Philips C221S3 Regulatory Information, Lead-free Product, GS EK1-20002011 GS mark requirement

5. Regulatory Infomation

5. Regulatory Information

Lead-free Product

Lead free display promotes environmentally sound recovery and disposal of waste from electrical and electronic equipment.Toxic

substances like Lead has been eliminated and compliance with European community’s stringent RoHs directive mandating restrictions on hazardous substances in electrical and electronic equipment have been adhered to in order to make Philips monitors safe to use throughout its life cycle.

CE Declaration of Conformity

This product is in conformity with the following standards

•EN60950-1:2006+A11:2009+A1:20 10+A12:2011 (Safety requirement of Information Technology Equipment)

•EN55022:2010 (Radio Disturbance requirement of Information Technology Equipment)

•EN55024:2010 (Immunity requirement of Information Technology Equipment)

•EN61000-3-2:2006 +A1:2009+A2:2009 (Limits for Harmonic Current Emission)

•EN61000-3-3:2008 (Limitation of Voltage Fluctuation and Flicker) following provisions of directives applicable.

•EN60601-1-2:2002 (Medical electrical equipment. General requirements for safety Collateral standard, Electromagnetic compatibility Requirements and tests)

•2006/95/EC (Low Voltage Directive)

•2004/108/EC (EMC Directive)

•2009/125/EC (ErP Directive, EC No. 1275/2008 Implementing Directive for Standby and Off mode power consumption)

•93/42/EEC, 2007/47/EC (Medical Device Directive)

•2011/65/EU (RoHS Directive)

and is produced by a manufacturing organization on ISO9000 level.

•ISO9241-307:2008 (Ergonomic requirement, Analysis and compliance test methods for electronic visual displays)

•GS EK1-2000:2011 (GS mark requirement)

•prEN50279:1998 (Low Frequency Electric and Magnetic fields for Visual Display)

•MPR-II (MPR:1990:8/1990:10 Low Frequency Electric and Magnetic fields)

•TUV IEC60601-1 (EN 60601-1:2006 Medical electrical equipment - Part 1: General requirements for basic safety and essential performance)

•EN 60601-1-2:2007 Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral standard: Electromagnetic compatibility - Requirements and tests

Federal Communications Commission (FCC) Notice (U.S. Only)

This equipment has been tested and found to comply with the limits for a Class B digital device, pursuant to Part 15 of the FCC Rules.These limits are designed to provide reasonable protection against harmful interference in a residential 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 radio communications. However, there is no guarantee that interference will not occur in a particular installation. If this equipment does cause harmful interference to radio or television reception, 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 antenna.

•Increase the separation between the equipment and receiver.

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