Samsung DI19PSQFV/EDC, DI19PSQAQ/EDC, DI19PSQRV/EDC Medical Requirement Classifications, Elkretsen

zThe product must be prepared for recycling and the manufacturer must have a certified environmental management system such as EMAS or ISO 14 000

zRestrictions 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.

	[U.S.A. Residents Only]		[European Residents Only]
	U.S.A.	SWEDEN	NORWAY	GERMANY
COMPANY	Solid Waste Transfer &	ELKRETSEN	Elektronikkretur AS	vfw AG
	Recycling Inc
	442 Frelinghuysen Ave	ELKRETSEN Box	6454 Etterstad 0602 Oslo	Max Plank Strasse 42
ADDRESS		1357, 111 83
				50858 Collogne
	Newark, NJ 07114	Stockholm	Fyrstikkalln 3B
				Germany
		Barnhusgatan 3, 4 tr.
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-	none	info@el-kretsen.se	adm@elektronikkretur.no	vfw.info@vfw-ag.de
MAIL
HOME	http://www.bcua.org/Solid	http://www.el-	http://www.elretur.no/
PAGE	Waste_Disposal.htm	kretsen.se/

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:

zReorient or relocate the receiving device.