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 General Electric
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 the inspection is not requested within this 14 day period.
GE Medical Systems – Americas
USA:(1) 800–437–1171
Canada:(1) 800–668–0732
Latin & South Am: (1) 305–735–2304
GE Medical Systems – Asia
Japan:(81) 426–48–2594
Korea(82)342–40–6000
GE Medical Systems – Europe
Germany(49) 212–2802–165
SAMSUNG GE MEDICAL SYSTEMS, LTD.
SERVICE TEAM
64–3, Sangdaewon–dong, Chungwon–ku, Sungnam–si
Kyunggido, KOREA
Stick along this line
(DO NOT TEAR) FOLD HERE AND SEAL (DO NOT
TEAR)
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(OMISSIONS,ERRORS,SUGGESTIONS)
PRODUCTPUBLICATION #
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PLEASE BE SPECIFIC IN YOUR CORRECTIONS AND SUGGESTIONS
FOLDFOLD
IF ADDITIONAL P AGES ARE INCLUDED, FOLD AND STAPLE TO LOWER PART OF THIS
SHEET BEFORE MAILING.
SERVICE REP
PHONE
FAX
COUNTRY
CITY
2184996
REV0
R & D Support Group Of SGMS
FAX Number: 82–342–420–420
2184997
REV. 0
GE MEDICAL SYSTEMS
WARNING
AVERTISSEMENT
D
THIS SERVICE MANUAL IS AVAILABLE IN ENGLISH ONLY.
D
IF A CUSTOMER’S SERVICE PROVIDER REQUIRES A LANGUAGE OTHER
THAN ENGLISH, IT IS THE CUSTOMER’S RESPONSIBILITY TO PROVIDE
TRANSLATION SERVICES.
D
DO NOT ATTEMPT TO SERVICE THE EQUIPMENT UNLESS THIS SERVICE
MANUAL HAS BEEN CONSULTED AND IS UNDERSTOOD.
D
F AILURE TO HEED THIS W ARNING MAY RESULT IN INJURY TO THE SER VICE
PROVIDER, OPERATOR OR PATIENT FROM ELECTRIC SHOCK,
MECHANICAL OR OTHER HAZARDS.
D
CE MANUEL DE MAINTENANCE N’EST DISPONIBLE QU’EN ANGLAIS.
D
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.
D
NE PAS TENTER D’INTERVENTION SUR LES ÉQUIPEMENTS TANT QUE LE
MANUEL SERVICE N’A PAS ÉTÉ CONSULTÉ ET COMPRIS.
D
LE NON-RESPECT DE CET AVERTISSEMENT PEUT ENTRAÎNER CHEZ LE
TECHNICIEN, L’OPÉRATEUR OU LE PATIENT DES BLESSURES DUES À DES
DANGERS ÉLECTRIQUES, MÉCANIQUES OU AUTRES.
WARNUNG
AVISO
D
DIESES KUNDENDIENST–HANDBUCH EXISTIERT NUR IN
ENGLISCHER SPRACHE.
D
FALLS EIN FREMDER KUNDENDIENST EINE ANDERE SPRACHE BENÖTIGT,
IST ES AUFGABE DES KUNDEN FÜR EINE ENTSPRECHENDE ÜBERSETZUNG
ZU SORGEN.
D
VERSUCHEN SIE NICHT, DAS GERÄT ZU REPARIEREN, BEVOR DIESES
KUNDENDIENST–HANDBUCH NICHT ZU RATE GEZOGEN UND VERST ANDEN
WURDE.
D
WIRD DIESE W ARNUNG NICHT BEACHTET , SO KANN ES ZU VERLETZUNGEN
DES KUNDENDIENSTTECHNIKERS, DES BEDIENERS ODER DES PATIENTEN
DURCH ELEKTRISCHE SCHLÄGE, MECHANISCHE ODER SONSTIGE
GEFAHREN KOMMEN.
D
ESTE MANUAL DE SERVICIO SÓLO EXISTE EN INGLÉS.
D
SI ALGÚN PROVEEDOR DE SERVICIOS AJENO A GEMS SOLICIT A UN IDIOMA
QUE NO SEA EL INGLÉS, ES RESPONSABILIDAD DEL CLIENTE OFRECER UN
SERVICIO DE TRADUCCIÓN.
D
NO SE DEBERÁ DAR SERVICIO TÉCNICO AL EQUIPO, SIN HABER
CONSULTADO Y COMPRENDIDO ESTE MANUAL DE SERVICIO.
D
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.
2184998REV. 0
GE MEDICAL SYSTEMS
ATENÇÃO
AVVERTENZA
D
ESTE MANUAL DE ASSISTÊNCIA TÉCNICA SÓ SE ENCONTRA
DISPONÍVEL EM INGLÊS.
D
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 TRADUÇÃO.
D
NÃO TENTE REPARAR O EQUIPAMENTO SEM TER CONSULTADO E
COMPREENDIDO ESTE MANUAL DE ASSISTÊNCIA TÉCNICA.
D
O NÃO CUMPRIMENTO DESTE AVISO PODE POR EM PERIGO A SEGURANÇA
DO TÉCNICO, OPERADOR OU PACIENTE DEVIDO A‘ CHOQUES ELÉTRICOS,
MECÂNICOS OU OUTROS.
D
IL PRESENTE MANUALE DI MANUTENZIONE È DISPONIBILE
SOLTANTO IN INGLESE.
D
SE UN ADDETTO ALLA MANUTENZIONE ESTERNO ALLA GEMS RICHIEDE IL
MANUALE IN UNA LINGUA DIVERSA, IL CLIENTE È TENUTO A PROVVEDERE
DIRETTAMENTE ALLA TRADUZIONE.
D
SI PROCEDA ALLA MANUTENZIONE DELL’APPARECCHIATURA SOLO DOPO
AVER CONSULTATO IL PRESENTE MANUALE ED AVERNE COMPRESO IL
CONTENUTO.
D
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.
This manual provides service information on the LOGIQα200 Ultrasound Scanning System. It contains the
following chapters:
1.Chapter 1, Introduction: Contains a content summary and warnings.
2.Chapter 2, Installation: Contains physical and electrical requirements that must be considered prior to
installation and a complete LOGIQα200 installation procedure with installation checklist.
3.Chapter 3, System Configuration: Contains system configuration and specifications.
4.Chapter 4, Functional Checks: Contains functional checks that must be performed as part of the
installation, or as required during servicing and periodic maintenance.
5.Chapter 5, Diagrams: Contains block diagrams and functional explanations of the LOGIQα200 electronics.
6.Chapter 6, Renewal Parts: Contains a complete list of replacement parts for the LOGIQα200 and
disassembly procedures for all changeable FRU.
7.Chapter 7, Periodic Maintenance: Provides periodic maintenance procedures for the LOGIQα200.
LOGIQα200 SERVICE MANUAL
2138853
8.Chapter 8, Installation for Options: is provided to keep the option installation instructions supplied with
each option.
1–3
INTRODUCTION
GE MEDICAL SYSTEMS
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LOGIQα200 SERVICE MANUAL
2138853
1–2SAFETY
1–2–1Warnings
W ARNING!
CAREFULLY READ ALL THE WARNINGS LISTED BELOW!
1.The operator manual should be fully read and understood before operating the LOGIQα200 and kept nearby
for quick reference.
2.Although the ultrasound energy transmitted from the LOGIQα200 transducer is within AIUM/NEMA
standards, unnecessary exposure should be avoided. Only trained personnel should operate the LOGIQ
α200.
3.To prevent electrical shock, the LOGIQ
α200 should be connected to a properly grounded power receptacle.
Do not use a three to two prong adapter. This defeats safety grounding.
4.Do not use with Defibrillator when LOGIQα200 is being operated .
5.Probes are fragile, please handle with care.
6.Concerning Outside Markings, refer to Illustration 1–1,1–2,1–3,1–4,1–5,1–6,1–7,1–8, and 1–9.
7.For the cleaning, disinfection, and sterilization, refer to Probe section in LOGIQ
α200 User Manual and
Caution Sheet supplied with each probe.
NOTICE
This medical equipment is approved, in terms of the prevention of radio wave interference, to be
used in hospitals, clinics and other institutions which are environmentally qualified. The use of
this equipment in an inappropriate environment may cause some electronic interference to radios
and televisions around the equipment. Proper handling of this equipment is required in order to
avoid such trouble according to the operator and service manuals.
This equipment can be used in residential areas only under the supervision of physicians or
qualified technicians.
1–4
INTRODUCTION
GE MEDICAL SYSTEMS
REV 0
1–2–1Warnings (Continued)
LOGIQα200 SERVICE MANUAL
2138853
OUTSIDE MARKINGS OF LOGIQα200 (FOR ALL UNITS)
ILLUSTRATION 1–1
1–5
INTRODUCTION
GE MEDICAL SYSTEMS
REV 0
1–2–1Warnings (Continued)
LOGIQα200 SERVICE MANUAL
2138853
OUTSIDE MARKINGS OFLOGIQα200 (FOR ALL UNITS)
ILLUSTRATION 1–2
Note
For further details regarding the cautions above, refer to 2–2–8 MOVING INTO POSITION in
Chapter 2.
1–6
INTRODUCTION
GE MEDICAL SYSTEMS
REV 0
1–2–1Warnings (Continued)
LOGIQα200 SERVICE MANUAL
2138853
OUTSIDE MARKINGS OFLOGIQα200 (FOR ALL UNITS)
ILLUSTRATION 1–3
1–7
INTRODUCTION
GE MEDICAL SYSTEMS
REV 3
1–2–1Warnings (Continued)
LOGIQα200 SERVICE MANUAL
2138853
MODEL NUMBER : 2205674
MANUFACTURED
LOCATION:SAMSUNG GE MEDICAL
S.N.:
VOLT: 220–240V~
AMP. LONG TERM : 2.1A
KVA: 0.5kVA
PHASE: 1
DESC.: LOGIQa 200
CISPR 11 / EN 55011
CLASS : A GROUP : 1
CLASSE : A GROUPE : 1
Class1/Classe1
SYSTEMS
KOREA
OUTSIDE MARKINGS OFLOGIQα200 (FOR EUROPE )
ILLUSTRATION 1–4
Note
For the symbols shown in the illustration above, refer to latter pages in this chapter.
1–8
INTRODUCTION
GE MEDICAL SYSTEMS
REV 3
1–2–1Warnings (Continued)
MADE FOR GE MEDICAL SYSTEMS
MILWAKEE, WISCONSIN BY
Do not use a Defibrillator simultaneously with the ECG, as its excessive voltage will
damage the signal input block of the ECG unit.
LOGIQα200 SERVICE MANUAL
2138853
CAUTION
OUTSIDE MARKINGS OF LOGIQα200 (FOR UNITS WITH ECG)
ILLUSTRATION 1–9
1–13
INTRODUCTION
GE MEDICAL SYSTEMS
REV 0
1–2–1Warnings (Continued)
LOGIQα200 SERVICE MANUAL
2138853
NOTE: Two labels are attached on rear of the SMPS assy box inside the rear cover
and front of HV Board Assy inside the front base cover.
MARKINGS OF LOGIQ 500 (INSIDE COVERS)
ILLUSTRATION 1–10
1–14
INTRODUCTION
GE MEDICAL SYSTEMS
REV 0
LOGIQα200 SERVICE MANUAL
2138853
1–2–1Warnings (Continued)
The following table describes the purpose and location of safety labels and other important information provided
on the equipment.
Label/IconPurpose/MeaningLocation
Identification and Rating Plate
Type/Class Label
IP Code
(IPX1)
Device Listing/
Certification Labels
Manufacturer’s name and address
Date of manufacture
Model and serial numbers
Electrical ratings (Volts, Amps, phase, and
frequency)
Used to indicate the degree of safety or protection.
Indicates the degree of protection provided
by the enclosure per IEC 529. IPX1
indicates drip proof.
Equipment Type BF (man in the box symbol)
IEC 878-02-03 indicates B Type equipment
having a floating applied part.
Equipment Type CF (heart in the box
symbol) IEC 878-02-05 indicate equipment
having a floating applied part having a
degree of protection suitable for direct
cardiac contact.
Laboratory logo or labels denoting
conformance with industry safety standards
such as UL or IEC.
Rear of console near power inlet
Foot Switch
Probe connectors
ECG connector and surgical probes
Rear of console
“DANGER – Risk of explosion used
in...”
The system is not designed for use with
flammable anesthetic gases.
“CAUTION” The equilateral triangle is usually
used in combination with other symbols to
advise or warn the user.
“ATTENTION – Consult accompanying
documents” is intended to alert the user to
refer to the operator manual or other
instructions when complete information
cannot be provided on the label.
1–15
Rear of console
Various
V arious
INTRODUCTION
GE MEDICAL SYSTEMS
REV 0
1–2–1Warnings (Continued)
Label/IconPurpose/MeaningLocation
LOGIQα200 SERVICE MANUAL
2138853
“CAUTION – Dangerous voltage” (the
lightning flash with arrowhead in equilateral
triangle) is used to indicate electric shock
hazards.
“Mains OFF” Indicates the power off position
of the mains power switch.
“Mains ON” Indicates the power on position
of the mains power switch.
“Equipotentiality” Indicates the terminal to be
used for connecting equipotential conductors
when interconnecting (grounding) with other
equipment.
CAUTION
This is only for ”FUNCTIONAL
GROUNDING”, NOT ”PROTECTIVE
EARTH”.
Indicates Main protective earth
terminal
Various
Front of system,
Main power switch
Front of system,
Main power switch
Rear of console
Various
1–16
INTRODUCTION
GE MEDICAL SYSTEMS
REV 3
1–2–2Specifications
Type of protection against electric shock:Class I EQUIPMENT (*1)
Degree of protection against electric shock: Type BF EQUIPMENT (*2) (Except ECG)
Type CF EQUIPMENT (*3) (ECG Only)
Ordinary Equipment
Continuous Operation
*1. Class I EQUIPMENT
EQUIPMENT in which protection against electric shock does not rely on BASIC INSULATION only, but
which includes an additional safety precaution in that means are provided for the connection of the
EQUIPMENT to the protective earth conductor in the fixed wiring of the installation in such a way that
ACCESSIBLE METAL PARTS cannot become LIVE in the event of a failure of the BASIC INSULATION.
*2. Type BF EQUIPMENT
TYPE B EQUIPMENT with an F–TYPE APPLIED P ART
TYPE B EQUIPMENT: EQUIPMENT providing a particular degree of protection against electric shock,
particularly regarding:
LOGIQα200 SERVICE MANUAL
2138853
– allowable LEAKAGE CURRENT;
Normal modeSingle failure mode
Patient leakage currentLess than 100µALess than 500µA
*3. Type CF EQUIPMENT
EQUIPMENT providing a particular degree of protection higher than that for TYPE OF BF EQUIPMENT
against electronic shock particularly regarding allowable LEAKAGE CURRENT, and having an F–TYPE
APPLIED P AR T.
– allowable LEAKAGE CURRENT;
Normal modeSingle failure mode
Patient leakage currentLess than 10µALess than 50µA
1–17
INTRODUCTION
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