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К этому устройству также есть другие инструкции:
Фрагмент инструкции
7. Szabályozási információk
CE Declaration of Conformity
Lead free display promotes
This product is in conformity with the following
environmentally sound recovery
standards
and disposal of waste from electrical
and electronic equipment. Toxic
EN60950-1:2006+A11:2009+A1:20
substances like Lead has been eliminated
10+A12:2011 (Safety requirement of
and compliance with European community’s
Information Technology Equipment)
on hazardous substances in electrical and
requirement of Information Technology
electronic equipment have been adhered to
Equipment)
in order to make Philips monitors safe to use
EN55024:2010 (Immunity requirement of
throughout its life cycle.
Information Technology Equipment)
EPEAT
EN61000-3-2:2006 +A1:2009+A2:2009
(Limits for Harmonic Current Emission)
(www.epeat.net)
EN61000-3-3:2008 (Limitation of Voltage
The EPEAT (Electronic
Fluctuation and Flicker) following provisions
Product Environmental
of directives applicable.
Assessment Tool) program
EN60601-1-2:2007 (Medical electrical
evaluates computer
equipment. General requirements for
environmental criteria developed through
an extensive stakeholder consensus process
2006/95/EC (Low Voltage Directive)
supported by US EPA.
2004/108/EC (EMC Directive)
EPEAT system helps purchasers in the public
1275/2008 Implementing Directive
for Standby and Off mode power
monitors based on their environmental
consumption)
attributes. EPEAT also provides a clear and
consistent set of performance criteria for the
and is produced by a manufacturing organization
for manufacturers to secure market recognition
on ISO9000 level.
for efforts to reduce the environmental impact
ISO9241-307:2008 (Ergonomic
of its products.
methods for electronic visual displays)
GS EK1-2000:2013 (GS mark requirement)
TUV IEC60601-1 (EN 60601-1:2006
Medical electrical equipment - Part 1:
Avoid the disposal of hazardous waste EPEAT’S
General requirements for basic safety and
requirement that all registered products meet
essential performance)
means that these products will consume less
EN 60601-1-2:2007 Medical electrical
energy throughout their life.
equipment - Part 1-2: General
requirements for basic safety and
essential performance - Collateral
standard: Electromagnetic compatibility -
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