• IF A CUSTOMER’S SERVICE PROVIDER REQUIRES A LANGUAGE OTHER
THAN ENGLISH, IT IS THE CUSTOMER’S RESPONSIBILITY TO PROVIDE
TRANSLATION SERVICES.
• DO NOT ATTEMPT TO SERVICE THE EQUIPMENT UNLESS THIS SERVICE
MANUAL HAS BEEN CONSULTED AND IS UNDERSTOOD.
• FAILURE TO HEED THIS WARNING MAY RESULT IN INJURY TO THE SERVICE
PROVIDER, OPERATOR OR PATIENT FROM ELECTRIC SHOCK, MECHANICAL
OR OTHER HAZARDS.
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.
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.
- i
Page 4
GELOGIQ P9/P7
AVISO
(ES)
ATENÇÃO
(PT-Br)
(PT-pt)
AVISO
AVVERTENZA
(IT)
D
IRECTION5604324, REVISION11 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.
• 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
RESPONSABILIDADE DO CLIENTE FORNECER OS SERVIÇOS DE TRADUÇÃO.
• NÃO TENTE REPARAR O EQUIPAMENTO SEM TER CONSULTADO E
COMPREENDIDO ESTE MANUAL DE ASSISTÊNCIA TÉCNICA.
• O NÃO CUMPRIMENTO DESTE AVISO PODE POR EM PERIGO A SEGURANÇA
DO TÉCNICO, OPERADOR OU PACIENTE DEVIDO A‘ CHOQUES ELÉTRICOS,
MECÂNICOS OU OUTROS.
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.
ii -
Page 5
GELOGIQ P9/P7
HOIATUS
(ET)
VAROITUS
(FI)
ΠΡΟΕΙ∆ΟΠΟΙΗΣΗ
(EL)
FIGYELMEZTETÉS
(HU)
D
IRECTION5604324, REVISION11 SERVICE MANUAL
KÄESOLEV TEENINDUSJUHEND ON SAADAVAL AINULT INGLISE KEELES.
• KUI KLIENDITEENINDUSE OSUTAJA NÕUAB JUHENDIT INGLISE KEELEST
ERINEVAS KEELES, VASTUTAB KLIENT TÕLKETEENUSE OSUTAMISE EEST.
• ÄRGE ÜRITAGE SEADMEID TEENINDADA ENNE EELNEVALT KÄESOLEVA
TEENINDUSJUHENDIGA TUTVUMIST JA SELLEST ARU SAAMIST.
• KÄESOLEVA HOIATUSE EIRAMINE VÕIB PÕHJUSTADA TEENUSEOSUTAJA,
OPERAATORI VÕI PATSIENDI VIGASTAMIST ELEKTRILÖÖGI, MEHAANILISE
VÕI MUU OHU TAGAJÄRJEL.
TÄMÄ HUOLTO-OHJE ON SAATAVILLA VAIN ENGLANNIKSI.
• JOS ASIAKKAAN PALVELUNTARJOAJA VAATII MUUTA KUIN
ENGLANNINKIELISTÄ MATERIAALIA, TARVITTAVAN KÄÄNNÖKSEN
HANKKIMINEN ON ASIAKKAAN VASTUULLA.
• ÄLÄ YRITÄ KORJATA LAITTEISTOA ENNEN KUIN OLET VARMASTI LUKENUT
JA YMMÄRTÄNYT TÄMÄN HUOLTO-OHJEEN.
• MIKÄLI TÄTÄ VAROITUSTA EI NOUDATETA, SEURAUKSENA VOI OLLA
PALVELUNTARJOAJAN, LAITTEISTON KÄYTTÄJÄN TAI POTILAAN
VAHINGOITTUMINEN SÄHKÖISKUN, MEKAANISEN VIAN TAI MUUN
VAARATILANTEEN VUOKSI.
ΤΟΠΑΡΟΝΕΓΧΕΙΡΙ∆ΙΟΣΕΡΒΙΣ∆ΙΑΤΙΘΕΤΑΙΣΤΑΑΓΓΛΙΚΑΜΟΝΟ.
• ΕΑΝΤΟΑΤΟΜΟΠΑΡΟΧΗΣΣΕΡΒΙΣΕΝΟΣΠΕΛΑΤΗΑΠΑΙΤΕΙΤΟΠΑΡΟΝ
ΕΓΧΕΙΡΙ∆ΙΟ 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
ΕΓΧΕΙΡΙ∆ΙΟ ΣΕΡΒΙΣ.
• ΕΑΝ ∆Ε ΛΑΒΕΤΕ ΥΠΟΨΗ ΤΗΝ ΠΡΟΕΙ∆ΟΠΟΙΗΣΗ ΑΥΤΗ, ΕΝ∆ΕΧΕΤΑΙ ΝΑ
ΠΡΟΚΛΗΘΕΙ ΤΡΑΥΜΑΤΙΣΜΟΣ ΣΤΟ ΑΤΟΜΟ ΠΑΡΟΧΗΣ ΣΕΡΒΙΣ, ΣΤΟ ΧΕΙΡΙΣΤΗ Ή
ΣΤΟΝ ΑΣΘΕΝΗ ΑΠΟ ΗΛΕΚΤΡΟΠΛΗΞΙΑ, ΜΗΧΑΝΙΚΟΥΣ Ή ΑΛΛΟΥΣ ΚΙΝ∆ΥΝΟΥΣ.
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.
- iii
Page 6
GELOGIQ P9/P7
VIÐVÖRUN
(IS)
VÝSTRAHA
(CS)
ADVARSEL
(DA)
WAARSCHUWING
(NL)
D
IRECTION5604324, REVISION11 SERVICE MANUAL
ÞESSI ÞJÓNUSTUHANDBÓK ER EINGÖNGU FÁANLEG Á ENSKU.
• EF ÞJÓNUSTUAÐILI VIÐSKIPTAMANNS ÞARFNAST ANNARS TUNGUMÁLS EN
ENSKU, ER ÞAÐ Á ÁBYRGÐ VIÐSKIPTAMANNS AÐ ÚTVEGA ÞÝÐINGU.
• REYNIÐ EKKI AÐ ÞJÓNUSTA TÆKIÐ NEMA EFTIR AÐ HAFA SKOÐAÐ OG
SKILIÐ ÞESSA ÞJÓNUSTUHANDBÓK.
• EF EKKI ER FARIÐ AÐ ÞESSARI VIÐVÖRUN GETUR ÞAÐ VALDIÐ MEIÐSLUM
ÞJÓNUSTUVEITANDA, STJÓRNANDA EÐA SJÚKLINGS VEGNA RAFLOSTS,
VÉLRÆNNAR EÐA ANNARRAR HÆTTU.
TENTO SERVISNÍ NÁVOD EXISTUJE POUZE V ANGLICKÉM JAZYCE.
•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
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.
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.
iv -
Page 7
GELOGIQ P9/P7
BRĪDINĀJUMS
(LV)
ĮSPĖJIMAS
(LT)
ADVARSEL
(NO)
OSTRZEŻENIE
(PL)
D
IRECTION5604324, REVISION11 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.
• 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.
•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.
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
ZAGROŻEŃ.
- v
Page 8
GELOGIQ P9/P7
ATE NŢIE
(RO)
ОСТОРОЖНО!
(RU)
(BG)
ПРЕДУПРЕЖДЕНИЕ
UPOZORENJE
(SR)
D
IRECTION5604324, REVISION11 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.
• 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.
ЧТО СПЕЦИАЛИСТ ПО ТЕХОБСЛУЖИВАНИЮ, ОПЕРАТОР ИЛИ ПАЦИЕНТ
ПОЛУЧАТ УДАР ЗЛЕКТРИЧЕСКИМ ТОКОМ, МЕХАНИЧЕСКУЮ ТРАВМУ ИЛИ
ДРУГОЕ ПОВРЕЖДЕНИЕ.
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.
vi -
Page 9
GELOGIQ P9/P7
OPOZORILO
(SL)
UPOZORENJE
(HR)
UPOZORNENIE
(SK)
VARNING
(SV)
D
IRECTION5604324, REVISION11 SERVICE MANUAL
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.
• 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.
• 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.
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.
- vii
Page 10
GELOGIQ P9/P7
DİKKAT
(TR)
(JA)
Traditional
Chinese
D
IRECTION5604324, REVISION11 SERVICE MANUAL
BU SERVİS KILAVUZU YALNIZCA İNGİLİZCE OLARAK SAĞLANMIŞTIR.
• BU UYARININ GÖZ ARDI EDİLMESİ, ELEKTRİK ÇARPMASI YA DA MEKANİK
VEYA DİĞER TÜRDEN KAZALAR SONUCUNDA TEKNİSYENİN, OPERATÖRÜN
YA DA HASTANIN YARALANMASINA YOL AÇABİLİR.
viii -
Page 11
GELOGIQ P9/P7
(ZH-CN)
(KO)
D
IRECTION5604324, REVISION11 SERVICE MANUAL
- ix
Page 12
GELOGIQ P9/P7
DANGER
WARNINGWARNING
D
IRECTION5604324, REVISION11 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 performed by qualified GE Healthcare personnel.
In performing all electrical work on these products, GE will use its own specially trained field engineers.
All of GE’s electrical work on these products will comply with the requirements of the applicable
electrical codes.
The purchaser of GE equipment shall only utilize qualified personnel (i.e., GE’s field engineers,
personnel of third-party service companies with equivalent training, or licensed electricians) to perform
electrical servicing on the equipment.
OMISSIONS & ERRORS
If there are any omissions, errors or suggestions for improving this documentation, please contact the
GE Healthcare Global Documentation Group with specific information listing the system type, manual
title, part number, revision number, page number and suggestion details.
Mail the information to:Service Documentation, 9900 Innovation Drive (RP-2123), Wauwatosa,
WI53226, USA.
GE Healthcare employees should use TrackWise to report service documentation issues. These issues
will then be in the internal problem reporting tool and communicated to the writer.
SERVICE SAFETY CONSIDERATIONS
DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH, ARE PRESENT IN
THIS EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING AND
ADJUSTING.
Use all Personal Protection Equipment (PPE) such as gloves, safety shoes, safety
glasses, and kneeling pad, to reduce the risk of injury.
For a complete review of all safety requirements, see the Chapter 1, Safety Considerations section in
the Service Manual.
x -
Page 13
GELOGIQ P9/P7
D
IRECTION5604324, REVISION11 SERVICE MANUAL
LEGAL NOTES
The contents of this publication may not be copied or duplicated in any form, in whole or in part, without
prior written permission of GE Healthcare.
GE Healthcare may revise this publication from time to time without written notice.
TRADEMARKS
All products and their name brands are trademarks of their respective holders.
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
Chapter 1
Introduction
Section 1-1
Overview
1-1-1Purpose of Chapter 1
This chapter describes important issues related to safely servicing the LOGIQ P9/P7 ultrasound
system. The service provider must read and understand all the information presented in this manual
before installing or servicing a unit.
Table 1-1 Contents in Chapter 1
SectionDescriptionPage Number
1-1
1-2
1-3
1-4
1-5
Overview
Important Conventions
Safety Considerations
Electromagnetic Compatibility (EMC)
Customer Assistance
1-1-2Purpose of Service Manual
This Service Manual is valid for LOGIQ P9/P7 ultrasound systems.
!! NOTICE:
This Service Manual provides installation and service information for LOGIQ P9/P7 Ultrasound
Scanning System and contains the following chapters:
1) Chapter 1 - Introduction: Contains a content summary and warnings.
2) Chapter 2 - Site Preparation: Contains pre-installation requirements.
procedures for all changeable Field Replaceable Units (FRU).
9) Chapter 9 - Renewal Parts: Contains a complete list of field replaceable parts.
10) Chapter 10 - Care & Maintenance: Provides care and maintenance procedures.
1-1
1-3
1-8
1-16
1-17
Chapter 1 - Introduction1-1
Page 42
GERAFTLOGIQ P9/P7
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
1-1-3Typical Users of the Basic Service Manual
•GE Service Personnel (installation, maintenance, etc.)
•Hospital’s Service Personnel
•Contractors (Some parts of Chapter 2 - Pre-Installation)
1-1-4Models Covered by this Manual
Table 1-2 LOGIQ P9/P7 - Model Designations
Part NumberDescription
5560941LOGIQ P7 Standard
5560939LOGIQ P7 Tall
5560938LOGIQ P9
5641296LOGIQ P7 with High Cabinet
5641037LOGIQ P9 with Articulating Monitor Arm
5724885LOGIQ P7 R2 with High Cabinet
5724886LOGIQ P9 R2 with Articulating Monitor Arm
5759916LOGIQ P7 R2.5
5759915LOGIQ P9 R2.5
5794264LOGIQ P9 R3
5795196LOGIQ P7 R3
NOTE:For LP9/P7 R3, the color of the system that is shown in this manual could look different from the real
system.
1-2Section 1-1 - Overview
Page 43
GEDRAFTLOGIQ P9/P7
DANGER
WARNINGWARNING
CAUTION
NOTICE
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
1-1-5Purpose of Operator Manual(s)
The Operator Manual(s) should be fully read and understood before operating the LOGIQ P9/P7 and
also kept near the unit for quick reference.
Section 1-2
Important Conventions
1-2-1Conventions Used in this Manual
Model Designations
This manual covers the LOGIQ P9/P7 ultrasound units listed on page 1-2.
Icons
Pictures, or icons, are used wherever they reinforce the printed message. The icons, labels and
conventions used on the product and in the service information are described in this chapter.
Safety Precaution Messages
Various levels of safety precaution messages may be found on the equipment and in the service
information. The different levels of concern are identified by a flag word that precedes the precautionary
message. Known or potential hazards are labeled in one of following ways:
INDICATES THE PRESENCE OF A HAZARD THAT WILL CAUSE SEVERE
!! DANGER:
!! WARNING:
!! CAUTION:
!! NOTICE:
NOTE:Notes provide important information about an item or a procedure.
PERSONAL INJURY OR DEATH IF THE INSTRUCTIONS ARE IGNORED.
INDICATES THE PRESENCE OF A HAZARD THAT CAN CAUSE SEVERE PERSONAL
INJURY AND PROPERTY DAMAGE IF INSTRUCTIONS ARE IGNORED.
Indicates the presence of a hazard that will or can cause minor personal injury and property
damage if instructions are ignored.
Equipment Damage Possible
Notice is used when a hazard is present that can cause property damage but has absolutely no
personal injury risk.
Example: Disk drive will crash.
Information contained in a NOTE can often save you time or effort.
Chapter 1 - Introduction1-3
Page 44
GERAFTLOGIQ P9/P7
LASER
LIGHT
Signed
Date
TAG
&
LOCKOUT
EYE
PROTECTION
or
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
1-2-2Standard Hazard Icons
Important information will always be preceded by the exclamation point contained within
a triangle, as seen throughout this chapter. In addition to text, several different graphical
icons (symbols) may be used to make you aware of specific types of hazards that could
cause harm. Even if a symbol isn’t used in this manual, it is included for your reference.
Table 1-3 Standard Hazard Icons
ELECTRICALMECHANICALRADIATION
LASERHEATPINCH
Other hazard icons make you aware of specific procedures that should be followed.
Table 1-4 Standard Icons Indicating a Special Procedure be Used
AVOID STATIC ELECTRICITYTAG AND LOCK OUTWEAR EYE PROTECTION
WEAR HAND PROTECTIONWEAR FOOT PROTECTION
1-4Section 1-2 - Important Conventions
Page 45
GEDRAFTLOGIQ P9/P7
xxxx
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
1-2-3Product Icons
The following table describes the purpose and location of safety labels and other important information
provided on the equipment.
Table 1-5 Product Icons
LABEL/SYMBOLPURPOSE/MEANINGLOCATION
Identification and Rating Plate
Device Listing/Certification Labels
Type/Class Label
IP Code (IPX 1)
IP Code (IPX 7)
Manufacturer's name and address
Model and serial numbers
Electrical ratings
Laboratory logo or labels denoting conformance with industry
safety standards such as UL or IEC.
Council Directive 93/42/EEC concerning medical devices: The
CE mark affixed to the equipment testifies compliance to the
directive.
Used to indicate the degree of safety or protection.
Indicates the degree of protection provided by the enclosure
per IEC 60529.
IPX 1 - protected against dripping water
IPX 7 - protected against the effects of immersion
Equipment Type BF (man in the box, symbol IEC 60878-5333)
indicates B Type equipment having even more electrical
isolation than standard Type B equipment because it is
intended for intimate patient contact.
To identify a defibrillation-proof type CF (heart in box with
“electrodes”, symbol IEC 60878-5336) applied part complying
with IEC 60601-1.
Rear side of the unit
on each probe
Rear side of the unit
Rear side of the unit
on the plug of each probe
Footswitch
Probes
Probe connectors
Main label on rear of system
Front side of the ECG-preamplifier
“CAUTION
This unit weighs...
Special care must be used to avoid..."
"DANGER Risk of explosion used in..."
This precaution is intended to prevent injury that may result if
one person attempt to move the unit considerable distances or
on an incline due to the weight of the unit.
The system is not designed for use with flammable anesthetic
gases.
"CAUTION" The equilateral triangle is usually used in
combination with other symbols to advise or warn the user.
ATTENTION - Consult accompanying documents " is
intended to alert the user to refer to the operator manual or
other instructions when complete information cannot be
provided on the label.
Chapter 1 - Introduction1-5
Used in the Service and User Manual
which should be adjacent to equipment
at all times for quick reference.
Indicated in the Service Manual.
various
Rear side of Power Supply
Page 46
GERAFTLOGIQ P9/P7
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
Table 1-5 Product Icons (Continued)
LABEL/SYMBOLPURPOSE/MEANINGLOCATION
"CAUTION - Dangerous voltage" (the lightning flash with
arrowhead in equilateral triangle) is used to indicate electric
shock hazards.
various
"Mains OFF" Indicates the power off position of the mains
power switch.
"OFF/Standby" Indicates the power off/standby position of the
power switch.
CAUTION
This Power Switch DOES NOT ISOLATE Mains Supply
"Mains ON" Indicates the power on position of the mains
power switch.
"Protective Earth" Indicates the protective earth (grounding)
terminal.
"Equipotentiality" Indicates the terminal to be used for
connecting equipotential conductors when interconnecting
(grounding) with other equipment.
Waste Electrical and Electronic Equipment (WEEE) Disposal.
This symbol indicates that waste electrical and electronic
equipment must not be disposed as unsorted municipal waste
and must be collected separately. Please contact an
authorized representative of the manufacturer for information
concerning the decommissioning of your equipment.
rear of system at mains switch
Adjacent to On-Off/Standby switch left
below the Control panel.
rear of system at mains switch
rear of system at mains switch
(on primary power supply - RTN)
rear of system at mains switch
(on primary power supply - RTN)
Rear side of the unit
on the plug of each probe
These symbols indicate that at least one of the six hazardous
substances of the China RoHS Labelling Standard is above
the RoHS limitation.
The number inside the circle is referred to as the
Environmental Friendly Use Period (EFUP). It indicates the
number of years that the product, under normal use, will
remain harmless to health of humans or the environment.
EFUP = 10 for Short Use Products
EFUP = 20 for Medium Use Products
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 and the
Touch Panel display, contain mercury.)
Loading prohibitedat top cover of the system
1-6Section 1-2 - Important Conventions
Rear side of the unit
on the plug of each probe
Rear side of the unit
not visible:
- below the cover on read side of Monitor
- on rear side of the Touch Panel
Page 47
GEDRAFTLOGIQ P9/P7
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
Table 1-5 Product Icons (Continued)
LABEL/SYMBOLPURPOSE/MEANINGLOCATION
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 P9/P7 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.
Rating Plate
Upgraded LOGIQ P9 systems, adjacent
to the Rating Plate
Chapter 1 - Introduction1-7
Page 48
GERAFTLOGIQ P9/P7
CAUTION
WARNINGWARNING
WARNINGWARNING
WARNINGWARNING
CAUTION
CAUTION
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
Section 1-3
Safety Considerations
1-3-1Introduction
The following safety precautions must be observed during all phases of operation, service and repair of
this equipment. Failure to comply with these precautions or with specific warnings elsewhere in this
manual, violates safety standards of design, manufacture and intended use of the equipment.
1-3-2Human Safety
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 P9/P7 Training are authorized to service the equipment.
1-3-3Mechanical Safety
The LOGIQ P9/P7 weighs 60 kg or more, depending on installed peripherals, (133 lbs or more)
!! CAUTION:
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).
USE EXTREME CAUTION WHEN ELEVATING THE UNIT, OR IF IT IS RAISED FOR A
!! WARNING:
REPAIR OR MOVED ALONG ANY INCLINE. THE LOGIQ P9/P7 SYSTEM MAY
BECOME UNSTABLE WHICH COULD CAUSE A TIP OVER.
ULTRASOUND PROBES ARE HIGHLY SENSITIVE MEDICAL INSTRUMENTS THAT
!! WARNING:
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.
!! WARNING:
!! CAUTION:
!! CAUTION:
NOTE:Special care should be taken when transporting the unit in a vehicle:
1-8Section 1-3 - Safety Considerations
EVEN IF IT LOOKS OK, IT MAY BE DAMAGED.
Always lower and center the Operator I/O Panel before moving the scanner.
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.
•Eject any DVD/CD from the drive.
•Place the probes in their carrying cases.
•DO NOT use the Control Panel as an anchor point.
•Secure the systems with straps in an upright position and lock the caster wheels (brake).
•Ensure that the LOGIQ P9/P7 system is firmly secured while inside the vehicle.
•Prevent vibration damage by driving cautiously. Avoid unpaved roads, excessive speeds, and
erratic stops or starts.
Page 49
GEDRAFTLOGIQ P9/P7
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
1-3-4Electrical Safety
1-3-4-1Safe 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 the system, make sure that the total
current rating of the system does not exceed the extension cord rating.
The power outlet used for this equipment should not be shared with other types of equipment.
Both the system power cable and the power connector meet international electrical standards.
This product is classified as Class I and INTERNALLY POWERED ME EQUIPMENT according to the
IEC/EN 60601-1.
1-3-4-2Probes
All the probes for the LOGIQ P9/P7 are designed and manufactured 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 against 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 and Seal.
•Do not use a cracked or damaged probe. In this event, call your field 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 LOGIQ P9/P7 Basic User Manual and the care
card supplied with the probe.
Chapter 1 - Introduction1-9
Page 50
GERAFTLOGIQ P9/P7
WARNINGWARNING
WARNINGWARNING
NOTICE
CAUTION
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
1-3-5Auxiliary Devices Safety
Power Supplies for additional equipment MUST comply with IEC 60601-1.
!! WARNING:
DO NOT attempt to use different peripherals and accessories (brand and model;
!! WARNING:
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!
The LOGIQ P9/P7 may be used with an isolation transformer to provide 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., printers) 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 / ANSI/AAMI
ES60601-1 for medical equipment).
Everybody who connects additional equipment to the signal input portion or signal output portion
configures a medical system, and is therefore responsible that the system complies with the
requirements of the system standard IEC 60601-1-1.
!! NOTICE:
!! CAUTION:
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 P9/P7 ultrasound system.
* IEC xxx stands for standards such as:
• IEC 60601 for medical devices
• IEC 60950 for information technology equipment etc.
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.
The leakage current of the entire system including any / all auxiliary equipment must not exceed
the limit values as per IEC 60601-1 / EN 60601-1 respectively other valid national or international
standards. All equipment must comply with UL, CSA and IEC requirements.
1-10Section 1-3 - Safety Considerations
Page 51
GEDRAFTLOGIQ P9/P7
CAUTION
CAUTION
CAUTION
WARNINGWARNING
NOTICE
2,5 m
1,5 m
1,5 m1,5 m
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
Please observe that some printers may not be medical devices! If the Bluetooth Printer and/or
!! CAUTION:
Line Printers are no medical devices, they have to be located outside of the patient environment
(according to IEC 60601-1 / ANSI/AAMI ES60601-1).
Auxiliary equipment must only be connected to the main console with the special main outlet
!! CAUTION:
provided for the electrical safety of the system.
Auxiliary equipment with direct main connection requires galvanic separation of the signal and/
!! CAUTION:
or control leads.
For hardware installation procedures see: Chapter 3 - Connection of Auxiliary Devices, on page 3-11.
After each installation, the leakage currents have to be measured according to
!! WARNING:
IEC 60601-1 respectively ANSI/AAMI ES60601-1.
!! NOTICE:
All peripherals mounted on the LOGIQ P9/P7 system chassis must be firmly secured in position.
Chapter 1 - Introduction1-11
Page 52
GERAFTLOGIQ P9/P7
CAUTION
WARNINGWARNING
CAUTION
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
1-3-6Battery Safety
NOTE:The LOGIQ P9/P7 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 batteries).
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.
USE ONLY BATTERIES APPROVED BY GE HEALTHCARE AS SUITABLE FOR USE WITH THE
LOGIQ P9/P7 ULTRASOUND SYSTEM.
THE LOGIQ P9/P7 BATTERY HAS A SAFETY DEVICE.
DO NOT ATTEMPT TO DIS-ASSEMBLE OR ALTER THE BATTERY!
ALWAYS OBSERVE THE FOLLOWING PRECAUTIONS:
•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 appears 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 35C (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.
1-12Section 1-3 - Safety Considerations
Page 53
GEDRAFTLOGIQ P9/P7
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
1-3-7Labels Locations
The LOGIQ P9/P7 ultrasound system comes equipped with product labels and icons.
These labels and icons represent pertinent information regarding the operation of the unit.
Figure 1-1 Label Location (R1, R2 and R2.5)
* Required for Asia.
1) LCD Caution Label
2) Gender Caution Label (Only for India, China, Korea)
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
1-3-8Dangerous Procedure Warnings
Warnings, such as the examples below, precede potentially dangerous procedures throughout this
manual. Instructions contained in the warnings must be followed.
DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH, ARE PRESENT
!! DANGER:
IN THIS EQUIPMENT.
USE EXTREME CAUTION WHEN HANDLING, TESTING AND ADJUSTING.
EXPLOSION WARNING
!! WARNING:
!! 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.
1-3-9Lockout/Tagout Requirements (For USA Only)
Follow OSHA Lockout/Tagout requirements to protect service personnel from injuries caused by
unexpected energizing or start-up of equipment during service, repair, or maintenance.
Energy Control and Power Lockout for LOGIQ P9/P7.
!! NOTICE:
When servicing parts of the system where there is exposure to voltage greater than 30 Volts:
Unplug the system.
Maintain control of the system power plug.
There are no test points to verify isolation, you must wait for at least 20 seconds for capacitors to
discharge.
Beware that the Power Supply, Front End Processor and Back End Processor may be energized even
if the power is turned off when the cord is still plugged into the AC Outlet.
1-3-10Returning/Shipping System, Probes and Repair Parts
When returning or shipping the LOGIQ P9/P7 system in the original packaging:
•system must be lowered to its minimum height with monitor flapped down (see Figure on page 3-8)
•the Control Console has to be centered and locked in “unextended” position.
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).
UT
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.
Chapter 1 - Introduction1-15
Page 56
GERAFTLOGIQ P9/P7
WARNINGWARNING
WARNINGWARNING
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
1-3-10Returning/Shipping System, Probes and Repair Parts (cont?)
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.
Section 1-4
Electromagnetic Compatibility (EMC)
1-4-1What 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 intended due interference from its environment or
when the device produces unacceptable levels of emission to its environment. This interference is often
referred to as radio–frequency or electromagnetic interference (RFI/EMI) and can be radiated through
space or conducted over interconnecting power of signal cables. In addition to electromagnetic energy,
EMC also includes possible effects from electrical fields, magnetic fields, electrostatic discharge and
disturbances in the electrical power supply.
For applicable standards please refer to Chapter 2 in the Basic User Manual of the LOGIQ P9/P7
ultrasound system.
1-4-2Compliance
The LOGIQ P9/P7 unit conforms to all applicable conducted and radiated emission limits and to
immunity from electrostatic discharge, radiated and conducted RF fields, magnetic fields and power line
transient requirements as mentioned in IEC 60601-1-2.
NOTE:For CE Compliance, it is critical that all covers, screws, shielding, gaskets, mesh, clamps, are in
good condition, installed tightly without skew or stress. Proper installation following all
comments noted in this service manual is required in order to achieve full EMC performance.
1-4-3Electrostatic Discharge (ESD) Prevention
DO NOT touch any boards with integrated circuits prior to taking the necessary ESD
!! WARNING:
!! WARNING:
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 replacement of ESD
sensitive parts. All parts that have the potential for storing energy must be discharged
or isolated before making contact.
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
Section 1-5
Customer Assistance
1-5-1Contact Information
If this equipment does not work as indicated in this service 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.
NOTE:Prepare vital system information (see: Section 7-2 on page 7-2) before you call:
•System Type
•System Serial number (also visible on label on back of the system)
•Application Software version
•Backup version
•additional information about installed software
Table 1-6 Phone Numbers for Customer Assistance
LocationPhone Number
USA
GE Healthcare
Ultrasound Service Engineering
9900 Innovation Drive (RP-2123)
Wauwatosa, WI 53226, USA
Canada1-800-668-0732
Latin America
Europe
GE Ultraschall Deutschland GmbH
Beethovenstraße 239
Postfach 11 05 60, D-42655 Solingen
Germany
This chapter provides the information required to plan and prepare for the installation of a LOGIQ P9/
P7 ultrasound unit. Included are descriptions of the facility and electrical needs to be met by the
purchaser.
Table 2-1 Contents in Chapter 2
SectionDescriptionPage Number
2-1
2-2
2-3
Overview
General Console Requirements
Facility Needs
2-1
2-2
2-7
Chapter 2 - Site Preparation2-1
Page 60
GERAFTLOGIQ P9/P7
CAUTION
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
Section 2-2
General Console Requirements
2-2-1Environmental Requirements
Table 2-2 System Environmental Requirements
Operational
(with probe)
o
10 - 35
Temperature
18- 30
Humidity
Pressure700 - 1060hPa700 - 1060hPa700 - 1060hPa
C (50 - 95 oF)
with 2D probe
o
C (64.4 - 86oF)
with 4D probe
10 - 80%
(non-condensing)
Storage
(LOGIQ P9/P7)
o
-10 - 50
(14 - 122
(non-condensing)
10 - 90%
C
o
F)
If the system has been in storage or has been transported, please see the acclimation requirements
!! CAUTION:
before powering
ON and/or using the system (see: Section 3-2-2 "Installation Warnings" on page 3-3).
2-2-1-1Cooling
The cooling requirement for the LOGIQ P9/P7 is 680 BTU/hr. This figure does not include cooling
needed for lights, people, or other equipment in the room.
NOTE:Each person in the room places an additional 300 BTU/hr. demand on the cooling system.
2-2-1-2Lighting
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 dimmers can be a source
of EMI which could degrade image quality. These controls should be selected to minimize possible
interference.
Transport
(LOGIQ P9/P7)
o
10 - 90%
C
o
F)
-10 - 50
(14 - 122
(non-condensing)
2-2-2Electrical Requirements
NOTE:GE Healthcare requires a dedicated power and ground for the proper operation of its Ultrasound
equipment. This dedicated power shall originate at the last distribution panel before the system.
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.
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 unit is only a conduit.
Table 2-3 Electrical Specifications for LOGIQ P9/P7
VoltageTolerancesCurrentFrequency
100 - 120 VAC±10%5.0 ... 4.1 A50, 60 Hz (±2%)
220 - 240 VAC±10%2.2 ... 2.0 A50, 60 Hz (±2%)
Power Consumption nominal 500 VA including all on-board peripherals.
2-2-2-2Inrush Current
Inrush current is not a factor to consider due to the inrush current limiting properties of the power
supplies.
2-2-2-3Site Circuit Breaker
It is recommended that the branch circuit breaker for the machine be readily accessible.
POWER OUTAGE MAY OCCUR.
!! CAUTION:
The LOGIQ P9/P7 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.
2-2-2-4Site Power Outlets
A dedicated AC power outlet must be within reach of the unit without extension cords. Other adequate
outlets for the external peripherals, medical and test equipment needed to support this unit must also
be present within 1 m (3.2 ft.) of the unit. Electrical installation must meet all current local, state, and
national electrical codes.
2-2-2-5Main Power Plug
The LOGIQ P9/P7 ultrasound system is supplied with a main power plug, as standard. In the event that
the unit arrives without a power plug, or with the wrong plug, contact your GE dealer. When necessary,
the installation engineer will supply the appropriate power plug to meet the applicable local regulations.
Chapter 2 - Site Preparation2-3
Page 62
GERAFTLOGIQ P9/P7
NOTICE
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
2-2-3EMI Limitations
Ultrasound systems are susceptible to Electromagnetic Interference (EMI) from radio frequencies,
magnetic fields, and transients in the air or wiring. Ultrasound machines also generate EMI.
The LOGIQ P9/P7 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.
!! NOTICE:
Electrical and electronic equipment may produce EMI unintentionally as the result of a defect.
Sources of EMI include the following:
•medical lasers
•scanners
•cauterizing guns
•computers
•monitors
•fans
•gel warmers
•microwave oven
•light dimmers
•portable phones
•broadcast stations and mobile broadcasting machines
Table 2-4 EMI Prevention/Abatement
EMI RuleDetails
Keep the unit at least 5 meters (16.4 feet) away from other EMI sources. Special shielding may be
Be aware of RF sources.
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.
required to eliminate interference problems caused by high frequency, high powered radio or video
broadcast signals.
Poor grounding is the most likely reason a unit will have noisy images.
Check grounding of the power cord and power outlet.
After you finish repairing or updating the system, replace all covers and tighten all screws.
Any cable with an external connection requires a magnet wrap at each end.
Install the shield over the front of card cage. Loose or missing covers or RF gaskets allow radio
frequencies to interfere with the ultrasound signals.
If more than 20% or a pair of the fingers on an RF gasket are broken, replace the gasket.
Do not turn ON the unit until any loose metallic part is removed 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.
SYSTEMS AND ELECTRONIC PROBES ARE DESIGNED FOR STORAGE TEMPERATURES OF
0 TO + 55 degrees C. WHEN EXPOSED TO LARGE TEMPERATURE VARIATIONS, THE
PRODUCT SHOULD BE KEPT IN ROOM TEMPERATURE FOR 10 HOURS BEFORE USE.
o
18
- 30oC
for 4D probe
2-2-5Time 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.
Have two people available to deliver and unpack the LOGIQ P9/P7 ultrasound system.
!! CAUTION:
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.
Chapter 2 - Site Preparation2-5
Page 64
GERAFTLOGIQ P9/P7
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
2-2-6System Specifications
2-2-6-1Physical Dimensions of LOGIQ P9/P7
The physical dimensions and weight (without Peripherals) of the LOGIQ P9/P7 unit are summarized in
Ta bl e 2 -6 .
NOTE:Physical dimensions (especially height and depth) depend on control console and monitor positioning.
For more details refer to Chapter 5 - OPIO Positioning, on page 5-20.
Table 2-6 Physical Dimensions and Weight (without Peripherals)
HeightWidthDepthWeight
1570 mm (max)
1375 mm (min) *
* with low cabinet option
2-2-6-2Acoustic Noise Output
max. 50 dB(A)
2-2-6-3Electrical Specifications
Please refer to Section 2-2-2-1 "LOGIQ P9/P7 Power Requirements" on page 2-3.
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.
Use the Pre-installation checklist (provided in Table 2-7) to verify that all needed steps have been taken.
Table 2-7 LOGIQ P9/P7 Pre-Installation Check List
ActionYesNo
Schedule at least 3 hours for installation of the system.
Notify installation team of the existence of any variances from the basic installation.
Make sure system and probes have been subject to acclimation period.
Environmental cooling is sufficient.
Lighting is adjustable to adapt to varying operational conditions of the scanner.
Electrical facilities meet system requirements.
EMI precautions have been taken and all possible sources of interference have been removed.
Mandatory site requirements have been met.
If a network is used, IP address has been set for the system and a dedicated network outlet is available.
Purchaser responsibility includes:
•Procuring the materials required.
•Completing the preparations before delivery of the ultrasound system.
•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 prepared for
the equipment must be performed by licensed electrical contractors. Other connections between pieces
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 product further
from the system than the interface kit allows presents challenges to the installation team. To avoid
delays during installation, such variances should be made known to the individuals or group performing
the installation at the earliest possible date (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.
Chapter 2 - Site Preparation2-7
Page 66
GERAFTLOGIQ P9/P7
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
2-3-2Mandatory Site Requirements
The following are mandatory site requirements. Additional (optional) recommendations, as well as a
recommended ultrasound room layout, are provided in Section 2-3-3 "Site Recommendations" .
•A dedicated single branch power outlet of adequate amperage (see Table 2-3 on page 2-3) that
meets all local and national codes and is located less than 2.5 m (8.2 ft) from the unit’s proposed
location. Refer to: Section 2-2-2 "Electrical Requirements" on page 2-2.
•A door opening of at least 76 cm (2.5 ft) in width.
•The proposed location for the unit is at least 0.2 m (0.67 ft) from the walls, to enable cooling.
•Clean and protected space for storage of probes (either in their case or on a rack).
•Material to safely clean probes (performed using a plastic container, never metal).
•Power outlet and place for any external peripheral are within 2 m (6.5 ft.) of each other with
peripheral within 1 m of the unit to connect cables.
NOTE:The LOGIQ P9/P7 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 3-46 on page 3-71 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.
2-3-3Site Recommendations
The following are (optional) site recommendations. Mandatory site requirements are provided in the
Mandatory Site Requirements section, above.
•Door opening of 90 cm (3 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.
Figure 2-1 below shows a floor plan illustrating the recommended layout of the Ultrasound Room and
depicting the minimal room layout requirements.
Figure 2-1 Recommended Floor Plan 4.3m x 5.2m (14ft x 17ft)
Chapter 2 - Site Preparation2-9
Page 68
GERAFTLOGIQ P9/P7
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
2-3-4Networking Setup Requirements
2-3-4-1Stand-alone Unit (without Network Connection)
None
2-3-4-2Unit Connected to Hospital’s Network
Supported networks:
•Ethernet network connection
•Up to 900 Mbps WLAN (optional)
2-3-4-3Purpose of the DICOM Network Function
DICOM (Digital Imaging and Communications in Medicine) services provide the operator with clinically
useful features for moving images and patient information over a hospital network.
Examples of DICOM services include the transfer of images to workstations for viewing or transferring
images to remote printers. As an added benefit, transferring images in this manner frees up the onboard monitor and peripherals, enabling viewing to be done while scanning continues.
With DICOM, images can be archived, stored, and retrieved faster, easier, and at a lower cost.
2-3-4-4DICOM Option Pre-installation Requirements
To configure the LOGIQ P9/P7 ultrasound unit to work with other network connections, the network
administrator must provide some necessary information.
Use the Agent Configuration (R3 only) on page 3-65 to record required information that must include:
• LOGIQ P9/P7
Details:
• Routing Information:IP addresses for default gateway and other routers in use at site.
• DICOM Application Information: Details of DICOM devices in use at the site, including the DICOM
Installation see: Section 3-13 "Configuring Connectivity" on page 3-58.
DICOM network details for the LOGIQ P9/P7 unit, including the
host name, local port, IP address, AE title and net mask.
host name, AE title, DICOM port number and IP addresses.
2-10Section 2-3 - Facility Needs
Page 69
GEDRAFTLOGIQ P9/P7
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
Chapter 3
Setup Instructions
Section 3-1
Overview
3-1-1The Purpose of Chapter 3
This chapter contains information needed to setup the LOGIQ P9/P7 ultrasound system. Included are
procedures to receive, unpack and configure the equipment.
A worksheet is provided (see: page 3-65 to page 3-71) to help ensure that all the required information
is available, prior to setup the system.
Table 3-1 Contents in Chapter 3
SectionDescriptionPage Number
3-1
3-2
3-3
3-4
3-5
3-6
3-7
3-8
3-9
3-10
3-11
3-12
3-13
3-14
3-15
3-16
Overview
Set Up Reminders
Receiving and Unpacking the Equipment
Packing materials - recycling information
Preparing for Set Up
Connection of Auxiliary Devices
Completing the Set Up
Printer Installation
System Configuration
Available Probes
Software/Option Configuration
Connectivity Setup
Configuring Connectivity
Agent Configuration (R3 only)
Connectivity Setup Worksheet
Paperwork
3-1
3-2
3-5
3-8
3-9
3-11
3-20
3-32
3-42
3-47
3-53
3-54
3-58
3-65
3-70
3-72
Chapter 3 - Setup Instructions3-1
Page 70
GERAFTLOGIQ P9/P7
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
Section 3-2
Set Up Reminders
3-2-1Average Installation Time
Once the site has been prepared, the average installation time required is shown in Tab le 3 -2 below.
Table 3-2 Average Installation Time
DescriptionAverage Installation TimeComments
Unpacking the scanner0.5 hours
Installing the scanner / options / printers0.5 to 1.5 hoursdepends on required configuration
DICOM Option (connectivity)0.5 - 1.5 hoursdepends on configuration amount
3-2Section 3-2 - Set Up Reminders
Page 71
GEDRAFTLOGIQ P9/P7
CAUTION
WARNINGWARNING
WARNINGWARNING
When moving or lifting the system, grasp it only at the rear
handle.
WARNING
WARNING
Do NOT pull or lift the system with the front handle
of the user interface (operator panel).
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
3-2-2Installation Warnings
1) Since the LOGIQ P9/P7 weighs approximately 90 kg (200 lbs.) without peripherals, two people are
required to unpack it.
2) There are no operator serviceable components. To prevent shock, do not remove any covers or
panels. Should problems or malfunctions occur, unplug the power cord.
Only qualified service personnel should carry out servicing and troubleshooting.
3-2-2-1Moving/Lifting the System
Figure 3-1 moving or lifting the system
3-2-2-2System Acclimation Time
After being transported, the LOGIQ P9/P7 system may be very cold or hot.
It requires one hour for each 2.5C increment if it's temperature is below 10C or above 40C.
Equipment damage possibility. Turning the system on without acclimation after arriving at site
If weight is placed on the OPIO (User Interface) in it’s extended position the console could tip over.
The system should NOT be moved with the OPIO (User Interface) extended. Move the
!! WARNING:
OPIO to it’s centered and locked position.
Monitor mounting mechanism may break if not properly supported (e.g., with packing
!! WARNING:
foam) during transportation.
Chapter 3 - Setup Instructions3-3
Page 72
GERAFTLOGIQ P9/P7
WARNINGWARNING
DANGER
CAUTION
CAUTION
CAUTION
CAUTION
CAUTION
CAUTION
CAUTION
CAUTION
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
3-2-2-4Brake Pedal Operation
REMEMBER: If the front wheel brakes are engaged for transportation, release brake
!! WARNING:
pedals (brakes on front wheels under the foot rest) to disengage the lock.
3-2-3Safety Reminders
WHEN USING ANY TEST INSTRUMENT THAT IS CAPABLE OF OPENING THE
!! DANGER:
AC GROUND LINE (I.E., METER’S GROUND SWITCH IS OPEN), DO NOT
TOUCH THE UNIT!
Two people should unpack the unit because of its weight.
!! CAUTION:
!! CAUTION:
!! CAUTION:
!! CAUTION:
Two people are required whenever a part weighing 16kg (35 lb.) or more must be lifted.
If the unit is very cold or hot, do NOT turn on its power until it has had sufficient time to
acclimate to its operating environment.
To prevent electrical shock, connect the unit to a properly grounded power outlet.
DO NOT use a three to two prong adapter. This defeats safety grounding.
DO NOT wear the ESD wrist strap when you work on live circuits and more than 30 V peak is
present.
!! CAUTION:
!! CAUTION:
!! CAUTION:
!! CAUTION:
DO NOT use a 20 Amp to 15 Amp adapter on the 120 Vac unit’s power cord.
This unit requires a dedicated 16 A circuit.
DO NOT operate this unit unless all board covers and frame panels are securely in place, to
ensure optimal system performance and cooling.
(When covers are removed, EMI may be present).
OPERATOR MANUAL(S)
The User Manual(s) should be fully read and understood before operating the LOGIQ P9/P7.
Keep manuals near the unit for reference.
ACOUSTIC OUTPUT HAZARD
Although the ultrasound energy transmitted from the LOGIQ P9/P7 ultrasound system is
within FDA limitations, avoid unnecessary exposure.
Ultrasound energy can produce heat and mechanical damage.
Figure 3-2 Environmental Labels
3-4Section 3-2 - Set Up Reminders
Page 73
GEDRAFTLOGIQ P9/P7
CAUTION
CAUTION
NOTICE
NOTICE
Indicator turns Red
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
Section 3-3
Receiving and Unpacking the Equipment
Please read this section carefully before unpacking the LOGIQ P9/P7 ultrasound system and its
!! CAUTION:
!! CAUTION:
(optional) peripherals.
The LOGIQ P9/P7 ultrasound system, together with peripherals, probes and accessories are shipped
from the factory in a single durable shipping crate which is mounted on a raised wooden platform base.
Transport only with forklift or stacker truck.
During transport pay attention to the point of gravity (“tilt and drop” indicator)!
Have two people available to unpack the LOGIQ P9/P7.
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.
Table 3-4 Shipping Carton - Dimensions and Weight
DescriptionHeightWidthDepth
LOGIQ P9/P7
incl. peripherals and accessories
* Weight is approximate and will vary depending upon the supplied peripherals
1550 mm / 61 inch 706 mm / 27.7 inch 904 mm / 35.6 inch120 kg / 267 lbs
Weight*
Before unpacking the unit:
•Inspect the crate for visible damage.
•Inspect the Drop and Tilt Indicator for evidence of accidental shock or tilting during transit (damage
incident, see: Figure 3-3 below).
Figure 3-3 Drop and Tilt Indicator
!! NOTICE:
!! NOTICE:
The device must only be transported in the original packaging!
Each shipping crate is composed of wooden base, cardboard box, re-usable plastic caps and cushions
inside. It is recommended to keep and store the shipping crate and all other packing materials (including
the support foams, anti-static plastic cover, etc.), in case the unit has to be moved to a different location.
Unpack the devices such a way that packaging can be reused.
For warranty purposes, storage of the above is required for one year from date of purchase.
If the shipping crate is damaged, please inform the GE sales representative immediately.
Chapter 3 - Setup Instructions3-5
Page 74
GERAFTLOGIQ P9/P7
Check whether delivery is complete
(according to packing list) and check visual damage!
The envelope with delivery address, packing list and
invoice is located on the front panel of the crate.
top cover
out sleeve
Option box on front of the system
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
Section 3-3 Receiving and Unpacking the Equipment (cont?)
Figure 3-4 envelope at front panel of the crate
Table 3-5 Unpacking Procedure
StepTask
1.
Remove the top cover, then remove the out sleeve.
2.
Remove the option box on front of the system.
3-6Section 3-3 - Receiving and Unpacking the Equipment
Page 75
GEDRAFTLOGIQ P9/P7
monitor pad
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
Table 3-5 Unpacking Procedure
StepTask
3.
Remove the monitor pads from the monitor and remove the 4 pads of the box bottom assy.
4.
Carefully remove foam packing material and plastic bag from the ultrasound unit and monitor.
Caution: Two people are needed in the next step due to the weight of the equipment.
5.
Unlock the casters and place the 4 caster's direction like the picture below and then using the incline plane
of the box bottom assy, slowly move the system from the box.
Note: Packing crate and material should be stored for future use.
Chapter 3 - Setup Instructions3-7
Page 76
GERAFTLOGIQ P9/P7
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
Section 3-4
Packing materials - recycling information
The packing materials for LOGIQ P9/P7 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).
3-8Section 3-4 - Packing materials - recycling information
Page 77
GEDRAFTLOGIQ P9/P7
NOTICE
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
Section 3-5
Preparing for Set Up
3-5-1Verify Customer Order
1) After unpacking the equipment, it is important to verify that all items ordered by the customer have
been received. Compare all items listed on the packing slip (delivery note) with those received.
It is recommended to keep and store the shipping carton and all other packing materials (including the
!! NOTICE:
StepItemRecommended Procedure
1
2
support foams, anti-static plastic cover, etc.), in case the unit has to be moved to a different location.
Unpack the devices such a way that packaging can be reused.
For warranty purposes, storage of the above is required for one year from date of purchase.
2) Visually inspect the system components using the following checklist.
Table 3-6 Damage Inspection Checklist - LOGIQ P9/P7 System
Main labelEnter Serial Number: __________________________ (printed on main label, see: Figure 1-1 on page 1-13)
ConsoleVerify that the system is switched OFF and unplugged. Clean the console and control panel.
3
Control Console
4
Probes
5
LCD Display
6
FansVerify that the system’s cooling fans and peripheral fans are operating.
7
Rear Panel
8
Covers
9
Peripherals
10
Power Cord
Physically inspect the control console for missing or damaged items.
After switching on the system, verify the proper illumination of all the control panel buttons.
Check all probes for wear and tear on the lens, cable, and connector. Look for bent or damaged pins on the
connector and in the connector socket on the unit. Verify that the EMI fingers around the probe connector
socket housing are intact. Check the probe locking mechanism and probe switch.
Clean the LCD display by gently wiping with a dry, soft, lint-free non-abrasive folded cloth. Inspect the monitor
for scratches and raster burn.
Check the rear panel connectors for bent pins, loose connections and loose or missing hardware. Screw all
the cable connectors tightly to the connector sockets on the panel. Verify that the labeling is in good condition.
Check that all screws are tightly secured in place, that there are no dents or scratches and that no internal
parts are exposed.
Check and clean the peripherals in accordance with the manufacturer’s directions.
To prevent EMI or system overheating, dress the peripheral cables inside the peripheral cover.
Check the power cord for cuts, loose hardware, tire marks, exposed insulation, or any deterioration.
Verify continuity. Replace the power cord, as required.
NOTE:Report any items that are missing, back-ordered, or damaged, to your GE sales representative. The
contact address is shown in Contact Information on page 1-17.
Chapter 3 - Setup Instructions3-9
Page 78
GERAFTLOGIQ P9/P7
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
3-5-2EMI Protection
This unit has been designed to minimize the effects of Electo-Magnetic Interference (EMI). Many of the
covers, shields, and screws are provided primarily to protect the system from image artifacts caused by
this interference. For this reason, it is imperative that all covers and hardware are installed and secured
before the unit is put into operation.
Ensure that the system is protected from electromagnetic interference (EMI), as follows:
•Operate the system at least 15 feet away from equipment that emits strong electromagnetic
radiation.
•Operate the system in an area enclosed by walls, floors and ceilings comprised of wood, plaster or
concrete, which help prevent EMI.
•Shield the system when operating it in the vicinity of radio broadcast equipment, if necessary.
•Do not operate mobile phones or other EMI emitting devices in the ultrasound room.
•Verify that all EMI rules listed in the following table are followed:
The LOGIQ P9/P7
qualified facilities, in terms of the prevention of radio wave interference. Operation of the ultrasound unit
in an inappropriate environment can cause electronic interference to radios and television sets situated
near the medical equipment.
For further details and EMI Prevention/Abatement refer to Section 2-2-3 "EMI Limitations" on page 2-4.
ultrasound unit is approved for use in hospitals, clinics and other environmentally
3-10Section 3-5 - Preparing for Set Up
Page 79
GEDRAFTLOGIQ P9/P7
WARNINGWARNING
CAUTION
2,5 m
1,5 m
1,5 m1,5 m
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
Section 3-6
Connection of Auxiliary Devices
NOTE:Normally auxiliary devices and peripherals come pre-installed with the system.
Table 3-7 below outlines hardware installation procedures described in the sub-sections.
Table 3-7 Connection Procedures
Sub-sectionDescriptionPage Number
3-6-1
3-6-2
3-6-3
3-6-3
3-6-4
3-6-5
3-6-6
3-6-7
Connecting the LCD Monitor
Connecting the Black & White Printer
Connecting the Color Printer
Connecting the Secondary “Patient” LCD Monitor
Connecting the Footswitch
Connecting the USB Flash Memory Stick
Connecting the external USB Hard disk (Handydrive)
General Remarks and Hints when using external USB-Devices
3-12
3-13
3-14
3-15
3-17
3-18
3-18
3-19
After each installation, the leakage currents have to be measured according to
!! WARNING:
!! CAUTION:
NOTE:For more detailed Safety Considerations when connecting auxiliary devices to the LOGIQ P9/P7
IEC 60601-1 respectively ANSI/AAMI ES60601-1.
Please observe that some printers may not be medical devices! If the Bluetooth Printer and/or
Line Printers are not medical devices, they have to be located outside of the patient
environment (according to IEC 60601-1 / ANSI/AAMI ES60601-1).
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
3-6-1Connecting the LCD Monitor
NOTE:The LCD monitor comes pre-installed with the system.
Figure 3-5 Connection Scheme - LCD Monitor
3-12Section 3-6 - Connection of Auxiliary Devices
Page 81
GEDRAFTLOGIQ P9/P7
WARNINGWARNING
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
3-6-2Connecting the Black & White Printer
1) Power OFF/Shutdown the system as described in: Section 3-7-3 on page 3-25.
2) Connect the Black & White printer according to correct connection scheme as described in
Figure 3-6 on page 3-14.
NOTE:There are three USB ports (stack) on rear panel. The BW printer may be connected to any of the 3x
USB stack connector.
3) When all the cables are connected, press the Power ON switch on the Black & White printer.
4) Power ON/Boot up the LOGIQ P9/P7 system as described in Section 3-7-2 on page 3-21. All
software drivers are pre-installed for the designated Black & White printer only.
5) Verify the correct settings in the printer “Properties”, see: Section 3-8-5 "Adjustment of Printer
Settings" on page 3-37.
After each installation, the leakage currents have to be measured according to
!! WARNING:
IEC 60601-1 respectively ANSI/AAMI ES60601-1.
Chapter 3 - Setup Instructions3-13
Page 82
GERAFTLOGIQ P9/P7
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
3-6-2-1Connection Scheme: B&W Printer
Figure 3-6 B&W Printer connection
3-14Section 3-6 - Connection of Auxiliary Devices
Page 83
GEDRAFTLOGIQ P9/P7
CAUTION
NOTICE
NOTICE
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
3-6-3Connecting the Secondary “Patient” LCD Monitor
Secondary LCD “Patient” Monitor MUST NEVER be connected to the LOGIQ P9/P7 ultrasound
!! CAUTION:
!! NOTICE:
!! NOTICE:
systems mains supply directly!
Always connect it to the supplied Isolation Transformer!
The Secondary Monitor is the only item to be connected to the Transformer.
Secondary Monitor is NOT intended for diagnostic use.
It is an additional device used to allow the patient to watch the proceedings.
Take your time to think about the best position of the monitor in your facilities.
Patients should be able to view the monitor easily and without having to bend or turn around.
Connection to Secondary Monitor is via HDMI cable, but HDMI connector output does NOT carry audio
signal.
1) Power OFF/Shutdown the system as described in: Section 3-7-3 on page 3-25.
2) Connect the Secondary Monitor according to connection scheme (see: Figure 3-7 on page 3-16).
Chapter 3 - Setup Instructions3-15
Page 84
GERAFTLOGIQ P9/P7
HDMI to DVI / HDMI to HDMI cable
connected to the
rear side of the
2nd Monitor
Secondary Monitor
appropriate
Transformer
A Secondary “Patient” Monitor MUST NEVER
be connected to the LOGIQ P9/P7 ultrasound systems mains
supply directly!
Always connect it to an appropriate Isolation Transformer
CAUTION
!! CAUTION:
Composite (BNC) Cable
S-Video Cable
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
3-6-3Connecting the Secondary “Patient” LCD Monitor (cont?)
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
3-6-4Connecting the Footswitch
The footswitch should be directly connected to any accessible USB-port on the LOGIQ P9/P7 (e.g., on
rear of the system).
NOTE:Connection of the Footswitch is always the same
(no differences between PC-Motherboard version of the system).
Figure 3-8 Connection Scheme - Footswitch
Chapter 3 - Setup Instructions3-17
Page 86
GERAFTLOGIQ P9/P7
NOTICE
NOTICE
NOTICE
NOTICE
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
3-6-5Connecting the USB Flash Memory Stick
Before connecting an USB device, please read General Remarks and Hints when using external USB-
!! NOTICE:
Devices on page 3-19.
The USB Flash Memory Stick may be connected to an accessible USB port of the LOGIQ P9/P7
system. Refer to Section 3-9-2 "External I/O Connectors" .
An external USB Flash Memory Stick can be connected once the system is powered ON, or after
shutdown. The LOGIQ P9/P7, Windows detects the device and automatically installs a driver. During
this process several dialogs may pop up, starting with the „Found New Hardware” dialog.
NOTE:Memory drives or sticks may be sensitive to EMC interference.
This may affect system performance and/or image quality.
Before disconnecting an external USB-device (e.g., USB Stick), the system has to be informed about
!! NOTICE:
the removal of the device! For this purpose press the EJECT
button on the keyboard.
For further details refer to: Section 3-6-7-2 "External USB-Devices - Disconnection" on page 3-19.
3-6-6Connecting the external USB Hard disk (Handydrive)
Before connecting an USB device, please read General Remarks and Hints when using external USB-
!! NOTICE:
Devices on page 3-19.
The external “Handydrive” HDD may be connected to an accessible USB port of the LOGIQ P9/P7
system. Refer to Section 3-9-2 "External I/O Connectors" .
An external USB Hard Disk Drive can be connected once the system is powered ON, or after shutdown.
The LOGIQ P9/P7, Windows detects the device and automatically installs a driver. During this process
several dialogs may pop up, starting with the „Found New Hardware“ dialog.
NOTE:Memory drives, sticks or HDD drives may be sensitive to EMC interference.
This may affect system performance and/or image quality.
Before disconnecting an external USB-device (e.g., USB Hard disk), the system has to be informed
!! NOTICE:
about the removal of the device! For this purpose press the EJECT
For further details refer to: Section 3-6-7-2 "External USB-Devices - Disconnection" on page 3-19.
button on the keyboard.
3-18Section 3-6 - Connection of Auxiliary Devices
Page 87
GEDRAFTLOGIQ P9/P7
WARNINGWARNING
NOTICE
CAUTION
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
3-6-7General Remarks and Hints when using external USB-Devices
Do not connect or disconnect any external USB-devices to or from the system while
!! WARNING:
3-6-7-1External USB-Devices - Connection
!! NOTICE:
3-6-7-2External USB-Devices - Disconnection
!! CAUTION:
scanning a patient! The appearing dialogs could distract you from the scan!
When an external USB-storage device (such as a USB-memory stick or an external hard disk) is
connected to the LOGIQ P9/P7, Windows detects the device and automatically installs a driver. During
this process, several dialogs may pop up, starting with the “Found New Hardware“ dialog.
The device is then accessible using the drive letter the system assigned to it.
When connecting external USB devices, be sure to execute Safety Directions found in the
LOGIQ P9/P7 Basic User Manual.
Unplugging or ejecting USB devices without first stopping them can often cause the system to
crash and possibly result in loss of valuable data.
To stop the external device, press F3 EJECT
button.
Chapter 3 - Setup Instructions3-19
Page 88
GERAFTLOGIQ P9/P7
CAUTION
WARNINGWARNING
CAUTION
CAUTION
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
Section 3-7
Completing the Set Up
3-7-1Connecting the Unit to a Power Source
The connection of the LOGIQ P9/P7 ultrasound unit to a power source should be performed by a
qualified person who has completed basic LOGIQ P9/P7 System User Training. Use only the power
cords, cables and plugs provided by or designated by GE to connect the unit to the power source.
Prior to connect the LOGIQ P9/P7 unit to a power source, verify compliance with all electrical
!! CAUTION:
!! WARNING:
!! CAUTION:
and safety requirements. Check the power cord to verify that it is intact and of hospital-grade.
Products equipped with a power source (wall outlet) plug should be connected to the fixed
power socket that has a protective grounding conductor. Never use an adapter or converter to
connect with a power source plug (for example, a three-prong to two-prong converter).
The unit’s power must be supplied from a separate, properly rated outlet to avoid risk
of fire. Refer to Section 2-2-2-1 "LOGIQ P9/P7 Power Requirements" on page 2-3 for
rating information. The power cord should not, under any circumstances, be altered to
a configuration rated less than that specified for the current.
Whenever disconnecting the LOGIQ P9/P7 system from the electrical outlet, always observe the
safety precautions. First unplug the main power cable from the wall outlet socket, then from the
unit itself. Remove by pulling on the cable connector - DO NOT pull on the cable.
!! CAUTION:
The LOGIQ P9/P7 requires all covers!
Operate this system only when all board covers and frame panels are securely in place.
The covers are required for safe operation, good system performance and cooling purposes.
3-20Section 3-7 - Completing the Set Up
Page 89
GEDRAFTLOGIQ P9/P7
Circuit Breaker
Main Power
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
3-7-2Power On / Boot Up
3-7-2-1Scanner Power On
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 Main Power Cable to the back of the system. Refer to Section 8-28 for details.
6) Connect the Main Power Cable to a hospital grade power outlet with the proper rated voltage.
Never use an adapter that would defeat the safety ground.
7) Switch ON the Circuit at the rear of the system.
Figure 3-9 Circuit and main power cable at rear of system
Chapter 3 - Setup Instructions3-21
Page 90
GERAFTLOGIQ P9/P7
NOTICE
On/Off Button
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
3-7-2-2Back End Processor Boot Up
When AC power is applied to the scanner, the ON/OFF button on the control panel illuminates blue,
!! NOTICE:
indicating that the System (including the Back-end Processor) is in Standby mode.
8) Hold down the On/Off
button (see: Figure 3-10) on the control panel for ~3 seconds.
NOTE:The mains outlet of the system for peripheral auxiliary equipment are commonly switched with the
ON/OFF 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.
When the ON/OFF button on the control panel is pressed, the System (including the Back-end
Processor) starts and the operating system is loaded which then leads the application software to
activate the scanner.
The system automatically performs an initialization sequence which includes the following:
-Loading the operating system.
-Running a quick diagnostic check of the system.
-Detecting connected probes
Figure 3-10 On/Off Button on Control Panel
As soon as the software has been loaded, the system enters 2D-Mode with the probe connected to port
nearest to a user.
NOTE:Total time used for start-up is about 2 minutes.
9) Adjust Height and position of control console.
3-22Section 3-7 - Completing the Set Up
Page 91
GEDRAFTLOGIQ P9/P7
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
3-7-2-3During a normal boot, you may observe
A) Power is distributed to Peripherals, Operator Panel (control panel), Monitor, Front-End and
Back-End Processor.
B) The Back-End Processor and rest of the scanner starts with the sequence listed in following steps:
1) “Boot Screen” is displayed.
2) Back-End Processor is turned ON and starts to load the software.
3) The Start Screen (LOGIQ?) is displayed on the monitor.
4) Start-up progress bars indicating software loading procedures, are displayed on the monitor,
as shown in Figure 3-11 below.Start-up progress bars indicating software loading procedures,
Figure 3-11 GE Healthcare wallpaper with progress bar (R1.x.x)
Figure 3-12 GE Healthcare wallpaper with progress bar (R2.x.x and later)
Chapter 3 - Setup Instructions3-23
Page 92
GERAFTLOGIQ P9/P7
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
5) Startup GE
NOTE:Startup GE Healthcare wallpaper with progress bar may differ depending on product type and release.
6) 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 PIL board).
7) The Keyboard backlight is lit.
8) As soon as the software has been loaded, the 2D screen is displayed on the monitor.
3-24Section 3-7 - Completing the Set Up
Page 93
GEDRAFTLOGIQ P9/P7
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
3-7-3Power Off / Shutdown
When you power off the unit, the system performs an automatic shutdown sequence
Figure 3-13 System Exit Window (R2 and R2.5)
Figure 3-14 System Exit Window (R3)
The SYSTEM - EXIT menu, used when power off the unit, gives you these choices:
Chapter 3 - Setup Instructions3-25
Page 94
GERAFTLOGIQ P9/P7
NOTICE
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
•Logoff
Use this button to log off the current user. The system remains ON and ready for 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. It is recommended to
perform a full shutdown at least once a week.
If the Shutdown button is dimmed, press the power button or Alt F10 to shut down the unit.
•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.
•Sleep (R2 and R2.5 Only)
Use Sleep Mode when you do a portable exam in order to reduce the time to start up the system.
When you use Sleep Mode, it takes ~90 seconds to start up the system versus 2-3 minutes.
•Change Password
Use this button to change User Password.
!! NOTICE:
Refer to Section 4-2-5-4 "Sleep Mode Check" on page 4-14.
After turning off a 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.
3-26Section 3-7 - Completing the Set Up
Page 95
GEDRAFTLOGIQ P9/P7
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
3-7-3-1Scanner Shutdown
1) If not already in read mode, freeze the image.
2) Press the ON/OFF button (see: Figure 3-10) on the control panel. Following dialog appears.
Figure 3-15 System - Exit (R2 and R2.5)
Figure 3-16 System - Exit (R3)
Chapter 3 - Setup Instructions3-27
Page 96
GERAFTLOGIQ P9/P7
WARNINGWARNING
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
3) Select the SHUTDOWN button. The system performs an automatic full shutdown sequence.
4) Switch OFF the Circuit at the rear of the system.
NOTE:The mains outlet of the system for peripheral auxiliary equipment are commonly switched with the
ON/OFF button. So the auxiliary equipment need not to be switched ON/OFF separately.
Disconnection of the Main Power Cable is necessary!
!! WARNING:
For Example: When repairing the system.
3-28Section 3-7 - Completing the Set Up
Page 97
GEDRAFTLOGIQ P9/P7
CAUTION
Circuit Breaker
Main Power
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
5) After complete power down, disconnect the main power cable from the system or unplug it from the
AC wall outlet socket.
Figure 3-17 Circuit and main power at rear of system
!! CAUTION:
6) Press on the brakes to block the front caster wheels.
7) Disconnect probes. (Turn the probe locking handle counterclockwise and then pull the connector
straight out of the probe port.)
DO NOT disconnect a probe while running (Live Scan “Write” mode)!
A software error may occur. In this case switch the unit OFF (perform a reset).
Chapter 3 - Setup Instructions3-29
Page 98
GERAFTLOGIQ P9/P7
CAUTION
CAUTION
CAUTION
CAUTION
a. Active probe port
b. Pencil probe port
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
3-7-4Transducer Connection
3-7-4-1Connecting the Probe
Inspect the probe before and after each use for damage or degradation to the housing, strain
!! CAUTION:
!! CAUTION:
!! CAUTION:
relief, lens, seal, cable and connector. DO NOT use a transducer which appears damaged until
functional and safe performance is verified. A thorough inspection should be conducted during
the cleaning process.
Remove any dust or foam rests from the probe pins.
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 touch the patient when
connecting or disconnecting a probe.
Probes can be connected at any time, regardless of whether the console is powered on or off. To ensure
that the ports are not active, place the system in the image freeze condition.
!! CAUTION:
Figure 3-18 Probe port
To connect a probe:
1) Place the probe's carrying case on a stable surface and open the case.
2) Carefully remove the probe and unwrap the probe cord.
3) Put the probe in the probe holder.
DO NOT allow the probe head to hang free. Impact to the probe head could result in irreparable
damage. Use the integrated cable management hook to wrap the cord.
4) Hold the probe connector vertically with the cable pointing upward.
5) Turn the connector locking handle to the left.
6) Align the connector with the probe port and carefully push into place.
7) Turn the connector locking handle to the right to secure the probe connector.
8) Carefully position the probe cord so it is free to move and is not resting on the floor.
3-30Section 3-7 - Completing the Set Up
Page 99
GEDRAFTLOGIQ P9/P7
CAUTION
CAUTION
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
3-7-4-2Connecting the CW Pencil Probe
Insert the probe connector into the probe port all the way seated in. Carefully position the probe cord so
it is free to move and is not resting on the floor.
3-7-4-3Cable Handling
Take the following precautions with probe cables:
•Keep free from wheels
•Do not bend the cable acutely
•Avoid crossing cables between probes.
3-7-4-4Activating the Probe
To activate the probe, select the appropriate probe from the probe indicators on the touch panel.
The probe's default settings for the mode and selected exam are used automatically.
Make sure that the probe and application names displayed on the screen correspond to the
!! CAUTION:
actual probe and application selection.
3-7-4-5Deactivating the Probe
When deactivating the probe, the probe is automatically placed in standby mode.
To deactivate a probe:
1) Ensure the LOGIQ™ P9/P7
2) Gently wipe the excess gel from the face of the probe.
3) Ensure that the probe is placed gently in the probe holder.
3-7-4-6Disconnecting the Probe
Probes can be disconnected at any time. However, the probe should not be active when disconnecting
the probe.
1) Ensure the probe is deactivated. Deactivate by selecting another probe or pressing Freeze.
2) Move the probe locking handle to the left.
3) Pull the probe connector straight out of the probe port carefully.
DO NOT allow the probe head to hang free. Impact to the probe head could result in irreparable
!! CAUTION:
damage. Use the integrated cable management hook to wrap the cord.
4) Ensure the cable is free.
5) Be sure that the probe head is clean before placing the probe in its storage box.
is in freeze mode. If necessary, press the Freeze key.
Chapter 3 - Setup Instructions3-31
Page 100
GERAFTLOGIQ P9/P7
NOTICE
D
IRECTION5604324, REVISION11DRAFT (JANUARY 24, 2019) SERVICE MANUAL
Section 3-8
Printer Installation
NOTE:For Connection schemes refer to Section 3-6 "Connection of Auxiliary Devices" on page 3-11.
For further installation instructions see:
•Section 3-8-1 "Installing Digital Black & White Printer Sony UP-D898" on page 3-32
•Section 3-8-2 "Installing Digital Color Printer Sony UP-D25MD" on page 3-27
•Section 3-8-5 "Adjustment of Printer Settings" on page 3-37
3-8-1Installing Digital Black & White Printer Sony UP-D898
1) Power off/Shutdown the system as described in: Section 3-7-3 on page 3-25.
2) Physically connect the printer cables as described on Section 3-6-2 on page 3-13.
After boot up of the system, verify the correct settings in the printer “Properties”,
!! NOTICE:
see: Section 3-8-4 "Adding Printer to the system" for assigning the Printer to the remote keys P1
P3
, P4, P5 and/or P6, and
see: Section 3-8-5 "Adjustment of Printer Settings" .
, P2,
3-32Section 3-8 - Printer Installation
Loading...
+ hidden pages
You need points to download manuals.
1 point = 1 manual.
You can buy points or you can get point for every manual you upload.