GE MEDICAL SYSTEMS
DIRECTION 2407381, REVISION 7LOGIQ™ 5 PRO SERVICE MANUAL
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GE MEDICAL SYSTEMS
GE Medical Systems: Telex 3797371
P.O. Box 414; Milwaukee, Wisconsin 53201, U.S.A.
(Asia, Pacific, Latin America, North America)
GE Ultraschall:Tel: +49 (0) 212 28 02 207
Deutschland GmbH & Co KG
Beethovenstrabe 239, Postfach 11 05 60
D-42655 Solingen, Germany
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GE MEDICAL SYSTEMS
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IRECTION 2380207, REVISION 7LOGIQ™ 5 PRO SERVICE MANUAL
Important Precautions
• THIS SERVICE MANUAL IS AVAILABLE IN ENGLISH ONLY.
• IF A CUSTOMER’S SERVICE PROVIDER REQUIRES A LANGUAGE OTHER THAN
ENGLISH, IT IS THE CUSTOMER’S RESPONSIBILITY TO PROVIDE
TRANSLATION SERVICES.
WARNING
AVERTISSEMENT
• 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, MéCA NIQUES OU AUTRES.
WARNUNG
• 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 D IE SES
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.
ii-i
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GE MEDICAL SYSTEMS
DIRECTION 2380207, REVISION 7LOGIQ™ 5 PRO SERVICE MANUAL
• ESTE MANUAL DE SERVICIO SóLO EXISTE EN INGLéS.
• SI ALGúN PROVEEDOR DE SERVICIOS AJENO A GEMS 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
AVISO
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
GEMS, SOLICITAR ESTES MANUAIS NOUTRO IDIOMA, é DA
RESPONSABILIDADE DO CLIENTE FORNECER OS SERVIçOS DE TRADUç ãO.
ATENÇÃO
• 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 SEGURANç A
DO TéCNICO, OPERADOR OU PACIENTE DEVIDO A‘ CHOQUES ELéTRICOS,
MECâNICOS OU OUTROS.
AVVERTENZA
• IL PRESENTE MANUALE DI MANUTENZIONE è DISPONIBILE SOLTANTO IN
INGLESE.
• SE UN ADDETTO ALLA MANUTENZIONE ESTERNO ALLA GEMS RICHIEDE IL
MANUALE IN UNA LINGUA DIVERSA, IL CLIENTE è TENUTO A PROVVEDERE
DIRETTAMENTE ALLA TRADUZIONE.
• SI PROCEDA ALLA MANUTENZIONE DELL’APPARECCHIATURA SOLO DOPO
AVER CONSULTATO IL PRESENTE MANUALE ED AVERNE COMPRESO IL
CONTENUTO.
• NON TENERE CONTO DELLA PRESENTE AVVERTENZA POTREBBE FAR
COMPIERE OPERAZIONI DA CUI DERIVINO LESIONI ALL’ADDETTO ALLA
MANUTENZIONE, ALL’UTILIZZATORE ED AL PAZIENTE PER FOLGORAZIONE
ELETTRICA, PER URTI MECCANICI OD ALTRI RISCHI.
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IRECTION 2380207, REVISION 7LOGIQ™ 5 PRO SERVICE MANUAL
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GE MEDICAL SYSTEMS
DIRECTION 2380207, REVISION 7LOGIQ™ 5 PRO 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 position ing of the equipment at the site prepared for the
equipment shall be performed by licensed electrical contractors. Othe r conn ections between pieces o f
electrical equipment, calibrations and testing sh all be perfo rm ed by qu a lifie d GE Me dic al Syst em s
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 Medical Systems Global Documentation Group with specific information listing the system type,
manual title, part number, revision number, page number and suggestion details. Ma il the information
to : Service Documentation, 9900 Innovation Drive (RP-2123), Wauwatosa, WI 53226, USA.
GE Medical Systems employees should use the iTrak System to report all documentation errors or
omissions.
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GE MEDICAL SYSTEMS
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IRECTION 2380207, REVISION 7LOGIQ™5 PRO 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 Medical Systems.
GE Medical Systems may revise this publication from time to time without written notice.
TRADEMARKS
All products and their name brands are trademarks of their respective holders.
IRECTION 2380207, REVISION 7LOGIQ™ 5 PRO 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™ 5 PRO scanner. 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
EMC, EMI, and ESD
Customer Assistance
1-1-2Purpose of Service Manual
This Service Manual provides installation and service information for the LOGIQ™ 5 PRO Ultrasound
Scanning System and contains the following chapters:
1.) Chapter 1 - Introduction: Contai ns a content summary and warnings.
2.) Chapter 2 - Pre-Installation: Contains pre-installation requirements for the LOGIQ™ 5 PRO.
4.) Chapter 4 - Functional Checks: Contains functional checks that are recommended as part of the
installation, or as required during servicing and periodic maintenance.
5.) Chapter 5 - Components and Functions (Theory): Contains block diagrams and functional
explanations of the electronics.
6.) Chapter 6 - Service Adjustments: Contains instructions on how to make availa ble adjustments to
the LOGIQ™ 5 PRO.
7.) Chapter 7 - Diagnostics/Troubleshooting: Provides procedu res for running diagnostic or related
routines for the LOGIQ™ 5 PRO.
8.) Chapter 8 - Replacement Procedures: Provides disassembly procedures and reassembly
procedures for all changeable Field Replaceable Units (FRU).
9.) Chapter 9 - Renewal Parts: Contains a complete list of field replaceable parts for the LOGIQ™ 5
PRO.
10.)Chapter 10 - Care & Maintenance: Provides periodic maintenance procedures for the LOGIQ™ 5
PRO.
1-1
1-3
1-12
1-18
1-19
Chapter 1 Introduction1-1
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GE MEDICAL SYSTEMS
DIRECTION 2380207, REVISION 7LOGIQ™ 5 PRO SERVICE MANUAL
•Contractors (Some parts of Chapter 2 - Pre-Installation)
1-1-4LOGIQ™ 5 PRO Models Covered by this Manual
Table 1-2 LOGIQ™ 5 PRO Model Designations
Part NumberDescription
2381304LOGIQ™ 5 PRO Console for Japan
2381301LOGIQ™ 5 PRO Console for USA
2381302LOGIQ™ 5 PRO Console for Europe
2381303LOGIQ™ 5 PRO Console for Korea
1-1-5Purpose of Operator Manual(s)
The Operator Manual(s) should be fully rea d and understood before operating the L OGIQ™ 5 PRO and
also kept near the unit for quick reference.
1-2Section 1-1 - Overview
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Section 1-2
Important Conventions
1-2-1Conventions Used in Book
Icons
Pictures, or icons, are used wherever they reinforce the printed message. The icons, labels and
conventions used on the product and in the service information are described in this chapter.
Safety Precaution Messages
Various levels of safety precaution messages may be found on the equipment and in the service
information. The different levels of concern are identi fied by a flag word that precedes the precautionary
message. Known or potential hazards are labeled in one of following ways:
DANGER
DANGER IS USED TO INDICATE THE PRESENCE OF A HAZARD THAT WILL
CAUSE SEVERE PERSONAL INJURY OR DEATH IF THE INSTRUCTIONS ARE
IGNORED.
WARNINGWARNING
CAUTION
NOTICE
NOTE:Notes provide important information about an item or a procedure.
WARNING IS USED TO INDICATE THE PRESENCE OF A HAZARD THAT CAN CAUSE
SEVERE PERSONAL INJURY AND PROPERTY DAMAGE IF INSTRUCTIONS ARE
IGNORED.
Caution is used to indicate the presence of a hazard that will or can cause minor personal injury
and property damage if instructions are ignored.
Equipment Damage Possible
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
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GE MEDICAL SYSTEMS
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DIRECTION 2380207, REVISION 7LOGIQ™ 5 PRO 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.
Table 1-3 Standard Hazard Icons
ELECTRICALMECHANICALRADIATION
LASERHEATPINCH
LASER
LIGHT
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
TAG
&
LOCKOUT
Date
Signed
EYE
PROTECTIO
1-4Section 1-2 - Important Conventions
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GE MEDICAL SYSTEMS
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IRECTION 2380207, REVISION 7LOGIQ™ 5 PRO SERVICE MANUAL
1-2-3Product Icons
The following table describes the purpose and locatio n of safety labe ls and other importan t 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 (IPX8)
Manufacturer's name and address
Date of manufacture
Model and serial numbers
Electrical ratings
Laboratory logo or labels denoting
conformance with industry safety standards
such as UL or IEC.
Used to indicate the degree of safety or protection.
Indicates the degree of protection provided by
the enclosure per IEC 529. IPX8 indicates drip
proof.
Equipment Type BF (man in the box symbol)
IEC 878-02-03 indicates B Type equipment
having even more electrical isolation than
standard Type B equipment because it is
intended for intimate patient contact.
Equipment Type CF (heart in the box symbol)
IEC 878-02-05 indicates equipment having a
high degree of protection suitable for direct
cardiac contact.
Rear of console near power inlet
Under monitor
On each probe
Rear of console
Under front of monitor
Footswitch
Probe connectors
PCG connector
or Rear of Console
ECG connector
Surgical probes
"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.
"CAUTION - Dangerous voltage" (the lightning
flash with arrowhead in equilateral triangle) is
used to indicate electric shock hazards.
Chapter 1 Introduction1-5
Various
Various
Various
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GE MEDICAL SYSTEMS
DIRECTION 2380207, REVISION 7LOGIQ™ 5 PRO SERVICE MANUAL
Table 1-5 Product Icons (Continued)
LABEL/SYMBOLPURPOSE/MEANINGLOCATION
"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.
"ON" Indicates the power on position of the
power switch.
CAUTION
This Power Switch DOES NOT ISOLATE
Mains Supply
"Protective Earth" Indicates the protective
earth (grounding) terminal.
Rear of system adjacent to mains switch
Adjacent to On-Off/Standby Switch
Front Panel Switch
Internal
"Equipotentiality" Indicates the terminal to be
used for connecting equipotential conductors
when interconnecting (grounding) with other
equipment.
Rear of console
1-6Section 1-2 - Important Conventions
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1-2-4WEEE Label
The following table describes the meaning of WEEE label and its translation provided on the equipment.
Table 1-6 WEEE Label
LABEL/SYMBOLLANGUAGEPURPOSE/MEANING
This symbol indicates that the waste of electrical and electronic equipme nt must
English
Czech (CZE)
not be disposed as unsorted municipal waste and must be collected separately.
Please contact an authorized representative of the manufactu rer for infor mation
concerning the decommissioning of your equi pme n t.
Tento symbol znamená, že díly elektrických nebo elektronických zařízení
nesmí být likvidovány do netříděného odpadu, ale musí být likvidovány
samostatně. Obraťte se prosím na autorizovaného představitele výrobce,
který poskytne informace týkající se likvidace vašeho přístroje.
Danish (DAN)
Dutch (DUT)
Catalan (CAT)
Chinese (CHN)
Dette symbol angiver, at elektrisk og elektronisk affald ikke må
bortskaffes som usorteret brændbart affald, men skal indsamles særskilt.
Kontakt venligst en autoriseret repræsentant for producenten for at få
oplysninger om, hvordan dit udstyr skal bortskaffes.
Dit symbool geeft aan dat het afval van elektrische en elektronische
apparatuur niet ongescheiden mag worden meegegeven met het
huisvuil, maar apart moet worden ingeleverd. Neem contact op met een
erkende vertegenwoordiger van de fabrikant voor informatie over het
inleveren van uw apparatuur.
Aquest símbol indica que els residus dels equips elèctrics i electrònics
s'han d'abocar per separat, no com a residus municipals no classificats.
Contacteu amb un representant autoritzat del fabricant per obtenir
informació sobre com desfer-vos del vostre equip.
Estonian (EST)
See märk näitab, et tarbetuks muutunud elektri- ja elektroonikaseadmeid
ei tohi ära visata sortimata olmejäätmetena, vaid need tuleb eraldi kokku
koguda. Seadmete käitlemise kohta küsige lisateavet tootja volitatud
esindajalt.
Chapter 1 Introduction1-7
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GE MEDICAL SYSTEMS
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DIRECTION 2380207, REVISION 7LOGIQ™ 5 PRO SERVICE MANUAL
Table 1-6 WEEE Label(Continued)
LABEL/SYMBOLLANGUAGEPURPOSE/MEANING
Tämä kuvatunnus ilmaisee, että sillä merkittyä sähkö- ja
Finnish (FIN)
elektroniikkalaitetta ei saa hävittää lajittelemattomana yhdyskuntajätteenä
vaan se on kerättävä talteen erikseen. Ota yhteyttä tuotteen valmistajan
valtuuttamaan myyntiedustajaan ja kysy lisätietoja laitteen käytöstä
poistosta.
Ce symbole indique que les déchets relatifs à l'équipement électrique et
French- France
(FRA)
électronique ne doivent pas être jetés comme les ordures ménagères
non-triées et doivent être collectés séparément. Contactez un repré
sentant agréé du fabricant pour obtenir des informations sur la mise au
rebut de votre équipement.
Dieses Symbol kennzeichnet elektrische und elektronische Geräte, die
nicht mit dem gewöhnlichen, unsortierten Hausmüll entsorgt werden dü
German (GER)
rfen, sondern separat behandelt werden müssen. Bitte nehmen Sie
Kontakt mit einem autorisierten Beauftragten des Herstellers auf, um
Informationen hinsichtlich der Entsorgung Ihres Gerätes zu erhalten.
Greek (GRE)
Hungarian
(HUN)
Icelandic (ICE)
Αυτό το σύµβολο υποδηλώνει ότι τα απόβλητα ηλεκτρικού και ηλεκτρονικού εξ
οπλισµού δεν πρέπει να απορρίπτονται ως κοινά απορρίµατα, αλλά να συλλέγον
ται ξεχωριστά. Παρακαλούµε επικοινωνήστε µε έναν εξουσιοδοτηµένο αντιπρό
σωπο του κατασκευαστή για πληροφορίες σχετικά µε την απόρριψη του εξοπλισ
ού.
A szimbólum azt jelzi, hogy az elektromos és elektronikus készülék hulladékát
tilos nem szelektív lakossági hulladékként kezelni, hanem elkülönítve kell gyű
jteni. Kérjük, a berendezés leselejtezését illetőleg lépjen kapcsolatba a gyártó
hivatalos ké
viseletével.
Merki þetta táknar að rafeindatækjum skal eytt á sérstakan máta, ekki m
á losa rafeindatæki í hefðbundin sorphirðuílát sem óflokkað sorp.
Vinsamlega hafið samband við umboðsmann framleiðanda fyrir upplý
singar um hvernig tækinu skal eytt.
1-8Section 1-2 - Important Conventions
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GE MEDICAL SYSTEMS
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IRECTION 2380207, REVISION 7LOGIQ™ 5 PRO SERVICE MANUAL
Table 1-6 WEEE Label(Continued)
LABEL/SYMBOLLANGUAGEPURPOSE/MEANING
Questo simbolo indica che i rifiuti derivanti da apparecchiature elettriche ed
Italian (ITA)
elettroniche non devono essere smaltiti come rifiuti municipali indifferenziati e
devono invece essere raccolti separatamente. Per informazioni relative alle
modalità di smantellamento delle apparecchiature fuori uso, contattare un
ra
resentante autorizzato del fabbricante.
Japanese
(JPN)
Šis apzīmējums norāda, ka no elektriskā un elektroniskā aprīkojuma
Latvian (LAT)
atkritumiem nedrīkst atbrīvoties kā no nešķirotiem mājsaimniecības
atkritumiem un tie ir jāsavāc atsevišķi. Lūdzu, sazinieties ar pilnvarotu raž
otāja pārstāvi, lai saņemtu informāciju par aprīkojuma ekspluatācijas pā
rtraukšanu.
Lithuanian
(LIT)
Norwegian
(NOR)
Polish (POL)
PortugueseBrazilian (POB)
Šis simbolis nurodo, kad elektros ir elektroninės įrangos atliekos turi būti
surenkamos atskirai ir negali būti šalinamos kaip nerūšiuotos savivaldybė
s tvarkomos atliekos. Informacijos apie įrangos veikimo sustabdymą
kreipkitės į įgaliotąjį gamintojo atstovą.
Dette symbolet angir at elektrisk og elektronisk utstyr ikke skal kastes
som restavfall, men må leveres inn separat. Ta kontakt med en autorisert
representant for produsenten hvis du vil ha informasjon om hvordan
utstyret skal avhendes.
Ten symbol oznacza, iż składowanie zużytych urządzeń elektrycznych i
elektronicznych wraz z ogólnymi odpadami miejskimi jest zabronione.
Informacji na temat miejsc składowania tego typu odpadów udziela
producent sprzętu.
Este símbolo indica que os resíduos do equipamento elétrico e eletrônico
não devem ser descartados no sistema de coleta de lixo municipal, e sim
coletados separadamente. Favor entrar em contato com um
representante autorizado do fabricante para obter informações sobre
como descartar seu equipamento.
Chapter 1 Introduction1-9
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DIRECTION 2380207, REVISION 7LOGIQ™ 5 PRO SERVICE MANUAL
Table 1-6 WEEE Label(Continued)
LABEL/SYMBOLLANGUAGEPURPOSE/MEANING
Acest simbol indică faptul că deşeurile de echipamente electrice şi
Romanian
(ROM)
electronice nu au voie să fie aruncate nediferenţiat ca gunoi menajer şi c
ă ele trebuie colectate separat. Vă rugăm să luaţi legătura cu un
reprezentant autorizat al producătorului pentru a obţine informaţii
referitoare la eliminarea ecologică a echipamentului dumneavoastră.
ктронное оборудование с неотсортированным бытовым мусором. Он
о должно собираться отдельно. Для получения сведений об утилиза
ции оборудования обратитесь к авторизованному представителю ко
мпании-производителя.
Ovaj simbol označava da se otpad električne i elektronske opreme ne
Serbian (SCC)
sme odlagati zajedno sa običnim gradskim smećem, već se mora
pokupiti posebno. Molimo vas da kontaktirate ovlašćenog predstavnika
proizvođača svoje opreme, kako bi ste se informisali o njenom pravilnom
rashodu.
Slovakian
(SLK)
Slovenian
(SLN)
Spanish-Spain
(SPA)
Swedish
(SWE)
Tento symbol označuje, že odpad elektrického a elektronického materiá
lu sa nesmie vyhadzovať do netriedeného komunálneho odpadu, ale mus
í sa likvidovať oddelene. Viac informácií o likvidácii vášho zariadenia vám
poskytne poverený zástupca výrobcu.
Ta simbol obeležava da se elektronski otpad in elektronska oprema ne sme
odlagati skup z navadnim mesnim otpadom, ter se mora pobrat posebej. Prosimo
vas da kontaktirate pooblaščenega prodajalca opreme, kako bi se informirali o
n
enem pravilnem rashodu.
Este símbolo indica que el equipo eléctrico y electrónico no debe tirarse
con los desechos domésticos y debe tratarse por separado. Contacte
con el representante local del fabricante para obtener más información
sobre la forma de desechar el equipo.
Denna symbol anger att elektriska oc h elektroniska utrustningar inte få r avyttras
som osorterat hushållsavfall och måste samlas in separat. Var god kontakta en
auktoriserad tillverkarrepresentant för information angående avyttring av
utrustnin
en.
1-10Section 1-2 - Important Conventions
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Table 1-6 WEEE Label(Continued)
LABEL/SYMBOLLANGUAGEPURPOSE/MEANING
Bu sembol, elektrikli ve elektronik ekipmanların sınıflandırılmamış çöp
Turkish (TUR)
olarak atılmaması ve ayrı olarak toplanması gerektiğini belirtir. Lütfen
ekipmanınızın imhasıyla ilgili olarak üreticinin yetkili temsilcisine baş
vurun.
The symbol is affixed to a battery to advise the user or owner thar it must be recycled or disposed of
in accordance with local, state, or country laws.
English
The letter below indicates the toxic element (Pb=Lead, Cd=Cadmium, Hg=Mercury) that is contained
in the battery that may require special recycling or disposal method, Please contact a GEHC
representative to facilitate servicing, removal and disposal options.
Chapter 1 Introduction1-11
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DIRECTION 2380207, REVISION 7LOGIQ™ 5 PRO SERVICE MANUAL
Section 1-3
Safety Considerations
1-3-1Introduction
The following safety precautions must be observed duri ng 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.
Servicing should be performed by authorized personnel only.
Only personnel who have participated in a LOGIQ™ 5 PRO Training are authorized to service the
equipment.
1-3-3Mechanical Safety
WARNINGWARNING
WARNINGWARNING
WARNINGWARNING
CAUTION
CAUTION
WHEN THE UNIT IS RAISED FOR A REPAIR OR MOVED ALONG ANY INCLINE, USE
EXTREME CAUTION SINCE IT MAY BECOME UNSTABLE AND TIP OVER.
ULTRASOUND PROBES ARE HIGHLY SENSITIVE MEDICAL INSTRUMENTS THAT
CAN EASILY BE DAMAGED BY IMPROPER HANDLING. USE CARE WHEN
HANDLING AND PROTECT FROM DAMAGE WHEN NOT IN USE. DO NOT USE A
DAMAGED OR DEFECTIVE PROBE. FAILURE TO FOLLOW THESE PRECAUTIONS
CAN RESULT IN SERIOUS INJURY AND EQUIPMENT DAMAGE.
NEVER USE A PROBE THAT HAS FALLEN TO THE FLOOR. EVEN IF IT LOOKS OK,
IT MAY BE DAMAGED.
Always lower and center the Opertaor I/O Panel before moving the scanner.
The LOGIQ™ 5 PRO weighs 180 kg or more, depending on installed periphera ls, (500 lbs., or
more) when ready for use. Care must be used when moving it or replacing its parts. Failure
to follow the precautions listed could result in injury, uncontrolled motion and costly
damage.
ALWAYS:
Be sure the pathway is clear.
Use slow, careful motions.
Use two people when moving on inclines or lifting more than 16 kg (35 lbs).
1-12Section 1-3 - Safety Considerations
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IRECTION 2380207, REVISION 7LOGIQ™ 5 PRO SERVICE MANUAL
1-3-3Mechanical Safety (cont’d)
NOTE:Special care should be taken when transporting the unit in a vehicle:
•Secure the unit in an upright position.
•Lock the wheels (brake)
•DO NOT use the Control Panel as an anchor point.
•Place the probes in their carrying case.
•Eject any Magneto Optical disk or CD from their drive.
CAUTION
Keep the heat venting holes on the monitor unobstructed to avoid overheating of the
monitor.
1-3-4Electrical Safety
To minimize shock hazard, the equipment chassis must be connected to an electrical ground. The
system is equipped with a three-conductor AC power cable. This must be plugged into an approved
electrical outlet with safety ground. 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.
WARNINGWARNING
DO NOT SERVICE OR DISASSEMBLE PARTS UNDER FRU UNIT LEVEL AT ANY
CIRCUMSTANCES.
Chapter 1 Introduction1-13
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GE MEDICAL SYSTEMS
DIRECTION 2380207, REVISION 7LOGIQ™ 5 PRO SERVICE MANUAL
1-3-5Label Locations
NOTE:For the symbols shown in the illustration below, refer to previous pages in this chapter.
(1)
(2)
(3)
Figure 1-1 OUTSIDE MARKINGS OF LOGIQ™ 5 PRO
(Monitor)
1.) Caution for Possible injury : “Never put any device onto the Monitor”
2.) Caution for Hazardous movement : (Inside of the OP rear Cover)
3.) Defibrillator Label ““Do not use with Defibrillator”(On optional ECG Module)
1-14Section 1-3 - Safety Considerations
Page 33
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IRECTION 2380207, REVISION 7LOGIQ™ 5 PRO SERVICE MANUAL
1-3-5Label Locations (cont’d).
(1)
(2)
(7)
220-240V 500VA Max
Including front printer panel
Europe/USA Console (220V)
100~120V 500VA Max
Including front printer panel
Japan/USA/Asia Console (100~120V)
(9)
(3)
(4)
(5)
(6)
(8)
Circuit Breaker
On
AC Line Input
100-120V~ 50/60Hz
1250VA Max
I
or
AC Line Input
220-240V~ 50/60Hz
Off
1250VA Max
Figure 1-2 OUTSIDE MARKINGS OF LOGIQ™ 5 PRO
1.) Possible Shock Hazard
2.) Label -”Do not use the following devices near this equ ipm e nt .”
3.) Label - “The equipment weighs approximately 180kg.
4.) Prescription Devices
5.) CE Mark Label
6.) CISPR Label
7.) Voltage Range Indication Label
8.) Power Indication Label
9.) Grounding reliability Label.
Circuit Breaker
On
I
Off
(Rear)
Chapter 1 Introduction1-15
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GE MEDICAL SYSTEMS
LOGIQ 5 PRO
DIRECTION 2380207, REVISION 7LOGIQ™ 5 PRO SERVICE MANUAL
1-3-5Label Locations (cont’d)
GE ULTRASOUND KOREA LTD.
LOGIQ 5 PRO
1250VA
(2)
LOGIQ 5 PRO
GE ULTRASOUND KOREA
(7)
(1)
(6)
China 220V Console
LOGIQ 5 PRO
(3)
(4)
(5)
1250VA
LOGIQ 5 PRO
120V
1250VA
GE ULTRASOUND Korea
LOGIQ 5 PRO
Korea 220V Console
Figure 1-3 OUTSIDE MARKINGS OF LOGIQ™ 5 PRO
1.) UL Label
2.) Identification and Rating Plate - USA/Asia 120V Console
3.) Identification and Rating Plate - Europe/Asia/Latin America 220V Console
4.) Identification and Rating Plate - Japan 100V Console
5.) Identification and Rating Plate - Korea 220V Console
6.) Caution EIAJ Label
7.) Identification and Rating Plate - China 220V Console
1-16Section 1-3 - Safety Considerations
Page 35
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IRECTION 2380207, REVISION 7LOGIQ™ 5 PRO SERVICE MANUAL
1-3-6Dangerous Procedure Warnings
Warnings, such as the examples below, precede potentially dangerous procedures throughout this
manual. Instructions contained in the warnings must be followed.
DANGER
DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH, ARE PRESENT
IN THIS EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING
AND ADJUSTING.
WARNINGWARNING
WARNINGWARNING
EXPLOSION WARNING
DO NOT OPERATE THE EQUIPMENT IN AN EXPLOSIVE ATMOSPHERE.
OPERATION OF ANY ELECTRICAL EQUIPMENT IN SUCH AN ENVIRONMENT
CONSTITUTES A DEFINITE SAFETY HAZARD.
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.
1-3-7Lockout/Tagout Requirements (For USA Only)
Follow OSHA Lockout/Tagout requirements by ensuring you are in total control of the electrical Mains
plug.
Chapter 1 Introduction1-17
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GE MEDICAL SYSTEMS
DIRECTION 2380207, REVISION 7LOGIQ™ 5 PRO SERVICE MANUAL
Section 1-4
EMC, EMI, and ESD
1-4-1Electromagnetic Compatibility (EMC)
Electromagnetic compatibility describes a level of performance of a device within its electromagnetic
environment. This environment consists of the device itself and its surroundings including other
equipment, power sources and persons with which the device must interface. Inadequate compatibility
results when a susceptible device fails to perform as intended due interference from its environment or
when the device produces unacceptable levels of emission to its environment. This interference is often
referred to as radio–frequency or electromagnetic interference (RFI/EM I) an d can be rad iated th rough
space or conducted over interconnecting power of signal cables. In ad dition to electromagnetic energy,
EMC also includes possible effects from electrical fields, magnetic fields, electrostatic discharge and
disturbances in the electrical power supply.
1-4-2CE Compliance
The LOGIQ™ 5 PRO unit conforms to all applicable conducted and radiated emission limits and to
immunity from electrostatic discharge, radiated and conducted RF fields, magnetic fields and power line
transient requirements.
For applicable standards refer to the Safety Chapter in the Basic User Manual.
NOTE:For CE Compliance, it is critical that all covers, screws, sh ielding, gaskets, mesh, clamps, a re 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
WARNINGWARNING
DO NOT TOUCH ANY BOARDS WITH INTEGRATED CIRCUITS PRIOR TO TAKING
THE NECESSARY ESD PRECAUTIONS:
1.ALWAYS CONNECT YOURSELF, VIA AN ARM-WRIST STRAP, TO THE ADVISED
ESD CONNECTION POINT LOCATED ON THE REAR OF THE SCANNER (TO THE
RIGHT OF THE POWER CONNECTOR).
2.FOLLOW GENERAL GUIDELINES FOR HANDLING OF ELECTROSTATIC
SENSITIVE EQUIPMENT.
1-18Section 1-4 - EMC, EMI, and ESD
Page 37
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IRECTION 2380207, REVISION 7LOGIQ™ 5 PRO 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 User Manual, or if you
require additional assistance, please contact the loca l distributor or appropriate support resource, as
listed below.
Prepare the following information before you call:
-System ID serial number.
-Software version.
Table 1-7 Phone Numbers for Customer Assistance
LocationPhone Number
1-800–437–1171
USA/ Canada
GE Medical Systems
Ultrasound Service Engineering
4855 W. Electric Avenue
Milwaukee, WI 53219
1-800-682-5327
Customer Answer Center
1-262-524-5698
Fax: +1-414-647-4125
Latin America
GE Medical Systems
Ultrasound Service Engineering
4855 W. Electric Avenue
Milwaukee, WI 53219
Customer Answer Center
Europe
GE Ultraschall Deutschland GmbH& Co. KG
BeethovenstraBe 239
Postfach 11 05 60, D-42665 Solingen
Germany
Asia (Singapore/ Japan)
GE Ultrasound Asia
Service Department - Ultrasound
298 Tiong Bahru Road #15-01/06
Central Plaza
Singapore 169730
1-262-524-5300
1-262-524-5698
Fax: +1-414-647-4125
Tel: +49 212 2802 208
+49 212 2802 207
Fax: +49 212 2802 431
Tel: +65 291-8528
+81 426-482950
Fax: +65 272-3997
+81 426-482902
Chapter 1 Introduction1-19
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GE MEDICAL SYSTEMS
DIRECTION 2380207, REVISION 7LOGIQ™ 5 PRO SERVICE MANUAL
1-5-2System Manufacturer
Table 1-8 System Manufacturer
ManufacturerFAX Number
GE Ultrasound Korea
462-120 65-1, Sangdaewon-dong, Joong-won-Gu,
Seongnam-Si, Gyeonggi-do,
Korea
82-31-740-6436
1-20Section 1-5 - Customer Assistance
Page 39
GE MEDICAL SYSTEMS
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IRECTION 2380207, REVISION 7 LOGIQ™5 PRO SERVICE MANUAL
Chapter 2
Pre-Installation
Section 2-1
Overview
2-1-1Purpose of chapter 2
This chapter provides the information required to plan and pr epare for the installatio n of a LOGIQ™ 5 .
Included are descriptions of the facility and electrical needs to be met by the purchaser of the unit. A
checklist is also provided at the end of this section to help determine whether the proper planning and
preparation is accomplished before the actual equipment installation is scheduled.
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
2-6
Chapter 2 Pre-Installation2-1
Page 40
GE MEDICAL SYSTEMS
DIRECTION 2380207, REVISION 7LOGIQ™5 PRO SERVICE MANUAL
Section 2-2
General Console Requirements
2-2-1Console Environmental Requirements
Table 2-2 Environmental Requirements for LOGIQ™ 5 Scanners
OperationalStorageTransport
Temperature
Humidity
Pressure
o
10 - 35 oC
50 - 104
30 - 85%
non-condensing
700 - 1060hPa700 - 1060hPa700 - 1060hPa
o
F
-10 - 60
14 - 140
30 - 90%
non-condensing
C
o
F
o
-40 - 60
-40 - 140
30 - 90%
non-condensing
C
Table 2-3 Environmental Requirements for an Ultrasound Room
ItemValues
Power Source
Current Rating
Radiation Shielding
Temperature
Humidity
Heat Dissipation
Floor Landing
Floor Condition
Weight
Refer to Table 2-4 on page 2-3.
15A (120V-100V); 8A (220-240V) CIRCUIT BREAKER
NONE REQUIRED for ULTRASOUND ENERGY
20-26 DEG. C (68-79 DEG F) for PATIENT COMFORT
50% to 70% for PATIENT COMFORT
2000 BTU/Hr.
Approximately 680 - 800 kg/m2 without Accessories
Gradient: WITHIN 5 degrees
180 kg (397lbs) without Accessories
o
F
2-2-1-1Cooling
The cooling requirement for the LOGIQ™ 5 is 3500 BTU/hr. This figure doe s not include cooling needed
for lights, people, or other equipment in the room. Each person in the room places an additiona l 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 diameters can be a sour ce
of EMI which could degrade image quality. These controls should be selected to minimize possible
interface.
2-2-2Electrical Requirements
NOTE:GE Medical Systems requires a dedicated power and ground for the proper operation of its
Ultrasound equipment. This dedicated power shall originate at the last distribution panel before
the system.
2-2Section 2-2 - General Console Requirements
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GE MEDICAL SYSTEMS
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IRECTION 2380207, REVISION 7 LOGIQ™5 PRO SERVICE MANUAL
2-2-2 Electrical Requirements (cont’d)
Sites with a mains power system with defined Neutral and Live:
The dedicated line shall consist of one phase, a neutral (not shared with any other circuit), and a full
size ground wire from the distribution panel to the Ultrasound outlet.
Sites with a mains power system without a defined Neutral:
The dedicated line shall consist of one phase (two lines), not shared with any other circuit, and a full
size ground wire from the distribution panel to the Ultrasound outlet.
NOTE:Please note that image artifacts can occur, if at any time within the facility, the ground from the
main facility's incoming power source to the Ultrasound unit is only a conduit.
2-2-2-1LOGIQ™ 5 Power Requirements
The following power line parameters should be monitored for on e week before installation. We
recommend that you use an analyzer Dranetz Model 606-3 or Dranetz Model 626:
Table 2-4 Electrical Specifications for LOGIQ™ 5
PARAMETERAREALIMITS
100V100 VAC ±10% (90-110 VAC)
Voltage Range
PowerAll applicationsMAX. 1250 VA
Line FrequencyAll applications50/60Hz (±2Hz)
Power TransientsAll applications
Decaying OscillationAll applications
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 ready accessible.
CAUTION
POWER OUTAGE MAY OCCURE.
The LOGIQ™ 5 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.
Less than 25% of nominal peak voltage
for less than 1 millisecond for any type of
transient, including line frequency,
synchronous, asynchronous, or
aperiodic transients.
Less than 15% of peak voltage for less
than 1 millisecond.
2-2-2-4Site Power Outlets
A desiccated AC power outlet must be within reach of the unit without extension cords. Other outlets
adequate for the external periphera ls, medical and test equipment neede d to support this unit must al so
be present within 1 m (3.2 ft.) of the unit. Electrical insta llatio n mus t meet all current local, state, and
national electrical codes.
Chapter 2 Pre-Installation2-3
Page 42
GE MEDICAL SYSTEMS
DIRECTION 2380207, REVISION 7LOGIQ™5 PRO SERVICE MANUAL
2-2-2-5Unit Power Plug
If the unit arrives without the power plug, or with the wrong plug, you must contact your GE dealer or
the installation engineer must supply what is locally required.
2-2-2-6Power Stability Requirements
Voltage drop-out
Max 10 ms.
Power Transients
(All applications)
Less than 25% of nominal peak voltage for less than 1 millisecond for any type of transient, including
line frequency, synchronous, asynchronous, or aperiodic transients.
2-2-3EMI Limitations
Ultrasound machines are susceptible to Electromagnetic Interference (EMI) from radio frequencies,
magnetic fields, and transient in the air wiring. The y also generate EMI. The LOGIQ™ 5 complies with
limits as stated on the EMC label. However there is no guarantee that interface will not occur in a
particular installation.
Possible EMI sources should be identified before the unit is installed.
Electrical and electronic equipment may produce EMI unintentionally as the result of defect.
These sources include:
•medical lasers,
•scanners,
•cauterizing guns,
•computers,
•monitors,
•fans,
•gel warmers,
•microwave ovens,
•light dimmers,
•portable phones.
The presence of broadcast station or broadcast van may also cause interference. See for EMI
Prevention tips.
See Table 2-5 for EMI Prevention tips.
Table 2-5 EMI Prevention/abatement
EMI RuleDetails
Be aware of RF sources
Ground the unit
Keep the unit at least 5 meters or 15 feet away from other EMI sources. Special shielding
may be required to eliminate interference problems caused by high frequency, high
powered radio or video broadcast signals.
Poor grounding is the most likely reason a unit will have noisy images. Check grounding of
the power cord and power outlet.
2-4Section 2-2 - General Console Requirements
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GE MEDICAL SYSTEMS
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IRECTION 2380207, REVISION 7 LOGIQ™5 PRO SERVICE MANUAL
Table 2-5 EMI Prevention/abatement
EMI RuleDetails
After you finish repairing or updating the system, replace all covers and tighten all screws.
Replace all screws, RF
gaskets, covers, cores
Any cable with an external connection requires a magnet wrap at each end. Install the
shield over the front of card cage. Loose or missing covers or RF gaskets allow radio
frequencies to interface with the ultrasound signals.
Replace broken RF gaskets
Do not place labels where RF
gaskets touch metal
Use GE specified harnesses
and peripherals
Take care with cellular phones Cellular phones may transmit a 5 V/m signal; that could cause image artifacts.
Properly dress peripheral
cables
If more than 20% or a pair of fingers on the RF gaskets are broken, replace the gaskets.
Do not turn on the unit until any loose metallic part is removed.
Never place a label where RF gaskets meet the unit. Otherwise, the gap created will permit
RF leakage. Or, if a label has been found in such a position, move the label.
The interconnect cables are grounded and require ferrite beads and other shielding. Also,
cable length, material, and routing are all important; do not change from what is specified.
Do not allow cables to lie across the top of the card cage or hang out of the peripheral bays.
Loop the excess length for peripheral cables inside the peripheral bays. Attach the monitor
cables to the frame.
2-2-4Scan Probe Environmental Requirements
Operation:10° to 35° C
Storage:--10° to 60° C
NOTE:Temperature in degrees C. Conversion to Degrees F = (Degrees C * 9/5) + 32).
NOTICE
SYSTEMS AND ELECTRONIC PROBES ARE DESIGNED FOR STORAGE TEMPERATURES
OF -20 TO + 50 degrees C. WHEN EXPOSED TO LARGE TEMPERATURE VARIATIONS, THE
PRODUCT SHOULD BE KEPT IN ROOM TEMPERATURE FOR 10 HOURS BEFORE USE.
Chapter 2 Pre-Installation2-5
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GE MEDICAL SYSTEMS
DIRECTION 2380207, REVISION 7LOGIQ™5 PRO SERVICE MANUAL
Section 2-3
Facility Needs
2-3-1Purchaser Responsibilities
The work and materials needed to prepare the site is the responsibility of the purchaser. Delay,
confusion, and waste of manpower can be avoided by completing pre installation work before delivery.
Use the PreInstallation checklist to verify that all needed steps have been taken.
Purchaser reasonability includes:
•Procuring the materials required.
•Completing the preparations befo re de livery of the ultrasound system.
•Paying the costs for any alternations and modifications not specifically provided in the sales
contract.
NOTE:All electrical installation that are preliminary to the positioning of the equipment at the site
prepared for the equipment must be performed by licensed electrical contractors. Other
connections between pieces of electrical equipment, products involved (and the accompanying
electrical installations) are highly sophisticated and special engineering competence is
required. All electrical work on these product must comply with the requirements of applicable
electrical codes. The purchaser of GE equipment must only utilize qualified personnel to
perform electrical servicing on the equipment.
The desire to use a non-listed or customer provided product or to place an approved product further
from the system than the interface kit allows pr esents challenges to the installation team. To avoid
delays during installation, such variances should be made known to the individuals or gr oup performing
the installation at the earliest possible date (preferable prior to purchase).
The ultrasound suite must be clean pr o of to delivery of the machine. Carpet is not recommended
because it collects dust and creates static. Potential sources of EMI (electromagnetic interference)
should also be investigated before delivery. Dirt, static, and EMI can negatively impact system.
2-3-2Required Features
NOTE:GE Medical Systems requires a dedicated power and ground for the proper operation of its
Ultrasound equipment. This dedicated power shall originate at the last distribution panel before
the system.
Sites with a mains power system with defined Neutral and Live:
The dedicated line shall consist of one phase, a neutral (not shared with any other circuit), and a full
size ground wire from the distribution panel to the Ultrasound outlet.
Sites with a mains power system without a defined Neutral:
The dedicated line shall consist of one phase (two lines), not shared with any other circuit, and a full
size ground wire from the distribution panel to the Ultrasound outlet.
Please note that image artifacts can occur, if at any time within the facility, the ground from the main
facility's incoming power source to the Ultrasound unit is only a conduit.
•Dedicated single branch power outlet of adequate amperage meeting all local and national codes
which is located less than 2.5 m (8 ft.) from the unit’s proposed location
•Door opening is at least 76 cm (30 in) wide
•Proposed location for unit is at least 0.3 m (1 ft.) from the wall for cooling
•Power outlet and place for any external peripheral are within 2 m (6.5 ft.) of each other with
peripheral within 1 m of the unit to connect cables.
2-6Section 2-3 - Facility Needs
Page 45
GE MEDICAL SYSTEMS
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IRECTION 2380207, REVISION 7 LOGIQ™5 PRO SERVICE MANUAL
NOTE:The LOGIQ™ 5 has four outlets inside the unit. One is for the monitor and three for on board
peripherals.
•Power outlets for other medical equipment and gel warmer
•Power outlets for test equipment and modem within 1 m (3.2 ft.) of unit
•Clean and protected space to store transducers (in their cases or on a rack)
•Material to safely clean probes (done with a plastic container, never metal)
Chapter 2 Pre-Installation2-7
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GE MEDICAL SYSTEMS
DIRECTION 2380207, REVISION 7LOGIQ™5 PRO SERVICE MANUAL
2-3-3Desirable Features
•Door is at least 92 cm (3 ft.) wide
•Circuit breaker for dedicated power outlet is easily accessible
•Sink with hot and cold water
•Receptacle for bio–hazardous waste, like used probe sheaths
•Emergency oxygen supply
•Storage for linens and equipment
•Nearby waiting room, lavatory, and dressing room
•Dual level lighting (bright and dim)
•Lockable cabinet ordered by GE for its software and proprietary manuals.
2-8Section 2-3 - Facility Needs
Page 47
GE MEDICAL SYSTEMS
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IRECTION 2380207, REVISION 7 LOGIQ™5 PRO SERVICE MANUAL
2-3-4Recommended and Alternate Ultrasound Room Layout
Recommended standard floor plan and a minimal floor plan for ultrasound equipment:
DEDICATED ALALOG TELEPHONE
LINE FOR CONNECTION TO INSITE
ROOM,
PROCESSING
FILM
DEDICATED
POWER
RECEPTACLE
18 IN.
(46 CM)
CONSOLE
LINEN SUPPLY
FILM VIEWER
FILM SUPPLIES
FILE
CABINET
SECRETARYS OR
DOCTOR’S DESK
SINK
FILM VIEWER
COUNTER TOP
COUNTER
TOP
SINK
SUCTION LINE
EMERGECY
OXYGEN
OVERHEAD
LIGHTS DIMMER
A 14 by 17 foot Recommended Floor Plan
LINEN SUPPLY
PROBES/SUPPLIES
FOOT
SW
STOOL
EXAMINATION
TABLE
76 IN.
(193 CM)
24 IN.
(61 CM)
PATIENT
TOILET
FACILITY
DOOR
42 IN.
(107 CM)
Scale : Each square equals one square foot
EXTERNAL
PERIPHERALS
DEDICATED POWER
OUTLETS
DEDICATED ANALOG TELEPHONE
LINE FOR CONNECTION TO INSITE
GE CABINET
FOT SOFTWARE
AND MANUALS
DOOR
30 IN.
(76 CM)
24 IN.
(61 CM)
FOOT
SW
STOOL
EXAMINARION
TABLE
LOGIQ 5
CONSOLE
76 IN.
(193 CM)
An 8 by 10 foot Minimal Floor Plan
Figure 2-1 RECOMMENDED ULTRASOUND ROOM LAYOUT
Chapter 2 Pre-Installation2-9
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GE MEDICAL SYSTEMS
DIRECTION 2380207, REVISION 7LOGIQ™5 PRO SERVICE MANUAL
2-3-5Networking Pre-installation Requirements
2-3-5-1Purpose of DICOM Network Function
DICOM services provide the operator with clinically useful features for moving images and patient
information over a hospital network. Examples of DICOM services include the transfer of images to
workstations for viewing or transferring images to remote printers. As an added benefit, transferring
images in this manner free up the o n-board monitor and peripherals, enabling viewing to be done while
scanning continues. With DICOM, images can be archived, stored, and retrie ve d faster, ea sie r, and at
a lower cost.
2-3-5-2DICOM Option Pre-installation Requirements
To configure the LOGIQ™ 5 to work with other network connections, the site’s network administrator
must provide some necessary information.
Information must include:
•A host name, local port number, AE Title, IP address and Net Mask for the LOGIQ™ 5 .
•The IP addresses for the default gateway and other routers at the site for ROUTING
INFORMATION.
•The host name, IP address, port and AE Title for each device the site wants connected to the
LOGIQ™ 5 for DICOM APPLICATION INFORMATION. A field for the make (manufacturer) and
the revision of the device, is also included. This information may be useful for solving errors.
2-10Section 2-3 - Facility Needs
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GE MEDICAL SYSTEMS
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IRECTION 2380207, REVISION 7 LOGIQ™5 PRO SERVICE MANUAL
Figure 2-2 Worksheet for DICOM Network Information
Chapter 2 Pre-Installation2-11
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GE MEDICAL SYSTEMS
DIRECTION 2380207, REVISION 7LOGIQ™5 PRO SERVICE MANUAL
2-12Section 2-3 - Facility Needs
Page 51
GE MEDICAL SYSTEMS
D
IRECTION2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
Chapter 3
Installation
Section 3-1
Overview
3-1-1Purpose of Chapter 3
This chapter contains information needed to install the unit. Included are references to a procedure that
describes how to receive and unpack the equipment and how to file a damage or loss claim.
How to prepare the facility and unit of the actual installation, and how to check and test the unit, probes,
and external peripherals for electrical safety are included in this procedure. Also included in this section
are guidelines for transporting the unit to a new site.
Table 3-1 Contents in Chapter 3
SectionDescriptionPage Number
3-1Overview3-1
3-2Installation Reminders3-2
3-3Receiving and Unpacking the Equipment3-4
3-4Preparing for Installation3-9
3-5Completing the Installation3-11
3-6System Configuration3-16
3-7Available Probes3-24
3-8Software/Option Configuration3-24
3-9Connectivity Installation Worksheet3-25
3-9Connectivity Installation Worksheet3-25
3-10Insite IP Address Configuration3-25
3-11Loading Base System Software3-25
3-10Paperwork3-26
Chapter 3 Installation3 - 1
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DIRECTION2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
Section 3-2
Installation Reminders
3-2-1Average Installation Time
Table 3-2 Average Installation Time
DescriptionAverage Installation TimeComments
Unpacking the scanner
Scanner wo/options
DICOM Option
InSite Option
0.5 hour
0.5 hour
0.5 hour
0.5 hour
Dependant on the configuration that is required
Dependant on the amount of configuration
The LOGIQ™ 5 PRO has been designed to be installed and checked out by an experienced service
technician in approximately four hours. LOGIQ™ 5 PRO consoles with optional equipment may take
slightly longer.
3-2-2Installation Warnings
1.) Since the LOGIQ™ 5 PRO weighs approximately 180 kg. (397 lb.) without options, preferably two
people should unpack it. Two people are also preferable for installing any additional bulky items.
2.) There are no operator serviceable components. To prevent shock, do not remove any covers or
panels. Should problems or malfunctions occur, unplug the power cord. Only qualified service
personnel should carry out servicing and troubleshooting.
NOTE:For information regarding packing labels, refer to LABELS ON PACKAGE.
3.) After being transported, the unit may be very cold or hot. If this is the case, allow the unit to
acclimate before you turn it on. It requires one hour for each 2.5°C increment if its temperature is
below 10°C or above 40°C.
CAUTION
Equipment damage possibility. Turning the system on without acc limati on af ter a rriving a t sit e
may cause the system to be damaged.
IRECTION2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
3-2-3Safety Reminders
DANGER
CAUTION
CAUTION
CAUTION
CAUTION
CAUTION
CAUTION
CAUTION
WHEN USING ANY TEST INSTRUMENT THAT IS CAPABLE OF OPENING THE
AC GROUND LINE (I.E., METER’S GROUND SWITCH IS OPEN), DON’T TOUCH
THE UNIT!
Two people should unpack the unit because of its weight. Two people are required whenev er
a part weighing 19kg (35 lb.) or more must be lifted.
If the unit is very cold or hot, do not turn on its power until it has had a chance to acclimate
to its operating environment.
To prevent electrical shock, connect the unit t o 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 c ircuits and more than 30 V pea k is
present.
Do not use a 20 Amp to 15 Amp adapter on the 120 Vac unit’s power cord. This unit requires
a dedicated 20 A circuit and can have a 15A plug if the on boa rd peripherals do not cause the
unit to draw more than 14.0 amps.
Do not operate this unit unless all board covers and frame panels are securely in place.
System performance and cooling require this.
OPERATOR MANUAL(S)
The User Manual(s) should be fully read and understood before operating the LOGIQ™ 5
PRO and kept near the unit for quick reference.
CAUTION
ACOUSTIC OUTPUT HAZARD
Although the ultrasound energy transmitted from the LOGIQ™ 5 PRO probe is within FDA
limits, avoid unnecessary exposure. Ultrasound energy can produce he at and mechanical
damage.
Figure 3-6 Environmental Labels
Chapter 3 Installation3 - 3
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DIRECTION2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
Section 3-3
Receiving and Unpacking the Equipment
When a new system arrives, check that any components are not d amaged and a re not in short su pply.
If shipping damage or shortage occurs, contact the address shown in Chapter 1.
CAUTION
CAUTION
Do not lift the unit by the Keyboard. Equipment damage may result.
The crate with the LOGIQ™ 5 PRO weighs approximately 180 kg. (397 lb.) Be prepared for a
sudden shift of weight as the unit is remove d from its base (pallet)
1.) Cut the three PLASTIC BANDs.
Plastic Bands
Figure 3-7 Cutting the Plastic Bands.
3 - 4Section 3-3 - Receiving and Unpacking the Equipment
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IRECTION2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
Section 3-3 Receiving and Unpacking the Equipment (cont’d)
2.) Lift the TOP COVER up and off.
Top Cover
Figure 3-8 Removing the top Cover
Chapter 3 Installation3 - 5
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DIRECTION2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
Section 3-3 Receiving and Unpacking the Equipment (cont’d)
3.) Remove the MONITOR CAP up and off..
Monitor Cap
Figure 3-9 Removing the monitor cap
3 - 6Section 3-3 - Receiving and Unpacking the Equipment
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IRECTION2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
Section 3-3 Receiving and Unpacking the Equipment (cont’d)
4.) Remove the three PLASTIC JOINTs from the OUTER SLEEVE
5.) Remove the OUTER SLEEVE.
6.) Remove the INNER SLEEVE.
Inner Sleeve
Plastic Joint
Outer Sleeve
Monitor Supporter
Palette Assy
Figure 3-10 Removing Plastic Joints and Sleeves
Chapter 3 Installation3 - 7
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DIRECTION2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
Section 3-3 Receiving and Unpacking the Equipment (cont’d)
7.) Remove the PLASTIC BAG.
8.) Lift the Monitor up by pressing the UP/Down Release Button.
9.) Remove the MONITOR SUPPORTER.
10.)Pull the Bottom Plate from the bottom so that it can be used as a ramp.
11.)Unlock the front caster and carefully put the console off the PALETTE.
PLASTIC BAG
Monitor
Supporter
Figure 3-11 Moving the LOGIQ™ 5 PRO from the crate
Console
Palette Base Assy
Bottom Plate
3 - 8Section 3-3 - Receiving and Unpacking the Equipment
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IRECTION2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
3-3-1Moving into Position
CAUTION
CAUTION
Do not lift the unit by the Keyboard.
Do not tilt the unit more than 5 degrees to avoid tipping it over.
To avoid injury by tipping over. Set the monitor to the lowest position before moving.
Equipment Damage Possibility. Lifting the console by holding covers may damage the covers.
Do not lift the console by holding any covers.
In general, a single adult can move the LOGIQ™ 5 PRO along an even surface with no steep grades.
At least two people should move the machine when large humps, grooves, or grades will be
encountered. (It is better to pull from the rear rather than push from the front of the unit). Before moving,
store all loose parts in the unit. Wrap transducers in soft cloth or foam to prevent damage.
Although LOGIQ™ 5 PRO is a compact and mobile machine, two people should move it over rough
surfaces or up and down grades.
3-3-2Adjusting System Clock
Set the system clock for the LOGIQ™ 5 PRO to the local time. For procedure of adjusting the system
clock, refer to section 3-6-1-1 on page 16.
Fill out proper customer Information the Product Locator Installation Card. Mail this Installation Card
“Product Locator” to the address corresponding to your pole.
3-3-3Product Locator Installation Card
NOTE:The Product Locator Installation Card shown may not be same as the provided Product Locator
card.
Figure 3-12 Product Locator Installation Card
Section 3-4
Preparing for Installation
3-4-1Verify Customer Order
Compare items received by the customer to that which is listed on the delivery order. Report any item s
that are missing, back ordered or damaged.
Chapter 3 Installation3 - 9
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DIRECTION2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
3-4-2Physical Inspection
3-4-2-1System Voltage Settings
Verify that the scanner is set to the correct voltage.
The Voltage settings for the LOGIQ™ 5 PRO Scanner is fou nd on a label to the right of the Power switch
and External I/O, on the rear of the system.For the Rating Plate example, refer to Figure 1-3 "OUTSIDE
MARKINGS OF LOGIQ™ 5 PRO" on page 1-16
WARNINGWARNING
Connecting a LOGIQ™ 5 PRO scanner to the wrong voltage level will most likely
destroy the scanner.
3-4-2-2Video Formats
Check that the video format is set to the locally used video standard, NTSC or PAL.
3-4-3EMI Protection
This Unit has been designed to minimize the effects of Electro Magnetic Interference (EMI). Many of th e
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 hard ware are installed and secure d
before the unit is put into operation.
3 - 10Section 3-4 - Preparing for Installation
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IRECTION2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
Section 3-5
Completing the Installation
3-5-1Power On/Boot Up
NOTE:After turning off the system, wait at least ten seconds before turning it on again. The system
may not be able to boot if power is recycled too quickly.
3-5-1-1Scanner Power On
1.) Connect the Main Power Cable at the rear of the System.
WARNINGWARNING
Protective earth must be taken when connecting AC power cable (200V) without its plug
to wall outlet.
2.) Connect the Main Power cable to an appropriate mains power outlet.
3.) Switch ON the Main Circuit Breaker at the rear of the System.
Main Circuit Breaker
Main Power Cable
Figure 3-13 Circuit Breaker
When power is applied to the Scanner, and the Rear Circuit breaker is turned ON, Power is dist ribute d
to the ATX smps in the Back End Processor and Power control circuit in the AC power assy . When the
Power ON/OFF key is pressed once, the power control circuit turn on the card cage and fans, and Back
End Processor ,Monitor. Backend Processor starts and its software code is distributed to initiate the
scanner.
4.) Press the ON/OFF
key at the keyboard paenl of the System once.
Chapter 3 Installation3 - 11
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DIRECTION2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
3-5-1-1 Scanner Power On (cont’d)
Composite
Serial
B/W
B/W Printer
Power
Figure 3-14 Power On/Off Switch Location
3-5-1-2Power Up Sequence
1.) The Start Up Screen will be shown on the Monitor display when the system is turned ON.
2.) After initialization is complete, default mode buttons on the keyboard are lit a nd the B-Mode screen
or Patient screen (no probes are connected) is displayed on the monitor.
Figure 3-15 Start Up Screen Display
3 - 12Section 3-5 - Completing the Installation
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IRECTION2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
3-5-1-3Maintanance Mode for Service
1.) If the service dongle is inserted in the USB port in the rear panel during system boot up,
Maintenance access window appears.
2.) Then key in the service pass word and click OK button.
3.) When the start application widow appear, click the “Maintenence” button
Figure 3-16 maintenance Window
NOTE:Start is selected automatically when it time out.
Chapter 3 Installation3 - 13
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DIRECTION2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
3-5-2Power Off/ Shutdown
NOTE:After turning off a system, wait at least ten seconds before turning it on again. The system may
not be able to boot if power is recycled too quickly.
3-5-2-1Power Shutdown
NOTICE
1.) Press once the ON/OFF
2.) Click the shutdown button in the Exit dialog box as Figure 3-17 on page 3-14
3.) Switch OFF the Main Circuit Breaker at the rear of the system Refer to Figure 3-13 on page 3-11 .
4.) Disconnect the Main Power Cable is necessary. For example : Relocating the scanner.
Disconnecting the Mains Power Cable before switching OFF the Circuit Breaker will activate the
uninterruptible power system (UPS) in the backend processor, forcing an ordered shutdown of the
system.
key at the front of the System.
Figure 3-17 System Exit Window
NOTICE
3 - 14Section 3-5 - Completing the Installation
The UPS serves only as a battery backup that allows for a soft shut-down of the scanner to prevent file
corruption. IT DOES NOT REGULATE INCOMING VOLTAGE.
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IRECTION2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
3-5-3Transducer Connection
1.) Connect a transducer to one of the three rightmost transducer receptacle as follows:
A.) Ensure that the transducer twist lock lever to the horizontal position.
B.) Insert the transducer connector on the receptacle guide pin until it touches the receptacle
mating surface.
C.) Twist the transducer twist lock lever to vertical position to lock it in place. Twist the lever
to the horizontal position to disconnect the transducer.
NOTE:It is not necessary to turn OFF power to connect or disconnect a transducer.
Chapter 3 Installation3 - 15
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DIRECTION2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
Section 3-6
System Configuration
3-6-1System Specifications
3-6-1-1System Settings
Table 3-1 System Configuration
Configuration CategoryDescription
Enables the user or service personnel to set the
Settings
1.) Press Power on/off switch.
2.) The SYSTEM EXIT window appears. Click on Logoff.
date, time, unit, language, basic information about
the organization such as the institution name and
department.
Figure 3-18 System EXIT window
3.) The message window appears. Click on OK.
4.) The OPERATOR LOGIN window appears.
Change the User level to Admin, then enter Password. Then click on Log on.
Figure 3-19 Operator LOGIN window
3 - 16Section 3-6 - System Configuration
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IRECTION2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
3-6-1-1 System Settings (cont’d)
5.) Press Utility > System.
6.) Set the Hospital name, Department, Date and Time, Language, and Units.
Click on Utilities to terminate the utility function.
3-6-1-2Physical Dimensions
The physical dimensions of the LOGIQ™ 5 PRO unit are summarized in Table 3-2 on page 3-17 .
The Size of LOGIQ™ 5 PRO, with monitor and peripherals
Table 3-2 Physical Dimensions of LOGIQ™ 5 PRO
HeightWidthDepthUnit
135 - 14552.099.0cm
53.1 - 57.0820.4738.9inches
Figure 3-20 Setting Display
Chapter 3 Installation3 - 17
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DIRECTION2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
3-6-1-2 Physical Dimensions (cont’d)
WEIGHT : 180Kg(397lbs)
including Monitor
520
NOTE: Length is in mm
Variation +/- 10%
Composite
Serial
B/W
B/W Printer
Power
1350~1450
800~900
Figure 3-21 Overall Dimensions
3-6-1-3Weight without Monitor and Peripherals
990
Table 3-3 Weight of LOGIQ™ 5 PRO With Monitor and Without Other Peripherals
ModelWeight [kg]Weight [lbs]
LOGIQ™ 5 PRO Approximately 180 Approximately 397
3-6-1-4Acoustic Noise Output:
Less than 70dB (A) according to DIN 45635 - 19 - 01 - KL2.
3-6-2Electrical Specifications
Table 3-4 Electrical Specifications for LOGIQ™ 5 PRO
IRECTION2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
3-6-3On-Board Optional Peripherals
Table 3-5 List of Recording Devices
DeviceManufacturerModelVideo Signal
B/W Video PrinterSONY
B/W Video PrinterMitsubishi
Video Cassette RecorderSONY
Video Cassette RecorderPana sonic
A6 Color Video PrinterSONY
A6 Color Video PrinterMitsubishi
A5 Color Video PrinterSONY
A5 Color PrinterMitsubishi
UP-895MDW
UPD-895
P-91(AP9500)
P91W
P91E
P91D
SVO-9500MD
SVO-9500-MDP
AG-MD835
AG-MD835P
AG-MD835E
UP-21MD
UP-21MDS
UP-D21MD
UP-D23MD
CP-900
CP900UM
CP-900E
CP-900D
UP-50
UP51MD
CP-800
CP-800UM
CP800E
NTSC/PAL
NTSC
NTSC/PAL
NTSC/PAL
NTSC
PAL
NTSC
NTSC
PAL
NTSC/PAL
NTSC
NTSC
NTSC/PAL
See each option installation instructions for installation and connection procedures.
NOTE:There are no external peripheral options for the LOGIQ™ 5 PRO
3-6-4External I/O Connector Panel
Located on the rear panel are video input and output connectors, audio input and output, camera
expose connectors, footswitch connector power connector and control connections for VCR, printer,
and service tools.
Chapter 3 Installation3 - 19
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DIRECTION2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
3-6-4 External I/O Connector Panel (cont’d)
This section indicates the pin assignment for each connector.
1
2
Serial
1 2
220-240V 500VA Max
Including front printer panel
Figure 3-22 Rear Connector Panel
NOTE:Each outer (case) ground line of peripheral/accessory connectors are protectively grounded.
Signal ground lines are not isolated, except the Service port (3). All of signal lines (include signal
GND) of the Service port are isolated.
3 - 20Section 3-6 - System Configuration
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3-6-4-1External I/O Pin Outs
Pin No.SignalPin No.Signal
1N/A6DSR
2RXD7RTS
3TXD8GTS
4DTR9 N/A
5GND
Table 3-6 Pin Assignments of RS232C for Remote 1 and Remote 2
Pin No.SignalPin No.Signal
1NC6NC
2RXD7 NC
3TXD8 NC
4NC9 RI
5GND
Table 3-7 Pin Assignments of RS232C for Service
Pin No.SignalPin No.Signal
1RED9N/A
2GREEN10SGND
3BLUE11 N/A
4N/A12N/A
5GND13HSYNC
6RGND14VSYNC
7GGND15N/A
8BGND
Table 3-8 Pin Assignments of DB15 connector for External VGA
Chapter 3 Installation3 - 21
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DIRECTION2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
3-6-4-1 External I/O Pin Outs (cont’d)
Pin No.SignalPin No.Signal
1+5 VDC3DATA +
2DATA -4GND
Table 3-9 Pin Assignments of USB
Pin No.SignalPin No.Signal
1TX+5 NC
2TX-6RX-
3RX+7 NC
4NC8NC
Table 3-10 Pin Assignments of InSite - RJ45 Male Connector
Pin No.SignalPin No.Signal
1TX+5 NC
2TX-6RX-
3RX+7 NC
4NC8NC
Table 3-11 Pin Assignments of Ethernet
Pin No.Output Signal
1PRINT*1
2Signal GND
Table 3-12 Pin Assignment of Mini-Jack for Controlling B/W Printer
Pin No.Output Signal
1SHUTTER*2
2Signal GND
Table 3-13 Pin Assignment of Mini-Jack for Controlling Color
3 - 22Section 3-6 - System Configuration
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3-6-5Video Specification
Video specifications may be needed to be able to connect laser cameras or other devices to the
LOGIQ™ 5 PRO.
Horizontal Period [µs]16.6632.0031.7826.4021.3320.68
Pixel Clock [MHz]78.7529.5024.5540.0049.5065.00
H Blank Width [µs]3.665.975.706.405.174.92
H Sync Width [µs]1.222.342.363.201.622.09
H Front Porch [µs]0.200.750.731.000.320.37
Active Horizontal Period [µs]13.0026.0326.0720.0016.1615.75
Vertical Rate [Hz]75.0350.0059.9460.3275.0060.00
Vertical Period [ms]13.3320.0016.6816.5813.3316.67
V Sync Width [lines=ms]32=0.5349=1.5745=1.4328=0.7425=0.5338=0.79
V Front Porch [lines=µs]3=50.005=160.006=190.704=105.603=64.006=124.10
GE MEDICAL SYSTEMS
DIRECTION2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
Section 3-7
Available Probes
See Specifications in the LOGIQ™ 5 PRO User Reference Manual for probes and intended use.
See Chapter 9, for part numbers to be used when ordering new or replacement probes.
Section 3-8
Software/Option Configuration
Refer to the LOGIQ™ 5 PRO Basic User Manual, Chapter 16, Customizing Your System for information
on configuring items like Hospital, Department, Language, Units (of measure), Date, Time and Date
Format.
For information on configuring Software Options, Refer to the LOGIQ™ 5 PRO Basic User Manual,
Chapter 16, Customizing Your System.
For information on configuring DICOM Connectivity, Refer to the LOGIQ™ 5 PRO Basic User Manual,
Chapter 16, Customizing Your System.
3 - 24Section 3-7 - Available Probes
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IRECTION2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
Section 3-9
Connectivity Installation Worksheet
Site System Information
Site:
Dept.:
LOGIQ SN:
CONTACT INFORMATION
Name
TCP/IP Settings
Name - AE Title:
Type:
Title
Floor:
Room:
REV:
Phone
Comments:
E-Mail Address
IP Settings
IP Address:
Subnet Mask:
Default Gateway:
Services (Destination Devices)
Device Type
1
2
3
4
5
6
7
8
9
10
11
12
Manufacturer
Name
Remote Archive Setup
Remote Archive IP:
Remote Archive Name:
IP Address
Port
AE Title
Chapter 3 Installation3 - 25
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DIRECTION2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
Section 3-10
Paperwork
NOTE:During and after installation, the documentation (i.e. User Manuals, Installation Manuals...) for the
peripheral units must be kept as part of the original system documentation. This will ensure that all
relevant safety and user information is availa b le du rin g th e op er a tion and ser vice of th e com p let e
system.
3-10-1Product Locator Installation
NOTE:The Product Locator Installation Card shown may not be same as the provided Product Locator
card.
Figure 3-23 Product Locator Installation Card
3-10-2User Manual(s)
Check that the correct User Manual(s) for the system and software revision, is included with the
installation. Specific language versions of the User Manual may also be available. Check with your GE
Sales Representative for availability.
3-10-2-1Reference off-board peripherals and options
None.
3 - 26Section 3-10 - Paperwork
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Chapter 4
Functional Checks
Section 4-1
Overview
4-1-1Purpose of Chapter 4
This chapter provides procedures for quickly checking major functions of the LOGIQ™ 5 PRO scanner
diagnostics by using the built-in service software, and power supply adjustments.
Table 4-15 Contents in Chapter 4
SectionDescriptionPage Number
4-1Overview4-1
4-2Required Equipment4-1
4-3General Procedure4-2
4-4Software Configuration Checks4-20
4-5Peripheral Checks4-21
4-6Peripheral Checks4-21
4-7Site Log4-24
\
NOTICE
Most of the information pertaining to this Functional Checks chapter is found in the LOGIQ™ 5 PRO
Quick Guide (Direction Number 2380205-100).
Section 4-2
Required Equipment
•An empty (blank) MO Disk.
•At least one transducer. See “Probe/Connectors Usage (QG)” on page 28. for an overview.
(normally you should check all the transducers used on the system.)
Chapter 4 Functional Checks4 - 1
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Section 4-3
General Procedure
CAUTION
SYSTEM REQUIRES ALL COVERS
Operate this unit only when all board covers and frame panels are securely in place. The
covers are required for safe operation, good system performance and cooling purposes.
NOTICE
Lockout/Tagout Requirements (For USA only)
Follow OSHA Lockout/Tagout requirements by ensuring you are in total co ntro l of the Po wer Ca ble
on the system.
TAG
&
LOCKOUT
Date
Signed
4-3-1Power On/Boot Up
NOTE:After turning off the system, wait at least ten seconds before turning it on again. The system
may not be able to boot if power is recycled too quickly.
4-3-1-1Scanner Power On
1.) Connect the Main Power Cable to the back of the System.
2.) Ensure the Cable Clip slips securely over the shoulders on the molded plug.
3.) Connect the Main Power cable to an appropriate mains power outlet.
4.) Switch ON the Main Circuit Breaker at the rear of the System.
4 - 2Section 4-3 - General Procedure
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4-3-1-1 Scanner Power On (cont’d)
Main Circuit Breaker
Main Power Cable
Figure 4-24 Circuit Breaker
NOTE:When power is applied to the Scanner, and the Rear Circuit breaker is turned ON, Power is
distributed to the ATX smps in the Back End Processor and Power control circuit in the AC
power assy . When the Power ON/OFF key is pressed once, the power control circuit turn on
the card cage and fans, and Back End Processor ,Monitor. Backend Processor starts and its
software code is distributed to initiate the scanner.
Chapter 4 Functional Checks4 - 3
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DIRECTION2380207, REVISION 7 LOGIQ™ 5 PRO SERVICE MANUAL
4-3-1-1 Scanner Power On (cont’d)
5.) Press the ON/OFF
key at the front of the System once.
Composite
Serial
B/W
B/W Printer
Power
Figure 4-25 Power On/Off Standby Switch Location
4-3-2Power Off / Shutdown
NOTE:After turning off a system, wait at least ten seconds before turning it on again. The system may not be
able to boot if power is recycled too quickly.
4-3-2-1Scanner shutdown
1.) Press the On/Off key at the front of the system once to display the SYSTEM - EXIT menu.
2.) Select Shutdown from the SYSTEM - EXIT menu.
Figure 4-26 System Exit Menu for System Shutdown
4 - 4Section 4-3 - General Procedure
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4-3-2-2Switch off the scanner
1.) Switch OFF the Circuit Breaker at the back of the scanner.
2.) Disconnect the Mains Power Cable is necessary. For example: Servicing or relocating the scanner.
NOTICE
Disconnecting the Mains Power Cable before switching OFF the Circuit Breaker will activate the
uninterruptible power system (UPS) in the Back End Processor, forcing an ordered shutdown of the
system.
4-3-3System Features
4-3-3-1Control Panel
Figure 4-27 Control Panel Tour
1.) Video
2.) Audio On/Off and Volume
3.) TGC
4.) Reverse
5.) Additional Feature Keys
6.) Keyboard
7.) Mode/Gain Keys
8.) Imaging/Measurement Keys
9.) Depth
Chapter 4 Functional Checks4 - 5
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4-3-3-1 Control Panel (cont’d)
10.)Imaging Feature Keys
11.)Freeze
12.)Probe and Cord Holder
13.)Gel Holder
14.)New Patient
15.)Application
16.)Report
17.)End Exam
18.)Mode Parameter
19.)Utility
20.)Top Menu control keys
21.)Submenu control keys
22.)Print keys
4-3-3-2Sub Menu Control KeysMenu Key Panel
Figure 4-28 Menu Key Tour
1.) Patient: Enter Patient screen
2.) Reports: Activates default report and Measurement Selection Menu of report choices.
3.) End Exam: Activates Image Management and Measurement Selection Menu with end of exam
options.
4.) Utility: Activates the configuration system.
5.) Applications: Select the application to use and Probe select.
6.) Mode Paramenters: To toggle between the Primary menus of different modes
7.) Top menu Controls : Activates the changes of functions in the Top menu.
8.) Sub menu controls: Activates Sub Menu for Modes and toggles/changes functions.
At the bottom of the Keypad, there are five combinat ion rotary dials/push buttons. The functionality of
these rotaries is changed, depending upon the currently displayed menu. Press the button to switch
between controls (as with Focus Position/Number), or rotate the dial to adjust the value.
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4-3-3-3Monitor Display
1234
1234
12
12
5
5
13
6
6
7
7
13
14
14
8
8
9
9
10
10
11
11
192021
192021
Figure 4-29 Monitor Display Tour
Table 4-16 Monitor Display Features
1. Institution/Hospital Name, Date, Time, Operator
Identification
3. Patient Name, Patient Identification4. GE Symbol : Probe Orientation Marker. Coincides with a
5. Image Preview6. Gray/Color Bar
7. Cine Gauge8. Measurement selection Menu
9. Image10. Measurement
11. Result window12. Imaging Paramenters by mode
13. Power Output Readout, system status14. Focal Zone
15. Depth Scale16. Body Pattern
17. TGC18. Image Management Menu : Menu, Delete, and Image
19. Image Palette20. System Messages Display
21. Trackball Fucntionality Status22.
2. Probe Identifier, Exam Study
probe orientation marking on the probe.
Manager
15
15
17
17
16
16
18
18
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4-3-4System B/M-Mode Checks
For a basic functional check of the system’s different modes, the Quick Guide will familiarize you with
image optimization for B-Mode, M-Mode, Color Flow, and Doppler.
Table 4-17 B/M-Mode Functions
Optimizes image quality and allows user to reduce beam
Power Output (Acoustic Power)
Dynamic Range
Focus Number and Position
intensity. 10% increments between 0-100%. Values greater
than 0.1 are displayed
Dynamic Range controls how echo intensities are converted to
shades of gray, thereby increasing the adjustable range of
contrast.
Increases the number of transmit focal zones or moves the
focal zone(s) so that you can tighten up the beam for a specific
area. A graphic caret corresponding to the focal zone
position(s) appears on the right edge of the image.
Rejection
Edge Enhance
Frame Average
Colorize
Gray Map
Rotation (Up/Down)Rotates the image by selecting the value from the pop up menu.
Frequency
Frame Rate/Resolution
B Flow
Selects a level below which echoes will not be amplified (an
echo must have a certain minimum amplitude before it will be
processed).
Edge Enhance brings out subtle tissue differences and
boundaries by enhancing the gray scale differences
corresponding to the edges of structures. Adjustments to M
Mode's edge enhancement affects the M Mode only.
Temporal filter that averages frames together. This has the
effect of presenting a smoother, softer image.
Enables gray scale image colorization. To deactivate, reselect
a Gray Map.
Determines how the echo intensity levels received are
presented as shades of gray.
Multi Frequency mode lets you
downshift to the probe's next lower
frequency or shift up to a higher
frequency.
Optimizes B Mode frame rate or spatial resolution for the best
possible image.
Provides intuitive representation of non-quantitative
hemodynamics in vascular structures.
Sensitivity/PRIAdjusts the sample rate for the flow signal.
Background On/Off
Sweep SpeedChanges the speed at which the timeline is swept.
Background On lets you view the anatomy roadmap;
Background Off lets you view just flow information.
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4-3-5System CFM and PWD Checks
Table 4-18 CFM and PWD Functions
Baseline
PRF/Wall Filter
Angle Correct
Threshold
Map
Invert
Packet Size
Quick Angle CorrectQuickly adjusts the angle by 60 degrees
Doppler Display Formats
Adjusts the baseline to accommodate faster or slower blood
flows to eliminate aliasing.
Velocity scale determines pulse repetition frequency. If the
sample volume gate range exceeds single gate PRF capability,
the system automatically switches to high PRF mode. Multiple
gates appear, and HPRF is indicated on the display.
Estimates the flow velocity in a direction at an angle to the
Doppler vector by computing the angle between the Doppler
vector and the flow to be measured
Threshold assigns the gray scale level at which color
information stops.
Allows a specific color map to be selected. After a selection has
been made, the color bar displays the resultant map.
Allows blood flow to be viewed from a different perspective, i.e.
red away (negative velocities) and blue toward (positive
velocities). The real-time or frozen image can be inverted.
Controls the number of samples gathered for a single color flow
vector.
Display layout can be preset to have B-Mode and Time-motion
side-by-side or over-under.
In the side-by-side layout, there are three display alternatives
defined: equal priority, time-motion priority or time-motion with
B-Mode reference.
In the over-under layout, there are three display alternatives
defined: time-motion priority, B Mode priority or equal priority.
Sample Volume Gate LengthSizes the sample volume gate
Scan Area
Slants the B-Mode or Color Flow linear image left or right to get
more information without moving the probe
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4-3-6Basic Measurements
NOTE:The following instructions assume that you first scan the patient and then press Freeze.
4-3-6-1Distance and Tissue Depth Measurements
1.) Press MEASURE
2.) To position the active caliper at the start point (distance) or the most anterior point (tissue
depth), move the TRACKBALL
3.) To fix the start point, press Set. The system fixes the first caliper and displays a seco nd active
caliper.
4.) To position the second active caliper at the end point (distance) or the most posterior point
(tissue depth), move the TRACKBALL
5.) To complete the measurement, press SET
value in the measurement results window.
Before you complete a measurement:
To toggle between active calipers, press MEAS URE
To erase the second caliper and the current data measured and start the measurement again, press
CLEAR
NOTE:To rotate through and activate previously fixed calipers, turn CURSOR SELECT
NOTE:After you complete the measurement, to erase all data that has been measured to this point,
but not data entered onto worksheets, press CLEAR
4-3-6-2Circumference/Area (Ellipse) Measurement
1.) Press MEASURE
2.) To position the active caliper, move the TRACKBALL
3.) To fix the start point, press SET
4.) To position the second caliper, move the TRACKBALL
5.) Turn the ELLIPSE
once.
caliper.
once; an active caliper displays.
.
.
. The system displays the distance or tissue depth
.
.
.
once; an active caliper displays.
.
. The system fixes the first caliper and displays a second active
.
control; an ellipse with an initial circle shape appears.
NOTE:Be careful not to press the Ellipse control as this activates the Body Pattern.
6.) To position the ellipse and to size the measured axes (move the calipers), move the
TRACKBALL
7.) To increase the size, turn the ELLIPSE
turn the ELLIPSE
8.) To toggle between active calipers, pr es s MEASURE
9.) To complete the measurement, press SET
in the measurement results window.
Before you complete a measurement:
-To erase the ellipse and the current data measured, press CLEAR
is displayed to restart the measurement.
-To exit the measurement function without completing the measurement, press CLEAR
second time.
4 - 10Section 4-3 - General Procedure
.
control in a clockwise direction. To decrease the size,
control in a counterclockwise direction.
.
. The system displays the circumference and area
once. The original caliper
a
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4-3-6-3Worksheets
Measurement/Calculation worksheets are available to display and edit measurements and calculations.
There are generic worksheets as well as Application specific worksheets. The worksheets are selected
from the Measurement icon on the monitor screen after pressing measurement key.
4-3-6-4Report Pages
Measurements/Calculations that are included on the worksheet can also be di splayed on Report Pages.
Report Pages can be customized to meet the appr o pr iate needs of the user.
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4-3-7Probe/Connectors Usage
4-3-7-1Connecting a probe
1.) Place the probe's carrying case on a stable surface and open the case.
2.) Carefully remove the probe and unwrap the probe cable.
3.) DO NOT allow the probe head to hang free. Impact to the probe head could result in irreparable
damage.
4.) Turn the connector locking handle counterclockwise.
5.) Align the connector with the probe port and carefully push into place.
6.) Turn the connector locking handle cloc kwise to secure the probe connector.
7.) Carefully position the probe cable in the probe cord holder spot so it is free to move, but not
resting on the floor.
4-3-7-2Activating the probe
Press the Appilcation button on the menu key panel in keyboard
Select the appropriate probe from the probe indicators on the monitor screen.
The probe activates in the currently-selected operati ng mode. The probe's default settings for the mode
and selected exam are used automatically.
4-3-7-3Deactivating the probe
When deactivating the probe, the probe is automatically placed in standby mode.
1.) Press the Freeze key.
2.) Gently wipe the excess gel from the face of the probe. (Refer to the Basic User Manual for
complete probe cleaning instructions.)
3.) Carefully slide the probe around the right side of the keyboard, toward the probe holder.
Ensure that the probe is placed gently in the probe holder.
4-3-7-4Disconnecting the probe
Probes can be disconnected at any time. However, the probe should not be selected as the active
probe.
1.) Move the probe locking handle counterclockwise. Pull the probe and connector straight out of
the probe port.
2.) Carefully slide the probe and connector away from the p robe port a nd arou nd the ri ght side of
the keyboard. Ensure the cable is free.
3.) Be sure that the probe head is clean before placing the probe in its storage box.
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4-3-8Using Cine
4-3-8-1Activating CINE
Press FREEZE
left most button on the menu key panel of keyboard. To stop CINE Loop playback. press Run/Stop.
4-3-8-2Quickly Move to Start/End Frame
Press FIRST
4-3-8-3Start Frame/End Frame
Turn the START FRAME
right to move forward through the CINE Loop.
, then roll the TRACKBALL to activate CINE. To start CINE Loop playback, press the
to move to the first CINE frame; press LAST to move to the last CINE frame.
dial to the left to move to the beginning of the CINE Loop. Turn the dial to the
Turn the END FRAME
move backward through the CINE Loop.
4-3-8-4Adjusting the CINE Loop Playback Speed
Turn the LOOP SPEED
4-3-8-5Disconnecting B-Mode CINE from Timeline CINE
To review the B-Mode CINE Loop only, press CINE MODE SELECTION
To review the Timeline CINE Loop only, press CINE MODE SELECTION
To return to linked B-Mode and Timeline CINE Loop review, press CINE MODE SELECTION
B/TL
.
4-3-8-6Moving through a CINE Loop Frame By Frame
Turn FRAME BY FRAME
dial to the right to move to the end of the CINE Loop. Turn the dial to the left to
dial right/left to increase/decrease the CINE Loop playback speed.
to move through CINE memory one frame at a time.
4-3-9Image Management (QG)
For Image Management functionality refer to the LOGIQ™ 5 PRO Quick Guide. It talks about several
topics:
•Clipboard
•Printing Images
•Browsing and Managing an Exam’s Stored Image
•Connectivity, and Dataflow Concept and Creation
•Starting an Exam
•Configuring Connectivity
•TCP/IP
•Services (Destinations)
•Buttons
•Views
Verifying and Pinging a Device
and select B ONLY.
and select TL ONLY.
and select
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4-3-10Using the CD-RW / MOD (Magneto-Optical Drive)
4-3-10-1Using the CD-RW
NOTICE
NOTICE
Never move the unit with a disk in the CD-RW because the drive actuator will not be locked
and the CD-RW could break.
1.) Push the EJECT
button, the disk tray will appear.
2.) Put the disk onto the disk tray.
3.) Press the EJECT
button to insert the disk into the CD-RW device.
4.) There are a number of methods to eject a disk from the CD-RW. Ejection is automatic in some
cases. Manual ejection methods, listed in preferred order of use, are:
a.) Press EJECT
b.) Press and hold EJECT
button on the CD-RW while system is ON.
button while the system is booting.
c.) Mechanical ejection. Insert the end of a paper clip into the hole next to the EJECT button while
system power is OFF.
Avoid mechanical ejection whenever possible. Mechanica l ejection leaves the actuator
unlocked and the MOD susceptible to d amage if moved. If forced to use t his method, r eboot
the system, then insert and eject a known good disk using one of the othe r methods.
CD-RW Drive
Eject Button
Figure 4-30 CD-RW drives
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4-3-10-2Using the MOD (Magneto-Optical Drive)
The 3.5 inch Magneto-Optical disk drive supports the following densities:
Standard: 1.3GB; 640MB; 540MB; 230MB; and 128MB
Overwrite: 1.3GB; 640MB; and 540MB
1.) Before installing an MO disk in the MOD, check the MO disk for loose hardware or damaged labels
which could jam inside the MOD. Also, ensure that the slide switch in one corner of the disk is set
so that the disk is write enabled (disk hole closed).
2.) Insert the disk into the MOD with the label facing up.
NOTICE
Never move the unit with a disk in the MOD because the drive actuator will not be lo cked and
the MOD could break.
3.) There are different methods to eject a disk from the MOD. In some cases disk ejection is automatic.
Manual ejection methods are listed below in preferred order from best (1 ) to worst (4).
a.) When in Archive Menu, use the softkey choice –or– click Image Presets up, then click the left
softkey switch up for ARCHIVE
b.) Press the EJECT
switch on the MOD while system is ON.
c.) Press and hold the EJECT
d.) Mechanical ejection. Insert the end of a paper clip into the h ole next to the EJECT
, then toggle the switch under EJECT MOD.
switch while the system is booting.
switch while
system power is OFF.
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4-3-11Backup and Restore Database, Preset Configurations and Images
NOTICE
4-3-11-1Formatting Media
Avoid mechanical ejection whenever possible. Mechanical ejection leaves the actuator
unlocked and the MOD susceptible to damage if mov ed. If forced to use this method, re boot the
system, then insert and eject a known good disk using one of the other manual ejection
methods.
1.) To format the backup media, CD-ROM or MOD, select the UTILITY
2.) Select CONNECTIVITY
monitor screen. Properly label and Insert the backup media.
3.) Select the media type from the drop down menu.
4.) Enter the label for the media as shown in Figure 4-31. It is best to use all capital letters with no
spaces or punctuation marks.
button on the Menu panel.
, then TOOL( in case of BT05 SW, REMOVABLE MEDIA )on the
Figure 4-31 Format and Verify Media
5.) The Ultrasound system displays a pop-up menu, as shown in Figure 4-32. When the formatting
has been completed, press OK
6.) If desired, verify that the format was successful by returning to Utility>Connectivity>Tools (in case of BT05 SW, Removable Media) and selecting VERIFY
Figure 4-32 Format Successful Pop-up Menu
4 - 16Section 4-3 - General Procedure
to continue.
as shown in Figure 4-31.
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4-3-11-2Backup System Presets and Configurations
NOTE:Always backup any preset configurations before a software reload. This ensures that if the presets need
to be reloaded, after the software update, they will be the same ones the customer was using prior to
service.
1.) Insert a formatted MOD (Magneto-Optical Disk) or CD-R into the drive.
2.) On the Touch Panel, press UTILITY
3.) On the Utility Touch Panel, press SYSTEM
4.) On the monitor display, select BACKUP/RESTORE
.
.
.
NOTE:If you are not logged in as GE Service or with administrator privileges, the Operator Login
window is displayed. Log on with administrator pr ivile ge s.
5.) In the Backup list, select Patient Archive, Report Archive, System Configuration and User Defined
Configuration.
6.) In the Media field, select MO or CD-RW.
7.) Select BACKUP
.
The system performs the backup. As it proceeds, status information is displayed on the Backup/Restore
screen.
Check here to
backup presets
and configurations
Figure 4-33 Backup/Restore Menu
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4-3-11-3Restore System Presets and Configurations
CAUTION
The restore procedure overwrites the existin g database on the local hard drive. Make sure to insert
the correct MOD or CD-R.
1.) Insert the Backup/Restore MOD (Magneto-Optical Disk) or CD-R into the drive.
2.) On the Touch Panel, press UTILITY
3.) On the Utility Touch Panel, press SYSTEM
4.) On the monitor display, select BACKUP/RESTORE
.
.
.
NOTE:If you are not logged in with administrator privileges, the Operator Login window is displayed.
Log on with administrator privileges.
5.) In the Restore list, select Patient Archive, Report Archive, System Con figuration and User Defined
Configuration.
6.) In the Media field, select the Backup/Restore MOD or CD-RW.
7.) Select RESTORE
.
The system performs the restore. As it proceeds, status information is displayed on the Backup/Restore
screen.
Figure 4-34 Backup/Restore Menu
Check here to
restore presets
and configurations
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4-3-11-4Archiving Images
To export an exam(s) to a compatible Ultrasound system:
1.) Format the removable media (MOD or CD-ROM) . Label the removable media. Answer Yes/OK
to the messages.Press Patient. Deselect any selected patient(s) in the search portion of the
Patient screen. Press Exam Data Transfer (located at the upper, left-hand corner of the Patient
menu).
Figure 4-35 Exam Data Transfer
2.) Select Export task Button.
Figure 4-36 Task button
3.) The [From] combo box is not active. It displays Local Archive. The [To] combo box is active.
Select the type of removable media MOD or CD Rom. Then please wait until the patient list is
visible.
Figure 4-37 To Combo Box
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4-3-11-4 Archiving Images (cont’d)
4.) In the patient list at the top of the Patient menu, select the patient(s) you want to export. You
can use Windows commands to select more than one patient. To select a consecutive list of
patients, click the cursor on the first name, move the cursor to the last name, then press and
hold down the Shift+right Set key to select all the names. To select a non-consecutive list of
patients, click the cursor at the first name, move the cursor to the next name, then press and
hold down the Ctrl+right Set key, move the cursor to the next name, then press and hold down
the Ctrl+right Set key again, etc. You can also search for patients via the Search key and string.
Or, Select All Button from the Patient Menu:
Figure 4-38 Source Section
NOTE:You need to use your best judgment when moving patients' images. If there are lots of images
or loops, then only move a few patients at a time.
5.) Once you have selected all of the patients to export, press Transfer Button as shown in Figure
4-38.
6.) The progress bar appears as the copy is taking place. Once transfer completed, the exported
patient list will be shown as Figure 4-39..
Figure 4-39 Destination Section of Patient Screen
7.) Press F3 to eject the media. Specify that you want to finalize the CD-ROM.
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4-3-12ECG Check Out (this option is currently not available on the LOGIQ™ 5 PRO
Connect the ECG Harness and check:
Table 4-19 ECG Harness Check
StepTask to doExpected Result(s)
Connect the ECG at the Connector on the Front of the
1.
scanner.
It will display a curve along the bottom edge of the image
sector
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Section 4-4
Application Turnover Checklist
Complete these checks before returning the scanner to customer for use:
1.) TBD
Section 4-5
Software Configuration Checks
Table 4-20 Software Configuration Checks
StepTask to doExpected Result(s)
1.
Check Date and Time settingDate and Time are correct
2.
Check that Location (Hospital Name) is correctLocation Name is correct
3.
Check Language settingsDesired Language is displayed
4.
Check assignment of Printer KeysPrint1-4 Keys are assigned as desired by the customer
5.
Check that all of the customer’s options are set up correct All authorized functions are enabled