Philips Brilliance Moniteur LCD avec D-image clinique - Manuel (Page 38)

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7. Regulatory Infomation
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.
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Reduce use of primary materials
Reduce use of toxic materials
Avoid the disposal of hazardous waste EPEAT’S
requirement that all registered products meet
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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