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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 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
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.
SWEDEN NORWAY GERMANY
COMPANY ELKRETSEN Elektronikkretur AS vfw AG
ADDRESS
ELKRETSEN Box 1357,
111 83 Stockholm
Barnhusgatan 3, 4 tr.
6454 Etterstad 0602 Oslo
Fyrstikkalln 3B
Max Plank Strasse 42
50858 Collogne
Germany
TELEPHONE 08-545 212 90 23 06 07 40 49 0 2234 9587 - 0
FAX 08-545 212 99 23 06 07 41
E-MAIL info@el-kretsen.se adm@elektronikkretur.no vfw.info@vfw-ag.de
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http://www.el-kretsen.se/
http://www.elretur.no/
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