Samsung 193P User Manual (user Manual) (ver.1.0) (English) - Page 50

Emissions, Ecology, Medical Requirement, Classifications

Page 50 highlights

Emissions z Electromagnetic fields z Noise emissions Ecology z The product must be prepared for recycling and the manufacturer must have a certified environmental management system such as EMAS or ISO 14 000 z Restrictions on o chlorinated and brominated flame retardants and polymers o heavy metals such as cadmium, mercury and lead. The requirements included in this label have been developed by TCO Development in cooperation with scientists, experts, users as well as manufacturers all over the world. Since the end of the 1980s TCO has been involved in influencing the development of IT equipment in a more userfriendly direction. Our labelling system started with displays in 1992 and is now requested by users and IT-manufacturers all over the world. For more information, Please visit www.tcodevelopment.com TCO'03 Recycling Information (TCO'03 applied model only) [European Residents Only] For recycling information for TCO'03 certified monitors, for the residents in the following countries, please contact the company corresponding to your region of residence. For those who reside in other countries, please contact a nearest local Samsung dealer for recycling information for the products to be treated in environmentally acceptable way. [U.S.A. Residents Only] [European Residents Only] U.S.A. COMPANY Solid Waste Transfer & Recycling Inc ADDRESS 442 Frelinghuysen Ave Newark, NJ 07114 TELEPHONE 973-565-0181 FAX Fax: 973-565-9485 EMAIL none HOME PAGE http://www.bcua.org/Solid Waste_Disposal.htm SWEDEN NORWAY ELKRETSEN Elektronikkretur AS ELKRETSEN Box 1357, 111 83 6454 Etterstad 0602 Oslo Stockholm Fyrstikkalln 3B Barnhusgatan 3, 4 tr. 08-545 212 90 23 06 07 40 08-545 212 99 23 06 07 41 [email protected] [email protected] http://www.elkretsen.se/ http://www.elretur.no/ GERMANY vfw AG Max Plank Strasse 42 50858 Collogne Germany 49 0 2234 9587 - 0 [email protected] 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

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Emissions
Electromagnetic fields
Noise emissions
Ecology
The product must be prepared for recycling and the manufacturer must have a certified
environmental management system such as EMAS or ISO 14 000
Restrictions on
o chlorinated and brominated flame retardants and polymers
o heavy metals such as cadmium, mercury and lead.
The requirements included in this label have been developed by TCO Development in cooperation
with scientists, experts, users as well as manufacturers all over the world. Since the end of the
1980s TCO has been involved in influencing the development of IT equipment in a more user-
friendly direction. Our labelling system started with displays in 1992 and is now requested by
users and IT-manufacturers all over the world.
For more information, Please visit
www.tcodevelopment.com
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
TCO'03 Recycling Information (TCO'03 applied model only)
[European Residents Only]
For recycling information for TCO'03 certified monitors, for the residents in the following countries,
please contact the company corresponding to your region of residence. For those who reside in
other countries, please contact a nearest local Samsung dealer for recycling information for the
products to be treated in environmentally acceptable way.
[U.S.A. Residents Only]
[European Residents Only]
U.S.A.
SWEDEN
NORWAY
GERMANY
COMPANY
Solid Waste Transfer &
Recycling Inc
ELKRETSEN
Elektronikkretur AS
vfw AG
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
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