GE Healthcare LOGIQ C3/C5 Premium Ultrasound System Basic Service Manual

Below you will find brief information for Ultrasound System LOGIQ C3/C5 Premium. The LOGIQ C3/C5 Premium is a high-performance ultrasound system designed for a wide range of clinical applications. It features a user-friendly interface, advanced imaging capabilities, and a comprehensive set of tools for diagnosis and treatment. It is well suited for applications in cardiology, obstetrics, gynecology, vascular, and abdominal imaging.

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GE Healthcare

LOGIQ C3/C5 Premium

Basic Service Manual

Part Number: 5341787-100

Revision: 8

GE H

EALTHCARE

LOGIQ C3/C5 P

REMIUM

IRECTION

5341787-100, R

EVISION

8 B

ASIC

ERVICE

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.

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,

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

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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ĪDINĀJUMS

(LV)

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.

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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

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(KO)

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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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LEGAL NOTES

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

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

PROPRIETARY TO GE HEALTHCARE

Permission to use this Advanced Service Software and related documentation (herein called the material) by persons other than GE Healthcare employees is provided only under an Advanced Service

Package License relating specifically to this Proprietary Material. This is a different agreement from the one under which operating and basic service software is licensed. A license to use operating or basic service software does not extend to or cover this software or related documentation.

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

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

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

Material now.

TRADEMARKS

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

COPYRIGHTS

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Revision History

Revision

Date

2009/05/02

2010/03/29

2010/05/27

2011/05/18

2011/11/08

2012/05/16

2012/12/05

Reason for change

Initial Release.

Update the Renewal Part List

Add PHI information

Add probe new probes information

Update for Software update

Update the FRU list

Update environmental labels 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 1-16

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

Chapter 3 - Installation pages 3-1 to 3-24

Chapter 4 - Functional

Checks pages 4-1 to 4-36

Revision

N/A

Pages

Chapter 5 - Theory pages 5-1 to 5-4

Chapter 6 - Service

Adjustments pages 6-1 to 6-2

Chapter 7 - Diagnostics/

Troubleshooting pages 7-1 to 7-14

Chapter 8 - Replacement

Procedures pages 8-1 to 8-8

Chapter 9 - Replacement

Parts pages 9-1 to 9-8

Chapter 10 - Periodic

Maintenance pages 10-1 to 10-16

Index pages I to II

Revision

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CHAPTER 1 Introduction

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

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

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

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

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

LOGIQ C3/C5 Premium Models Covered by this Manual . . . . . . . . . . . . . 1 - 2

Important Conventions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 4

Conventions Used in Book . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 4

Standard Hazard Icons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 5

Product Icons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 6

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

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

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

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

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

Label Locations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 10

Dangerous Procedure Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 11

Returning/Shipping Probes and Repair Parts . . . . . . . . . . . . . . . . . . . . . . . 1 - 11

EMC, EMI, and ESD . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 12

Electromagnetic Compatibility (EMC) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 12

CE Compliance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 12

Electrostatic Discharge (ESD) Prevention . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 12

Lockout/Tagout (LOTO) requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 13

Customer Assistance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 14

Contact Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 14

System Manufacturer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 15

Factory Site . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 15

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Setup Reminders . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 2

Average Installation Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 2

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

Safety Reminders . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 4

Receiving and Unpacking the Equipment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 5

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

Product Locator Installation Card . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 6

Preparing for Installation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 7

Verify Customer Order . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 7

Physical Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 7

EMI Protection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 7

Completing the Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 8

Power On / Boot Up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 8

Power Off/ Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 8

Transducer Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 9

System Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 10

System Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 10

Electrical Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 11

On-Board Optional Peripherals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 11

Connecting Cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 12

Peripherals/Accessories Connector Panel . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 12

Available Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 19

Software/Option Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 19

Connectivity Installation Worksheet . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 20

Loading Base Image Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 21

Software Version check out . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 22

Functional Check-out . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 22

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

Product Locator Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 23

User Manual(s) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 23

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

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

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

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

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

Power Off/ Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 2

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

Adjusting the Display Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 5

System Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 6

B Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 9

M Mode Controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 12

Doppler Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 15

Color Flow Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 19

Basic Measurements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 23

Probe/Connectors Usage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 24

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

Image Management (QG) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 25

Backup and Restore Database, Preset Configurations and Images . . . . . . 4 - 26

Software Configuration Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 36

Peripheral Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 36

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

Purpose of Chapter 5 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 1

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

System Diagram . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 2

Software Diagram . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 3

Common Service Platform . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 4

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 4

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CHAPTER 6 Service Adjustments

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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

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

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

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

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

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

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

USB Quick Save . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 4

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 4

Check and Record the Print or Store Key Function . . . . . . . . . . . . . . . . . . 7 - 4

Setting the Print or Store Key to USB Quick Save . . . . . . . . . . . . . . . . . . . 7 - 5

Screen Captures. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 6

Check and Record the Store Key Function . . . . . . . . . . . . . . . . . . . . . . . . 7 - 6

Setting the Store Key to Screen Capture . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 6

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

Reset the Store Key to Customer’s Functionality . . . . . . . . . . . . . . . . . . . . 7 - 8

Common Diagnostics . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 9

Utilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 9

PC Diagnostics (Non-Interactive Tests) . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 10

PC Diagnostics (Interactive Tests) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 11

Restart LOGIQ C3/C5 Premium After Diagnostics . . . . . . . . . . . . . . . . . . . 7 - 11

Network Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 12

Network Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 12

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

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

DISASSEMBLY/RE-ASSEMBLY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 2

Warning and Caution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 2

Returning/Shipping for repairs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 2

Air filter and Knob Screw . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 3

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

Loading Base Image Software. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 6

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CHAPTER 9 Renewal Parts

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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

Accessories and kits. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 4

Manuals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 6

Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 7

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CHAPTER 10 Care & Maintenance

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

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

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

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

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

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

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

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

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

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

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

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

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

Physical Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 7

Outlet Test -Wiring Arrangement - USA & Canada . . . . . . . . . . . . . . . . . . . 10 - 8

Grounding Continuity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 9

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

Isolated Patient Lead (Source) Leakage–Lead to Lead . . . . . . . . . . . . . . . . 10 - 11

Isolated Patient Lead (Sink) Leakage-Isolation Test . . . . . . . . . . . . . . . . . . 10 - 11

Probe Leakage Current Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 13

When There's Too Much Leakage Current... . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 15

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Chapter 1 Introduction

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Section 1-1

Overview

1-1-1 Purpose of Chapter 1

This chapter describes important issues related to safely servicing the LOGIQ C3/C5 Premium. The service provider must read and understand all the information presented in this manual before installing or servicing a unit.

Table 1-1 Contents in Chapter 1

Section

1-1

1-2

1-3

1-4

1-5

1-6

Overview

Important Conventions

Safety Considerations

EMC, EMI, and ESD

Lockout/Tagout (LOTO) requirements

Customer Assistance

Description Page Number

1-1

1-4

1-9

1-12

1-13

1-14

1-1-2 Purpose of Service Manual

This Service Manual provides installation and service information for the LOGIQ C3/C5 Premium and contains the following chapters:

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

2.) Chapter 2 - Site Preparations: Contains pre-installation requirements for the LOGIQ C3/C5

Premium.

3.) Chapter 3 - System Setup: 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 C3/C5 Premium.

7.) Chapter 7 - Diagnostics/Troubleshooting: Provides procedures for running diagnostic or related routines for the LOGIQ C3/C5 Premium.

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 C3/

C5 Premium.

10.)Chapter 10 - Care & Maintenance: Provides periodic maintenance procedures for the LOGIQ C3/

C5 Premium.

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1-1-3 Typical Users of the Basic Service Manual

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

• Hospital’s Service Personnel

• Contractors (Some parts of Chapter 2 - Site Preparation)

1-1-4

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Purpose of Operator Manual(s)

The Operator Manual(s) should be fully read and understood before operating the LOGIQ C3/C5

Premium and also kept near the unit for quick reference.

Probe information displayed on screen does not necessarily reflect the probes available on your ultrasound system. Please refer to the probe list for available probes and features.

1-1-5 LOGIQ C3/C5 Premium Models Covered by this Manual

Table 1-2 LOGIQ C3 Model Designations (For Software Version R2.0.1, R 2.0.2, R2.0.3 )

Part Number

5346769

5346771

5346772

5346774

Description

LOGIQ C3 Premium Console for Europe

LOGIQ C3 Premium Console for India

LOGIQ C3 Premium Console for Argentina

LOGIQ C3 Premium Console for 110V

Table 1-3 LOGIQ C5 Model Designations (For Software Version R2.0.1, R 2.0.2, R2.0.3 )

Part Number

5346775

5346777

5346778

5346779

Description

LOGIQ C5 Premium Console for Europe

LOGIQ C5 Premium Console for India

LOGIQ C5 Premium Console for Argentina

LOGIQ C5 Premium Console for 110V

Table 1-4 LOGIQ C3 Model Designations (For Software Version R2.0.6)

Part Number

5430949

5431009

5430951

5430952

Description

LOGIQ C3 Premium Console for Europe

LOGIQ C3 Premium Console for India

LOGIQ C3 Premium Console for Argentina

LOGIQ C3 Premium Console for 110V

Table 1-5 LOGIQ C5 Model Designations (For Software Version R2.0.6)

Part Number

5430954

5431010

5430958

5430960

Description

LOGIQ C5 Premium Console for Europe

LOGIQ C5 Premium Console for India

LOGIQ C5 Premium Console for Argentina

LOGIQ C5 Premium Console for 110V

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1-1-5 LOGIQ C3/C5 Premium Models Covered by this Manual

(cont’d)

Table 1-6 LOGIQ C3 Model Designations (For Software Version R2.1.0)

Part Number

5433023

5433034

5433035

Description

LOGIQ C3 Premium Console for Europe (220V)

LOGIQ C3 Premium Console for Latin America (220V)

LOGIQ C3 Premium Console for Latin America (110V)

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Table 1-7 LOGIQ C5 Model Designations (For Software Version R2.1.0)

Part Number

5433036

5433038

5433039

5433043

5433046

Description

LOGIQ C5Premium Console for Europe (220V)

LOGIQ C5 Premium Console for Latin America (220V)

LOGIQ C5 Premium Console for Latin America (110V)

LOGIQ C5 Premium 4D Console for Latin America (220V)

LOGIQ C5 Premium 4D Console for Latin America (110V)

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Section 1-2

Important Conventions

1-2-1

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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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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 1-8 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 1-9 Standard Icons Indicating a Special Procedure Be Used

AVOID STATIC ELECTRICITY TAG AND LOCK OUT WEAR EYE PROTECTION

TAG

LOCKOUT

Signed Date

EYE

PROTECTION

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Product Icons

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

Table 1-10: Product Icons

Label/Icon

Identification and Rating

Plate

Purpose/Meaning

• Manufacture’s name and address

• Date of manufacture

• Model and serial numbers

Location

Type/Class Label

IP Code (IPX8)

IPX8: FSU-1000

Amps, phase, and frequency)

Used to indicate the degree of safety or protection.

Indicates the degree of protection provided by the enclosure per IEC60 529.

Type BF Applied Part (man in the box) symbol is in accordance with IEC 60878-

02-03.

General Warning.

Bottom of footswitch

Beside the probe connector

Various

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

Indicates the power on and power off position of the power switch.

CAUTION: This Power Switch

DOES NOT ISOLATE Mains

Supply.

“Protective Earth” indicates the protective earth

(grounding) terminal.

Various

See the Console Overview section for location information.

Inside PowerBox and

Console

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Label/Icon

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Table 1-10: Product Icons

Purpose/Meaning

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

Indicates the presence of hazardous substance(s) above the maximum concentration value. Maximum concentration values for electronic information products, as set by the

People’s Republic of China

Electronic Industry Standard

SJ/T11364-2006, include the hazardous substances of lead, mercury, hexavalent chromium, cadmium, polybrominated biphenyl

(PBB), and polybrominated diphenyl ether (PBDE). “10” indicates the number of years during which the hazardous substance(s) will not leak or mutate so that the use of this product will not result in any severe environmental pollution, bodily injury, or damage to any assets.

Type CF Defib-Proof Applied

Part (heart in the box with paddle) symbol is in accordance with IEC 60878-

02-06.

Utilize additional care and personnel when moving on steep inclines (>5 degrees) or loading into vehicle for transport.

Location

Bottom

Probe and Rear Panel,

China Rating Plate

ECG module

Back of LCD

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Label/Icon

Table 1-10: Product Icons

Purpose/Meaning

Do not place any objects on the monitor.

Location

Back of LCD

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Do not force the LCD monitor with your hands.

Back of LCD

There is a pinch point on the

LCD monitor. Take care to avoid injuring hands or fingers when flipping down the LCD monitor.

Use the rear handle for horizontal movement only..

Back of LCD

“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.

Do not push the system

Various

Back of LCD

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Section 1-3

Safety Considerations

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1-3-2

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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

Servicing should be performed by authorized personnel only.

Only personnel who have participated in a LOGIQ C3/C5 Premium Training are authorized to service the equipment.

1-3-3

CAUTION

Mechanical Safety

WHEN THE UNIT IS RAISED FOR A REPAIR OR MOVED ALONG ANY INCLINE, USE

EXTREME CAUTION SINCE IT MAY BECOME UNSTABLE AND TIP OVER.

ULTRASOUND PROBES ARE HIGHLY SENSITIVE MEDICAL INSTRUMENTS THAT

CAN EASILY BE DAMAGED BY IMPROPER HANDLING. USE CARE WHEN

HANDLING AND PROTECT FROM DAMAGE WHEN NOT IN USE. DO NOT USE A

DAMAGED OR DEFECTIVE PROBE. FAILURE TO FOLLOW THESE PRECAUTIONS

CAN RESULT IN SERIOUS INJURY AND EQUIPMENT DAMAGE.

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

IT MAY BE DAMAGED.

The LOGIQ C3/C5 Premium weighs 75 kg or more, depending on installed peripherals, when ready for use. Care must be used when moving it or replacing its parts. Failure to follow the precautions listed could result in injury, uncontrolled motion and costly damage.

ALWAYS:

Be sure the pathway is clear.

Use slow, careful motions.

Use two people when moving on inclines or lifting more than 75 kg (169 lbs).

AFTER UNPLUG POWER CORD, WAIT FOR AT LEAST 20 SECONDS FOR

CAPACITORS TO DISCHARGE AS THERE ARE NO TEST POINTS TO VERIFY

ISOLATION.

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1-3-3 Mechanical Safety

(cont’d)

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

• Secure the unit in an upright position.

• Lock the wheels (brake)

1-3-4

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Electrical Safety

To minimize shock hazard, the equipment chassis must be connected to an electrical ground. The system is equipped with a three-conductor AC power cable. This must be plugged into an approved electrical outlet with safety ground. The power outlet used for this equipment should not be shared with other types of equipment.

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

1-3-5

DO NOT SERVICE OR DISASSEMBLE PARTS UNDER FRU UNIT LEVEL AT ANY

CIRCUMSTANCES.

Label Locations

Refer to LOGIQ C3/LOGIQ C5 Premium Basic User Manual Section Warning Label Location at page

2-31.

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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.

1-3-7

NOTE:

EXPLOSION WARNING

DO NOT OPERATE THE EQUIPMENT IN AN EXPLOSIVE ATMOSPHERE.

OPERATION OF ANY ELECTRICAL EQUIPMENT IN SUCH AN ENVIRONMENT

CONSTITUTES A DEFINITE SAFETY HAZARD.

DO NOT SUBSTITUTE PARTS OR MODIFY EQUIPMENT

BECAUSE OF THE DANGER OF INTRODUCING ADDITIONAL HAZARDS, DO NOT

INSTALL SUBSTITUTE PARTS OR PERFORM ANY UNAUTHORIZED MODIFICATION

OF THE EQUIPMENT.

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

DAMAGE OF SYSTEM FILES.

AFTER UNPLUG POWER CORD, WAIT FOR AT LEAST 20 SECONDS FOR

CAPACITORS TO DISCHARGE AS THERE ARE NO TEST POINTS TO VERIFY

ISOLATION.

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.

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

Section 1-3 - Safety Considerations 1 - 11

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Section 1-4

EMC, EMI, and ESD

1-4-1

1-4-2

NOTE:

1-4-3

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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 C3/C5 Premium 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.

1 - 12 Section 1-4 - EMC, EMI, and ESD

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Section 1-5

Lockout/Tagout (LOTO) requirements

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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 C3/C5 Premium

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.

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

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

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

NOTE:

The US Department of Transportation (DOT) has ruled that “items that were saturated and/or dripping with human blood that are now caked with dried blood; or which were used or intended for use in patient care” are “regulated medical waste” for 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.

Section 1-5 - Lockout/Tagout (LOTO) requirements 1 - 13

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Section 1-6

Customer Assistance

1-6-1

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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 1-11 Phone Numbers for Customer Assistance

Location

USA

GE Vingmed Ultrasound

Ultrasound Service Engineering

9900 Innovation Drive

Wauwatosa, WI 53226

Canada

Service: On-site

Service Parts

Application Support

Latin America

Service

Application Support

Europe (OLC- EMEA)

GE Ultraschall Deutschland GmbH

Beethovenstraße 239

Postfach 11 05 60, D-42655 Solingen

Germany

Online Services Ultrasound Asia

Australia

China

India

Japan

Korea

Singapore

Phone Number

1-800-437-1171

OLC - EMEA

Phone: +49 (0)212 2802 - 652

Fax:

+33 1 3083 1300

+49 (0) 212 2802 - 431

+(86) 800-810-8188

+(91) 1-800-11-4567

+(81) 42-648-2924

+(82) 2620 13585

+(95) 6277-3444

1-800-558-2040

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

1-800-668-0732

1-800-321-7937

1-262-524-5698

1 - 14 Section 1-6 - Customer Assistance

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1-6-2 System Manufacturer

1-6-3

Table 1-12 System Manufacturer

Manufacturer

GE Medical Systems (China) Co., Ltd.

No.19, Changjiang Road, Wuxi National Hi-Tech Development Zone,

Jiangsu, P.R. China 214028

Factory Site

Table 1-13 Factory Site

Factory Site

GE Medical Systems (China) Co., Ltd.

No.19, Changjiang Road, Wuxi National Hi-Tech Development Zone,

Jiangsu, P.R. China 214028

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FAX Number

TEL: +86 510-85225888

FAX: +86 510-85226688

FAX Number

TEL: +86 510-85225888

FAX: +86 510-85226688

Section 1-6 - Customer Assistance 1 - 15

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1 - 16 Section 1-6 - Customer Assistance

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Chapter 2 Site Preparations

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Section 2-1

Overview

2-1-1 Purpose of chapter 2

This chapter provides the information required to plan and prepare for the installation of LOGIQ C3/C5

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

Table 2-1 Contents in Chapter 2

Section

2-1

2-2

2-3

Description

Overview

General Console Requirements

Facility Needs

Page Number

2-1

2-2

2-6

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Section 2-2

General Console Requirements

2-2-1

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Console Environmental Requirements

Table 2-2 Environmental Requirements for LOGIQ C3/C5 Premium Scanners

Temperature

Humidity

Pressure

Operational

10 - 40 o

50 - 104 o

30 - 75% non-condensing

700 - 1060hPa

Storage

-5 - 50 o

23 - 122 o

10 - 90% non-condensing

700 - 1060hPa

Transport

-5 - 50 o

23 - 122 o

10 - 90% non-condensing

700 - 1060hPa

NOTE:

2-2-1-1

2-2-2

NOTE:

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

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 Healthcare requires a dedicated power and ground for the proper operation of its Ultrasound equipment. This dedicated power shall originate at the last distribution panel before the system.

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

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

Sites with a mains power system without a defined Neutral:

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

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

2 - 2 Section 2-2 - General Console Requirements

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2-2-2 Electrical Requirements

(cont’d)

2-2-2-1

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LOGIQ C3/C5 Premium Power Requirements

The following power line parameters should be monitored for one week before installation. We recommend that you use an analyzer Dranetz Model 606-3 or Dranetz Model 626:

Table 2-3 Electrical Specifications for LOGIQ C3/C5 Premium

PARAMETER AREA

Voltage Range

Power

Line Frequency

Power Transients

Decaying Oscillation

100-120V~

220-240V~

All applications

LIMITS

500VA

MAX. 750 VA

50/60Hz (

±2Hz)

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

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

2-2-2-2 Inrush Current

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

2-2-2-3 Site Circuit Breaker

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

CAUTION

POWER OUTAGE MAY OCCURE.

The LOGIQ C3/C5 Premium requires a dedicated single branch circuit. To avoid circuit overload and possible loss of critical care equipment, make sure you DO NOT have any other equipment operating on the same circuit.

2-2-2-4

2-2-2-5

2-2-2-6

Site Power Outlets

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

Unit Power Plug

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

Power Stability Requirements

Voltage drop-out

Max 10 ms.

Power Transients

(All applications)

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

Section 2-2 - General Console Requirements 2 - 3

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2-2-3

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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 C3/C5 Premium complies with limits as stated on the EMC label. However there is no guarantee that interface will not occur in a particular installation.

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

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

These sources include:

• medical lasers,

• scanners,

• cauterizing guns,

• computers,

• monitors,

• fans,

• gel warmers,

• microwave ovens,

• light dimmers,

• portable phones.

The presence of broadcast station or broadcast van may also cause interference. See for EMI

Prevention tips.

See Table 2-4 for EMI Prevention tips.

2 - 4

Table 2-4 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 interface with the ultrasound signals.

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

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

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.

Section 2-2 - General Console Requirements

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2-2-4 Scan Probe Environmental Requirements

Operation:10° to 40° C

Storage:-5° to 50° C

NOTE:

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

NOTICE

SYSTEMS AND ELECTRONIC PROBES ARE DESIGNED FOR STORAGE TEMPERATURES OF

-10 TO + 60 degrees C. WHEN EXPOSED TO LARGE TEMPERATURE VARIATIONS, THE

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

Section 2-2 - General Console Requirements 2 - 5

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Section 2-3

Facility Needs

2-3-1

NOTE:

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

2 - 6 Section 2-3 - Facility Needs

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2-3-2 Required Features

NOTE:

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

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

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

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

Sites with a mains power system without a defined Neutral:

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

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

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

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

• Proposed location for unit is at least 0.3 m (1 ft.) from the wall for cooling

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

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2-3-3 Recommended and Alternate Ultrasound Room Layout

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

DEDICATED

POWER

RECEPTACLE

DEDICATED ALALOG TELEPHONE

LINE FOR CONNECTION TO INSITE

18 IN.

(46 CM)

LINEN SUPPLY

CONSOLE

FILM VIEWER

COUNTER TOP

FOOT

STOOL

SINK

76 IN.

(193 CM)

SUCTION LINE

EMERGECY

OXYGEN

24 IN.

(61 CM)

SECRETARYS OR

DOCTOR’S DESK

FILM VIEWER

FILM SUPPLIES

SINK

OVERHEAD

LIGHTS DIMMER

PATIENT

TOILET

FACILITY

DOOR

42 IN.

(107 CM)

A 14 by 17 foot Recommended Floor Plan

Scale : Each square equals one square foot

LINEN SUPPLY

PROBES/SUPPLIES

EXTERNAL

PERIPHERALS

DEDICATED POWER

OUTLETS

STOOL

FOOT

LOGIQ 5

CONSOLE

DEDICATED ANALOG TELEPHONE

LINE FOR CONNECTION TO INSITE

24 IN.

(61 CM)

EXAMINARION

TABLE

76 IN.

(193 CM)

DOOR

30 IN.

(76 CM)

An 8 by 10 foot Minimal Floor Plan

GE CABINET

FOT SOFTWARE

AND MANUALS

Figure 2-1 RECOMMENDED ULTRASOUND ROOM LAYOUT

2 - 8 Section 2-3 - Facility Needs

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2-3-4 Networking Pre-installation Requirements

2-3-4-1

2-3-4-2

2-3-4-3

2-3-4-4

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Stand Alone Scanner (without Network Connection)

None.

Scanner Connected to Hospital’s Network

Supported networks:

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

DICOM Option Pre-installation Requirements

To configure the LOGIQ C3/C5 Premium 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 C3/C5 Premium.

• 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 C3/C5 Premium for DICOM APPLICATION INFORMATION. A field for the make

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

Section 2-3 - Facility Needs 2 - 9

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2-3-4-4 DICOM Option Pre-installation Requirements (cont’d)

LOGIQ C3/

Host Name

AE Title

Local Port

ROUTING INFORMATION

ROUTER1

ROUTER2

ROUTER3

Destination

IP Addresses

DICOM APPLICATION INFORMATION

NAME MAKE/REVISION

AE TITLE

Store 1

IP Address

Net Mask

Default

GATEWAY IP Addresses

IP ADDRESSES

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PORT

Store 2

Store 3

Store 4

Store 5

Store 6

Worklist

Storage

Commit

MPPS

Figure 2-2 Worksheet for DICOM Network Information

2 - 10 Section 2-3 - Facility Needs

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Chapter 3 System Setup

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Section 3-1

Overview

3-1-1 Purpose of Chapter 3

This chapter contains information needed to install the unit. Included are references to a procedure that describes how to receive and unpack the equipment and how to file a damage or loss claim.

How to prepare the facility and unit of the actual installation, and how to check and test the unit and external peripherals for electrical safety are included in this procedure. Also included LOGIQ C3/C5

Premium in this section are guidelines for transporting the unit to a new site.

Table 3-1 Contents in Chapter 3

Section

3-5

3-6

3-7

3-8

3-1

3-2

3-3

3-4

3-9

3-10

3-11

Description

Overview

Setup Reminders

Receiving and Unpacking the Equipment

Preparing for Installation

Completing the Installation

System Configuration

Software/Option Configuration

Connectivity Installation Worksheet

Loading Base Image Software

Software Version check out

Paperwork

Page Number

3-5

3-6

3-7

3-8

3-1

3-2

3-3

3-4

3-9

3-10

3-11

Chapter 3 System Setup 3 - 1

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Section 3-2Setup Reminders

3-2-1 Average Installation Time

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Table 3-2 Average Installation Time

Description

Unpacking the scanner

Scanner wo/options

DICOM Option

Average Installation Time

0.5 hour

Comments

Dependant on the configuration that is required

Dependant on the amount of configuration

The LOGIQ C3/C5 Premium has been designed to be installed and checked out by an experienced service technician in approximately 1 hour. LOGIQ C3/C5 Premium consoles with optional equipment may take slightly longer.

3 - 2 Section 3-2 - Setup Reminders

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Installation Warnings

1.) Since the LOGIQ C3/C5 Premium weighs approximately 75 kg without options, preferably two people should unpack it. Two people are also preferable for installing any additional bulky items.

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

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

3.) After being transported, the unit may be very cold or hot. If this is the case, allow the unit to acclimate before you turn it on. It requires one hour for each 2.5

°C increment it's temperature is below 10

°C or above 30°C.

CAUTION

Equipment damage possibility. Turning the system on without acclimation after arriving at site may cause the system to be damaged.

Table 3-3 Acclimation Time

°C

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

°F

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

hrs

8 6 4 2 0 0 0 0 0 0 0 2 4 6 8 10 12 14 16 18 20

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3-2-3 Safety Reminders

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DANGER

CAUTION

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!

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

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

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

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

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

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

System performance and cooling require this.

OPERATOR MANUAL(S)

The User Manual(s) should be fully read and understood before operating the LOGIQ C3/C5

Premium and kept near the unit for quick reference.

3 - 4

Figure 3-1 Environmental Labels

Section 3-2 - Setup Reminders

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Section 3-3

Receiving and Unpacking the Equipment

VIVID FIVE

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When a new system arrives, check that any components are not damaged and are not in short supply.

If shipping damage or shortage occurs, contact the address shown in Chapter 1.

CAUTION

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

CAUTION

The crate with the LOGIQ C3/C5 Premium weighs approximately 75kg. Be prepared for a sudden shift of weight as the unit is removed from its base (pallet)

Unpacking the the equipment

1.) Remove all the strapping tapes from the packing box.

2.) Remove the upper cover of the packing box and then rotate the knob to the right to open the packing box.

3.) Remove the PE bag and plastic film from the system.

4.) Remove Accessories Carton from the system.

5.) Remove the PE bag and plastic film from the syste

6.) Remove strapping tapes .

7.) Lift down the system .

Figure 3-2 Open the box

Chapter 3 System Setup 3 - 5

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3-3-1 Moving into Position

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CAUTION

Do not tilt the unit more than 5 degrees to avoid tipping it over.

To avoid injury by tipping over. Set the monitor to the lowest position before moving.

In general, a single adult can move the LOGIQ C3/C5 Premium along an even surface with no steep grades. At least two people should move the machine when large humps, grooves, or grades will be encountered. (It is better to pull from the rear rather than push from the front of the unit). Before moving, store all loose parts in the unit. Wrap transducers in soft cloth or foam to prevent damage.

Although LOGIQ C3/C5 Premium is a mobile machine, two people should move it over rough surfaces or up and down grades.

3-3-2

NOTE:

Product Locator Installation Card

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

Figure 3-3 Product Locator Installation Card

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

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Section 3-4

Preparing for Installation

3-4-1

3-4-2

3-4-2-1

3-4-2-2

3-4-3

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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 Docking Cart is set to the correct voltage.

The Voltage settings for the LOGIQ C3/C5 Premium is found on a label to the right of the Power switch and External I/O, on the rear of the system.

Connecting a LOGIQ C3/C5 Premium to the wrong voltage level will most likely destroy it.

Video Formats

Check that the video format is set to the locally used video standard, NTSC or PAL.

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.

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Section 3-5

Completing the Installation

3-5-1

NOTE:

3-5-1-1

3-5-1-2

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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.

Scanner Power On

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

Peripherals and the Back-end Processor.

Turn on the system

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

3-5-2

NOTE:

3-5-2-1

3 - 8

Figure 3-4 Power On/Off Switch

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

No status messages are displayed during this process.

Power Off/ Shutdown

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.

Back-end Processor Power Down

To power down the system:

1.) Press the Power On/Off switch once.

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3-5-2-1 Back-end Processor Power Down (cont’d)

2.) The System-Exit window is displayed.

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3-5-2-2

3-5-3

NOTE:

Figure 3-5 System Exit Window

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

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

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

Scanner Shutdown

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

Transducer Connection

1.) Plug the probe connector into the probe port, then lock the probe.

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

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

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Section 3-6

System Configuration

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System Specifications

Physical Dimensions

The physical dimensions of the LOGIQ C3/C5 Premium unit are summarized in Table 3-4 on page 3-10 .

The Size of LOGIQ C3/C5 Premium.

Table 3-4 Physical Dimensions of LOGIQ C3/C5 Premium

Height

1400

55.16

Width

500

19.70

Depth

700

27.58

Unit

mm inches

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3-6-1-2 Weight

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Table 3-5 Weight of LOGIQ C3/C5 Premium With Monitor and Without Other Peripherals

Weight [kg] Weight [lb] Model

LOGIQ C3/C5

Premium

Approximately 75 Approximately 165

3-6-2

3-6-3

Electrical Specifications

Table 3-6 Electrical Specifications for LOGIQ C3/C5 Premium

System

Voltage Current

500VA

110 -120 V AC

220- 240 V AC

500VA

On-Board Optional Peripherals

Frequency

50/60Hz

Table 3-7 List of Optional Peripherals

Device

B/W Printer

HP Printer

USB Memory

1-Pedal Footswitch

3-Pedal Footswitch

USB Hard Disk

Color Printer

ECG

Manufacturer

SONY

SanDisk

Whanam

Seagate

SONY

MITSUBISHI

NORAV

Model

UP-D897MD

UP-D897

HP 470 Officejet

HP8000

HP6000

SanDisk 4G

FSU1000

MKF 2-MED GP26

USBHDD 250G

USBHDD 500G

UP-D23MD

UP-D25MD

P95D

CP30DW-Z

ECG -USB1

Video Signal

USB

NOTE:

ECG are only supported by LOGIQ C5 Premium.

For detailed installation information and connection procedures, please refer to Peripheral Installation

Instruction manual (5266280-100).

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3-6-4

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Connecting Cables

Equipment damage possibility. Be sure to use the following recommended connecting cables to connect recording devices and a network with LOGIQ C3/C5 Premium console.

Table 3-8 List of Connecting Cables

Name Part No.

Figure NOTE

USB Cable 5122305

For USB Printer

3-6-5

3-6-5-1

Peripherals/Accessories Connector Panel

LOGIQ C3/C5 Premium peripherals and accessories can be properly connected using the side connector panel.

Rear Panel Connector

Located on the rear panel are Network port, 2 USB port, S-Video Out, VGA, Audio Out, Composite Out.

3 - 12

Figure 3-6 Rear Connector Panel

1.) 2 USB Ports (Printers, Footswitch, etc)

2.) Network Port

3.) VGA

4.) Audio Out

5.) S-Video Out

6.) Composite Out

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3-6-5-2 Left Panel Connector

1 USB port is Located on the left panel.

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3-6-5-3

Figure 3-7 Left Connector Panel

1.) 1 USB Ports (Printers, Footswitch, etc)

Printer Box Rear Panel connector

NOTE:

Figure 3-8 Printer Box Rear Connector Panel

1.) 1 USB Ports only for B/W Printer

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

Signal ground lines are not isolated, except the Service port (3). All of signal lines (include signal

GND) of the Service port are isolated.

ANUAL

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3-6-5-4 Pin assignment for each connector

Table 3-9 Pin Assignments of External VGA

Pin No.

Signal

RED

GREEN

BLUE

GND

Pin No.

Signal

HSY

VSY

Table 3-10 Pin Assignments of USB

Pin No.

Signal

+5 VDC

DATA

GND

Pin No.

Table 3-11 Pin Assignments of Audio

Pin No.

Signal

GND

L+

Speaker L

Pin No.

Signal

+5 VDC

DATA

GND

Signal

R+

Speaker R

Table 3-12 Pin Assignment of S-Video

Pin No.

Output Signal

GND

Pin No.

Output Signal

Table 3-13 Pin Assignment of Composite Video Out

Pin No.

Output Signal

Composite Out

Pin No.

Output Signal

GND

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3-6-5-5 Connect Peripherals

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

B/W Printer can be properly connected using USB Ports.

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Figure 3-9 Connect B/W printer to the system

B.) Connect UP-D23 color printer to the system.UP-D23 Color Printer can be properly connected using

USB Ports.

Figure 3-10 Connect color printer to the system

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3-6-5-5 Connect Peripherals (cont’d)

C.) Connect the B/W printer (Sony UP-897MD)to the system

The B/W printer can be properly connected using the Composite Out Port.

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Figure 3-11 Connect B/W Printer (Sony UP-897MD) to the system

D.) Connect Foot Switch to the system.

Foot Switch can be properly connected using USB Ports.

1-Pedal Footswitch 3-Pedal Footswitch

Figure 3-12 Connect Foot Switch to the system

3 - 16 Section 3-6 - System Configuration

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3-6-5-5 Connect Peripherals (cont’d)

E.) Connect the USB Memory to the system. The USB Memory can be properly connected using USB ports.

Figure 3-13 USB Memory Connection

F.) ECG can be properly connected using USB ports. (ECG only supported by LOGIQ C5 Premium)

Figure 3-14 ECG Connection

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3-6-5-5 Connect Peripherals (cont’d)

G.) Connect HP 470 Officejet printer to the system. HP 470b Officejet Printer can be properly connected using USB Ports.

Figure 3-15 HP 470b Officejet printer to the system

H.) Connect the USB HDD to the system. The USB Harddisk can be properly connected using USB ports.

Figure 3-16 USB Hard Disk Connection

3 - 18 Section 3-6 - System Configuration

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3-6-6 Available Probes

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See in specification in the LOGIQ C3/C5 Premium User Reference Manual for Probes and intended use.

Table 3-14 List of Probes on LOGIQ C3/C5 Premium

Probe Name Material of Headshell

4C-RC

NORYL

6.5C-RC

E7C-RC

7.5L-RC

3S-RC

L6-12-RC

C2-5-RC

VALOX

NORYL

Area of Using

GENERAL PURPOSE

VETERINARY

PEDIATRIC

NEONATAL

TRANSVAGINAL

TRANSRECTAL

SMALL PARTS

PERIPHERAL VASCULAR

CARDIAC

SMALL PARTS

PERIPHERAL VASCULAR

GENERAL PURPOSE

TYPE

CONVEX

MICRO-CONVEX

LINEAR

SECTOR

LINEAR

CONVEX

Catalog Number Part Number

H48102LE 5315581

H48102LF

H48102LG 5315686

H48102LJ

H40452LA

H40462LJ

H40462LH

5315685

5315683

5213343

5399465

5401243

Section 3-7

Software/Option Configuration

Refer to the LOGIQ C3/C5 Premium 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 C3/C5 Premium Basic User

Manual, Chapter 16, Customizing Your System.

For information on configuring DICOM Connectivity, Refer to the LOGIQ C3/C5 Premium Basic User

Manual, Chapter 16, Customizing Your System.

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Section 3-8

Connectivity Installation Worksheet

Site System Information

Site:

Dept:

LOGIQ SN: Type:

Floor:

Room:

REV:

CONTACT INFORMATION

Name Title

Phone

Comments:

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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

Device Type

Name

3 - 20

IP Address Port

Section 3-8 - Connectivity Installation Worksheet

AE Title

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Section 3-9

Loading Base Image Software

Refer to

Section 8-4 "Loading Base Image Software" on page 8-6 .

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Section 3-10Software Version check out

3-10-1

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Functional Check-out

1.) Power on LOGIQ C3/C5 Premium scanner and wait until system booting to main screen.

2.) Press UTILITY key on control panel.

3.) Choose the About button on the right.

Figure 3-17 About and Software version

3 - 22 Section 3-10 - Software Version check out

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Section 3-11

Paperwork

NOTE:

3-11-1

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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.

3-11-2

Figure 3-18 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.

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This page was intentionally left blank.

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3 - 24 Section 3-11 - Paperwork

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Chapter 4 Functional Checks

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Section 4-1

Overview

4-1-1 Purpose for Chapter 4

This chapter provides procedures for quickly checking major functions of the LOGIQ C3/C5 Premium console, diagnostics by using the built-in service software, and power supply.

Table 4-1 Contents in Chapter 4

Section

4-1

4-2

4-3

4-4

4-5

Description

Overview

Required Equipment

General Procedure

Software Configuration Checks

Peripheral Checks

4-1

4-2

4-36

Page Number

Section 4-2

Required Equipment

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

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

Chapter 4 Functional Checks 4 - 1

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Section 4-3

General Procedure

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CAUTION

SYSTEM REQUIRES ALL COVERS

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

4-3-1

4-3-1-1

Power On/Boot Up

After connect the system to the electrical supply, the power is applied to the scanner. When the Control panel Power On/Off key is pressed once, the System starts.

Scanner Power On

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

Peripherals and the Back-end Processor.

4-3-1-2 Turn on the system

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

4-3-2

NOTE:

4-3-2-1

Figure 4-19 Power On/Off Switch

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

No status messages are displayed during this process.

Power Off/ Shutdown

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.

Back-end Processor Power Down

To power down the system:

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

4 - 2 Section 4-3 - General Procedure

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4-3-2-1Back-end Processor Power Down (cont’d)

2.) The System-Exit window is displayed.

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Figure 4-20 System Exit Window

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

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

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

4-3-2-2 Scanner Shutdown

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

CAUTION

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

Failure to do so may result in corrupted patient files.

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4-3-3 Archiving and Loading Presets

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NOTE:

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

The system may crash if use a DVD for Archive/Backup/EZBackup/Restore, so always use a

CD-R or USB HDD for Archive/Backup/EZBackup/Restore. DVD only can be used for upgrade.

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

R disk (or USB memory device) for reloading on the system.

NOTICE

Presets should NOT be saved on the same CD-R disk (or USB memory device) as images. The Archive

Menu lists the images but does NOT list the presets stored on a CD-R disk (or USB memory device).

4-3-3-1 Archiving Presets to an CD-R Disk (or USB memory device)

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

2.) Access to the Utility Menu, and select System. The Backup sheet will be shown on the LCD display.

4 - 4

Figure 4-21 Backup Sheet

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

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

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

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Loading Presets from an CD-R disk (or USB memory device)

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

2.) Access to the Utility Menu, and select System. The Restore sheet will be shown on the LCD display.

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

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

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

4-3-4 Adjusting the Display Monitor

Please refer to Section 6-2 "Monitor Adjustments" on page 6-2

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4-3-5 System Features

4-3-5-1 Control Panel

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4 - 6

NOTE:

Figure 4-22 Control Panel Tour

1.) Power On/Off Switch

2.) Probe Key

3.) Top Menu Controls

4.) Keyboard

5.) Preset, Comment, Harmonics keys

6.) Patient key

7.) Mode keys: B-Mode, M-Mode, PW-Mode, PDI,CF Mode.

8.) Gain/Auto key

9.) Zoom key

10.)Ellipse key

11.)Depth key

12.)Reverse, Print, Store keys

13.)Left, Right key

14.)Freeze key

15.)Trackball

16.)Imaging/Measurement keys

17.)TGC

18.)Gel Holder

19.)Probe Holder

LOGIQ C3 Premium does not support PW Mode and CF Mode.

Section 4-3 - General Procedure

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4-3-5-2 LOGIQ C3/C5 Premium SoftMenu Key Tour

1.) Top Menu Controls op Menu Controls

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Figure 4-23 SoftMenu Key Tour

2.) Sub menu Controls: Activates Sub Menu for Modes and toggles/changes functions

A.) Press F5 on the keyboard to activate Sub Menu,

B.) Use the Direction keys to toggle/change functions

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Figure 4-24 Sub Menu Controls

Chapter 4 Functional Checks 4 - 7

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4-3-5-3 Monitor Display

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4 - 8

Figure 4-25 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. Grey/Color Bar.

7. Cine Gauge.

8. Measurement Summary Window.

9. Image.

10. Measurement.

11. Results Window.

12. Probe Identifier. Exam Study.

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

14. Focal Zone.

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

16. Body Pattern.

17. Depth Scale.

18. SoftMenu

19. Caps Lock: On/Off.

20. Start menu icon.

21. Card icon.

Section 4-3 - General Procedure

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4-3-6 B Mode Checks

4-3-6-1

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Preparations

1.) Connect one of the probes listed in 3-6-6 "Available Probes" on page 3-19 , in Chapter 3 Installation to the System probe connector.

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

SoftMenu Key

Frequency

Virtual Convex

Edge Enhance

Colorize

Dynamic Range

Gray Map

Rotation

Rejection

Focus Position

Focus Number

Secondary Menu

Biopsy Kit

Frame Average

Line Density

Focus Width

B softener

Power Output

Suppression

Range Focus

TGC

B Mode

Depth

Freeze

Scan Area

Zoom

Figure 4-26 Controls available in B Mode

Figure 4-27 B Mode Screen Picture Example

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4-3-6-2 B Mode OP Panel Controls

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Table 4-3 B Mode Control Panel Controls

Step

Press B Mode key

Task

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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4-3-6-3 B Mode Softmenu

Table 4-4 B Mode Softmenu

Step Task

Activate Colorize

Adjust Edge Enhance

Activate Grey Map

Adjust Frequency

Adjust Frame Average

Adjust Rotation

Power output

Dynamic Range

Focus Number and Position

Adjust Rejection

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Expected Result(s)

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

Edge Enhance brings out subtle tissue differences and boundaries by enhancing the gray scale differences corresponding to the edges of structures. Adjustments to M Mode's edge enhancement affects the M Mode only.

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

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

Temporal filter that averages frames together.

This has the effect of presenting a smoother, softer image.

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

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

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

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

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

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Chapter 4 Functional Checks 4 - 11

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4-3-7 M Mode Controls

4-3-7-1

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Preparations

1.) Connect one of the probes listed in 3-6-6 "Available Probes" on page 3-19 , in Chapter 3 Installation to the System probe connector.

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

Secondary Menu

Primary Menu

Power Output

Anatomical M

Dynamic Range

Colorize

Rejection

Full Timeline

Sweep Speed

Display Format

TGC

M Cursor

M-Mode

Gain

Figure 4-28 Controls available in M Mode

4 - 12

Figure 4-29 M Mode Screen Picture Example

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

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Table 4-5 M Mode OP Panel Controls

Step

Press M Mode key

Task

Adjust Gain

Display M-Mode Cursor

Expected Result(s)

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).

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

M-Mode Cursor.

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4-3-7-3 M Mode Softmenu

Table 4-6 M Mode Softmenu

Step Task

Adjust Sweep Speed

Adjust Edge Enhance

Activate Grey Map

Activate Colorize

Activate Full Timeline

Select Display Format

Adjust Dynamic Range

Power output

Anatomical M

Adjust Rejection

LOGIQ C3/C5 P

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Expected Result(s)

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

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

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

Displays only timeline screen. Press the Full

Timescreen to activate.

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

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

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

Enter into AMM Mode (Option).

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

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4-3-8 Doppler Mode Checks

4-3-8-1

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Preparations

1.) Connect one of the probes listed in 3-6-6 "Available Probes" on page 3-19 , in Chapter 3 Installation to the System probe connector.

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

Primary Menu

Frequency

SV Length

Sweep Speed

Angle Steer

Angle Correct

Quick Angle

Baseline

Invert

PRF

Wall Filter

PW-Mode

Gain

Figure 4-30 Controls available in Doppler Mode

TGC

Secondary Menu

Rejection

Dynamic Range

Display Format

Full Timeline

Trace Method

Trace Sensitivity

Trace direction

Modify, Auto Calcs

PW/CF Ratio

Duplex

Time Resolution

Colorize

Gray Map

Power Output

Auto Calcs

Spectral Average

Cycles, to Average

M/D Cursor

B Pause Cursor

Figure 4-31 Doppler Mode Screen Picture Example

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

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Table 4-7 Doppler Mode OP Panel Controls

Step

Task

Press PW Mode key

Adjust Gain

Display M/D-Mode Cursor

B-Pause

Expected Result(s)

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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4-3-8-3 Doppler Mode OP Panel Controls

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Table 4-8 Doppler Mode Touch Panel Controls

Step Task

Adjust Rejection

Adjust Sweep Speed

Activate Full Timeline

Select Display Format

Adjust Frequency

Trace Direction

Invert

Auto Calculation

Modify Calcs

Trace Method

Activate Colorize

Activate Gray Map

Dynamic Range

Adjust Angle Correct

Adjust Angle Steer

Move Baseline

Expected Result(s)

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

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

Displays only timeline screen. Press the Full

Timescreen to activate.

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

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

Allows to select different trace direction.

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.

Enables or disables auto calculation.

Activates the window to modify the auto calculation items.

Allows to select different trace method.

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.

Slant the Color Flow linear image left or right to get more information without moving probes. Click Angle Steer to the left to slant the linear image.

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

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Table 4-8 Doppler Mode Touch Panel Controls

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Step

Task Expected Result(s)

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

Adjusts the sensitivity to get more accurate envelope trace.

Adjusts the resolution in frequency domain.

Spectral Average

Power output

SV Length

Optimizes the smoothness of the spectrum.

Different levels can be selected.

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

Sizes the sample volume gate.

Wall Filter

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

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4-3-9 Color Flow Mode Checks

NOTE: Color Flow Mode only support by LOGIQ C5 Premium

4-3-9-1

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Preparations

1.) Connect one of the probes listed in 3-6-6 "Available Probes" on page 3-19 , in Chapter 3 Installation to the System probe connector.

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

Primary Menu

Frequency

Spatial Filter

Angle Steer

Packet Size

PRF

Map

Threshold

Invert

Wall Filter

Virtual Convex

CF Mode

Gain

Secondary Menu

Baseline

Line Density

Flash Suppression

Transparency Map

Focus Position

Frame Average

Power Output

TGC

Figure 4-32 Controls available in Color Flow Mode

Figure 4-33 CFM Mode Screen Picture Example

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

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Table 4-9 Color Flow Mode OP Panel Controls

Step

Task

Press CFM-Mode key

Adjust Gain

Expected Result(s)

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 Softmenu Key

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Table 4-10 Color Flow Mode Softmenu Key

Step Task

Threshold

Packet Size

Select Color maps

Adjust Frequency

Set Frame Average

Color Invert

Adjust LIne Density

Expected Result(s)

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.

Activate Spatial Filter

Adjust Dynamic Range

Activate ACE

Adjust Angle Steer

Move Baseline

Change PRF

(Pulse Repetition Frequency)

Transparency Map

Focus Position

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

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.

Allows to select specific transparency map

Capture

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Table 4-10 Color Flow Mode Softmenu Key

Step

Power output

Wall Filter

Task

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Expected Result(s)

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

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

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4-3-10 Basic Measurements

NOTE:

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The following instructions assume that you first scan the patient and then press Freeze.

4-3-10-1

NOTE:

4-3-10-2

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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4-3-10-3

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Worksheets

Measurement/Calculation worksheets are available to display and edit measurements and calculations.

There are generic worksheets as well as Application specific worksheets. The worksheets are selected from the Measurement Touch Panel.

4-3-10-4 Report Pages

Measurements/Calculations that are included on the worksheet can also be displayed on Report Pages.

Report Pages can be customized to meet the appropriate needs of the user.

4-3-11

4-3-11-1

Probe/Connectors Usage

4-3-11-2

4-3-11-3

4-3-11-4

Connecting a probe

1.) Place the probe's carrying case on a stable surface and open the case.

2.) Carefully remove the probe and unwrap the probe cable.

3.) DO NOT allow the probe head to hang free. Impact to the probe head could result in irreparable damage.

4.) Align the connector with the probe port and carefully push into place.

5.) Lock the probe.

6.) Carefully position the probe cord so it is free to move and is not resting on the floor.

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

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.

2.) Pull the probe and connector straight out of the probe port.

3.) Carefully slide the probe and connector away from the probe port and around the right side of the keyboard.

4.) Ensure the cable is free.

5.) Be sure that the probe head is clean before placing the probe in its storage box.

Take the following precautions with the probe cables: Do not bend, be sure to keep probe cables free from the wheels.

4-3-12

4-3-12-1

4 - 24

Using Cine

Activating CINE

Press Freeze, then roll the Trackball to activate CINE. To start CINE Loop playback, press Run/Stop.

To stop CINE Loop playback. press Run/Stop.

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4-3-12-2 Quickly Move to Start/End Frame

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Press First to move to the first CINE frame; press Last to move to the last CINE frame.

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4-3-12-3 Start Frame/End Frame

Press the Start Frame Two-Button Softkey to move to the beginning of the CINE Loop. Adjust the Start

Frame up/down Two-Button Softkey upward to move forward through the CINE Loop. Adjust the

Softkey downward to move backward through the CINE Loop.

Press the End Frame Two-Button Softkey to move to the end of the CINE Loop. Adjust the End Frame up/down Two-Button Softkey upward to move forward through the CINE Loop. Adjust the Softkey downward to move backward through the CINE Loop.

4-3-12-4

4-3-12-5

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.

4-3-13 Image Management (QG)

For Image Management functionality refer to the LOGIQ C3/C5 Premium 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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4-3-14

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Backup and Restore Database, Preset Configurations and Images

4-3-14-1

NOTE:

Formatting Media

The system may crash if use a DVD for Archive/Backup/EZBackup/Restore, so always use a

CD-R or USB HDD for Archive/Backup/EZBackup/Restore.You only can use DVD for upgrade.

1.) To format the backup media, select the UTILITY button on the Keyboard.

2.) Select CONNECTIVITY, then REMOVABLE MEDIA. Properly label and Insert the backup media.

3.) Select the media type from the drop down menu.

4.) Enter the label for the media as shown in Figure 4-34. It is best to use all capital letters with no spaces or punctuation marks. Press Format.

Figure 4-34 Format and Verify Media

5.) The Ultrasound system displays a pop-up menu, as shown in Figure 4-35. When the formatting has been completed, press OK to continue.

6.) If desired, verify that the format was successful by returning to Utility->Connectivity-

>Removable Media and selecting VERIFY as shown in Figure 4-34.

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4-3-14-2 Backup System Presets and Configurations

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NOTE:

Figure 4-35 Format Successful Pop-up Menu

Always backup any preset configurations before a software reload. This ensures that if the presets need to be reloaded, after the software update, they will be the same ones the customer was using prior to service.

1.) Insert a formatted CD into the drive.

2.) On the Keyboard, press UTILITY.

3.) On the LCD display, press SYSTEM.

4.) On the LCD display, select BACKUP/RESTORE.

If you are not logged in as GE Service or with administrator privileges, the Operator Login window is displayed. Log on with administrator privileges.

5.) In the Backup list, select Patient Archive, Report Archive and User Defined Configuration.

6.) In the Media field, select CD/DVD (or USB memory device).

7.) Select BACKUP.

The system performs the backup. As it proceeds, status information is displayed on the Backup/Restore screen.

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4-3-14-2Backup System Presets and Configurations (cont’d)

Check here to backup presets and configurations

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Figure 4-36 Backup/Restore Menu

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4-3-14-3 Restore System Presets and Configurations

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CAUTION

The restore procedure overwrites the existing database on the local hard drive. Make sure to insert the correct CD (or USB memory device).

NOTE:

1.) Insert the Backup/Restore CD (or USB memory device) into the drive.

2.) On the Keyboard, press UTILITY.

3.) On the LCD display, press SYSTEM.

4.) On the LCD display, select BACKUP/RESTORE.

If you are not logged in with administrator privileges, the Operator Login window is displayed.

Log on with administrator privileges.

5.) In the Restore list, select Patient Archive, Report Archive and User Defined Configuration.

6.) In the Media field, select the Backup/Restore CD/DVD (or USB memory device).

7.) Select RESTORE.

The system performs the restore. As it proceeds, status information is displayed on the Backup/Restore screen.

Check here to restore presets and configurations.

Figure 4-37 Backup/Restore Menu

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4-3-14-4

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Archiving Images

1.) Insert the archive media. To format the archive media, select the Utility button on the

Keyboard.

2.) Select Connectivity, then Removable Media.

3.) Format the CD. Verify the format if desired.

4.) Images will be moved from the hard drive by date. Therefore, the best way is to label media by date.

NOTE: Images will be moved from the hard drive by date. Therefore, the best way to label media is by date. When images are moved to the archive media, they will be deleted from the system hard drive. However, the patient database (backed up earlier) maintains pointers to the location of the images on the archive media.

Choose the days which want to older than current exam date.

Figure 4-38 Format CD Screen

5.) Select Backup/Restore, then EZBackup/Move.

6.) Select “Backup File Older Than in Days”.

4 - 30

Figure 4-39 EZBackup/Move

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4-3-14-4

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Archiving Images (cont’d)

7.) Press PATIENT and set the Dataflow to store images directly to CD-ROM.

8.) From the image screen, press EZBACKUP/MOVE. The Move Images pop-up appears.

ANUAL

Figure 4-40 Image Archive Move Pop-up Menu

9.) Press Next on pop-up message.

10.)A media check message appears. Press OK to continue.

Figure 4-41 Media check message

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4-3-14-4

Archiving Images (cont’d)

11.)Press Finish after Backup/Move complete.

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4-3-14-5

Figure 4-42 EZBackup/Move complete

All databases, presets and images should now be saved to removable media.

Full Backup

1.) Connect the USB HDD to system.

2.) Select Backup/Restore, then Emergency Repair Disk.

3.) Select “Reminder Dialog Interval Days”.

Reminder Dialog

Interval Days

4 - 32

Figure 4-43 Emergency Repair Disk

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4-3-14-5

Full Backup (cont’d)

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4.) Return to scan mode. Press Ctrl + B, the Emergency Disk Making window pop-up appears.

Figure 4-44 Emergency Disk Making Pop-up Menu

5.) Press Next on pop-up message.

6.) A storage information message appears. Press Next to continue.

Figure 4-45 Storage Information message

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4-3-14-5

Full Backup (cont’d)

7.) Press Finish after Emergency Disk Making complete.

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Figure 4-46 Emergency Disk Making Complete

All databases, presets and images should now be saved to Emergency Disk.

8.) Press Ctrl + R, Emergency Disk Recovery window pop-up appear.

4 - 34

Figure 4-47 Emergency Disk Recovery

9.) Press Next on pop-up message.

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4-3-14-5

Full Backup (cont’d)

10.)A recovery information message appears. Press Next to continue.

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Figure 4-48 Recovery Information message

11.)Press Finish after Emergency Disk Recovery complete.

Figure 4-49 Emergency Disk Recovery Complete

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Section 4-4

Software Configuration Checks

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Table 4-11 Software Configuration Checks

Step

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 Store and Print Keys are Store

(store image), Print (print). Store and Print Keys 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

Press (FREEZE)

Press (PRINT) on the Control Panel

Expected Result(s)

Stop image acquisition.

The image displayed on the screen is printed on B&W printer.

Connect with Foot Switch on USB port and press once.

To start image acquisition (the same function as (FREEZE) key).

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Chapter 5 Components and Functions (Theory)

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Section 5-1

Overview

5-1-1 Purpose of Chapter 5

This chapter explains LOGIQ C3/C5 Premium' system concepts, component arrangement, and subsystem function.

Section

5-1

5-2

5-3

Table 5-1 Contents in Chapter 5

Description

Overview

Block Diagram

Common Service Platform

Page Number

5-1

5-2

5-4

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Section 5-2Block Diagram

5-2-1 System Diagram

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Figure 5-50 LOGIQ C3/C5 Premium System Diagram

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5-2-2 Software Diagram

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Figure 5-51 LOGIQ C3/C5 Premium Software Diagram

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Section 5-3

Common Service Platform

5-3-1

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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.

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Chapter 6 Service Adjustments

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Section 6-1

Overview

6-1-1 Purpose of this chapter 6

This section describes how to test and adjust the scanner. These tests are optional. You may use them to check the system for errors.

Table 6-2 Contents in chapter

Section

6-1

6-2

Overview

Monitor Adjustments

Description Page Number

6-1

6-2

Chapter 6 Service Adjustments 6 - 1

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Section 6-2

Monitor Adjustments

6-2-1

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Adjustments Procedures

To adjust the brightness:

For LOGIQ C3/LC5 Premium: Adjust the LCD monitor’s button, located the right side of the LCD

Monitor.

For LOGIQ C3/LC5 Premium: Adjust the LCD monitor’s button, located the bottom of the LCD Monitor.

6 - 2

NOTE:

Figure 6-52 LCD Monitor

To adjust the light:

If the left side button of the LCD has the light symbol, the LCD has the lights to light the keyboard.

For LOGIQ C3/C5 Premium: Adjust the left side button of the monitor to turn on/off the light.

Figure 6-53 Light Adjustment

Section 6-2 - Monitor Adjustments

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Chapter 7 Diagnostics/Troubleshooting

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Section 7-1

Overview

7-1-1 Purpose of Chapter 7

This section describes how to setup and run the tools and software that help maintain image quality and system operation. Very basic host, system and board level diagnostics are run whenever power is applied. Some Service Tools may be run at the application level. However most software tests are required.

Table 7-3 Contents in Chapter 7

Section

7-1

7-2

7-3

7-4

7-5

7-6

Overview

Gathering Trouble Data

USB Quick Save

Screen Captures

Common Diagnostics

Network Configuration

Description Page Number

7-1

7-2

7-4

7-6

7-9

7-12

Section 7-1 - Overview 7 - 1

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Section 7-2

Gathering Trouble Data

7-2-1

7-2-2

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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 C3/C5 Premium

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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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 C3/C5

Premium.

This Alt-D function is available at all times.

Figure 7-54 ALT-D Dialog Box

When Alt-D is pressed, a menu box appears that allows for:

A place to enter a description of the problem

A choice to store to a pre-formatted CD-R, RD (Removable Disk) or to the Export directory D: drive.

The subsequent file is compressed and time stamped. The screen capture is a bitmap which eliminates the possibility of artifacts from compression.

Section 7-2 - Gathering Trouble Data 7 - 3

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Section 7-3

USB Quick Save

7-3-1

NOTE:

7-3-2

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Overview

There may be times when the customer or field engineer will want to directly save images into USB memory. This is accomplished by saving individual Cine clips (moving images- avi format) or still images

(jpg format) directly to a USB memory disk by pressing Print or Store Key.

There’s no factory default print key to accomplish USB Quick Save. However, customer may have customize Print and Store Key function.

When performing a USB Quick Save, you can only define one USB Quick Save operation with either

Print or Store keys.

The print key that has been assigned to the USB Quick Save function should not have any other service functions assigned to it.

Check and Record the Print or Store Key Function

Check the function of the Print or Store Key in the event that the customer may have made some custom settings.

1.) Click Utility on the keyboard.

2.) Select Connectivity from the Utilities Menu.

3.) Select the Buttons tab on the Connectivity screen.

4.) In the Physical Print Buttons field, select Print or Store.

The Connectivity/Buttons Screen will be displayed like the one shown below.

7 - 4

Figure 7-55 Defining Print or Store Key Operation

If Print or Store key is not set to Image Area, proceed to step 5 to record the customer’s customized settings.

5.) In the Destinations section, record the service that is displayed.

6.) In the Physical Print Buttons section, record the parameters related to the service.

Section 7-3 - USB Quick Save

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7-3-3

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Setting the Print or Store Key to USB Quick Save

If the Print or Store Key is not set to screen capture:

1.) While on the Connect screen, with the Buttons tab displayed, go to the Destinations list.

2.) From the list select USB Quick Save. Press [>>] to add the selection to the Printflow View section.

3.) Ensure that the Physical Print Buttons section for capture Area is set to Image Area and No

Image Compression.

4.) The Print and Store Key should now be set up for USB Quick Save, sending the images directly to the USB memory.

NOTICE

It is unable to get full screen using USB Quick Save, just Image Area is available.

Section 7-3 - USB Quick Save 7 - 5

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Section 7-4

Screen Captures

7-4-1

7-4-2

7-4-3

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There may be times when the customer or field engineer will want to capture a presentation on the screen. This is accomplished by first saving the image(s) to the clipboard using a Print or Store Key.

The Store key is the factory default print key to accomplish a secondary Screen Capture. However, the customer may have customized the Store Key function.

Check and Record the Store Key Function

Check the function of the Store Key in the event that the customer may have made some custom settings.

1.) Click Utility on the keyboard.

2.) Select Connectivity from the Utilities Menu.

3.) Select the Buttons tab on the Connectivity screen.

4.) In the Physical Print Buttons field, select Store.

The Connectivity/Buttons Screen will be displayed like the one shown in Figure 7-55 on page 7-4 .

If Store key is not set to Whole Screen, as shown in Figure 7-55 , proceed to step 5 to record the customer’s customized settings.

5.) In the Destinations section, record the service that is displayed.

6.) In the Physical Print Buttons section, record the parameters related to the service.

Setting the Store Key to Screen Capture

If the Store Key is not set to screen capture:

1.) While on the Connect screen, with the Buttons tab displayed, go to the Destinations list.

2.) From the list select Copy To Dataflow. Press [>>] to add the selection to the Printflow View section.

3.) Ensure that the Physical Print Buttons section for capture Area is set to Whole Screen, secondary Capture and No Image Compression.

4.) The Store Key should now be set up for whole screen capture, sending the screens to the image buffer (clipboard).

Capturing a Screen

The following is a generic process to capture any screen from the scanner:

1.) Navigate to and display the image/screen to be captured.

2.) Press STORE. This will place a snapshot of the screen on the “clipboard” displayed at the bottom of the scan image display.

7 - 6 Section 7-4 - Screen Captures

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7-4-3 Capturing a Screen

(cont’d)

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Clipboard

Thumbnai ls

Figure 7-56 Select Image to Capture

3.) Click FREEZE to unfreeze the image to view the image screen and the snapshots displayed on the bottom.

4.) Highlight the snapshot to be stored to RD (Removable Disk) or CD-R.

5.) Select Menu on the right side of the image screen, then highlight and select SAVE AS.

Save As

Figure 7-57 Menu > Save As

Section 7-4 - Screen Captures 7 - 7

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7-4-3 Capturing a Screen

(cont’d)

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7-4-4

Figure 7-58 Save Dialog Box

6.) A Save dialog box will be opened. Choose d:\export folder as the archive location to save the image on the hard disk or CD-R.

NOTICE

After capture the snapshot of the screen to the “clipboard” and save it to the hard disk or other media, it is not full screen image on the hard disk or media.

Reset the Store Key to Customer’s Functionality

If the customer had programmed the Store Key to a function other than screen capture, restore that functionality recorded in section 7-3-2 on page 4 . Refer to Figure 7-55 .

1.) Click Utility on the keyboard.

2.) Select Connectivity from the Utilities Menu.

3.) Select the Buttons tab on the Connectivity screen.

4.) In the Physical Print Button field, select Store.

5.) In the Destinations list, select the service(s) recorded in step 5 , Section 7-3-2 .

6.) In the Physical Print Buttons section, select the parameters related to the service recorded in step 6 , Section 7-3-2 .

7 - 8 Section 7-4 - Screen Captures

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Section 7-5

Common Diagnostics

7-5-1

7-5-1-1

7-5-1-2

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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.

Section 7-5 - Common Diagnostics 7 - 9

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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

7-5-2-7

7-5-2-8

7-5-2-9

7-5-2-10

Essential Tests

System Board

Hard Disk Surface Scan

Hard Disk Quick Test

PCIBus

Video Card

Network Interface

CMOS

DRAM Memory

Parallel Port

LOGIQ C3/C5 P

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7 - 10 Section 7-5 - Common Diagnostics

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7-5-3 PC Diagnostics (Interactive Tests)

7-5-3-1

7-5-3-2

7-5-4

Keyboard Test

Mouse Test

Restart LOGIQ C3/C5 Premium After Diagnostics

Always shutdown the system and reboot after a diagnostics session.

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Section 7-5 - Common Diagnostics 7 - 11

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Section 7-6

Network Configuration

7-6-1

7-6-1-1

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Network Configuration

Wire-LAN Network

1.) Connect system with network.

2.) Press Utility -> Connectivity -> TCPIP, in IP Settings window check the Enable DHCP box. In

Network Speed box, choose the proper speed available.

Figure 7-59 Enable DHCP

7 - 12 Section 7-6 - Network Configuration

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7-6-1-1

Wire-LAN Network (cont’d)

NOTE:

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If user want to setup static IP address, uncheck Enable DHCP option, input static address in IP-

Address box, Subnet Mask and Default Gateway box. In Network Speed box, choose the proper speed available.

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Figure 7-60 Input static address

3.) Click Save, in popped-up dialog choose Shutdown.

Figure 7-61 Save and reboot inquiry dialog

4.) After the system shutdown, reboot the system.

5.) After reboot, the network icon at the left bottom of screen turns green.

Figure 7-62 Network icon

Section 7-6 - Network Configuration 7 - 13

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This page was intentionally left blank.

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7 - 14 Section 7-6 - Network Configuration

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Chapter 8 Replacement Procedures

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Section 8-1

Overview

8-1-1 Purpose of Chapter 8

This chapter describes replacement procedures for the following modules and subsystems.

Table 8-1 Contents in Chapter 8

Section

8-1

8-2

8-2-1

8-2-2

8-2-3

8-4

Description

Overview

DISASSEMBLY/RE-ASSEMBLY

Warning and Caution

Returning/Shipping for repairs

Air filter and Knob Screw

Loading Base Image Software

Page Number

8-1

8-2

8-3

8-6

Section 8-1 - Overview 8 - 1

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Section 8-2

DISASSEMBLY/RE-ASSEMBLY

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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 not wear the ESD wrist strap when you remove a part of power supply unit. Turn OFF power and unplug the power cord before removing a part of power supply unit. However be sure to turn off power and wear the strap before you remove a circuit boards.

DO NOT SERVICE OR DISASSEMBLE PARTS UNDER FRU UNIT LEVEL AT ANY

CIRCUMSTANCES.

8-2-2

NOTE:

Returning/Shipping for repairs

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

GEHC policy states that body fluids must be properly removed from any part or equipment prior to shipment. GEHC 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.

If the LOGIC3/C5 Premium needs to be sent for repair, ensure that any patient information is erased from the Harddisk/Storage Device. In case that any patient information is still residing on the LOGIC3/

C5 Premium, GE will contact the customer and request for urgent collection of that patient information.

GE will keep this patient information in a secure environment for a maximum period of 1 month. All patient information will be permanently deleted at that point.

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

GE will ascertain agreement from the customer. The paitent information shall only be transfered 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.

8 - 2 Section 8-2 - DISASSEMBLY/RE-ASSEMBLY

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8-2-3 Air filter and Knob Screw

8-2-3-1

8-2-3-2

8-2-3-3

8-2-3-4

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Tools

• Common phillips screwdrivers

Preparations

• Shut Down the System and disconnect the power cord.

Removal Procedure

1.) Unscrew the knob screw which fix air filter on the edge of power box, refer to 8-2-3 "Air filter and

Knob Screw" on page 8-3 .

2.) Pull rightward the knob screw out the air filter, refer to 8-2-3 "Air filter and Knob Screw" on page 8-3 .

3.) Lift down the air filter and plastic frame, refer to 8-2-3 "Air filter and Knob Screw" on page 8-3 .

4.) Remove the plastic frame , refer to 8-2-3 "Air filter and Knob Screw" on page 8-3

Mounting procedure

Install the new parts in the reverse order of removal.

Figure 8-63 Air filter and Knob Screw Disassembly

Section 8-2 - DISASSEMBLY/RE-ASSEMBLY 8 - 3

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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

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Purpose: This is a description on how to remove the trackball and clean the roller.

Tools

• No need.

Needed Manpower

• 1 person, 3 minutes + travel

Preparations

• Shut down the system.

Procedure

Refer to Figure 8-64 on page 8-5

1.) Turn the ring counterclockwise.

2.) Remove the ring.

3.) Using hand, carefully grab and remove the trackball.

4.) Carefully clean the roller using swab.

8 - 4 Section 8-3 - Trackball Roller Cleaning

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Section 8-3 Trackball Roller Cleaning

(cont’d)

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1) 2)

3)

Figure 8-64 Trackball Roller Cleaning

4)

Section 8-3 - Trackball Roller Cleaning 8 - 5

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Section 8-4Loading Base Image Software

NOTE:

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

Please ensure power cable is connected during system upgrade!

1.) Insert the disk labeled “System & Application Software” into the DVD ROM drive.

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

Down” from the System Exit menu.

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

4.) Turn on the system. System will detect the DVD-RW automatically.

5.) Press any key to continue when below message display as shown below.

Figure 8-65 Upgrade message

8 - 6 Section 8-4 - Loading Base Image Software

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Section 8-4 Loading Base Image Software

(cont’d)

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6.) Select one of the options for loading the system. Select choice 1] to load the complete disk.

Figure 8-66 Selection for loading the system

While the software install procedure is designed to preserve data, you should select choice [2] to format disk C only.

7.) Press any key to continue when below message display as shown below.

Figure 8-67 Upgrade continue message

Section 8-4 - Loading Base Image Software 8 - 7

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Section 8-4 Loading Base Image Software

(cont’d)

8.) System CD will be loaded as shown in the screen below.

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Figure 8-68 Upgrading message

9.) System updating finished, refer to Figure 8-69 on page 8-8 .

Figure 8-69 System upgrade complete

10.)Press power key to reboot system, then remove the CDROM from the drive immediately. When system first time boot up after upgrading complete, type Serial Number and Option Key before starting up.

8 - 8 Section 8-4 - Loading Base Image Software

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Chapter 9 Renewal Parts

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Section 9-1

Overview

9-1-1 Purpose of Chapter 9

This chapter gives you an overview of Renewal Parts for LOGIQ C3/C5 Premium.

Table 9-1 Contents in Chapter 9

Section

9-1

9-2

9-3

9-4

9-5

9-7

Overview

List of Abbreviations

Renewal Parts Lists

Operator Console Assy

Accessories and kits

Probes

Description Page Number

9-1

9-2

9-3

9-4

9-7

Section 9-2

List of Abbreviations

• Assy - Assembly

• Ctrl - Control

• FRU 1 - Replacement part available in part hub

• FRU 2 - Replacement part available from the manufacturer (lead time involved)

• Int - Internal

• I/O - Input/Output

• LCD - Liquid Crystal Display

• MON - Monitor

• PAT. - Patient

• PC - Personal Computer (Back End Processor)

Chapter 9 Renewal Parts 9 - 1

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Section 9-3Renewal Parts Lists

9-3-1 Equipment Models Covered in this Chapter

Table 9-2 Renewal Parts List for Customer

Part Name

AC Power Cord

Probe ,Gel Holder and Cable

Hook Kit

Probe ,Gel Holder and Cable

Hook Kit

Part Number

5177123

5176304

5176773

5177195

5176907

5177153

5177154

5177187-2

5177146

5400868

5176753

5315730

Description

Power cord Europe Class

Power cord China Class

Power cord India Class

Power cord Argentina Class

Power cord UK Class

Power cord Denmark Class

Power cord Switzerland Class

Power cord Australia Class

Power cord USA Class

Power cord Brazilian Class

Power cord Israel Class

Probe ,Gel Holder and Cable Hook Kit

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FRU

Quantity

9 - 2 Section 9-3 - Renewal Parts Lists

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Section 9-4Operator Console Assy

LCD Assy

Keyboard Assy

Boay Assy

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Base Assy

LOGIQ C3 Premium

LOGIQ C5 Premium

Figure 9-70 Operator Console Assy

Chapter 9 Renewal Parts 9 - 3

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Section 9-5Accessories and kits

Item

5000

5001

5001A

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Table 9-3 Accessories ,Cables and Kits

Part Number

5352411

5352549

5426738

Description

Cable Kit for Upper Part (including the following cables)

5332380

Cable from KBDTRSF board to Main

5333069

5333070

Cable from MainKBD to PWRSW board for probe key

LCD Power Cable

5333070

5220407

LCD DVI Cable

Encoder Cable

5220410

TGC Cable

Cable Kit Underside (including the following cables)

5332371

5332373

5340119

5340734

5333465

MTK

HDD_SATA

DVD_SATA

Cable from MST PWA to TX and Relay

5333468

5224314

5332370

System DC Cable

Printer Cable

Printer Power Cable From Power Box

MTM (MST 2 rear panel)

5341010

LAN Cable

Cable Kit Underside (including the following cables)

5332371

5332373

5340119

5340734

5333465

MTK

HDD_SATA

DVD_SATA

Cable from MST PWA to TX and Relay

5333468

5224314

5332370

System DC Cable

Printer Cable

Printer Power Cable From Power Box

MTM (MST 2 rear panel)

5341010

5416388

LAN Cable

LC_Premium 4D control cable

Qty

FRU

9 - 4 Section 9-5 - Accessories and kits

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Table 9-3 Accessories ,Cables and Kits

Item Part Number

5003

5012

5013

5014

5015

5008

5009

5010

5011

5016

5017

5018

5328133

5324832

5315697

5343395-3

5343395-4

5343395-7

5343395-8

5343395-9

5343395-10

5426284-2

5426284-3

5426284-4

Description

Service Tools for LOGIQ C (including the following tools)

5262716

5324751

5324786

Caster Spanner

TBJMA Screw Driver FJ6-40

SATA Hex Blade 80108

Support Jig for Service

EMC Sheet Kit

LOGIQ C Premium R2.0.2 System and Application DVD

LOGIQ C Premium R2.0.3 System and Application DVD

LOGIQ C Premium R2.0.6 System and Application DVD

LOGIQ C Premium R2.0.7 System and Application DVD

LOGIQ C Premium R2.0.8 System and Application DVD

LOGIQ C Premium R2.0.9 System and Application DVD

LOGIQ C Premium R2.1.1 System and Application DVD

LOGIQ C Premium R2.1.2 System and Application DVD

LOGIQ C Premium R2.1.3 System and Application DVD

VIVID FIVE

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ANUAL

Qty

FRU

Chapter 9 Renewal Parts 9 - 5

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Section 9-6Manuals

Item

6000

Part Number

5341787-100

6001

6002

6003

6004

6005

6006

6007

6008

5341361 -100

5341361 -101

5341361 -106

5341361 -108

5341361 -111

5341361 -127

5341361 -141

5341784-100

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Description

LOGIQ C3/C5 Premium Service Manual

System User Manuals

User Manual, LOGIQ C3/C5 Premium, English

User Manual, LOGIQ C3/C5 Premium, French

User Manual, LOGIQ C3/C5 Premium, Spanish

User Manual, LOGIQ C3/C5 Premium, German

User Manual, LOGIQ C3/C5 Premium, Italian

User Manual, LOGIQ C3/C5 Premium, portuguese

User Manual, LOGIQ C3/C5 Premium, Chinese

System Quick Start Guide

Quick Start Guide, LOGIQ C3/C5 Premium

Qty FRU

1 N

9 - 6 Section 9-6 - Manuals

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Section 9-7Probes

Item

7004

7005

7006

7007

7008

7000

7001

7002

7003

Table 9-4 Probes on LOGIQ C3/C5 Premium

Part Name

4C-RC

7.5C-RC

6.5C-RC

E7C-RC

3S-RC

L6-12-RC

C2-5-RC

E8CS-RC

RAB4-8-RC

Part Number

5315581

5315683

5315685

5315686

5213343

5399465

5401243

5395336

KTZ157074

Description

Probe (Center Frequency: 3.75MHz)

Probe (Center Frequency: 7.5MHz)

Probe (Center Frequency: 6.5MHz)

Probe (Center Frequency: 2.0MHz)

Probe (Center Frequency: 7.75MHz)

Probe (Center Frequency: 3.2MHz)

Probe (Center Frequency: 6.5MHz)

Probe (Center Frequency: 4.4MHz)

VIVID FIVE

ASIC

ERVICE

ANUAL

Quantity FRU

NOTICE

All the spare parts should be disposed according to local laws.

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VIVID FIVE

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ANUAL

9 - 8 Section 9-7 - Probes

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Chapter 10 Care & Maintenance

LOGIQ C3/C5 P

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Section 10-1

Overview

10-1-1

10-1-2

Periodic Maintenance Inspections

It has been determined by engineering that your system does not have any high wear components that fail with use, therefore no Periodic Maintenance Inspections are mandatory. Some Customers Quality

Assurance Programs may require additional tasks and or inspections at a different frequency than listed in this manual.

Purpose of Chapter 10

This chapter describes Care & Maintenance on the scanner and peripherals. These procedures are intended to maintain the quality of the ultrasound systems performance. Read this chapter completely and familiarize yourself with the procedures before performing a task.

Table 10-1 Contents in Chapter 10

Section Description

10-1

Overview

10-2

Why do Maintenance

10-3

Maintenance Task Schedule

10-4

Tools Required

Section 10-5

When There's Too Much Leakage Current...

Page Number

10-1

10-2

10-4

10-15

CAUTION

Practice good ESD prevention. Wear an anti–static strap when handling electronic parts and even when disconnecting/connecting cables.

DANGER

THERE ARE SEVERAL PLACES ON THE BACKPLANE, THE AC DISTRIBUTION,

AND DC DISTRIBUTION THAT ARE DANGEROUS. BE SURE TO DISCONNECT

THE SYSTEM POWER PLUG AND OPEN THE MAIN CIRCUIT BREAKER

BEFORE YOU REMOVE ANY PARTS. BE CAUTIOUS WHENEVER POWER IS

STILL ON AND COVERS ARE REMOVED.

CAUTION

Do not pull out or insert circuit boards while power is ON.

CAUTION

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

Section 10-1 - Overview 10 - 1

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Section 10-2

Why do Maintenance

10-2-1

10-2-2

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Keeping Records

It is good business practice that ultrasound facilities maintain records of quality checks and corrective maintenance. The Ultrasound Inspection Certificate (provided on page 10-16 ) provides the customer with documentation that the ultrasound scanner is maintained on a periodic basis.

A copy of the Ultrasound Periodic Maintenance Inspection Certificate should be kept in the same room or near the scanner.

Quality Assurance

In order to gain accreditation from organizations such as the American College of Radiology (USA), it is the customer’s responsibility to have a quality assurance program in place for each scanner. The program must be directed by a medical physicists, the supervising radiologist/physician or appropriate designee.

Routine quality control testing must occur regularly. The same tests are performed during each period so that changes can be monitored over time and effective corrective action can be taken.

Testing results, corrective action and the effects of corrective action must be documented and maintained on the site.

Your GE service representative can help you with establishing, performing and maintaining records for a quality assurance program. Please contact us for coverage information and/or price for service.

Section 10-3

Maintenance Task Schedule

10-3-1

NOTE:

How often should care & maintenance tasks be performed?

The Care & Maintenance Task Schedule (provided on page 10-3 ) specifies how often your LOGIQ C3/

C5 Premium should be serviced and outlines items requiring special attention.

It is the customer’s responsibility to ensure the LOGIQ C3/C5 Premium 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 C3/C5 Premium 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 C3/C5 Premium for an average patient load (10-12 per day) and not 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

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Section 10-3 Maintenance Task Schedule

(cont’d)

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Table 10-2 Customer Care Schedule

Service at Indicated Time

Clean Probe Holders

Clean Air Filter

Inspect AC Mains Cable

Inspect Cables and Connectors

Clean Console

Inspect Wheels, Casters, brakes and

Swivel Locks

Check Control Panel Movement

Console Leakage Current Checks

Peripheral Leakage Current Checks

Surface Probe Leakage Current Checks

Endocavity Probe Leakage

Current Checks

Transesphongeal Probe Leakage

Current Checks

Surgical Probe Leakage

Current Checks

Measurement Accuracy Checks

Functional Checks

Daily Weekly Monthly

•

Per Facilities

QA Program

•

Notes

more frequently depending on your environment

•

Mobile Unit Check Weekly

•

Mobile Unit Check Daily

•

Mobile Unit Check Daily also after corrective maintenance also after corrective maintenance also after corrective maintenance also after corrective maintenance also after corrective maintenance also after corrective maintenance also after corrective maintenance also after corrective maintenance

NOTE:

PMs are not mandatory, the table above is for reference only.

May require specialized equipment to complete.

Section 10-3 - Maintenance Task Schedule 10 - 3

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Section 10-4

Tools Required

10-4-1

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Standard GE Tool Kit

The following is a description of the “Standard” GE tool kit in the USA. Not all tools are required for PMs.

Table 10-3 Overview of GE-1 Tool Kit Contents

Tool ID

9-GH807

68-412

9-GH130

9-41584

9-4118

9-41293

9-41294

9-41295

9-46677

9-34701

9-43499

9-4355

9-43523

9-43531

9-4518

9-44776

9-44601

9-4151

9-41421

9-41594

9-41581

9-39451

9-45358

9-4078

9-44572

9-44579

9-45385

9-45378

9-4518

Description

Pliers Retaining Ring

Scribe

Wrench Open End 3/8 - 7/16

Wrench Open End 1/2 - 9/16

Pliers, Arc Joint 7 inch

Pliers, Slip Joint

Pliers, Long Nose, Miniature

Ignition Wrench Set, 10 pc.

Wrench, Adj., 4 inch

Screwdriver, Blade, Stubby

Screwdriver, Blade, Pocket clip

Screwdriver, Blade 1/8 in. x 4 in.

Screwdriver, Blade 3/16 in. x 4 in.

20' Steel Tape, locking Spring load

Ratchet, Offset, Slotted

Ratchet, Offset, Phillips

Tapered Reamer

Screwdriver, slotted 1/4 in.X 6 in.

Screwdriver, Phillips #2, Stubby

Screwdriver, Phillips #0

Screwdriver, Phillips #1

Screwdriver, Phillips #2

Hex Keys, 20 pc., Metric

1/4 in. Standard.Socket set (19 pc)

1/2 inch Socket 1/4 inch drive

Flex Spinner

Breaker

6 inch Ext.

Tool ID

9-HT62002

9-4099

9-GH3001

9-GH300ME

9-XL9920

9-XL9921

9-XL9922

9-XL9923

9-XL9924

9-XL9925

9-XL9926

9-XL99764

9-XL99964

9-XLM60

9-XL9971MM

9-XL9972MM

9-XL9973MM

9-XL9974MM

9-XL9975MM

9-XL9976MM

9-XL9977MM

9-XL991CM

C2356E

BLBO

DWL4283T

9-41322

9-6757

9-9487

9-45341

9-3001

Description

Xcelite-hex Blade 1.27mm

Xcelite-hex Blade 1.5mm

Xcelite-hex Blade 2 mm

Xcelite-hex Blade 2.5mm

Xcelite-hex Blade 3mm

Xcelite-hex Blade 4mm

Xcelite-hex Blade 5mm

Handle

Screw starter - Kedman Quick Wedge

Box - 18 Compartment

Box - 5 Compartment

Pickup Tool, Claw type

6 pc Needle File Set

Utility Knife

Pliers Vice Grip 10 inch

Xacto Pen Knife

Solder Aid, Fork and Hook

Mirror, Round, Telescoping

Steel Rule Decimal 6 inch

Steel Rule Metric 6 inch

Xcelite-hex Blade.050 inch

Xcelite-hex Blade 1/16 inch

Xcelite-hex Blade 5/16 inch

Xcelite-hex Blade 3/32 inch

Xcelite-hex Blade 1/8 inch

Xcelite-hex Blade 5/32 inch

Xcelite-hex Blade 3/16 inch

Xcelite-hex Blade 7/64

Xcelite-hex Blade 9/64

Mini-screwdriver kit

10 - 4 Section 10-4 - Tools Required

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Table 10-3 Overview of GE-1 Tool Kit Contents (Continued)

Tool ID

9-65283

9-46696

9-39829

9-38461

9-4280

9-WEW60P3

9-WECT5B6

9-WEWDP12

93383

9-GH408

21576

9-4516

Description

Case 8.5 in. x 4.5 in. x 2 in. Deep

Hex Keys

Torpedo Level, Magnetic

Hammer, Ball Peen, 4 oz

Universal Joint 1/4 inch

Weller - Soldering Iron, 3 wire

Weller - Soldering Iron Tip

Weller - Desoldering Pump

Flashlight Mini-Mag Lite (AAA Bat.)

Tweezers

Brush - Bristle

Pliers 4 1/4 inch Diagonal

Tool ID

9-45072

9-XL100X

9-XL87CG

9-WEWDT-07

9-WS175-E

KH174

KH175

9-Z9480121

LOGIQ C3/C5 P

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Description

Pliers 6 inch Diagonal

Wire Stripper/Cutter 5 inch - 100X

Pliers - very fine needle nose-87CG

Weller-Soldering-Replacement Tip(1)

Wiss - Surgical Scissors

Hemostat 5 inch Straight

Hemostat 5 inch curved

Alignment tool (red)

ANUAL

Table 10-4 Overview of GE-2 Tool Kit Contents(Continued)

Tool ID

9-45381

9-45092

9-42882

9-42884

9-42886

9-42973

9-GH77

9-GH890

9-31276

9-31277

9-31263

21045C

9-44604

9-41587

9-41586

9-GH19512

9-44741

Description

Pliers, Arc Joint 9 1/2 inch

Pliers, Linesman 8 1/2 inch

Punch, Pin 3/32 inch

Punch, Pin 5/32 inch

Punch, Pin 1/4 inch

Cold Chisel 1/2 inch

Center Punch Automatic

File Handle, Adj.

File, Round, Bastard 8 inch

File, Half Round, Bastard 8 inch

File, Flat Mill 8 inch

Close Quarter Saw

Wrench, Adj 10 inch

Screwdriver 5/16 inch x 8 inch

Screwdriver, Stubby 5/16 inch

Countersink 1/2 inch

12 PC Combination Wrench Set

GE-2 Sears Kit (#99034)

Tool ID

9-44067

9-42679

9-44262

9-4258

9-34374

9-44311

9-33485

9-33484

9-52068

9-52722

9-52723

9-44046

Description

Socket 1 1/16 in. for 1/2 in. drive

Socket 10MM Hex for 1/2 in. drive (2273333)

Extension 10 inch for 1/2 in. drive (2273405)

3/8 inch to 1/2 inch Adapter

3/8 inch Metric Socket Set - 12 PT

16mm Socket 12 pt.

Metal Socket Tray

Tap and Drill Set

#6 Tap

#8 Tap

High Speed Drill Set

#36 Drill

#29 Drill

3/8 inch Socket Set

Section 10-4 - Tools Required 10 - 5

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10-4-2 Special Tools, Supplies and Equipment

10-4-2-1 Specific Requirements for Care & Maintenance

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Table 10-5 Overview of Requirements for Care & Maintenance

Part Number Tool

Digital Volt Meter (DVM)

Leakage Current Ultrasound Kit

Anti Static Kit

Anti Static Vacuum Cleaner

Air Filter

Safety Analyzer

SVHS VCR Cassette

SVHS VCR Head Cleaner

2113015

46–194427P231

46–194427P279

46–194427P369

46–194427P373

46–194427P370

46–194427P278

46–194427P279

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

air intake

The Safety Analyzer tool should be calibrated and compliant with

AAMI/ESI 1993 or IEC 60601 or AS/NZS 3551

60 minute

120 minute

See VCR user manual for requirements blank 128 M disk blank 230 M disk

3.5” MOD MEDIA

E7010GG

E7010GF

E8381AA

E8381AB

5.25” MOD Media

3.5” MOD Media Cleaner

5.25” MOD Media Cleaner

3.5” MOD Head Cleaner Kit

5.25” MOD Head Cleaner Kit

QIQ Phantom

B/W Printer Cleaning Sheet

Color Printer Cleaning Sheet

Disposable Gloves

2117811

2148392

E8370RB

cleans the diskettes cleans the diskettes

cleans the drive heads cleans the drive heads

RMI Grayscale Target Model 403GS

See printer user manual for requirements

10 - 6 Section 10-4 - Tools Required

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10-4-3 Input Power

10-4-3-1

PROPRIETARY TO GE LOGIQ C3/C5 P

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ANUAL

Mains Cable Inspection

Table 10-6 Mains Cable Inspection

Step

Item Description

Unplug Cord Disconnect the mains cable from the wall and system.

Inspect

Inspect it and its connectors for damage of any kind.

Verify

Verify that the LINE, NEUTRAL and GROUND wires are properly attached to the terminals, and that no strands may cause a short circuit.

Inlet connector retainer is functional.

10-4-4

10-4-4-1

Cleaning

General Cleaning

Table 10-7 General Cleaning

Step Item Description

1 Console

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).

NOTE:

10-4-5

For your convenience or of the air filter is too dirty, replacement filters are available. refer to

Chapter 9 for the air filter replacement part number.

Physical Inspection

Table 10-8 Physical Checks

Step Item Description

1 Labeling

Verify that all system labeling is present and in readable condition. refer to the LOGIQ C3/C5

Premium User Manual for details.

2 Scratches & Dents Inspect the console for dents, scratches or cracks.

Wheels & Brakes

Check all wheels and casters for wear and verify operation of foot brake, to stop the unit from moving, and release mechanism. Check all caster locks and caster swivel locks for proper operation.

Cables &

Connectors

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.

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 and verify that the labeling is good.

Op Panel Lights

Check for proper operation of all operator panel and TGC lights.

Monitor Light

Check for proper operation of any monitor lights if available.

External

Microphone

Check for proper operation of any external microphones by recording an audio test.

Section 10-4 - Tools Required 10 - 7

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10-4-6

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Outlet Test -Wiring Arrangement - USA & Canada

Test all outlets in the area for proper grounding and wiring arrangment 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 10-1 Typical 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.

10 - 8 Section 10-4 - Tools Required

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10-4-7 Grounding Continuity

CAUTION

Electric Shock Hazard. The patient must not be contacted to the equipment during this test.

Measure the resistance from the third pin of the attachment plug to the exposed metal parts of the case.

The ground wire resistance should be less than 0.2 ohms. Reference the procedure in the IEC 601-1.1.

10-4-7-1

Figure 10-2 Ground Continuity Test

Meter Procedure

Follow these steps to test the ground wire resistance.

1.) Turn the LOGIQ C3/C5 Premium unit OFF.

2.) Plug the unit into the meter, and the meter into the tested AC wall outlet.

3.) Plug the black chassis cable into the meter’s “CHASSIS” connector and attach the black chassis cable clamp to an exposed metal part of the LOGIQ C3/C5 Premium unit.

4.) Set the meter’s “FUNCTION” switch to the RESISTANCE position.

5.) Set the meter’s “POLARITY” switch to the OFF (center) position.

6.) Measure and record the ground wire resistance.

Section 10-4 - Tools Required 10 - 9

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10-4-8 Chassis Leakage Current Test

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10-4-8-1

Definition

This test measures the current that would flow in a grounded person who touched accessible metal parts of the bedside station if the ground wire should break. The test verifies the isolation of the power line from the chassis. The meter is connected from accessible metal parts of the case to ground.

Measurements should be made with the unit On and Off, with the power line polarity Normal and

Reversed. Record the highest reading.

CAUTION

Electric Shock Hazard. When the meter's ground switch is OPEN, don't touch the unit!

CAUTION

Equipment damage possibility. Never switch the Polarity and the status of Neutral when the unit is powered ON. Be sure to turn the unit power OFF before switching them using the POLARITY switch and/or the NEUTRAL switch. Otherwise, the unit may be damaged.

10-4-8-2 Generic Procedure

The test verifies the isolation of the power line from the chassis. The testing meter is connected from accessible metal parts of the case to ground. Measurements should be made with the unit ON and OFF, with the power line polarity Normal and Reversed. Record the highest reading of current.

10 - 10

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 10-12 .

Section 10-4 - Tools Required

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10-4-9

PROPRIETARY TO GE LOGIQ C3/C5 P

REMIUM

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ANUAL

Isolated Patient Lead (Source) Leakage–Lead to Lead

Reference the procedure in the IEC 60601-1. Select and test each of the five ECG lead positions

(except ALL) on the LEAD selector, testing each to the power condition combinations found in the table.

Record the highest leakage current measured.

10-4-10 Isolated Patient Lead (Sink) Leakage-Isolation Test

reference the procedure in the IEC 60601-1. Select the ALL position on the lead selector. Depress the rocker switch to ISO TEST to test lead isolation.

CAUTION

Line voltage is applied to the ECG leads during this test. To avoid possible electric shock hazard, the system being tested must not be touched by patients, users or anyone while the ISO

TEST switch is depressed.

NOTE: It is not necessary to test each lead individually or power condition combinations as required in previous tests.

Section 10-4 - Tools Required 10 - 11

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10-4-10-1 Data Sheet for ECG Leakage Current

The test passes when all readings measure less than the value shown in the table below. Record all data on the PM Inspection Certificate.

Table 10-9 Maximum Allowance Limit for ECG Leakage Current

Patient Lead to Ground Leakage Current Test and

Patient Lead to Lead Leakage Current Test

AC Power

Source

115V

220/240V

Maximum

Allowance Limit

GROUND OPEN

10uA

GROUND

CLOSED

10uA

500uA 10uA

Table 10-10 Maximum Allowance Limit for ECG Leakage Current

Patient Lead Isolation Current Test

AC Power

Source

115V

220/240V

Maximum

Allowance Limit

20uA

5mA

ECG

Power

OFF

Table 10-11 Typical Data Sheet for ECG Leakage Current

Tester Lead Selector Tester

Polarity

Switch

NORM

REVERSE

NORM

REVERSE

NORM

REVERSE

NORM

REVERSE

Tester

Ground

Switch

CLOSED

OPEN

CLOSED

OPEN

RL RA LA LL C

10 - 12 Section 10-4 - Tools Required

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10-4-11 Probe Leakage Current Test

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10-4-11-1 Definition

This test measures the current that would flow to ground from any of the probes through a patient who is being scanned and becomes grounded by touching some other grounded surface.

10-4-11-2 Generic Procedure

Measurements should be made with the ground open and closed, with power line polarity normal and reversed, and with the unit Off and On. For each combination, the probe must be active to find the worst case condition.

POWER

OUTLET

H (BLACK)

N (WHITE)

G (GREEN)

POLARITY REVERSING SWITCH

MOMENTARY

SWITCH

CONSOLE

PROBE

LEAKAGE TEST

METER

NOTE:

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.

10-4-11-3 Meter Procedure Using Probe Adapter

Follow the Safety Analyzer tool instruction to test each transducer for leakage current.

The electrical Safety Analyzer tool should be calibrated and compliant with AMMI/ESI 1993 or IEC

60601 or AS/NZS 3551.

10-4-11-4 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 AMMI/ESI 1993 or IEC

60601 or AS/NZS 3551.

Section 10-4 - Tools Required 10 - 13

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10-4-11-5 Data Sheet for Transducer Source Leakage Current

The test passes when all readings measure less than the values. Record all data on the PM Inspection

Certificate.

CAUTION

Table 10-12 Typical Data Sheet For Transducer Source Leakage Current

Unit Power

OFF

Transducer Tested:

Tester Power Polarity

Switch

NORM

REV

NORM

REV

Tester GROUND or

NEUTRAL Switch

OPEN

CLOSED

OPEN

CLOSED

OPEN

CLOSED

OPEN

CLOSED

Measurement

10 - 14 Section 10-4 - Tools Required

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PROPRIETARY TO GE

Section 10-5

When There's Too Much Leakage Current...

LOGIQ C3/C5 P

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ANUAL

CHASSIS FAILS

Check the ground on the power cord and plug for continuity. Ensure the ground is not broken, frayed, or intermittent. Replace any defective part.

Tighten all grounds. Ensure star washers are under all ground studs.

Inspect wiring for bad crimps, poor connections, or damage.

Test the wall outlet; verify it is grounded and is free of other wiring abnormalities. Notify the user or owner to correct any deviations. As a work around, check the other outlets to see if they could be used instead.

NOTE: No outlet tester can detect the condition where the white neutral wire and the green grounding wire are reversed. If later tests indicate high leakage currents, this should be suspected as a possible cause and the outlet wiring should be visually inspected.

PROBE FAILS

Test the probe in another connector to isolate if the fault lies with the probe or the scanner.

NOTE: Each probe will have some amount of leakage, dependent on its design. Small variations in probe leakage currents are normal from probe to probe. Other variations will result from differences in line voltage and test lead placement. The maximum allowable leakage current for body surface contact probe differs from inter-cavity probe. Be sure to enter the correct probe type in the appropriate space on the check list.

If excessive leakage current is slot dependent, inspect the system connector for bent pins, poor connections, and ground continuity.

If the problem remains with the probe, replace the probe.

PERIPHERAL FAILS

Tighten all grounds. Ensure star washers are under all ground studs.

Inspect wiring for bad crimps, poor connections, or damage.

STILL FAILS

If all else fails, begin isolation by removing the probes, external peripherals, then the on board ones, one at a time while monitoring the leakage current measurement.

NEW UNIT

If the leakage current measurement tests fail on a new unit and if situation can not be corrected, submit a Safety Failure Report to document the system problem. Remove unit from operation.

ECG FAILS

Inspect cables for damage or poor connections.

Section 10-5 - When There's Too Much Leakage Current...

10 - 15

Probe 4:

Probe 5:

Probe 6:

Probe 7:

Probe 8:

Probe 9:

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ULTRASOUND INSPECTION CERTIFICATE

Customer Name: System ID:

System Type

Probe 1:

Probe 2:

Probe 3:

Frequency:

Model Number:

Scan Format*:

Frequency:

Scan Format*:

Dispatch Number / Date Performed:

Serial Number:

Model Number:

LOGIQ C3/C5 P

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Warranty/Contract/HBS

Manufacture Date:

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

Monitor

Touch Panel

OK? or

N/A

PHYSICAL INSPECTION AND CLEANING

Physical Inspection and Cleaning

(if applicable)

Console

Monitor

Touch Panel

Air Filter

Probe Holders

External I/O

Wheels, Brakes & Swivel Locks

Cables and Connectors

GE Approved Peripherals (VCR, CD-RW, MOD,

Printers)

Inspect

Measurement Accuracy

GE Approved Peripherals

Clean

COMMENTS:

______________________________________________________________________________

10 - 16 Section 10-5 - When There's Too Much Leakage Current...

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ELECTRICAL SAFETY

PROPRIETARY TO GE LOGIQ C3/C5 P

REMIUM

ASIC

ERVICE

ANUAL

Electrical Test Performed

Outlet (correct ground &wiring config.)

System Ground Continuity

Chassis Source Leakage Current - Probe

Chassis Source Leakage Current - Caster

Chassis Source Leakage Current - CRT

Patient Lead Source Leakage

(Lead to Ground)

Patient Lead Source Leakage

(Lead to Lead)

Patient Lead Source Leakage

(Isolation)

Peripheral 1 Leakage Current

Peripheral 1Ground Continuity

Peripheral 2 Leakage Current

Peripheral 2Ground Continuity

Peripheral 3 Leakage Current

Peripheral 3Ground Continuity

Max Value

Allowed

Value

Measured OK?

Comments

PROBES

Probe Number

(from previous page)

Probe 1:

Probe 2:

Probe 3:

Probe 4:

Probe 5:

Probe 6:

Probe 7:

Max Value

Allowed

Max Value

Measured OK?

Comments

Probe 8:

Probe 9:

Final Check. All system covers are in place. System scans with all probes as expected.

Section 10-5 - When There's Too Much Leakage Current...

10 - 17

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EVISION

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LOGIQ C3/C5 P

REMIUM

ASIC

ERVICE

ANUAL

10 - 18 Section 10-5 - When There's Too Much Leakage Current...

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EVISION

A,B

Abbreviations, 9-1

Archiving Images

Move, 4-30

Backup

Patient Database, 4-26

Preset Configurations, 4-26

Basic Measurements

Functional Checks, 4-23

Body pattern display location, 4-8

Boot Up, 3-8

Caps lock display location, 4-8

CE Compliance, 1-12

Cine gauge display location, 4-8

Color Mode

Overview, 4-15

Connectivity

Worksheet, 3-20

Contact Information, 1-14

Control Panel, 4-6

Customer Assistance, 1-14

Dangerous Procedure Warnings, 1-11

Date/Time display location, 4-8

Depth scale display location, 4-8

DICOM Network Function, 2-9

Electrical Safety, 1-10

Electrostatic Discharge Warning, 1-12

EMI, 1-12

ESD, 1-12

Exam study display location, 4-8

Focal zone display location, 4-8

VIVID FIVE

LOGIQ™ 9 P

ROPRIETARY

ANUAL

INDEX

Functional Checks, 4-1

Basic Measurements, 4-23

Control Panel, 4-6

Image Management, 4-25

Monitor Display, 4-8

Peripherals, 4-36

Probes/Connector Usage, 4-24

Gathering Trouble Data, 7-2

General Cleaning, 10-7

Gray/color bar display location, 4-8

Hazard Icons, 1-5

Hospital name display location, 4-8

Human Safety, 1-9

Image Management

Functional Checks, 4-25

Image preview display location, 4-8

Imaging parameters display location, 4-8

Institution name display location, 4-8

LOTO, 1-13

Measurement summary window display location, 4-8

Mechanical Safety, 1-9

Models Covered, 1-2

Monitor Display

Functioanl Checks, 4-8

Monitor display location, 4-8

Move

Archiving Images, 4-30

Index I

GE H

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IRECTION

5273008-100, R

EVISION

Operator identification display location, 4-8

P4 Key Function, 7-4, , 7-6

Patient identification display location, 4-8

Patient name display location, 4-8

PC Diagnostics, 7-10

Hard Drive Tests, 7-10

Keyboard Test, 7-11

Memory Tests, 7-10

PC Diagnostics (Interactive Tests), 7-11

Peripherals

Functional Checks, 4-36

Power On, 3-8

Power-up Procedures

Voltage Settings, 3-7

Probe identifier display location, 4-8

Probe orientation marker display location, 4-8

Probes/Connector Usage

Functional Checks, 4-24

Product Icons, 1-6

Required Features, 2-7

Restore

Patient Database, 4-29

Preset Configurations, 4-29

Safety Considerations, 1-9

Screen Captures, 7-6

Service Manual

Purpose of, 1-1

System Manufacturer, 1-15

Touch Panel

Functional Checks, 4-6

Trouble Image with Logs, 7-3

Troubleshooting

Gathering Trouble Data, 7-2

Screen Captures, 7-6

Trouble Image with Logs, 7-3

Vital System Information, 7-2

II Index

VIVID FIVE

LOGIQ™ 9 P

ROPRIETARY

ANUAL

Ultrasound Room Layout, 2-8

Voltage Settings, 3-7

Warnings and Cautions, 1-9

2009-2012, General Electric Company.

GE Healthcare-GEMedical Systems Ultrasound.

9900 Innovation Drive

Wawautosa, Wisconsin 53226

USA

Key features

High-performance ultrasound system
User-friendly interface
Advanced imaging capabilities
Comprehensive set of tools for diagnosis and treatment
Wide range of clinical applications

Frequently asked questions

The LOGIQ C3/C5 Premium console requires a temperature range of 10°C to 35°C (50°F to 95°F), a relative humidity of 30% to 80%, and a barometric pressure of 700 to 1060 hPa.

The LOGIQ C3/C5 Premium requires a 100 to 240 VAC, 50/60 Hz, single-phase power supply.

The LOGIQ C3/C5 Premium contains dangerous voltages that can cause death. Use extreme caution when handling, testing and adjusting the system. Always use Personal Protection Equipment (PPE) such as gloves, safety shoes, safety glasses, and a 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.