Samsung 173P user manual download (Page 51 of 54)

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ADDRESS
442 Frelinghuysen Ave
Newark, NJ 07114
ELKRETSEN
Box 1357,
111 83
Stockholm
Barnhusgatan
3, 4 tr.
6454 Etterstad 0602
Oslo
Fyrstikkalln 3B
Max Plank
Strasse 42
50858
Collogne
Germany
TELEPHONE
973-565-0181
08-545 212
90
23 06 07 40
49 0 2234
9587 - 0
FAX
Fax: 973-565-9485
08-545 212
99
23 06 07 41
E-
MAIL
none
info@el-
kretsen.se
adm@elektronikkretur.no
vfw.info@vfw-
ag.de
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Medical Requirement
Classifications:
In accordance with UL 2601-1/IEC 60601-1, the product is cssified as Continuous duty Class I
equipment, which is not protected against ingress of liquids. The product is not suitable for use
in the presence of a flammable anaesthetic mixture with air or with oxygen or nitrous oxide.
EMC
This equipment has been tested and found to comply with the limits for medical devices to the
IEC 601-1-2:1994. These limits are designed to provide reasonable protection against harmful
interference in a typical medical installation. This equipment generates, uses and can radiate
radio frequency energy and, if not installed and used in accordance with the instructions, may
cause harmful interference to other devices in the vicinity. However, there is no guarantee that
interference will not occur in a particular installation. If this equipment does cause harmful
interference to other devices, which can be determined by turning the equipment off and on, the
user is encouraged to try to correct the interference by one or more of the following measures:
Reorient or relocate the receiving device.
Increase the separation between the equipment.
Connect the equipment into an outlet on a circuit different from that to which the other
device(s) are connected.
Consult the manufacturer or field service technician for help.
Video In / RS 232 / Video Out
Accessories equipment connected to the analog and digital interfaces must be certified to the
respective IEC standards (i.e. IEC 950 for data processing equipment and IEC 601-1 for
medical equipment.) Furthermore all configurations shall comply with the system standard IEC
601-1-1. Everybody who connects additional equipment to the signal input part or signal output
part configures a medical system, and is therefore, responsible that the system complies with
the requirements of the system standard IEC 601-1-1. If in doubt, consult the technical services
department or your local representative.
Transport and Storage Limitations:
Temperature Range of -40
°
C to +70
°
C
Relative Humidity of 10 -95%, non-condensing
* Bio-accumulative is defined as substances which accumulate within living organisms.
** Lead, Cadmium and Mercury are heavy metals which are Bio-accumulative.
Sample
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