Bedienungsanleitung Philips C272P4 (Seite 44 von 63) (Holländisch)

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8. Informatie over voorschriften

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.

EPEAT

(www.epeat.net)

The EPEAT (Electronic

Product Environmental

Assessment Tool) program

evaluates computer

desktops, laptops, and monitors based on 51

environmental criteria developed through

an extensive stakeholder consensus process

supported by US EPA.

EPEAT system helps purchasers in the public

and private sectors evaluate, compare and

select desktop computers, notebooks and

monitors based on their environmental

attributes. EPEAT also provides a clear and

consistent set of performance criteria for the

design of products, and provides an opportunity

for manufacturers to secure market recognition

for efforts to reduce the environmental impact

of its products.

BeneÀts of EPEAT

Reduce use of primary materials

Reduce use of toxic materials

Avoid the disposal of hazardous waste EPEAT’S

requirement that all registered products meet

(1(5*<67$5·VHQHUJ\HIÀFLHQF\VSHFLÀFDWLRQV

means that these products will consume less

energy throughout their life.

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.

 EN60601-1-2:2007 (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 EK1-2000:2013 (GS mark requirement).

 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

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