GE Healthcare LOGIQ e, Vet, LOGIQ i, Vivid e Ultrasound System Basic Service Manual
Below you will find brief information for Ultrasound System LOGIQ e, Ultrasound System LOGIQ e Vet, Ultrasound System LOGIQ i, Ultrasound System Vivid e. This manual contains basic information and procedures for understanding system operation, system setup, system diagnostics and troubleshooting, and system part identification.
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GE Healthcare
LOGIQ e/LOGIQ e Vet/LOGIQ i/
Vivid e
Basic Service Manual
Part Number: 5370626-100
Revision: 7
GE H
EALTHCARE
D
IRECTION
5370626-100, R
EVISION
7 LOGIQ
E
/LOGIQ
E
V
ET
/LOGIQ
I
/V
IVID E
B
ASIC
S
ERVICE
M
ANUAL
Important Precautions
WARNING
(EN)
THIS SERVICE MANUAL IS AVAILABLE IN ENGLISH ONLY.
• IF A CUSTOMER’S SERVICE PROVIDER REQUIRES A LANGUAGE OTHER
THAN ENGLISH, IT IS THE CUSTOMER’S RESPONSIBILITY TO PROVIDE
TRANSLATION SERVICES.
• DO NOT ATTEMPT TO SERVICE THE EQUIPMENT UNLESS THIS SERVICE
MANUAL HAS BEEN CONSULTED AND IS UNDERSTOOD.
• FAILURE TO HEED THIS WARNING MAY RESULT IN INJURY TO THE SERVICE
PROVIDER, OPERATOR OR PATIENT FROM ELECTRIC SHOCK, MECHANICAL
OR OTHER HAZARDS.
AVERTISSEMENT
(FR)
CE MANUEL DE MAINTENANCE N’EST DISPONIBLE QU’EN ANGLAIS.
• SI LE TECHNICIEN DU CLIENT A BESOIN DE CE MANUEL DANS UNE AUTRE
LANGUE QUE L’ANGLAIS, C’EST AU CLIENT QU’IL INCOMBE DE LE FAIRE
TRADUIRE.
• NE PAS TENTER D’INTERVENTION SUR LES é QUIPEMENTS TANT QUE LE
MANUEL SERVICE N’A PAS é Té CONSULTé ET COMPRIS.
• LE NON-RESPECT DE CET AVERTISSEMENT PEUT ENTRAîNER CHEZ LE
TECHNICIEN, L’OPé RATEUR OU LE PATIENT DES BLESSURES DUES à DES
DANGERS é LECTRIQUES, Mé CANIQUES OU AUTRES.
WARNUNG
(DE)
DIESES KUNDENDIENST-HANDBUCH EXISTIERT NUR IN ENGLISCHER
SPRACHE.
• FALLS EIN FREMDER KUNDENDIENST EINE ANDERE SPRACHE BENö TIGT,
IST ES AUFGABE DES KUNDEN Fü R EINE ENTSPRECHENDE ÜBERSETZUNG
ZU SORGEN.
• VERSUCHEN SIE NICHT, DAS GERä T ZU REPARIEREN, BEVOR DIESES
KUNDENDIENST-HANDBUCH NICHT ZU RATE GEZOGEN UND VERSTANDEN
WURDE.
• WIRD DIESE WARNUNG NICHT BEACHTET, SO KANN ES ZU VERLETZUNGEN
DES KUNDENDIENSTTECHNIKERS, DES BEDIENERS ODER DES PATIENTEN
DURCH ELEKTRISCHE SCHLä GE, MECHANISCHE ODER SONSTIGE
GEFAHREN KOMMEN.
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AVISO
(ES)
ESTE MANUAL DE SERVICIO Só LO EXISTE EN INGLé S.
• SI ALGú N PROVEEDOR DE SERVICIOS AJENO A GEHC SOLICITA UN IDIOMA
QUE NO SEA EL INGLé S, ES RESPONSABILIDAD DEL CLIENTE OFRECER UN
SERVICIO DE TRADUCCIó N.
• NO SE DEBERá DAR SERVICIO Té CNICO 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 ELé CTRICAS, MECá NICAS O DE
OTRA NATURALEZA.
ATENÇÃO
(PT-Br)
ESTE MANUAL DE ASSISTê NCIA Té CNICA Só SE ENCONTRA DISPONíVEL EM
INGLê S.
• SE QUALQUER OUTRO SERVIç O DE ASSISTê NCIA Té CNICA, QUE Nã O A
GEHC, SOLICITAR ESTES MANUAIS NOUTRO IDIOMA, é DA
RESPONSABILIDADE DO CLIENTE FORNECER OS SERVIç OS DE TRADUç ã O.
• Nã O TENTE REPARAR O EQUIPAMENTO SEM TER CONSULTADO E
COMPREENDIDO ESTE MANUAL DE ASSISTê NCIA Té CNICA.
• O Nã O CUMPRIMENTO DESTE AVISO PODE POR EM PERIGO A SEGURANç A
DO Té CNICO, OPERADOR OU PACIENTE DEVIDO A‘ CHOQUES ELé TRICOS,
MECâ NICOS OU OUTROS.
AVISO
(PT-pt)
ESTE MANUAL DE ASSISTÊNCIA ESTÁ DISPONÍVEL APENAS EM INGLÊS.
• SE QUALQUER OUTRO SERVIÇO DE ASSISTÊNCIA TÉCNICA, QUE NÃO A
GEHC, SOLICITAR ESTES MANUAIS NOUTRO IDIOMA, É DA
RESPONSABILIDADE DO CLIENTE FORNECER OS SERVIÇOS DE TRADUÇÃO.
• NÃO TENTE EFECTUAR REPARAÇÕES NO EQUIPAMENTO SEM TER
CONSULTADO E COMPREENDIDO PREVIAMENTE ESTE MANUAL.
• A INOBSERVÂNCIA DESTE AVISO PODE RESULTAR EM FERIMENTOS NO
TÉCNICO DE ASSISTÊNCIA, OPERADOR OU PACIENTE EM CONSEQUÊNCIA
DE CHOQUE ELÉCTRICO, PERIGOS DE ORIGEM MECÂNICA, BEM COMO DE
OUTROS TIPOS.
ii
AVVERTENZA
(IT)
IL PRESENTE MANUALE DI MANUTENZIONE è DISPONIBILE SOLTANTO IN
INGLESE.
• SE UN ADDETTO ALLA MANUTENZIONE ESTERNO ALLA GEHC RICHIEDE IL
MANUALE IN UNA LINGUA DIVERSA, IL CLIENTE è TENUTO A PROVVEDERE
DIRETTAMENTE ALLA TRADUZIONE.
• SI PROCEDA ALLA MANUTENZIONE DELL’APPARECCHIATURA SOLO DOPO
AVER CONSULTATO IL PRESENTE MANUALE ED AVERNE COMPRESO IL
CONTENUTO.
• NON TENERE CONTO DELLA PRESENTE AVVERTENZA POTREBBE FAR
COMPIERE OPERAZIONI DA CUI DERIVINO LESIONI ALL’ADDETTO ALLA
MANUTENZIONE, ALL’UTILIZZATORE ED AL PAZIENTE PER FOLGORAZIONE
ELETTRICA, PER URTI MECCANICI OD ALTRI RISCHI.
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HOIATUS
(ET)
KÄESOLEV TEENINDUSJUHEND ON SAADAVAL AINULT INGLISE KEELES.
• KUI KLIENDITEENINDUSE OSUTAJA Nõ UAB JUHENDIT INGLISE KEELEST
ERINEVAS KEELES, VASTUTAB KLIENT Tõ LKETEENUSE OSUTAMISE EEST.
• ä RGE ü RITAGE SEADMEID TEENINDADA ENNE EELNEVALT Kä ESOLEVA
TEENINDUSJUHENDIGA TUTVUMIST JA SELLEST ARU SAAMIST.
• Kä ESOLEVA HOIATUSE EIRAMINE Võ IB Põ HJUSTADA TEENUSEOSUTAJA,
OPERAATORI Võ I PATSIENDI VIGASTAMIST ELEKTRILö ö GI, MEHAANILISE
Võ I MUU OHU TAGAJä RJEL.
VAROITUS
(FI)
TÄMÄ HUOLTO-OHJE ON SAATAVILLA VAIN ENGLANNIKSI.
• JOS ASIAKKAAN PALVELUNTARJOAJA VAATII MUUTA KUIN
ENGLANNINKIELISTä MATERIAALIA, TARVITTAVAN Kä ä NNö KSEN
HANKKIMINEN ON ASIAKKAAN VASTUULLA.
• ä Lä YRITä KORJATA LAITTEISTOA ENNEN KUIN OLET VARMASTI LUKENUT
JA YMMä RTä NYT Tä Mä N HUOLTO-OHJEEN.
• MIKä LI Tä Tä VAROITUSTA EI NOUDATETA, SEURAUKSENA VOI OLLA
PALVELUNTARJOAJAN, LAITTEISTON Kä YTTä Jä N TAI POTILAAN
VAHINGOITTUMINEN Sä HKö ISKUN, MEKAANISEN VIAN TAI MUUN
VAARATILANTEEN VUOKSI.
ΠΡΟΕΙΔΟΠΟΙΗΣΗ
(EL)
ΤΟ ΠΑΡΟΝ ΕΓΧΕΙΡΙΔΙΟ ΣΕΡΒΙΣ ΔΙΑΤΙΘΕΤΑΙ ΣΤΑ ΑΓΓΛΙΚΑ ΜΟΝΟ.
•
ΕΑΝ ΤΟ ΑΤΟΜΟ ΠΑΡΟΧΗΣ ΣΕΡΒΙΣ ΕΝΟΣ ΠΕΛΑΤΗ ΑΠΑΙΤΕΙ ΤΟ ΠΑΡΟΝ
ΕΓΧΕΙΡΙΔΙΟ ΣΕ ΓΛΩΣΣΑ ΕΚΤΟΣ ΤΩΝ ΑΓΓΛΙΚΩΝ, ΑΠΟΤΕΛΕΙ ΕΥΘΥΝΗ ΤΟΥ
ΠΕΛΑΤΗ ΝΑ ΠΑΡΕΧΕΙ ΥΠΗΡΕΣΙΕΣ ΜΕΤΑΦΡΑΣΗΣ.
•
ΜΗΝ ΕΠΙΧΕΙΡΗΣΕΤΕ ΤΗΝ ΕΚΤΕΛΕΣΗ ΕΡΓΑΣΙΩΝ ΣΕΡΒΙΣ ΣΤΟΝ ΕΞΟΠΛΙΣΜΟ
ΕΚΤΟΣ ΕΑΝ ΕΧΕΤΕ ΣΥΜΒΟΥΛΕΥΤΕΙ ΚΑΙ ΕΧΕΤΕ ΚΑΤΑΝΟΗΣΕΙ ΤΟ ΠΑΡΟΝ
ΕΓΧΕΙΡΙΔΙΟ ΣΕΡΒΙΣ.
•
ΕΑΝ ΔΕ ΛΑΒΕΤΕ ΥΠΟΨΗ ΤΗΝ ΠΡΟΕΙΔΟΠΟΙΗΣΗ ΑΥΤΗ, ΕΝΔΕΧΕΤΑΙ ΝΑ
ΠΡΟΚΛΗΘΕΙ ΤΡΑΥΜΑΤΙΣΜΟΣ ΣΤΟ ΑΤΟΜΟ ΠΑΡΟΧΗΣ ΣΕΡΒΙΣ, ΣΤΟ ΧΕΙΡΙΣΤΗ Ή
ΣΤΟΝ ΑΣΘΕΝΗ ΑΠΟ ΗΛΕΚΤΡΟΠΛΗΞΙΑ, ΜΗΧΑΝΙΚΟΥΣ Ή ΑΛΛΟΥΣ ΚΙΝΔΥΝΟΥΣ.
FIGYELMEZTETÉS
(HU)
EZEN KARBANTARTÁSI KÉZIKÖNYV KIZÁRÓLAG ANGOL NYELVEN ÉRHET
Ő EL.
• HA A VEV
Ő SZOLGÁLTATÓJA ANGOLTÓL ELTÉRŐ NYELVRE TART IGÉNYT,
AKKOR A VEV
Ő FELELŐSSÉGE A FORDÍTÁS ELKÉSZÍTTETÉSE.
• NE PRÓBÁLJA ELKEZDENI HASZNÁLNI A BERENDEZÉST, AMÍG A
KARBANTARTÁSI KÉZIKÖNYVBEN LEÍRTAKAT NEM ÉRTELMEZTÉK.
• EZEN FIGYELMEZTETÉS FIGYELMEN KÍVÜL HAGYÁSA A SZOLGÁLTATÓ,
M
ŰKÖDTETŐ VAGY A BETEG ÁRAMÜTÉS, MECHANIKAI VAGY EGYÉB
VESZÉLYHELYZET MIATTI SÉRÜLÉSÉT EREDMÉNYEZHETI.
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VIÐVÖRUN
(IS)
VÝSTRAHA
(CS)
ÞESSI ÞJÓNUSTUHANDBÓK ER EINGÖNGU FÁANLEG Á ENSKU.
• EF ÞJÓNUSTUAÐILI VIÐSKIPTAMANNS ÞARFNAST ANNARS TUNGUMÁLS EN
ENSKU, ER ÞAÐ Á ÁBYRGÐ VIÐSKIPTAMANNS AÐ ÚTVEGA ÞÝÐINGU.
• REYNIÐ EKKI AÐ ÞJÓNUSTA TÆKIÐ NEMA EFTIR AÐ HAFA SKOÐAÐ OG
SKILIÐ ÞESSA ÞJÓNUSTUHANDBÓK.
• EF EKKI ER FARIÐ AÐ ÞESSARI VIÐVÖRUN GETUR ÞAÐ VALDIÐ MEIÐSLUM
ÞJÓNUSTUVEITANDA, STJÓRNANDA EÐA SJÚKLINGS VEGNA RAFLOSTS,
VÉLRÆNNAR EÐA ANNARRAR HÆTTU.
TENTO SERVISNÍ NÁVOD EXISTUJE POUZE V ANGLICKé M JAZYCE.
• V P ř íPADě, ŽE POSKYTOVATEL SLUŽEB ZÁKAZNÍKŮM POTř EBUJE Ná VOD
V JINé M JAZYCE, JE ZAJIšT ěNí Př EKLADU DO ODPOVíDAJíCíHO JAZYKA
ú KOLEM Zá KAZNíKA.
• NEPROVÁD
ĚJTE úDRŽBU TOHOTO ZAř íZENí, ANIŽ BYSTE SI Př Eč ETLI
TENTO SERVISNÍ NÁVOD A POCHOPILI JEHO OBSAH.
• V P ř íPADě NEDODRŽOVá Ní Té TO VýSTRAHY MůŽE DOJíT ÚRAZU
ELEKTRICKÁM PROUDEM PRACOVNíKA POSKYTOVATELE SLUŽEB,
OBSLUŽNé HO PERSONá LU NEBO PACIENT ů VLIVEM ELEKTRICKéHOP
PROUDU, RESPEKTIVE VLIVEM K RIZIKU MECHANICKÉHO POŠKOZENÍ NEBO
JINÉMU RIZIKU.
ADVARSEL
(DA)
DENNE SERVICEMANUAL FINDES KUN PÅ ENGELSK.
• HVIS EN KUNDES TEKNIKER HAR BRUG FOR ET ANDET SPROG END
ENGELSK, ER DET KUNDENS ANSVAR AT SØRGE FOR OVERSÆTTELSE.
• FORSØG IKKE AT SERVICERE UDSTYRET MEDMINDRE
DENNE SERVICEMANUAL ER BLEVET LÆST OG FORSTÅET.
• MANGLENDE OVERHOLDELSE AF DENNE ADVARSEL KAN MEDF
ŘRE SKADE
P
Ĺ GRUND AF ELEKTRISK, MEKANISK ELLER ANDEN FARE FOR
TEKNIKEREN, OPERAT
ŘREN ELLER PATIENTEN.
WAARSCHUWING
(NL)
DEZE ONDERHOUDSHANDLEIDING IS ENKEL IN HET ENGELS VERKRIJGBAAR.
• ALS HET ONDERHOUDSPERSONEEL EEN ANDERE TAAL VEREIST, DAN IS DE
KLANT VERANTWOORDELIJK VOOR DE VERTALING ERVAN.
• PROBEER DE APPARATUUR NIET TE ONDERHOUDEN VOORDAT DEZE
ONDERHOUDSHANDLEIDING WERD GERAADPLEEGD EN BEGREPEN IS.
• INDIEN DEZE WAARSCHUWING NIET WORDT OPGEVOLGD, ZOU HET
ONDERHOUDSPERSONEEL, DE OPERATOR OF EEN PATIËNT GEWOND
KUNNEN RAKEN ALS GEVOLG VAN EEN ELEKTRISCHE SCHOK,
MECHANISCHE OF ANDERE GEVAREN.
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ĪDINĀJUMS
(LV)
š
Ī APKALPES ROKASGRĀMATA IR PIEEJAMA TIKAI ANGĻU VALODĀ.
• JA KLIENTA APKALPES SNIEDZ
ĒJAM NEPIECIEŠAMA INFORMĀCIJA CITĀ
VALOD
Ā, NEVIS ANGĻU, KLIENTA PIENĀKUMS IR NODROŠINĀT TULKOŠANU.
• NEVEICIET APR
ĪKOJUMA APKALPI BEZ APKALPES ROKASGRĀMATAS
IZLAS
ĪŠANAS UN SAPRAŠANAS.
• Š
Ī BRĪDINĀJUMA NEIEVĒROŠANA VAR RADĪT ELEKTRISKĀS STRĀVAS
TRIECIENA, MEH
ĀNISKU VAI CITU RISKU IZRAISĪTU TRAUMU APKALPES
SNIEDZ
ĒJAM, OPERATORAM VAI PACIENTAM.
ĮSPĖJIMAS
(LT)
ŠIS EKSPLOATAVIMO VADOVAS YRA IŠLEISTAS TIK ANGL
Ų KALBA.
• JEI KLIENTO PASLAUG
Ų TEIKĖJUI REIKIA VADOVO KITA KALBA – NE ANGLŲ,
VERTIMU PASIR
ŪPINTI TURI KLIENTAS.
• NEM
ĖGINKITE ATLIKTI ĮRANGOS TECHNINĖS PRIEŽIŪROS DARBŲ, NEBENT
VADOVAUTUM
ĖTĖS ŠIUO EKSPLOATAVIMO VADOVU IR JĮ SUPRASTUMĖTE
• NEPAISANT ŠIO PERSP
ĖJIMO, PASLAUGŲ TEIKĖJAS, OPERATORIUS AR
PACIENTAS GALI B
ŪTI SUŽEISTAS DĖL ELEKTROS SMŪGIO, MECHANINIŲ AR
KIT
Ų PAVOJŲ.
ADVARSEL
(NO)
DENNE SERVICEHÅNDBOKEN FINNES BARE PÅ ENGELSK.
• HVIS KUNDENS SERVICELEVERANDØR TRENGER ET ANNET SPRÅK, ER DET
KUNDENS ANSVAR Å SØRGE FOR OVERSETTELSE.
• IKKE FORSØK Å REPARERE UTSTYRET UTEN AT DENNE
SERVICEHÅNDBOKEN ER LEST OG FORSTÅTT.
• MANGLENDE HENSYN TIL DENNE ADVARSELEN KAN FØRE TIL AT
SERVICELEVERANDØREN, OPERATØREN ELLER PASIENTEN SKADES PÅ
GRUNN AV ELEKTRISK STØT, MEKANISKE ELLER ANDRE FARER.
OSTRZE
ŻENIE
(PL)
NINIEJSZY PODR
ĘCZNIK SERWISOWY DOSTĘPNY JEST JEDYNIE W JĘZYKU
ANGIELSKIM.
• JE ś LI FIRMA śWIADCZĄCA KLIENTOWI USłUGI SERWISOWE WYMAGA
UDOST ę PNIENIA PODRęCZNIKA W Ję ZYKU INNYM NIŻ ANGIELSKI,
OBOWI
ĄZEK ZAPEWNIENIA STOSOWNEGO TłUMACZENIA SPOCZYWA NA
KLIENCIE.
• NIE PRó BOWA 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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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)
Да н н о е руко в о дс т во п о о бс луж ива н ию ПРЕДОСТАВЛЯЕТСЯ т о лько н а а н г лийс ко м Яз ы ке .
•
Ес ли с ервис н о МУ ПЕРСОНАЛУ клиен т а н ео бхо димо руко во дс т во н е н а а н г лийс ко м ЯЗЫКЕ, клиен т у с ледует с а мо с т о Ят ельн о
ОБЕСПЕЧИТЬ п ерево д.
•
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 Mô ŽE VYÚSTI
Ť DO ZRANENIA
POSKYTOVATE
ĽA SLUŽIEB, OBSLUHUJúCEJ OSOBY ALEBO PACIENTA
ELEKTRICKýM PRú DOM, PRÍPADNE DO MECHANICKé HO ALEBO INé HO
NEBEZPE č ENSTVA.
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 contact the product's Lead Service Integrator (LSI) to report service documentation issues. DO NOT use TrackWise for this purpose. The LSI will then use the internal problem reporting tool to communicate these issues 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.
TRADEMARKS
All products and their name brands are trademarks of their respective holders.
COPYRIGHTS
All Material Copyright© 2004 to 2011 by General Electric Company Inc. All Rights Reserved.
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Revision History
Revision
5
6
7
3
4
1
2
Date
23, Qct. 2009
13, May 2010
29, June 2010
30, November 2010
25, April 2011
25, Sep 2011
5, Oct 2011
Reason for change
Initial Release
Update for Software update and adding new probes
Update to add Isolation Cart enhanced Version
Update LOGIQ e Spare Parts and add USA CKD address
Add Vivid e R6.x.x
Update for LOGIQ e Vet R6.x.x
Update for LOGIQ e R7.x.x
List of Effected Pages (LOEP)
Pages
Title Page
Warnings i to -xii
TOC
1-1 to 1-20
2-1 to 2-10
Revision
7
7
7
7
7
Pages
3-1 to 3-32
4-1 to 4-38
5-1 to 5-20
6-1 to 6-2
7-1 to 7-28
Revision
7
7
7
7
7
Pages
8-1 to 8-10
9-1 to 9-32
10-1 to 10-21
Index
Back Cover
Revision
7
7
7
7
N/A
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Table of Contents
CHAPTER 1
Introduction
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 1
Purpose of Chapter 1 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 1
Chapter Contents . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 1
Purpose of Service Manual . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 1
Typical Users of the Basic Service Manual . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 2
LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e Models Covered by this Manual . . 1 - 3
Purpose of Operator Manual(s) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 5
Important Conventions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 5
Conventions Used in Book . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 5
Standard Hazard Icons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 6
Product Icons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 7
Safety Considerations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 11
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 11
Human Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 11
Mechanical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 11
Electrical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 12
Label Location . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 13
Battery Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 14
Dangerous Procedure Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 16
Lockout/Tagout (LOTO) requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 16
Returning/Shipping Probes and Repair Parts . . . . . . . . . . . . . . . . . . . . . . . 1 - 17
EMC, EMI, and ESD . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 18
Electromagnetic Compatibility (EMC) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 18
CE Compliance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 18
Electrostatic Discharge (ESD) Prevention . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 18
Customer Assistance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 19
Contact Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 19
System Manufacturer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 20
Factory Sites . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 20
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CHAPTER 2
Site preparations
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 1
Purpose of this chapter 2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 1
Chapter Contents . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 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
Recommended Ultrasound Room Layout . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 6
Required Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 7
Desirable Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 7
Networking Pre-installation Requirements . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 9
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CHAPTER 3
System Setup
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 1
Purpose of Chapter 3 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 1
Average Installation Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 2
Installation Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 3
Safety Reminders . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 3
Receiving and Unpacking the Equipment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 4
Moving into Position . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 7
Packing the Equipment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 7
Preparing for Installation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 8
Verify Customer Order . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 8
Physical Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 8
EMI Protection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 8
Completing the Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 9
Power On / Boot Up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 9
Power Off/ Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 10
Transducer Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 11
System Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 12
System Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 12
Electrical Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 12
Approved peripherals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 13
Connecting Cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 14
Peripherals/Accessories Connector Panel . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 14
Available Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 25
Software/Option Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 27
Connectivity Installation Worksheet . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 28
Loading Base Image Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 29
Software Version check out . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 30
Functional Check-out . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 30
Paperwork . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 31
Product Locator Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 31
User Manual(s) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 31
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Functional Checks
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 1
Purpose for Chapter 4 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 1
Required Equipment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 1
General Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 2
Power On/Boot Up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 2
Power Off/ Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 3
Archiving and Loading Presets . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 5
Adjusting the Display Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 6
Lockout/Tagout (LOTO) requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 6
System Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 7
B Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 10
M Mode Controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 13
Color Flow Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 16
Doppler Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 20
CWD Functional Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 24
Basic Measurements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 25
Probe/Connectors Usage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 25
Using Cine . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 26
Image Management (QG) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 27
Backup and Restore Database, Preset Configurations and Images . . . . . 4 - 28
Software Configuration Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 37
Peripheral Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 37
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CHAPTER 5
Components and Functions (Theory)
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 1
Block Diagrams and Theory . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 2
Block Diagram . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 2
General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 3
External I/O . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 4
Peripherals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 4
Wiring . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 5
Power Diagrams . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 6
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 6
AC Power . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 6
Battery charging . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 7
Air Flow Distribution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 8
Fans . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 9
Common Service Platform . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 10
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 10
Global Service User Interface (GSUI) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 10
Service Home Page . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 12
Error Logs Tab . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 13
Diagnostics . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 17
Image Quality . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 18
Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 18
Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 19
Utilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 19
Replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 20
PM . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 20
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CHAPTER 6
Service Adjustments
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 1
Purpose of this chapter 6 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 1
Monitor Adjustments. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 2
Adjustments Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 2
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Diagnostics/Troubleshooting
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 1
Purpose of Chapter 7 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 1
Gathering Trouble Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 2
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 2
Collect Vital System Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 2
Collect a Trouble Image with Logs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 3
USB Quick Save . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 4
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 4
Check and Record the P3 Key Function . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 4
Setting the P3 Key to USB Quick Save . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 5
Screen Captures. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 6
Check and Record the P1 Key Function . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 6
Setting the P1 Key to Screen Capture . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 6
Capturing a Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 6
Reset the P1 Key to Customer’s Functionality . . . . . . . . . . . . . . . . . . . . . . 7 - 8
Global Service User Interface (GSUI) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 9
Enter global service user interface . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 9
Active Diagnostic Function . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 10
Control Frame . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 10
Common Diagnostics . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 12
Utilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 12
PC Diagnostics (Non-Interactive Tests) . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 13
PC Diagnostics (Interactive Tests) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 14
Restart the system after diagnostics . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 14
Network and Insite II Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 15
Network Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 15
Insite II Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 19
Insite II Configuration (For LOGIQ e R6.x.x) . . . . . . . . . . . . . . . . . . . . . . . 7 - 24
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CHAPTER 8
Replacement Procedures
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 1
Purpose of Chapter 8 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 1
Disassembly/Re-assembly of LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e . . . . . . . . . 8 - 1
Warning and Caution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 1
Handle Assy (FRU No. 313) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 2
Loading Base Image Software. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 4
Checks after FRU replacement (Debrief Guidelines). . . . . . . . . . . . . . . . . . . . . . . . 8 - 9
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CHAPTER 9
Renewal Parts
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 1
Purpose of Chapter 9 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 1
List of Abbreviations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 1
Renewal Parts Lists . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 2
Equipment Models Covered in this Chapter . . . . . . . . . . . . . . . . . . . . . . . . 9 - 2
Operator Console Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 3
LCD Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 4
Keyboard Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 6
Bottom Assy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 9
Cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 14
Isolation Cart Components . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 15
Isolation Cart Enhanced Version Components. . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 17
Accessories and Kits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 19
Manuals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 24
Probe . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 29
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CHAPTER 10
Care & Maintenance
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 1
Periodic Maintenance Inspections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 1
Purpose of Chapter 10 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 1
Why do Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 2
Keeping Records . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 2
Quality Assurance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 2
Maintenance Task Schedule . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 2
How often should care & maintenance tasks be performed? . . . . . . . . . . . . 10 - 2
Tools Required. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 4
Special Tools, Supplies and Equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 4
System Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 5
Preliminary Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 5
Functional Checks (See Also Chapter 4) . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 6
Input Power . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 7
Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 7
Physical Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 8
Optional Diagnostic Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 9
Probe Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 9
Battery Performance Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 10
Electrical Safety Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 11
Safety Test Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 11
GEMS Leakage Current Limits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 12
Outlet Test - Wiring Arrangement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 13
Chassis Leakage Current Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 14
Probe Leakage Current Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 16
When There's Too Much Leakage Current... . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 19
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Chapter 1
Introduction
Section 1-1
Overview
1-1-1
1-1-2
Purpose of Chapter 1
This chapter describes important issues related to safely servicing this ultrasound machine. The service provider must read and understand all the information presented here before installing or servicing a unit.
Chapter Contents
Table 1-1 Contents in Chapter 1
Section
1-1
1-2
1-3
1-4
1-5
Overview
Important Conventions
Safety Considerations
EMC, EMI, and ESD
Customer Assistance
Description Page Number
1-1
1-6
1-12
1-16
1-17
1-1-3 Purpose of Service Manual
This Service Manual provides service information for the LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e
Ultrasound Scanning System. It 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 e/LOGIQ e
Vet/LOGIQ i/Vivid e .
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 e/LOGIQ e Vet/LOGIQ i/Vivid e .
7.) Chapter 7 - Diagnostics/Troubleshooting: Provides procedures for running diagnostic or related routines for the LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e .
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 e/
LOGIQ e Vet/LOGIQ i/Vivid e .
10.)Chapter 10 - Care & Maintenance: Provides periodic maintenance procedures for the LOGIQ e/
LOGIQ e Vet/LOGIQ i/Vivid e .
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1-1-4 Typical Users of the Basic Service Manual
• Service Personnel (installation, maintenance, etc.).
• Hospital’s Service Personnel
• Contractors (Some parts of Chapter 2 - Site Preparations)
1-2 Section 1-1 - Overview
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1-1-5 LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e Models Covered by this Manual
Table 1-2 LOGIQ e R4.x.x Model Designations
Part Number
5151219
5151220
5151243
5151247
5151252
5151253
5151251
Description
LOGIQ e R4.x.x Console for USA
LOGIQ e R4.x.x Console for Argentina
LOGIQ e R4.x.x Console for Europe
LOGIQ e R4.x.x Console for China
LOGIQ e R4.x.x Console for Japanese
LOGIQ e R4.x.x Console for Australia
LOGIQ e R4.x.x Console for India
Table 1-3 LOGIQ e R5.0.x / LOGIQ e Vet Model Designations
Part Number
5199260
5198329
5199670
5198793
5198161
5199693
5212841
Description
LOGIQ e / LOGIQ e Vet R5.0.x Console for USA
LOGIQ e / LOGIQ e Vet R5.0.x Console for Argentina
LOGIQ e / LOGIQ e Vet R5.0.x Console for Europe
LOGIQ e / LOGIQ e Vet R5.0.x Console for China
LOGIQ e / LOGIQ e Vet R5.0.x Console for Japanese
LOGIQ e / LOGIQ e Vet R5.0.x Console for Australia
LOGIQ e / LOGIQ e Vet R5.0.x Console for India
Table 1-4 LOGIQ e R5.2.x Model Designations
Part Number
5323370
5323375
5323371
5323380
5323378
5323377
Description
LOGIQ e R5.2.x Console for USA
LOGIQ e R5.2.xConsole for Argentina
LOGIQ e R5.2.xConsole for Europe
LOGIQ e R5.2.xConsole for Japanese
LOGIQ e R5.2.xConsole for Australia
LOGIQ e R5.2.x Console for India
Table 1-5 LOGIQ e R6.x.x Model Designations
Part Number
5389028
5389808
5389810
5389811
5389812
5389813
5389814
5410642
5410642
Description
LOGIQ e R6.x.x Console for USA
LOGIQ e R6.x.x Console for Argentina
LOGIQ e R6.x.x Console for Europe
LOGIQ e R6.x.x Console for Chinese
LOGIQ e R6.x.x Console for Japanese
LOGIQ e R6.x.x Console for Australia
LOGIQ e R6.x.x Console for India
LOGIQ e R6.x.x Console for CKD USA
LOGIQ e R6.x.x Console for CKD Taiwan
Chapter 1 Introduction 1-3
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Table 1-6 LOGIQ e R6.x.x Model Designations
Part Number
5432745
5432746
5432747
Description
LOGIQ e R7.x.x Console for USA
LOGIQ e R7.x.x Console for Europe
LOGIQ e R7.x.x Console for Japan
Table 1-7 LOGIQ i R4.x.x Model Designations
Part Number
5176830
5179969
5179685
5179209
5179748
5179191
5179176
Description
LOGIQ i R4.1.x Console for USA
LOGIQ i R4.1.x Console for Argentina
LOGIQ i R4.1.x Console for Europe
LOGIQ i R4.1.x Console for China
LOGIQ i R4.1.x Console for Japanese
LOGIQ i R4.1.x Console for Australia
LOGIQ i R4.1.x Console for India
Table 1-8 LOGIQ i R5.x.x Model Designations
Part Number
5245475
5245476
5245477
5245478
5245480
5245481
Description
LOGIQ i R5.x.x Console for USA
LOGIQ i R5.x.x Console for Argentina
LOGIQ i R5.x.x Console for Europe
LOGIQ i R5.x.x Console for China
LOGIQ i R5.x.x Console for Australia
LOGIQ i R5.x.x Console for India
Table 1-9 Vivid e R4.x.x Model Designations
Part Number
5171613
5172528
5171633
5171603
5171755
5172272
5172286
5183318
Description
Vivid e R4.x.x Console for USA
Vivid e R4.x.x Console for Argentina
Vivid e R4.x.x Console for Europe
Vivid e R4.x.xConsole for China
Vivid e R4.x.x Console for Japanese
Vivid e R4.x.x Console for Australia
Vivid e R4.x.x Console for India/South Africa
Vivid e R4.x.x Console with SKD ECG
Table 1-10 Vivid e R5.x.x Model Designations
Part Number
5198601
5212203
5212894
Description
Vivid e R5.x.x Console for USA
Vivid e R5.x.x Console for Argentina
Vivid e R5.x.x Console for Asia
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Table 1-10 Vivid e R5.x.x Model Designations
Part Number
5199815
5213329
5212851
5199644
5183318
Description
Vivid e R5.x.x Console for China
Vivid e R5.x.x Console for Japan
Vivid e R5.x.x Console for Australia
Vivid e R5.x.x Console for India/South Africa
Vivid e R5.x.x Console with SKD ECG for Europe
Table 1-11 Vivid e R6.x.x Model Designations
Part Number
5411312
5411381
5411382
5411383
5411384
5411385
5411386
5411388
5410641
Description
Vivid e R6.x.x Console for EU
Vivid e R6.x.x Console for USA
Vivid e R6.x.x Console for China
Vivid e R6.x.x Console for Argentina
Vivid e R6.x.x Console for Japan
Vivid e R6.x.x Console for Australia
Vivid e R6.x.x Console for India
Vivid e R6.x.x Console for SKD ECG
Vivid e R6.x.x Console for CKD Taiwan
1-1-6
Table 1-12 LOGIQ e Vet R6.x.x Model Designations
Part Number
5198415-2
5199518-2
Description
LOGIQ e Vet R6.x.x Console for EU
LOGIQ e Vet R6.x.x Console for USA
Purpose of Operator Manual(s)
The Operator Manual(s) should be fully read and understood before operating the LOGIQ e/LOGIQ e
Vet/LOGIQ i/Vivid e and also kept near the unit for quick reference.
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Section 1-2
Important Conventions
1-2-1 Conventions Used in Book
Icons
Pictures, or icons, are used wherever they reinforce the printed message. The icons, labels and conventions used on the product and in the service information are described in this chapter.
Safety Precaution Messages
Various levels of safety precaution messages may be found on the equipment and in the service information. The different levels of concern are identified by a flag word that precedes the precautionary message. Known or potential hazards are labeled in one of following ways:
DANGER
DANGER IS USED TO INDICATE THE PRESENCE OF A HAZARD THAT WILL
CAUSE SEVERE PERSONAL INJURY OR DEATH IF THE INSTRUCTIONS ARE
IGNORED.
WARNING IS USED TO INDICATE THE PRESENCE OF A HAZARD THAT CAN CAUSE
SEVERE PERSONAL INJURY AND PROPERTY DAMAGE IF INSTRUCTIONS ARE
IGNORED.
CAUTION
Caution is used to indicate the presence of a hazard that will or can cause minor personal injury and property damage if instructions are ignored.
NOTICE
Equipment Damage Possible
Notice is used when a hazard is present that can cause property damage but has absolutely no personal injury risk.
Example: Disk drive will crash.
NOTE: Notes provide important information about an item or a procedure.
Information contained in a NOTE can often save you time or effort.
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1-2-2 Standard Hazard Icons
Important information will always be preceded by the exclamation point contained within a triangle, as seen throughout this chapter. In addition to text, several different graphical icons (symbols) may be used to make you aware of specific types of hazards that could cause harm.
Table 1-13 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 1-14 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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1-2-3 Product Icons
The following table describes the purpose and location of safety labels and other important information provided on the equipment.
Table 1-15 Warnings
LABEL/SYMBOL
Identification and Rating Plate
PURPOSE/MEANING LOCATION
• Manufacture’s name and address
• Date of manufacture
• Model and serial numbers
• Electrical ratings (Volts, Amps, phase, and frequency)
Bottom panel of the console
Type/Class Label
IP Code (IPX1 or IPX8)
IPX1: FSU-2001
IPX8: MKF 2-MED GP26, FSU-1000
Used to indicate the degree of safety or protection.
Bottom panel of the adapter.
Indicates the degree of protection provided by the enclosure per IEC60
529. IPX1 cannot be used in operating room environment;
IPX8 can be used in operating room environment.
Bottom of Footswitch
Authorized European Representative address
Bottom panel
United States only Prescription
Requirement label
Bottom panel
Equipment Type BF (man in the box symbol) IEC 878-02-03 indicates B
Type equipment having a floating applied part.
Probe connectors
General Warning.
Various
“CAUTION - Dangerous voltage” (the lightning flash with arrowhead in equilateral triangle) is used to indicate electric shock hazards.
Various
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Table 1-15 Warnings
LABEL/SYMBOL PURPOSE/MEANING LOCATION
“Protective Earth” indicates the protective earth (grounding) terminal.
Inside of AC adapter
“ON” indicates the power on position of the power switch.
CAUTION
This Power Switch DOES NOT
ISOLATE Mains Supply
Stick to Power Switch
“TUV” Listing and Certification Mark is used to designate conformance to nationally recognized product safety standards. The Mark bears the name and /or logo of the testing laboratory, product category, safety standard is assessed and a control number.
Bottom panel of the console
Date of manufacture.
The date could be a year, year and month, or year, month and day, as appropriate. See ISO 8601 for date formates.
Rating Plate
Catalog or model number.
Rating Plate
Serial number Rating Plate
Direct Current.
For products to be powered from a DC supply.
Rating Plate
Input Rating Plate
For use with adapter model TWADP
100
Rating Plate
Description Rating Plate
Type CF Defib-Proof Applied Part (heart in the box with paddle) symbolis in accordance with IEC 60878-02-06.
ECG Module
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Table 1-15 Warnings
LABEL/SYMBOL PURPOSE/MEANING LOCATION
“Consult accompanying documents” is intended to alert the user to refer to the operator manual or other instructions when complete information cannot be provided on the label.
Various
Do not push the system.
Rear of Docking Cart and rear of
Isolation Cart.
This symbol indicates that the waste of electrical and electronic equipment must not be disposed as unsorted municipal waste and must be collected separately. Please contact an authorized representative of the manufacturer for information concerning the decommissioning of your equipment.
Rating Plate
When closing the LCD cover, use caution to avoid injuring hands or fingers as there is a closing mechanism which allows the LCD cover to automatically close.
Rating Plate
Indicates the product contains hazardous materials in excess of the limits established by Chinese standard
SJ/T11363-2006 Requirements for
Concentration Limits for Certain
Hazardous Substances in Electronic
Information Products. The number in the symbol is the Environment-friendly
Use Period (EFUP), which indicates the period during which the toxic or hazardous substances or elements contained in electronic information products will not leak or mutate under normal operating conditions so that the use of such electronic information products will not result in any severe environmental pollution, any bodily injury or damage to any assets.
Rear panel, rating plate
This product consists of devices that may contain mercury, which must be recycled or disposed of in accordance with local, state, or country laws. (Within this system, the backlight lamps in the monitor display contain mercury.)
Bottom panel of the console
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Table 1-15 Warnings
LABEL/SYMBOL PURPOSE/MEANING
The separate collection symbol is affixed to a battery, or its packaging, to advise you that the battery must be recycled or disposed of in accordance with local or country laws. The letters below the separate collection symbol indicate whether certain elements
(Pb=Lead, Cd=Cadmium, Hg=Mercury) are contained in the battery. To minimize potential effects on the environment and human health, it is important that all marked batteries that you remove from the product are properly recycled or disposed. For information on how the battery may be safely removed from the device, please consult the service manual or equipment instructions.
Information on the potential effects on the environment and human health of the substances used in batteries is available at this url: http:// www.gehealthcare.com/euen/weeerecycling/index.html
Battery Pack
LOCATION
No hazardous substance, above the maximum concentration value, is present. 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).
Do not connect the DVD-RW to the system while scanning.
DVD-RW
GOST Symbol. Russia Regulatory
Country Clearance.
Bottom
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Section 1-3
Safety Considerations
1-3-1
1-3-2
1-3-3
Introduction
The following safety precautions must be observed during all phases of operation, service and repair of this equipment. Failure to comply with these precautions or with specific warnings elsewhere in this manual, violates safety standards of design, manufacture and intended use of the equipment.
Human Safety
Operating personnel must not remove the system covers.
Servicing should be performed by authorized personnel only.
Only personnel who have participated in a LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e Training are authorized to service the equipment.
Mechanical Safety
Ultrasound probes are highly sensitive medical instruments that can easily be damaged by improper handling. Use care when handling and protect from damage when not in use. Do not use a damaged or defective probe. Failure to follow these precautions can result in serious injury and equipment damage.
Never use a probe that has fallen to the floor. Even if it looks ok, it may be damaged.
CAUTION
The LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e weights 4.6kg or more, depending on installed peripherals, when ready for use. To avoid possible injury and equipment damage:
ALWAYS:
• Use the handle to move the system.
• Do not let the system strike walls or door frame.
• Limit movement to a slow careful walk.
NOTE: Special care should be taken when transporting the unit in a vehicle:
• Before transporting, place the system in its special storage case.
• Ensure that the system is firmly secured while inside the vehicle.
• Secure system with straps or as directed otherwise to prevent motion during transport.
• Prevent vibration damage by driving cautiously. Avoid unpaved roads, excessive speeds, and erratic stops or starts.
1-3-4
1-3-5
Electrical Safety
To minimize shock hazard, the equipment chassis must be connected to an electrical ground. The system is equipped with a three-conductor AC power cable. This must be plugged into an approved electrical outlet with protective ground.
The power outlet used for this equipment should not be shared with other types of equipment.
Both the system power cable and the power connector meet international electrical standards.
Label Location
Please refer to Basic User Manual for label location information.
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1-3-6 Battery Safety
To avoid the risk of injury, follow the warning and cautions to make sure that the battery does not burst, ignite, or generate heat of fumes.
• The battery has a safety device. Do not disassemble or alter the battery.
• Charge and discharge the batteries only when the ambient temperature is between 10 and
40 C (50 F and 122 F).
• Do not short-circuit the battery by directly connecting the negative terminals with metal objects.
• Do not heat the battery or discard it in a fire.
• Do not expose the battery to temperature over 50
° C (122° F). Keep it away from fire and other
heat sources.
• Do not charge the battery near a heat source, such as a fire or heater.
• Do not leave the battery in direct sunlight.
• Do not drop packs from height to prevent them from possible malfunction damage.
• Do not pierce the battery with a sharp object, hit it, or step on it.
• Do not use a damaged battery.
• Do not solder a battery.
• Do not connect the battery to an electrical power outlet.
• Do not contact PCM ( Power Control and Monitor, it’s a small board in the battery) directly to prevent packs from ESD damage.
• In case of longer non-use of the LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e , please make sure the battery is removed.
CAUTION
To avoid the battery bursting, igniting, or fumes from the battery causing equipment damage, observe the following precautions:
• Do not immerse the battery in water or allow it to get wet.
• Do not put the battery into a microwave oven or pressurized container.
• If the battery leaks or emits an odor, remove it from all possible flammable sources.
• If the battery emits an odor or heat, is deformed or discolored, or in a way appears abnormal during use, recharging or storage, immediately remove it and stop using it. If you have any questions about the battery, consult GE or your local representative.
• Short term (less than one month) storage of battery pack:
•
Store the battery in a temperature range between 0
° C (32° F) and 50° C (122°F).
• Use only GE recognized batteries.
• In case of the long term (3 months or more) storage:
•
Store the battery in a temperature range of -20
° C (-4° F) and 45° C (113°F).
• When charging for the first time after long-term storage. Recover such packs to original performance through repeating several cycles of full charging and discharging.
• When store packs for more than 6 months, charge at lease once charging require per 6 months to prevent leakage and deterioration in performance due to selfdischarging.
• When the system isn't powered on continuously more than 6 months, in order to prevent leakage and deterioration in performance of CMOS battery, power on the system at least once per 6 months for more than 10 hours to have CMOS battery fully charged. Time and date need to be re-setup.
NOTICE
The battery shall be shipped in about 30% charged state. Those packs have to be fully charged and discharged up to 3 times to utilize Li-lon smart packs before use.
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1-3-7 Dangerous Procedure Warnings
Warnings, such as the examples below, precede potentially dangerous procedures throughout this manual. Instructions contained in the warnings must be followed.
DANGER
DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH, ARE PRESENT
IN THIS EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING
AND ADJUSTING.
1-3-8
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.
Lockout/Tagout (LOTO) requirements
Follow OSHA Lockout/Tagout requirements (USA) or local Lockout/Tagout requirements by ensuring you are in total control of the AC power plug at all times during the service process.
To apply Lockout/Tagout:
1.) Plan and prepare for shutdown.
2.) Shutdown the equipment.
3.) Isolate the equipment.
4.) Apply Lockout/Tagout Devices.
5.) Remove battery.
6.) Control all stored and residual energy.
7.) Verify isolation.
All potentially hazardous stored or residual energy is relieved.
Signed
NOTICE
TAG
&
LOCKOUT
Date
Energy Control and Power Lockout for LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e
WHEN SERVICING PARTS OF THE SYSTEM WHERE THERE IS EXPOSURE TO VOLTAGE
GREATER THAN 30 VOLTS:
1. TURN OFF THE SCANNER.
2. UNPLUG THE SYSTEM.
3. MAINTAIN CONTROL OF THE SYSTEM POWER PLUG.
4. WAIT FOR AT LEAST 20 SECONDS FOR CAPACITORS TO DISCHARGE AS THERE ARE NO
TEST POINTS TO VERIFY ISOLATION. THE AMBER LIGHT ON THE OP PANEL ON/OFF BUTTON
WILL TURN OFF.
5. REMOVE THE SYSTEM BATTERY.
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1-3-9 Returning/Shipping Probes and Repair Parts
Equipment being returned must be clean and free of blood and other infectious substances.
GEMS policy states that body fluids must be properly removed from any part or equipment prior to shipment. GEMS employees, as well as customers, are responsible for ensuring that parts/equipment have been properly decontaminated prior to shipment. Under no circumstance should a part or equipment with visible body fluids be taken or shipped from a clinic or site (for example, body coils or an ultrasound probe).
The purpose of the regulation is to protect employees in the transportation industry, as well as the people who will receive or open this package.
NOTE:
NOTE:
The US Department of Transportation (DOT) has ruled that “items that were saturated and/or dripping with human blood that are now caked with dried blood; or which were used or intended for use in patient care” are “regulated medical waste” for transportation purposes and must be transported as a hazardous material.
The USER/SERVICE staff should dispose all the waste properly as per federal, state, and local waste disposal regulation.
The ultrasound system is not meant to be long term storage of patient data or images. The user us responsible for the date on the system and a regular backup is highly recommended.
If the system is sent for repair, please ensure that any patient information is backup and erased from the system before shipping. It is always possible during system failure and repair to lose patient data.
GE is not responsible for the loss of this data.
If PHI (Patient Healthcare Information) data needs to be sent to GE employees for service purposes,
GE will ascertain agreement from the customer. The patient information shall only be transferred by approved service processes, tools and devices restricting access, protecting or encrypting data where required, and providing traceability in the form of paper or electronic documents at each stage of the procedure while maintaining compliance with cross-border restrictions of patient information transfers.
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Section 1-4
EMC, EMI, and ESD
1-4-1
1-4-2
NOTE:
1-4-3
Electromagnetic Compatibility (EMC)
Electromagnetic compatibility describes a level of performance of a device within its electromagnetic environment. This environment consists of the device itself and its surroundings including other equipment, power sources and persons with which the device must interface. Inadequate compatibility results when a susceptible device fails to perform as intended due interference from its environment or when the device produces unacceptable levels of emission to its environment. This interference is often referred to as radio–frequency or electromagnetic interference (RFI/EMI) and can be radiated through space or conducted over interconnecting power of signal cables. In addition to electromagnetic energy,
EMC also includes possible effects from electrical fields, magnetic fields, electrostatic discharge and disturbances in the electrical power supply.
CE Compliance
The LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e 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.
1-16 Section 1-4 - EMC, EMI, and ESD
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Section 1-5
Customer Assistance
1-5-1 Contact Information
If this equipment does not work as indicated in this service manual or in the User Manual, or if you require additional assistance, please contact the local distributor or appropriate support resource, as listed below.
Prepare the following information before you call:
-
-
System ID serial number.
Software version.
Table 1-16 Phone Numbers for Customer Assistance
Location
USA
GE Medical Systems
Ultrasound Service Engineering
9900 Innovation Drive
Wauwatosa, WI 53226
Service: On-site
Service: Parts
Applications support
Phone Number
1-800–437–1171
1-800-558-2040
1-800-682-5327 or 1-262-524-5698
Canada
Latin America
Service
Applications support
1-800-668-0732
1-800-321-7937
1-262-524-5698
Europe
GE Ultraschall Deutschland GmbH& Co. KG
BeethovenstraBe 239
Postfach 11 05 60, D-42665 Solingen
Germany
Asia (Singapore)
GE Ultrasound Asia
Service Department - Ultrasound
298 Tiong Bahru Road #15-01/06
Central Plaza
Singapore 169730
Japan Support Center
Phone: +33 (0)130-831-300 (General Imaging and Cardiac)
Fax: +49 (0)212-2802-431
Tel: +65 291-8528
Fax: +65 6291-7006
Phone: 81-42-648-2944
Fax: 81-42-648-2905
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1-5-2 System Manufacturer
Table 1-17 System Manufacturer
Manufacturer
GE Medical Systems (China) Co., Ltd.
No.19, Changjiang Road, Wuxi National Hi-Tech Dev. Zone, Jiangsu,
P.R.China 214028
Phone Number
TEL: +86 510-85225888
FAX: +86 510-85226688
1-5-3 Factory Sites
Table 1-18 Factory Sites
Manufacturer
GE Medical Systems (China) Co., Ltd.
No.19, Changjiang Road, Wuxi National Hi-Tech Dev. Zone, Jiangsu,
P.R.China 214028
GE Ultrasound Korea:
65-1, Sangdaewon-dong, Jungwon-gu, Seongnam-si, Gyeonggi-do,
Korea 462-120
GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC
DBA GE Healthcare
9900 Innovation Drive
Wauwatosa, WI 53226
U.S.A
Phone Number
TEL: +86 510-85225888
FAX: +86 510-85226688
TEL: +82-31-740-6112
FAX: +82-31-740-6435
TEL: (1) 800-437-1171
FAX: (1) 414-721-3865
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Chapter 2
Site preparations
Section 2-1
Overview
2-1-1
2-1-2
Purpose of this chapter 2
This chapter provides the information required to plan and prepare for the installation of a LOGIQ e/
LOGIQ e Vet/LOGIQ i/Vivid e . Included are descriptions of the facility and electrical needs to be met by the purchaser of the unit.
Chapter Contents
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
Chapter 2 Site preparations 2-1
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Section 2-2
General Console Requirements
2-2-1 Console Environmental Requirements
Table 2-2 Environmental Requirements for LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e Scanners
Operational Storage Transport
Temperature
Humidity
Pressure
10 - 40 degree C
30 - 75% non-condensing
700 - 1060hPa
-5 - 50 degree C
10 - 90% non-condensing
700 - 1060hPa
Temperatures in degree C, conversion to degree F =(degree C*(9/5) + 32)
-5 - 50 degree C
10 - 90% non-condensing
700 - 1060hPa
2-2-1-1
2-2-2
NOTE:
2-2-2-1
Lighting
Bright light is needed for system installation, updates and repairs. However, operator and patient comfort may be optimized if the room light is subdued and indirect. Therefore a combination lighting system (dim/bright) is recommended. Keep in mind that lighting controls and diameters can be a source of EMI which could degrade image quality. These controls should be selected to minimize possible interface.
Electrical Requirements
GE Medical Systems requires a dedicated power and ground for the proper operation of its
Ultrasound equipment. This dedicated power shall originate at the last distribution panel before the system.
Sites with a mains power system with defined Neutral and Live:
The dedicated line shall consist of one phase, a neutral (not shared with any other circuit), and a full size ground wire from the distribution panel to the Ultrasound outlet.
Sites with a mains power system without a defined Neutral:
The dedicated line shall consist of one phase (two lines), not shared with any other circuit, and a full size ground wire from the distribution panel to the Ultrasound outlet.
Please note that image artifacts can occur, if at any time within the facility, the ground from the main facility's incoming power source to the Ultrasound unit is only a conduit.
LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e Power Requirements
Table 2-3 Electrical Specifications for LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e
Adapter
TWADP100
Voltage
100-240 VAC
Power
130VA max.
Current
1.3 A (max.)
Frequency
50/ 60HZ
2-2 Section 2-2 - General Console Requirements
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2-2-2-2 Inrush Current
Inrush current is not a factor to consider due to the inrush current limiting properties of the power supplies.
Table 2-4 Inrush Current
Voltage
100V
240V
Console Only
0.38A
0.20A
Inrush Current
Console with all peripherals
0.41A
0.21A
2-2-2-3
2-2-2-4
2-2-2-5
2-2-2-6
Site Circuit Breaker
It is recommended that the branch circuit breaker for the machine be readily accessible.
Site Power Outlets
A dedicated AC power outlet must be within reach of the unit without extension cords. Other adequate outlets for the external peripherals, medical and test equipment needed to support this unit must also be present within 1 m (3.2 ft.) of the unit. Electrical installation must meet all current local, state, and national electrical codes.
Unit Power Plug
If the unit arrives without a power plug, or with the wrong plug, you must contact your GE dealer or the installation engineer must supply what is locally required.
Power Stability Requirements
Voltage drop-out
Max 10 ms.
Power Transients
(All applications)
Less than 25% of nominal peak voltage for less than 1 millisecond for any type of transient, including line frequency, synchronous, asynchronous, or aperiodic transients.
Chapter 2 Site preparations 2-3
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2-2-3 EMI Limitations
Ultrasound machines are susceptible to Electromagnetic Interference (EMI) from radio frequencies, magnetic fields, and transient in the air wiring. They also generate EMI. The LOGIQ e/LOGIQ e Vet/
LOGIQ i/Vivid e complies with limits as stated on the EMC label. However there is no guarantee that interface will not occur in a particular installation.
Possible EMI sources should be identified before the unit is installed.
Electrical and electronic equipment may produce EMI unintentionally as the result of defect.
These sources include:
• medical lasers,
• scanners,
• cauterizing guns,
• computers,
• monitors,
• fans,
• gel warmers,
• microwave ovens,
• light dimmers,
• portable phones.
The presence of a broadcast station or broadcast van may also cause interference.
See Table 2-5 for EMI Prevention tips.
Table 2-5 EMI Prevention/abatement
EMI Rule Details
Be aware of RF sources
Ground the unit
Replace all screws, RF gaskets, covers, cores
Replace broken RF gaskets
Keep the unit at least 5 meters or 15 feet away from other EMI sources. Special shielding may be required to eliminate interference problems caused by high frequency, high powered radio or video broadcast signals.
Poor grounding is the most likely reason a unit will have noisy images. Check grounding of the power cord and power outlet.
After you finish repairing or updating the system, replace all covers and tighten all screws.
Any cable with an external connection requires a magnet wrap at each end. Install the shield over the front of card cage. Loose or missing covers or RF gaskets allow radio frequencies to interfere with the ultrasound signals.
If more than 20% or a pair of the fingers on an RF gasket are broken, replace the gasket.
Do not turn on the unit until any loose metallic part is removed.
Do not place labels where RF gaskets touch metal
Never place a label where RF gaskets meet the unit. Otherwise, the gap created will permit
RF leakage. Or, if a label has been found in such a position, move the label.
Use GE specified harnesses and peripherals
The interconnect cables are grounded and require ferrite beads and other shielding. Also, cable length, material, and routing are all important; do not change from what is specified.
Take care with cellular phones Cellular phones may transmit a 5 V/m signal; that could cause image artifacts.
Properly dress peripheral cables
Do not allow cables to lie across the top of the card cage or hang out of the peripheral bays.
Loop the excess length for peripheral cables inside the peripheral bays. Attach the monitor cables to the frame.
2-4 Section 2-2 - General Console Requirements
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2-2-4 Scan Probe Environmental Requirements
Operation:10° to 40° C
Storage:-10° to 50° C
NOTE:
NOTE:
The recommended storage temperature range of 6Tc-RS is between 0°C and 45°C.
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.
Chapter 2 Site preparations 2-5
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Section 2-3
Facility Needs
2-3-1
2-3-1-1
NOTE:
Recommended Ultrasound Room Layout
Purchaser Responsibilities
The work and materials needed to prepare the site is the responsibility of the purchaser. Delay, confusion, and waste of manpower can be avoided by completing pre installation work before delivery.
User the Pre Installation checklist to verify that all needed steps have been taken,
Purchaser reasonability includes:
• Procuring the materials required.
• Completing the preparations before delivery of the ultrasound system.
• Paying the costs for any alternations and modifications not specifically provided in the sales contract.
All electrical installation that are preliminary to the positioning of the equipment at the site prepared for the equipment must be performed by licensed electrical contractors. Other connections between pieces of electrical equipment, products involved (and the accompanying electrical installations) are highly sophisticated and special engineering competence is required. All electrical work on these product must comply with the requirements of applicable electrical codes. The purchaser of GE equipment must only utilize qualified personnel to perform electrical servicing on the equipment.
The desire to use a non-listed or customer provided product or to place an approved product further from the system than the interface kit allows presents challenges to the installation team. To avoid delays during installation, such variances should be made known to the individuals or group performing the installation at the earliest possible date (preferable prior to purchase).
The ultrasound suite must be clean prior to delivery of the machine. Carpet is not recommended because it collects dust and creates static. Potential sources of EMI (electromagnetic interference) should also be investigated before delivery. Dirt, static, and EMI can negatively impact system.
2-6 Section 2-3 - Facility Needs
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2-3-2 Required Features
NOTE: GE Medical Systems requires a dedicated power and ground for the proper operation of its
Ultrasound equipment. This dedicated power shall originate at the last distribution panel before the system.
Sites with a mains power system with defined Neutral and Live:
The dedicated line shall consist of one phase, a neutral (not shared with any other circuit), and a full size ground wire from the distribution panel to the Ultrasound outlet.
Sites with a mains power system without a defined Neutral:
The dedicated line shall consist of one phase (two lines), not shared with any other circuit, and a full size ground wire from the distribution panel to the Ultrasound outlet.
Please note that image artifacts can occur, if at any time within the facility, the ground from the main facility's incoming power source to the Ultrasound unit is only a conduit.
• Dedicated single branch power outlet of adequate amperage meeting all local and national codes which is located less than 2.5 m (8 ft.) from the unit’s proposed location
• Door opening is at least 76 cm (30 in) wide
• Proposed location for unit is at least 0.2m (0.67 ft.) from the wall for cooling
• Power outlet and place for any external peripheral are within 2 m (6.5 ft.) of each other with peripheral within 1 m of the unit to connect cables.
• Power outlets for other medical equipment and gel warmer
• Power outlets for test equipment and modem within 1 m (3.2 ft.) of unit
• Clean and protected space to store transducers (in their cases or on a rack)
• Material to safely clean probes (done with a plastic container, never metal)
2-3-3 Desirable Features
• Door is at least 92 cm (3 ft.) wide
• Circuit breaker for dedicated power outlet is easily accessible
• Sink with hot and cold water
• Receptacle for bio–hazardous waste, like used probe sheaths
• Emergency oxygen supply
• Storage for linens and equipment
• Nearby waiting room, lavatory, and dressing room
• Dual level lighting (bright and dim)
• Lockable cabinet ordered by GE for its software and proprietary manuals.
Chapter 2 Site preparations 2-7
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2-3-3-1 Recommended and Alternate Ultrasound Room Layout
Recommended standard floor plan and a minimal floor plan for ultrasound equipment:
D E D IC AT E D
P O W E R
R E C EP TA C LE
18 IN.
(46 C M )
LINEN SUPPLY
C O NS O LE
FILM V IEW E R
C O UN T E R TO P
FOOT
S W
S TOO L
SIN K
SU C T IO N LINE
E M E R G E C Y
OX Y G EN
76 IN.
(193 C M )
24 IN.
(61 C M )
SE CR E TA R YS O R
D O C TO R ’S D ES K
O V E R H E A D
LIG H T S D IMM E R
P AT IEN T
TO ILET
D OO R
42 IN.
(107 C M )
A 14 by 17 foot R ecommended Floor Plan
S cale : Each square equals one square foot
LINEN SUPPLY
P R OB ES /SUPPLIES
FILM V IEW E R
FILM SUPPLIES
SIN K
E XT E R N A L
PE R IPH E R A LS
S TOO L
FOOT
S W
LO G IQ B oo k X P
C O NS O LE
D E D IC AT E D PO W E R
O U T LE T S
24 IN.
(61 C M )
E XAM INA R IO N
TAB LE
76 IN.
(193 C M )
D OO R
30 IN.
(76 C M )
A n 8 by 10 foot M inimal Floor Plan
G E C AB INE T
FOT SO FT W A R E
A N D MA NU A LS
Figure 2-1 RECOMMENDED ULTRASOUND ROOM LAYOUT
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
Stand Alone Scanner (without Network Connection)
None.
Scanner Connected to Hospital’s Network
Supported networks:
Wireless LAN
Purpose of DICOM Network Function
DICOM services provide the operator with clinically useful features for moving images and patient information over a hospital network. Examples of DICOM services include the transfer of images to workstations for viewing or transferring images to remote printers. As an added benefit, transferring images in this manner frees up the 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 e/LOGIQ e Vet/LOGIQ i/Vivid e 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 e/LOGIQ e Vet/
LOGIQ i/Vivid e .
• 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 e/LOGIQ e Vet/LOGIQ i/Vivid e 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.
Chapter 2 Site preparations 2-9
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2-3-4-4
.
DICOM Option Pre-installation Requirements (cont’d)
LOGIQ e/
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
.
.
.
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
Section 3-1
Overview
3-1-1 Purpose of Chapter 3
This chapter contains information needed to install the unit. Included are references to a procedure that describes how to receive and unpack the equipment and how to file a damage or loss claim.
How to prepare the facility and unit of the actual installation, and how to check and test the unit, probes, and external peripherals for electrical safety are included in this procedure. Also included in this section are guidelines for transporting the unit to a new site.
Table 3-1 Contents in Chapter 3
Section
3-1
3-6
3-7
3-8
3-9
3-2
3-3
3-4
3-5
3-10
3-11
Description
Overview
Receiving and Unpacking the Equipment
Packing the Equipment
Preparing for Installation
Completing the Installation
System Configuration
Software/Option Configuration
Connectivity Installation Worksheet
Loading Base Image Software
Software Version check out
Paperwork
Page Number
3-1
3-12
3-27
3-28
3-29
3-4
3-7
3-8
3-9
3-30
3-31
Chapter 3 System Setup 3-1
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3-1-2 Average Installation Time
Table 3-2 Average Installation Time
Description
Unpacking the scanner
Scanner wo/options
DICOM Option
Average Installation Time
20 minutes
30 minutes
30 minutes
Comments
Dependent on the configuration that is required
Dependent on the amount of configuration
The LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e installation and functional checkout will take approximately one hour. LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e consoles with optional equipment may take slightly longer.
3-2 Section 3-1 - Overview
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3-1-3 Installation Warnings
8.) There are no operator serviceable components. To prevent shock, do not remove any covers or panels. Should problems or malfunctions occur, unplug the power cord. Only qualified service personnel should carry out servicing.
NOTE: For information regarding packing labels, refer to LABELS ON PACKAGE.
9.) After being transported, the unit may be very cold or hot. If this is the case, allow the unit to acclimate before you turn it on. It requires one hour for each 2.5×C increment it's temperature is below 10×C or above 40×C.
DANGER
Equipment damage possibility. Turning the system on without acclimation after arriving at site may cause the system to be damaged.
Table 3-3 Time for Settlement
°C
60 55 50 45 40 35 30 25 20 15 10 5 0 -5 -10 -15 -20 -25 -30 -35 -40
°F
140 131 122 113 104 95 86 77 68 59 50 41 32 23 14 5 -4 -13 -22 -31 -40
hrs
8 6 4 2 0 0 0 0 0 0 0 2 4 6 8 10 12 14 16 18 20
3-1-4 Safety Reminders
DANGER
WHEN USING ANY TEST INSTRUMENT THAT IS CAPABLE OF OPENING THE
AC GROUND LINE (I.E., METER’S GROUND SWITCH IS OPEN), DON’T TOUCH
THE UNIT!
CAUTION
If the unit is very cold or hot, do not turn on its power until it has had a chance to acclimate to its operating environment.
DANGER
To prevent electrical shock, connect the unit to a properly grounded power outlet. Do not use a three to two prong adapter. This defeats safety grounding.
DANGER
Do not operate this unit unless all board covers are securely in place.
DANGER
OPERATOR MANUAL(S)
The User Manual(s) should be fully read and understood before operating the LOGIQ e/LOGIQ e
Vet/LOGIQ i/Vivid e and kept near the unit for quick reference.
DANGER
ACOUSTIC OUTPUT HAZARD
Although the ultrasound energy transmitted from the LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e probe is within FDA limits, avoid unnecessary exposure. Ultrasound energy can produce heat and mechanical damage
Chapter 3 System Setup 3-3
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Section 3-2
Receiving and Unpacking the Equipment
When a new system arrives, check that any components are not damaged and are not in short supply.
If shipping damage or shortage occurs, contact the address shown in Chapter 1.
1.) Cut the four PLASTIC BANDs.
2.) Cut the adhesive tape and open top covers of paper carton.
Adhesive tape
Plastic Bands
1
2
Figure 3-1 Open top covers of paper carton.
3-4 Section 3-2 - Receiving and Unpacking the Equipment
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Section 3-2 Receiving and Unpacking the Equipment
(cont’d)
3.) Take out the Paper pad.
4.) Take out console together with 2 interleavers from console package.
5.) Take out the interleavers beside Accessories Package.
6.) Take out Accessories Package.
Paper Pad
Console and interleavers
Console Package
Accessories Package
Figure 3-2 Unpacking the equipment
CAUTION
Do not lift the unit by the rubber band. Equipment damage may result.
Chapter 3 System Setup 3-5
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Section 3-2 Receiving and Unpacking the Equipment
(cont’d)
7.) Remove 2 interleavers.
8.) Remove plastic bag.
Interleaver
Console
Figure 3-3 Removing interleavers and plastic bag
Interleaver
3-6 Section 3-2 - Receiving and Unpacking the Equipment
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Section 3-2 Receiving and Unpacking the Equipment
(cont’d)
NOTE: Check the shipping container for special instructions. Verify that the container is intact. In some cases a secondary container may be used. If so, ask the carrier for unpacking instructions.
Figure 3-4 Labels on Package
CAUTION
Please carefully unpack the system, and do not dispose the package of LOGIQ e/LOGIQ e Vet/
LOGIQ i/Vivid e , so that it can be reused for service.
3-2-1
CAUTION
Moving into Position
Do not lift the unit by the rubber band. Use handle to move system.
CAUTION
Equipment Damage Possibility. Lifting the console by holding covers may damage the covers.
Do not lift the console by holding any covers.
In general, a single adult can move the LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e . Before moving, store all loose parts in original accessory box or in back pack. Return probes to original box.
Section 3-3
Packing the Equipment
Please pack LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e in the reverse order of unpacking.
Chapter 3 System Setup 3-7
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Section 3-4
Preparing for Installation
3-4-1
3-4-2
3-4-2-1
3-4-3
Verify Customer Order
Compare items received by the customer to that which is listed on the delivery order. Report any items that are missing, back ordered or damaged.
Physical Inspection
System Voltage Settings
• Verify that the scanner is set to the correct voltage. The Voltage settings for the LOGIQ e/LOGIQ e
Vet/LOGIQ i/Vivid e Scanner is found on a label located on the AC adapter.
• 220-240VAC(China); 100-120VAC(USA/Japan); 220-240VAC(Europe, Latin America).
Connecting a LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e scanner to the wrong voltage level will most likely destroy the scanner.
EMI Protection
This Unit has been designed to minimize the effects of Electro Magnetic Interference (EMI). Many of the covers, shields, and screws are provided primarily to protect the system from image artifacts caused by this interference. For this reason, it is imperative that all covers and hardware are installed and secured before the unit is put into operation.
3-8 Section 3-4 - Preparing for Installation
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Section 3-5
Completing the Installation
3-5-1
NOTE:
3-5-1-1
Power On / Boot Up
After turning off a system, wait at least ten seconds before turning it on again. The system may not be able to boot if power is recycled too quickly.
Scanner Power On
Lower the handle. Plug the AC adapter output connector into the system DC input port (located on the system’s rear panel) with the arrow side upward. Plug the AC adapter power cord into a grounded, protective earth outlet.
UP UP
Figure 3-5 Connect AC adapter
When power is applied to the scanner, power is distributed to the Cooling Unit, Control Panel, LCD,
Peripherals and the Back-end Processor.
Chapter 3 System Setup 3-9
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3-5-1-2 Turn on the system
Press the Power On/Off switch at the front of the system once.
Power On/Off switch
3-5-2
NOTE:
3-5-2-1
Figure 3-6 Power On/Off Switch
When the Power On/Off switch on the Control Panel is pressed once, the Back-end Processor starts and the software code is distributed to initiate the 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.
2.) The System-Exit window is displayed.
3-10
Figure 3-7 System Exit Window
3.) Using the Trackball or Select key, select Shutdown.
4.) The shutdown process takes a few seconds and is complete when the power status LED is turned off.
5.) Disconnect the probes.Clean or disinfect all probes as necessary. Store them in their shipping cases to avoid damage.
6.) Close LCD cover.
Section 3-5 - Completing the Installation
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3-5-2-2 Scanner Shutdown
Disconnect the Mains Power Cable if necessary. For example: Relocating the scanner.
3-5-3
NOTE:
Transducer Connection
1.) Carefully open the system LCD display, plug the probe connector into the probe port, then lock the probe latch upward.
Please ensure that the probe latch is in an unlocked position before you connect the probe to the system.
Probe Latch
NOTE:
Figure 3-8 Connect the probe
It is not necessary to turn OFF power to connect or disconnect a probe.
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Section 3-6
System Configuration
3-6-1
3-6-1-1
System Specifications
Physical Dimensions
The physical dimensions of the LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e console are summarized in
Figure 3-9 on page 3-12 .
Table 3-4 Physical Dimensions of LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e
Height
Console
Only
Console with handle
61
2.4
100
3.9
Width
Console
Only
Console with handle
Depth
Console Only
Console with handle
340
13.4
375
14.8
287
11.3
337
13.3
Unit
Unit
mm inches
WEIGHT: 4.6KG
NOTE: Length is in mm
3-6-2
Figure 3-9 Overall Dimensions
Electrical Specifications
Table 3-5 Electrical Specifications for LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e
Adapter
TWADP100
Voltage
100-240 VAC
Tolerances
+/-10%
Current
1.3A (max)
Frequency
50/60Hz
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3-6-3 Approved peripherals
Table 3-6 Approved on-board peripherals
Device
B/W Printer
Digital Color Printer
HP Color Printer
DVD-RW
Wireless Lan Adapter
3-pedal footswitch
1-pedal footswitch
1-pedal footswitch
USB Memory
USB HUB
ECG
USB HDD
DVD-Recorder
Video Transfer
BarCode Reader*
Manufacturer
LITEON
NetGear
NetGear
Linksys
Steute
Whanam
Whanam
SanDisk
SanDisk
SONY
SONY
SONY
HP
HP
HP
LITEON
LITEON
SanDisk
Shenzhen Gaojian
Shenzhen Gaojian
NORAV
Seagate
Seagate
Seagate
Panasonic
Pinnacle
Handheld
Handheld
Model
UP-D897
UP-D23MD
UP-D25MD
HP Officejet Pro K5400
HP Officejet Pro K8600
HP Deskjet 470
LITEON DX-20A4P
LITEON Model eHAU 120
LITEON Model eHAU 324
WN111V2
WG111V3
Linksys WUSB54G
MKF 2-MED GP26
FSU2001
FSU-1000
CRUZER 2G
CRUZER 4G
CRUZER 4G with U3
Application
HE 702A
HE420GE
ECG-USB1
USB HDD 80G
USB HDD 250G
USB HDD 500G
MD-800E
MD-800U
Interface
USB
USB
USB
USB
USB
USB
USB
USB
USB
USB
USB
USB
USB
USB
USB
USB
USB
USB
USB
USB
USB
USB
USB
USB
USB
Remark
Only supported by LOGIQ e R6.x.x and LOGIQ e R7.x.x.
Not supported by LOGIQ e R4.x.x,
LOGIQ e R6.x.x, Vivid e R4.x.x,
LOGIQ i R4.x.x
Pinnacle Video Transfer -
8230-10022-11
USB
Not supported by LOGIQ e R5.0.x,
LOGIQ e Vet R5.0.x, Vivid e
R5.0.x, LOGIQ i R5.0.x
Handheld 3800G
Handheld 4600G
USB
USB
Only supported by LOGIQ e R5.2.x,
R6.x.x, R7.x.x, LOGIQ e Vet 6.x.x
NOTE:
NOTE:
For detailed installation information and connection procedures, please refer to Peripheral
Installation manual.
BarCode Reader* is supported by LOGIQ e Software version R5.2.x, R6.x.x only.
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3-6-4 Connecting Cables
Equipment damage possibility. Be sure to use the following recommended connecting cables to connect recording devices and a network with LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e console.
Table 3-7 List of Connecting Cables
Name Part No.
Figure NOTE
USB Cable 5122305
For USB Printer & USB DVD-RW
3-6-5
3-6-5-1
Peripherals/Accessories Connector Panel
LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e peripherals and accessories can be properly connected using the side connector panel.
Rear Panel Connector
Located on the rear panel are video input and output connectors, power connector and ethernet port.
1
2
Figure 3-10 Rear Connector Panel
3
1.) Port for DC input (AC Adapter)
2.) Docking Connector
3.) SVGA Output
4.) Ethernet port
4
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3-6-5-2 Left Panel Connector
Located on the left side panel are two USB Ports for control connections for printer, service tools and earphone port.
1
2
NOTE:
Figure 3-11 Left Side Panel
1.) Two interchangeable USB Port (Digital Printers, DVD-RW and/or FootSwitch, etc)
2.) Earphone Port.
Each outer (case) ground line of peripheral/accessory connectors are protectively grounded.
Signal ground lines are not isolated.
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3-6-5-3 This section indicates the pin assignment for each connector.
1. Pin Assignment of DC input
Connector: 4 Pin, Female
Table 3-8 Pin Assignments of DC input
Pin No.
1
2
Signal
+20V
+20V
Pin No.
3
4
2. Pin Assignment of USB
Table 3-9 Pin assignment of USB1
Signal
GND
GND
Pin No.
1
2
Pin No.
1
2
Signal
+5VDC
DATA-
Signal
+5VDC
DATA-
Pin No.
3
4
Table 3-10 Pin assignment of USB2
Pin No.
3
4
Signal
DATA+
GND
Signal
DATA+
GND
3-16
3. Pin assignment of RS232C for external VGA
Connector: D-SUB, 15Pin, Female
Table 3-11 Pin Assignments of RS232C for External VGA
Pin No.
7
8
5
6
3
4
1
2
Signal
RED
GREEN
BLUE
N/A
GND
RGND
GGND
BGND
Pin No.
13
14
15
16
9
10
11
12
Signal
N/A
SGND
N/A
N/A
HSYNC
VSYNC
N/A
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3-6-5-4 Connect peripherals
A.) Connect B/W printer to the system.
B/W Printer can be properly connected using USB Port1 or USB Port 2 ( Figure 3-12 on page 3-17 ).
Figure 3-12 Connect B/W printer to the system
B.) Connect UP-D23MD color printer to the system.
UP-D23MD Color Printer can be properly connected using USB Port1 or USB Port 2 ( Figure 3-13 on page 3-17 ).
Figure 3-13 Connect digital color printer to the system
NOTICE
HP Deskjet 470 /HP Officejet Pro K5400 Color Printer must connect with PIT (Printer Isolation
Transformer) when being used.
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3-6-5-4
Connect peripherals (cont’d)
C.) Connect DVD-RW to the system.
DVD-RW can be properly connected using USB Port1 or USB Port2 ( Figure 3-14 on page 3-18 ).
3-18
Figure 3-14 Connect DVD-RW to the system
CAUTION
DO NOT connect DVD-RW to the system while scanning.
LITEON DVD-RW drive recommended media list
Media issues are common throughout the DVD-RW drive industry. Because DVD media vendors often change disc suppliers, quality levels may change due to manufacturing differences. This means that you may encounter DVD/CD creation problems with media that may have worked successfully before.
Overall system configuration and other factors may also affect the success of creating a DVD/CD.
The following media types have been tested. LITEON highly recommends that you use the media types on this list when creating your DVDs/CDs.
Not all brands of media have been tested and, therefore, you may encounter success with other brands not listed. This list will be updated as other media is tested and approved.
Table 3-12 LITEON DVD-RW drive recommended media list
Brand Name
SONY
SONY
SONY
Mitsubishi
Mitsubishi
Mitsubishi
Mitsubishi
JVC
MBI
MBI
Taiyo Yuden
Taiyo Yuden
Type
DVD-R
CD-R
DVD-RW
CD-R
CD-RW
DVD-R
DVD-RW
DVD-R
CD-R
DVD-R
CD-R
DVD-R
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3-6-5-4
Connect peripherals (cont’d)
D.) Connect FootSwitch to the system.
FootSwitch can be properly connected using USB Port1 or USB Port2.
1-pedal footswitch
3-pedal footswitch
Figure 3-15 Connect Foot Switch to the system
E.) Connect Wireless LAN Adapter to the system.
Wireless LAN Adapter can be properly connected using USB port.
Wireless Lan
Adapter
Figure 3-16 Connect Wireless LAN Adapter to the system
F.) Connect the CRT to the system.
CRT can be properly connected using the SVGA output.
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3-6-5-4
Connect peripherals (cont’d)
G.) Connect the USB Memory to the system. The USB Memory can be properly connected using USB port 1 or 2.
Figure 3-17 USB Memory Connection
H.) Connect the ECG to the system. ECG can be properly connected using USB port 1 or 2.
Figure 3-18 ECG
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3-6-5-4
Connect peripherals (cont’d)
I.) Connect the USB HDD to the system. The USB Harddisk can be properly connected using USB port 1 and 2.
Figure 3-19 Emergency Disk Connection
J.) Connect the BarCode Reader to the system, the BarCode Reader can be properly connected via
USB port 1 or 2.
Figure 3-20 BarCode Reader Connection
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3-6-5-4
Connect peripherals (cont’d)
K.) Connect the Sandisk U3 USB Flash Drive to the system. The Sandisk U3 USB Flash Drive can be properly connected using USB port 1 and 2.
NOTE:
NOTE:
Figure 3-21 Sandisk U3 USB Flash Drive Connection
The Password of the Sandisk U3 USB Flash Drive is Predefined.
The Sandisk U3 USB Flash Drive is only available on LOGIQ e R6.x.x and LOGIQ e R7.x.x.
Connect the security enabled Sandisk U3 USB Flash Drive into the system, input the password in the pop-up dialog. Click OK to login, click Cancel to cancel.
Figure 3-22 Input the password
The Sandisk U3 USB Flash Drive can be used if the right password is entered. An error message will display if the wrong password is entered.
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3-6-5-4
Connect peripherals (cont’d)
Figure 3-23 Wrong password error
Click OK, input the password again.
The Sandisk U3 USB Flash Drive will be locked if reaching the maximum number of failed password attempts.
NOTE:
Figure 3-24 Sandisk U3 USB Flash Drive locked
Please refer to the operation manual of each peripheral for information needed by the user to operate the system safely.
For detailed installation information, please refer to the LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e
Peripheral Installation Instruction manual.
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3-6-5-4
Connect peripherals (cont’d)
L.) Connect the external monitor to the system. The monitor can be properly connected using the VGA port.
Figure 3-25 VGA Connection
Press Ctrl+Alt+V on the keyboard, a dialog box appears.
For LOGIQ e R5.x.x, R6.x.x, R7.x.x, LOGIQ i R5.x.x,
Vivid e R5.x.x/R6.x.x
For LOGIQ e R4.x.x, LOGIQ i R4.x.x, Vivid e R4.x.x
Figure 3-26 Graphics Controller Properties
NOTE:
NOTE:
Select Intel(R) Dual Display Clone; check the Same display configuration driver on both display box and select OK.
Please refer to the operation manual of each peripheral for information needed by the user to operate the system safely.
For LOGIQ e R5.2.x, R6.x.x, R7.x.x, the default set is dual, it will not pop up Figure 3-26 .
For detailed installation information, please refer to the LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e
Peripheral Installation manual.
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3-6-6 Available Probes
See in specification in the LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e User Reference Manual for Probes and intended use.
For LOGIQ e R4.0.x, the system supports 4C-RS, E8C-RS, 8C-RS, i12L-RS, 8L-RS, 3S-RS, 12L-RS
Probes.
For LOGIQ e R5.0.x, the system supports 4C-RS, E8C-RS, 8C-RS, i12L-RS, 8L-RS, 3S-RS, 12L-RS, i/t739-RS, 9L-RS Probes.
For LOGIQ e R5.2.x, the system supports 4C-RS, E8C-RS, 8C-RS, i12L-RS, 8L-RS, 3S-RS, 12L-RS, i/t739-RS, 9L-RS, 16L-RS Probes.
For LOGIQ e R6.x.x, the system supports 4C-RS, E8C-RS, 8C-RS, i12L-RS, 8L-RS, 3S-RS, 12L-RS, i/t739-RS, 9L-RS, 16L-RS, 6Tc-RS, 6S-RS Probes.
For LOGIQ e R7.x.x, the system supports 4C-RS, E8C-RS, 8C-RS, i12L-RS, 8L-RS, 3S-RS, 12L-RS, i/t739-RS, 9L-RS, 16L-RS, 6Tc-RS, 6S-RS, L8-18i-RS,P2D Probes.
For LOGIQ i R4.x.x, the system supports 4C-RS, E8C-RS, 8C-RS, i12L-RS, 8L-RS, 3S-RS, 12L-RS
Probes.
For LOGIQ i R5.x.x, the system supports 4C-RS, E8C-RS, 8C-RS, i12L-RS, 8L-RS, 3S-RS, 6S-RS,
12L-RS, i/t739-RS, P2D, 9L-RS Probes.
For Vivid e R4.x.x, the system supports 4C-RS, i12L-RS, 8L-RS, 3S-RS Probes.
For Vivid e R5.0.x, the system supports 4C-RS, i12L-RS, 8L-RS, 3S-RS, 8C-RS, 9L-RS, P2D Probes.
For Vivid e R5.2.x, the system supports 4C-RS, 8C-RS, E8C-RS, 8L-RS, 9L-RS, 12L-RS, i12L-RS, 3S-
RS, 6S-RS, P2D Probes.
For Vivid e R6.x.x, the system supports 4C-RS, 8C-RS, E8C-RS, 8L-RS, 9L-RS, 12L-RS, i12L-RS, 3S-
RS, 6S-RS, P2D, 6Tc-RS Probes.
For LOGIQ e Vet R5.0.x, the system supports 4C-RS Vet, E8C-RS Vet, 8C-RS Vet, i12L-RS Vet, 8L-
RS Vet, 3S-RS Vet, 12L-RS Vet, 9L-RS Vet, i739-RS LC, 6S Vet-RS
For LOGIQ e Vet R5.2.x, the system supports 4C-RS Vet, E8C-RS Vet, 8C-RS Vet, i12L-RS Vet, 8L-
RS Vet, 3S-RS Vet, 12L-RS Vet, 9L-RS Vet
For LOGIQ e Vet R6.x.x, the system supports 4C-RS Vet, E8C-RS Vet, 8C-RS Vet, i12L-RS Vet, 8L-
RS Vet, 3S-RS Vet, 12L-RS Vet, 9L-RS Vet, 6S Vet-RS, i739-RS-LC, 6Tc-RS Vet
NOTE: 16L-RS is not available in China.
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3-6-6 Available Probes
(cont’d)
Table 3-13 List of Probes for LOGIQ e/LOGIQ i/Vivid e
Probe Name Material of Headshell
4C-RS
E8C-RS
NORYL
VALOX
Area of Using TYPE
GENERAL PURPOSE CONVEX
TRANSVAGINAL TRANSRECTAL MICRO-CONVEX
8C-RS i12L-RS
8L-RS
3S-RS
12L-RS
9L-RS i739-RS t739-RS
P2D
6S-RS
16L-RS
6Tc-RS
VALOX
ABS (GE)
VALOX
VALOX
NORYL
VALOX
VALOX
VALOX
VALOX
VALOX
VALOX
VETERINARY
PEDIATRIC NEONATAL
MICRO-CONVEX
INTRAOPERATIVE SMALL PARTS
VASCULAR PEDIATRICS
SMALL PARTS
PERIPHERAL VASCULAR
CARDIOLOGY
TRANSVAGINAL ABDOMEN
SMALL PARTS
PERIPHERAL VASCULAR
SMALL PATS VASCULAR
INTRAOPERATIVE
INTRAOPERATIVE
CARDIOLOGY
CARDIOLOGY PEDIATRICS
SMALL PARTS
PERIPHERAL VASCULAR
TRANSESOPHAGEAL FOR ADULT
LINEAR
LINEAR
SECTOR
LINEAR
LINEAR
LINEAR
LINEAR
Non-Imaging CW
SECTOR
LINEAR
SECTOR
Catalog Number Part Number
H4000SR
H40402LN
5131629
2290777
H40402LS
H40402LW
H40402LT
H4000PD
H40402LY
H40442LL
H40402LJ
H40412LP
H45551CA
H45021RP
H40452LJ
H45551ZE
2354971
2377942
2376127
2355686
5154514
5213143
2404995
2404999
KE100003
47236956
5317271
KN100104
NOTE: 16L-RS is not available in China.
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3-6-6 Available Probes
(cont’d)
Table 3-14 List of Probes for LOGIQ e Vet
Probe Name Material of Headshell
4C-RS Vet NORYL
E8C-RS Vet
8C-RS Vet i12L-RS Vet
8L-RS Vet
3S-RS Vet
12L-RS Vet
9L-RS Vet i739-RS-LC
6SVet-RS
6Tc-RS Vet
VALOX
VALOX
ABS (GE)
VALOX
VALOX
NORYL
VALOX
VALOX
VALOX
VALOX
Area of Using
GENERAL PURPOSE
TRANSVAGINAL
TRANSRECTAL
VETERINARY
PEDIATRIC
NEONATAL
INTRAOPERATIVE SMALL
PARTS VASCULAR
PEDIATRICS
SMALL PARTS
PERIPHERAL VASCULAR
CARDIOLOGY
TRANSVAGINAL
ABDOMEN
SMALL PARTS
PERIPHERAL VASCULAR
SMALL PARTS VASCULAR
INTRAOPERATIVE
CARDIOLOGY
PEDIATRICS
TRANSVAGINAL FOR
ADULT
TYPE
CONVEX
MICRO-CONVEX
MICRO-CONVEX
LINEAR
LINEAR
SECTOR
LINEAR
LINEAR
LINEAR
SECTOR
SECTOR
Catalog Number Part Number
H40442LY 5198378
H41562LL
H41562LK
H41562LN
H41562LM
H41562LR
H40442LZ
H40442LW
H41482LS
H40452L
H48922LB
5134643
5134642
5134645
5134644
5134647
5212304
5220453
5136420
5198571
5430790
NOTE: i739-RS-LC , 6SVet-RS and 6Tc-RS Vet probes are only availble for R6.x.x.
Section 3-7
Software/Option Configuration
Refer to the LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e 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 e/LOGIQ e Vet/LOGIQ i/Vivid e
Basic User Manual, Chapter 16, Customizing Your System.
For information on configuring DICOM Connectivity, Refer to the LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e 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:
Comments:
CONTACT INFORMATION
Name Title
Phone E-Mail Address
TCP/IP Settings
Name - AE Title:
IP Settings
IP Address:
Subnet Mask:
Default Gateway:
Remote Archive Setup
Remote Archive IP:
Remote Archive Name:
Services (Destination Devices)
Manufacturer
7
8
5
6
3
4
1
2
9
10
11
12
Device Type
Name
3-28
IP Address Port
Section 3-8 - Connectivity Installation Worksheet
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Section 3-9
Loading Base Image Software
This information has been moved, please refer to:
Section 8-3 "Loading Base Image Software" on page 8-4
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Section 3-10Software Version check out
3-10-1 Functional Check-out
1.) Power on LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e scanner and wait until system booting to main screen.
2.) Press Utility/Config key on control panel.
3.) Choose the About button on the right.
Figure 3-27 About
4.) Check whether "Software version" is the right version for use.
3-30
Figure 3-28 Software version
Section 3-10 - Software Version check out
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Section 3-11
Paperwork
NOTE:
3-11-1
NOTE:
During and after installation, the documentation (i.e. User Manuals, Installation Manuals...) for the peripheral units must be kept as part of the original system documentation. This will ensure that all relevant safety and user information is available during the operation and service of the complete system.
Product Locator Installation
The Product Locator Installation Card shown may not be same as the provided Product Locator card.
3-11-2
Figure 3-29 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.
Chapter 3 System Setup 3-31
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3-32 Section 3-11 - Paperwork
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Chapter 4
Functional Checks
Section 4-1
Overview
4-1-1 Purpose for Chapter 4
This chapter provides procedures for quickly checking major functions of the LOGIQ e/LOGIQ e Vet/
LOGIQ i/Vivid e console, diagnostics by using the built-in service software, and power supply adjustments.
Table 4-1 Contents in chapter 4
Section
4-1
4-2
4-3
4-4
4-5
Overview
Required Equipment
General Procedure
Software Configuration Checks
Peripheral Checks
Description Page Number
4-1
4-1
4-2
4-37
4-37
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
CAUTION
SYSTEM REQUIRES ALL COVERS
Operate this unit only when all board covers and frame panels are securely in place. The covers are required for safe operation, good system performance and cooling purposes.
NOTICE
Lockout/Tagout Requirements (For USA only)
Follow OSHA Lockout/Tagout requirements by ensuring you are in total control of the Power Cable on the system.
TAG
&
LOCKOUT
Signed Date
4-3-1
4-3-1-1
Power On/Boot Up
After AC/DC is connected correctly to the scanner, the power is applied to the scanner. When the
Control panel Power On/Off key is pressed once, the System starts.
Scanner Power On
Lower the handle. Plug the AC adapter output connector into the system DC input port (located on the system’s rear panel) with the arrow side upward. Plug the AC adapter power cord into a grounded, protective earth outlet.
4-2
UP UP
Figure 4-30 connect AC adapter
Section 4-3 - General Procedure
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4-3-1-1
Scanner Power On (cont’d)
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.
Power On/Off switch
4-3-2
NOTE:
4-3-2-1
Figure 4-31 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.
2.) The System-Exit window is displayed.
Figure 4-1 System Exit Window
3.) Using the Trackball or Select key, select Shutdown.
Chapter 4 Functional Checks 4-3
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4-3-2-1
Back-end Processor Power Down (cont’d)
4.) The shutdown process takes 15 seconds and the power off sequence is complete when the power status LED is turned off.
5.) Disconnect the probes.Clean or disinfect all probes as necessary. Store them in their shipping cases to avoid damage.
6.) Close LCD cover.
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.
4-3-2-3
NOTE:
Full Maintenance Reboot
Full Maintenance Reboot will fully restart the whole system for performance improvement.
It’s recommended to do Full Maintenance Reboot at least daily or when system starts to slow down or lag in its reaction.
1.) Press the Power On/Off switch at the front of the system once.
2.) Click “Full Maintenance Reboot”.
3.) Full Maintenance Reboot dialog is displayed.
4-4
4-3-2-4
Figure 4-2 “Full Maintenance Reboot” dialog
Exit (only activated for LOGIQ e R6.0.2)
Exit will reboot application.
1.) Press the Power On/Off switch at the front of the system once.
2.) Click “Exit”.
3.) The application will reboot.
Section 4-3 - General Procedure
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4-3-3 Archiving and Loading Presets
NOTE: Always save presets before any software reload. This ensures the presets loaded after the software reload are as up–to–date as possible.
All user presets except changes to Summary, Anatomy, and Biometry pages, can be saved on an DVD-
R disk (or USB memory device) for reloading on the system.
NOTICE
Presets should NOT be saved on the same DVD-R disk (or USB memory device) as images. The
Archive Menu lists the images but does NOT list the presets stored on a DVD-R disk (or USB memory device).
4-3-3-1 Archiving Presets to an DVD-R Disk (or USB memory device)
1.) Insert an empty (blank) DVD-R disk into the DVD-RW.
2.) Access to the Utility/Config Menu, and select System. The Backup sheet will be shown on the LCD display.
Figure 4-3 Backup Sheet
3.) Select the item to Backup/Restore.
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.
Chapter 4 Functional Checks 4-5
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4-3-3-2 Loading Presets from an DVD-R disk (or USB memory device)
1.) Insert the DVD-R disk with the archived Presets into the DVD-RW.
2.) Access to the Utility/Config Menu, and select System. The Restore sheet will be shown on the LCD display. (see Figure 4-3 on page 4-5 )
3.) Select the item to restore either from Resource Files.
4.) Enter restore destination or browse through the disk to locate the destination.
5.) Select Restore. The restore status for each item is displayed on the Result column.
4-3-4
4-3-5
Adjusting the Display Monitor
Please refer to Section 6-2 "Monitor Adjustments" on page 6-2 .
Lockout/Tagout (LOTO) requirements
Follow OSHA Lockout/Tagout requirements (USA) or local Lockout/Tagout requirements by ensuring you are in total control of the AC power plug at all times during the service process.
To apply Lockout/Tagout:
1.) Plan and prepare for shutdown.
2.) Shutdown the equipment.
3.) Isolate the equipment.
4.) Apply Lockout/Tagout Devices.
5.) Remove battery.
6.) Control all stored and residual energy.
7.) Verify isolation.
All potentially hazardous stored or residual energy is relieved.
Signed
NOTICE
TAG
&
LOCKOUT
Date
Energy Control and Power Lockout for LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e
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.
4-6 Section 4-3 - General Procedure
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4-3-6 System Features
4-3-6-1 Control Panel
1
11
5 3
6
2
4
Figure 4-4 Control Panel Tour
1.) TGC
2.) New Patient
3.) End Exam
4.) Mode/Gain/Auto Keys
5.) Preset Key
6.) Imaging/Measurement Keys
7.) Depth/Zoom/Ellipse
8.) Image Keys
9.) Print Keys
10.)Freeze
11.)Keyboard
Chapter 4 Functional Checks
7
8
9
10
4-7
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4-3-6-2 LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e SoftMenu Key Tour
In general, there are two types of softMenu keys: Paddle Switch and adjustable knobs.
2
3
Figure 4-5 SoftMenu Key Tour
1.) The Paddle Switch is used to access and adjust the Sub SoftMenu.
2.) Press the adjustable knobs to toggle option menu between line one and line two.
3.) Rotate the adjustable knobs to adjust the corresponding parameters.
1
4-8 Section 4-3 - General Procedure
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4-3-6-3 Monitor Display
1 2 3
4
12
5
6
13
7
8
9
10
14
15
17
16
18
11
20 21
19 22
23
24
Figure 4-6 Monitor Display Tour
Table 4-2 Monitor Display Features
1. Institution/Hospital Name, Date, Time, Operator
Identification, system status (real-time of frozen).
2. Patient Name, Patient Identification.
3. Acoustic Output Readout,
4. GE Symbol: Probe Orientation Marker. Coincides with a probe orientation marking on the probe.
5. Image Preview.
6. Gray/Color Bar.
7. Cine Gauge.
8. Measurement Summary Window.
9. Image.
10. Measurement.
11. Results Window.
12. Probe Identifier. Exam Study.
13. Imaging Parameters by Mode (current mode highlighted).
14. Focal Zone.
15. TGC (not shown on the image).
16. Body Pattern.
17. Depth Scale.
18. SoftMenu
19. Caps Lock: On/Off.
20. Start menu icon.
21. Battery icon.
22. Network icon.
23. Trackball Functionality Status: Scroll, M&A (Measurement and Analysis), Position, Size, Scan Area Width and Tilt.
24. Active key for Depth/Zoom/Ellipse
Chapter 4 Functional Checks 4-9
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4-3-7
4-3-7-1
NOTE:
B Mode Checks
Preparations
1.) Connect one of the probes listed in 3-6-6 "Available Probes" on page 3-25 , in Chapter 3 Installation to the System probe connector.
2.) Turn ON the scanner (if it isn’t turned on already)
The keyboard layout varies from each Product, the following figures show LOGIQ e R5.x.x as an example.
SoftMenu Key
Primary Menu
Secondary Menu
B Mode
Figure 4-7 Controls available in B Mode
Zoom/Depth
Scan Area
Freeze
4-10
Figure 4-8 B Mode Screen Picture Example
Section 4-3 - General Procedure
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4-3-7-2 B Mode OP Panel Controls
Table 4-3 B Mode Control Panel Controls
Step
1
Press B Mode key
Task
2
3
4
5
7
8
9
10
Adjust Depth
Adjust Gain
Adjust Focus
Activate Auto Optimize
Adjust Time Gain Compensation (TGC)
Adjust Scan Area
Adjust Zoom
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 Gn (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.
Toggles the left/right orientation of the scan image.
Comments
Chapter 4 Functional Checks 4-11
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4-3-7-3 B Mode Softmenu Key
4-12
Table 4-4 B Mode Softmenu Key
Step
1
2
3
4
5
6
7
8
9
10
11
12
13
Task Expected Result(s) comments
Adjust Rejection
Activate Colorize
Adjust Frequency
Adjust Frame Average
Selects a level below which echoes will not be amplified (an echo must have a certain minimum amplitude before it will be processed).
Enables gray scale image colorization. To deactivate, reselect a Gray Map.
Adjust Edge Enhance
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.
For LOGIQ e, LOGIQ e Vet and
LOGIQ i
Adjust Edge Enhance/Contour
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.
For Vivid e
Activate Gray Map
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.
For LOGIQ e, LOGIQ e Vet and
LOGIQ i
Adjust DDP
Adjust Rotation
Adjust Line Density
Adjust Frame Rate
Power output
Dynamic Range
Focus Number and Position
Virtual Convex
Virtual Apex
Temporal filter that averages frames together.
This has the effect of presenting a smoother, softer image.
For Vivid e
Rotates the image by selecting the value from the pop-up menu.
Optimizes B Mode frame rate or spatial resolution for the best possible image.
For LOGIQ e, LOGIQ e Vet and
LOGIQ i
Optimizes B Mode frame rate or spatial resolution for the best possible image.
Optimizes image quality and allows user to reduce beam intensity. 2% 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.
For Vivid e
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.
Virtual Convex for linear probe
Virtual Convex for Sector probe
Only for LOGIQ e R5.x.x/R6.x.x/
R7.x.x, LOGIQ e Vet, LOGIQ i R5.x.x,
Vivid e R5.x.x, Vivid e R6.x.x
Section 4-3 - General Procedure
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4-3-8 M Mode Controls
4-3-8-1 Preparations
1.) Connect one of the probes listed in 3-6-6 "Available Probes" on page 3-25 , in Chapter 3 Installation to the System probe connector.
2.) Turn ON the scanner (if it isn’t turned on already).
Primary Menu Secondary Menu
Gain
M Mode
Figure 4-9 Controls available in M Mode
M/D Cursor
Figure 4-10 M Mode Screen Picture Example
Chapter 4 Functional Checks 4-13
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4-3-8-2 M Mode OP Panel Controls
Table 4-5 M Mode OP Panel Controls
Step
1
Press M Mode key
Task
2
3
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 Gn (dB).
Displays the M-Mode cursor on the B-Mode image. Press Cursor and Trackball to position
M-Mode Cursor.
Comments
4-14 Section 4-3 - General Procedure
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4-3-8-3 M Mode Softmenu Key
Table 4-6 M Mode Softmenu Key
Step Task
1
Adjust Rejection
2
Adjust Sweep Speed
3
4
Activate Gray Map
6
Activate Colorize
7
Activate Full Timeline
8
Adjust Edge Enhance
Adjust Edge Enhance/Contour
Select Display Format
Select Layout
9
Adjust Dynamic Range
10
Power output
Expected Result(s) Comments
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 the time line is swept. The following speed values are available, 1, 2, 3, 4, 6, 8, 12, 16.
Edge Enhance brings out subtle tissue differences and boundaries by enhancing the gray scale differences corresponding to the edges of structures. Adjustments to M Mode's edge enhancement affects the M Mode only.
For LOGIQ e, LOGIQ e Vet and LOGIQ i
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.
For Vivid e
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.
For LOGIQ e, LOGIQ e Vet and LOGIQ i
Select the Layout to display B image and M image on the LCD. Press Display Format, and select from the pop up menu.
For Vivid e
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. 2% increments between 0-100%. Values greater than 0.1 are displayed.
Chapter 4 Functional Checks 4-15
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4-3-9 Color Flow Mode Checks
4-3-9-1 Preparations
1.) Connect one of the probes listed in 3-6-6 "Available Probes" on page 3-25 , in Chapter 3 Installation to the System probe connector.
2.) Turn ON the scanner (if it isn’t turned on already).
Primary Menu
Secondary Menu
CF Mode
Gain
Figure 4-11 Controls available in Color Flow Mode
4-16
Figure 4-12 CFM Mode Screen Picture Example
Section 4-3 - General Procedure
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4-3-9-2 Color Flow Mode OP Panel Controls
Table 4-7 Color Flow Mode OP Panel Controls
Step
1
Task
Press CFM-Mode key
2
Adjust Gain
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.
comments
Chapter 4 Functional Checks 4-17
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4-3-9-3 Color Flow Mode Softemenu Key
Table 4-8 Color Flow Mode Softmenu Key
Step Task
1
2
3
4
5
6
7
8
9
10
11
12
Threshold
Packet Size
Select Color maps
Adjust Frequency
Set Frame Average
Color Invert
Adjust LIne Density
Adjust Frame Rate
Activate Spatial Filter
Adjust Dynamic Range
Activate ACE
Adjust Angle Steer
Move Baseline
Expected Result(s) Comments
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.
For LOGIQ e, LOGIQ e Vet and LOGIQ i
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.
For Vivid e
Adjust Spatial Filter to smooth out the color, makes it look less pixely.
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.
4-18 Section 4-3 - General Procedure
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Table 4-8 Color Flow Mode Softmenu Key
Step
13
14
15
16
17
18
Change PRF
(Pulse Repetition Frequency)
Change scale
Transparency Map
Focus Position
Power output
Wall Filter
Low Vel Reject
Angio
Task Expected Result(s) Comments
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.
For LOGIQ e, LOGIQ e Vet and LOGIQ i
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.
For Vivid e
Allows to select specific transparency map
Increases the number of transmit focal zones or moves the focal zone(s) so that you can tighten up the beam for a specific area. A graphic caret corresponding to the focal zone position(s) appears on the right edge of the image.
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.
For LOGIQ e, LOGIQ e Vet and LOGIQ i
Low Vel Reject insulates the Doppler signal from excessive noise caused from vessel movement.
For Vivid e
To enter PDI (Power Doppler Imaging) mode while not in CARD application. For CARD application, there’s no “Angio“ rotary on primary menu.
For Vivid e
Chapter 4 Functional Checks 4-19
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4-3-10 Doppler Mode Checks
4-3-10-1 Preparations
1.) Connect one of the probes listed in 3-6-6 "Available Probes" on page 3-25 , in Chapter 3 Installation to the System probe connector.
2.) Turn ON the scanner (if it isn’t turned on already).
Primary Menu Secondary Menu
PW Mode
Gain
B Pause
Figure 4-13 Controls available in Doppler Mode
M/D Cursor
4-20
Figure 4-14 Doppler Mode Screen Picture Example
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4-3-10-2 Doppler Mode OP Panel Controls
Table 4-9 Doppler Mode OP Panel Controls
Step
1
Press PW Mode key
Task
2
3
4
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.
Comments
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4-3-10-3 Doppler Mode OP Panel Controls
4-22
Table 4-10 Doppler Mode Touch Panel Controls
Step Task
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
Adjust Rejection
Adjust Sweep Speed
Activate Full Timeline
Select Display Format
Select Layout
Adjust Frequency
Trace Direction
Invert
Auto Calculation
Modify Calcs
Trace Method
Activate Colorize
Activate Gray Map
Dynamic Range
Adjust Angle Correct
Adjust Angle Steer
Expected Result(s) comments
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.
For LOGIQ e, LOGIQ e
Vet and LOGIQ i
Display layout can be preset to have B-Mode and Time-motion side-by-side or over-under.
For Vivid e
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.
For LOGIQ e, LOGIQ e
Vet and LOGIQ i
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.
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Table 4-10 Doppler Mode Touch Panel Controls
Step Task
16
17
18
19
20
21
22
23
Move Baseline
Change PRF (Pulse Repetition
Frequencies) - (Wall Filter)
Change Scale - (Low Vel Reject)
Trace Sensitivity
Time Resolution
Spectral Average
Power output
SV Length
Wall Filter
Low Vel Reject
Expected Result(s) comments
Adjusts the baseline to accommodate faster or slower blood flows to eliminate aliasing.
Velocity scale determines pulse repetition frequency. If the sample volume gate range exceeds single gate PRF capability, the system automatically switches to high PRF mode. Multiple gates appear, and HPRF is indicated on the display.
For LOGIQ e, LOGIQ e
Vet and LOGIQ i
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.
For Vivid e
Adjusts the sensitivity to get more accurate envelope trace.
Adjusts the resolution in frequency domain.
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%.
Sizes the sample volume gate.
Wall Filter insulates the Doppler signal from excessive noise caused from vessel movement.
For LOGIQ e, LOGIQ e
Vet and LOGIQ i
Wall Filter insulates the Doppler signal from excessive noise caused from vessel movement.
For Vivid e
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4-3-11 CWD Functional Check
4-3-11-1
4-3-11-2
Preparations
1.) Connect 3S-RS/6S-RS/6Tc-RS Probe to the system, see in Chapter 3 Installation.
2.) Turn ON the scanner (if it isn’t turned on already).
Activating CW Doppler
To activate CW Doppler Mode:
Ensure that the appropriate CW probe is connected.
• For LOGIQ e, LOGIQ e Vet and LOGIQ i, press F6 on the keyboard to enter CW mode. F6 is the predefined function key for CW, which can be configured in Utility/Config -> Admin -> Function Key preset menu.
• For Vivid e, press CW Key on the keyboard.
The Doppler Spectrum appears, along with the CW Top/Sub Menu Menu.
4-3-11-3
Figure 4-1.
CWD Screen
The following CW parameters are displayed: Frequency, Gain, Acoustic Output, Scale, Wall Filter and
Dynamic Range.
Exiting CW Doppler
To exit CW Doppler Mode,
• For LOGIQ e, LOGIQ e Vet and LOGIQ i, press F6.
• For Vivid e, press CW.
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4-3-12 Basic Measurements
NOTE:
The following instructions assume that you first scan the patient and then press Freeze.
4-3-12-1
4-3-12-2
4-3-12-3
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.
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.
6.) To position the ellipse and to size the measured axes (move the calipers), move the
TRACKBALL.
7.) To increase the size, rotate the ELLIPSE button clockwise. To decrease the size, contrarotate the ELLIPSE button.
8.) To complete the measurement, press SET. The system displays the circumference and area in the measurement results window.
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.
4-3-13
4-3-13-1
4-3-13-2
Probe/Connectors Usage
Connecting a probe
1.) Place the probe's carrying case on a stable surface and open the case.
2.) Carefully remove the probe and unwrap the probe cable.
3.) DO NOT allow the probe head to hang free. Impact to the probe head could result in irreparable damage.
4.) Align the connector with the probe port and carefully push into place.
5.) Lock the probe latch upward.
6.) Carefully position the probe cord so it is free to move and is not resting on the floor.
Activating the probe
The probe activates in the currently-selected operating mode. The probe's default settings for the mode and selected exam are used automatically.
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4-3-13-3 Deactivating the probe
1.) Press the Freeze key.
2.) Gently wipe the excess gel from the face of the probe. (Refer to the Basic User Manual for complete probe cleaning instructions.)
3.) Carefully slide the probe around the right side of the keyboard, toward the probe holder.
Ensure that the probe is placed gently in the probe holder.
4-3-13-4 Disconnecting the probe
Probes can be disconnected at any time. However, the probe should not be selected as the active probe.
1.) Unlock the probe latch downward.
2.) Pull the probe and connector straight out of the probe port.
3.) Carefully slide the probe and connector away from the probe port and around the right side of the keyboard.
4.) Ensure the cable is free.
5.) Be sure that the probe head is clean before placing the probe in its storage box.
Take the following precautions with the probe cables: Do not bend. If you have purchased the cart option, be sure to keep probe cables free from the wheels.
Be careful not to trip on the probe cables if using the device without the optional cart.
4-3-14
4-3-14-1
4-3-14-2
4-3-14-3
4-3-14-4
4-3-14-5
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.
Quickly Move to Start/End Frame
Press First to move to the first CINE frame; press Last to move to the last CINE frame.
Start Frame/End Frame
Press the Start Frame Two-Button Softkey to move to the beginning of the CINE Loop. Adjust the Start
Frame up/down Two-Button Softkey upward to move forward through the CINE Loop. Adjust the
Softkey downward to move backward through the CINE Loop.
Press the End Frame Two-Button Softkey to move to the end of the CINE Loop. Adjust the End Frame up/down Two-Button Softkey upward to move forward through the CINE Loop. Adjust the Softkey downward to move backward through the CINE Loop.
Adjusting the CINE Loop Playback Speed
Adjust the Loop Speed up/down Two-Button Softkey to increase/decrease the CINE Loop playback speed.
Moving through a CINE Loop Frame By Frame
Adjust the Frame by Frame up/down Two-Button Softkey to move through CINE memory one frame at a time.
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4-3-15 Image Management (QG)
For Image Management functionality refer to the LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e 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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4-3-16 Backup and Restore Database, Preset Configurations and Images
4-3-16-1 Formatting Media
1.) To format the backup media, DVD-RW, select the UTILITY/CONFIG 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 4-15. It is best to use all capital letters with no spaces or punctuation marks. Press Format.
Figure 4-15 Format and Verify Media
5.) The Ultrasound system displays a pop-up menu, as shown in Figure 4-16. When the formatting has been completed, press OK to continue.
6.) If desired, verify that the format was successful by returning to Utility/Config->Connectivity-
>Tools->Removable Media and selecting VERIFY as shown in Figure 4-15.
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Figure 4-16 Format Successful Pop-up Menu
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Backup System Presets and Configurations 4-3-16-2
NOTE:
NOTE:
Always backup any preset configurations before a software reload. This ensures that if the presets need to be reloaded, after the software update, they will be the same ones the customer was using prior to service.
1.) Insert a formatted DVD into the drive.
2.) On the Keyboard, press UTILITY/CONFIG.
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 DVD-RW (or USB memory device).
7.) Select BACKUP.
The system performs the backup. As it proceeds, status information is displayed on the Backup/Restore screen.
Check here to backup presets and configurations
Figure 4-17 Backup/Restore Menu
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4-3-16-3 Restore System Presets and Configurations
CAUTION
The restore procedure overwrites the existing database on the local hard disk drive. Make sure to insert the correct DVD (or USB memory device).
NOTE:
1.) Insert the Backup/Restore DVD (or USB memory device) into the drive.
2.) On the Keyboard, press UTILITY/CONFIG.
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 DVD-RW (or USB memory device).
7.) Select RESTORE.
The system performs the restore. As it proceeds, status information is displayed on the Backup/Restore screen.
After the Restore completes, the system will automatically reboot.
Check here to restore presets and configurations.
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Figure 4-18 Backup/Restore Menu
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4-3-16-4
NOTE:
NOTE:
Archiving Images
1.) Insert the archive media. To format the archive media, DVD-RW, select the Utility/Config button on the Keyboard.
For LOGIQ e R5.x.x, LOGIQ e R6.x.x, LOGIQ e R7.x.x, LOGIQ e Vet, Vivid e R5.x.x, Vivid e
R6.x.x and LOGIQ i R5.x.x, USB HDD also can be used as archive media.
2.) Select Connectivity, then Removable Media.
3.) Format the DVD-RW. Verify the format if desired.
4.) Images will be moved from the hard disk drive by date. Therefore, the best way is to label media by date.
Images will be moved from the hard disk 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 disk drive. However, the patient database (backed up earlier) maintains pointers to the location of the images on the archive media.
NOTE:
Figure 4-19 Format DVD-RW Screen
5.) Select Backup/Restore, then EZBackup/Move.
For LOGIQ e R4.x.x, LOGIQ i R4.x.x and Vivid e R4.x.x, there is one buttons for EZBackup/
Move, while for LOGIQ e R5.x.x, LOGIQ e R6.x.x, LOGIQ e R7.x.x, LOGIQ e Vet, LOGIQ i
R5.x.x, Vivid e R5.x.x, and Vivid e R6.x.x, there are two buttons for EZBackup and EZMove.
6.) Select “Backup File Older Than in Days”.
Choose the days which want to older than current exam date.
Figure 4-20 EZBackup/Move
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4-3-16-4
Archiving Images (cont’d)
7.) Press PATIENT and set the Dataflow to store images directly to DVD-ROM.
8.) From the image screen, press EZBACKUP/MOVE. The Move Images pop-up appears.
Figure 4-21 Image Archive Move Pop-up Menu
9.) Press Next on pop-up message.
10.)A media check message appears. Press OK to continue.
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Figure 4-22 Media check message
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4-3-16-4
Archiving Images (cont’d)
11.)Press Finish after Backup/Move complete.
4-3-16-5
Figure 4-23 EZBackup/Move complete
All databases, presets and images should now be saved to removable media.
Emergency Repair Disk
1.) Connect the USB HDD to system.
2.) Select Backup/Restore, then Emergency Repair Disk.
3.) Select “Reminder Dialog Interval Days”.
Reminder Dialog
Interval Days
Figure 4-24 Emergency Repair Disk
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4-3-16-5
Emergency Repair Disk (cont’d)
4.) Return to scan mode. Press Ctrl + B, the Emergency Disk Making window pop-up appears.
Figure 4-25 Emergency Disk Making Pop-up Menu
5.) Press Next on pop-up message.
6.) A storage information message appears. Press Next to continue.
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Figure 4-26 Storage Information message
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4-3-16-5
Emergency Repair Disk (cont’d)
7.) Press Finish after Emergency Disk Making complete.
Figure 4-27 Emergency Disk Making Complete
All databases, presets and images should now be saved to Emergency Disk.
8.) Press Ctrl + R, Emergency Disk Recovery will pop-up.
Figure 4-28 Emergency Disk Recovery
9.) Press Next on pop-up message.
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4-3-16-5
Emergency Repair Disk (cont’d)
10.)A recovery information message appears. Press Next to continue.
Figure 4-29 Recovery Information message
11.)Press Finish after Emergency Disk Recovery complete.
4-36
Figure 4-30 Emergency Disk Recovery Complete
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Section 4-4
Software Configuration Checks
Table 4-11 Software Configuration Checks
Step
1.
2.
3.
4.
5.
Task to do Expected Result(s)
Check Date and Time setting
Check that Location (Hospital Name) is correct
Date and Time are correct
Location Name is correct
Check Language settings
Check assignment of Printer Keys
Desired Language is displayed
For LOGIQ e, LOGIQ e Vet, LOGIQ i, the default function for Print1-3 Keys is P1 (store image); P2 (print); P3 (USB
Quick Save). Print1-3 Keys can also be assigned as desired by the customer
For Vivid e, the default function for Store Key and Print1-
2 Keys is Store (store image); P1 (print); P2 (USB Quick
Save). Store Key and Print1-2 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
NOTE: Please refer to Peripherals Manual for detail procedures of each peripheral check.
Check that peripherals work as described below:
Table 4-12 Peripheral Checks
Step Task to do
1.
Press (FREEZE)
2.
Press the default print key on the Control
Panel
3.
Connect with Foot witch on USB port and press once.
Stop image acquisition.
Expected Result(s)
The image displayed on the screen is printed on printer.
To start image acquisition (the same function as (FREEZE) key).
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Chapter 5
Components and Functions (Theory)
Section 5-1
Overview
This chapter explains LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e ’s system concepts, component arrangement, and subsystem function. It also describes the Power Distribution System (PDS) and probes.
Table 5-1 Contents in Chapter 5
Section
5-1
5-2
5-3
5-3
5-4
Overview
Block Diagrams and Theory
Power Diagrams
Power Diagrams
Common Service Platform
Description Page Number
5-1
5-2
5-6
5-6
5-10
Chapter 5 Components and Functions (Theory) 5-1
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Section 5-2
Block Diagrams and Theory
5-2-1 Block Diagram
128
TX64
64
RX64
On board
Distributed
Power
LV unit
HV unit
CWD
(option)
USC
Battery Charger and MUX
AC
Adapter
Li-Ion
Battery
SMBus
TMST(RFI/Carrier)
Keyboard
A/N key
PS2 USB
Trackball
U/S key
Soft menu key
TGC
Limited backlit
I/O
USB2.0
Audio
Ethernet
VGA
Docking
LCD
15” XGA
Speaker
Peripherals
DVD-RW
USB-Wireless
LAN
Printer
Foot SW
ECG
VCR
Cart
Figure 5-1 LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e System Block Diagram
• Pre Amp: Preamplifier
• OQX2: Beamforming ASIC
• CHACOM: B/M/CFM/DOP mode signal processor ASIC
• DSP: Digital Signal Processor with PCI interface between CPU and TMST
• HV unit: High voltage unit
• LV unit: Low voltage unit
• DC/DC & HV Ctrl, SMBUS I/F: DC/DC high voltage control smart bus interface
• TUSC FPGA: LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e Ultrasound controlling and Image data transfer FPGA
5-2 Section 5-2 - Block Diagrams and Theory
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5-2-2 General Information
• LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e is an ultrasound imaging scanner.
• The system can be used for:
2D Black and White imaging
-
-
-
-
2D Color Flow
M-Mode Black and White imaging
Doppler
A number of combinations of the above
• LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e is a digital beam forming system that can handle up to 128 elements linear probes.
• Signal flow from the Probe Connector Panel to the Front End, to the Mid Processors and Back End
Processor and finally to the LCD and peripherals.
• System configuration is stored on a hard disk drive and all necessary software is loaded from the hard disk drive on power up.
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5-2-3 External I/O
5-2-4
Figure 5-2 External I/O module overview
External I/O:
The external I/O is the interface between the scanner and all external items. Examples: wireless network, USB interface medical grade printer and external medical grade SVGA displayer.
Peripherals
DVD-RW, and a Black & White Video Printer can be connected to the external I/O.
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5-2-5 Wiring
Figure 5-3 Wiring Diagram
• TX64: Transmit board
• RX64: Front end processing board
• TMST: Master board
• PWR SW: Power Switch
• FPC: Flexible Print Circuit board
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Section 5-3
Power Diagrams
5-3-1
5-3-2
Overview
The AC Power assy’s main tasks are to isolate and output to the DC/DC unit which is inside the system console. The input of AC power pack will be the AC outlet and it’s universal, the range is AC 90V-264V,
47-63Hz. And no main power switch located on this power pack.
AC Power
TMST & TX64
5-6
Figure 5-4 AC Power Distribution Block Diagram
The mains cord has plugs in one side end. A male plug connects to the mains outlet on site.
The mains voltage is routed to the AC power pack through a Circuit Breaker located on the site.
The Circuit Breaker is of the auto fuse type, if for some reason the current grows to high, the switch will automatically break the power.
From the Main Circuit Breaker, the AC power is routed via an Inrush Current Limiter to a internal outlet connector for the Mains Transformer.
Section 5-3 - Power Diagrams
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5-3-3 Battery charging
The charging circuit is lithium-Ion battery charge and discharge controller. This block can switch the power between the battery and the output of AC Pack. If the output of AC Pack is available, the power input of Charge Board Unit should be from the AC Pack and the battery will be charged if it’s not full.
This block will be also in charge of the battery charging monitor to avoid the battery over heat and over charging, charging will be shut off automatically if battery is charged fully. The battery will discharge to provide the power to the system when out of AC power pack output or AC line.
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5-3-4 Air Flow Distribution
A
B
A
B
Figure 5-5 Air Flow Inside the Scanner
The two air flow passes allow the scanner to be cooled down as shown in the figure above.
• Path A (Bottom front > CPU Assy > Bottom left) for TMST & CPU Assy cooling.
• Path B (Bottom front > TX64/RX64 > Bottom right) for TX64/RX64 cooling.
5-8 Section 5-3 - Power Diagrams
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5-3-5 Fans
Figure 5-6 Left & Right Fans
The scanner contains the four fans at the following positions for producing an air flow.
-
-
One fan assy: On the Left side for air flow path A.
One fan assy: On the Right side for air flow path B.
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Section 5-4
Common Service Platform
5-4-1
5-4-2
5-4-2-1
5-4-2-2
Introduction
The Service Platform contains a set of software modules that are common to all PC backend ultrasound and cardiology systems. The Common Service Platform will increase service productivity and reduce training and service costs.
Global Service User Interface (GSUI)
Internationalization
The user interface provided by the service platform is designed for GE personnel and as such is in
English only. There is no multi-lingual capability built into the Service Interface.
Service Login
Select Utility/Config->Service. This button links the user to the service login screen.
5-4-2-3
Figure 5-7 Service Login Screen
Access / Security
The service interface has different access and security user levels. Each user is only granted access to the tools that are authorized for their use.
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5-4-2-3
Access / Security (cont’d)
Table 5-2 Service Login User Levels
User Level
Operator
Administrator
External Service
Access Authorization
Authorized access to specified diagnostics, error logs and utilities. Same acquisition diagnostic tests as GE Service.
Password
uls uls gogems
5-4-2-4
Every access request, whether successful or not, will be logged into a service access log that is viewable to authorized users.
The usage for security cable
The ultrasound system equipped with Kensington security slot which is compatible with a Kensington security cable, refer to Figure 5-8 on page 5-11 .
Figure 5-8 Kensington security slot
How to prevent unauthorized removal of the ultrasound system?
1.) Wrap the cable around the immovable object, refer to Figure 5-9 on page 5-11 ;
2.) Make sure and rotate the key to the right (unlocked position);
3.) Insert the lock into the Kensington security slot in the system side cover, refer to Figure 5-9 on page
5-11 ;
4.) Rotate the key to the left (locked position).
5.) For more information, visit www.kensington.com.
NOTE:
Figure 5-9 Kensington security slot and system
Full maintenance reboot should be selected after the service dongle is used on the system.
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5-4-3 Service Home Page
The navigation bar at the top of the screen allows the user to select from several tools and utilities.
Figure 5-10 Customer Service Home Page
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5-4-4 Error Logs Tab
From the Error Logs Tab the Log Viewer displays four categories with pull-down sub-menus and an Exit selection. The Service Interface allows scanner logs to be viewed by all service users.
The log entries are color-coded to identify the error level severity at a glance.
Table 5-3 Log Entry Key
Severity
1
2
3
Error Level
Information
Warning
Error
Color Code
Green
Blue
Red
The Service Interface supports the transfer of these logs to local destinations such as the CD-ROM drive.
Figure 5-11 Log Viewer / Logs / Log Entries
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5-4-4-1 Logs
The seven sub-menus of the Logs category are System, Power, Infomatics, Temperature, Probe,
Board, and DICOM.
NOTE: Figure 5-11 provides a graphical example of the log entries for the System Logs.
Log table headings for the different logs are as follows:
• System
Log entry headings include Time Stamp; Error Level; Package; and Error Message.
• Power
Log entry headings include Time Stamp; Error Level; Package; and Error Message.
• Infomatics
Log entry headings include TimeStamp, Revision, PtID, PtDOB, PtSex, PtWeight, PtHeight,
ExamID, Exam Category, ExamCurDate, ExamStartTime, ExamEndTime, FreezeTime,
TimeOfImageArchived, AccessionNumber, RefPhyName, ReadingPhyName, Operator, RoomNo,
BodyPatternSelected, InstitutionName, ActiveModeTime, CalculationMade, CalculationTime,
HelpUsage, ProductName, SystemSWRev, NoOfSWModules, SystemPowerOnTime,
SystemIdleTime, NoOfBoards, ProbeChangedDate, ProbeChangedTime, ProbeChangedStatus,
NoOfProbeSlots, NoOfProbes, ProbeID, ProbeSerialNumber, and ActiveExamProbes.
• Temperature
Log entry headings include Time Stamp; Error Level; Package; CPU Internal Temp, TMST Process
Temp, TMST Internal Temp, TMST Remote Temp, TX64 Process Temp, TX64 Internal Temp,
TX64 Remote Temp, TMST 3.3V, TMST 5V, TMST 12V, TMST 1.2V, TMST 1.5V, TMST 1.8V,
TX64 1.5V, TX64 1.8V, TX64 3.3V, TX 64 5V, TX649V, TX64 12V, TX 64 +THV, TX64-THV,
TX64+SHV, and TX64-SHV.
• Probe
Log entry headings include Time Stamp; Error Level; Package; Error Message; Severity; Revision; and three new labels that have not yet been named.
• Board
Log entry headings include Time Stamp; Error Level; Package; Board; Severity; Revision and two new labels that have yet been named.
• DICOM
Log entry headings include Time Stamp; Error Level; Package; and Error Message.
• Touch Screen (only for LOGIQ e R5.2.x)
Log entry headings include Touch Screen operation events.
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5-4-4-2 Utilities
The two sub-menus of the Utilities category are Plot Log, and Plot Page.
Plot Log Plot Page
5-4-4-3
Figure 5-12 Utilities Sub-Menus
• Plot Log
Allows for the color coded plot of all Log contents with the package on the ‘x’ axis and incident count on the ‘y’ axis.
• Plot Page
Allows for the color coded plot of all Page contents with the package on the ‘x’ axis and incident count on the ‘y’ axis.
Search
On the Text Search sub-menu of the Search category, users enter case-sensitive text they wish to find.
This filter field works well for filtering the Sys log file for the word “fail”.
Figure 5-13 Search Sub-Menu
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5-4-4-4 Exit
The sub-menu, Exit Log Viewer, returns the user to the Service Desktop home page.
Figure 5-14 Exit Log Sub-Menu
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5-4-5 Diagnostics
Detailed Diagnostic information is found in Chapter 7 .
5-4-5-1
5-4-5-2
Figure 5-15 User Diagnostic Page
Diagnostics Execution
Diagnostic tests are executable by both local and remote users. The Service Platform provides top-level diagnostic selection based on the user’s level and login access permissions. Remote access will require disruptive diagnostic permissions to run Acquisition diagnostics.
Diagnostic Reports
Diagnostic tests return a report to the Service Platform. The platform retains the report and allows for future viewing of the diagnostic logs.
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5-4-6 Image Quality
The Image Quality page is intended to contain tools for troubleshooting image quality issues.
5-4-7
FIELD IS NOT YET POPULATED
Figure 5-16 Image Quality Page
Calibration
The Calibration page is intended to contain the tools used to calibrate the system.
FIELD IS NOT YET POPULATED
Figure 5-17 Calibration Page
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5-4-8 Configuration
The Configuration page is intended to be used to setup various configuration files on the system.
The Service Platform is the access and authorization control for remote access to the configuration subsystem.
The enable/disable of software options can be done from this Configuration page.
5-4-9
Figure 5-18 Configuration Page
Utilities
The Utilities page contains several miscellaneous tools.
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5-4-10 Replacement
The Replacement page is intended to contain the tools used to track replacement parts used in the system.
5-4-11
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Figure 5-19 Part Replacement Page
PM
The PM page is intended to contain the tools used in periodic maintenance of the system.
FIELD IS NOT YET POPULATED
Figure 5-20 Planned Maintenance Page
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Chapter 6
Service Adjustments
Section 6-1
Overview
6-1-1 Purpose of this chapter 6
This section describes how to test and adjust the scanner. These tests are optional. You may use them to check the system for errors.
Table 6-1 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 Adjustments Procedures
To adjust the brightness and volume:
1.) Press Ctrl + brightness key together (up/down), located on the keyboard.
1.) Press Ctrl + volume key together (left/right), located on the keyboard.
Figure 6-1 LCD Monitor
6-2 Section 6-2 - Monitor Adjustments
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Chapter 7
Diagnostics/Troubleshooting
Section 7-1
Overview
7-1-1 Purpose of Chapter 7
This section describes how to setup and run the tools and software that help maintain image quality and system operation. Very basic host, system and board level diagnostics are run whenever power is applied. Some Service Tools may be run at the application level. However most software tests are required.
Table 7-1 Contents in Chapter 7
Section
7-1
7-2
7-3
7-4
7-5
7-6
7-7
Description
Overview
Gathering Trouble Data
USB Quick Save
Screen Captures
Global Service User Interface (GSUI)
Common Diagnostics
Network and Insite II Configuration
Page Number
7-1
7-2
7-4
7-6
7-9
7-12
7-15
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Section 7-2
Gathering Trouble Data
7-2-1
7-2-2
Overview
There may be a time when it would be advantageous to capture trouble images and system data (logs) for acquisition to be sent back to the manufacturer for analysis. There are different options to acquire this data that would give different results.
Collect Vital System Information
The following information is necessary in order to properly analyze data or images being reported as a malfunction or being returned to the manufacturer:
Product Name = LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e
From the Utility>System>About screen:
Applications Software
-
-
-
-
Software Version
Software Part Number
System Image Software
Image Revision
Image Part Number
7-2 Section 7-2 - Gathering Trouble Data
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7-2-3 Collect a Trouble Image with Logs
If the system should malfunction, press the Alt-D keys simultaneously. This will collect a screen capture of the image monitor, system presets and the following logs:
-
-
-
-
-
Keyboard Shadow Log
Error Logs
Crash Log
Power Supply
Temperature
NOTE: Power Supply and Temperature logs are not currently being updated by the LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e .
This Alt-D function is available at all times.
Figure 7-1 ALT-D Dialog Box
When Alt-D is pressed, a menu box appears that allows for:
A place to enter a description of the problem
A choice to store to a pre-formatted DVD-R, RD (Removable Disk) or to the Export directory
D: export.
The subsequent file is compressed and time stamped. The screen capture is a bitmap which eliminates the possibility of artifacts from compression.
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Section 7-3
USB Quick Save
7-3-1
7-3-2
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 a Print Key.
For LOGIQ e, LOGIQ e Vet and LOGIQ i, the P3 key is the factory default print key to accomplish the
USB Quick Save; for Vivid e, the P2 key is the factory default print key to accomplish the USB Quick
Save. However, the default is for the Image Area only or the customer may have customized the default
Key function.
Here, take LOGIQ e for example and the P3 key is the factory default print key to accomplish the USB
Quick Save.
Check and Record the P3 Key Function
Check the function of the default Key in the event that the customer may have made some customized settings.
1.) Click Utility/Config 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 Print3 key.
The Connectivity/Buttons Screen will be displayed like the one shown in Figure 7-2 on page 7-4 .
7-4
Figure 7-2 Buttons Set Up Screen
P3 is the factory default USB Quick Save key. If it is not set to Image Area, proceed to step 5 to record the customer’s customized settings.
Section 7-3 - USB Quick Save
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7-3-2 Check and Record the P3 Key Function
(cont’d)
5.) In the Destinations section, record the service that is displayed.
6.) In the Physical Print Buttons section, record the parameters related to the service.
7-3-3 Setting the P3 Key to USB Quick Save
If the P3 Key is not set to USB Quick Save:
1.) While on the Connectivity 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 P3 Key should now be set up for USB Quick Save, sending the images directly to the USB memory.
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Section 7-4
Screen Captures
7-4-1
7-4-2
7-4-3
There may be times when the customer or field engineer will want to capture a presentation on the screen. This is accomplished by first saving the image(s) to the clipboard using a Print Key.
There’s no factory default print key to accomplish a secondary screen capture. However, customer may have customize any of Print Key function. Here, take Print1 button for example, for LOGIQ e, LOGIQ e
Vet, LOGIQ i, Print1, Print 2 and Print3 are the same, for Vivid e, Store, Print1 and Print2 are the same.
Therefore, screen capture should involve the following steps:
1.) Check and record any custom settings for the Print1 button.
2.) Set the Print1 button to Whole Screen, Secondary Capture.
3.) Capture the required screens to the Hard Disk Drive or DVD-R.
4.) Restore the Print1 button to it’s original settings.
Check and Record the P1 Key Function
Check the function of the Print1 Key in the event that the customer may have made some custom settings.
1.) Click Utility/Config 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 Print1.
The Connectivity/Buttons Screen will be displayed like the one shown in Figure 7-2 on page 7-4 .
If P1 is not set to Whole Screen, as shown in Figure 7-2 , 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 P1 Key to Screen Capture
If the P1 Key is not set to screen capture:
1.) While on the Connectivity 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 P1 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 P1. This will place a snapshot of the screen on the “clipboard” displayed at the bottom of the scan image display.
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7-4-3 Capturing a Screen
(cont’d)
Clipboard
Thumbnai ls
Menu
Figure 7-3 Select Image to Capture
3.) Click FREEZE to unfreeze the image to view the image screen and the snapshots displayed on the bottom.
4.) Highlight the snapshot to be stored.
5.) Select Menu on the right side of the image screen, then highlight and select SAVE AS.
Save As
Figure 7-4 Menu > Save As
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7-4-3 Capturing a Screen
(cont’d)
For LOGIQ e R4.x.x, LOGIQ i R4.x.x, Vivid e R4.x.x
For LOGIQ e R5.x.x, R6.x.x, R7.x.x, LOGIQ i R5.x.x, Vivid e R5.x.x,
Figure 7-5 Save Dialog Box
7-4-4
6.) A Save dialog box will be opened.
• For LOGIQ e R4.x.x, LOGIQ i R4.x.x, Vivid e R4.x.x, choose d:\export folder as the archive location to save the image on the DVD-R.
• For LOGIQ e R5.x.x, LOGIQ e R6.x.x, LOGIQ e R7.x.x, LOGIQ i R5.x.x, Vivid e R5.x.x, Vivid e
R6.x.x, select Save first, and Select Transfer to CD/DVD to save the image on the CD/DVD.
Reset the P1 Key to Customer’s Functionality
If the customer had programmed the P3 Key to a function other than screen capture, restore that functionality recorded in section 7-4-1 on page 6 . Refer to Figure 7-2 .
1.) Click Utility/Config 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 Print1.
5.) In the Destinations list, select the service(s) recorded in step 5 , Section 7-4-1 .
6.) In the Physical Print Buttons section, select the parameters related to the service recorded in step 6 , Section 7-4-1 .
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Section 7-5
Global Service User Interface (GSUI)
7-5-1 Enter global service user interface
1.) Press Utility/Config - Service, see Figure 7-6 on page 7-9 .
Figure 7-6 system Service button
1.) Select GE Service in option of User Level of GEMS Service Home page and input correct password, press OK button. See Figure 7-7 on page 7-9 .
Figure 7-7 Service Login Page
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7-5-2 Active Diagnostic Function
2.) Choose Diagnostic in Global Service Interface to active diagnostic functions, choose options to activate various functions correspondingly.
7-5-3
7-5-3-1
7-5-3-2
7-5-3-3
7-10
Figure 7-8 Active Diagnostic Function
Control Frame
Contains the user interface elements used for:
• Diagnostic control, and
• Operator feedback
Button
This button has two modes each with appropriate text:
• Execute - to start the diagnostic, and
• Abort - to stop a diagnostic
The button can also be disabled.
Loop Count
This is an editable text field that will only accept numeric values with 4 digits or less. When the button is configured as an “execute” button and pressed, the loop count field will be queried to determine the number of times to execute the diagnostic.
Progress Indicator
Displays a graphical progress indication to the user.
Section 7-5 - Global Service User Interface (GSUI)
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7-5-3-4 Short Text Message
Displays either a starting message or aborting message, as well as the diagnostic completion status.
7-5-3-5 Background Color
Initially gray, the Control Frame background color changes upon completion of a diagnostic to indicate completion status.
• Fail = Red
• Pass = Green
• Neither pass nor fail = Set back to Gray (for example, final code status is Aborted).
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Section 7-6
Common Diagnostics
7-6-1
7-6-1-1
7-6-1-2
Utilities
Provides two selections:
Disruptive Mode
Allows you to enable or disable disruptive mode troubleshooting.
System Shutdown
Allows for system shutdown from the diagnostic menu. Select to Restart System or Shutdown System.
Also, select to retain Disruptive Mode or Not.
After submitting to restart or shutdown a confirmation screen gives one last chance to confirm or cancel the request.
7-12 Section 7-6 - Common Diagnostics
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7-6-2 PC Diagnostics (Non-Interactive Tests)
7-6-2-1
7-6-2-2
7-6-2-3
7-6-2-4
7-6-2-5
7-6-2-6
7-6-2-7
7-6-2-8
7-6-2-9
7-6-2-10
Essential Tests
System Board
Hard Disk Drive Surface Scan
Hard Disk Drive Quick Test
PCIBus
Video Card
Network Interface
CMOS
DRAM Memory
Parallel Port
Chapter 7 Diagnostics/Troubleshooting 7-13
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7-6-3 PC Diagnostics (Interactive Tests)
7-6-3-1
7-6-3-2
7-6-3-3
7-6-4
Keyboard Test
Mouse Test
Audio Card Test (only for LOGIQ e R5.2.x and R6.x.x)
Restart the system after diagnostics
Always shutdown the system and reboot after a diagnostics session.
7-14 Section 7-6 - Common Diagnostics
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Section 7-7
Network and Insite II Configuration
7-7-1
7-7-1-1
Network Configuration
Wire-LAN Network
1.) Connect system with network.
2.) Press Utility/Config -> Connectivity -> TCPIP, in IP Settings window check the Enable DHCP box.
In Network Speed box, choose the proper speed available.
Figure 7-9 Enable DHCP
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7-7-1-1
Wire-LAN Network (cont’d)
NOTE: If user want to setup static IP address, uncheck Enable DHCP option, input static address in
IP-Address box, Subnet Mask and Default Gateway box. In Network Speed box, choose the proper speed available.
Figure 7-10 Input static address
3.) Click Save, in popped-up dialog choose Ok.
7-16
Figure 7-11 Save and reboot inquiry dialog
4.) After reboot, the network icon at the left bottom of screen turns green.
Figure 7-12 Network icon
Section 7-7 - Network and Insite II Configuration
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7-7-1-2 Wireless LAN Network
1.) Connect wireless LAN card with system.
2.) Click Start at the left bottom of screen, and select “ Network Connections.
Figure 7-13 Start menu
3.) In the pop-up window choose Wireless Network Connection. Click it with cursor key, then select
View Available Wireless Networks.
For LOGIQ e R5.x.x/R6.x.x/R7.x.x, Vivid e R5.x.x/R6.x.x,
LOGIQ i R5.x.x
For LOGIQ e R4.x.x, LOGIQ i R4.x.x, Vivid e R4.x.x
Figure 7-14 Wireless Network Connection configuration
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7-7-1-2
Wireless LAN Network (cont’d)
4.) The Wireless Network Connection dialog box displays. Select the proper wireless network in
Available wireless networks window, check the Allow me to connect... box, and click Connect.
For LOGIQ e R5.x.x/R6.x.x/R7.x.x, Vivid e R5.x.x/R6.x.x
LOGIQ i R5.x.x
For LOGIQ e R4.x.x, LOGIQ i R4.x.x, Vivid e R4.x.x
Figure 7-15 Wireless Network Connection dialog box
NOTE: If an encrypted network has been selected, input Network key in Wireless Network Connection dialog box displayed, and click Connect.
Figure 7-16 Network key input
5.) The network icon at the left bottom of screen turns green.
Type network key here.
7-18
NOTE:
Figure 7-17 Network icon
To manually configure a wireless network, the involvement of the IT department is mandatory.
Section 7-7 - Network and Insite II Configuration
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7-7-2 Insite II Configuration
6.) Enter global service user interface, and log in as GE Service. See section 7-5-1 on page 9 .
7.) To use Pilot Server, on Configuration page, choose Questra Agent Configuration in left column.
Select Advanced Configuration, then choose “Others” as server type, and manually input pilot address, and click SAVE.
NOTE:
Figure 7-18 Advanced_Configuration page (out of GE network)
If system is within GE network, choose Development as server type, and do not need step 9.) enter
Proxy Server address.
Figure 7-19 Advanced_Configuration page (within GE network)
Chapter 7 Diagnostics/Troubleshooting 7-19
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7-7-2 Insite II Configuration
(cont’d)
8.) Change to Device Information page, enter Device and Serial Number as the serial number of that system, then press Modify Device Configurations.
NOTE:
Figure 7-20 Device_Information page
The Device name and Serial Number entered should be unique on server. It can be read from the rating plate label.
Figure 7-21 Rating plate label
7-20 Section 7-7 - Network and Insite II Configuration
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7-7-2 Insite II Configuration
(cont’d)
9.) Change to Proxy_Configuration page, enter Proxy Server Address as 3.20.128.6 and Proxy Server
Port as 88, then press SAVE.
Figure 7-22 Proxy_Configuration page
Chapter 7 Diagnostics/Troubleshooting 7-21
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7-7-2 Insite II Configuration
(cont’d)
10.)Change to Diagnostics page. Enable Disruptive Mode at Service side by pressing Yes.
Figure 7-23 Enable Disruptive Mode
11.)Customer will receive a request of Service side, click Yes to accept.
7-22
Figure 7-24 Accept requirement of Service
Section 7-7 - Network and Insite II Configuration
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7-7-2 Insite II Configuration
(cont’d)
12.)Service can do Remote Diagnostics successfully.
Figure 7-25 Remote Diagnostic successful
13.)Press power switch, and choose Full Maintenance Reboot to reboot system.
Figure 7-26 Full Maintenance Reboot window
Chapter 7 Diagnostics/Troubleshooting 7-23
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7-7-3 Insite II Configuration (For LOGIQ e R6.x.x and LOGIQ e R7.x.x)
1.) Enter global service user interface, and log in as GE Service. See section 7-5-1 on page 9 .
2.) On Configuration page, select Insite ExC Agent Configuration in the left column, fill in the information in Agent Configuration, choose “PPODUCT” as Enterprise server in Advanced
Configuration, please keep the default settings for other items, then click Submit Changes.
NOTE:
Figure 7-27 Choose Enterprise server
The BOLD items can not be left blank.
7-24 Section 7-7 - Network and Insite II Configuration
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7-7-3 Insite II Configuration (For LOGIQ e R6.x.x and LOGIQ e R7.x.x)
(cont’d)
3.) Set Disruptive Mode Status as Enabled. Change to Utilities page. select Disruptive Mode in the left column, Check whether the Disruptive Mode Status is Enabled, if not, click Yes to change the
Disruptive Mode Status as Enabled. See Figure 7-28 on page 7-25 .
Figure 7-28 Device_Information page
There is another way to Set Disruptive Mode Status as Enabled. Click Insite Icon in system status bar, choose Connect clinical Lifeline, the Insite Icon will change to RED, do not need to change if the insite icon is already RED. See Figure 7-29 on page 7-25 .
Figure 7-29 Set Disruptive Mode Status
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7-7-3 Insite II Configuration (For LOGIQ e R6.x.x and LOGIQ e R7.x.x)
(cont’d)
4.) Customer will receive a request of Service side, click Yes to accept. See Figure 7-30 on page 7-26
Figure 7-30 Accept requirement of Service
5.) Service can do Remote Diagnostics successfully. See Figure 7-31 on page 7-26
Figure 7-31 Remote Diagnostic successful
7-26 Section 7-7 - Network and Insite II Configuration
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7-7-3 Insite II Configuration (For LOGIQ e R6.x.x and LOGIQ e R7.x.x)
(cont’d)
6.) Press power switch, select Full Maintenance Reboot to reboot system, see Figure 7-32 on page 7-
27 .
Figure 7-32 Full Maintenance Reboot window
7.) In remote server side, select the device type in DEVICE TYPE.
Figure 7-33 device type window
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7-7-3 Insite II Configuration (For LOGIQ e R6.x.x and LOGIQ e R7.x.x)
(cont’d)
8.) Select Update Software in the category of SERVICE.
Figure 7-34 Update software
9.) The page of software package shows up, select the correct software package in the list. Then select
SCHEDULE to set a proper time to upgrade the software.
7-28
Figure 7-35 software package
Section 7-7 - Network and Insite II Configuration
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7-7-3 Insite II Configuration (For LOGIQ e R6.x.x and LOGIQ e R7.x.x)
(cont’d)
10.)Click “+” icon on the schedule page to set up a schedule. Fill in the name and time, then click Add.
Figure 7-36 New schedule page
11.)Then the active schedule is shown on the SCHEDULE page.
Figure 7-37 Active Schedule
Chapter 7 Diagnostics/Troubleshooting 7-29
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7-7-3 Insite II Configuration (For LOGIQ e R6.x.x and LOGIQ e R7.x.x)
(cont’d)
12.)In device side, if the device is connected to network, a mail icon will show in the status bar.
Figure 7-38 Status bar
13.)Press Power buuton. The SYSTEM-EXIT window shows up. Click Decline, the system will not download the software, and the Insite icon in the status bar will not shown. Click Download, the system will begin to download the software.
NOTE:
Figure 7-39 System-Exit window
If the administrator is in remote side, press Alt+F1 to display the frontpanel simulator. Select the On/Off button, and the system-exit window shows up.
7-30
Figure 7-40 Frontpanel Simulator window
Section 7-7 - Network and Insite II Configuration
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7-7-3 Insite II Configuration (For LOGIQ e R6.x.x and LOGIQ e R7.x.x)
(cont’d)
NOTE: Make sure the system administrator is logged on as ADM, or the system will indicate such message.
Figure 7-41 System-exit error
14.)The system begins to download the software, and wait until the process complete.
If you click Pause, the download process will be paused. Click Download to re-start the process.
If you click Cancel, the download process will stop.
Figure 7-42 Software download process
Chapter 7 Diagnostics/Troubleshooting 7-31
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7-7-3 Insite II Configuration (For LOGIQ e R6.x.x and LOGIQ e R7.x.x)
(cont’d)
15.)When the download is complete, it will show the window below.
Figure 7-43 Download Complete window
16.)Restart the system, and the system CD will be loaded as shown in Figure 7-44 on page 7-32 .
Figure 7-44 System CD loading
7-32 Section 7-7 - Network and Insite II Configuration
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7-7-3 Insite II Configuration (For LOGIQ e R6.x.x and LOGIQ e R7.x.x)
(cont’d)
17.)After the system is on, login as ADM. Press Power button, and the system-exit window displays.
Select Verify.
Figure 7-45 System-exit verify window
18.)It will show the verify items. Select Passed, and sign the signature, the upgrade completes. If any of the 10 items fails, the system will remind the user to restart the system to rollback to the previous version.
Figure 7-46 Verify item
Chapter 7 Diagnostics/Troubleshooting 7-33
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7-34 Section 7-7 - Network and Insite II Configuration
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Chapter 8
Replacement Procedures
Section 8-1
Overview
8-1-1 Purpose of Chapter 8
This chapter describes replacement procedures for the following modules and subsystems.
Table 8-1 Contents in Chapter 8
Section
8-1
Page Number
8-1
8-2
8-2-1
8-2-2
8-3
8-4
Description
Overview
Disassembly/Re-assembly of LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e
Warning and Caution
Handle Assy (FRU No. 313)
Loading Base Image Software
Checks after FRU replacement (Debrief Guidelines)
8-1
8-1
8-2
8-4
8-9
Section 8-2
Disassembly/Re-assembly of LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e
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 work on live circuits and more than 30V peak is present.
Chapter 8 Replacement Procedures 8-1
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8-2-2 Handle Assy (FRU No. 313)
Purpose: This is a description on how to remove and replace the Handle Assy (FRU No.313).
8-2-2-1
8-2-2-2
8-2-2-3
8-2-2-4
8-2-2-5
Tools
• Plier
Needed Manpower
• 1 person, 2 minutes + travel
Preparations
• Shut Down the System.
Removal Procedure
Refer to Figure 8-1 on page 8-3 .
1.) Unscrew the two handle caps on both sides of the system, the rotation direction is counterclockwise.
2.) Pull out the Handle.
Mounting procedure
1.) Install the new parts in the reverse order of removal.
8-2 Section 8-2 - Disassembly/Re-assembly of LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e
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8-2-2 Handle Assy (FRU No. 313)
(cont’d)
1)
Figure 8-1 Handle Assy Disassembly
2)
Chapter 8 Replacement Procedures 8-3
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Section 8-3
Loading Base Image Software
NOTE:
NOTE:
While it is believed to be unnecessary, It would not hurt to disconnect the system from the network and remove all transducers.
Please ensure AC adapter 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 “Full
Maintenance Reboot” 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.
Figure 8-2 Shutdown Dialog Box
4.) Turn on the scanner. System will detect the DVD-RW automatically.
5.) Press any key to continue when below message display as shown in Figure 8-3 on page 8-4 .
8-4
Figure 8-3 Update message
Section 8-3 - Loading Base Image Software
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Section 8-3 Loading Base Image Software
(cont’d)
6.) Select one of the options for loading the system. Select choice [a] to load the complete disk.
Refer to Figure 8-4 on page 8-5 .
Figure 8-4 Selection for loading the system
While the software install procedure is designed to preserve data, you should select choice [b] to format disk C only.
7.) Press “Yes” or “No” to continue.
Figure 8-5 Confirmation on loading the system
Chapter 8 Replacement Procedures 8-5
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Section 8-3 Loading Base Image Software
(cont’d)
8.) System CD will be loaded as shown in Figure 8-6 on page 8-6 .
Figure 8-6 System CD loading
If the screen displays as show in Figure 8-7 on page 8-6 after input “Yes”, wait about 1 minute until
Figure 8-6 on page 8-6 displays.
NOTE:
Figure 8-7 System CD loading blank message
System CD will be loaded twice, and it will need about 20 minutes.
8-6 Section 8-3 - Loading Base Image Software
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Section 8-3 Loading Base Image Software
(cont’d)
9.) After finish updating system, refer to Figure 8-8 on page 8-7 .
Figure 8-8 System upgrade complete
10.)Press any key to reboot system. When system first time boot up after upgrading complete, you will see the following message.
Figure 8-9 Windows start
11.)Make a region selection when below message display as show in Figure 8-10 on page 8-7 .
NOTE:
Figure 8-10 Region selection message
Step 11.) is only for LOGIQ e R4.x.x, LOGIQ i R4.x.x and Vivid e R4.x.x.
Chapter 8 Replacement Procedures 8-7
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Section 8-3 Loading Base Image Software
(cont’d)
NOTE: For LOGIQ e R5.x.x, R6.x.x, please select a package to run the application.
For Emergency&Critical For Nerve&Needle
For General Imaging
Figure 8-11 Package selection message
NOTE: For LOGIQ e R5.x.x, you need to select a package to run the application.
8-8 Section 8-3 - Loading Base Image Software
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Section 8-4Checks after FRU replacement (Debrief Guidelines)
Perform required Functional tests based upon the FRU being replaced.
Table 8-2 Functional Tests Matrix of LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e
Section
FRU
No.
8-2-2
Section
8-3
313
Description Functional Tests
Basic Functional
Checks
4-3-1 , 4-3-2 , 4-3-7 , 4-3-8 , 4-3-9 , 4-3-10
Handle Assy
Handle function check:
1. The system can be carried with the handle;
2. The handle can rotate from +90 to -110 degree
Loading Base Image
Software
4-3-1 , 4-3-2 , 4-3-7 , 4-3-8 , 4-3-9 , 4-3-10 , Section 4-4
Table 8-3 Functional Test key of LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e
Key
4-3-1
4-3-2
4-3-7
4-3-8
4-3-9
4-3-10
Section 4-4
Functional Test/Diagnostics/Leakage Current
Power On/Boot Up
Power Off/ Shutdown
B Mode Checks
M Mode Controls
Color Flow Mode Checks
Doppler Mode Checks
Software Configuration Checks
Chapter 8 Replacement Procedures 8-9
GE H
EALTHCARE
D
IRECTION
5370626-100, R
EVISION
7 LOGIQ
E
/LOGIQ
E
V
ET
/LOGIQ
I
/V
IVID E
B
ASIC
S
ERVICE
M
ANUAL
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8-10 Section 8-4 - Checks after FRU replacement (Debrief Guidelines)
GE H
EALTHCARE
D
IRECTION
5370626-100, R
EVISION
7 LOGIQ
E
/LOGIQ
E
V
ET
/LOGIQ
I
/V
IVID E
B
ASIC
S
ERVICE
M
ANUAL
Chapter 9
Renewal Parts
Section 9-1
Overview
9-1-1 Purpose of Chapter 9
This chapter gives an overview of Spare Parts available for the LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e .
Table 9-1 Contents in Chapter 9
Section
9-1
9-6
9-7
9-8
9-9
9-2
9-3
9-4
9-5
9-10
9-11
9-12
9-13
Description
Overview
List of Abbreviations
Renewal Parts Lists
Operator Console Assy
LCD Assy
Keyboard Assy
Bottom Assy
Cables
Isolation Cart Components
Isolation Cart Enhanced Version Components
Accessories and Kits
Manuals
Probe
Page Number
9-1
9-6
9-7
9-15
9-16
9-1
9-2
9-3
9-4
9-18
9-21
9-26
9-31
Section 9-2
List of Abbreviations
• Assy - Assembly
• Ctrl - Control
• FRU 1 - Replacement part available in part hub
• FRU 2 - Replacement part available from the manufacturer (lead time involved)
• KBD - Keyboard
• LCD - Liquid Crystal Display
• BnV - Brightness and Volume
• RX64- Dragon Front Processor Board
• TMST - Master Board
• TX64 - Dragon Transmit Board
Chapter 9 Renewal Parts 9-1
GE H
EALTHCARE
D
IRECTION
5370626-100, R
EVISION
7 LOGIQ
E
/LOGIQ
E
V
ET
/LOGIQ
I
/V
IVID E
B
ASIC
S
ERVICE
M
ANUAL
Section 9-3Renewal Parts Lists
9-3-1 Equipment Models Covered in this Chapter
Table 9-2 ACDC Power Pack & ACDC Power Cable list
Item
007
008
009
010
011
012
013
003
004
005
006
001
001A
002
002A
Part
Number
5196783
5196783-2
2409198
2409198-2
5120411
5120412
5120439
5120440
5125218
5125219
5125221
5125223
5125227
5125228
5400793
Part Name
ACDC adapter with clamp filter
ACDC adapter with clamp filter
ACDC Power Pack unit 100W AC Adapter
ACDC Power Pack unit 110W AC Adapter
ACDC Power Cable for USA
ACDC Power Cable for Europe
ACDC Power Cable for China
ACDC Power Cable for Japan
ACDC Power Cable for Australia/New Zealand
ACDC Power Cable for United Kingdom and Ireland
ACDC Power Cable for India/South Africa
ACDC Power Cable for Argentina
ACDC Power Cable for Israel
ACDC Power Cable for Switzerland
ACDC Power Cable for Brazil
Quantity FRU
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1 x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x
9-2 Section 9-3 - Renewal Parts Lists
GE H
EALTHCARE
D
IRECTION
5370626-100, R
EVISION
7 LOGIQ
E
/LOGIQ
E
V
ET
/LOGIQ
I
/V
IVID E
B
ASIC
S
ERVICE
M
ANUAL
Section 9-4 Operator Console Assy
LCD Assy
Bottom Assy
Figure 9-1 OPERATOR CONSOLE ASSY
Keyboard Assy
Chapter 9 Renewal Parts 9-3
GE H
EALTHCARE
D
IRECTION
5370626-100, R
EVISION
7 LOGIQ
E
/LOGIQ
E
V
ET
/LOGIQ
I
/V
IVID E
B
ASIC
S
ERVICE
M
ANUAL
Section 9-5 LCD Assy
100
102
101
104
9-4
105
Figure 9-2 LCD Assy
Section 9-5 - LCD Assy
103
GE H
EALTHCARE
D
IRECTION
5370626-100, R
EVISION
7 LOGIQ
E
/LOGIQ
E
V
ET
/LOGIQ
I
/V
IVID E
B
ASIC
S
ERVICE
M
ANUAL
Section 9-5 LCD Assy
(cont’d)
Table 9-3 LCD Assy
5133509-3
5199553
5190010-2
5419292
5149676
5212061
5190008
5190009
5147731-2
5244921
5147473-2
5244918
5190011
5244920
5419295
5418452
Item
100
101
102
103
Part
Number
5147731
104
105
106
106A
107
108
5251801
5146747
5125944-3
5184890
5184890-2
5244561
5366398
Part Name
LCD Assy for LOGIQ e R5.0.x /LOGIQ e R5.2.x/LOGIQ e R6.x.x/ LOGIQ e Vet /
Vivid e R4.x.x
LCD Assy for LOGIQ e R4.x.x/Vivid e R4.x.x
LCD Assy for Vivid e R5.x.x / Vivid e R6.x.x
LCD Assy for LOGIQ i R4.x.x
LCD Assy for LOGIQ i R5.x.x
LCD Assy for LOGIQ e R7.x.x
LCD Front Cover for LOGIQ e R7.x.x
LCD Front Cover for LOGIQ e R4.x.x / LOGIQ e R5.0.x / LOGIQ e R5.2.x/
LOGIQ e R6.x.x /LOGIQ e Vet / Vivid e R4.x.x
LCD Front Cover for Vivid e R5.x.x / Vivid e R6.x.x
Front Cover for LOGIQ i R4.x.x /LOGIQ i R5.x.x
LCD Back Cover for LOGIQ e R7.x.x
LCD Back Cover for LOGIQ e R4.x.x / LOGIQ e R5.0.x / LOGIQ e R5.2.x/
LOGIQ e R6.x.x /LOGIQ e Vet / Vivid e R4.x.x
LCD Back Cover for Vivid e R5.x.x / Vivid e R6.x.x
Back Cover for LOGIQ i R4.x.x
Back Cover for LOGIQ i R5.x.x
Inverter Assy LOGIQ e R5.0.x / LOGIQ e R5.2.x/LOGIQ e R6.x.x /LOGIQ e Vet /
Vivid e R5.x.x / Vivid e R6.x.x
Inverter Assy for LOGIQ e R4.x.x / Vivid e R4.x.x / LOGIQ i R4.x.x /
LOGIQ i R5.x.x
LCD panel for LOGIQ e R5.0.x / LOGIQ e R5.2.x/LOGIQ e R6.x.x / LOGIQ e Vet/
Vivid e R4.x.x / Vivid e R5.x.x / Vivid e R6.x.x / LOGIQ i R5.x.x
LCD panel for LOGIQ e R4.x.x /Vivid e R4.x.x / LOGIQ i R4.x.x
LCD cable
Cable Kit (LCD cable, KBD cables) for LOGIQ e R4.x.x / Vivid e R4.x.x
Cable Kit (LCD cable, KBD cables) for LOGIQ e R4.x.x / LOGIQ i R5.x.x
Hg label for Vivid e R4.x.x
LCD Cable Kit (LCD Cable and LCD Cable with JAE connector
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1 x x
1
1
1
1
1
1 x x x x x x x x
1 x x
1
1
1 x x x x
1 x x
1
1
1 x x
1 x x x x x
1 x x x x
2 x x
2
2
2
2
2
2 x x x x x x x x x x x x x x x x x x
Chapter 9 Renewal Parts 9-5
GE H
EALTHCARE
D
IRECTION
5370626-100, R
EVISION
7 LOGIQ
E
/LOGIQ
E
V
ET
/LOGIQ
I
/V
IVID E
B
ASIC
S
ERVICE
M
ANUAL
Section 9-6Keyboard Assy
203
200
9-6
201
Figure 9-3 Keyboard Assy
202
Section 9-6 - Keyboard Assy
GE H
EALTHCARE
D
IRECTION
5370626-100, R
EVISION
7 LOGIQ
E
/LOGIQ
E
V
ET
/LOGIQ
I
/V
IVID E
B
ASIC
S
ERVICE
M
ANUAL
Section 9-6 Keyboard Assy
(cont’d)
205
206
204
Figure 9-4 Keyboard Assy (cont’d)
Table 9-4 Keyboard Assy
Item
200
Part
Number
5419297
5198176
5148753
5172817
5199342
5184814
Part Name
Keyboard Assy for LOGIQ e R7.x.x
Keyboard Assy for LOGIQ e R5.0.x / LOGIQ e R5.2.x /LOGIQ e R6.x.x / LOGIQ e Vet
Keyboard Assy for LOGIQ e R4.x.x
Keyboard Assy for Vivid e R4.x.x
Keyboard Assy Vivid e R5.x. x/ Vivid e R6.x.x
Keyboard Assy for LOGIQ i R4.x.x / LOGIQ i R5.x.x
1
1
1
1
1
1
1
1
1
1
1
1 x x x x x x x
Chapter 9 Renewal Parts 9-7
GE H
EALTHCARE
D
IRECTION
5370626-100, R
EVISION
7 LOGIQ
E
/LOGIQ
E
V
ET
/LOGIQ
I
/V
IVID E
B
ASIC
S
ERVICE
M
ANUAL
Table 9-4 Keyboard Assy
Item
201
Part
Number
5160471
5420742
202
203
5123732
5175936
5252489
5419296
5199756
5148760
5173857
5199973
5190002
Part Name
Trackball Assy
A/N Key Assy for LOGIQ e R7.x.x
A/N Key Assy for LOGIQ e R4.x.x / LOGIQ e R5.0.x / LOGIQ e R5.2.x /
LOGIQ e R6.x.x/ LOGIQ e Vet / LOGIQ i R4.x.x / LOGIQ i R5.x.x
A/N Key Assy for Vivid e R4.x.x
A/N Key Assy for Vivid e R5.x.x / Vivid e R6.x.x
Keyboard cover Assy for LOGIQ e R7.x.x
Keyboard cover Assy for LOGIQ e R5.0.x / LOGIQ e R5.2.x /LOGIQ e R6.x.x/
LOGIQ e Vet
Keyboard cover Assy for LOGIQ e R4.x.x
Keyboard cover Assy for Vivid e R4.x.x
Keyboard cover Assy for Vivid e R5.x.x / Vivid e R6.x.x
Keyboard cover Assy for LOGIQ i R4.x.x / LOGIQ i R5.x.x
KBD cable kits for LOGIQ e R4.x.x / LOGIQ e R5.0.x / LOGIQ e R5.2.x/LOGIQ e
R6.x.x / LOGIQ e Vet /Vivid e R5.x.x / Vivid e R6.x.x /LOGIQ i R5.x.x
1
1
1
2 x x x x x
1
1
1
1
2 x
2
2
2 x x x x x
1
1
1
1
1
2 x
2
2
2
2 x x x x x
1 1 x x x x 5154621-2
204
205
206
207
5154621
5155123
5173672
5224534
5155004
5125106-4
5125106-3
KBD cable kits for LOGIQ e R4.x.x / Vivid e R4.x.x / LOGIQ i R4.x.x
Keyboard PWA kits for LOGIQ e R4.x.x / LOGIQ e R5.0.x / LOGIQ e R5.2.x/LOGIQ e R6.x.x / LOGIQ e Vet / LOGIQ i R4.x.x / LOGIQ i R5.x.x
Keyboard PWA kits for Vivid e R4.x.x
Keyboard PWA kits for Vivid e R5.x.x / Vivid e R6.x.x
Speaker Kits
Main KBD to MST Cable for LOGIQ e R7.x.x
Main KBD to MST Cable
1
1
2
1
1
1
1
1 x
1 x
1
2
2
1
2 x x x x x x x x x x x x x x x
9-8 Section 9-6 - Keyboard Assy
GE H
EALTHCARE
D
IRECTION
5370626-100, R
EVISION
7 LOGIQ
E
/LOGIQ
E
V
ET
/LOGIQ
I
/V
IVID E
B
ASIC
S
ERVICE
M
ANUAL
Section 9-7Bottom Assy
309
301
312
310
303
304
300
303
301
302
302A
Figure 9-5 Bottom Assy
Chapter 9 Renewal Parts
304
9-9
GE H
EALTHCARE
D
IRECTION
5370626-100, R
EVISION
7 LOGIQ
E
/LOGIQ
E
V
ET
/LOGIQ
I
/V
IVID E
B
ASIC
S
ERVICE
M
ANUAL
Section 9-7 Bottom Assy
(cont’d)
305
306
9-10
309
Figure 9-6 Bottom Assy (cont’d)
310
Section 9-7 - Bottom Assy
307
308
GE H
EALTHCARE
D
IRECTION
5370626-100, R
EVISION
7 LOGIQ
E
/LOGIQ
E
V
ET
/LOGIQ
I
/V
IVID E
B
ASIC
S
ERVICE
M
ANUAL
Section 9-7 Bottom Assy
(cont’d)
312
311
316
313
317
Figure 9-7 Bottom Assy (cont’d)
318
Chapter 9 Renewal Parts 9-11
GE H
EALTHCARE
D
IRECTION
5370626-100, R
EVISION
7 LOGIQ
E
/LOGIQ
E
V
ET
/LOGIQ
I
/V
IVID E
B
ASIC
S
ERVICE
M
ANUAL
Section 9-7 Bottom Assy
(cont’d)
Table 9-5 Bottom Assy
Item
Part
Number
5422185
5148765
300
301
5148764
5213129
5182370
2406640
2406640-2
2406640-3
2406640-3R
2406640-4
302
2404903
302A
2404903-2
302B
2404903-3
302C
302D
303
303A
304
304A
304B
305
2404903-6
2404903-7
2404906
2404906-3
5148771
5389034
5422449
5124847-2
5124847-3
Part Name
Bottom Cover Assy for LOGIQ e R4.x.x / LOGIQ e R5.0.x / LOGIQ e R5.2.x /
LOGIQ e R6.x.x / LOGIQ e R7.x.x / LOGIQ e Vet
Bottom Cover Assy for LOGIQ e R4.x.x / LOGIQ e R5.0.x / LOGIQ e R5.2.x /
LOGIQ e R6.x.x/ LOGIQ e Vet
Bottom Cover Assy for Vivid e R4.x.x
Bottom Cover Assy for Vivid e R5.x.x / Vivid e R6.x.x
Bottom Cover Assy for LOGIQ i R4.x.x / LOGIQ i R5.x.x
TMST Board
TMST Board
TMST Board
TMST Board
TMST Board
TX64 Board for LOGIQ e R4.x.x / LOGIQ e R5.x.x / Vivid e R4.x.x / Vivid e
R5.x.x / LOGIQ i R4.x.x / LOGIQ i R5.x.x / LOGIQ e Vet
TX64 Board for LOGIQ e R4.x.x / LOGIQ e R5.x.x / Vivid e R4.x.x / Vivid e
R5.x.x / LOGIQ i R4.x.x / LOGIQ i R5.x.x / LOGIQ e Vet
TX64 Board for LOGIQ e R4.x.x / LOGIQ e R5.x.x / Vivid e R4.x.x / Vivid e
R5.x.x / LOGIQ i R4.x.x / LOGIQ i R5.x.x / LOGIQ e Vet
TX64 Board for LOGIQ e R6.x.x / Vivid e R6.x.x
TX64 Board for LOGIQ e R6.x.x / LOGIQ e R7.x.x / Vivid e R6.x.x
RX64 Board
RX64 Board
Probe Connector Assy
Probe Connector Assy for LOGIQ e R6.x.x
Probe Connector Assy for LOGIQ e R6.x.x / LOGIQ e R7.x.x
CWD Board
CWD Board
1
1
2
2
1
1
1
1
2
1
2
2
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1 x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x
9-12 Section 9-7 - Bottom Assy
GE H
EALTHCARE
D
IRECTION
5370626-100, R
EVISION
7 LOGIQ
E
/LOGIQ
E
V
ET
/LOGIQ
I
/V
IVID E
B
ASIC
S
ERVICE
M
ANUAL
Table 9-5 Bottom Assy
Item
306
307
309
310
311
312
313
314
315
316
317
Part
Number
5419298
5212013
5148773
5212340
5184871
5155175
307A
308
5392210
5392210-2
5159620
5162038-3
5162038-2
5148768
5173403-3
5155166
2406733
5154937
5234933
5154486
5154731
5255230
5255231-2
5148772
5174862-5
5190005
5145407
Part Name
Menu Panel Assy for LOGIQ e R7.x.x
Menu Panel Assy for LOGIQ e R5.0.x / LOGIQ e R5.2.x/LOGIQ e R6.x.x/
LOGIQ e Vet
Menu Panel Assy for LOGIQ e R4.x.x / Vivid e R4.x.x
Menu Panel Assy for Vivid e R5.x.x / Vivid e R6.x.x
Menu Panel Assy for LOGIQ i R4.x.x / LOGIQ i R5.x.x
PM1.4G ETX CPU Module for LOGIQ e R4.x.x / LOGIQ e R5.x.x / Vivid e R4.x.x
/ Vivid e R5.x.x / LOGIQ i R4.x.x / LOGIQ i R5.x.x / LOGIQ e Vet
U7500 CPU kits for LOGIQ e R6.x.x / Vivid e R6.x.x
U7500 CPU kits only for LOGIQ e R6.x.x / Vivid e R6.x.x
512MB DDR Memory
Charger Board and Cable Kits for LOGIQ e R5.0.x / LOGIQ e R5.2.x /LOGIQ e
R6.x.x/ LOGIQ e Vet / Vivid e R5.x.x / Vivid e R6.x.x / LOGIQ i R5.x.x
Charger Board and Cable Kits for LOGIQ e R4.x.x / Vivid e R4.x.x / LOGIQ i
R4.x.x
Left FAN Assy (2 Fans)
Right FAN Assy (2 Fans)
LCD and Handle Hinge kits
TMST2TX64 Assy
Handle Assy for LOGIQ e R4.x.x / LOGIQ e R5.0.x /LOGIQ e R5.2.X/LOGIQ e
R6.x.x / LOGIQ e Vet / Vivid e R4.x.x / LOGIQ i R4.x.x / LOGIQ i R5.x.x
Handle Assy for Vivid R5.x.x / Vivid e R6.x.x
Screw Kits
Rubber Kits
80G HDD without Program Assy
160G HDD without Program Assy
HDD Assy for LOGIQ e R4.x.x
HDD Assy for Vivid e R4.x.x
HDD Assy for LOGIQ i R4.x.x / LOGIQ i R5.x.x
CMOS Battery
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
2
1
2
1
1
2
1
1
1
1
1
2
1
2
2
1
1
1
1
1
1
1
1
1
2 x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x
Chapter 9 Renewal Parts 9-13
GE H
EALTHCARE
D
IRECTION
5370626-100, R
EVISION
7 LOGIQ
E
/LOGIQ
E
V
ET
/LOGIQ
I
/V
IVID E
B
ASIC
S
ERVICE
M
ANUAL
Table 9-5 Bottom Assy
Item
318
319
Part
Number
5422180
5135311
5234927
Part Name
Battery Clip for LOGIQ e R5.0.x / LOGIQ e R5.2.x / LOGIQ e R6.x.x / LOGIQ e
R7.x.x /LOGIQ e Vet / Vivid e R5.x.x / Vivid e R6.x.x
Battery Clip for LOGIQ e R5.0.x / LOGIQ e R5.2.x //LOGIQ e R6.x.x LOGIQ e
Vet / Vivid e R5.x.x / Vivid e R6.x.x
HDD Shelf kits for LOGIQ i R4.x.x / LOGIQ i R5.x.x
1
1
1
2
2
1 x x x x x x x
9-14 Section 9-7 - Bottom Assy
GE H
EALTHCARE
D
IRECTION
5370626-100, R
EVISION
7 LOGIQ
E
/LOGIQ
E
V
ET
/LOGIQ
I
/V
IVID E
B
ASIC
S
ERVICE
M
ANUAL
Section 9-8
Cables
Chapter 9 Renewal Parts 9-15
GE H
EALTHCARE
D
IRECTION
5370626-100, R
EVISION
7 LOGIQ
E
/LOGIQ
E
V
ET
/LOGIQ
I
/V
IVID E
B
ASIC
S
ERVICE
M
ANUAL
Section 9-9Isolation Cart Components
502
501
503
504
506
507
505
509
Figure 9-8 Isolation Cart Components
Table 9-6 Isolation Cart Components
Item
501
502
503
504
505
Part
Number
5183729
5180439-2
5180376
5180376-2
5183627
5183958
5183719
Part Name
Wheels
Isolation transformer 110V
Isolation transformer 200V~240V
Isolation transformer 220V
Handle kits
Probe holder kits
Hardware kits
508
1
1
1
1
1
1
1
2
2
2
2
2
2
2 x x x x x x x x x x x x x x x x x x x x x x x x x x x x
9-16 Section 9-9 - Isolation Cart Components
GE H
EALTHCARE
D
IRECTION
5370626-100, R
EVISION
7 LOGIQ
E
/LOGIQ
E
V
ET
/LOGIQ
I
/V
IVID E
B
ASIC
S
ERVICE
M
ANUAL
Table 9-6 Isolation Cart Components
Item
506
507
508
509
Part
Number
5182671
5182937
5182252
5182323
5182095
5182890
5182310
5182038
5182881
5182625
5182631
5183906
5176271-2
5177329-2
5195546
Part Name
USA class cable kits
European class cable kits
Chinese class cable kits
Japanese class cable kits
Australia/New Zealand class cable kits
United Kingdom and Ireland class cable kits
Denmark class cable kits
India/South Africa class cable kits
Argentina class cable kits
Israel class cable kits
Switzerland class cable kits
Security lock
Isolation Cart (110V)
Isolation Cart (220V)
Isolation Cart 250V T 5A Fuse for Tranformer
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
2
2
1
2
2
2
2
2
2
2
2
2
2
2
2 x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x
Chapter 9 Renewal Parts 9-17
GE H
EALTHCARE
D
IRECTION
5370626-100, R
EVISION
7 LOGIQ
E
/LOGIQ
E
V
ET
/LOGIQ
I
/V
IVID E
B
ASIC
S
ERVICE
M
ANUAL
Section 9-10
Isolation Cart Enhanced Version Components
511
512
515
513
514
518
519
516
517
522
521
Figure 9-9 Isolation Cart Components
524
523
9-18 Section 9-10 - Isolation Cart Enhanced Version Components
GE H
EALTHCARE
D
IRECTION
5370626-100, R
EVISION
7 LOGIQ
E
/LOGIQ
E
V
ET
/LOGIQ
I
/V
IVID E
B
ASIC
S
ERVICE
M
ANUAL
Table 9-7 Isolation Cart Components
Item
510
511
512
513
513A
Part
Number
5384810
5423269
5384811
5426642
5394065
5391606
5394036
5426645
5394032
5426644
5394021
5215494
5423270
5394023
5391829
5394060
5394061
5426649
5426650
5394028
5394064
5426643
5394067
5426646
514
514A
515
516
517
517A
518
518A
519
521
522
522A
523
523A
Part Name
Isolation Cart (110V)
Isolation Cart (110V)
Isolation Cart (220V)
Isolation Cart (220V)
Castor kits
Gas Spring lever
Isolation cart transformer 110V (Dark Steel Blue)
Isolation cart transformer 220V (Dark Steel Blue)
Isolation cart transformer 110V (Onyx Black)
Isolation cart transformer 220V (Onyx Black)
Cable hook kit (Dark Steel Blue)
Cable hook kit (Onyx Black)
Isolation Cart Rear Handle
Spring Cable Assy
Locate block and Screw cap (GE Pearl Metallic)
Locate block and Screw cap (GE N9)
Probe and gel holder kit (Dark Steel Blue)
Probe and gel holder kit (Onyx Black)
Handle clip kit
Security lock with package
Isolation Cart Front handle (Dark Steel Blue)
Isolation Cart Front handle (Onyx Black)
Gas Spring Assy (Dark Steel Blue)
Gas Spring Assy (Onyx Black)
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1 x x x x x x x x x x x x x x x x x x x x x
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2 x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x
Chapter 9 Renewal Parts 9-19
GE H
EALTHCARE
D
IRECTION
5370626-100, R
EVISION
7 LOGIQ
E
/LOGIQ
E
V
ET
/LOGIQ
I
/V
IVID E
B
ASIC
S
ERVICE
M
ANUAL
Table 9-7 Isolation Cart Components
Item
524
525
525A
526
526A
Part
Number
5177154
5176753
5177195
5176773
5177153
5176907
5177187-2
5177126
5176304
5177123
5177146
5393025
5426647
5393026
5426648
Part Name
AC Power Cord Switzerland
AC Power Cord Israel
AC Power Cord Argentina
AC Power Cord India
AC Power Cord Denmark
AC Power Cord UK
AC Power Cord Australia
AC Power Cord Japan
AC Power Cord China
AC Power Cord Europe
AC Power Cord USA
Isolation Cart Drawer Kits (GE Pearl Metallic)
Isolation Cart Drawer Kits (GE N9)
Isolation Cart Basket Kits (GE Pearl Metallic)
Isolation Cart Basket Kits (GE N9)
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1 x x x x x x x x x x x x x x x
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2 x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x
9-20 Section 9-10 - Isolation Cart Enhanced Version Components
GE H
EALTHCARE
D
IRECTION
5370626-100, R
EVISION
7 LOGIQ
E
/LOGIQ
E
V
ET
/LOGIQ
I
/V
IVID E
B
ASIC
S
ERVICE
M
ANUAL
Section 9-11
Accessories and Kits
Table 9-8 Accessories and Kits
Item Part Number
601
602
602A
602B
602C
603
603A
603B
603C
604
605A
605B
606
607
604A
604B
604C
605
607A
608
5422172
5120410-2
5120410
5183459
5151233
5151233-2
5151233-3
5151233-4
5151255
5151255-2
5151255-3
5151255-4
5151234
5151234-2
5151234-3
5151234-4
5182891-2
5182891-3
5182891-4
5151236
2327703
5338419
5172876-2
Part Name
Battery Pack for LOGIQ e R4.x.x / LOGIQ e R5.0.x / LOGIQ e R5.2.x /
LOGIQ e R6.x.x / LOGIQ e R7.x.x / LOGIQ e Vet /Vivid e R4.x.x / LOGIQ i R4.x.x
Battery Pack for LOGIQ e R4.x.x / LOGIQ e R5.0.x / LOGIQ e R5.2.x /
LOGIQ e R6.x.x/LOGIQ e Vet /Vivid e R4.x.x / LOGIQ i R4.x.x
Battery Pack for LOGIQ e R4.x.x / LOGIQ e R5.0.x / LOGIQ e R5.2.x /
LOGIQ e R6.x.x/LOGIQ e Vet /Vivid e R4.x.x / LOGIQ i R4.x.x
Battery Pack Vivid e R5.x.x / Vivid e R6.x.x / LOGIQ i R5.x.x
DVD-RW (USA) LG DVD-RW for LOGIQ e R4.x.x / Vivid e R4.x.x
/ LOGIQ i R4.x.x
DVD-RW (USA) LITEON DVD-RW
DVD-RW (USA) LITEON DVD-RW
DVD-RW (USA) LITEON DVD-RW
DVD-RW (CHN) LG DVD-RW LOGIQ e R4.x.x / Vivid e R4.x.x / LOGIQ i
R4.x.x
DVD-RW (CHN) LITEON DVD-RW
DVD-RW (CHN) LITEON DVD-RW
DVD-RW (CHN) LITEON DVD-RW
DVD-RW (EUR) LG DVD-RW LOGIQ e R4.x.x / Vivid e R4.x.x / LOGIQ i
R4.x.x
DVD-RW (EUR) LITEON DVD-RW
DVD-RW (EUR) LITEON DVD-RW
DVD-RW (EUR) LITEON DVD-RW
DVD-RW (JPN) LITEON DVD-RW
DVD-RW (JPN) LITEON DVD-RW
DVD-RW (JPN) LITEON DVD-RW
USB Footswitch 3 Pedal Footswitch
USB Footswitch FSU 2001 1 Pedal Footswitch
USB Footswitch FSU-1000
USB Wireless Card
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
2 x x x x
2 x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2 x x x x x x x x x x x x x x x x x x x x
Chapter 9 Renewal Parts 9-21
GE H
EALTHCARE
D
IRECTION
5370626-100, R
EVISION
7 LOGIQ
E
/LOGIQ
E
V
ET
/LOGIQ
I
/V
IVID E
B
ASIC
S
ERVICE
M
ANUAL
Table 9-8 Accessories and Kits
Item Part Number
617
618
619
620
613A
614A
615A
616A
613
614
615
616
609
610
611
612
5133107-2
5133108-2
5133106-2
5133109-2
5175689
5175988
5175350
5175546
5151259
5151261
5151262
5151263
5133107
5133108
5133106
5133109
621
621A
621B
622
622A
622B
623
623A
623B
624
624A
5175122
5175122-2
5175122-3
5175833
5175833-2
5175833-3
5175554
5175554-2
5175554-3
5175898
5175898-2
Part Name
UP-D897 Digital B/W Printer (USA)
UP-D897 Digital B/W Printer (EU)
UP-D897 Digital B/W Printer (CHN)
UP-D897 Digital B/W Printer (JPN)
UP-D23MD Digital Color Printer (US)
UP-D23MD Digital Color Printer (EU)
UP-D23MD Digital Color Printer (CN)
UP-D23MD Digital Color Printer (JP)
UP-D25MD Digital Color Printer (US)
UP-D25MD Digital Color Printer (EU)
UP-D25MD Digital Color Printer (CN)
UP-D25MD Digital Color Printer (JP)
HP470 Printer Kits (HP470+PIT) -US
HP470 Printer Kits (HP470+PIT) -EU
HP470 Printer Kits (HP470+PIT) -CN
HP470 Printer Kits (HP470+PIT) -JP
HP K550 PC Printer -US for LOGIQ e R4.x.x / Vivid e R4.x.x / LOGIQ i
R4.x.x
HP K5400 PC Printer -US
HP K8600 PC Printer -US
HP K550 PC Printer -EU for LOGIQ e R4.x.x / Vivid e R4.x.x / LOGIQ i
R4.x.x
HP K5400 PC Printer -EU
HP K8600 PC Printer -EU
HP K550 PC Printer -CN for LOGIQ e R4.x.x / Vivid e R4.x.x / LOGIQ i
R4.x.x
HP K5400 PC Printer -CN
HP K8600 PC Printer -CN
HP K550 PC Printer-JP for LOGIQ e R4.x.x / Vivid e R4.x.x / LOGIQ i
R4.x.x
HP K5400 PC Printer-JP
9-22 Section 9-11 - Accessories and Kits
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1 x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2 x x x x x x x
GE H
EALTHCARE
D
IRECTION
5370626-100, R
EVISION
7 LOGIQ
E
/LOGIQ
E
V
ET
/LOGIQ
I
/V
IVID E
B
ASIC
S
ERVICE
M
ANUAL
Table 9-8 Accessories and Kits
Item Part Number
624B 5175898-3
625
626
627
634
636
637
638
639
635
635A
635B
635C
632
632A
633
633A
628
629
630
631
633B
633C
5183418
5146055
5129487
5234932
5183684
5183684
5191678
5173797
5173797-2
5173797-3
5173797-4
5322237
5322752
5322231
5324784
5146056
5146739
5149641
5195563
5184951
5184951-2
5168040
5168040-2
5168040-3
5168040-4
5181598
Part Name
HP K8600 PC Printer-JP
Loop Connector service tool for channel diagnostic used for LOGIQ e
R5.0.x / LOGIQ e R5.2.x/LOGIQ e R6.x.x / LOGIQ e Vet / Vivid e R5.x.x/
Vivid e R6.x.x/ LOGIQ i R4.x.x / LOGIQ i R5.x.x
ECG USB Cable
ECG Module from Norav Isral ECG Module, not for applicable for Muslim countries and China
ECG Detachable Cable AHA
ECG Detachable Cable IEC
ECG Module with Chinese Label
ECG Module with SKD Label, only applicable for Muslim countries
USB Hub
4 Ports HUB (USB 2.0)
USB Memory 512M
USB Memory 1G
USB Memory 2G
USB Memory 4G
LOGO Kit for LOGIQ e R4.x.x / LOGIQ e R5.0.x / LOGIQ e R5.2.x/LOGIQ e R6.x.x
LOGO Kit for LOGIQ e Vet
LOGO Kit for Vivid e R4.x.x
LOGO Kit for Vivid e R5.x.x / Vivid e R6.x.x
LOGO Kit for LOGIQ i R4.x.x / LOGIQ i R5.x.x
USB Harddisk 40G
USB Harddisk 80G
USB Harddisk 250G
USB Harddisk 500G
Barcode Reader 4600G for LOGIQ e R5.2.x/LOGIQ e R6.x.x
Barcode Reader 3800G for LOGIQ e R5.2.x/LOGIQ e R6.x.x
Barcode Reader Cable for Service for LOGIQ e R5.2.x/LOGIQ e R6.x.x
3-meter Internet Cable for Service
Chapter 9 Renewal Parts
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
2 x x x x
2 x x x x
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2 x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x
9-23
GE H
EALTHCARE
D
IRECTION
5370626-100, R
EVISION
7 LOGIQ
E
/LOGIQ
E
V
ET
/LOGIQ
I
/V
IVID E
B
ASIC
S
ERVICE
M
ANUAL
Table 9-8 Accessories and Kits
Item Part Number
644
644A
645
646
640
641
642
643
647
648
649
650
655
651
5235031-3
5322236
5322457-4
5322457-6
5322457-7
5396928-3
5396928-4
5396928-5
5396928-6
5423626
5248829
5248829-2
5248829-3
5173474
5173474-2
5173474-3
5173474-4
5173474-5
5173474-6
5235031
5235031-2
5199293
5196495
5268864
5248284
5264324
5264324-2
5172876-3
5324784
9-24
Part Name
Shoulder Bag
Clamp Filter for LOGIQ i R5.1.x
Peripheral Driver Patch CD Installation kit
Software Upgrade DVD for R5.1.0 for LOGIQ i
USB Wireless adapter WG111v3 Installation kit
USB Wireless adapter WN111v2 Installation kit
NetGear USB Wireless Adapter WG111 V3
3m Lan Cable
System and Application software DVD for LOGIQ e (R4.0.0)
System and Application software DVD for LOGIQ e (R4.0.1)
System and Application software DVD for LOGIQ e (R4.0.2)
System and Application software DVD for LOGIQ e (R4.0.3)
System and Application software DVD for LOGIQ e (R4.0.4)
System and Application software DVD for LOGIQ e (R4.0.4)
System and Application software DVD for LOGIQ e (R 5.0.0)
System and Application software DVD for LOGIQ e (R 5.0.1)
System and Application software DVD for LOGIQ e (R 5.0.1)
System and Application software DVD for LOGIQ e (R 5.2.0)
System and Application software DVD for LOGIQ e (R 5.2.1)
System and Application software DVD for LOGIQ e (R 5.2.2)
System and Application software DVD for LOGIQ e (R 5.2.3)
System and Application software DVD for LOGIQ e (R 6.0.1)
System and Application software DVD for LOGIQ e (R 6.0.2)
System and Application software DVD for LOGIQ e (R 6.0.3)
System and Application software DVD for LOGIQ e (R 6.0.4)
System and Application software DVD for LOGIQ e (R 7.0.0)
System and Application software DVD for LOGIQ e Vet (R 5.0.0)
System and Application software DVD for LOGIQ e Vet (R 5.0.1)
System and Application software DVD for LOGIQ e Vet (R 5.0.1)
Section 9-11 - Accessories and Kits
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2
2 x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
GE H
EALTHCARE
D
IRECTION
5370626-100, R
EVISION
7 LOGIQ
E
/LOGIQ
E
V
ET
/LOGIQ
I
/V
IVID E
B
ASIC
S
ERVICE
M
ANUAL
Table 9-8 Accessories and Kits
Item Part Number
652
653
654
5248828
5248828-2
5248828-3
5248828-4
5248828-5
5248828-6
5191713-3
5191713-6
5191713-7
5248829-4
5248829-5
5175298
5175298-2
5175298-3
5175298-4
5175298-5
5175298-6
Part Name
System and Application software DVD for LOGIQ e Vet (R 5.2.0)
System and Application software DVD for LOGIQ e Vet (R 6.0.3)
System and Application software DVD for Vivid e (R4.0.0)
System and Application software DVD for Vivid e (R4.0.1)
System and Application software DVD for Vivid e (R4.0.2)
System and Application software DVD for Vivid e (R4.0.3)
System and Application software DVD for Vivid e (R4.0.4)
System and Application software DVD for Vivid e (R4.0.4)
System and Application software DVD for Vivid e (R 5.0.0)
System and Application software DVD for Vivid e (R 5.0.1)
System and Application software DVD for Vivid e (R 5.0.1)
System and Application software DVD for Vivid e (R 5.2.0)
System and Application software DVD for Vivid e (R 5.2.1)
System and Application software DVD for Vivid e (R 6.0.0)
System and Application software DVD for LOGIQ i (R4.1.1)
System and Application software DVD for LOGIQ i (R5.1.0)
System and Application software DVD for LOGIQ i (R5.1.1)
1
1
2
2 x x x x x x x x x x x x x x x x x
Chapter 9 Renewal Parts 9-25
GE H
EALTHCARE
D
IRECTION
5370626-100, R
EVISION
7 LOGIQ
E
/LOGIQ
E
V
ET
/LOGIQ
I
/V
IVID E
B
ASIC
S
ERVICE
M
ANUAL
Section 9-12Manuals
Table 9-9 MANUALS for LOGIQ e R4.x.x
Item Part Name Part Number
LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e Service
Manual
5370626 -100
LOGIQ e R4.x.x User Manual, English
LOGIQ e R4.x.x User Manual, French
LOGIQ e R4.x.x User Manual, Spanish
LOGIQ e R4.x.x User Manual, German
LOGIQ e R4.x.x User Manual, Italian
System User Manuals
5118586-100
5118586-101
5118586-106
5118586-108
5118586-111
5118586-127
5118586-140
5118586-141
LOGIQ e R4.x.x User Manual, Portuguese
LOGIQ e R4.x.x User Manual, Japanese
LOGIQ e R4.x.x User Manual, Chinese
LOGIQ e R4.x.x Quick Start Guide, English
LOGIQ e R4.x.x Quick Start Guide, French
LOGIQ e R4.x.x Quick Start Guide, Spanish
LOGIQ e R4.x.x Quick Start Guide, German
LOGIQ e R4.x.x Quick Start Guide, Italian
LOGIQ e R4.x.x Quick Start Guide, Portuguese
LOGIQ e R4.x.x Quick Start Guide, Japanese
LOGIQ e R4.x.x Quick Start Guide, Chinese
System Quick Start Guide
5130174 -100
5130174 -101
5130174 -106
5130174 -108
5130174 -111
5130174 -127
5130174 -140
5130174 -141
Description
Service Manual
Basic User Manual
Basic User Manual
Basic User Manual
Basic User Manual
Basic User Manual
Basic User Manual
Basic User Manual
Basic User Manual
Quick Start Guide
Quick Start Guide
Quick Start Guide
Quick Start Guide
Quick Start Guide
Quick Start Guide
Quick Start Guide
Quick Start Guide
Quantity FRU
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
N
N
N
N
N
N
N
N
N
N
N
N
N
N
N
N
N
Table 9-10 MANUALS for LOGIQ e R5.0.x / LOGIQ e R5.2.x / LOGIQ e R6.x.x/ LOGIQ e Vet
Part Number Description Quantity FRU Item Part Name
LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e
Service Manual
5370626 -100 Service Manual 1 N
LOGIQ e User Manual, English
LOGIQ e User Manual, French
LOGIQ e User Manual, Spanish
LOGIQ e User Manual, German
LOGIQ e User Manual, Italian
System User Manuals
5199656 -100
5199656 -101
5199656 -106
5199656 -108
5199656 -111
Basic User Manual (for R5.0.x)
Basic User Manual (for R5.0.x)
Basic User Manual (for R5.0.x)
Basic User Manual (for R5.0.x)
Basic User Manual (for R5.0.x)
1
1
1
1
1
N
N
N
N
N
9-26 Section 9-12 - Manuals
GE H
EALTHCARE
D
IRECTION
5370626-100, R
EVISION
7 LOGIQ
E
/LOGIQ
E
V
ET
/LOGIQ
I
/V
IVID E
B
ASIC
S
ERVICE
M
ANUAL
Table 9-10 MANUALS for LOGIQ e R5.0.x / LOGIQ e R5.2.x / LOGIQ e R6.x.x/ LOGIQ e Vet
Item Part Name
LOGIQ e User Manual, Portuguese
LOGIQ e User Manual, Japanese
LOGIQ e User Manual, Chinese
LOGIQ e Vet User Manual English
LOGIQ e Vet User Manual, French
LOGIQ e Vet User Manual, Spanish
LOGIQ e Vet User Manual, German
LOGIQ e Vet User Manual, Italian
LOGIQ e Vet User Manual, Portuguese
LOGIQ e Vet User Manual, Japanese
LOGIQ e Vet User Manual, Chinese
LOGIQ e R5.0.x CKD User Manual,
English
LOGIQ e User Manual, English
LOGIQ e User Manual, French
LOGIQ e User Manual, Spanish
LOGIQ e User Manual, German
LOGIQ e User Manual, Italian
LOGIQ e User Manual, Portuguese
LOGIQ e User Manual, Japanese
LOGIQ e User Manual, Chinese
Part Number
5199656 -127
5199656 -140
5199656 -141
5198506 -100
5198506 -101
5198506 -106
5198506 -108
5198506 -111
5198506 -127
5198506 -140
5198506 -141
5268200-100
Description
Basic User Manual (for R5.0.x)
Basic User Manual (for R5.0.x)
Basic User Manual (for R5.0.x)
Basic User Manual (for R5.0.x/5.2.x)
Basic User Manual (for R5.0.x/5.2.x)
Basic User Manual (for R5.0.x/5.2.x)
Basic User Manual (for R5.0.x/5.2.x)
Basic User Manual (for R5.0.x/5.2.x)
Basic User Manual (for R5.0.x/5.2.x)
Basic User Manual (for R5.0.x)
Basic User Manual (for R5.0.x)
Basic User Manual (for R5.0.x)
5314622 -100
5314622 -101
5314622 -106
5314622 -108
5314622 -111
5314622 -127
5314622 -140
5314622 -141
System Quick Start Guide
Basic User Manual (for R5.2.x/R6.x.x)
Basic User Manual (for R5.2.x/R6.x.x)
Basic User Manual (for R5.2.x/R6.x.x)
Basic User Manual (for R5.2.x/R6.x.x)
Basic User Manual (for R5.2.x/R6.x.x)
Basic User Manual (for R5.2.x/R6.x.x)
Basic User Manual (for R5.2.x/R6.x.x)
Basic User Manual (for R5.2.x/R6.x.x)
1
1
1
1
1
1
1
1
Quantity FRU
1 N
1
1
N
N
N
N
N
N
N
N
N
N
1
1
1
1
1
1
1
1
1
N
N
N
N
N
N
N
N
N
LOGIQ e R5.0.x / LOGIQ e Vet Quick
Start Guide, English
LOGIQ e R5.0.x / LOGIQ e Vet Quick
Start Guide, French
LOGIQ e R5.0.x / LOGIQ e Vet Quick
Start Guide, Spanish
LOGIQ e R5.0.x / LOGIQ e Vet Quick
Start Guide, German
LOGIQ e R5.0.x / LOGIQ e Vet Quick
Start Guide, Italian
LOGIQ e R5.0.x / LOGIQ e Vet Quick
Start Guide, Portuguese
5212024 -100
5212024 -101
5212024 -106
5212024 -108
5212024 -111
5212024 -127
Quick Start Guide (for R5.0.x)
Quick Start Guide (for R5.0.x)
Quick Start Guide (for R5.0.x)
Quick Start Guide (for R5.0.x)
Quick Start Guide (for R5.0.x)
Quick Start Guide (for R5.0.x)
1
1
1
1
1
1
N
N
N
N
N
N
Chapter 9 Renewal Parts 9-27
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Table 9-10 MANUALS for LOGIQ e R5.0.x / LOGIQ e R5.2.x / LOGIQ e R6.x.x/ LOGIQ e Vet
Part Number Description Quantity FRU Item Part Name
LOGIQ e R5.0.x / LOGIQ e Vet Quick
Start Guide, Japanese
LOGIQ e R5.0.x / LOGIQ e Vet Quick
Start Guide, Chinese
LOGIQ e R5.2.x/R6.x.x Quick Start
Guide
LOGIQ e Vet R5.2.x Quick Start Guide,
English
5212024 -140
5212024 -141
5314624-100
5329881-100
Quick Start Guide (for R5.0.x)
Quick Start Guide (for R5.0.x)
Quick Start Guide (for R5.2.x/R6.x.x)
Quick Start Guide (for R5.2.x)
1
1
1
1
N
N
N
N
Table 9-11 MANUALS for Vivid e R4.x.x
Item Part Name Part Number
LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e Service
Manual
5370626 -100
Vivid e R4.x.x User Manual, English
Vivid e R4.x.x User Manual, French
Vivid e R4.x.x User Manual, Spanish
Vivid e R4.x.x User Manual, German
Vivid e R4.x.x User Manual, Italian
Vivid e R4.x.x User Manual, Portuguese
Vivid e R4.x.x User Manual, Japanese
Vivid e R4.x.x User Manual, Chinese
System User Manuals
5165247-100
5165247-101
5165247-106
5165247-108
5165247-111
5165247-127
5165247-140
5165247-141
Vivid e R4.x.x Quick Start Guide, English
Vivid e R4.x.x Quick Start Guide, French
Vivid e R4.x.x Quick Start Guide, Spanish
Vivid e R4.x.x Quick Start Guide, German
Vivid e R4.x.x Quick Start Guide, Italian
Vivid e R4.x.x Quick Start Guide, Portuguese
Vivid e R4.x.x Quick Start Guide, Japanese
Vivid e R4.x.x Quick Start Guide, Chinese
System Quick Start Guide
5175726 -100
5175726 -101
5175726 -106
5175726 -108
5175726 -111
5175726 -127
5175726 -140
5175726 -141
Description
Service Manual
Basic User Manual
Basic User Manual
Basic User Manual
Basic User Manual
Basic User Manual
Basic User Manual
Basic User Manual
Basic User Manual
Quick Start Guide
Quick Start Guide
Quick Start Guide
Quick Start Guide
Quick Start Guide
Quick Start Guide
Quick Start Guide
Quick Start Guide
Quantity FRU
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
N
N
N
N
N
N
N
N
N
N
N
N
N
N
N
N
N
9-28 Section 9-12 - Manuals
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Table 9-12 MANUALS for Vivid e R5.x.x / Vivid e R6.x.x
Description Quantity FRU Item Part Name Part Number
LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e Service
Manual
5370626-100
System User Manuals
5198874 -100
Vivid e R5.x.x/R6.x.x User Manual, English
Vivid e R5.x.x/R6.x.x User Manual, French
5198874 -101
Vivid e R5.x.x/R6.x.x User Manual, Spanish
Vivid e R5.x.x/R6.x.x User Manual, German
Vivid e R5.0.x Quick Start Guide, Italian
5198874 -106
5198874 -108
Vivid e R5.x.x/R6.x.x User Manual, Italian
5198874 -111
Vivid e R5.x.x/R6.x.x User Manual, Portuguese
Vivid e R5.x.x/R6.x.x User Manual, Japanese
Vivid e R5.0.x Quick Start Guide, Spanish
Vivid e R5.0.x Quick Start Guide, German
5198874 -127
5198874 -140
Vivid e R5.x.x/R6.x.x User Manual, Chinese
Vivid e R5.0.x Quick Start Guide, French
5198874 -141
Vivid e R5.x.x/R6.x.x Quick Start Guide, English
System Quick Start Guide
5212811 -100
5212811 -101
5212811 -106
5212811 -108
5212811 -111
Vivid e R5.0.x Quick Start Guide, Portuguese
Vivid e R5.0.x Quick Start Guide, Japanese
5212811 -127
5212811 -140
Vivid e R5.0.x Quick Start Guide, Chinese
5212811 -141
Service Manual
Basic User Manual
Basic User Manual
Basic User Manual
Basic User Manual
Basic User Manual
Basic User Manual
Basic User Manual
Basic User Manual
Quick Start Guide
Quick Start Guide
Quick Start Guide
Quick Start Guide
Quick Start Guide
Quick Start Guide
Quick Start Guide
Quick Start Guide
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
N
N
N
N
N
N
N
N
N
N
N
N
N
N
N
N
N
Item
Table 9-13 MANUALS for LOGIQ i R4.x.x / LOGIQ i R5.x.x
Part Name Part Number
Manuals
Description
LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e Service
Manual
5370626-100 Service Manual
LOGIQ i R4.x.x User Manual, English
LOGIQ i R4.x.x User Manual, French
LOGIQ i R4.x.x User Manual, Spanish
LOGIQ i R4.x.x User Manual, German
LOGIQ i R4.x.x User Manual, Italian
System User Manuals
5179205-100
5179205-101
5179205-106
5179205-108
5179205-111
Basic User Manual
Basic User Manual
Basic User Manual
Basic User Manual
Basic User Manual
Quantity FRU
1
1
1
1
1
1
N
N
N
N
N
N
Chapter 9 Renewal Parts 9-29
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Table 9-13 MANUALS for LOGIQ i R4.x.x / LOGIQ i R5.x.x
Item Part Name Part Number
5179205-127
LOGIQ i R4.x.x User Manual, Portuguese
LOGIQ i R4.x.x User Manual, Japanese
LOGIQ i R4.x.x User Manual, Chinese
5179205-140
5179205-141
LOGIQ i R5.x.x User Manual, English
LOGIQ i R5.x.x User Manual, French
LOGIQ i R5.x.x User Manual, Spanish
LOGIQ i R5.x.x User Manual, German
LOGIQ i R5.x.x User Manual, Italian
LOGIQ i R5.x.x User Manual, Portuguese
LOGIQ i R5.x.x User Manual, Chinese
System User Manuals
5212229-100
5212229-101
5212229-106
5212229-108
5212229-111
5212229-127
5179205-141
LOGIQ i R4.x.x Quick Start Guide, English
LOGIQ i R4.x.x Quick Start Guide, French
LOGIQ i R4.x.x Quick Start Guide, Spanish
LOGIQ i R4.x.x Quick Start Guide, German
LOGIQ i R4.x.x Quick Start Guide, Italian
LOGIQ i R4.x.x Quick Start Guide, Portuguese
LOGIQ i R4.x.x Quick Start Guide, Japanese
LOGIQ i R4.x.x Quick Start Guide, Chinese
System Quick Start Guide
5180949 -100
5180949 -101
5180949 -106
5180949 -108
5180949 -111
5180949 -127
5180949 -140
5180949 -141
LOGIQ i R5.x.x Quick Start Guide, English
System Quick Start Guide
5245368 -100
Description
Basic User Manual
Basic User Manual
Basic User Manual
Basic User Manual
Basic User Manual
Basic User Manual
Basic User Manual
Basic User Manual
Basic User Manual
Basic User Manual
Quick Start Guide
Quick Start Guide
Quick Start Guide
Quick Start Guide
Quick Start Guide
Quick Start Guide
Quick Start Guide
Quick Start Guide
Quick Start Guide
Quantity FRU
1 N
1
1
N
N
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
N
N
N
N
N
N
N
N
N
N
N
N
N
N
N
N
9-30 Section 9-12 - Manuals
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Section 9-13Probe
Table 9-14 Probes for LOGIQ e, Vivid e and LOGIQ i
Item
701
702
703
704
705
706
707
708
709
710
711
712
713
714
Part
Name
E8C-RS
8C-RS i12L-RS
8L-RS
3S-RS
12L-RS i739-RS
T739-RS
P2D
9L-RS
6S-RS
16L-RS
6Tc-RS
715 L8-18i-RS
Part
Number
4C-RS 5131629
2290777
2354971
2377942
2376127
2355686
5154514
2404995
2404999
KE100003
5213143
47236867
5317271
KN100104
5397810
Description
Probe
(Center Frequency: 3.2MHz)
Probe
(Center Frequency: 6.5MHz)
Probe
(Center Frequency: 6.5MHz)
Probe
(Center Frequency: 5.6MHz)
Probe
(Center Frequency: 6.2MHz)
Probe
(Center Frequency: 2.0MHz)
Probe
(Center Frequency: 7.5MHz)
Probe
(Center Frequency: 7.4MHz)
Probe
(Center Frequency: 6.5MHz)
Probe
(Center Frequency:2.0MHz)
Probe
(Center Frequency: 7.5MHz)
Probe
(Center Frequency: 4.8MHz)
Probe
(Center Frequency: 12.0MHz)
Probe
(Center Frequency: 4.8MHz)
Probe
(Center Frequency: 9.5MHz)
1 1 x
1 1 x
1 1 x
1 1 x
1 1 x
1 1 x
1 1 x
1 1
1 1
1 1
1 1
1 1
1 1 x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x
NOTE: 16L-RS is not available in China.
x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x
Chapter 9 Renewal Parts 9-31
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Section 9-13 Probe
(cont’d)
Table 9-15 Probes for LOGIQ e Vet
Item
754
755
756
757
750
751
752
753
758
759
760
Part Name
4C-RS Vet
E8C-RS Vet
8C-RS Vet i12L-RS Vet
8L-RS Vet
3S-RS Vet
12L-RS Vet
9L-RS Vet i739-RS-LC
6S Vet-RS Vet
6Tc-RS Vet
Part
Number
5198378
5134643
5134642
5134645
2376127
5134647
5212304
5220453
5136420
5198571
5430790
Description
Probe (Center Frequency: 3.2MHz)
Probe (Center Frequency: 6.5MHz)
Probe (Center Frequency: 6.5MHz)
Probe (Center Frequency: 5.6MHz)
Probe (Center Frequency: 6.2MHz)
Probe (Center Frequency: 2.0MHz)
Probe (Center Frequency: 7.5MHz)
Probe (Center Frequency: 7.5MHz)
Probe (Center Frequency: 6.4MHz)
Probe (Center Frequency:4.8MHz)
Probe (Center Frequency: 4.8 MHz)
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1 x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x
9-32 Section 9-13 - Probe
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Chapter 10
Care & Maintenance
Section 10-1
Overview
10-1-1
10-1-2
Periodic Maintenance Inspections
It has been determined by engineering that your LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e 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
10-1
10-2
10-3
10-4
10-5
10-6
10-7
Description
Overview
Why do Maintenance
Maintenance Task Schedule
Tools Required
System Maintenance
Electrical Safety Tests
When There's Too Much Leakage Current...
Page Number
10-1
10-2
10-2
10-4
10-5
10-11
10-18
CAUTION
Practice good ESD prevention. Wear an anti–static strap when handling electronic parts and even when disconnecting/connecting cables.
DANGER
BE SURE TO DISCONNECT THE SYSTEM POWER PLUG BEFORE YOU
REMOVE ANY PARTS. BE CAUTIOUS WHENEVER POWER IS STILL ON AND
COVERS ARE REMOVED.
CAUTION
Do not pull out or insert circuit boards while power is ON.
CAUTION
Do not operate this unit unless all board covers and frame panels are securely in place. System performance and cooling require this.
Chapter 10 Care & Maintenance 10-1
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Section 10-2
Why do Maintenance
10-2-1
10-2-2
Keeping Records
It is good business practice that ultrasound facilities maintain records of periodic and corrective maintenance. The Ultrasound Periodic Maintenance Inspection Certificate provides the customer with documentation that the ultrasound 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:
NOTE:
How often should care & maintenance tasks be performed?
The Care & Maintenance Task Schedule (provided on page 10-3 ) specifies how often your LOGIQ e/
LOGIQ e Vet/LOGIQ i/Vivid e should be serviced and outlines items requiring special attention.
It is the customer’s responsibility to ensure the LOGIQ e/LOGIQ e Vet/LOGIQ i/Vivid e 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 knowlegde of your LOGIQ e/LOGIQ e Vet/LOGIQ i/
Vivid e 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 e/LOGIQ e Vet/LOGIQ i/Vivid e for an average patient load (10-12 per day) and use it as a primary mobile unit which is transported between diagnostic facilities.
If conditions exist which exceed typical usage and patient load, then it is recommended to increase the maintenance frequencies.
10-2 Section 10-2 - Why do Maintenance
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NOTE:
NOTE:
Table 10-2 Customer Care Schedule
Service at Indicated Time
Clean Probes
Inspect AC Mains Cable
Inspect Cables and Connectors
Clean Console
Clean LCD
Console Leakage Current Checks
Peripheral Leakage Current Checks
Surface Probe Leakage Current Checks
Endocavity Probe Leakage
Current Checks
Measurement Accuracy Checks
Daily
•*
Weekly Monthly
Per Facilities
QA Program Notes
* or before each use
•
•
•
•
Mobile Unit Check Weekly
See Note
See Note
See Note
See Note
See Note
Twice
Annually
Twice
Annually
Twice
Annually
Quarterly
Annually
Twice
Annually
May require specialized equipment to complete
PMs are not mandatory, the table above is for reference only.
Chapter 10 Care & Maintenance 10-3
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Section 10-4
Tools Required
10-4-1
10-4-1-1
Special Tools, Supplies and Equipment
Specific Requirements for Care & Maintenance
Table 10-3 Overview of Requirements for Care & Maintenance
Tool
Digital Volt Meter (DVM)
Part Number Comments
Anti Static Kit
Anti Static Vacuum Cleaner
Safety Analyzer
QIQ Phantom
B/W Printer Cleaning Sheet
Color Printer Cleaning Sheet
Disposable Gloves
46–194427P231
46–194427P279
46–194427P369
46–194427P373
46–194427P370
46–194427P278
46–194427P279
46–285652G1
E8370RB
Kit includes anti–static mat, wrist strap and cables for 200 to 240
V system
3M #2204 Large adjustable wrist strap
3M #2214 Small adjustable wrist strap
3M #3051 conductive ground cord
120V
230V
The satety Analyzer tool should be calibrated abd compliant with
AAMI/ESI 1993 or IEC 60601 or AS/NZS 3551.
RMI Grayscale Target Model 403GS
See printer user manual for requirements
See printer user manual for requirements
10-4 Section 10-4 - Tools Required
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Section 10-5
System Maintenance
10-5-1 Preliminary Checks
The preliminary checks take about 15 minutes to perform. Refer to the system user documentation whenever necessary.
Table 10-4 System Checks
Step
1
2
3
4
5
6
Item
Ask & Listen
Paperwork
Power up
Probes
Displays
Presets
Description
Ask the customer if they have any problems or questions about the equipment.
Fill in the top of the Ultrasound Inspection Certificate (see page 19). Note all probes and system options.
With AC input.
Turn the system power on and verify that all fans and peripherals turn on. Watch the displays during power up to verify that no warning or error messages are displayed.
Check the Battery recharging.
Without AC input, use internal battery.
Verify that the system properly recognizes all probes.
Verify proper display on the LCD.
Backup all customer presets on an DVD-RW.
Chapter 10 Care & Maintenance 10-5
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10-5-2 Functional Checks (See Also Chapter 4)
The functional checks take about 60 minutes to perform. Refer to the system user documentation whenever necessary.
10-5-2-1 System Checks
Table 10-5 System Functional Checks
÷ Step Description
B-Mode
CF-Mode
Verify basic B-Mode (2D) operation. Check the basic system controls that affect this mode of operation.
Verify basic CF-Mode (Color Flow Mode) operation. Check the basic system controls that affect this mode of operation.
Doppler Modes
Verify basic Doppler operation (PW if available). Check the basic system controls that affect this mode of operation.
M-Mode
Verify basic M-Mode operation. Check the basic system controls that affect this mode of operation.
*Applicable
Software Options
Verify the basic operation of all optional modes such as Multi-Image, 3D, Harmonics, Cine,... etc.
Check the basic system controls that affect each options operation.
Xmit/Recv
Elements
Use the Visual Channel Utility on the loop connect to verify that all system xmit/recv channels are functional.
Keyboard Test
Perform the Keyboard Test Procedure to verify that all keyboard controls are OK.
LCD
Verify basic LCD display functions. Refer to Chapter 3 of the User Manual.
Software Menu check
Verify Software Menu display functions. Refer to Chapter 3 of the User Manual.
Measurements
In measurement mode, make distance measurement, get result in result window. Verify the distance by graduate rule. Distance Accuracy should be within
±5%. (Name result from result window Result
A, result from graduate rule Result B; Distance Accuracy= (Result B-Result A)/Result A)
NOTE: * Some software may be considered standard depending upon system model configuration.
10-6 Section 10-5 - System Maintenance
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10-5-2-2 Peripheral/Option Checks
If any peripherals or options are not part of the system configuration, the check can be omitted. Refer to the User Manual for a list of approved peripherals/options.
10-5-3
10-5-3-1
10-5-4
10-5-4-1
Table 10-6 GE Approved Peripheral/Hardware Option Functional Checks
Step Item Description
1 B/W Printer
Verify hardcopy output of the B/W video page printer. Clean heads and covers if necessary.
2 Color Printer Verify hardcopy output of the Color video page printer. Clean heads and covers if necessary.
3 DICOM
Verify that DICOM is functioning properly. Send an image to a DICOM device.
4
5
Footswitch
Verify that the footswitch is functioning as programed. Clean as necessary.
ECG
Verify basic operation with customer.
6 DVD
Verify that the DVD is functioning properly. Clean heads and covers if necessary.
Input Power
AC/DC Adapter Inspection
Table 10-7 AC/DC Adapter Inspection
Step
1
2
3
Item Description
Unplug Cord Disconnect the mains cable from the wall and system.
Inspect
Inspect it and its connectors for damage of any kinds.
Verify
Verify that the LINE wires are properly attached to the terminals, and that no strands may cause a short circuit.
Cleaning
General Cleaning
Table 10-8 General Cleaning
Step Item Description
1 Console
Remove the battery. Use a fluid detergent in warm water on a soft, damp cloth to carefully wipe the entire system. Be careful not to get the cloth too wet so that moisture does not enter the console.
2 Probe Holder Clean probe holders. (they may need to be soaked to remove excess gel).
3 LCD
Use a soft, non-abrasive folder cloth. Gently wipe the LCD face. DO NOT use a glass cleaner that has a hydrocarbon base (such as Benzene, Methy Alcohol or Methy Ethyl Ketone) on LCD with the filter (antiglare shield).
Chapter 10 Care & Maintenance 10-7
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10-5-5 Physical Inspection
Table 10-9 Physical Checks
Step Item Description
1 Labeling
Verify that all system labeling is present and in readable condition. Refer to User Manual,...... for details.
2 Scratches & Dents Inspect the console for dents, scratches or cracks.
3 Control Panel
Inspect keyboard and control panel. Note any damaged or missing items.
4
5
6
7
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.
Op Panel Lights
Check for proper operation of all operator panel and Freeze Key light.
10-8 Section 10-5 - System Maintenance
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10-5-6 Optional Diagnostic Checks
Optionally you can access the diagnostic software as described in Chapter 5 or 7. View the error logs and run desired diagnostics.
10-5-6-1
10-5-7
10-5-7-1
View the Logs
1.) Review the system error log for any problems.
2.) Check the temperature log to see if there are any trends that could cause problems in the future.
3.) Check the Configuration Log; update if needed.
Probe Maintenance
Probe Related Checks
Table 10-10 Probe Related Checks
Step
1
2
Item Description
Probe Holder
Clean probe holders (they may need to be soaked to remove excess gel).
Probes
Thoroughly check the system probe connectors and remove dust from inside the connector sockets if necessary. Visually check for bent, damaged or missing pins
10-5-7-2
10-5-7-3
NOTE:
NOTE:
NOTE:
Basic Probe Care
The system user manuals and various probe handling cards provide a complete description of probe care, maintenance, cleaning and disinfection. Ensure that you are completely familiar with the proper care of GE probes.
Ultrasound probes can be easily damaged by improper handling. See the User Manual and probe care cards for more details. Failure to follow these precautions can result in serious injury and equipment damage. Failure to properly handle or maintain a probe may also void its warranty.
Any evidence of wear indicates the probe cannot be used.
Do a visual check of the probe pins and system sockets before plugging in a probe.
Basic Probe Cleaning
Refer to the User’s Manual for details on probe cleaning.
To help protect yourself from blood borne diseases, wear approved disposable gloves. These are made of nitrile derived from vegetable starch to prevent allergic latex reactions.
Failure to follow the prescribed cleaning or disinfection procedures will void the probe’s warranty. DO NOT soak or wipe the lens with any product not listed in the User Manual. Doing so could result in irreparable damage to the probe. Follow care instructions that came with the probe.
Disinfect a defective probe before you return it. Be sure to tag the probe as being disinfected.
Chapter 10 Care & Maintenance 10-9
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10-5-8 Battery Performance Maintenance
Battery replacement every three years is recommended.
It is recommended to do battery performance maintenance one time per year.
Please follow the flow chart below to carry out battery performance maintenance.
Battery discharge
>45 minutes?
Yes
Battery charge > 3 hour
No
Battery charge > 3 hour
No
Replace battery
Battery power > 90%?
Yes
Battery is Ok
Battery power > 90%?
Yes
Discharge
No
Replace battery
>45 minutes?
Yes
Battery is Ok
NOTE:
NOTE:
Figure 10-1 Flow chart of Battery Performance Maintenance
Disconnect all probes when discharge battery.
Discharge the battery to let the system automatically shut down.
10-10 Section 10-5 - System Maintenance
No
Replace battery
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Section 10-6
Electrical Safety Tests
10-6-1 Safety Test Overview
The electrical safety tests in this section are based on and conform to IEC 60601-1 Medical Equipment
Safety Standards. They are intended for the electrical safety evaluation of cord-connected, electrically operated, patient care equipment. If additional information is needed, refer to the IEC 60601-1 documents.
THE USER MUST ENSURE THAT THE SAFETY INSPECTIONS ARE PERFORMED AT
LEAST EVERY 6 MONTHS ACCORDING TO THE REQUIREMENTS OF THE PATIENT
SAFETY STANDARD IEC-EN 60601-1. ONLY TRAINED PERSONS ARE ALLOWED TO
PERFORM THE SAFETY INSPECTIONS MENTIONED ABOVE.
CAUTION
To avoid electrical shock, the unit under test must not be connected to other electrical equipment. The unit under test must not be contacted by users or patients while performing these tests.
CAUTION
Possible risk of infection. Do not handle soiled or contaminated probes and other components that have been in patient contact. Follow appropriate cleaning and disinfecting procedures before handling the equipment.
Test the system, peripherals and probes for leakage current. Excessive leakage current can cause injury or death in sensitive patients. High leakage current can also indicate degradation of insulation and a potential for electrical failure. Do not use probes or equipment having excessive leakage current.
To minimize the risk that a probe may shock someone the customer should:
• Not use a probe that is cracked or damaged in any way
• Check probe leakage current:
* Based on your facilities QA program for surface probes
* Based on your facilities QA program for endocavitary probes
* whenever probe damage is suspected
Chapter 10 Care & Maintenance 10-11
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10-6-2 GEMS Leakage Current Limits
The following limits are summarized for IEC 60601-1 Medical Equipment Safety Standards. These limits are GEMS standards and in some cases are lower than the above standards listed.
Table 10-11 Chassis Leakage Current Limits—Accessible Metal Surfaces
Country
All (Except USA &
Canada)
USA & Canada
Normal Condition
0.1 mA
0.1 mA
Open Ground
0.5 mA
0.3 mA
Reverse Polarity
0.5 mA
0.3 mA
Open Neutral
0.5 mA
0.3 mA
Table 10-12 Type BF Applied Part Leakage Current Limits - Probes surface
Country
All
Normal
Condition
0.1 mA
Open Ground Reverse Polarity Open Neutral *Mains Applied
0.5 mA 0.5 mA 0.5 mA 5.0 mA
NOTE:
Table 10-13 Type CF Applied Part Leakage Current Limits - ECG Connections
Country
All
Normal Condition Open Ground Reverse Polarity Open Neutral *Mains Applied
0.01 mA 0.05 mA 0.05 mA 0.05 mA 0.05 mA
*Mains Applied refers to the sink leakage test where mains (supply) voltage is applied to the part to determine the amount of current that will pass (or sink) to ground if a patient contacted mains voltage.
The following tests are performed at the factory and should be performed at the site. These tests are: chassis leakage current, and probe leakage current. All measurements are made with an electrical safety analyzer which should be calibrated and compliant with AAMI/ESI 1993 or IEC 60601 or AS/NZS
3551.
10-12 Section 10-6 - Electrical Safety Tests
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10-6-3 Outlet Test - Wiring Arrangement
Test all outlets in the area for proper grounding and wiring arrangement by plugging in the neon outlet tester and noting the combination of lights that are illuminated. Any problems found should be reported to the hospital immediately and the receptacle should not be used.
NOTE:
Figure 10-2 Typical Alternate Outlet Tester
No outlet tester can detect the condition where the Neutral (grounded supply) conductor and the
Grounding (protective earth) conductor are reversed. If later tests indicate high leakage currents, this should be suspected as a possible cause and the outlet wiring should be visually inspected.
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10-6-4 Chassis Leakage Current Test
10-6-4-1 Definition
This test measures the current that would flow in a grounded person who touched accessible metal parts of the bedside station if the ground wire should break. The test verifies the isolation of the power line from the chassis. The meter is connected from accessible metal parts of the case to ground.
Measurements should be made with the unit On and Off, with the power line polarity Normal and
Reversed. Record the highest reading.
CAUTION
Electric Shock Hazard. When the meter's ground switch is OPEN, don't touch the unit!
CAUTION
Equipment damage possibility. Never switch the Polarity and the status of Neutral when the unit is powered ON. Be sure to turn the unit power OFF before switching them using the POLARITY switch and/or the NEUTRAL switch. Otherwise, the unit may be damaged.
10-6-4-2 Generic Procedure
The test verifies the isolation of the power line from the chassis. The testing meter is connected from accessible metal parts of the case to ground. Measurements should be made with the unit ON and OFF, with the power line polarity Normal and Reversed. Record the highest reading of current.
10-14
Figure 10-3 Set Up for Chassis Source Leakage Current,
IEC 601-1 Clause 19 - Continuos Leakage Currents and
Patient, Auxiliary Currents
When using the Microguard or a similar test instrument, its power plug may be inserted into the wall outlet and the equipment under test is plugged into the receptacle on the panel of the meter. This places the meter in the grounding conductor and the current flowing from the case to ground will be indicated in any of the current ranges. The maximum allowable limit for chassis source leakage is shown in
Table 10-11 .
Section 10-6 - Electrical Safety Tests
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10-6-4-3 Data Sheet for enclosure Source Leakage Current
The test passes when all readings measure less than the value shown in Table 10-11 . Record all data on the PM Inspection Certificate.
Table 10-14 Typical Data Sheet for enclosure Source Leakage Current
Unit Power
Tester Polarity
Switch
Tester Neutral or Ground
Switch
Enter Name of tested peripheral here:
ON
ON
ON
ON
OFF
OFF
OFF
OFF
NORM
NORM
REV
REV
NORM
NORM
REV
REV
OPEN
CLOSED
OPEN
CLOSED
OPEN
CLOSED
OPEN
CLOSED
Test 1
Speaker
Cover
Test 2
Real Panel
Metal
Parts
Optional
Test 3
Optional
Test 4
Chapter 10 Care & Maintenance 10-15
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10-6-5 Probe Leakage Current Test
10-6-5-1
10-6-5-2
Definition
This test measures the current that would flow to ground from any of the probes through a patient who is being scanned and becomes grounded by touching some other grounded surface.
Generic Procedure
Measurements should be made with the ground open and closed, with power line polarity normal and reversed, and with the unit Off and On. For each combination, the probe must be active to find the worst case condition.
POWER
OUTLET
H (BLACK)
N (WHITE)
G (GREEN)
POLARITY REVERSING SWITCH
MOMENTARY
SWITCH
CONSOLE
LEAKAGE TEST
METER
PROBE
NOTE:
10-6-5-3
Figure 10-4 Set Up for Probe Leakage Current
Each probe will have some amount of leakage current, dependent on its design. Small variations in probe leakage currents are normal from probe to probe. Other variations will result from differences in line voltage and test lead placement.
No Meter Probe Adapter Procedure
Follow the Safety Analyzer tool instruction to test each transducer for leakage current.
The electrical Safety Analyzer tool should be calibrated and compliant with AAM/ESI 1993 or IEC 60601 or AS/NZS 3551.
10-16 Section 10-6 - Electrical Safety Tests
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10-6-5-4 Data Sheet for Transducer Source Leakage Current
The test passes when all readings measure less than the values shown in Table 10-11 . Record all data on the PM Inspection Certificate.
CAUTION
Equipment damage possibility. Never switch the Polarity and the status of Neutral when the unit is powered ON. Be sure to turn the unit power OFF before switching them using the POLARITY switch and/or the NEUTRAL switch. Otherwise, the unit may be damaged
.
Table 10-15 Typical Data Sheet For Transducer Source Leakage Current
Unit Power
OFF
OFF
OFF
OFF
ON
ON
ON
ON
Transducer Tested:
Tester Power Polarity
Switch
NORM
NORM
REV
REV
NORM
NORM
REV
REV
Tester GROUND or
NUETRAL Switch
OPEN
CLOSED
OPEN
CLOSED
OPEN
CLOSED
OPEN
CLOSED
Measurement
Chapter 10 Care & Maintenance 10-17
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Section 10-7
When There's Too Much Leakage Current...
AC/DC FAILS
Check any broken of the AC/DC adapter and its cable. Replace a new one if any portion defective.
ENCLOSURE FAILS
Check any broken of the enclosure. Replace any defective part.
Inspect wiring for bad crimps, poor connections, or damage.
Test the wall outlet; verify it is grounded and is free of other wiring abnormalities. Notify the user or owner to correct any deviations. As a work around, check the other outlets to see if they could be used instead.
NOTE: No outlet tester can detect the condition where the white neutral wire and the green grounding wire are reversed. If later tests indicate high leakage currents, this should be suspected as a possible cause and the outlet wiring should be visually inspected.
PROBE FAILS
Change another probe to confirm if the fail is caused by console.
NOTE: Each probe will have some amount of leakage, dependent on its design. Small variations in probe leakage currents are normal from probe to probe. Other variations will result from differences in line voltage and test lead placement. The maximum allowable leakage current for body surface contact probe differs from inter-cavity probe. Be sure to enter the correct probe type in the appropriate space on the check list.
If excessive leakage current is slot dependent, inspect the system connector for bent pins, poor connections, and ground continuity.
If the problem remains with the probe, replace the probe.
PERIPHERAL FAILS
Inspect wiring for bad crimps, poor connections, or damage.
STILL FAILS
If all else fails, begin isolation by removing the probes, external peripherals, then the on board ones, one at a time while monitoring the leakage current measurement.
NEW UNIT
If the leakage current measurement tests fail on a new unit and if situation can not be corrected, submit a Safety Failure Report to document the system problem. Remove unit from operation.
10-18 Section 10-7 - When There's Too Much Leakage Current...
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ULTRASOUND INSPECTION CERTIFICATE
Customer Name: System ID: Dispatch Number / Date Performed: Warranty/Contract/HBS
System Type
Probe 1:
Probe 2:
Probe 3:
Frequency:
Frequency:
Frequency:
Model Number:
Scan Format*:
Scan Format*:
Scan Format*:
Serial Number:
Model Number:
Model Number:
Model Number:
Manufacture Date:
Serial Number:
Serial Number:
Serial Number:
Probe 4:
Probe 5:
Frequency:
Frequency:
Scan Format*:
Scan Format*:
Model Number:
Model Number:
Serial Number:
Serial Number:
* Scan Format: Phased Array, Linear Array, Curved Array, Mechanical Array or Other
FUNCTIONAL CHECKS
Functional Check (if applicable)
B-Mode Function
Doppler Modes Function
CF-Mode Function
M-Mode Function
Applicable Software Options
Applicable Hardware Options
Control Panel
LCD
Measurement Accuracy
GE Approved Peripherals
OK? or
N/A
PHYSICAL INSPECTION AND CLEANING
Physical Inspection and Cleaning
(if applicable)
Console
LCD
External I/O
Cables and Connectors
GE Approved Peripherals (DVD-RW, Printer)
Labeling (see User Manual for Labeling)
Inspect Clean
COMMENTS:
______________________________________________________________________________
______________________________________________________________________________
Chapter 10 Care & Maintenance 10-19
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______________________________________________________________________________
______________________________________________________________________________
ELECTRICAL SAFETY
Electrical Test Performed
Outlet (correct ground &wiring config.)
Type BF Applied Part Leakage Current
Limits- Probe enclosure Source Leakage Current -
Chassis Leakage Current Limits
Peripheral 1 Leakage Current
Peripheral 2 Leakage Current
Max Value
Allowed
Value
Measured OK?
Comments
PROBES
Probe Number
(from previous page)
Probe 1:
Max Value
Allowed
Max Value
Measured OK?
Comments
Probe 2:
Probe 3:
Final Check. All system covers are in place. System scans with all probes as expected.
Accepted by: ______________________________________________________________________
10-20 Section 10-7 - When There's Too Much Leakage Current...
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Chapter 10 Care & Maintenance 10-21
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10-22 Section 10-7 - When There's Too Much Leakage Current...
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A,B
Abbreviations, 9-1
Archiving Images
Move, 4-31
Backup
Patient Database, 4-28
Preset Configurations, 4-28
Basic Measurements
Functional Checks, 4-25
Body pattern display location, 4-9
Boot Up, 3-9
INDEX
EMI, 1-18
ESD, 1-18
Exam study display location, 4-9
F
Focal zone display location, 4-9
Functional Checks
Basic Measurements, 4-25
Control Panel, 4-7
Image Management, 4-27
Monitor Display, 4-9
Peripherals, 4-37
Probes/Connector Usage, 4-25
C
Caps lock display location, 4-9
CE Compliance, 1-18
Cine gauge display location, 4-9
Color Mode
Overview, 4-20
Configuration, 5-19
Connectivity
Worksheet, 3-28
Contact Information, 1-19
Control Panel, 4-7
Conventions
Conventions Used in Book, 1-5
Customer Assistance, 1-19
CW Doppler activating, 4-24 exiting, 4-24
G
Gathering Trouble Data, 7-2
General Cleaning, 10-7
Gray/color bar display location, 4-9
H
Hazard Icons, 1-6
Hospital name display location, 4-9
Human Safety, 1-11
D
Dangerous Procedure Warnings, 1-16
Date/Time display location, 4-9
Depth scale display location, 4-9
Diagnostics, 5-17
DICOM Network Function, 2-9
I
Image Management
Functional Checks, 4-27
Image preview display location, 4-9
Imaging parameters display location, 4-9
Inrush Current, 2-2, , 2-3
Institution name display location, 4-9
E
Electrical requirements, 2-2
Electrical Safety, 1-12
Electrostatic Discharge Warning, 1-18
L
Logs, 5-14
LOTO, 1-16, , 4-6
Index 1
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M
Measurement summary window display location, 4-9
Mechanical Safety, 1-11
Media
Formatting, 4-28
Models Covered, 1-3
Monitor Display
Functioanl Checks, 4-9
Monitor display location, 4-9
Move
Archiving Images, 4-31
O
Operator identification display location, 4-9
S
Safety Considerations, 1-11
Screen Captures, 7-6
System Maintenance, 10-5
System Manufacturer, 1-20
System messages display location, 4-9
T
TGC display location, 4-9
Touch Panel
Functional Checks, 4-7
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
P
P4 Key Function, 7-4, , 7-6
Patient identification display location, 4-9
Patient name display location, 4-9
PC Diagnostics, 7-13
Hard Drive Tests, 7-13
Keyboard Test, 7-14
Memory Tests, 7-13
PC Diagnostics (Interactive Tests), 7-14
Peripherals
Functional Checks, 4-37
Power On, 3-9
Power Requirements, 2-2 electrical, 2-2 stability, 2-3
Power Stability Requirements, 2-3
Probe Connector Cleaning, 10-9
Probe identifier display location, 4-9
Probe orientation marker display location, 4-9
Probes/Connector Usage
Functional Checks, 4-25
U
Utilities, 5-19
W
Warnings and Cautions, 1-11
R
Required Features, 2-7
Restore
Patient Database, 4-30
Preset Configurations, 4-30
Index 2
©
2004 to 2011, General Electric Company.
GE Medical Systems, a General Electric Company, going to market as GE Healthcare.
3200 N. Grandview Boulevard
Waukesha, Wisconsin 53149
USA www.gehealthcare.com

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Key features
- System operation
- System setup
- System diagnostics
- Troubleshooting
- System part identification