic Measurements

NOTE:


The following instructions assume that you first scan the patient and then press Freeze.

4-3-11-1

NOTE:

NOTE:

4-3-11-2

NOTE:

Distance and Tissue Depth Measurements

1.) Press MEASURE once; an active caliper displays.

2.) To position the active caliper at the start point (distance) or the most anterior point (tissue depth), move the TRACKBALL.

3.) To fix the start point, press Set. The system fixes the first caliper and displays a second active caliper.

4.) To position the second active caliper at the end point (distance) or the most posterior point

(tissue depth), move the TRACKBALL.

5.) To complete the measurement, press SET. The system displays the distance or tissue depth value in the measurement results window.

Before you complete a measurement:

To toggle between active calipers, press MEASURE.

To erase the second caliper and the current data measured and start the measurement again, press CLEAR once.

To rotate through and activate previously fixed calipers, adjust CURSOR SELECT.

After you complete the measurement, to erase all data that has been measured to this point,

but not data entered onto worksheets, press CLEAR.

Circumference/Area (Ellipse) Measurement

1.) Press MEASURE once; an active caliper displays.

2.) To position the active caliper, move the TRACKBALL.

3.) To fix the start point, press SET. The system fixes the first caliper and displays a second active caliper.

4.) To position the second caliper, move the TRACKBALL.

5.) Adjust the ELLIPSE; an ellipse with an initial circle shape appears.

Be careful not to press the Ellipse control as this activates the Body Pattern.

6.) To position the ellipse and to size the measured axes (move the calipers), move the

TRACKBALL.

7.) To increase the size, adjust the ELLIPSE upward button. To decrease the size, adjust the

ELLIPSE downward button.

8.) To toggle between active calipers, press MEASURE.

9.) To complete the measurement, press SET. The system displays the circumference and area in the measurement results window.

Before you complete a measurement:

-

-

To erase the ellipse and the current data measured, press CLEAR once. The original caliper is displayed to restart the measurement.

To exit the measurement function without completing the measurement, press CLEAR a second time.


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4-3-11-3


Worksheets

Measurement/Calculation worksheets are available to display and edit measurements and calculations.

There are generic worksheets as well as Application specific worksheets. The worksheets are selected from the Measurement Touch Panel.

4-3-11-4 Report* Pages

Measurements/Calculations that are included on the worksheet can also be displayed on Report Pages.

Report Pages can be customized to meet the appropriate needs of the user.

NOTICE * Report is not available on LOGIQ Book XP PRO.

4-3-12

4-3-12-1

4-3-12-2

4-3-12-3

4-3-12-4

Probe/Connectors Usage

Connecting a probe

1.) Place the probe's carrying case on a stable surface and open the case.

2.) Carefully remove the probe and unwrap the probe cable.

3.) DO NOT allow the probe head to hang free. Impact to the probe head could result in irreparable damage.

4.) Align the connector with the probe port and carefully push into place.

5.) Lock the probe latch upward.

6.) Carefully position the probe cord so it is free to move and is not resting on the floor.

Activating the probe

The probe activates in the currently-selected operating mode. The probe's default settings for the mode and selected exam are used automatically.

Deactivating the probe

When deactivating the probe, the probe is automatically placed in standby mode.

1.) Press the Freeze key.

2.) Gently wipe the excess gel from the face of the probe. (Refer to the Basic User Manual for complete probe cleaning instructions.)

3.) Carefully slide the probe around the right side of the keyboard, toward the probe holder.

Ensure that the probe is placed gently in the probe holder.

Disconnecting the probe

Probes can be disconnected at any time. However, the probe should not be selected as the active probe.

1.) Unlock the probe latch downward.

2.) Pull the probe and connector straight out of the probe port.

3.) Carefully slide the probe and connector away from the probe port and around the right side of the keyboard.

4.) Ensure the cable is free.

5.) Be sure that the probe head is clean before placing the probe in its storage box.

Take the following precautions with the probe cables: Do not bend. If you have purchased the cart option, be sure to keep probe cables free from the wheels.

Be careful not to trip on the probe cables if using the device without the optional cart.


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4-3-13 Using Cine

4-3-13-1

4-3-13-2

4-3-13-3

4-3-13-4

4-3-13-5


Activating CINE

Press Freeze, then roll the Trackball to activate CINE. To start CINE Loop playback, press Run/Stop.

To stop CINE Loop playback. press Run/Stop.

Quickly Move to Start/End Frame

Press First to move to the first CINE frame; press Last to move to the last CINE frame.

Start Frame/End Frame

Press the Start Frame Two-Button Softkey to move to the beginning of the CINE Loop. Adjust the Start

Frame up/down Two-Button Softkey upward to move forward through the CINE Loop. Adjust the

Softkey downward to move backward through the CINE Loop.

Press the End Frame Two-Button Softkey to move to the end of the CINE Loop. Adjust the End Frame up/down Two-Button Softkey upward to move forward through the CINE Loop. Adjust the Softkey downward to move backward through the CINE Loop.

Adjusting the CINE Loop Playback Speed

Adjust the Loop Speed up/down Two-Button Softkey to increase/decrease the CINE Loop playback speed.

Moving through a CINE Loop Frame By Frame

Adjust the Frame by Frame up/down Two-Button Softkey to move through CINE memory one frame at a time.

4-3-14 Image Management (QG)

For Image Management functionality refer to the LOGIQ Book XP Series Quick Guide. It talks about several topics:

• Clipboard

• Printing Images

• Browsing and Managing an Exam’s Stored Image

• Connectivity, and Dataflow Concept and Creation

• Starting an Exam

• Configuring Connectivity

• TCP/IP

• Services (Destinations)

• Buttons

• Views

• Verifying and Pinging a Device


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4-3-15


Backup and Restore Database, Preset Configurations and Images

4-3-15-1 Formatting Media

1.) To format the backup media, CD-RW, select the UTILITY button on the Keyboard.

2.) Select CONNECTIVITY, then TOOLS. Properly label and Insert the backup media.

3.) Select the media type from the drop down menu.

4.) Enter the label for the media as shown in Figure 4-17 on page 4-25 . It is best to use all capital letters with no spaces or punctuation marks. Press Format.

Media Selection

Media Label

Verify Format

Format

Figure 4-17 Format and Verify Media

5.) The Ultrasound system displays a pop-up menu, as shown in Figure 4-18 on page 4-25 . When the formatting has been completed, press OK to continue.

6.) If desired, verify that the format was successful by returning to

Utility>Advanced>Connectivity>Tools and selecting VERIFY as shown in Figure 4-17 on page

4-25 .

Figure 4-18 Format Successful Pop-up Menu


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4-3-15-2 Backup System Presets and Configurations


NOTE:

NOTE:

Always backup any preset configurations before a software reload. This ensures that if the presets need to be reloaded, after the software update, they will be the same ones the customer was using prior to service.

1.) Insert a formatted CD-R into the drive.

2.) On the Keyboard, press UTILITY.

3.) On the LCD display, press SYSTEM.

4.) On the LCD display, select BACKUP/RESTORE.

If you are not logged in as GE Service or with administrator privileges, the Operator Login window is displayed. Log on with administrator privileges.

5.) In the Backup list, select Patient Archive, Report* Archive and User Defined Configuration.

6.) In the Media field, select CD-RW.

7.) Select BACKUP.

The system performs the backup. As it proceeds, status information is displayed on the Backup/Restore screen.

NOTICE * This function is not available on LOGIQ Book XP PRO.

Check here to backup presets and configurations

4-26

Figure 4-19 Backup/Restore Menu


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4-3-15-3 Restore System Presets and Configurations


CAUTION

The restore procedure overwrites the existing database on the local hard drive. Make sure to insert the correct CD.

NOTE:

1.) Insert the Backup/Restore CD-R into the drive.

2.) On the Keyboard, press UTILITY.

3.) On the LCD display, press SYSTEM.

4.) On the LCD display, select BACKUP/RESTORE.

If you are not logged in with administrator privileges, the Operator Login window is displayed.

Log on with administrator privileges.

5.) In the Restore list, select Patient Archive, Report* Archive and User Defined Configuration.

6.) In the Media field, select the Backup/Restore CD-RW.

7.) Select RESTORE.

The system performs the restore. As it proceeds, status information is displayed on the Backup/Restore screen.

NOTICE * This function is not available on LOGIQ Book XP PRO.

Check here to restore presets and

Figure 4-20 Backup/Restore Menu


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4-3-15-4


Archiving Images

1.) Insert the archive media. To format the archive media, CD-RW, select the Utility button on the

Keyboard.

2.) Select Connectivity, then Tools.

3.) Format the CD-RW. Verify the format if desired.

4.) Images will be moved from the hard drive by date. Therefore, the best way is to label media by date.

NOTE: Images will be moved from the hard drive by date. Therefore, the best way to label media is by date. When images are moved to the archive media, they will be deleted from the system hard drive. However, the patient database (backed up earlier) maintains pointers to the location of the images on the archive media.

Media Selection

Media Label

Verify Format

Format

Figure 4-21 Format CD-ROM Screen

5.) Press PATIENT and set the Dataflow to store images directly to CD-RW.

6.) From the patient screen, press MORE, then select Move Images. The Move Images pop-up appears.


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4-3-15-4 Archiving Images (cont’d)


Figure 4-22 Image Archive Move Pop-up Menu

7.) Fill in the From Date and To Date. Specify to Keep days together.

8.) Press RECALCULATE.

9.) Press OK. An in-progress message appears. The archive operation is complete when you receive the message shown in Figure 4-23 on page 4-29 .

Figure 4-23 Archive Operation Complete Message

10.)Repeat the image move steps until all images have been archived.

All databases, presets and images should now be saved to removable media.


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Section 4-4

Software Configuration Checks


Table 4-11 Software Configuration Checks

Step

1.

2.

3.

4.

5.

Task to do Expected Result(s)

Check Date and Time setting

Check that Location (Hospital Name) is correct

Date and Time are correct

Location Name is correct

Check Language settings

Check assignment of Printer Keys

Desired Language is displayed

The default function for Print1-3 Key is P1 (store image);

P2 (print); P3 (capture screen). Print1-3 Key can also be assigned as desired by the customer

Check that all of the customer’s options are set up correct All authorized functions are enabled

Section 4-5

Peripheral Checks

Check that peripherals work as described below:

Table 4-12 Peripheral Checks

Step Task to do

1.

Press (FREEZE)

2.

Press (PRINT 2) on the Control Panel

3.

Connect with Footswitch on USB port and press once.


Stop image acquisition.

The image displayed on the screen is printed on B&W printer.

To start image acquisition (the same function as (FREEZE) key).

4-30 Section 4-4 - Software Configuration Checks

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D IRECTION 5194296-100, R EVISION A LOGIQ B OOK XP S ERIES B ASIC S ERVICE M ANUAL

Chapter 5

Components and Functions (Theory)

Section 5-1

Overview

This chapter explains LOGIQ Book XP Series’s system concepts, component arrangement, and subsystem function. It also describes the Power Distribution System (PDS) and probes.


Section

5-1

5-2

5-3

5-4

Overview

Block Diagrams and Theory

Power Diagrams

Common Service Platform


5-1

5-2

5-4

5-7

Chapter 5 Components and Functions (Theory) 5-1

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D IRECTION 5194296-100, R EVISION A

Section 5-2

Block Diagrams and Theory

5-2-1 Block Diagram


Figure 5-1 LOGIQ Book XP Series System Block Diagram

• Pre Amp: Preamplifier

• OQX2: Beamforming ASIC

• CHACOM: B/M/CFM/DOP mode signal processor ASIC

• SH-PCI: PCI bridge located between SH4 and PCI bus

• HV unit: High voltage unit

• LV unit: Low voltage unit

• DC/DC & HV Ctrl, SMBUS I/F: DC/DC high voltage control smart bus interface

• IMGD FPGA: Image data processing FPGA

• DUSC FPGA: LOGIQ Book XP Series Ultrasound controlling FPGA

5-2 Section 5-2 - Block Diagrams and Theory

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5-2-2


General Information

• LOGIQ Book XP Series is a linear array ultrasound imaging scanner.

• The system can be used for:

2D Black and White imaging

-

-

-

-

2D Color Flow

M-Mode Black and White imaging

Color M-Mode

Doppler

A number of combinations of the above

• LOGIQ Book XP Series is a digital beam forming system that can handle up to 128 element linear probes.

• Signal flow from the Probe Connector Panel to the Front End, to the Mid Processors and Back End

Processor and finally to the LCD and peripherals.

• System configuration is stored on a hard disk and all necessary software is loaded from the hard disk on power up.


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Section 5-3

Power Diagrams

5-3-1

5-3-2


Overview

The AC Power assy’s main tasks are to isolate and output to the DC/DC unit which is inside the system console. The input of AC power pack will be the AC outlet and it’s universal, the range is AC 90V-264V,

47-63Hz. And no main power switch located on this power pack.

AC Power

Figure 5-2 AC Power Distribution Block Diagram

The mains cord has plugs in one side end. A male plug connects to the mains outlet on site.

The mains voltage is routed to the AC power pack through a Circuit Breaker located on the site.

The Circuit Breaker is of the auto fuse type, if for some reason the current grows to high, the switch will automatically break the power.

From the Main Circuit Breaker, the AC power is routed via an Inrush Current Limiter to a internal outlet connector for the Mains Transformer.

5-4 Section 5-3 - Power Diagrams

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5-3-3 Air Flow Distribution


A

A

B

C

C

B A

Figure 5-3 Air Flow Inside the System

The three air flow passes allow the system to be cooled down as shown in the figure above.

• Pass A (Rear Fan> MST, DFP Assy> Bottom front/Bottom left) for MST, DFP Assy cooling.

• Pass B (Bottom> Bottom Fan> DCDC> Bottom left) for DCDC cooling.

• Pass C (Bottom> CPU Fan> Bottom left) for CPU cooling.


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5-3-4 Fans


5-6

Figure 5-4 Fans

The system contains the eight fans at the following positions for producing an air flow.

-

-

-

One fan: Inside the CPU for air flow pass C

One fan: On the Rear for air flow pass A

One fan: On the Bottom for air flow pass B

Section 5-3 - Power Diagrams

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Section 5-4

Common Service Platform

5-4-1

5-4-2

5-4-2-1

5-4-2-2


Introduction

The Service Platform contains a set of software modules that are common to all PC backend ultrasound and cardiology systems. The Common Service Platform will increase service productivity and reduce training and service costs.

Global Service User Interface (GSUI)

Internationalization

The user interface provided by the service platform is designed for GE personnel and as such is in

English only. There is no multi-lingual capability built into the Service Interface.

Service Login

Select Service Platform from Start menu.

This menu links the user to the service login screen.

5-4-2-3

Figure 5-5 Service Login Screen

Access / Security

The service interface has different access and security user levels. Each user is only granted access to the tools that are authorized for their use.

Table 5-2 Service Login User Levels

User Level

Operator

Administrator

External Service

Access Authorization

Authorized access to specified diagnostics, error logs and utilities. Same acquisition diagnostic tests as GE Service.

Password uls uls gogems

Every access request, whether successful or not, will be logged into a service access log that is viewable to authorized users.


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5-4-2-4


The usage for security cable

The ultrasound system equipped with Kensington security slot which is compatible with a Kensington security cable, refer to Figure 5-6 on page 8 .

Figure 5-6

How to prevent unauthorized removal of the ultrasound system?

1.) Wrap the cable around the immovable object, refer to Figure 5-7 on page 8 ;

2.) Make sure and rotate the key to the right (unlocked position);

3.) Insert the lock into the Kensington security slot in the system side cover, refer to Figure 5-7 ;

4.) Rotate the key to the left (locked position).

5.) For more information, visit www.kensington.com.

Figure 5-7

5-8 Section 5-4 - Common Service Platform

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5-4-3 Service Home Page


The navigation bar at the top of the screen allows the user to select from several tools and utilities.

Figure 5-8 Customer Service Home Page


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5-4-4


Error Logs Tab (Not available on LOGIQ Book XP Series now)

From the Error Logs Tab the Log Viewer displays four categories with pull-down sub-menus and an Exit selection. The Service Interface allows scanner logs to be viewed by all service users.

The Filter Error log is not available to customer level analysis.

The log entries are color-coded to identify the error level severity at a glance.

Table 5-3 Log Entry Key

Severity

1

2

3

Error Level

Information

Warning

Error

Color Code

Green

Blue

Red

The Service Interface supports the transfer of these logs to local destinations such as the CD-ROM drive.

5-10

Figure 5-9 Log Viewer / Logs / Log Entries

Section 5-4 - Common Service Platform

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5-4-4-1


Logs

The seven sub-menus of the Logs category are System, Power, Infomatics, Temperature, Probe,

Board, and DICOM*.

NOTE: Figure 5-9 provides a graphical example of the log entries for the System Logs.

Log table headings for the different logs are as follows:

• System

Log entry headings include Time Stamp; Error Level; Package; and Error Message.

• Power


• Infomatics

Log entry headings include TimeStamp, Revision, PtID, PtDOB, PtSex, PtWeight, PtHeight,

ExamID, Exam Category, ExamCurDate, and ExamStartTime.

• Temperature

Log entry headings include Time Stamp; Error Level; Package; Upper FEC Sensor; and Lower FEC

Sensor.

• Probe

Log entry headings include Time Stamp; Error Level; Package; Error Message; Severity; Revision; and three (3) new labels that have not yet been named.

• Board

Log entry headings include Time Stamp; Error Level; Package; Board; Severity; and two (2) new labels that have yet been named.

• DICOM*




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5-4-4-2 Utilities

LOGIQ B OOK XP S ERIES

The two sub-menus of the Utilities category are Plot Log, and Plot Page.

B ASIC S ERVICE M ANUAL

Plot Log Plot Page

5-4-4-3

Figure 5-10 Utilities Sub-Menus

• Plot Log

Allows for the color coded plot of all Log contents with the package on the ‘x’ axis and incident count on the ‘y’ axis.

• Plot Page

Allows for the color coded plot of all Page contents with the package on the ‘x’ axis and incident count on the ‘y’ axis.

Search

On the Text Search sub-menu of the Search category, user can select Text Search, then enter casesensitive text they wish to find. This filter field works well for filtering the Sys log file for the word “fail”.

5-12

Figure 5-11 Search Sub-Menu

Section 5-4 - Common Service Platform

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5-4-4-4 Exit

LOGIQ B OOK XP S ERIES B ASIC S

The sub-menu, Exit Log Viewer, returns the user to the Service Desktop home page.

ERVICE M ANUAL

Figure 5-12 Exit Log Sub-Menu


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5-4-5 Diagnostics


Detailed Diagnostic information is found in Chapter 7 .

5-4-5-1

5-4-5-2

Figure 5-13 User Diagnostic Page

Diagnostics Execution

Diagnostic tests are executable by both local and remote users. The Service Platform provides top-level diagnostic selection based on the user’s level and login access permissions. Remote access will require disruptive diagnostic permissions to run Acquisition diagnostics.

Diagnostic Reports

Diagnostic tests return a report to the Service Platform. The platform retains the report and allows for future viewing of the diagnostic logs.


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5-4-6 Image Quality


The Image Quality page is intended to contain tools for troubleshooting image quality issues.

5-4-7

FIELD IS NOT YET POPULATED

Figure 5-14 Image Quality Page

Calibration

The Calibration page is intended to contain the tools used to calibrate the system.

FIELD IS NOT YE POPULATED

Figure 5-15 Calibration Page


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5-4-8


Configuration

The Configuration page is intended to be used to setup various configuration files on the system.

The Service Platform is the access and authorization control for remote access to the configuration subsystem.

The enable/disable of software options can be done from this Configuration page.

5-4-9

Figure 5-16 Configuration Page

Utilities

The Utilities page contains several miscellaneous tools.

5-4-10 Replacement

The Replacement page is intended to contain the tools used to track replacement parts used in the system.


Figure 5-17 Part Replacement Page


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5-4-11


PM

The PM page is intended to contain the tools used in periodic maintenance of the system.


Figure 5-18 Planned Maintenance Page


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This page was intentionally left blank.


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Chapter 6

Service Adjustments


Section 6-1

Overview

6-1-1 Purpose of this chapter 6

This section describes how to test and adjust the system. These tests are optional. You may use them to check the system for errors.

Table 6-4 Contents in chapter

Section

6-1

6-2

Overview

Monitor Adjustments


6-1

6-2

Chapter 6 Service Adjustments 6-1

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Section 6-2

Monitor Adjustments

6-2-1


Adjustments Procedures

To adjust the brightness:

1.) Adjust the LCD monitor’s toggle, located beside the Primary and Secondary Control (on the right side of the LCD Monitor).

Brightness Toggle

Figure 6-19 LCD Monitor

6-2 Section 6-2 - Monitor Adjustments

GE H EALTHCARE


Chapter 7

Diagnostics/Troubleshooting

Section 7-1

Overview


This section describes how to setup and run the tools and software that help maintain image quality and system operation. Very basic host, system and board level diagnostics are run whenever power is applied. Some Service Tools may be run at the application level. However most software tests are required.


Section

7-1

7-2

7-3

7-4

7-5

7-6

Description

Overview

Gathering Trouble Data

Screen Captures

Global Service User Interface (GSUI)

Common Diagnostics

LOGIQ Book XP Series Diagnostic Descriptions

Page Number

7-1

7-2

7-4

7-8

7-17

7-19

Chapter 7 Diagnostics/Troubleshooting 7-1

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Section 7-2

Gathering Trouble Data

7-2-1

7-2-2


Overview

There may be a time when it would be advantageous to capture trouble images and system data (logs) for acquisition to be sent back to the manufacturer for analysis. There are different options to acquire this data that would give different results.

Collect Vital System Information

The following information is necessary in order to properly analyze data or images being reported as a malfunction or being returned to the manufacturer:

Product Name = LOGIQ Book XP

From the Utility>System>General>About screen:

Applications Software

-

-

-

-

Software Version

Software Part Number

System Image Software

Image Revision

Image Part Number

7-2 Section 7-2 - Gathering Trouble Data

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7-2-3


Collect a Trouble Image with Logs

If the system should malfunction, press the Alt-D keys simultaneously. This will collect a screen capture of the image monitor, system presets and the following logs:

-

-

-

-

-

Keyboard Shadow Log

Error Logs

Crash Log

Power Supply

Temperature

NOTE: Power Supply and Temperature logs are not currently being updated by the LOGIQ Book XP

Series.

This Alt-D function is available at all times.

Figure 7-1 ALT-D Dialog Box

When Alt-D is pressed, a menu box appears that allows for:

-

-

A place to enter a description of the problem

A choice to store to a pre-formatted CD-R, RD (Removable Disk) or to the Export directory E: drive.

The subsequent file is compressed and time stamped. The screen capture is a bitmap which eliminates the possibility of artifacts from compression.


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Section 7-3

Screen Captures

7-3-1


There may be times when the customer or field engineer will want to capture a presentation on the screen. This is accomplished by first saving the image(s) to the clipboard using a Print Key.

The P3 key is the factory default print key to accomplish a secondary screen capture. However, the default is for the video area only or the customer may have customized the P3 Key function. Therefore, screen capture should involve the following steps:

1.) Check and record any custom settings for the Print3 button.

2.) Set the Print3 button to Whole Screen, Secondary Capture.

3.) Capture the required screens to the Hard Drive or CD-R.

4.) Restore the Print3 button to it’s original settings.

Check and Record the P3 Key Function

Check the function of the Print 3 Key in the event that the customer may have made some custom settings.

1.) Click Utility on the keyboard.

2.) Select Advanced>Connectivity from the Utilities Menu.

3.) Select the Buttons tab on the Connectivity screen.

4.) In the Button field, select Print3.

The Connectivity/Buttons Screen will be displayed like the one shown in Figure 7-2 on page 7-4 .

7-4

Figure 7-2 Buttons Set Up Screen

P3 is the factory default Screen Capture Key. If it is not set to Whole Screen or Screen Capture, as shown in Figure 7-2 , proceed to step 5 to record the customer’s custom settings.

Section 7-3 - Screen Captures

GE H EALTHCARE


7-3-1


Check and Record the P3 Key Function

(cont’d)

5.) In the Destinations section, record the service that is displayed. The destinations list displays the following information:

* Name: user defined during service configuration

* Type: the type of service

* Destination Device: the device for which the service was configured

* Dir: direction: output, input, or both (I+O)

6.) In the Image generated section, record the parameters related to the service.

7-3-2 Setting the P3 Key to Screen Capture

If the P3 Key is not set to screen capture:

1.) While on the Connectivity screen, with the Buttons tab displayed, go to the drop down selection menu in the Destinations section.

2.) From the drop down menu select CopyToWflow_01>Image to Buffer>MyComputer>Out.

3.) Ensure that the Image generated section for capture Area is set to Whole Screen, secondary

Capture and No Image Compression.

4.) The P3 Key should now be set up for whole screen capture, sending the screens to the image buffer (clipboard).


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7-3-3


Capturing a Screen

The following is a generic process to capture any screen from the scanner:

1.) Navigate to and display the image/screen to be captured.

2.) Press P3. This will place a snapshot of the screen on the “clipboard” displayed at the bottom of the scan image display.

7-6

Clipboard

Thumbnails

Menu

Figure 7-3 Select Image to Capture

3.) Click FREEZE to unfreeze the image to view the image screen and the snapshots displayed on the bottom.

4.) Highlight the snapshot to be stored to the system RD (Removable Disk) or CD-R.

5.) Select Menu on the right side of the image screen, then highlight and select SAVE AS.

Save As

Figure 7-4 Menu > Save As

Section 7-3 - Screen Captures

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7-3-3 Capturing a Screen

(cont’d)


7-3-4

NOTE:

Figure 7-5 Save Dialog Box

6.) A Save dialog box will be opened. Save the image on the Removable disk or CD-R.

Reset the P3 Key to Customer’s Functionality

If the customer had programmed the P3 Key to a function other than screen capture, restore that functionality recorded in section 7-3-1 on page 4 . Refer to Figure 7-2 .

1.) Click Utility on the keyboard.

2.) Select Advanced>Connectivity from the Utilities Menu.

3.) Select the Buttons tab on the Connectivity screen.

4.) In the Button field, select Print3.

5.) In the Destinations section, select the service(s) recorded in step 5 , Section 7-3-1 . The destinations list displays the following information:

* Name: user defined during service configuration

* Type: the type of service

* Destination Device: the device for which the service was configured

* Dir: direction: output, input, or both (I+O)

Only output services can be associated to the print keys.

6.) In the Image generated section, select the parameters related to the service recorded in step

6 , Section 7-3-1 .


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Section 7-4

Global Service User Interface (GSUI)

7-4-1


Enter global service user interface

1.) When system is running, there is a start icon in the system status bar, see Figure 7-6 on page 7-8

Figure 7-6 system status bar

2.) Click start Icon, appears the selection menu, choose Service Platform icon in the bar, see Figure

7-7 on page 7-8

Figure 7-7

Click OK or wait 5 seconds after starting information appears. See Figure 7-8 on page 7-8 .

7-8

Figure 7-8 Information

Section 7-4 - Global Service User Interface (GSUI)

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7-4-1


Enter global service user interface

(cont’d)

3.) Select GE Service in option of User Level of GEMS Service Home page and input correct password, press OK button. See Figure 7-9 on page 7-9

Figure 7-9 Service Login Page


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7-4-2


Active Diagnostic Function

4.) Choose Diagnostic in Global Service Interface to active diagnostic functions, choose options to activate various functions correspondingly.

Figure 7-10 Active Diagnostic Function

7-10 Section 7-4 - Global Service User Interface (GSUI)

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7-4-3


Reset Database

5.) Choose Utilities in Global Service Interface. Click Scanner Utilities.

6.) Choose “Reset Database” to start Database reset tool.

Figure 7-11

7.) Click ”Reset Database” to Database reset tool.


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7-4-3


Reset Database

(cont’d)

8.) Click “OK” to start reset.

9.) Restart system after completing Database Reset.

Figure 7-12 Database Reset


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7-4-4


Clean Userdefs

10.)Choose Utilities in Global Service Interface. Click Scanner Utilities.

11.)Choose “Clean Userdefs” to start Userdefs clean tool.

Figure 7-13

12.)Click ”Clean Userdefs” to Userdefs clean tool.


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7-4-4 Clean Userdefs

(cont’d)

13.)Click “OK” to start clean.

14.)Restart system after completing Userdefs Clean.


Figure 7-14 Userdefs Clean


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7-4-5


Update FPGA

15.)Choose Utilities in Global Service Interface.

16.)Click “LOGIQ Book XP FPGA Update” to active Fpga update tool.

Figure 7-15

17.)Click “Update” to Fpga Update tool.

18.)Restart system after completing Fpga upgrade.

7-4-6

7-4-6-1

7-4-6-2

Figure 7-16 Reset Database

Control Frame

Contains the user interface elements used for:

• Diagnostic control, and

• Operator feedback

Button

This button has two modes each with appropriate text:

• Execute - to start the diagnostic, and

• Abort - to stop a diagnostic

The button can also be disabled.

Loop Count

This is an editable text field that will only accept numeric values with 4 digits or less. When the button is configured as an “execute” button and pressed, the loop count field will be queried to determine the number of times to execute the diagnostic.


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7-4-6-3 Progress Indicator

Displays a graphical progress indication to the user.


7-4-6-4

7-4-6-5

Short Text Message

Displays either a starting message or aborting message, as well as the diagnostic completion status.

Background Color

Initially gray, the Control Frame background color changes upon completion of a diagnostic to indicate completion status.

• Fail = Red

• Pass = Green

• Neither pass nor fail = Set back to Gray (for example, final code status is Aborted).


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Section 7-5

Common Diagnostics

7-5-1

7-5-1-1

7-5-1-2


Utilities

Provides two selections:

Disruptive Mode

Allows you to enable or disable disruptive mode troubleshooting.

System Shutdown

Allows for system shutdown from the diagnostic menu. Select to Restart System or Shutdown System.

Also, select to retain Disruptive Mode or Not.

After submitting to restart or shutdown a confirmation screen gives one last chance to confirm or cancel the request.


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7-5-2 PC Diagnostics (Non-Interactive Tests)


7-5-2-1

7-5-2-2

7-5-2-3

7-5-2-4

7-5-2-5

7-5-2-6

CPU Tests

Hard Drive Tests

Memory Tests

CD Drive Test

Video Test

USB Test

7-5-3

7-5-3-1

7-5-3-2

PC Diagnostics (Interactive Tests)

Keyboard Test

LCD Test

7-18 Section 7-5 - Common Diagnostics

GE H EALTHCARE


Section 7-6

LOGIQ Book XP Series Diagnostic Descriptions

7-6-1 Troubleshooting

These programs are provided for performing troubleshooting of the system.

Table 7-2 Troubleshooting Menu

Menu

Overall Test

Image Trouble

(Digital) Test

Image Trouble

(Analog) Test

Descriptions

Performs all of the troubleshooting tests listed below.

N/A

N/A

Error Code


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7-6-2 FRU Test

7-6-2-1


MST

These programs are provided for testing the MST board.

Table 7-3 FRU Test, MST Diagnostics Menu

Menu Descriptions

Overall Test

Assy Revision Test

Performs all of the MST board tests listed below.

Error Code

10001

TRIG Test

The PC sends the command to the SH4 to generate the trigger for self test. Then the results are returned to the PC.

10002

SH-4 Memory Test The PC sends the command to the SH4 to check the memory especially for SH-4.

10003

SH-PCI Test 1 The PC sends the command to the SH4 to check the SDRAM in MST.

10004

SH-4 Test

COMSO BM Test

Transmit HV Test

Supply HV Test

LV Test

Test the watchdog of SH4.

Use test mode of OQ card to check COMSO.

10005

10006

The HV unit outputs Plus and Minus THV, which is adjustable (variable).

This test checks if HVs can be read at A/D and adjusted by SH4.

The LV unit outputs four kinds of DC Voltage.

This test checks if they can be read at A/D and D/A in MST.

10007

The HV unit generates Plus and Minus SHV for HVSW, which is adjusted to follow

THV.

Checks if it can be read at A/D in MST.

10008

10009

D/A-A/D channel test.

10010 D/A-A/D Test

USCBus Test

Check USCBus

Checks if the SH4 writes the data properly to USC Register or PMX Register.

PCI/F1 Test (EUSC) N/A

10011

10012

PCI/F2 Test (IMGD) N/A

Memory Test N/A

10013

10014

7-20 Section 7-6 - LOGIQ Book XP Series Diagnostic Descriptions

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7-6-2-2 DFP

LOGIQ B

These programs are provided for testing the DFP board.


Table 7-4 FRU Test, DFP Diagnostics Menu

Menu Descriptions

Overall Test

Assy Revision

Test

DUSC I/F Test

Performs all of the DFP board tests listed below.

OQCARD Test

Check if the SH4 in the MST can access the DFP board via DUSC bus.

Local Bus Test Check if SH4 can read and write register of DFP board via DUSC bus.

WRAM Test The SH4 in MST reads and writes the register of WRAM in DFP via DUSC bus.

The SH4 in MST reads and writes the OQCARD registers in DFP via bus.

Error Code

20001

20002

20003

20004

20005


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7-6-2-3 DTX

LOGIQ B

These programs are provided for testing the DTX board.


Table 7-5 FRU Test, DTX Diagnostics Menu

Descriptions Menu

Overall Test

Assy Revision

Test

Performs all of the DTX board tests listed below.

Error Code

30001


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7-6-2-4


DCNN

These programs are provided for testing the DCNN board.

The PC sends the command to the SH4 in the MST, which brings DCNN into test then gets test report from DCNN via DUSC Bus and sends it back to the PC.

Table 7-6 FRU Test, DCNN Diagnostics Menu

Descriptions Menu

Overall Test

Assy Revision

Test

Performs all of the DCNN board tests listed below.

N/A

Error Code

40001


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7-6-2-5 PC

These programs are provided for testing the PC.


Table 7-7 FRU Test, PC Diagnostics Menu

Descriptions

CPU

Menu

Hard Drive

Memory

CDRW

Video

USB

CPU test

Hard Drive test

Memory test

CDRW test

Video test

USB test

PCI Board PCI Board test

AGP Video Card AGP Video Card test

Error Code

50001

50002

50003

50004

50005

50006

50007

50008


GE H EALTHCARE


Chapter 8

Replacement Procedures


Section 8-1

Overview


This chapter describes replacement procedures for the following modules and subsystems.


Section

8-1

8-2

8-2-1

8-2-2

8-3

8-4

Description

Overview

Disassembly/Re-assembly

Warning and Caution

Handle Assy (FRU No. 312)

Trackball Roller Cleaning

Loading the System Software

Page Number

8-1

8-1

8-1

8-2

8-4

8-6

Section 8-2

Disassembly/Re-assembly

8-2-1 Warning and Caution

ONLY QUALIFIED SERVICE PERSONNEL SHOULD REMOVE ANY COVERS OR

PANELS. ELECTRICAL HAZARDS EXISTS AT SEVERAL POINTS INSIDE. BECOME

THOROUGHLY FAMILIAR WITH ALL HAZARDOUS VOLTAGES AND HIGH CURRENT

LEVELS TO AVOID ACCIDENTAL CONTACT

CAUTION

Do wear the ESD wrist strap when you work on live circuits and more than 30V peak is present.

Chapter 8 Replacement Procedures 8-1

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8-2-2 Handle Assy (FRU No. 312)


Purpose: This is a description on how to remove and replace the Handle Assy (FRU No.312).

8-2-2-1

8-2-2-2

8-2-2-3

8-2-2-4

8-2-2-5

Tools

• Plier

Needed Manpower

• 1person, 2 minutes + travel

Preparations

• Shut Down the System, disconnect the AC/DC power cord and remove the battery.

Removal Procedure

Refer to Figure 8-1 on page 8-3 .

1.) Unscrew the two handle caps on both sides of the system, the rotation direction is counterclockwise.

2.) Pull out the Handle.

Mounting procedure

1.) Install the new parts in the reverse order of removal.

8-2 Section 8-2 - Disassembly/Re-assembly

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8-2-2 Handle Assy (FRU No. 312)

(cont’d)


1)

Figure 8-1 Handle Assy DISASSEMBLY

2)


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Section 8-3

Trackball Roller Cleaning

8-3-0-1

8-3-0-2

8-3-0-3

8-3-0-4


Purpose: This is a description on how to remove the trackball and clean the roller.

Tools

• No need.

Needed Manpower

• 1persons, 2 minutes + travel

Preparations

• Shut Down the System, disconnect the AC/DC power cord and remove the battery.

Procedure

Refer to Figure 8-2 on page 8-5 .

1.) Open LCD Assy.

2.) Turn other ring counterclockwise.

3.) Remove the ring.

4.) Using hand, carefully grab and remover trackball.

5.) Carefully clean roller using Qtip.

8-4 Section 8-3 - Trackball Roller Cleaning

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Section 8-3 Trackball Roller Cleaning

(cont’d)


2)

3)

4)

Figure 8-2 Trackball Roller Cleaning

5)


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Section 8-4Loading the System Software


Please refer to Section 3-9 "Loading the System Software" from page 3-27 to page 3-49.


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Chapter 9

Renewal Parts


Section 9-1

Overview


This chapter gives you an overview of Spare Parts available for the LOGIQ Book XP Series.


Section

9-1

9-6

9-7

9-8

9-9

9-2

9-3

9-4

9-5

9-10

9-11

Description

Overview

List of Abbreviations

Renewal Parts Lists

Operator Console Assy

Keyboard Assy

Bottom Assy

Isolation Cart Components

Isolation Cart Enhanced Version Components

Accessories and Kits

Manuals

Probes

Section 9-2

List of Abbreviations

• Assy - Assembly

• Ctrl - Control

• FRU 1 - Replacement part available in part hub

• FRU 2 - Replacement part available from the manufacturer (lead time involved)

• KBD - Keyboard

• LCD - Liquid Crystal Display

• BnV - Brightness and Volume

• DFP - Dragon Front Processor Board

• MST - Master Board

• DTX - Dragon Transmit Board

• FPC - Flexible Print Circuit Board

Chapter 9 Renewal Parts

Page Number

9-1

9-4

9-5

9-7

9-10

9-1

9-2

9-3

9-4

9-15

9-16

9-1

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Section 9-3Renewal Parts Lists

9-3-1


Equipment Models Covered in this Chapter

Table 9-2 ACDC Power Pack & ACDC Power Cable list

Part Name

ACDC Power Pack unit

ACDC Power Cable

ACDC Power Cable

ACDC Power Cable

ACDC Power Cable

ACDC Power Cable

ACDC Power Cable

ACDC Power Cable

ACDC Power Cable

ACDC Power Cable

ACDC Power Cable

ACDC Power Cable

Part Number

5124447

5120411

5120412

5120439

5120440

5125218

5125219

5125221

5125223

5125227

5125228

5400793

Description

100-240V AC INPUT/20V DC OUTPUT

ACDC Power Cable for USA

ACDC Power Cable for Europe

ACDC Power Cable for China

ACDC Power Cable for Japan

ACDC Power Cable for Australia/New Zealand

ACDC Power Cable for United Kingdom and Ireland

ACDC Power Cable for India/South Africa

ACDC Power Cable for Argentina

ACDC Power Cable for Israel

ACDC Power Cable for Switzerland

ACDC Power Cable for Brazil

Quantity

1

1

1

1

1

1

1

1

1

1

1

1

FRU

1

1

1

1

1

1

1

1

1

1

1

1

9-2 Section 9-3 - Renewal Parts Lists

GE H EALTHCARE


Section 9-4 Operator Console Assy


LCD Assy

Bottom Assy

Keyboard Assy

Figure 9-1OPERATOR CONSOLE ASSY

Chapter 9 Renewal Parts 9-3

GE H EALTHCARE


Section 9-5Keyboard Assy

Item

201

Table 9-3 Keyboard Assy

Part Name Part Number

Trackball 2326353

Section 9-6Bottom Assy

Item

312

Table 9-4 Bottom Assy

Part Name

Handle Kits

Part Number

5121679


Description

Trackball

Description

Handle

Quantity FRU

1 1

Quantity

1

FRU

2

9-4 Section 9-5 - Keyboard Assy

GE H EALTHCARE


Section 9-7Isolation Cart Components


502

501

503

504

505

506

507

Figure 9-2 Isolation Cart Components

Table 9-5 Isolation Cart Components

Item

501

502

503

504

505

506

Part Name

Wheels

Isolation transformer 110V


Handle kits

Probe holder kits

Hardware kits

USA class cable kits

European class cable kits

Chinese class cable kits

Japanese class cable kits

Australia/New Zealand class cable kits

United Kingdom and Ireland class cable kits

Denmark class cable kits

India/South Africa class cable kits

Argentina class cable kits

Israel class cable kits

Switzerland class cable kits

Part Number

5183729

5180439-2

5180376

5183627

5183958

5183719

5182671

5182937

5182252

5182323

5182095

5182890

5182310

5182038

5182881

5182625

5182631

Description

Wheels



Handle kits

Probe holder kits

Hardware kits

USA class cable kits

European class cable kits

Chinese class cable kits

Japanese class cable kits

Australia/New Zealand class cable kits

United Kingdom and Ireland class cable kits

Denmark class cable kits

India/South Africa class cable kits

Argentina class cable kits

Israel class cable kits

Switzerland class cable kits


508

Quantity

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

FRU

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

9-5

GE H EALTHCARE



Item

507

508

Part Name

Security lock

Isolation Cart (110V)


Part Number

5183906

5177673-2

5177558-2


Description

Security lock for Twin



Quantity

1

1

1

FRU

2

2

2

9-6 Section 9-7 - Isolation Cart Components

GE H EALTHCARE


Section 9-8Isolation Cart Enhanced Version Components

511 512

515

513

514

517

516

518

519

525

521

522

526

Figure 9-3 Isolation Cart Components


524

523

9-7

GE H EALTHCARE



Item

510

511

511A

512

512A

Part Name



Isolation cart (110V)

Isolation cart (220V)

Castor kits

Castor kits

Gas Spring lever

Gas Spring lever

Part Number

5384810

5384811

5423269

5423270

5394023

5451500

5391829

5434960

513

513A

514

514A

515

515A

516

517

517A

518

518A

519

521

522

522A

523

523A

Isolation cart transformer 110V




Cable hook kit

Cable hook kit

Isolation Cart Rear Handle

Isolation Cart Rear Handle

Spring Cable Assy

Locate block and Screw cap

Locate block and Screw cap

Probe and gel holder kit

Probe and gel holder kit

Handle clip kit

Security lock with package

Isolation Cart Front handle

Isolation Cart Front handle

Gas Spring Assy

Gas Spring Assy

5394060

5394061

5240781-2

5240780-2

5394028

5426642

5394065

5461076

5391606

5394036

5426645

5394032

5426644

5394021

5215494

5394064

5426643

5394067

5426646


Description



Isolation cart BT12 (110V)

Isolation cart BT12 (220V)

Castor kits (Dark Steel Blue)

Castor kits (Onyx Black)

Gas Spring lever (Dark Steel Blue)

Gas Spring lever (Onyx Black)

Isolation cart transformer 110V (Dark

Steel Blue)

Isolation cart transformer 220V (Dark

Steel Blue)

Isolation cart transformer 110V (Onyx

Black)

Isolation cart transformer 220V (Onyx

Black)

Cable hook kit (Dark Steel Blue)

Cable hook kit (Onyx Black)

Isolation Cart Rear Handle (Dark Steel

Blue)

Isolation Cart Rear Handle (Onyx Black)

Spring Cable Assy

Locate block and Screw cap (GE Pearl

Metallic)

Locate block and Screw cap (GE N9)

Probe and gel holder kit (Dark Steel

Blue)

Probe and gel holder kit (Onyx Black)

Handle clip kit

Security lock with package

Isolation Cart Front handle (Dark Steel

Blue)

Isolation Cart Front handle (Onyx Black)

Gas Spring Assy (Dark Steel Blue)

Gas Spring Assy (Onyx Black)

Quantity FRU

1

1

1

1

1

1

1

1

2

2

2

2

2

2

2

2

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

9-8 Section 9-8 - Isolation Cart Enhanced Version Components

GE H EALTHCARE



Item

524

525

526

Part Name

AC Power Cord Switzerland

AC Power Cord Israel

AC Power Cord Argentina

AC Power Cord India

AC Power Cord Denmark

AC Power Cord UK

AC Power Cord Australia

AC Power Cord Japan

AC Power Cord China

AC Power Cord Europe

AC Power Cord USA

Isolation Cart Drawer Kits

Isolation Cart Basket Kits

Part Number

5177154

5176753

5177195

5176773

5177153

5176907

5177187-2

5177126

5176304

5177123

5177146

5426647

5426648


Description

AC Power Cord Switzerland

AC Power Cord Israel

AC Power Cord Argentina

AC Power Cord India

AC Power Cord Denmark

AC Power Cord UK

AC Power Cord Australia

AC Power Cord Japan

AC Power Cord China

AC Power Cord Europe

AC Power Cord USA

Isolation Cart Drawer Kits (GE N9)

Isolation Cart Basket Kits (GE N9)

Quantity FRU

1

1

1

1

1

1

1

1

1

1

1

2

2

2

2

2

2

2

2

2

2

2

1

1

2

2


608

609

610

611

612

613

614

Item

604B

604C

605

605A

603B

603C

604

604A

602B

602C

603

603A

601

601A

602

602A

605B

605C

605D

605E

606

606A

GE H EALTHCARE


Section 9-9Accessories and Kits

Table 9-7 Accessories and Kits

Part Name

Battery Pack

Battery Pack

USB CD-RW CN Ver

USB CD-RW CN Ver

USB CD-RW CN Ver

USB CD-RW CN Ver

USB CD-RW US Ver

USB CD-RW US Ver

USB CD-RW US Ver

USB CD-RW US Ver

USB CD-RW JP Ver

USB CD-RW JP Ver

USB CD-RW JP Ver

USB CD-RW JP Ver

USB CD-RW EU Ver

USB CD-RW EU Ver

USB CD-RW EU Ver

USB CD-RW EU Ver

LITEON eSAU108 DVDRW Kit

LITEON eUAU108 DVDRW Kit

USB Footswitch

USB Footswitch

Part Number

5251789-3

5251789-4

5251787

5251787-2

5251787-3

5251787-4

5251788

5251788-2

2325369-7

2325369-8

5251790

5251790-2

5251790-3

5251790-4

5251789

5251789-2

5251788-3

5251788-4

5456273

5456273-2

2327703

5338419

Cisco Wireless LAN Adapter

USB Connector

B&W printer (UP-D897) CHN kit

B&W printer (UP-D897) USA kit

B&W printer (UP-D897) EUP kit

B&W printer (UP-D897) JPN kit

Color printer (UP-D23MD) CHN Kit

5124101

2393636

5151262

5151259

5151261

5151263

5133106


Description

Battery Pack

Battery Pack

DVD-RW with China power cord




DVD-RW with America power cord




DVD-RW with Japan power cord




DVD-RW with Europe power cord




LITEON eSAU108 DVDRW Kit

LITEON eUAU108 DVDRW Kit

Footswitch with USB port

Footswitch with USB port

Option part (Not available on LOGIQ Book XP

PRO)

Option part

Option part

Option part

Option part

Option part

Option part

1

1

1

1

1

1

Qty FRU

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

1 2

2

2

2

2

2

2

9-10 Section 9-9 - Accessories and Kits

GE H EALTHCARE



Item

616A

617

617A

618

614A

615

615A

616

Part Name

Color printer (UP-D25MD) CHN Kit

Color printer (UP-D23MD) USA Kit

Color printer (UP-D25MD) USA Kit

Color printer (UP-D23MD) EUP Kit

Color printer (UP-D25MD) EUP Kit

Color printer (UP-D23MD) JPN Kit

Color printer (UP-D25MD) JPN Kit

Hardware Kit

Part Number

5133106-2

5133107

5133107-2

5133108

5133108-2

5133109

5133109-2

5123493

619 Basic system software load image 5194306

619A

620

620A

621

621A

622

622A

626

627

628

629

623

623A

624

625

630

631

632

Basic system software load image

Application software






USB HUB Assy

USB HUB Assy

3M USB Cable Assy

USA type Power cord for Printer

China type Power cord for Printer

German type Power cord for Printer

Japan type Power cord for Printer

LV Carrying Case Assy

LOGIQ Book Carrying Case hard cover

Sterile Monitor Covers Assy

PIT Assy for EU and CN

5194306-2

5194307

5194307-2

5196082

5196082-2

5196081

5196081-2

5117263

5184951-2

5135661

5118339

5118340

5118341

5118960

5151240

5136143

5136142

5146884


Description

Option part

Option part

Option part

Option part

Option part

Option part

Option part

Include all screws and washers

LOGIQ Book XP Base system software CD

(R2.2.0)

LOGIQ Book XP Base system software CD

(R2.2.1)

LOGIQ Book XP Application software CD

(R2.2.0)

LOGIQ Book XP Application software CD

(R2.2.1)

LOGIQ Book XP Vet Application software CD

(R2.2.0)

LOGIQ Book XP Vet Application software CD

(R2.2.1)

LOGIQ Book XP PRO Application software

CD(R2.2.0)

LOGIQ Book XP PRO Application software

CD(R2.2.1)

Option Part

Option Part

Option Part

Option Part

Option Part

Option Part

Option Part

Option Part

Option Part

Option Part

PIT Assy for EU and CN

Qty FRU

1

1

1

1

1

1

1

1

2

2

2

2

2

2

2

2

1

1

1

1

1

1

1

1

2

2

2

2

2

2

2

2

1

1

1

1

1

1

1

1

1

1

1

2

2

2

2

2

2

2

2

2

2

2


GE H EALTHCARE



Item

607

649

650

650A

650B

651

651A

647B

648

648A

648B

646A

646B

647

647A

645

645A

645B

646

641

642

643

644

637

638

639

640

633

634

635

636

Part Name

PIT Assy for US

PIT Assy for JP

ECG Module

ECG USB Cable

ECG AHA Cable

ECG IEC Cable

ECG Module with Chinese Label

ECG Module with SKD label

HP470 Printer (HP470+PIT) USA Kits

HP470 Printer (HP470+PIT) EUP Kits

HP470 Printer (HP470+PIT) CHN Kits

HP470 Printer (HP470+PIT) JAP Kits

PC Printer (HP K550) JAP



PC Printer (HP K550) USA



PC Printer (HP K550) EUP



PC Printer (HP K550) CHN



Net Card

Net Card

USB Memory 1G

USB Memory 2G

USB Memory 4G

LOGIQ BOOK XP Software DVD

LOGIQ BOOK XP Software DVD


Part Number

5401755

5401756

5168040-2

5168040-3

5168040-4

5441508

5441508-2

5175122-2

5175122-3

5175833

5175833-2

5175833-3

5175554

5175554-2

5175554-3

5175689

5175988

5175546

5175350

5175898

5175898-2

5175898-3

5175122

5146885

5146887

5129487

5146055

5146056

5146739

5149641

5199563

Description

PIT Assy for US

PIT Assy for JP

Option Part

Option Part

Option Part

Option Part

Option Part

Option Part

HP470 Printer (HP470+PIT) without power cord




PC Printer (HP K550) without power cord












Option part (Not available for Japanese)

Option part (Only for Japanese)

USB Memory 1G

USB Memory 2G

USB Memory 4G

LOGIQ BOOK XP software DVD (R2.2.2)

LOGIQ BOOK XP software DVD (R2.2.3)

Qty FRU

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2


GE H EALTHCARE



Part Number

668

669

670

671

664

665

666

667

672

673

674

660

661

662

663

656

657

658

659

653A

653B

654

655

652

652A

652B

653

Item

651B

651C

651D

Part Name

LOGIQ BOOK XP Software DVD (Chinese

Version)

LOGIQ BOOK XP Software USB

LOGIQ BOOK XP Software USB (Chinese

Version)

LOGIQ BOOK XP PRO software DVD

LOGIQ BOOK XP PRO software DVD

LOGIQ BOOK XP PRO software USB

LOGIQ BOOK XP VET software DVD

LOGIQ BOOK XP VET software DVD

LOGIQ BOOK XP VET software USB

Measure Transfer Connection Kit

LB XP NetCard USA

LB XP NetCard JAP

Sony UPP-110HG B/W Printer Paper 1 roll

Mitsubishi P95D BW PRINTER USA KIT

Mitsubishi P95D BW PRINTER EUP KIT

Mitsubishi P95D BW PRINTER CHN KIT

Mitsubishi P95D BW PRINTER JPN KIT

Sony UP-D25MD Color paper printer CHN kit

Sony UP-D25MD Color paper printer USA kit

Sony UP-D25MD Color paper printer EU kit

Sony UP-D25MD Color paper printer JPN kit

HP Officejet 100 Printer CHN Kit

HP Officejet 100 Printer EUP Kit

HP Officejet 100 Printer JPN Kit

HP Officejet 100 Printer USA Kit

ECG module (AHA) USA

ECG module (IEC) Eur

ECG Assy w/Chinese Lable

USB Memory Stick

Cisco Wireless LAN Card

5456030

5455196

5451875

5398063

5398064

5426594

5426595

5426596

5426597

5146763

5146764

5147166

5395754

5251776

5401682

5130409

5420904

5420902

5420901

5420903

5398061

5398062

5458136

5458136-2

5441763

5446367

5446367-2

5447435

5304711

5401735

LOGIQ B OOK XP S

Description

ERIES B ASIC S

LOGIQ BOOK XP R2.2.2 China software DVD

LOGIQ BOOK XP Software USB (R2.2.3)

LOGIQ BOOK XP Software USB Chinese

Version (R2.2.2)

LOGIQ BOOK XP PRO software DVD (R2.2.2)

LOGIQ BOOK XP PRO software DVD (R2.2.3)

LOGIQ BOOK XP PRO software USB (R2.2.3)

LOGIQ BOOK XP VET software DVD (R2.2.2)

LOGIQ BOOK XP VET software DVD (R2.2.3)

LOGIQ BOOK XP VET software USB (R2.2.3)

Measure Transfer Connection Kit

LB XP NetCard USA

LB XP NetCard JAP

Sony UPP-110HG B/W Printer Paper 1 roll

Mitsubishi P95D BW PRINTER USA KIT

Mitsubishi P95D BW PRINTER EUP KIT

Mitsubishi P95D BW PRINTER CHN KIT

Mitsubishi P95D BW PRINTER JPN KIT

Sony UP-D25MD Color paper printer CHN kit

Sony UP-D25MD Color paper printer USA kit

Sony UP-D25MD Color paper printer EU kit

Sony UP-D25MD Color paper printer JPN kit

HP Officejet 100 Printer CHN Kit

HP Officejet 100 Printer EUP Kit

HP Officejet 100 Printer JPN Kit

HP Officejet 100 Printer USA Kit

ECG module (AHA) USA

ECG module (IEC) Eur

ECG Assy w/Chinese Lable

USB Memory Stick (SanDisk USB Stick 4G)

Cisco Wireless LAN Card (for Japan only)

ERVICE

Qty FRU

1

1

1

M ANUAL

2

2

2

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2

2


GE H EALTHCARE



Item Part Name

675

675A

675B

676

Peripheral Driver Patch CD Installation Kit

Peripheral Driver Patch USB Installation Kit


TU2-ET100Net Card Kit for LOGIQ BOOK XP

Series

Part Number

5455722

5453562

5453562-2

5460107


Description

Peripheral Driver Patch CD Installation kit



TU2-ET100Net Card Kit for LOGIQ BOOK XP

Series

Qty FRU

1

1

1

2

2

2

1 2


GE H EALTHCARE


Section 9-10Manuals

Item


Table 9-8 MANUALS

Part Name

LOGIQ Book XP Series Basic Service Manual

Part Number

5194296-100

System User Manuals

LOGIQ Book XP Series Basic User Manual - English

LOGIQ Book XP Series Basic User Manual - French

LOGIQ Book XP Series Basic User Manual -Spanish

LOGIQ Book XP Series Basic User Manual - German

LOGIQ Book XP Series Basic User Manual -Italian

LOGIQ Book XP Series Basic User Manual -Portuguese

LOGIQ Book XP Series Basic User Manual -Japanese

LOGIQ Book XP Series Basic User Manual - Chinese

5194291-100

5194291-101

5194291-106

5194291-108

5194291-111

5194291-127

5194291-140

5194291-141

System Quick Guide

LOGIQ Book XP Series Guick Guide - English

LOGIQ Book XP Series Guick Guide - French

LOGIQ Book XP Series Guick Guide - Spanish

LOGIQ Book XP Series Guick Guide - German

LOGIQ Book XP Series Guick Guide - Italian

LOGIQ Book XP Series Guick Guide - Portuguese

LOGIQ Book XP Series Guick Guide - Japanese

LOGIQ Book XP Series Guick Guide - Chinese

5194294-100

5194294-101

5194294-106

5194294-108

5194294-111

5194294-127

5194294-140

5194294-141

Description

Service Manual

Basic User Manual

Basic User Manual

Basic User Manual

Basic User Manual

Basic User Manual

Basic User Manual

Basic User Manual

Basic User Manual

Quick Start Guide

Quick Start Guide

Quick Start Guide

Quick Start Guide

Quick Start Guide

Quick Start Guide

Quick Start Guide

Quick Start Guide

Quantity FRU

1 N

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

N

N

N

N

N

N

N

N

N

N

N

N

N

N

N

N


GE H EALTHCARE


Section 9-11Probes

Item

705

706

707

708

701

702

703

704

Item

705

706

707

708

701

702

703

704

Table 9-9 Probes on LOGIQ Book XP

Part Name

3C-RS

E8C-RS

8C -RS i12L-RS

8L-RS

3S-RS i739-RS

T739-RS

Part Number

2290776

2290777

2354971

2377942

2376127

2323337

2404995

2404999


Description

Probe (Center Frequency: 3.8MHz)








Table 9-10 Probes on LOGIQ Book XP Vet/XP PRO

Part Name

3C-RS

E8C-RS

8C -RS i12L-RS

8L-RS

3S-RS i739-RS LC

T739-RS

Part Number

5134641

5134643

5134642

5134645

5134644

5134647

5136420

5134646

Description









Quantity FRU

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

Quantity FRU

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

9-16 Section 9-11 - Probes

GE H EALTHCARE


Chapter 10

Care & Maintenance


Section 10-1

Overview

10-1-1

10-1-2

Periodic Maintenance Inspections

It has been determined by engineering that your LOGIQ Book XP Series system does not have any high wear components that fail with use, therefore no Periodic Maintenance Inspections are mandatory.

Some Customers Quality Assurance Programs may require additional tasks and or inspections at a different frequency than listed in this manual.

Purpose of Chapter 10

This chapter describes Care & Maintenance on the system and peripherals. These procedures are intended to maintain the quality of the ultrasound systems performance. Read this chapter completely and familiarize yourself with the procedures before performing a task.


Section

10-1

10-2

10-3

10-4

10-5

10-6

10-7

Description

Overview

Why do Maintenance

Maintenance Task Schedule

Tools Required

System Maintenance

Electrical Safety Tests

When There's Too Much Leakage Current...

Page Number

10-1

10-2

10-2

10-4

10-5

10-11

10-18

CAUTION

Practice good ESD prevention. Wear an anti–static strap when handling electronic parts and even when disconnecting/connecting cables.

DANGER

BE SURE TO DISCONNECT THE SYSTEM POWER PLUG BEFORE YOU

REMOVE ANY PARTS. BE CAUTIOUS WHENEVER POWER IS STILL ON AND

COVERS ARE REMOVED.

CAUTION

Do not pull out or insert circuit boards while power is ON.

CAUTION

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

Chapter 10 Care & Maintenance 10-1

GE H EALTHCARE


Section 10-2

Why do Maintenance

10-2-1

10-2-2


Keeping Records

It is good business practice that ultrasound facilities maintain records of periodic and corrective maintenance. The Ultrasound Periodic Maintenance Inspection Certificate provides the customer with documentation that the ultrasound system is maintained on a periodic basis.

A copy of the Ultrasound Periodic Maintenance Inspection Certificate should be kept in the same room or near the system.

Quality Assurance

In order to gain accreditation from organizations such as the American College of Radiology (USA), it is the customer’s responsibility to have a quality assurance program in place for each system. The program must be directed by a medical physicists, the supervising radiologist/physician or appropriate designee.

Routine quality control testing must occur regularly. The same tests are performed during each period so that changes can be monitored over time and effective corrective action can be taken.

Testing results, corrective action and the effects of corrective action must be documented and maintained on the site.

Your GE service representative can help you with establishing, performing and maintaining records for a quality assurance program. Please contact us for coverage information and/or price for service.

Section 10-3

Maintenance Task Schedule

10-3-1

NOTE:

NOTE:

How often should care & maintenance tasks be performed?

The Care & Maintenance Task Schedule (provided on page 10-3 ) specifies how often your LOGIQ Book

XP Series should be serviced and outlines items requiring special attention.

It is the customer’s responsibility to ensure the LOGIQ Book XP Series care & maintenance is performed as scheduled in order to retain its high level of safety, dependability and performance.

Your GE Service Representative has an in-depth knowledge of your LOGIQ Book XP Series ultrasound scanning system and can best provide competent, efficient service. Please contact us for coverage information and/or price for service.

The service procedures and recommended intervals shown in the Care & Maintenance Task Schedule assumes that you use your LOGIQ Book XP Series for an average patient load (10-12 per day) and use it as a primary mobile unit which is transported between diagnostic facilities.

If conditions exist which exceed typical usage and patient load, then it is recommended to increase the maintenance frequencies.

10-2 Section 10-2 - Why do Maintenance

GE H EALTHCARE


Section 10-3 Maintenance Task Schedule

(cont’d)

Table 10-2 Customer Care Schedule

Service at Indicated Time

Clean Probes

Clean ECG

Inspect AC Mains Cable

Inspect Cables and Connectors

Clean Console

Clean LCD

Console Leakage Current Checks

Peripheral Leakage Current Checks

Surface Probe Leakage Current Checks

Endocavity Probe Leakage

Current Checks

Measurement Accuracy Checks

Probe/Phantom Checks

Daily

•*

•*

Weekly Monthly

Per Facilities

QA Program Notes

* or before each use

* or before each use

Mobile Unit Check Weekly

•

•

•

•

See Note

See Note

See Note

See Note

See Note

See Note

Annually

Annually

Annually

Quarterly

Annually

Annually

Quarterly

Annually

NOTE:

NOTE:

May require specialized equipment to complete.

PMs are not mandatory, the table above is for reference only.


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Section 10-4

Tools Required

10-4-1

10-4-1-1

Special Tools, Supplies and Equipment

Specific Requirements for Care & Maintenance


Table 10-3 Overview of Requirements for Care & Maintenance

Part Number Tool

Digital Volt Meter (DVM)

Leakage Current Ultrasound Kit

Anti Static Kit

Anti Static Vacuum Cleaner

Safety Analyzer

QIQ Phantom

B/W Printer Cleaning Sheet

Color Printer Cleaning Sheet

Disposable Gloves

2113015

46–194427P231

46–194427P279

46–194427P369

46–194427P373

46–194427P370

46–194427P278

46–194427P279

E8370RB

Comments

For 120V and 220V Units

Kit includes anti–static mat, wrist strap and cables for 200 to 240

V system

3M #2204 Large adjustable wrist strap

3M #2214 Small adjustable wrist strap

3M #3051 conductive ground cord

120V

230V

The safety Analyzer tool should be calibrated and compliant with

AAMI/ESI 1993 or IEC 60601 or AS/NZS 3551

RMI Grayscale Target Model 403GS

See printer user manual for requirements

See printer user manual for requirements

10-4 Section 10-4 - Tools Required

GE H EALTHCARE


Section 10-5

System Maintenance

10-5-1


Preliminary Checks

The preliminary checks take about 15 minutes to perform. Refer to the system user documentation whenever necessary.

Table 10-4 System Checks

Step

1

2

3

4

5

6

Item

Ask & Listen

Paperwork

Power up

Probes

Displays

Presets

Description

Ask the customer if they have any problems or questions about the equipment.

Fill in the top of the Ultrasound Inspection Certificate (see page 10- 19 ). Note all probes and system options.

With AC input.

Turn the system power on and verify that all fans and peripherals turn on. Watch the displays during power up to verify that no warning or error messages are displayed.

Check the Battery recharging.

Without AC input, use internal battery.

Verify that the system properly recognizes all probes.

Verify proper display on the LCD.

Backup all customer presets on an CD-RW.


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10-5-2


Functional Checks (See Also Chapter 4)

The functional checks take about 60 minutes to perform. Refer to the system user documentation whenever necessary.

10-5-2-1 System Checks

Table 10-5 System Functional Checks

÷ Step Description

B-Mode

CF-Mode*

Verify basic B-Mode (2D) operation. Check the basic system controls that affect this mode of operation.

Verify basic CF-Mode (Color Flow Mode) operation. Check the basic system controls that affect this mode of operation.

Doppler Modes*

Verify basic Doppler operation (PW if available). Check the basic system controls that affect this mode of operation.

M-Mode Verify basic M-Mode operation. Check the basic system controls that affect this mode of operation.

*Applicable

Software Options

Verify the basic operation of all optional modes such as Multi-Image, 3D*, Harmonics, Cine,... etc.

Check the basic system controls that affect each options operation.

Xmit/Recv

Elements

Use the Visual Channel Utility on the loop connect to verify that all system xmit/recv channels are functional.

Keyboard Test Perform the Keyboard Test Procedure to verify that all keyboard controls are OK.

LCD Verify basic LCD display functions. Refer to Chapter 3 of the User Manual.

Software Menu check

Verify Software Menu display functions. Refer to Chapter 3 of the User Manual.

Measurements

Scan a gray scale phantom and use the measurement controls to verify distance and area calculation accuracy. Refer to the User Manual, Chapter 18, for measurement accuracy specifications.

NOTE: * Some software may be considered standard depending upon system model configuration.

NOTICE * 3D is option on LOGIQ Book XP Vet, but not available on LOGIQ Book XP PRO.

NOTICE * CF and Doppler mode are option on LOGIQ Book XP PRO/XP Vet.

10-6 Section 10-5 - System Maintenance

GE H EALTHCARE


10-5-2-2


Peripheral/Option Checks

If any peripherals or options are not part of the system configuration, the check can be omitted. Refer to the User Manual for a list of approved peripherals/options.

Table 10-6 GE Approved Peripheral/Hardware Option Functional Checks

Step Item Description

1 B/W Printer Verify hardcopy output of the B/W video page printer. Clean heads and covers if necessary.

2 Color Printer Verify hardcopy output of the Color video page printer. Clean heads and covers if necessary.

3

4

DICOM* Verify that DICOM is functioning properly. Send an image to a DICOM device.

Footswitch Verify that the footswitch is functioning as programed. Clean as necessary.

5 CD-RW Verify that the CD-RW is functioning properly. Clean heads and covers if necessary.

NOTICE * This function is option on LOGIQ Book XP Vet, but not available on LOGIQ Book XP PRO.

10-5-3

10-5-3-1

10-5-4

10-5-4-1

Input Power

AC/DC Adapter Inspection

Table 10-7 AC/DC Adapter Inspection

Step

1

2

Item Description

Unplug Cord Disconnect the mains cable from the wall and system.

Inspect Inspect it and its connectors for damage of any kinds.

3 Verify

Verify that the LINE wires are properly attached to the terminals, and that no strands may cause a short circuit.

Cleaning

General Cleaning

Table 10-8 General Cleaning


1 Console

Remove the battery. Use a fluid detergent in warm water on a soft, damp cloth to carefully wipe the entire system. Be careful not to get the cloth too wet so that moisture does not enter the console.

2 Probe Holder Clean probe holders. (they may need to be soaked to remove excess gel).

3 LCD

Use a soft, non-abrasive folder cloth. Gently wipe the LCD face. DO NOT use a glass cleaner that has a hydrocarbon base (such as Benzene, Methy Alcohol or Methy Ethyl Ketone) on LCD with the filter (antiglare shield).


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10-5-5 Physical Inspection


Table 10-9 Physical Checks


1

2 Scratches & Dents Inspect the console for dents, scratches or cracks.

3 Control Panel Inspect keyboard and control panel. Note any damaged or missing items.

4

Labeling

Cables &

Connectors

Verify that all system labeling is present and in readable condition. Refer to User Manual,...... for details.

Check all internal cable harnesses and connectors for wear and secure connector seating. Pay special attention to footswitch assembly and probe strain or bend reliefs.

5

6

7

Shielding &

Covers

Check to ensure that all EMI shielding, internal covers, air flow panels and screws are in place.

Missing covers and hardware could cause EMI/RFI problems while scanning.

External I/O Check all connectors for damage.

Op Panel Lights Check for proper operation of all operator panel and Freeze Key light.


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10-5-6


Optional Diagnostic Checks

Optionally you can access the diagnostic software as described in Chapters 5 or 7. View the error logs and run desired diagnostics.

10-5-6-1

10-5-7

10-5-7-1

View the Logs

1.) Review the system error log for any problems.

2.) Check the temperature log to see if there are any trends that could cause problems in the future.

3.) Check the Configuration Log; update if needed.

Probe Maintenance

Probe Related Checks

Table 10-10 Probe Related Checks

Step

1

2

Item Description

Probe Holder Clean probe holders (they may need to be soaked to remove excess gel).

Probes

Thoroughly check the system probe connectors and remove dust from inside the connector sockets if necessary. Visually check for bent, damaged or missing pins

10-5-7-2

10-5-7-3

NOTE:

NOTE:

NOTE:

Basic Probe Care

The system user manuals and various probe handling cards provide a complete description of probe care, maintenance, cleaning and disinfection. Ensure that you are completely familiar with the proper care of GE probes.

Ultrasound probes can be easily damaged by improper handling. See the User Manual and probe care cards for more details. Failure to follow these precautions can result in serious injury and equipment damage. Failure to properly handle or maintain a probe may also void its warranty.

Any evidence of wear indicates the probe cannot be used.

Do a visual check of the probe pins and system sockets before plugging in a probe.

Basic Probe Cleaning

Refer to the User’s Manual for details on probe cleaning.

To help protect yourself from blood borne diseases, wear approved disposable gloves. These are made of nitrile derived from vegetable starch to prevent allergic latex reactions.

Failure to follow the prescribed cleaning or disinfection procedures will void the probe’s warranty. DO NOT soak or wipe the lens with any product not listed in the User Manual. Doing so could result in irreparable damage to the probe. Follow care instructions that came with the probe.

Disinfect a defective probe before you return it. Be sure to tag the probe as being disinfected.


GE H EALTHCARE


10-5-8


Battery Performance Maintenance

It is recommended to do battery performance maintenance one time per year.

Please follow the flow chart below to carry out battery performance maintenance.

Battery discharge

>45 minutes?

Yes

Battery charge > 3 hour

No

Battery charge > 3 hour

No

Replace battery

Battery power > 90%?

Yes

Battery is Ok

Battery power > 90%?

Yes

Discharge

No

Replace battery

>45 minutes?

Yes

Battery is Ok

NOTE:

NOTE:

Figure 10-1 Flow chart of Battery Performance Maintenance

Disconnect all probes when discharge battery.

Discharge the battery to let the system automatically shut down.

No

Replace battery


GE H EALTHCARE


Section 10-6

Electrical Safety Tests


10-6-1 Safety Test Overview

The electrical safety tests in this section are based on and conform to IEC 60601-1 Medical Equipment

Safety Standards. They are intended for the electrical safety evaluation of cord-connected, electrically operated, patient care equipment. If additional information is needed, refer to the IEC 60601-1 documents.

THE USER MUST ENSURE THAT THE SAFETY INSPECTIONS ARE PERFORMED AT

LEAST EVERY 6 MONTHS ACCORDING TO THE REQUIREMENTS OF THE PATIENT

SAFETY STANDARD IEC-EN 60601-1. ONLY TRAINED PERSONS ARE ALLOWED TO

PERFORM THE SAFETY INSPECTIONS MENTIONED ABOVE.

CAUTION

To avoid electrical shock, the unit under test must not be connected to other electrical equipment. The unit under test must not be contacted by users or patients while performing these tests.

CAUTION

Possible risk of infection. Do not handle soiled or contaminated probes and other components that have been in patient contact. Follow appropriate cleaning and disinfecting procedures before handling the equipment.

Test the system, peripherals and probes for leakage current. Excessive leakage current can cause injury or death in sensitive patients. High leakage current can also indicate degradation of insulation and a potential for electrical failure. Do not use probes or equipment having excessive leakage current.

To minimize the risk that a probe may shock someone the customer should:

• Not use a probe that is cracked or damaged in any way

• Check probe leakage current:

* Based on your facilities QA program for surface probes

* Based on your facilities QA program for endocavitary probes

* whenever probe damage is suspected


GE H EALTHCARE


10-6-2


GEMS Leakage Current Limits

The following limits are summarized for IEC 60601-1 Medical Equipment Safety Standards. These limits are GEMS standards and in some cases are lower than the above standards listed.

Table 10-11 Chassis Leakage Current Limits—Accessible Metal Surfaces

Country

All (Except USA &

Canada)

USA & Canada

Normal Condition

0.1 mA

0.1 mA

Open Ground

0.5 mA

0.3 mA

Reverse Polarity

0.5 mA

0.3 mA

Open Neutral

0.5 mA

0.3 mA

Table 10-12 Type BF Applied Part Leakage Current Limits - Probes surface

Country

All

Normal

Condition

0.1 mA

Open Ground Reverse Polarity Open Neutral *Mains Applied

0.5 mA 0.5 mA 0.5 mA 5.0 mA

NOTE:

Table 10-13 Type CF Applied Part Leakage Current Limits - ECG Connections

Country

All

Normal

Condition

0.01 mA

Open Ground Reverse Polarity Open Neutral *Mains Applied

0.05 mA 0.05 mA 0.05 mA 0.05 mA

*Mains Applied refers to the sink leakage test where mains (supply) voltage is applied to the part to determine the amount of current that will pass (or sink) to ground if a patient contacted mains voltage.

The following tests are performed at the factory and should be performed at the site. These tests are: chassis leakage current, and probe leakage current. All measurements are made with an electrical safety analyzer.

10-12 Section 10-6 - Electrical Safety Tests

GE H EALTHCARE


10-6-3


Outlet Test - Wiring Arrangement

Test all outlets in the area for proper grounding and wiring arrangement by plugging in the neon outlet tester and noting the combination of lights that are illuminated. Any problems found should be reported to the hospital immediately and the receptacle should not be used.

NOTE:

Figure 10-2 Typical Alternate Outlet Tester

No outlet tester can detect the condition where the Neutral (grounded supply) conductor and the

Grounding (protective earth) conductor are reversed. If later tests indicate high leakage currents, this should be suspected as a possible cause and the outlet wiring should be visually inspected.


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10-6-4 Chassis Leakage Current Test


10-6-4-1 Definition

This test measures the current that would flow in a grounded person who touched accessible metal parts of the bedside station if the ground wire should break. The test verifies the isolation of the power line from the chassis. The meter is connected from accessible metal parts of the case to ground.

Measurements should be made with the unit On and Off, with the power line polarity Normal and

Reversed. Record the highest reading.

CAUTION

Electric Shock Hazard. When the meter's ground switch is OPEN, don't touch the unit!

CAUTION

Equipment damage possibility. Never switch the Polarity and the status of Neutral when the unit is powered ON. Be sure to turn the unit power OFF before switching them using the POLARITY switch and/or the NEUTRAL switch. Otherwise, the unit may be damaged.

10-6-4-2 Generic Procedure

The test verifies the isolation of the power line from the chassis. The testing meter is connected from accessible metal parts of the case to ground. Measurements should be made with the unit ON and OFF, with the power line polarity Normal and Reversed. Record the highest reading of current.

10-14

Figure 10-3 Set Up for Chassis Source Leakage Current,

IEC 601-1 Clause 19 - Continuos Leakage Currents and

Patient, Auxiliary Currents

When using the Microguard or a similar test instrument, its power plug may be inserted into the wall outlet and the equipment under test is plugged into the receptacle on the panel of the meter. This places the meter in the grounding conductor and the current flowing from the case to ground will be indicated in any of the current ranges. The maximum allowable limit for chassis source leakage is shown in

Table 10-11 .

Section 10-6 - Electrical Safety Tests

GE H EALTHCARE


10-6-4-3


Data Sheet for enclosure Source Leakage Current

The test passes when all readings measure less than the value shown in Table 10-11 . Record all data on the PM Inspection Certificate.

Table 10-14 Typical Data Sheet for enclosure Source Leakage Current

Unit Power

Tester Polarity

Switch

Tester Neutral or Ground

Switch

Enter Name of tested peripheral here:

ON

ON

ON

ON

OFF

OFF

OFF

OFF

NORM

NORM

REV

REV

NORM

NORM

REV

REV

OPEN

CLOSED

OPEN

CLOSED

OPEN

CLOSED

OPEN

CLOSED

Test 1

Speaker

Cover

Test 2

Real Panel

Metal

Parts

Optional

Test 3

Optional

Test 4


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10-6-5 Probe Leakage Current Test

10-6-5-1

10-6-5-2


Definition

This test measures the current that would flow to ground from any of the probes through a patient who is being scanned and becomes grounded by touching some other grounded surface.

Generic Procedure

Measurements should be made with the ground open and closed, with power line polarity normal and reversed, and with the unit Off and On. For each combination, the probe must be active to find the worst case condition.

POWER

OUTLET

H (BLACK)

N (WHITE)

G (GREEN)

POLARITY REVERSING SWITCH

MOMENTARY

SWITCH

CONSOLE

PROBE

LEAKAGE TEST

METER

NOTE:

10-6-5-3

Figure 10-4 Set Up for Probe Leakage Current

Each probe will have some amount of leakage current, dependent on its design. Small variations in probe leakage currents are normal from probe to probe. Other variations will result from differences in line voltage and test lead placement.

No Meter Probe Adapter Procedure

Follow the Safety Analyzer tool instruction to test each transducer for leakage current.

The electrical Safety Analyzer tool should be calibrated and compliant with AAMI/ESI 1993 or IEC

60601 or AS/NZS 3551.

10-16 Section 10-6 - Electrical Safety Tests

GE H EALTHCARE


10-6-5-4


Data Sheet for Transducer Source Leakage Current

The test passes when all readings measure less than the values shown in Table 10-11 . Record all data on the PM Inspection Certificate.

CAUTION

Equipment damage possibility. Never switch the Polarity and the status of Neutral when the unit is powered ON. Be sure to turn the unit power OFF before switching them using the POLARITY switch and/or the NEUTRAL switch. Otherwise, the unit may be damaged

.

Table 10-15 Typical Data Sheet For Transducer Source Leakage Current

Unit Power

OFF

OFF

OFF

OFF

ON

ON

ON

ON

Transducer Tested:

Tester Power Polarity

Switch

NORM

NORM

REV

REV

NORM

NORM

REV

REV

Tester GROUND or

NUETRAL Switch

OPEN

CLOSED

OPEN

CLOSED

OPEN

CLOSED

OPEN

CLOSED

Measurement


GE H EALTHCARE


Section 10-7

When There's Too Much Leakage Current...


AC/DC FAILS

Check any broken of the AC/DC adapter and its cable. Replace a new one if any portion defective.

ENCLOSURE FAILS

Check any broken of the enclosure. Replace any defective part.

Inspect wiring for bad crimps, poor connections, or damage.

Test the wall outlet; verify it is grounded and is free of other wiring abnormalities. Notify the user or owner to correct any deviations. As a work around, check the other outlets to see if they could be used instead.

NOTE: No outlet tester can detect the condition where the white neutral wire and the green grounding wire are reversed. If later tests indicate high leakage currents, this should be suspected as a possible cause and the outlet wiring should be visually inspected.

PROBE FAILS

Change another probe to confirm if the fail is caused by console.

NOTE: Each probe will have some amount of leakage, dependent on its design. Small variations in probe leakage currents are normal from probe to probe. Other variations will result from differences in line voltage and test lead placement. The maximum allowable leakage current for body surface contact probe differs from inter-cavity probe. Be sure to enter the correct probe type in the appropriate space on the check list.

If excessive leakage current is slot dependent, inspect the system connector for bent pins, poor connections, and ground continuity.

If the problem remains with the probe, replace the probe.

PERIPHERAL FAILS

Inspect wiring for bad crimps, poor connections, or damage.

STILL FAILS

If all else fails, begin isolation by removing the probes, external peripherals, then the on board ones, one at a time while monitoring the leakage current measurement.

NEW UNIT

If the leakage current measurement tests fail on a new unit and if situation can not be corrected, submit a Safety Failure Report to document the system problem. Remove unit from operation.

10-18 Section 10-7 - When There's Too Much Leakage Current...

GE H EALTHCARE


ULTRASOUND INSPECTION CERTIFICATE

Customer Name: System ID:

System Type

Probe 1:

Probe 2:

Probe 3:

Frequency:

Frequency:

Frequency:

Model Number:

Scan Format*:

Scan Format*:

Scan Format*:

Probe 4:

Probe 5:

Frequency:

Frequency:

Scan Format*:

Scan Format*:


Dispatch Number / Date Performed:

Serial Number:

Model Number:

Model Number:

Model Number:

Model Number:

Model Number:

Warranty/Contract/HBS

Manufacture Date:

Serial Number:

Serial Number:

Serial Number:

Serial Number:

Serial Number:

* Scan Format: Phased Array, Linear Array, Curved Array, Mechanical Array or Other

FUNCTIONAL CHECKS

Functional Check (if applicable)

B-Mode Function

Doppler Modes Function

CF-Mode Function

M-Mode Function

Applicable Software Options

Applicable Hardware Options

Control Panel

LCD

Measurement Accuracy

GE Approved Peripherals

OK? or

N/A

PHYSICAL INSPECTION AND CLEANING

Physical Inspection and Cleaning

(if applicable)

Console

LCD

External I/O

Cables and Connectors

GE Approved Peripherals (CD-RW, Printer)

Labeling (see User Manual for Labeling)

Inspect Clean

COMMENTS:

______________________________________________________________________________

______________________________________________________________________________

______________________________________________________________________________

______________________________________________________________________________


GE H EALTHCARE


ELECTRICAL SAFETY


Electrical Test Performed

Outlet (correct ground &wiring config.)

Type BF Applied Part Leakage Current

Limits- Probe enclosure Source Leakage Current -

Chassis Leakage Current Limits

Peripheral 1 Leakage Current

Peripheral 2 Leakage Current

Max Value

Allowed

Value

Measured OK?

Comments

PROBES

Probe Number

(from previous page)

Probe 1:

Max Value

Allowed

Max Value

Measured OK?

Comments

Probe 2:

Probe 3:

Final Check. All system covers are in place. System scans with all probes as expected.

Accepted by: ______________________________________________________________________

10-20 Section 10-7 - When There's Too Much Leakage Current...

GE H EALTHCARE


A,B

Abbreviations, 9-1

Archiving Images

Move, 4-28

Backup

Patient Database, 4-25

Preset Configurations, 4-25

Basic Measurements

Functional Checks, 4-22

Body pattern display location, 4-9

Boot Up, 3-9

C

Caps lock display location, 4-9

CE Compliance, 1-16

Cine gauge display location, 4-9

Color Mode

Overview, 4-19

Configuration, 5-16

Connectivity

Worksheet, 3-26

Contact Information, 1-17

Control Panel, 4-7

Conventions

Conventions Used in Book, 1-3

Customer Assistance, 1-17

D

Dangerous Procedure Warnings, 1-13

Date/Time display location, 4-9

Depth scale display location, 4-9

Diagnostics, 5-14

DICOM Network Function, 2-9

E

Electrical requirements, 2-2

Electrical Safety, 1-10

Electrostatic Discharge Warning, 1-16

EMI, 1-16

ESD, 1-16

Exam study


INDEX

display location, 4-9

F

Focal zone display location, 4-9

Functional Checks

Basic Measurements, 4-22

Control Panel, 4-7

Image Management, 4-24

Monitor Display, 4-9

Peripherals, 4-30

Probes/Connector Usage, 4-23

G

Gathering Trouble Data, 7-2

General Cleaning, 10-7

Gray/color bar display location, 4-9

H

Hazard Icons, 1-4

Hospital name display location, 4-9

Human Safety, 1-9

I

Image Management


Image preview display location, 4-9

Imaging parameters display location, 4-9

Inrush Current, 2-2, , 2-3

Institution name display location, 4-9

L

Logs, 5-11

LOTO, 4-6

M

Measurement summary window display location, 4-9

Index 1

GE H EALTHCARE


Mechanical Safety, 1-9

Media

Formatting, 4-25

Monitor Display

Functioanl Checks, 4-9

Monitor display location, 4-9

Move

Archiving Images, 4-28

O

Operator identification display location, 4-9

P

P4 Key Function, 7-4

Patient identification display location, 4-9

Patient name display location, 4-9

PC Diagnostics, 7-18

CD/DVD Drive Test, 7-18

CPU Tests, 7-18

Hard Drive Tests, 7-18

Keyboard Test, 7-18

Memory Tests, 7-18

Monitor Test, 7-18

USB Test, 7-18

Video Test, 7-18

PC Diagnostics (Interactive Tests), 7-18

Peripherals


Power On, 3-9

Power Requirements, 2-2 electrical, 2-2 stability, 2-3

Power Stability Requirements, 2-3

Probe Connector Cleaning, 10-9

Probe identifier display location, 4-9

Probe orientation marker display location, 4-9

Probes/Connector Usage


R

Required Features, 2-7


INDEX

Restore

Patient Database, 4-27

Preset Configurations, 4-27

S

Safety Considerations, 1-9

Screen Captures, 7-4

System Maintenance, 10-5

System Manufacturer, 1-18

System messages display location, 4-9

T

TGC display location, 4-9

Touch Panel


Trouble Image with Logs, 7-3

Troubleshooting

Gathering Trouble Data, 7-2

Screen Captures, 7-4

Trouble Image with Logs, 7-3

Vital System Information, 7-2

U

Utilities, 5-16

W

Warnings and Cautions, 1-9

Index 2

©

2009-2012, General Electric Company.

GE Healthcare-GEMedical Systems Ultrasound.

9900 Innovation Drive

Wawautosa, Wisconsin 53226

USA

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