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GE Voluson E6

GE Voluson E6
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GE HEALTHCAREDRAFT VOLUSON E8 / VOLUSON E6
D
IRECTION KTD102576, REVISION 7 DRAFT (AUGUST 23, 2012) SERVICE MANUAL
Chapter 1 - Introduction 1-9
Manufacturer’s name and address
Identification and Rating Plate
(rear side of system / on plug of each probe)
Date of manufacture
Identification and Rating Plate
(rear side of system / on plug of each probe)
Serial number
Identification and Rating Plate
(rear side of system / on plug of each probe)
Catalog or model number
Identification and Rating Plate
(rear side of system / on plug of each probe)
Device Listing /
Certification Labels
Laboratory logo or labels denoting conformance with industry safety
standards such as UL or IEC.
rear side of system
CE Conformity mark according to Medical Device Directive 93/42/EEC.
0123: Identification number of notified body TÜV Süd Product Service.
Identification and Rating Plate
(rear side of system / on plug of each probe)
“Tested and production monitored by TÜV Product Service NRTL
with respect to ELECTRICAL SHOCK, FIRE and MECHANICAL
HAZARDS only in accordance with UL2601-1 and CAN/CSA C22.2
NO.601.1.”
Identification and Rating Plate
(rear side of system)
Type/Class Label
Used to indicate the degree of safety or protection.
IP Code (IPX 0)
IP Code (IPX 1)
IP Code (IPX 7)
degree of protection provided by the enclosure per IEC 60529:
IPX 0 - no protection against ingress of water
IPX 1 - protected against dripping water
IPX 7 - protected against the effects of immersion
various
Equipment Type BF (man in box, symbol IEC 60878-5333) indicates
B Type equipment having even more electrical isolation than standard
Type B equipment because it is intended for intimate patient contact.
Identification and Rating Plate
(rear side of system / on plug of each probe)
Defibrillator-proof Type CF equipment (heart in box with “electrodes”,
symbol IEC 60878-5336) identifies a defibrillation-proof type CF
applied part complying with IEC 60601-1.
front side of the ECG-preamplifier
"DANGER -
Risk of explosion used in..."
The system is not designed for use with flammable anesthetic gases. Indicated in the Service Manual.
This precaution is intended to prevent injury that may result if one
person attempt to move the system considerable distances or on an
incline due to the weight of the system.
Used in the Service and User Manual which
should be adjacent to equipment at all times
for quick reference.
Pushing prohibited.
Do not lean on the system. Tipping danger.
Take special care when moving the system.
various
Loading prohibited.
Do not put any items on this shelf. Danger of breaking.
Also items might be crushed when lowering the user interface.
at top cover of system
“ATTENTION” - Read and understand all instructions for use”
This symbol advises the reader to consult the accompanying
documents (operator manual or other instructions).
rear side of system
Table 1-6 Product Labels and Icons
LABEL/SYMBOL PURPOSE/MEANING LOCATION
0123

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