GE LOGIQ S8_LOGIQ E8 Service Manual_SM_5349227_12 DUCO-SLIDE Cabinet Operation Manual

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GE Healthcare

(FEBRUARY 28, 2019)

PRELIMINARY

LOGIQ S8/LOGIQ E8

Service Manual

COVER.FM

Document Number: 5394227

Revision: 12

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This manual is a reference for the LOGIQ S8/LOGIQ E8 and LOGIQ S8 Vet ultrasound systems (Hereafter listed as LOGIQ S8). All information provided in this manual is relevant for all three systems unless otherwise

specified.

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GE HEALTHCARE DIRECTION 5394227, 12 LOGIQ S8/LOGIQ E8 SERVICE MANUAL

Important Precautions

TRANSLATION POLICY

THIS SERVICE MANUAL IS AVAILABLE IN ENGLISH ONLY.

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

WARNING

(EN)

AVERTISSEMENT

(FR)

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

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

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

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

• NE PAS TENTER D’INTERVENTION SUR LES ÉQUIPEMENTS TANT QUE LE MANUEL SERVICE N’A PAS ÉTÉ CONSULTÉ ET COMPRIS.

• LE NON-RESPECT DE CET AVERTISSEMENT PEUT ENTRAÎNER CHEZ LE TECHNICIEN, L’OPÉRATEUR OU LE PATIENT DES BLESSURES DUES À DES DANGERS ÉLECTRIQUES, MÉCANIQUES OU AUTRES.

WARNUNG

(DE)

DIESES KUNDENDIENST-HANDBUCH EXISTIERT NUR IN ENGLISCHER SPRACHE.

• FALLS EIN FREMDER KUNDENDIENST EINE ANDERE SPRACHE BENÖTIGT, IST ES AUFGABE DES KUNDEN FÜR EINE ENTSPRECHENDE ÜBERSETZUNG ZU SORGEN.

• VERSUCHEN SIE NICHT, DAS GERÄT ZU REPARIEREN, BEVOR DIESES KUNDENDIENST-HANDBUCH NICHT ZU RATE GEZOGEN UND VERSTANDEN WURDE.

• WIRD DIESE WARNUNG NICHT BEACHTET, SO KANN ES ZU VERLETZUNGEN DES KUNDENDIENSTTECHNIKERS, DES BEDIENERS ODER DES PATIENTEN DURCH ELEKTRISCHE SCHLÄGE, MECHANISCHE ODER SONSTIGE GEFAHREN KOMMEN.

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GE HEALTHCARE DIRECTION 5394227, 12 LOGIQ S8/LOGIQ E8 SERVICE MANUAL

ESTE MANUAL DE SERVICIO SÓLO EXISTE EN INGLÉS.

• SI ALGÚN PROVEEDOR DE SERVICIOS AJENO A GEHC SOLICITA UN IDIOMA QUE NO SEA EL INGLÉS, ES RESPONSABILIDAD DEL CLIENTE OFRECER UN SERVICIO DE TRADUCCIÓN.

AVISO

(ES)

• NO SE DEBERÁ DAR SERVICIO TÉCNICO AL EQUIPO, SIN HABER CONSULTADO Y COMPRENDIDO ESTE MANUAL DE SERVICIO.

• LA NO OBSERVANCIA DEL PRESENTE AVISO PUEDE DAR LUGAR A QUE EL PROVEEDOR DE SERVICIOS, EL OPERADOR O EL PACIENTE SUFRAN LESIONES PROVOCADAS POR CAUSAS ELÉCTRICAS, MECÁNICAS O DE OTRA NATURALEZA.

ESTE MANUAL DE ASSISTÊNCIA TÉCNICA SÓ SE ENCONTRA DISPONÍVEL EM INGLÊS.

• SE QUALQUER OUTRO SERVIÇO DE ASSISTÊNCIA TÉCNICA, QUE NÃO A GEHC, SOLICITAR ESTES MANUAIS NOUTRO IDIOMA, É DA

ATENÇÃO

(PT-Br)

RESPONSABILIDADE DO CLIENTE FORNECER OS SERVIÇOS DE TRADUÇÃO.

• NÃO TENTE REPARAR O EQUIPAMENTO SEM TER CONSULTADO E COMPREENDIDO ESTE MANUAL DE ASSISTÊNCIA TÉCNICA.

• O NÃO CUMPRIMENTO DESTE AVISO PODE POR EM PERIGO A SEGURANÇA DO TÉCNICO, OPERADOR OU PACIENTE DEVIDO A‘ CHOQUES ELÉTRICOS, MECÃNICOS OU OUTROS.

AVISO

(PT-pt)

AVVERTENZA

(IT)

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.

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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GE HEALTHCARE DIRECTION 5394227, 12 LOGIQ S8/LOGIQ E8 SERVICE MANUAL

KÄESOLEV TEENINDUSJUHEND ON SAADAVAL AINULT INGLISE KEELES.

• KUI KLIENDITEENINDUSE OSUTAJA NÕUAB JUHENDIT INGLISE KEELEST ERINEVAS KEELES, VASTUTAB KLIENT TÕLKETEENUSE OSUTAMISE EEST.

HOIATUS

(ET)

• ÄRGE ÜRITAGE SEADMEID TEENINDADA ENNE EELNEVALT KÄESOLEVA TEENINDUSJUHENDIGA TUTVUMIST JA SELLEST ARU SAAMIST.

• KÄESOLEVA HOIATUSE EIRAMINE VÕIB PÕHJUSTADA TEENUSEOSUTAJA, OPERAATORI VÕI PATSIENDI VIGASTAMIST ELEKTRILÖÖGI, MEHAANILISE VÕI MUU OHU TAGAJÄRJEL.

TÄMÄ HUOLTO-OHJE ON SAATAVILLA VAIN ENGLANNIKSI.

• JOS ASIAKKAAN PALVELUNTARJOAJA VAATII MUUTA KUIN ENGLANNINKIELISTÄ MATERIAALIA, TARVITTAVAN KÄÄNNÖKSEN HANKKIMINEN ON ASIAKKAAN VASTUULLA.

VAROITUS

(FI)

• ÄLÄ YRITÄ KORJATA LAITTEISTOA ENNEN KUIN OLET VARMASTI LUKENUT JA YMMÄRTÄNYT TÄMÄN HUOLTO-OHJEEN.

• MIKÄLI TÄTÄ VAROITUSTA EI NOUDATETA, SEURAUKSENA VOI OLLA PALVELUNTARJOAJAN, LAITTEISTON KÄYTTÄJÄN TAI POTILAAN VAHINGOITTUMINEN SÄHKÖISKUN, MEKAANISEN VIAN TAI MUUN VAARATILANTEEN VUOKSI.

ΠΡΟΕΙΔΟΠΟΙΗΣΗ

(EL)

FIGYELMEZTETÉS

(HU)

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.

EZEN KARBANTARTÁSI KÉZIKÖNYV KIZÁRÓLAG ANGOL NYELVEN ÉRHETŐ EL.

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

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

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

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ÞESSI ÞJÓNUSTUHANDBÓK ER EINGÖNGU FÁANLEG Á ENSKU.

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

VIÐVÖRUN

(IS)

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

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

TENTO SERVISNÍ NÁVOD EXISTUJE POUZE V ANGLICKÉM JAZYCE.

•VPŘÍPADĚ, ŽE POSKYTOVATEL SLUŽEB ZÁKAZNÍKŮM POTŘEBUJE NÁVOD V JINÉM JAZYCE, JE ZAJIŠTĚNÍ PŘEKLADU DO ODPOVÍDAJÍCÍHO JAZYKA ÚKOLEM ZÁKAZNÍKA.

• NEPROVÁDĚJTE ÚDRŽBU TOHOTO ZAŘÍZENÍ, ANIŽ BYSTE SI PŘEČETLI

VÝSTRAHA

(CS)

TENTO SERVISNÍ NÁVOD A POCHOPILI JEHO OBSAH.

•VPŘÍPADĚ NEDODRŽOVÁNÍ TÉTO VÝSTRAHY MŮŽE DOJÍT ÚRAZU ELEKTRICKÁM PROUDEM PRACOVNÍKA POSKYTOVATELE SLUŽEB, OBSLUŽNÉHO PERSONÁLU NEBO PACIENTŮ VLIVEM ELEKTRICKÉHOP PROUDU, RESPEKTIVE VLIVEM K RIZIKU MECHANICKÉHO POŠKOZENÍ NEBO JINÉMU RIZIKU.

ADVARSEL

(DA)

WAARSCHUWING

(NL)

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 MEDFØRE SKADE PÅ GRUND AF ELEKTRISK, MEKANISK ELLER ANDEN FARE FOR TEKNIKEREN, OPERATØREN ELLER PATIENTEN.

DEZE ONDERHOUDSHANDLEIDING IS ENKEL IN HET ENGELS VERKRIJGBAAR.

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

• PROBEER DE APPARATUUR NIET TE ONDERHOUDEN VOORDAT DEZE 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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GE HEALTHCARE DIRECTION 5394227, 12 LOGIQ S8/LOGIQ E8 SERVICE MANUAL

ŠĪ APKALPES ROKASGRĀMATA IR PIEEJAMA TIKAI ANGĻU VALODĀ.

• JA KLIENTA APKALPES SNIEDZĒJAM NEPIECIEŠAMA INFORMĀCIJA CITĀ VALODĀ, NEVIS ANGĻU, KLIENTA PIENĀKUMS IR NODROŠINĀT TULKOŠANU.

BRĪDINĀJUMS

(LV)

• NEVEICIET APRĪKOJUMA APKALPI BEZ APKALPES ROKASGRĀMATAS IZLASĪŠANAS UN SAPRAŠANAS.

•ŠĪ BRĪDINĀJUMA NEIEVĒROŠANA VAR RADĪT ELEKTRISKĀS STRĀVAS TRIECIENA, MEHĀNISKU VAI CITU RISKU IZRAISĪTU TRAUMU APKALPES SNIEDZĒJAM, OPERATORAM VAI PACIENTAM.

ŠIS EKSPLOATAVIMO VADOVAS YRA IŠLEISTAS TIK ANGLŲ KALBA.

• JEI KLIENTO PASLAUGŲ TEIKĖJUI REIKIA VADOVO KITA KALBA – NE ANGLŲ, VERTIMU PASIRŪPINTI TURI KLIENTAS.

ĮSPĖJIMAS

(LT)

•NEMĖGINKITE ATLIKTI ĮRANGOS TECHNINĖS PRIEŽIŪROS DARBŲ, NEBENT VADOVAUTUMĖTĖS ŠIUO EKSPLOATAVIMO VADOVU IR JĮ SUPRASTUMĖTE

• NEPAISANT ŠIO PERSPĖJIMO, PASLAUGŲ TEIKĖJAS, OPERATORIUS AR PACIENTAS GALI BŪTI SUŽEISTAS DĖL ELEKTROS SM

ŪGIO, MECHANINIŲ AR

KITŲ PAVOJŲ.

ADVARSEL

(NO)

OSTRZEŻENIE

(PL)

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.

NINIEJSZY PODRĘCZNIK SERWISOWY DOSTĘPNY JEST JEDYNIE W JĘZYKU ANGIELSKIM.

•JEŚLI FIRMA ŚWIADCZĄCA KLIENTOWI USłUGI SERWISOWE WYMAGA UDOSTĘPNIENIA PODRĘCZNIKA W JĘZYKU INNYM NIŻ ANGIELSKI, OBOWIĄZEK ZAPEWNIENIA STOSOWNEGO TłUMACZENIA SPOCZYWA NA KLIENCIE.

• NIE PRÓBOWAĆ SERWISOWAĆ NINIEJSZEGO SPRZĘTU BEZ UPRZEDNIEGO ZAPOZNANIA SIĘ Z PODRĘCZNIKIEM SERWISOWYM.

• NIEZASTOSOWANIE SIĘ DO TEGO OSTRZEŻENIA MOŻE GROZIĆ OBRAŻENIAMI CIAłA SERWISANTA, OPERATORA LUB PACJENTA W WYNIKU PORAŻENIA PRĄDEM, URAZU MECHANICZNEGO LUB INNEGO RODZAJU ZAGROŻEUŃ.

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GE HEALTHCARE DIRECTION 5394227, 12 LOGIQ S8/LOGIQ E8 SERVICE MANUAL

ACEST MANUAL DE SERVICE ESTE DISPONIBIL NUMAI ÎN LIMBA ENGLEZĂ.

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

ATE NŢIE

(RO)

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

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

ДАННОЕ РУКОВОДСТВО ПО ОБСЛУЖИВАНИЮ ПРЕДОСТАВЛЯЕТСЯ ТОЛЬКО НА АНГЛИЙСКОМ ЯЗЫКЕ.

• ЕСЛИ СЕРВИСНОМУ ПЕРСОНАЛУ КЛИЕНТА НЕОБХОДИМО РУКОВОДСТВО НЕ НА АНГЛИЙСКОМ ЯЗЫКЕ, КЛИЕНТУ СЛЕДУЕТ САМОСТОЯТЕЛЬНО ОБЕСПЕЧИТЬ ПЕРЕВОД.

ОСТОРОЖНО!

(RU)

• 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)

UPOZORENJE

(SR)

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.

OVAJ PRIRUČNIK ZA SERVISIRANJE DOSTUPAN JE SAMO NA ENGLESKOM JEZIKU.

• AKO KLIJENTOV SERVISER ZAHTEVA JEZIK KOJI NIJE ENGLESKI,

ODGOVORNOST JE NA KLIJENTU DA PRUŽI USLUGE PREVOĐENJA.

• NEMOJTE POKUŠAVATI DA SERVISIRATE OPREMU AKO NISTE PROČITALI I RAZUMELI PRIRUČNIK ZA SERVISIRANJE.

• AKO NE POŠTUJETE OVO UPOZORENJE, MOŽE DOĆI DO POVREĐIVANJA SERVISERA, OPERATERA ILI PACIJENTA UZROKOVANOG ELEKTRIČNIM UDAROM, MEHANIČKIM I DRUGIM OPASNOSTIMA.

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TA SERVISNI PRIROČNIK JE NA VOLJO SAMO V ANGLEŠČINI.

• ČE PONUDNIK SERVISNIH STORITEV ZA STRANKO POTREBUJE NAVODILA V

DRUGEM JEZIKU, JE ZA PREVOD ODGOVORNA STRANKA SAMA.

OPOZORILO

(SL)

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

RAZUMELI SERVISNI PRIROČNIK.

• ČE TEGA OPOZORILA NE UPOŠTEVATE, OBSTAJA NEVARNOST ELEKTRIČNEGA UDARA, MEHANSKIH ALI DRUGIH NEVARNOSTI IN POSLEDIČNIH POŠKODB PONUDNIKA SERVISNIH STORITEV, UPORABNIKA OPREME ALI PACIENTA.

OVAJ SERVISNI PRIRUČNIK DOSTUPAN JE SAMO NA ENGLESKOM JEZIKU.

• AKO KLIJENTOV SERVISER ZAHTIJEVA JEZIK KOJI NIJE ENGLESKI, ODGOVORNOST KLIJENTA JE PRUŽITI USLUGE PREVOĐENJA.

UPOZORENJE

(HR)

• NEMOJTE POKUŠAVATI SERVISIRATI OPREMU AKO NISTE PROČITALI I RAZUMJELI SERVISNI PRIRUČNIK.

• AKO NE POŠTUJETE OVO UPOZORENJE, MOŽE DOĆI DO OZLJEDE SERVISERA, OPERATERA ILI PACIJENTA PROUZROČENE STRUJNIM UDAROM, MEHANIČKIM I DRUGIM OPASNOSTIMA.

UPOZORNENIE

(SK)

VARNING

(SV)

TÁTO SERVISNÁ PRÍRUČKA JE K DISPOZÍCII LEN V ANGLIČTINE.

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

• NEPOKÚŠAJTE SA VYKONÁVAŤ SERVIS ZARIADENIA SKÔR, AKO SI NEPREČÍTATE SERVISNÚ PRÍRUČKU A NEPOROZUMIETE JEJ.

• ZANEDBANIE TOHTO UPOZORNENIA MÔŽE VYÚSTIŤ DO ZRANENIA POSKYTOVATEĽA SLUŽIEB, OBSLUHUJÚCEJ OSOBY ALEBO PACIENTA ELEKTRICKÝM PRÚDOM, PRÍPADNE DO MECHANICKÉHO ALEBO INÉHO NEBEZPEČENSTVA.

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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GE HEALTHCARE DIRECTION 5394227, 12 LOGIQ S8/LOGIQ E8 SERVICE MANUAL

BU SERVİS KILAVUZU YALNIZCA İNGİLİZCE OLARAK SAĞLANMIŞTIR.

•EĞER MÜŞTERİ TEKNİSYENİ KILAVUZUN İNGİLİZCE DIŞINDAKİ BİR DİLDE OLMASINI İSTERSE, KILAVUZU TERCÜME ETTİRMEK MÜŞTERİNİN

DİKKAT

(TR)

SORUMLULUĞUNDADIR.

•SERVİS KILAVUZUNU OKUYUP ANLAMADAN EKİPMANLARA MÜDAHALE ETMEYİNİZ.

• BU UYARININ GÖZ ARDI EDİLMESİ, ELEKTRİK ÇARPMASI YA DA MEKANİK VEYA DİĞER TÜRDEN KAZALAR SONUCUNDA TEKNİSYENİN, OPERATÖRÜN YA DA HASTANIN YARALANMASINA YOL AÇABİLİR.

(JA)

Traditional

Chinese

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(ZH-CN)

(KO)

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GE HEALTHCARE DIRECTION 5394227, 12 LOGIQ S8/LOGIQ E8 SERVICE MANUAL

DAMAGE IN TRANSPORTATION

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

CERTIFIED ELECTRICAL CONTRACTOR STATEMENT - 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 perfor med 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 sys tem type, manual title, part number, revision number, page number and suggestion details.

Mail the information to: Service Documentation, 9900 Innovation Drive (RP-2123), Wauwatosa, WI53226, USA. GE Healthcare employees should use Application Lifecycle Management (ALM) to report service

documentation issues. These issues will then be in the internal problem reporting tool and communicated to the writer.

SERVICE SAFETY CONSIDERATIONS

DANGER

DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH, ARE PRESENT IN THIS EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING AND ADJUSTING.

WARNINGWARNING

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 Chap te r 1, Saf et y Con sid er at ion s sec tio n in the Service Manual.

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LEGAL NOTES

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

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

PROPRIETARY TO GE HEALTHCARE

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

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

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

If you are not party to such a license agre em e nt or a GE Healthcare Employee, you must exit this Material now.

TRADEMARKS

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

COPYRIGHTS

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Revision History

Revision Date Reason for change

1 Jun. 2011 Initial Release 2 Jul. 2011 Correction 3 Mar. 2012 Correction 4 May. 2013 Initial release for R2.x 5 March.. 2014 Minor correctionfor R2.x 6 July, 2015 Release for R3 7 September, 2015 Update 8 November, 2015 Update BW Printer setup

9 Februry, 2016 Add UDI label information 10 Februry, 2017 Update adding R4 information 11 June, 2017 Revise with Service Note information 12 October, 2017 Add Installation Instruction information 13 March, 2019 Update for R4.2.5x release

List of Effected Pages (LOEP)

Pages Revision Pages Revision Pages Revision

Title Page 12 Chapter 3 12 Chapter 8 12

Warnings i to xii 12 Chapter 4 12 Chapter 9 12

TOC 12 Chapter 5 12 Chapter 10 12 Chapter 1 12 Chapter 6 12 Back Cover N/A Chapter 2 12 Chapter 7 12

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Table of Contents

CHAPTER 1

Introduction

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

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

Contents in this chapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 1

Service manual overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 2

Contents in this service manual . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 2

Typical users of the Service Manual . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 3

Models covered by this manual . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 4

Product description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 6

Important conventions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 7

Conventions used in this manual . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 7

Standard Hazard Icons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 8

Product Icons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 10

Safety Considerations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 15

Contents in this section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 15

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 15

Human Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 15

Mechanical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 17

Electrical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 19

Auxiliary Devices Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 20

Battery Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 22

Labels Locations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 23

The labels on the cover . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 23

Rating plate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 26

Dangerous Procedure Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 27

Lockout/Tagout (LOTO) Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 28

Returning/Shipping System, Probes and Repair Parts . . . . . . . . . . . . . . . . . . . . . .1 - 29

For LOGIQ S8 Vet system . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 29

Electromagnetic Compatibility (EMC) and Electrostatic Discharge (ESD). . . . . . . .1 - 30

What is EMC? . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 30

Compliance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 30

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Electrostatic Discharge (ESD) Prevention . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 30

Customer Assistance. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 31

Contact Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 31

System Manufacturer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 32

Authorized EU Representative . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 32

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CHAPTER 2

Site preparations

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

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

Contents in this chapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 1

General console requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 2

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

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

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

Probe Environmental Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 6

Time and Manpower Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 6

Facility needs. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 7

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

Required Facility Needs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 8

Privacy and Security . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 8

Desirable features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 9

Minimal floor plan suggestions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 9

Networking setup requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 10

Environmental Dangers. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 12

Patient Vicinity UL60601-1 (USA) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 12

Patient Environment IEC60601-1 (IEC60601-1-1) and ANSI AAMI ES60601-1 2 - 13

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CHAPTER 3

System Setup

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

Purpose of this chapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 1

Contents in this chapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 1

Setup reminders . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 2

Average Setup Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 2

Setup warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 3

Receiving and unpacking the equipment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 5

Receiving and unpacking warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 5

Receiving the LOGIQ S8 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 6

Transportation Box Label . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 8

Unpacking the LOGIQ S8 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 9

Packing materials - recycling information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 10

Preparing for setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 11

Verify Customer Order . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 11

Physical inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 11

EMI Protection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 11

Completing the Set Up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 12

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

Electrical specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 13

Connection the I/O Rear Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 14

Connecting Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 15

Power On/Off. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 17

Connect AC (mains) Power to the LOGIQ S8 . . . . . . . . . . . . . . . . . . . . . . .3 - 18

Power ON . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 19

Logoff/Shutdown/Exit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 21

Complete shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 22

Sleep Mode (R1 to R4) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 23

To change your password . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 24

Password policies . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 25

Disk encryption . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 29

System Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 32

Purpose of this section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 32

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System Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 32

Software Option installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 35

Optional Peripherals/Peripheral Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 37

Connecting the Secondary “Patient” LCD Monitor . . . . . . . . . . . . . . . . . . . .3 - 38

Connecting the Off-Board/On-Board UVC . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 42

Connecting the Footswitch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 46

ECG connector . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 47

Connecting the USB Flash Drive and USB External Hard disk drive . . . . .3 - 48

Printer Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 49

Installing Digital Black & White Printer Sony UP-D897/D898 . . . . . . . . . . .3 - 49

Installing Digital Color Printer Sony UP-D25MD . . . . . . . . . . . . . . . . . . . . .3 - 58

Adding the printer to the system . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 64

Setting the printer to print reports . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 65

PC printer setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 65

Connectivity Setup. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 66

Connectivity Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 66

The Dataflow Concept . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 66

Stand-alone LOGIQ S8 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 68

LOGIQ S8 + PC within a “Sneaker Net” . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 68

Connection between LOGIQ S8 and DICOM Server . . . . . . . . . . . . . . . . . .3 - 68

Wired Ethernet from LOGIQ S8 to a Workstation . . . . . . . . . . . . . . . . . . . .3 - 69

Connection using Wireless Option (R2.x.x or later) . . . . . . . . . . . . . . . . . . .3 - 69

Network icon . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 70

Configuring Connectivity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 72

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 72

Contents in this section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 72

Structured Reporting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 72

Connectivity Functions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 73

TCPIP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 74

Device . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 76

Service . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 77

Instructions for setting up Network Storage on LOGIQ S8 R4 . . . . . . . . . .3 - 79

Setting up InSite Connection (R1 to R4) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 82

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 82

Contents in this section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 82

Prerequisites for InSite Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 82

Configuration Steps . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 83

Configuring InSite . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 83

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Configuring Agent Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 83

Configuring Advanced Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 86

Configuring Request for Service (RFS) . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 90

Verifying InSite Connection - CSD . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 91

Verifying InSite Connection - VCO . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 92

Agent Configuration (R4.2.5x and later) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 93

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 93

Verifying back office connection - CSD . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 93

Verifying Back Office Connection - VOC . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 94

Connectivity Setup Worksheet . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 95

Paperwork . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 97

Product Locator Installation Card . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 97

User Manual(s) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 97

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CHAPTER 4

Functional Checks

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

Purpose of this chapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 1

Contents in this chapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 1

Required equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 1

General procedures. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 2

Power ON . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 3

Logoff/Shutdown/Exit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 5

Complete shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 6

Monitor Positions Adjustment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 7

Operator panel position adjustment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 9

Caster . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 11

Moving and Transporting the LOGIQ S8 . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 13

Service Platform Confirmation (R1 to R4) . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 17

Functional Checks. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 18

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 18

Contents in this section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 18

Preparation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 18

Basic Controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 19

Performance Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 22

B-Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 23

M-Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 25

Color Flow Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 27

PW/CW Doppler Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 29

Tissue Velocity Imaging (TVI) Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 31

SWE (Shear Wave “Shear Elasto”) Functional Check . . . . . . . . . . . . . . . . .4 - 32

Cineloop Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 32

Basic Measurements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 33

System Integration Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 35

Probe/Connectors Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 37

ECG Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 38

Peripheral Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 39

System Exterior Visual Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 41

Mechanical Functions Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 46

Extended Battery (Option) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 46

3D/4D (Option) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 46

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Volume Navigation (Option) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 46

FibroScan module (Option) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 47

Application Turnover Check List . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 48

Software Configuration Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 48

Power supply test and adjustments. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 48

Power Supply Test Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 48

Power Supply Adjustment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 48

Site Log . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 - 49

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CHAPTER 5

Components and Functions (Theory)

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

Purpose of this chapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 1

Contents in this chapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 1

General Information. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 2

System Exterior . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 3

System Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 6

USB Ports . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 7

Rear panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 10

Power Distribution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 11

Purpose of this section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 11

Power Up Sequence Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 11

Power Loss description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 12

Software Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 13

Purpose of this section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 13

Contents in this section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 13

LOGIQ S8 software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 13

Software Options. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 14

Hardware Options.. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 17

LOGIQ S8 R4 - FibroScan Option . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 21

Regional and Peripheral Options. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 25

Regional Options. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 25

Peripheral Options. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 25

Air Flow Distribution. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 26

Air Flow Distribution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 26

Product Manuals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 27

Purpose of the operator manual(s) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 27

User documentation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 27

Basic Service documentation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 27

Service/Proprietary documentation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 27

Advanced Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 27

LOGIQ E8 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 28

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CHAPTER 6

Service Adjustments

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

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

Monitor Adjustment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6 - 2

19” LCD Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6 - 2

22” (OLED) and 23” Wide Monitor Adjustment . . . . . . . . . . . . . . . . . . . . . .6 - 8

Volume Navigation Calibration Procedure. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6 - 10

Purpose of this section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6 - 10

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6 - 10

Equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6 - 10

Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6 - 11

Measure Initial Accuracy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6 - 12

Perform Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6 - 13

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CHAPTER 7

Diagnostics/Troubleshooting

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

Purpose of this chapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 1

Contents in this chapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 1

Service Platform . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 2

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 2

Access / Security . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 2

Local Access (R1 to R4) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 2

Remote Access to Service Platform . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 3

Customer Granting Full Remote Access Permission to GE Service Technician 7 - 4

Gathering Troubleshooting Data (R1 to R4) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 5

Purpose of this Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 5

Contents in this section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 5

Collecting Vital System Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 6

Collecting a Screen Capture with Logs . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 9

Capturing Service Logs with ALT+D . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 12

Screen captures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 13

Capturing Network Logs with Network Sniffer . . . . . . . . . . . . . . . . . . . . . . .7 - 14

Service Desktop (CSD) - R1 to R4 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 20

Purpose of this Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 20

Contents in this chapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 20

Global Service User Interface (GSUI) . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 21

CSD Top Page . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 22

Error Logs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 23

Diagnostics . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 24

Image Quality . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 25

Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 25

Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 26

Utilities - Common Utilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 27

Utilities - Scanner Utilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 35

Replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 37

PM . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 37

Gathering Troubleshooting Data (R4.2.5x and later). . . . . . . . . . . . . . . . . . . . . . . .7 - 38

Purpose of this section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 38

Collecting vital system information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 38

Shortcut keys . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 39

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Collecting a screen capture with logs . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 40

Capturing network logs to use for troubleshooting . . . . . . . . . . . . . . . . . . .7 - 44

Service Desktop (R4.2.5x and later) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 46

Purpose of this section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 46

Disruptive mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 47

Color statuses . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 47

Licenses . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 48

Home . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 49

Utilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 54

Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 65

Agent Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 66

Troubleshooting Trees, Instructions and Tech Tips . . . . . . . . . . . . . . . . . . . . . . . .7 - 68

Contents in this section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 68

Shortcut Keys . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 68

System does not boot up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 69

Noise disturbs the Image . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 70

Trackball - Impaired sensitivity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 71

Printer Malfunction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 73

19” Monitor Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 74

Universal Video Converter Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . .7 - 75

4D Option Trouble shooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 75

Power Assistant Option Trouble Shooting . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 75

Extended Battery Option Trouble Shooting . . . . . . . . . . . . . . . . . . . . . . . . .7 - 76

Mode encoder works twice when pushed button once . . . . . . . . . . . . . . . .7 - 77

Sticky buttons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 77

Mode button failure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 77

PC Printer Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 78

FibroScan Module (FSIM) Trouble Shooting . . . . . . . . . . . . . . . . . . . . . . . .7 - 79

Fibroscan Probe . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 81

Privacy and Security Trouble Shooting . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 82

Slow response rate between the LOGIQ™ S8 and a DICOM (PACS) server 7 - 82

When the touch panel does not response . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 83

Limitation message during AFI Analysis . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 83

Noise Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 84

Electromagnetic Interference (EMI) Troubleshooting . . . . . . . . . . . . . . . . .7 - 86

Connectivity Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 87

User Group Management and User Right Control (For R4) . . . . . . . . . . . .7 - 89

Error messages. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7 - 91

FibroScan Module Error messages and Logs . . . . . . . . . . . . . . . . . . . . . . .7 - 93

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GE HEALTHCARE DIRECTION 5394227, 12 LOGIQ S8/LOGIQ E8 SERVICE MANUAL

CHAPTER 8

Renewal Parts

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

Contents in this chapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 1

Optional Peripherals and Accessories. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 2

Printers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 2

Probes. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 4

Power Cord . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 8

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GE HEALTHCARE DIRECTION 5394227, 12 LOGIQ S8/LOGIQ E8 SERVICE MANUAL

CHAPTER 9

Care & Maintenance

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

Periodic maintenance inspections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 1

Purpose of this chapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 1

Contents in this chapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 1

Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 2

Why do maintenance. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 2

Keeping records . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 2

Quality assurance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 2

Maintenance task schedule. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 3

How often should maintenance tasks be performed? . . . . . . . . . . . . . . . . .9 - 3

Tools required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 6

Special tools, supplies and equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 6

System maintenance. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 7

Preliminary checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 7

Functional checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 8

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

Physical inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 13

Probe maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 14

Using a Phantom. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 16

Electrical Safety Tests. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 17

Safety test overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 17

GEHC Leakage Current Limits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 18

Outlet Test - Wiring Arrangement - USA & Canada . . . . . . . . . . . . . . . . . .9 - 20

Grounding Continuity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 21

Chassis leakage current test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 22

Data sheet for enclosure/chassis leakage current . . . . . . . . . . . . . . . . . . . .9 - 23

Isolated patient lead (source) leakage-lead to ground . . . . . . . . . . . . . . . . .9 - 24

Isolated patient lead (source) leakage–lead to lead . . . . . . . . . . . . . . . . . .9 - 26

Isolated patient lead (sink) leakage-isolation test . . . . . . . . . . . . . . . . . . . .9 - 27

Probe leakage current test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 28

Mains on applied part . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 31

e-TRAX (source) Leakage Current Test . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 33

e-TRAX Leakage current - Mains to CF Applied part . . . . . . . . . . . . . . . . .9 - 34

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GE HEALTHCARE DIRECTION 5394227, 12 LOGIQ S8/LOGIQ E8 SERVICE MANUAL

When There’s Too Much Leakage Current... . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 35

Chassis Fails . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 35

Probe Fails . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 35

Peripheral Fails . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 35

Still Fails . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 35

ECG Fails . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 36

Ultrasound Equipment Quality Check (EQC and IQC) . . . . . . . . . . . . . . . .9 - 36

- 15

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GE HEALTHCARE DIRECTION 5394227, 12 LOGIQ S8/LOGIQ E8 SERVICE MANUAL

Chapter 1 Introduction

Section 1-1 Overview

1-1-1 Purpose of this chapter

This chapter describes important issues related to safely servicing LOGIQ S8. The service provider must read and understand all the information presented here before installing or servicing a unit.

Attention

This manual contains necessary and sufficient information for the Field Service Engineer or Biotech Engineer to maintain and service the system safely. Advanced equipment training may be provided b y factory trained Field Service trainers for the agreed-upon time period.

This service manual provides installation and service information for the LOGIQ S8 ultrasound system as shown in Table 1-1 "Contents in this service manual" on page 1- 2.

NOTE: Ensure you are working with the latest version of the Proprietary Service Manual. Consult the

CDL and OnBase to confirm and to download the latest version.

1-1-2 Contents in this chapter

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

1-2 Service manual overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-2

1-3 Important conventions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-7

1-4 Safety Considerations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-15

1-5 Labels Locations. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-23

1-6 Dangerous Procedure Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-27

1-7 Lockout/Tagout (LOTO) Requirements. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-28

1-8 Returning/Shipping System, Probes and Repair Parts. . . . . . . . . . . . . . . . . . . . . . . . . . 1-29

1-9 Electromagnetic Compatibility (EMC) and Electrostatic Discharge (ESD) . . . . . . . . . . . 1-30

1-10 Customer Assistance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-31

Section 1-1 - Overview 1 - 1

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GE HEALTHCARE DIRECTION 5394227, 12 LOGIQ S8/LOGIQ E8 SERVICE MANUAL

Section 1-2 Service manual overview

1-2-1 Contents in this service manual

The service manual is divided into ten chapters. In the beginning of the manual, before chapter 1, you will find the language policy for GE Healthcare’s

service documentation, legal information , a re visio n over vie w, an d th e Ta b le of Contents (TOC).

Table 1-1 Contents in this service manual

CHAPTER

NUMBER

CHAPTER TITLE DESCRIPTION

1 2 3

N/A

Introduction Contains a content summary and warnings. Site preparations System Setup Contains setup procedure with procedure checklist.

Functional Checks

Components and Functions (Theory)

Service Adjustments

Diagnostics/Troubleshooting

Replacement Procedures

Renewal Parts Care & Maintenance Index A quick way to the topic you’re looking for.

Contains pre-setup requirements for the LOGIQ S8.

Contains functional checks that must be performed as part of the installation, or as required during servicing and periodic maintenance.

Contains block diagrams and functional explanations of the electronics.

Contains instructions on how to make any available adjustments to the LOGIQ S8.

Provides procedures for running diagnostic or related routines for the LOGIQ S8.

Provides disassembly procedures and reassembly procedures for all changeable FRUs, available option installation instructions, and upgrade installation instructions.

Contains a complete list of replacement parts for the LOGIQ S8. Provides periodic maintenance procedures for LOGIQ S8.

1 - 2 Section 1-2 - Service manual overview

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GE HEALTHCARE DIRECTION 5394227, 12 LOGIQ S8/LOGIQ E8 SERVICE MANUAL

1-2-2 Typical users of the Service Manual

• GE Service Personnel (Setup, maintenance, etc.)

• Hospital Service Personnel

• Architectural Planners/Installation Planners (some parts of Chapter 2 - Site preparations)

Section 1-2 - Service manual overview 1 - 3

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GE HEALTHCARE DIRECTION 5394227, 12 LOGIQ S8/LOGIQ E8 SERVICE MANUAL

1-2-3 Models covered by this manual

Table 1-2 LOGIQ S8 Models

MODEL NUMBER DESCRIPTION R1 R2 R3 R4 R4.2.5x

5418099 5418100 5418101 5418102 5418103 5418104 5418105 5478057 5478058 5669845 5669847 5756373 5815518 5808841

LOGIQ S8 Console, BASIC configuration Y U U* N N LOGIQ S8 Console, CHINA configuration Y U U* N N LOGIQ S8 Console, JAPAN configuration Y U U* N N LOGIQ S8 Console, KOREA configuration Y U U* N N LOGIQ S8 Console, INDIA configuration Y U U* N N LOGIQ S8 Console, USA configuration Y U U* N N LOGIQ S8 Console, CANADA configuration Y U U* N N LOGIQ S8 R2 - 110V N Y U* N N LOGIQ S8 R2 - 220V N Y U* N N LOGIQ S8 R3 N N Y U N LOGIQ S8 R3 with OLED monitor N N Y U N LOGIQ S8 R4 with OLED monitor N N N Y U LOGIQ S8 R4.2.5x with OLED monitor NNNN Y LOGIQ S8 R4.2.5x with LCD monitor NNNN Y

Table 1-3 LOGIQ S8 Vet Models

MODEL NUMBER DESCRIPTION R1 R2 R3 R4 R4.2.5x

5459532 5478475 5478476 5604017

LOGIQ S8 Vet - USA Y N N N N LOGIQ S8 Vet R2 - 110V N Y U* N N LOGIQ S8 Vet R2 - 220V N Y U* N N LOGIQ S8 Vet Upgrade kit N N U* U* U*

1 - 4 Section 1-2 - Service manual overview

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GE HEALTHCARE DIRECTION 5394227, 12 LOGIQ S8/LOGIQ E8 SERVICE MANUAL

1-2-3 Models covered by this manual (cont’d)

Table 1-4 LOGIQ E8 Model (ship only for People's Republic of China)

MODEL NUMBER DESCRIPTION R1 R2 R3 R4.2.5x

5486788 5669848

5818169

LOGIQ E8 R2 N Y U* N LOGIQ E8 R3 OLED N N Y N LOGIQ E8 R4.2.5x OLED N N N Y

Software Configurations and Hardware/Software Compatibility - Upgrade Options Y: Original, U: Upgrade available, N: Not supported U*:

Upgrade available. (No LCD upgrade)

Section 1-2 - Service manual overview 1 - 5

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GE HEALTHCARE DIRECTION 5394227, 12 LOGIQ S8/LOGIQ E8 SERVICE MANUAL

1-2-4 Product description

1-2-4-1 Overview of the LOGIQ S8/LOGIQ E8 ultrasound system

The LOGIQ S8/LOGIQ E8 ultrasound system is a high performance digital ultrasound imaging system with total data management.

This system provides image generation in B-Mode, Color Doppler, Power Doppler, M-Mode, Color MMode, PW/CW and 3D/4D, Tissue Velocity imaging, Volume-Guided Ultrasound, Elastograph y, and Contrast applications.

The fully digital architecture of the LOGIQ S8/LOGIQ E8 allows optimal usage of all scanning modes and probe types throughout the full spectrum of operating frequencies.

Signal flows from the Probe Connector Panel to the Front End, and then over to the Back End Pro cessor and finally to the monitor and peripherals.

System configuration is stored on the hard drive in the Back End Processor. All necessary software is loaded from the hard drive on power up.

1 - 6 Section 1-2 - Service manual overview

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GE HEALTHCARE DIRECTION 5394227, 12 LOGIQ S8/LOGIQ E8 SERVICE MANUAL

Section 1-3 Important conventions

1-3-1 Conventions used in this manual

1-3-1-1 Icons

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

1-3-1-2 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 precautionar y message. Known or potential hazards to personnel are labeled in one of three ways:

DANGER

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

WARNINGWARNING

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

CAUTION

NOTICE

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

CAUTION IS USED TO INDICATE THE PRESENCE OF A HAZARD THAT WILL OR CAN CAUSE MINOR PERSONAL INJURY AND PROPERTY DAMAGE IF INSTRUCTIONS ARE IGNORED. EQUIPMENT DAMAGE POSSIBLE.

When a hazard is present that can cause property damage, but has absolutely no personal injury risk, a NOTICE is used.

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

Notice Example: Disk drive may crash.

the notes; the information contained in a note can of te n sav e yo u tim e or effo rt .

Section 1-3 - Important conventions 1 - 7

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GE HEALTHCARE DIRECTION 5394227, 12 LOGIQ S8/LOGIQ E8 SERVICE MANUAL

1-3-2 Standard Hazard Icons

Important information will always be preceded by the exclamation point (!) contained within a triangle, or the symbols for “Danger”, “Warning” or “Caution”, as see n throughout this chapter. In addition to te xt, several different graphical icons (symbols) may be used to make you aware of specific types of hazards that could cause harm.

Even if a symbol isn’t used in this manual, it is included for your reference.

Table 1-5 Standard Hazard Icons

ELECTRICAL BIOHAZARD RADIATION

LASER HEAT PINCH

LASER

LIGHT

ACOUSTIC OUTPUT EXPLOSION

DANGER/WARNING/

MOVING

CAUTION SMOKE/FIRE

1 - 8 Section 1-3 - Important conventions

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GE HEALTHCARE DIRECTION 5394227, 12 LOGIQ S8/LOGIQ E8 SERVICE MANUAL

1-3-2-1 Standard Icons that indicate that a special procedure is to be used

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

Table 1-6 Standard Icons Indicating a Special Procedure be Used

AVOID STATIC ELECTRICITY TAG AND LOCK OUT WEAR EYE PROTECTION

WEAR HAND PROTECTION WEAR FOOT PROTECTION

Section 1-3 - Important conventions 1 - 9

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GE HEALTHCARE DIRECTION 5394227, 12 LOGIQ S8/LOGIQ E8 SERVICE MANUAL

1-3-3 Product Icons

The following table describes the purpose and location of safety labels and ot her important inform ation provided on the equipment.

Table 1-7 Label Icons

Label/Icon Purpose/Meaning Location

Identification and Rating Plate Manufacturer’s name and address

Identification and Rating Plate Date of manufacture

Serial Number Rating Plate

Catalog Number Rating Plate

United States only Prescription Requirement label

CE Mark The CE Mark of Conformity indicates this equipment conforms with

the Council Directive 93/42/EEC.

Authorized European Representative address Rear of the system

Rating Plate

Rear of the system

IP Code (IPX8)

Indicates the degree of protection provided by the enclosure per IEC60 529. Can be used in operating room environment.

Type B Applied Part symbol is in accordance with IEC 60878-02-03.

Type BF Applied Part (man in the box) symbol is in accordance with IEC 60878-02-03.

Defibrillation-proof applied part type BF. ECG connector

Type CF Applied Part (heart in the box) symbol is in accordance with IEC 60878-02-03.

1 - 10 Section 1-3 - Important conventions

Footswitch

Probe marked Type B

Probe marked Type BF

eTrax Needle

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GE HEALTHCARE DIRECTION 5394227, 12 LOGIQ S8/LOGIQ E8 SERVICE MANUAL

Table 1-7 Label Icons(Continued)

Label/Icon Purpose/Meaning Location

Follow instruction for use.

Symbol indicating that the Instructions for Use are supplied in electronic form.

“General Warning Sign” Rear of the system

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

“Mains OFF” indicates the power off position of the mains power breaker.

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

Rear of the system Probe connector

Rear Panel

Internal

Rear of the system

“ON” indicates the power on position of the power button. CAUTION: This Power button DOES NOT ISOLATE Mains Supply.

Stand-by. The standby symbol (line partially within a broken circle), indicates a sleep mode or low power state. Blue: Stand-by or sleep mode Green: Power on

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

R1/R2/R3 Operator control panel

R4 Operator control panel

Section 1-3 - Important conventions 1 - 11

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GE HEALTHCARE DIRECTION 5394227, 12 LOGIQ S8/LOGIQ E8 SERVICE MANUAL

Table 1-7 Label Icons(Continued)

Label/Icon Purpose/Meaning Location

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

Connection of additional protective earth conductors or potential equalization conductors is not necessary in most cases and is only recommended for situations involving multiple equipment in a highrisk patient environment to provide assurance that all equipment is at the same potential and operates within acceptable leakage current limits. An example of a high-risk patient would be a special procedure where the patient has an accessible conductive path to the heart such as exposed cardiac pacing leads.

Rear of the system

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

The separate collection symbol is affixed to a battery, or its packaging, to advise you that the battery must be recycled or disposed of in accordance with local or country laws. The letters below the separate collection symbol indicate whether certain elements (Pb=Lead, Cd=Cadmium, Hg=Mercury) are contained in the battery. To minimize potential effects on the environment and human health, it is important that all marked batteries that you remove from the product are properly recycled or disposed. For information on how the battery may be safely removed from the device, please consult the service manual or equipment instructions. Information on the potential effects on the environment and human health of the substances used in batteries is available at this url: http:/ /www.gehealthcare.com/euen/weee-recycling/index.html

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

Rear of the system

Probe connector

Battery Pack if contains Pb/Cd/Hg

Probe connector

1 - 12 Section 1-3 - Important conventions

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Table 1-7 Label Icons(Continued)

Label/Icon Purpose/Meaning Location

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

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

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.)

Rear of the system

UL conformity mark according to UL 60601-1 and CAN/CSA C22/2 NO. 601.1:.

UL conformity mark according to ANSI/AAMI ES60601-1:2005/ (R)2012, CAN/CSA-C22.2 No. 60601-1:14.

ISO 7010 - P007 Volume Navigation Pacemaker Warning. No access for person with pacemaker.

How to lock Operator Panel prior to transport Rear of the system.

DO NOT place a finger, hand or any object on the joint of the monitor or monitor arm to avoid injury when moving the monitor and monitor arm.

DO NOT push the system. Use the handle to push/pull the system, e.g., DO NOT use the LCD. Failure to do so may cause serious injury or system damage.

R1 to R3 Leg of the rear caster

R4 and later Leg of the rear caster

V Nav Transmitter

Rear of the LCD monitor.

Rear of the system

Section 1-3 - Important conventions 1 - 13

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Table 1-7 Label Icons(Continued)

Label/Icon Purpose/Meaning Location

Caution Probe connector

Neck of Monitor arm, on

Non-Ionizing Electromagnetic Radiation

equipped with Wireless LAN

This system is for animal use only. Do not mix up with human diagnosis.

Rear of the LS8 Vet system

GOST Symbol. Russia Regulatory Country Clearance. Under the rating plate

EAC Mark of Conformity. Image of the Common Mark of Products Circulation in the market of the Customs Un io n memb e r-states.

Every system has a unique marking for identification, the Unique Device Identification (UDI) Label. The UDI label consists of a series of alpha-numeric characters and barcode which uniquely identify the LOGIQ S8 system as a medical device manufactured by General Electric. Scan or enter the UDI information into the patient health record as required by country-specific laws.

Under the rating plate

Rating Plate

1 - 14 Section 1-3 - Important conventions

Upgraded LOGIQ S8 systems, UDI label is on the left-rear caster.

Probe UDI label

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Section 1-4 Safety Considerations

1-4-1 Contents in this section

1-4-1 Contents in this section. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-15

1-4-2 Introduction. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-15

1-4-3 Human Safety. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-15

1-4-4 Mechanical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-17

1-4-5 Electrical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-19

1-4-6 Auxiliary Devices Safety. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-20

1-4-7 Battery Safety. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-22

1-4-2 Introduction

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

1-4-3 Human Safety

DANGER

WARNINGWARNING

• Operating personnel must not remove the system covers, except for removing front cover to clean air filter.

• Servicing should be performed by authorized personnel only.

Only personnel who have participated in a LOGIQ S8 Training are authorize d to service the equipment.

DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH, ARE PRESENT IN THIS EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING AND ADJUSTING.

IF THE COVERS ARE REMOVED FROM AN OPERATING LOGIQ S8, SOME METAL SURFACES MAY BE WARM ENOUGH TO POSE A POTENTIAL HEAT HAZARD IF TOUCHED, EVEN WHILE IN SHUTDOWN MODE.

BECAUSE OF THE LIMITED ACCESS TO CABINETS AND EQUIPMENT IN THE FIELD, PLACING PEOPLE IN AWKWARD POSITIONS, GE HAS LIMITED THE LIFTING WEIGHT FOR ONE PERSON IN THE FIELD TO 16 KG (35 LBS). ANYTHING OVER 16 KG (35 LBS) REQUIRES 2 PEOPLE.

USE ALL PERSONAL PROTECTION EQUIPMENT (PPE) SUCH AS GLOVES, SAFETY SHOES, SAFETY GLASSES, AND KNEELING PAD, TO REDUCE THE RISK OF INJURY.

WEAR ALL PPE INCLUDING GLOVES AS INDICATED IN THE CHEMICAL MSDS.

WARNINGWARNING

EXPLOSION WARNING DO NOT OPERATE THE EQUIPMENT IN AN EXPLOSIVE ATMOSPHERE. OPERATION

OF ANY ELECTRICAL EQUIPMENT IN SUCH AN ENVIRONMENT CONSTITUTES A DEFINITE SAFETY HAZARD.

Section 1-4 - Safety Considerations 1 - 15

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WARNINGWARNING

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.

ENSURE THAT THE SYSTEM IS TURNED OFF AND UNPLUGGED.

WAIT FOR AT LEAST 20 SECONDS FOR CAPACITORS TO DISCHARGE AS THERE ARE NO TEST POINTS TO VERIFY ISOLATION. THE BLUE LIGHT ON THE POWER BUTTON WILL TURN OFF.

RISK OF ELECTRICAL SHOCK, SYSTEM MUST BE TURNED OFF AND DISCONNECTED FROM POWER SOURCE. CORD MUST BE CONTROLLED AT ALL TIMES.

USE EXTREME CAUTION AS LONG AS THE LOGIQ S8/LOGIQ E8 IS UN-STABLE, NOT RESTING ON ALL FOUR CASTERS.

TILTING THE CONSOLE REQUIRES TWO PEOPLE IN ORDER TO AVOID INJURY TO SERVICE PERSONNEL AND DAMAGE TO THE EQUIPMENT.

BEWARE OF POSSIBLE SHARP EDGES ON ALL MECHANICAL PARTS. IF SHARP EDGES ARE ENCOUNTERED, THE APPROPRIATE PPE SHOULD BE USED TO REDUCE THE RISK OF INJURY.

1 - 16 Section 1-4 - Safety Considerations

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1-4-4 Mechanical Safety

WARNINGWARNING

CAUTION

USE EXTREME CAUTION WHEN ELEVATING THE UNIT, OR IF IT IS RAISED FOR A REPAIR OR MOVED ALONG ANY INCLINE. THE LOGIQ S8 SYSTEM MAY BECOME UNSTABLE WHICH COULD CAUSE A TIP OVER.

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

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

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

The system weighs approximately 85 kg (LOGIQ S8) / 97 kg (LOGIQ E8) or more, depending on installed peripherals, when ready for use.

Care must be used when moving it or replacing its parts. Failure to follow the precautions listed could result in injury, uncontrolled motion and costly damage.

ALWAYS:

• Use the handle to move the system.

• Be sure the pathway is clear.

• Use slow, careful motions.

• Do not let the system strike walls or door frames. Two people are required when moving on inclines or lifting more than 16 kg (35 lbs).

CAUTION

THE SYSTEM SHOULD NOT BE MOVED WITH THE OPERATOR I/O PANEL EXTENDED. MOVE THE OPERATOR I/O PANEL TO ITS CENTERED AND LOCKED POSITION. LOWER THE OPERATOR I/O PANEL AS MUCH AS POSSIBLE BEFORE MOVING THE SYSTEM.

Before you move or transport the system, make sure to lock the LCD monitor firmly and flip down the monitor to prevent damage to the system.

To avoid injury when you move the LCD monitor and the monitor arm, DO NOT put your finger, hand, or object on the joint of the monitor or the monitor arm.

To avoid injury or damage to the monitor, make sure there is nothing within range of the LCD before moving the monitor and monitor arm. This includes people as well as things.

Ensure that nobody touches the console arm/frogleg when moving the Operator Panel.

Section 1-4 - Safety Considerations 1 - 17

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CAUTION

Use Protective Glasses during drilling, filing and during all other work where eyes need protection.

CAUTION

NOTICE

Be careful not to pinch any of the cables.

Use Safety Shoes when doing work where there is any chance of foot damage.

Use Protective Gloves when drilling and cutting.

NOTE: Special care should be taken when transp orting the unit in a vehicle, se e 4-3-8-3 "Transporting

the System" on page 4-16.

1 - 18 Section 1-4 - Safety Considerations

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1-4-5 Electrical Safety

1-4-5-1 Safe Practices

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

electrical outlet with safety ground. If an extension cord is used with th e system, make sure that the total current rating of the system does not exceed the extension cord rating.

The power outlet used for this equipment should not be shared with other types of equipment. Both the system power cable and the power connector meet international electrical standards.

WARNINGWARNING

CONNECTING A LOGIQ S8/LOGIQ E8 SCANNER TO THE WRONG VOLTAGE LEVEL WILL MOST LIKELY DESTROY IT.

1-4-5-2 Probes

All the probes for the LOGIQ S8 are designed and ma nufactured to provide trouble-free, reliable service. To ensure this, correct handling of probes is important and the following points should be noted:

• Do not drop a probe or strike it agai nst a hard surface, as this may damage the transducer elements, acoustic lens, or housing.

• Inspect the probe prior to each use for damage or degradation to the housing, cable strain relief, lens, seal, connector pins and locking mechanism.

• Do not use a cracked or damaged probe. In this event, call your fiel d service representative immediately to obtain a replacement.

• Avoid pulling, pinching or kinking the probe cable, since a damaged cable may compromise the electrical safety of the probe.

• To avoid the risk of a probe accidentally falling, do not allow the probe cables to become entangled, or to be caught in the machine’s wheels.

• Never immerse the probe connector or adapter into any liquid.

NOTE: For detailed information on handling probes, refer to the Basic User Manual and the care card supplied

with the probe.

Section 1-4 - Safety Considerations 1 - 19

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1-4-6 Auxiliary Devices Safety

WARNINGWARNING

Power Supplies for additional equipment MUST comply with IEC 60601-1.

DO NOT attempt to use different peripherals and accessories (brand and model; connected via USB ports) other than approved and provided by GE Healthcare! The ultrasound system is an extremely sensitive and complex medical system. Any unauthorized peripherals may cause system failure or damage!

After each installation, the leakage currents have to be measured according to IEC 60601-1 respectively UL 60601-1.

The LOGIQ S8 may be used with an isolation transformer to pr ovide the required separation from mains for both, the system and the auxiliary devices.

One AUX main outlet is located at the primary power supply. It is used for connecting the two-fold splitter whose outlets are led to the shelves intend for auxiliary devices (e.g., printer s) and the AUX main outlet that is accessible on the back of the control console.

The IEC 60601-1-1 standard provides a guideline for safely interconnecting medical devices in systems. “Equipment connected to the analog or digital interface must comply with the respective IEC/UL standards (e.g. IEC 60950 / UL 60950 for data processing equipment and IEC 60601-1 / UL 60601-1 for medical equipment).

Everybody who connects additional equipment to the signal input portion or signal output portion configures a medical system, and is therefore re sp on sib le th at the system complies with the requirements of the system standard IEC 60601-1-1.

Special care has to be taken, if the device is connected to computer network (e.g., Ethernet), because other devices could be connected without any control. There could be a potential difference between the protective earth and any line of the computer network including the shield.

In this case the only way to operate the system safely is to use an isolated signal link with minimum 4mm creepage distance, 2.5mm air clearance of the isolation device. For computer networks there are media converters available which convert the electrical to optical signals. Please consider that this converter has to comply with IEC xxx standards* and is battery operated or connected to the isolation mains output of the LOGIQ S8.

* IEC xxx stands for standards such as:

• IEC 60601 for medical devices

• IEC 60950 for information technology equipment etc.

CAUTION

1 - 20 Section 1-4 - Safety Considerations

The leakage current of the entire system including any / all auxiliary equipment must not exceed the limit values as per EN 60601-1-1:1990 (IEC 60601-1-1) respectively other valid national or international standards. All equipment must comply with UL, CSA and IEC requirements.

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CAUTION

NOTICE

Please observe that some printers may not be medical devices! If the Bluetooth Printer and/or Line Printers are no medical devices, they have to be located outside of the patient environment (according to IEC 60601-1 / UL 60601-1).

Auxiliary equipment must only be connected to the main console with the special main outlet provided for the electrical safety of the system.

Auxiliary equipment with direct main connection requires galvanic separation of the signal and/ or control leads.

The system integrator (any person connecting the medical device to other devices) is responsible that the connections are safe.

If in doubt, consult the technical service department or your local representative.

NOTICE

All peripherals mounted on the LOGIQ S8 system chassis must be firmly secured in position.

Each signal output (DVI, D-SUB (VGA), S-VIDEO, COMPOSITE (BNC), COMPOSITE (RCA)) of UVC (Universal Video Converter) is insulated.

Section 1-4 - Safety Considerations 1 - 21

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1-4-7 Battery Safety

NOTE: The LOGIQ S8 ultrasound system is supplied with a lithium ion battery in the power supply

module, as option.

The lithium ion technology used in the system’s battery is significantly less hazardous to the environment than the lithium metal technology used in some other batteries (such as watch batte ries) . Used batteries should not be placed with common household waste products. Contact local authorities for the location of a chemical waste collection program nearest you.

NOTE: Regulations vary for different countries. Dispose of a used battery in accordance with local

regulations.

WARNINGWARNING

CAUTION

THE LOGIQ S8 BATTERY HAS A SAFETY DEVICE. DO NOT ATTEMPT TO DIS-ASSEMBLE OR ALTER THE BATTERY! ALWAYS OBSERVE THE FOLLOWING PRECAUTIONS:

USE ONLY BATTERIES APPROVED BY GE HEALTHCARE AS SUITABLE FOR USE WITH THE LOGIQ S8/LOGIQ E8 ULTRASOUND SYSTEM.

• 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 temperatures over 50 °C. Keep the battery 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 pierce the battery with a sharp object, hit it, or step on it.

• DO NOT use a damaged battery.

• DO NOT apply solder to a battery.

• DO NOT connect the battery to an electrical power outlet.

TO PREVENT THE BATTERY BURSTING, IGNITING, OR FUMES FROM THE BATTERY CAUSING EQUIPMENT DAMAGE, ALWAYS OBSERVE THE FOLLOWING PRECAUTIONS:

• DO NOT immerse the battery in water or allow it to get wet.

• DO NOT place 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 appe ars abnormal during use, recharging or storage, immediately remove it and stop using it.

NOTE: If you have any questions about the battery, consult your local GE representative.

• Storage of the battery pack: Short-term (less than 1 month): between 0 °C (32 °F) and 50 °C (122 °F)

Long-term (more than 3 months): between 10 °C (50 °F) and 35 °C (95 °F)

When charging the battery for the first time after long-term storage, recover the battery pack to original performance through repeating several cycles of full charging and discharging.

1 - 22 Section 1-4 - Safety Considerations

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Section 1-5Labels Locations

1-5-1 The labels on the cover

The LOGIQ S8 comes equipped with product labels and icons. These labels and icons represent pertinent information regarding the operation of the unit.

NOTE: The rating label is located on the rear of R1/R2/R3 system.

19” Monitor

LOGIQ S8/LOGIQ E8

LOGIQ S8 Vet

23”/22” Wide Monitor

Figure 1-1 Label location - R1/R2/R3 system

Section 1-5 - Labels Locations 1 - 23

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Figure 1-2 Label location - R4 and later system

1. LCD Caution label

2. LOGIQ S8 rating label

3. Gender Caution (only for India, China, Korea)

4. Multi Caution label

5. LOGIQ S8 Rating label (only for China, Korea, Japan)

6. UL label

NOTE: * Depending on country, “Gender Label” is attached.

1 - 24 Section 1-5 - Labels Locations

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1-5-1-1 WLAN label location (if WLAN option installed)

Figure 1-3 WLAN Label location (R1 to R3 system)

Figure 1-4 WLAN Label location (R4 and later system)

Section 1-5 - Labels Locations 1 - 25

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1-5-2 Rating plate

The following information prints on the rating plate.

1. Catalogue number

2. Manufacturing date

3. Manufacturer

4. System Serial Number

Figure 1-5 Rating plate and UL label - example

5. Power Supply Voltage

6. Power Input

7. Power Supply Frequency

8. Model Name

Rating plate UL label

NOTE: The rating label is located on the rear of R1/R2/R3 system.

Figure 1-6 Rating plate and UL label - R4 example

1 - 26 Section 1-5 - Labels Locations

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Section 1-6 Dangerous Procedure Warnings

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

DANGER

WARNINGWARNING

DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH, ARE PRESENT IN THIS EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING AND ADJUSTING.

IF THE COVERS ARE REMOVED FROM AN OPERATING LOGIQ S8/LOGIQ E8, SOME METAL SURFACES MAY BE WARM ENOUGH TO POSE A POTENTIAL HEAT HAZARD IF TOUCHED, EVEN WHILE IN SHUT DOWN MODE.

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.

Section 1-6 - Dangerous Procedure Warnings 1 - 27

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Section 1-7 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.) Control all stored and residual energy.

6.) Verify isolation. All potentially hazardous stored or residual energy is relieved.

NOTICE

Energy Control and Power Lockout for LOGIQ S8 When servicing parts of the system where there is exposure to voltage greater than 30 Volts:

1. Remove the front cover and confirm the power status LED. If ON, then turn off the system.

2. Unplug the system.

3. Maintain control of the system power plug.

4. Wait for at least 20 seconds for capacitors to discha rge as there are no test po ints to verify isolation. The Power On/Off button LED turns off.

5. Confirm the Power Status LEDs are OFF.

- If the LEDs are turned ON, attempt to shut down the system again.

- If unable to turn off the system, press and hold the POWER on/off button to force shutdown .

Power Status LED

1 - 28 Section 1-7 - Lockout/Tagout (LOTO) Requirements

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Section 1-8 Returning/Shipping System, Probes and Repair Parts

Equipment being returned must be clean and free of blood and other infectious substances. GEHC policy states that body fluids must be properly removed from any part or equipment prior to

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

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

NOTE: The US Department of Transportation (DOT) has ruled that “items what 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 purpose and must be transported as a hazardous material.

When returning or shipping the LOGIQ S8 system in the original packaging:

1.) Adjust the LCD monitor and control panel using Up/Down control and Swivel control to their centered and lowest positions.

2.) Flip down the LCD monitor and lock the monitor arm.

See 4-3-8 "Moving and Transporting the LOGIQ S8" on page 4-13 for more information.

NOTICE

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

1-8-1 For LOGIQ S8 Vet system

Return used/unused spare parts from a veterinary environment with the purple recycling label (regardless of its actual condition) and add a description on the label stating that the items were removed from a LOGIQ S8 Vet in a veterinary environment.

This apply for Probes and covers labeled as Vet used. If purple recycling label is not used in your region, use local recycling label.

Section 1-8 - Returning/Shipping System, Probes and Repair Parts 1 - 29

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Section 1-9 Electromagnetic Compatibility (EMC) and

1-9-1 What is 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 inte nded due interferen ce from its environment or when the device produces unacceptable levels of emission to its environmen t. 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 ele ctromagnetic energy, EMC also includes possible effects from electrical fields, magnetic fields, electrostatic discharge and disturbances in the electrical power supply.

For applicable standards please refer to Chapter 2 in the Basic User Manual of the each system.

1-9-2 Compliance

The LOGIQ S8 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 as mentioned in IEC 60601-1-2.

Electrostatic Discharge (ESD)

NOTE: For CE Compliance, it is crit ical that all covers, screws, shielding, gaskets, mesh, clamps, ar e in

good condition, installed tightly without skew or stress. Proper installation following all comments noted in this service manual is required in order to achieve full EMC performance.

1-9-3 Electrostatic Discharge (ESD) Prevention

WARNINGWARNING

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

ALWAYS CONNECT YOURSELF, VIA AN ARM-WRIST STRAP, TO THE ADVISED ESD CONNECTION POINT LOCATED ON THE REAR OF THE SCANNER (NEAR THE POWER CONNECTOR).

FOLLOW GENERAL GUIDELINES FOR HANDLING OF ELECTROSTATIC SENSITIVE EQUIPMENT.

DO NOT touch any boards with integrated circuits prior to taking the necessary ESD precautions:

1.) When installing boards, ESD may cause damage to a board. ALWAYS connect yourself, via an arm-wrist strap, to the advised ESD connection point located on the rear of the system (to the right of the power connector).

2.) Follow general guidelines for handling of electrostatic sensitive equipment.

Risk of electrical shock: System must be turned off. Avoid all contact with electrical contacts, conductors and components. Always use non-conductive handles designed for the removal and rep lacement of ESD sensitive parts. All parts that have the potential for storing energy must be discharged or isolated before making contact.

1 - 30 Section 1-9 - Electromagnetic Compatibility (EMC) and Electrostatic Discharge (ESD)

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Section 1-10 Customer Assistance

1-10-1 Contact Information

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

Before you call, identify the following information, and acquire image (Alt+D) to send to the Customer Care team:

1.) System ID serial number (also visible on label on back of the system).

2.) Software version.

3.) Date and time of occurrence.

4.) Sequence of events leading to issue.

5.) Is the issue repeatable?

6.) Imaging mode, probe, preset/application.

7.) Media brand, speed, capacity, type.

8.) Save secondary image capture, cine loop.

NOTE: Restart the application before resuming clinical scanning.

Table 1-8 Phone Numbers for Customer Assistance

Location Phone Number

USA GE Healthcare Ultrasound Service Engineering 9900 Innovation Drive (RP-2123) Wauwatosa, WI 53226, USA

Canada 1-800-668-0732

Latin America

Europe GE Ultraschall Deutschland GmbH Beethovenstraße 239 Postfach 11 05 60, D-42655 Solingen Germany

EAGM

Asia (Singapore) GE Ultrasound Asia Service Department -

Ultrasound 1 Maritime Square #13-01 HarbourFront Centre Singapore 099253

Service On-site Service: Parts Applications support

Service Applications support

Support Phone: +49 (0) 212-2802-652 Support Fax: +49 (0) 212-2802-431

Egypt Service Center UAE Service Center

Tel: 800 1012882 Fax: +65 6291-7006

1-800–437–1171 1-800-558-2040 1-800-682-5327 or 1-262-524-5698

1-800-524-5300 1-262-524-5698

00202 2322 1252 00971 8003646

ANZ -Service Support 1 800 647 855

Japan Support Center

Phone: 81-42-648-2940 Fax: 81-42-648-2905

Section 1-10 - Customer Assistance 1 - 31

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Table 1-8 Phone Numbers for Customer Assistance

Location Phone Number

86-800-810 8188

China

India

86-400-812 8188 86-10-6788 2652

1-800-425-8025 1-800-425-7255 1-800-102-7750

1-10-2 System Manufacturer

Table 1-9 System Manufacturer

Manufacturer FAX Number

GE Ultrasound Korea

9, Sunhwan-ro 214beon-gil, Jungwon-gu, Seongnam-Si, Gyeonggi-do

Korea

+82 (0) 31-740-6436

1-10-3 Authorized EU Representative

Table 1-10 Authorized EU Representative

Manufacturer TEL/FAX Number

The location of the CE marking is shown in the Safety chapter of this manual.

Authorized EU Representative European registered place of business: GE Medical Systems Information Technologies GmbH (GEMS IT GmbH) Munzinger Strasse 3, D-79111 Freiburg, GERMANY

+49 761 45 43 -0 /

+49 761 45 43 -233

1 - 32 Section 1-10 - Customer Assistance

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Chapter 2 Site preparations

Section 2-1 Overview

2-1-1 Purpose of this chapter

This chapter provides the informatio n re qu ir ed to plan and prepare for the setup of a LOGIQ S8. Included are descriptions of the facility and electrical needs to be met by the purchaser of the unit.

2-1-2 Contents in this chapter

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

2-2 General console requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-2

2-3 Facility needs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-7

Section 2-1 - Overview 2 - 1

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Section 2-2 General console requirements

2-2-1 Environmental Requirements

Table 2-1 System Environmental Requirements

Operational Storage Transport

Temperature

Humidity 30 - 80% (non-condensin g) 10 - 90% (non-condensing) 10 - 90% (non-condensing) Pressure 700 - 1060 hPa 700 - 1060 hPa 700 - 1060 hPa

Heat Dissipation 680BTU/hr n/a n/a

10 - 35

2-2-1-1 Cooling

The cooling requirement for the LOGIQ S8 is 680 BTU/hr. This figure does no t include coolin g needed for lights, people, or other equipment in the room.

Each person in the room places an additional 300 BTU/hr. demand on the cooling system.

C /50 - 95 oF -10 - 50 oC/14 - 122 oF -10 - 50 oC/14 - 122 oF

2-2-1-2 Lighting

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

2 - 2 Section 2-2 - General console requirements

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2-2-2 Electrical Requirements

2-2-2-1 General requirements

NOTE: GE Healthcare requires a dedicated power and ground for the proper operation of its Ultrasound

system. This dedicated power shall originate at the last distribution panel before the system. Sites with a mains power system with defined Neutral and Live:

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

Sites with a mains power system without a defined Neutral:

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

NOTE: Please note that image artifacts can occur, if at any time within the facility, the Ground from the main

facility's incoming power source to the Ultrasound system is only a conduit.

2-2-2-2 Electrical requirements

In the table below, the electrical specifications for LOGIQ S8 include LCD and on board peripherals.

Table 2-2 Electrical Specifications

Model Voltage Tolerances Current Frequency

LOGIQ S8

Power Consumption nominal 900 VA including all on-board peripherals.

2-2-2-3 Inrush Current

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

2-2-2-4 Site Circuit Breaker

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

CAUTION

!! CAUTION:

POWER OUTAGE MAY OCCUR. The LOGIQ S8 requires a dedicated single branch circuit. To avoid circuit overload and possible

loss of critical care equipment, make sure you DO NOT have any other equipment operating on the same circuit.

2-2-2-5 Site Power Outlets

A dedicated AC power outlet must be within reach of the unit without extension cord s. Other adequ ate 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 insta llatio n mus t meet all current local, state, and national electrical codes.

100 - 120 VAC ±10% 9.0 ... 7.0 A 50/60 Hz (±2%) 220 - 240 VAC ±10% 4.0 ... 3.7 A 50/60 Hz (±2%)

2-2-2-6 Power Plug

The LOGIQ S8 is supplied with a main power plug, as standard. 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.

Section 2-2 - General console requirements 2 - 3

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2-2-3 EMI Limitations

Ultrasound systems are susceptible to Electromagnetic Interference (EMI) from radio frequencies, magnetic fields, and transients in the air or wiring. Ultrasound systems also generate EMI. The LOGIQ S8 complies with limits as stated on the EMC label. However, there is no guarantee that interference 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 a de fect. These

sources include:

• Medical lasers

• Scanners

• Cauterizing guns

•Computers

•Monitors

•Fans

• Gel warmers

• Microwave oven

• Light dimmers

• Mobile phones

• In-house wireless phones (DECT phones)

• Wireless computer keyboard and mouse

• Air conditioning system

• High frequency (HF) surgery equipmen t

• General AC/DC adapters

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

2 - 4 Section 2-2 - General console requirements

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See table below for EMI Prevention tips.

Table 2-3 EMI Prevention/Abatement

EMI Rule Details

Keep the unit at least 5 meters (16.4 feet) away from other EMI sources. Special shielding may be

Be aware of RF sources.

required to eliminate interference problems caused by high frequency, high powered radio or video broadcast signals.

Ground the unit.

Replace and/or reassemble all screws, RF gaskets, covers and cores.

Replace broken RF gaskets.

Do not place labels where RF gaskets touch metal.

Use GE- specified harnesses and peripherals.

Take care with cellular phones.

Properly dress peripheral cables.

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 and replaced, if required.

Never place a label where RF gaskets meet the unit. Otherwise, the gap created will permit RF leakage. In case a label has been found in such a location, move the label to a different, appropriate location.

The interconnect cables are grounded and require ferrite beads and other shielding. Cable length, material, and routing are all important; do not make any changes that do not meet all specifications.

Cellular phones may transmit a 5 V/m signal that causes image artifacts.

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

Section 2-2 - General console requirements 2 - 5

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2-2-4 Probe Environmental Requirements

Probes should be operated, stored, or transported within the parameters outlined below.

NOTE: See attached TEE probe user manual for the environmental requirements of 6Tc-RS probe. NOTE: See attached FibroScan user manual for the environmental requirements of FibroScan probe.

Table 2-4 Probe Environmental Requirements

Probe Operation Storage Transport

Temperature 2D probe

10C-D -10°- 55° C/14°-131° F-40° - 55° C/-40° - 131° F 4D probe 18° - 30° C/64.4° - 86° F-10° - 50° C/14° - 122° F

Humidity 2D probe 10 - 90% non-condensing

4D probe 30 - 75% non-condensing 10 - 85% non-condensing

Pressure 2D/4D probe 700 - 1060hPa

10C-D 680 - 1060hPa

10° - 35° C/50° - 95° F

-40° - 60° C/-40° - 140° F

NOTICE

!! NOTICE:

WHEN EXPOSED TO LARGE TEMPERATURE VARIATIONS, THE PRODUCT SHOULD BE KEPT IN ROOM TEMPERATURE FOR 10 HOURS BEFORE USE.

NOTE: Refer to Table 3-2 Acclim ate Time on page 3-4 to determine the needed settlement time.

2-2-5 Time and Manpower Requirements

Site preparation takes time. Begin Pre-installation checks as soon as possible. If possible, allow six weeks before delivery, for enough time to make necessary changes.

CAUTION

!! CAUTION:

Have two people available to deliver and unpack the LOGIQ S8. Attempts to move the unit considerable distances (or on an incline) by one person alone, could

result in personal injury and/or damage to the system.

2 - 6 Section 2-2 - General console requirements

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Section 2-3 Facility needs

2-3-1 Purchaser Responsibilities

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

• Procuring the materials required.

• Completing the preparations before deliver y of th e ultr a so un d sys tem .

• Paying the costs for any alterations and modifications not specifically provided in the sales contract.

NOTE: All electrical installations that are preliminary to the positioning of the equipment at the site pr epared for

the equipment must be performed by licensed electr ical contractors. Other connections between p ieces of electrical equipment, calibrations, and testing must also be performed by qualified personnel. The products involved (and the accompanying electrical installations) are highly sophisticated and special engineering competence is required. All electrical work on these products 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 prod uct further from the system than the interface kit allows pres ents challenges to the installation team. To avoid delays during installation, such variances should be m ade known to the individuals or group performing the installation at the earliest possible date (preferably prior to the 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 reliability.

Section 2-3 - Facility needs 2 - 7

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2-3-2 Required Facility Needs

NOTE: GE Healthcare requires a dedicated power and gr ound for the proper operation of its Ultrasound

system. 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.

The following are mandatory site requirements. Additional (optional) recommendations, as well as a recommended ultrasound room layout, are provided in Section 2-3-4 "Desirable features" .

• Dedicated single branch power outlet of adequate amperage (see Table 2-2 Electrical

Specifications on page 2-3) that meets all local and national codes and is located less than 2.5 m

(8.2 ft.) from the LOGIQ S8 proposed location.

• Door opening of at least 76 cm (2.5 ft.) in width.

• Proposed location for the LOGIQ S8 is at least 0.2 m (0.67 ft.) from the walls, to enable 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.

• Clean and protected space for storage of probes (either in their case or on a rack).

• Material to safely clean probes (perform ed usin g a pla stic con tain e r, ne ve r me ta l).

NOTE: The LOGIQ S8 has one outlet for on board peripherals.

In case of network option:

• An active network outlet in the vicinity of the ultrasound unit.

• A network cable of appropriate length (regular Pin-to-Pin network cable).

• An IT administrator who will assist in configuring the unit to work with your local network.

A fixed IP address is required. Refer to the form provided in Figure 3-61 Worksheet for DICOM

Network Information on page 3-96 for network details that are required.

NOTE: All relevant preliminary network port installations at the prepared site must be performed by

authorized contractors. The purchaser of GE equipment must utilize only qualified personnel to perform servicing of the equipment.

2-3-3 Privacy and Security

Since the LOGIQ systems are integrated into your IT-network, GE wants to make sure that you are aware of the proactive measures we are taking to secure the system.

For more information on privacy and security, refer to LOGIQ S8 Priva cy and Se curity manual in eDoc CD.

2 - 8 Section 2-3 - Facility needs

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2-3-4 Desirable features

The followings are (optional) site recommendations.

• Door opening of at least 76 cm (2.5 ft.) in width.

• Accessible circuit breaker for a dedicated power outlet.

• Sink with hot and cold running water.

• Receptacle for bio–hazardous waste, for example, used probe sheaths.

• Emergency oxygen supply.

• Storage area for linens and equipment.

• Nearby waiting room, lavatory, and dressing room.

• Dual level lighting (bright and dim).

• Lockable cabinet for software and manuals.

2-3-5 Minimal floor plan suggestions

Dedicated Power Outlets

LOGIQ S8

Cabinet for Software and Manuals (optional)

Figure 2-1 Minimal Floor Plan 4.3m x 5.2m (14ft x 17ft)

Hospital Network

Section 2-3 - Facility needs 2 - 9

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2-3-6 Networking setup requirements

For detail of Connectivity setup information, refer to the Basic User Manual supplied with the each system.

2-3-6-1 Stand alone scanner (without network connection)

None.

2-3-6-2 Scanner connected to hospital’s network

Supported networks:

• Ethernet network connection (R1.x.x/R2 and later)

• Up to 900 Mbps WLAN (R2 and later, optional)

• 10/100/1000 Mbps Ethernet/DICOM network connection is required.

2-3-6-3 InSite Requirements

Need internet access available to be able to connect to Insite. Insite requires an Ethernet connection with a 10/100 Mbps or 10/100/1000 Mbps interface.

2-3-6-4 Purpose of the 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 tra nsferri ng images to remote printers.

As an added benefit, transferring images in this manner frees up the on-board LCD and peripherals, enabling viewing to be done while scanning continues.

With DICOM, images can be archived, stored, and retrieved faster, easier, and at a lower cost.

2-3-6-5 DICOM Option Pre-installation Requirements

To configure the LOGIQ S8 to work with other network connections, the site’s network administrator must provide information to complete the form in Figure 2-2 Worksheet for DICOM Networ k Information

on page 2-11. Ensure that there are no spaces in any field of the form.

Entries must include:

• A host name, local port number, AE Title, IP address and Net Mask for the LOGIQ S8.

• 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 S8 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 error solving.

2 - 10 Section 2-3 - Facility needs

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2-3-6-5 DICOM Option Pre-installation Requirements (cont’d)

Figure 2-2 Worksheet for DICOM Network Information

Site System Information

Site:

Dept:

LOGIQ™ S8

SN:

CONTACT INFORMATION Name

Type:

TCP/IP Settings

System IP Settings

Name - AE Title:

IP Address:

Subnet Mask:

Default Gateway:

Title

Floor:

Room:

REV:

Phone

Remote Archive Setup

Name - AE Title:

IP Address:

Subnet Mask:

Default Gateway:

Server Name:

Remote DB User Name:

Comments:

E-Mail Address

Services (Destination Devices)

Device Type

1 2 3 4 5 6 7 8

9 10 11 12

Manufacturer

Name

IP Address

Port

AE Title

Section 2-3 - Facility needs 2 - 11

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Section 2-4 Environmental Dangers

Commercial devices such as laser cameras, printers, VCRs and external monitors, usually exceed allowable leakage current limits and, when plugge d in to sep arate AC ou tlet s, are in viola tion of pa tie nt safety standards. Suitable electrical isolation of such external AC outlets, or providing the device with extra protective earth, will be required in order to meet UL60601-1 and IEC60601-1 / IEC60601-1-1 standards for electrical leakage.

2-4-1 Patient Vicinity UL60601-1 (USA)

2.12.20DV (UL60601-1:2003) In area in which patients are normally cared for, the patient vicinity is the space with surfaces likely to

be contacted by the patient or attendant who can touch the patient. This encloses a space within the room 1.83 m (6 ft.) beyond the perimeter of the bed (examination table, dental chair, treatment booth, and the like) in its intended location, and extending vertically 2.29 m (7.5 ft.) above the floor.

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2-4-2 Patient Environment IEC60601-1 (IEC60601-1-1) and ANSI AAMI ES60601-1

Sub Clause 2.202 and figure 201 (IEC60601-1-1:2000) Sub Clause 3.79 and figure A.9 (IEC60601-1:2005 and ANSI AAMI ES60601-1:2005) Such an area is an environment in which medical diagnosis, monitoring or treatment is carried out. It is

very difficult to attach unique dimensions to the PATIENT ENVIROMENT. In practice, a distance of 2,5 m (8.2 ft.) above the floor on which the medical personnel stand and a horizontal distance of 1,5 m (4.9 ft.) have justified themselves as indicative of the dimensions of the Patient Environment.

The patient environment/vicinity will be depicted as a dashed line in this procedure. See example below.

Section 2-4 - Environmental Dangers 2 - 13

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Chapter 3 System Setup

Section 3-1 Overview

3-1-1 Purpose of this chapter

This chapter contains information needed to set up the LOGIQ S8. Included is 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 setup, and how to check and test the unit, probes, and external peripherals for electrical safety are included in this procedure.

3-1-2 Contents in this chapter

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

3-2 Setup reminders . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-2

3-3 Receiving and unpacking the equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5

3-4 Packing materials - recycling information. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-10

3-5 Preparing for setup. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-11

3-6 Completing the Set Up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-12

3-8 System Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-32

3-9 Optional Peripherals/Peripheral Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-37

3-10 Printer Installation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-49

3-11 Connectivity Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-66

3-12 Configuring Connectivity. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-72

3-13 Setting up InSite Connection (R1 to R4) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-82

3-14 Agent Configuration (R4.2.5x and later). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-93

3-15 Connectivity Setup Worksheet . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-95

3-16 Paperwork . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-97

Section 3-1 - Overview 3 - 1

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Section 3-2 Setup reminders

3-2-1 Average Setup Time

Once the site has been prepared, the average installation time required is shown in table below.

Table 3-1 Average Installation Time

Description Average Setup Time Comments

Unpacking the scanner Setup the scanner / options / printers DICOM Option (connectivity) Install Insite/iLink

0.5 hours

0.5 to 1.5 hours Dependent on the configuration

0.5 - 1.5 hours Dependent on the configuration

0.5 hours

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3-2-2 Setup warnings

!! WARNING:

!! CAUTION:

DANGER

WARNINGWARNING

CAUTION

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

DO NOT PULL OR LIFT THE SYSTEM WITH THE FRONT HANDLE OF THE USER INTERFACE (OPERATOR PANEL).

THE SYSTEM SHOULD NOT BE MOVED WITH THE OPERATOR CONTROL PANEL EXTENDED. MOVE THE OPERATOR CONTROL PANEL TO IT’S CENTERED AND LOCKED POSITION. REFER TO Section 8-2-3 "Returning/Shipping Probes and

Repair Parts" on page 8-4.

TO PREVENT ELECTRICAL SHOCK, CONNECT THE UNIT TO A PROPERLY GROUNDED POWER OUTLET. DO NOT USE A THREE TO TWO PRONG ADAPTER. THIS DEFEATS SAFETY GROUNDING.

DO NOT WEAR THE ESD WRIST STRAP WHEN YOU WORK ON LIVE CIRCUITS AND MORE THAN 30 V PEAK IS PRESENT.

DO NOT OPERATE THIS ULTRASOUND SYSTEM UNLESS ALL BOARD COVERS AND FRAME PANELS ARE SECURELY IN PLACE. SYSTEM PERFORMANCE AND COOLING REQUIRE THIS. (When covers are removed, EMI may be present).

CAUTION

OPERATOR MANUAL(S) THE USER MANUAL(S) SHOULD BE FULLY READ AND UNDERSTOOD BEFORE

OPERATING THE LOGIQ S8/LOGIQ E8 AND KEPT NEAR THE UNIT FOR QUICK REFERENCE.

ACOUSTIC OUTPUT HAZARD ALTHOUGH THE ULTRASOUND ENERGY TRANSMITTED FROM THE LOGIQ S8 PROBE IS

WITHIN AIUM/NEMA STANDARDS, AVOID UNNECESSARY EXPOSURE. ULTRASOUND ENERGY CAN PRODUCE HEAT AND MECHANICAL DAMAGE.

• The system weighs approximately 85 kg (LOGIQ S8) / 97 kg (LOGIQ E8) without peripherals, two people are required to unpack it.

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

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3-2-2-1 If the unit is very cold or hot

CAUTION

!! CAUTION:

Turning the system ON after arrival at the site - without allowing time for acclimation - may cause system damage!

Following transport, the system may be very cold, or ho t. Allow time for the system to acclimate before

being switched ON. Acclimation requires 1 hour for each 2.5 system is below 10

C or above 40oC..

C increment, when the temperature of the

Table 3-2 Acclimate Time

-40-35-30-25-20-15-10-5 0 5 1015202530354045505560

-40-31-22-13-4 5 14233241505968778695104113122131140

Hrs 201816141210864200000002468

NOTE: After a long period of storage, or after transportation of the system with the monitor in the fold ed-

down position, it is highly recommended to place the monitor in the upright position - and to leave it in this position for a period of longer than 1 hour before use. This will enable it to properly adjust to the environmental conditions.

3 - 4 Section 3-2 - Setup reminders

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Section 3-3 Receiving and unpacking the equipment

3-3-1 Receiving and unpacking warnings

WARNINGWARNING

CAUTION

DO NOT PULL OR LIFT THE SYSTEM WITH THE FRONT HANDLE OF THE USER INTERFACE (OPERATOR PANEL).

Two people are needed to unpack the unit because of its weight. Attempts to move the unit considerable distances or on an incline by one person could result in injury or damage or both.

Two people are required whenever a part weighing 16 kg (35 lbs.) or more must be lifted.

Remember to use relevant personal protecting equipment (pre) during packing/unpacking. Check with your local EHS representative.

Section 3-3 - Receiving and unpacking the equipment 3 - 5

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3-3-2 Receiving the LOGIQ S8

3-3-2-1 Overview

Improper handling during transportation may harm the equipment inside the package even if the package itself is undamaged.

3-3-2-2 Examine package

Examine package closely at time of delivery.

Table 3-3 Examine all packages

STEP TASK

Is damage apparent? If YES, continue with the instruction in Section 3-3-2-3 "Damage in

transportation" on page 3-6.

If NO, continue with the next step.

Before cutting the straps, check the tilt indicator. Is the tilt Indicator red colored (1) inside the middle of the indicator?

• If YES: The tilt Indicator has been activated. Continue with the instructions in Section 3-3-2-3 "Damage in transportation" on page 3-6.

• If NO: continue with the instruction in Section 3-3-4 "Unpacking the

LOGIQ S8" on page 3-9.

3-3-2-3 Damage in transportation

Follow this procedure if damage is apparent:

Table 3-4 Damage in transportation

STEP TASK

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.

Report the damage to the carrier.

• 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.

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3-3-2-4 The Tilt & Shock indicators (if applied)

NOTE: Tilt and Shock Indicators are removed in later product shipments.

3-3-2-4-1 Overview

Improper handling during transportation may harm the equipment inside the package even if the package itself is undamaged.

To make it easier to detect if the handling during transportation has been improper, a set of Tilt & Shock indicators have been attached to the transportation box.

3-3-2-4-2 Position of the Tilt & Shock indicators

Inspect the Drop and Tilt Indicator for evidence of accidental shock or tilting during transit (damage incident, as illustrated in the figure below.

Figure 3-1 Tilt & Shock indicators

NOTE: Before cutting the straps, check the Shock and Tilt Tags to make sure they have not been triggered.

If damaged, report it to the carrier. If not, then cut the straps around the crate.

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3-3-3 Transportation Box Label

Figure 3-2 Label 1

Figure 3-3 Label 2

Figure 3-4 Label 3

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3-3-4 Unpacking the LOGIQ S8

The instruction manual describes the best method for unpacking the LOGIQ S8 ultrasound scanning unit. Images are ONLY for reference; wear proper PPE when handling packaging (gloves, safety shoes,

etc....).

Table 3-5 Unpacking Procedure

Step Task

1. Cut the straps around the crate.

2. Remove the top cover.

3. Remove three P-Joint, then remove the out sleeve.

4. Remove the option box.

5. Carefully remove foam packing material and plastic bag from the ultrasound unit and monitor

6. Remove the box bottom assy..

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Table 3-5 Unpacking Procedure

Step Task

7. Unlock the casters and align the orientation of the 4 caster's direction (refer to 4-3-7 "Caster" on page 4-11) and then using the incline plane of the box bottom assy., slowly move the system from the box.

Note: Place all of the filling inside the Transportation Box. Close the box, and store the filling for possible future use.

Section 3-4 Packing materials - recycling information

The packing materials for LOGIQ S8 are recyclable:

• The Transportation Box is made of cardboard.

• The inner reinforcements are made of Ethafoam (Polyethylene foam).

• The plastic foil is made of LDPE (Low Density Polyethylene).

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Section 3-5 Preparing for setup

3-5-1 Verify Customer Order

Compare all items listed on the packing slip (delivery note) with those received. Report any items that are missing, back ordered, or damaged.

The envelope with delivery address, packing list and invoice is located on the front panel of the crate.

Check whether delivery is complete (according to packing list) and check visual damage!

Figure 3-5 envelope at front panel of the crate

3-5-2 Physical inspection

Verify that the system arrived intact (visual inspection). If the system has been damaged, please refer to 3-3-2-3 "Damage in transport ation" on pa ge 3-6 in the

beginning of this manual.

3-5-3 EMI Protection

This unit has been designed to minimize the effects of Electo-Magnetic Interference (EMI). Ma ny 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 secu red before the unit is put into operation.

Refer to Section 2-2-3 "EMI Limitations" on page 2-4.

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Section 3-6 Completing the Set Up

3-6-1 System Specifications

3-6-1-1 System requirements verification

• Verify that the site meets the requirements listed in (see: Section 2-3 "Facility needs" on p age 2-7).

• Verify that the specifications below don’t conflict with any on-site conditions.

3-6-1-2 Physical Dimensions

Table 3-6 LOGIQ S8 R1 to R3 (without Peripherals)

Height Width Depth Weight

1720 mm, 67.7 in (max)

1150 mm, 45.3 in (min) *

* with low cabinet option.

Table 3-7 LOGIQ S8 R4 and later (without Peripherals)

500 mm, 19.7 in (Keyboard)

620 mm, 24.4 in (Caster)

865 mm, 34.1 in (max)

795 mm, 31.3 in (Caster)

85 kg

(187.4 lbs.)

Height Width Depth Weight

1760 mm, 69.3 in (max)

1150 mm, 45.3in (min, 23” LCD)

1100 mm, 43.3in (min, 22” OLED)

Table 3-8 LOGIQ E8 R2 and R3 (without Peripherals)

Height Width Depth Weight

1750 mm (max)

1250 mm (min)

Table 3-9 LOGIQ E8 R4 and later (without Peripherals)

Height Width Depth Weight

1760 mm (max)

1240 mm (min)

3-6-1-3 Acoustic Noise Output

max. 50 dB(A)

520 mm, 20.5 in (Keyboard)

530 mm, 20.9 in (Caster) 561 mm, 22.1 in (23” LCD Monitor) 527mm, 20.7in (22” OLED Monitor)

500 mm (Keyboard)

620 mm (Caster)

520 mm (Keyboard)

530 mm (Caster)

527mm (22” OLED Monitor)

865 mm, 34.1 in (max)

795 mm, 31.3 in (Caster) 85 kg

(187.4 lbs.)

865 mm (max)

795 mm (Caster)

865 mm (max)

795 mm (Caster)

97 kg

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3-6-2 Electrical specifications

WARNINGWARNING

CONNECTING A LOGIQ S8 TO THE WRONG VOLTAGE LEVEL WILL MOST LIKELY DESTROY THE UNIT.

3-6-2-1 Verification of the LOGIQ S8’s voltage setting

Verify that the mains voltage specified for the unit is available on-site. The voltage setting for the unit is found on a label on the back of the system on lower r ear frame of the

LOGIQ S8.

3-6-2-2 Electrical Specifications

In the table below, the electrical specifications for LOGIQ S8 include LCD and on board peripherals.

Table 3-10 Electrical Specifications

Model Voltage Tolerances Current Frequency

LOGIQ S8

Power Consumption nominal 900 VA including all on-board peripherals.

100 - 120 VAC ±10% 9.0 ... 7.0 A 50/60 Hz (±2%) 220 - 240 VAC ±10% 4.0 ... 3.7 A 50/60 Hz (±2%)

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3-6-3 Connection the I/O Rear Panel

Accessory equipment connected to the analog an d d igital interfaces must be certified according to the respective IEC standards (i.e., IEC60950 for data processing equipment and IEC60601-1 for medical equipment). Furthermore, all complete configurations shall comply with the valid version of the system standard IEC60601-1-1. Everyone who connects add itional equipment to the signal in put part or signal output part of the LOGIQ S8 system configures a medical system, and is therefore resp onsible to ensure that the system complies with the requirements of the valid version of IEC60601-1-1. If in doubt, consu lt the technical service department or your local GE Healthcare representative.

Figure 3-6 External I/O Connectors - on Rear of System

Table 3-11 External I/O Connector - Description

Item Connector Name Section number Description

USB Port

HDMI Connector

Ethernet

AUDIO

5-2-3-2

5-2-4-1 5-2-4-2 5-2-4-3

R1/R2: USB2.0 Full Speed (Isolated) R3/R4: USB2.0 Full Speed (No isolated)

Connector for external Monitor.

LAN for InSite Connection (RJ45).

Connector for External Speaker .

Audio line out (3.5mm pin jack)

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3-6-4 Connecting Probes

3-6-4-1 Introduction

Probes can be connected at any time, regardless of whether the unit is on or off. To ensure that the ports are not active, place the system in the image freeze condition

LOGIQ S8/LOGIQ S8 Vet

LOGIQ E8

a. Active probe port b. Parking probe port

c. Pencil probe port

Figure 3-7 Probe port

3-6-4-2 Cable Handling

Take the following precautions with probe cable s:

• Keep free from wheels

• Do not bend the cable acutely

• Avoid crossing cables between probes.

3-6-4-3 Connect a probe

CAUTION

!! CAUTION:

CAUTION

!! CAUTION:

CAUTION

!! CAUTION:

DO NOT use a probe which appears damaged until functional and safe performance is verified.

Fault conditions can result in electric shock hazard. Do not touch the surface of probe connectors which are exposed when the probe is removed.

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

1.) Before connecting the probe: a.) Do a visual check of the probe pins and system sockets.

b.) Remove any dust or foam rests from the probe pins. c.) Inspect the probe for damage or degradation to the housing, strain relief, lens, seal, cable and

connector.

2.) Put the probe in the pr obe holder. Use the integrated cable management hook to wrap the cord.

3.) Ensure that the probe locking handle is at horizontal position.

4.) Hold the probe connector vertically with the cable pointing upward.

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

6.) Turn the connector locking handle clockwise (to vertical position) to secure the probe connector.

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

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3-6-4-4 Connecting the CW Pencil Probe (LOGIQ S8/LOGIQ S8 Vet)

Insert the probe connector into the pencil probe port all the way seated in. Carefully position the probe cable so it is free to move and is not resting on the floor.

3-6-4-5 Connecting the TEE Probe

Type of this connector is “RS”, connect to the system by TEE probe adapter. TEE RS-DLP probe adapter has 2 connection ports. On e is “RS” type for TEE pr obe, the other is “DLP”

type for LOGIQ S8 system.

DLP Connector lock knob

RS Connector (Probe side)

DLP Connector (System side)

RS Connector lock knob

Figure 3-8 DLP-RS Connector

1.) Hold the probe connector and TEE DLP-RS adapter with the cable pointing DLP connector lock knob.

2.) Turn the RS connector lock knob to release side.

Release

RS Connector lock knob

Lock

DLP Connector lock knob

Release

Figure 3-9 Lock/Release position

3.) Align the connector with the RS port and carefully push into place.

4.) Turn the RS connector lock knob to the lock side.

5.) Hold the adapter + probe connector vertically with the cable pointing upward.

6.) Turn the DLP connector lock knob to lock side to secure the probe connecto r.

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

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Section 3-7 Power On/Off

DANGER

ALWAYS CONNECT THE UNIT TO A FIXED POWER SOCKET WHICH HAS THE PROTECTIVE GROUNDING CONNECTOR.

DANGER

NEVER USE A THREE-TO-TWO PRONG ADAPTER; THIS DEFEATS THE SAFETY GROUND.

DANGER

ENSURE THAT THE POWER CORD AND PLUG ARE INTACT AND THAT THE POWER PLUG IS THE PROPER HOSPITAL-GRADE TYPE (WHERE REQUIRED).

CAUTION

NOTICE

NOTE: If the battery option is installed (R4 or later)

LOGIQ S8 REQUIRES ALL COVERS. OPERATE THIS UNIT ONLY WHEN ALL BOARD COVERS AND FLAME PANELS ARE SECURELY

IN PLACE. THE COVERS ARE REQUIRED FOR SAFE OPERATION, GOOD SYSTEM PERFORMANCE AND COOLING PURPOSES.

User only power supply cords, cables and plugs provided by or designated by GE Healthcare.

After turning off the system, wait at least 10 seconds before turning it on again. The system may not be able to boot if power is recycled too quickly.

The extended battery/small battery is charged automatically when the LOGIQ S8 is connected to the wall outlet via the power cable and circuit breaker i s turned on wh ether the LOGIQ S8 is turned on or in standby-mode.

But you can turn off the circuit breaker and disconnect the power cable when the battery is charging.

• While the extended battery/small battery charging, a fan is running. a fan stops automatically when battery is fully charged.

• While the extended battery charging, the LED is blinking and turn off when the battery is fully charged.

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3-7-1 Connect AC (mains) Power to the LOGIQ S8

Connecting AC Power to the LOGIQ S8 involves preliminary checks of the power cord, voltage level and compliance with electrical safety requirements.

WARNINGWARNING

CAUTION

POWER OUTAGE MAY OCCUR. THE ULTRASOUND UNIT REQUIRES A DEDICATED SINGLE BRANCH CIRCUIT. TO AVOID CIRCUIT OVERLOAD AND POSSIBLE LOSS OF CRITICAL CARE EQUIPMENT, MAKE SURE YOU DO NOT HAVE OTHER EQUIPMENT OPERATING ON THE SAME CIRCUIT.

Disconnect the plug from the wall outlet in case an emergency should occur. Ensure easy access to the power outlet.

1.) Ensure that the wall outlet is of appropriate type, and that the Circuit Breaker is turned off.

2.) Uncoil the power cable, allowing sufficient slack so that the unit can be moved slightly.

3.) Verify that the power cable is without any visible scratches or any sign of damage.

4.) Verify that the on-site mains voltage is within the limits indicated on the rating label on the right side of the rear panel.

5.) Connect the Power Cable’s female plug to the Power Inlet at the rear of the unit.

6.) Lock the plug in position with the Retaining Clamp.

7.) Verify that the Mains Power Circuit Breaker is in OFF position, if not, switch it OFF.

Circuit Breaker

Screw

Pull Out Protection

(Metal Bracket)

Mains Power Cable

Screw

Figure 3-10 Circuit breaker and main power cable at rear of system

8.) Connect the Power Cable’s other end (male plug) to a hospital grade mains power outlet with the proper rated voltage, and the unit is ready for Power ON/Boot Up.

NOTE: The power for on-board peripheral auxiliary equipment are commonly switched with the power button.

The power switch of any attached printer(s) needs to be in ON position before starting the system. However, be aware some auxiliary equipment may switch itself to standby mode (e.g., Color video printer) and must therefore be switched on separately.

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3-7-2 Power ON

NOTE: The mains outlet of the system for peripheral auxiliary equipment are commonly switched with

the ON/OFF standby button. So the auxiliary equipment need not to be switched ON/OFF separately.

1.) Switch ON the Mains Power Circuit Breaker at the rear of the system. The power button turns on a light as blue.

2.) Press once the power button on the Operator Contro l Panel to boot the system . Th e powe r b utton

turns on a light as green.

Off/Stand-by

Figure 3-11 Power Button

3.) The System (including the Back-end Processor) starts and the operating system is loaded which

then leads the application software to activate the scanner. During a normal boot, you may observe

- Power is distributed to Peripherals, Operator Panel (control panel), Monitor, Front-End and Back-End Processor.

- The Back-End Processor and rest of the scanner starts with the sequence listed in following steps:

a.) “Boot Screen” is displayed. b.) Back-End Processor is turned ON and starts to load the software. c.) The Start Screen is displayed on the monitor. d.) Start-up progress bars indicating software loading procedures, are displayed on the

monitor.

e.) The software initiates and sets up the Front-End electronics and the rest of the scanner

(incl. the clicking sound of the relays on the PID board).

f.) The Keyboard backlight is lit.

4.) As soon as the software has been loaded, the system enters B-Mode with the probe connected to port nearest to a user. Total time used for start-up is about 2 minutes. The power button on the Control Panel and indicator color.

ON (Power Assistant mode)

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3-7-3 Login

At login, you are notified that “You are accessing a diagnostic medical device that is provided by authorized usage only. Data stored on this device may be subject to various regulations including but not limited to regulations which govern disclosure and privacy of this data. By using this device you are acknowledging that you are authorized to do so and are trained in appropriate use and regulatory guidelines.”

NOTICE

The System Administrator manages system groups, users, and permissions. After you have been added as a valid user, the System Administrator assigns you a temporary password . When you log into the system for the first time, you will be prompted to change your password.

Figure 3-12 Login Window (Example of R4.2.5x)

After you have established your password, follow these steps to login.

1.) Type your user name in the Operator field.

2.) Type your password in the Password field.

3.) Press OK to login, or Cancel to cancel login.

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3-7-4 Logoff/Shutdown/Exit

1.) When you lightly press the Power On/Off switch once. The System-Exit window is displayed.

System Exit Window - R1 System Exit Window - R2 and later

2.) The SYSTEM - EXIT menu, used when power off the unit, gives you these choices:

• Logoff

Use this button to log off the current user. The system remains ON and ready fo r a new user to log on. If the Logoff button is dimmed, it indicates that no user is logged on to the unit at the moment.

• Shutdown

Use this button to shut down the system. The entire system will shut down. The power button turns on blue indicated Standby- mode (refer to Section Figure 3-11 "Power Button" on page 3-19).

For the system with R4.2.5x and later, press Power On/Off button three (3) times to shutdown.

NOTE: If the system has Small/Extended battery (Option), the system automatically starts battery-charging

when goes to Standby-mode.

•Cancel

Use this button to exit from the System-Exit menu and return to the previous operation.

• Exit (Only available when logged in as GE Service with Service Dongle) Select this button when you want to exit to the Windows Desktop. Refer to Section Section 7-3 "Exit

to Windows Desktop" on page 7-5.

• Sleep (R1 to R4)

Select this button to go to SLEEP mode. Refer to Section 3-7-6 "Sleep Mode (R1 to R4)" on page

3-23.

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3-7-5 Complete shutdown

NOTICE

!! NOTICE:

After turning off the system, wait at least 10 seconds before turning it on again. The system may not be able to boot if power is recycled too quickly.

NOTE: The mains outlet of the system for peripheral auxiliary equipment are commonly switched with the power

button. So the auxiliary equipment need not to be switched ON/OFF separately.

1.) Enter the scan screen and lightly press the Power On/Off switch once. The System-Exit window is displayed.

2.) Select Shutdown. The system performs an automatic full shutdown sequence.

NOTICE

The

NOTICE

The system will go to Power Assistant Mode (Optional, R2 or later) if above procedures are skipped.

Be sure to wait with the next step until the system has finished its shut-down. Failing to do so may destroy data on the Hard Disk Drive, making the system fail later.

3.) Switch OFF the Circuit breaker on the rear panel of the system.

4.) After complete power down, disconnect the main po wer cable from the system or unplug it from the

AC wall outlet socket.

WARNINGWARNING

Confirmation of LED status is necessary when repairing the system.

Confirm the Power Status LEDs are OFF.

- If the LEDs are turned ON, attempt to shut down the system again.

- If unable to turn off the system, press and hold the Power on/off button to force shutdown.

NOTE: For R4 or later system with Extended Battery option, the extended battery is charged when the LOGIQ S8 in Standby-mode. While battery charging, LED is blinking and main fan is operating. But you can turn off the circuit breaker and disconnect the power cable when the battery is charging.

3 - 22 Section 3-7 - Power On/Off

Power Status LED