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manual abstract
7. Informations règlementaires
7. Informations
and is produced by a manufacturing organization
on ISO9000 level.
règlementaires
ISO9241-307:2008 (Ergonomic
requirement, Analysis and compliance test
Lead-free Product
methods for electronic visual displays)
Lead free display promotes
GS EK1-2000:2013 (GS mark requirement)
environmentally sound recovery
and disposal of waste from electrical
TUV IEC60601-1 (EN 60601-1:2006
and electronic equipment. Toxic
Medical electrical equipment - Part 1:
substances like Lead has been eliminated
General requirements for basic safety and
and compliance with European community’s
essential performance)
stringent RoHs directive mandating restrictions
EN 60601-1-2:2007 Medical electrical
on hazardous substances in electrical and
equipment - Part 1-2: General
electronic equipment have been adhered to
requirements for basic safety and
in order to make Philips monitors safe to use
essential performance - Collateral
throughout its life cycle.
standard: Electromagnetic compatibility -
Requirements and tests
CE Declaration of Conformity
This product is in conformity with the following
However, there is no guarantee that
standards
interference will not occur in a particular
installation. If this equipment does cause
EN60950-1:2006+A11:2009+A1:20
harmful interference to radio or television
10+A12:2011 (Safety requirement of
reception, which can be determined by
Information Technology Equipment)
turning the equipment off and on, the
EN55022:2010 (Radio Disturbance
user is encouraged to try to correct
requirement of Information Technology
the interference by one or more of the
Equipment)
following measures:
EN55024:2010 (Immunity requirement of
Reorient or relocate the receiving antenna.
Information Technology Equipment)
Increase the separation between the
EN61000-3-2:2006 +A1:2009+A2:2009
equipment and receiver.
(Limits for Harmonic Current Emission)
Connect the equipment into an outlet on
EN61000-3-3:2008 (Limitation of Voltage
a circuit different from that to which the
Fluctuation and Flicker) following provisions
receiver is connected.
of directives applicable.
Consult the dealer or an experienced
EN60601-1-2:2007 (Medical electrical
radio/TV technician for help.
equipment. General requirements for
safety Collateral standard, Electromagnetic
compatibility Requirements and tests)
approved by the party responsible for
2006/95/EC (Low Voltage Directive)
compliance could void the user's authority
to operate the equipment.
2004/108/EC (EMC Directive)
2009/125/EC (ErP Directive, EC No.
Use only RF shielded cable that was supplied
1275/2008 Implementing Directive
with the monitor when connecting this monitor
for Standby and Off mode power
to a computer device.
consumption)
2011/65/EU (RoHS Directive)
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