Samsung PO24FSSSS/EDC manual TCO03 Recycling Information TCO03 applied model only

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.

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TCO'03 Recycling Information (TCO'03 applied model 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
		ELKRETSEN Box		Max Plank Strasse
	442 Frelinghuysen Ave	1357, 111 83	6454 Etterstad 0602 Oslo
				42
ADDRESS		Stockholm
	Newark, NJ 07114		Fyrstikkalln 3B	50858 Collogne
		Barnhusgatan 3, 4
				Germany
		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.

zIncrease the separation between the equipment.

zConnect the equipment into an outlet on a circuit different from that to which the other device(s) are connected.

zConsult 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