Philips Moniteur LCD - Manuel (Page 24)

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5. Informations Concernant es Réglementations
5. Informations Concernant
es Réglementations
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: