Philips C221S3 用户手册

下载
页码 37
22
5. Regulatory Infomation
5.  Regulatory Information
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: 
•  Reorient or relocate the receiving antenna.
•  Increase the separation between the 
equipment and receiver.