LABEL/SYMBOL PURPOSE/MEANING
LOCATION
Serial number
Identification and Rating Plate
(rear side of the system / on plug of each probe)
Catalog or model number
Identification and Rating Plate
(rear side of the 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 the 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 the 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 the 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 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 60417-5333)
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 the system / on plug of each probe)
Defibrillator-proof Type CF equipment (heart in box with paddle,
symbol IEC 60417-5336) 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 the 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 the system
This symbol indicates that in the United States of America, federal
law restricts this device to sale by or on the order of a physician.
Identification and Rating Plate
(rear side of the system)
Waste Electrical and Electronic Equipment (WEEE) Disposal. This
symbol indicates that waste electrical and electronic equipment
must not be disposed as unsorted municipal waste and must be
collected separately. Please contact an authorized representative
of the manufacturer for information concerning the
decommissioning of your equipment.
Identification and Rating Plate
(rear side of the system / on plug of each probe)
Introduction
Voluson E-Series Service Manual
KTD106657 Revision 2
1-17
Содержание H48681XB
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Страница 366: ...GE Healthcare Austria GmbH Co OG Tiefenbach 15 4871 Zipf Austria www gehealthcare com ...