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This declaration applies to all specimens
manufactured identical to the samples submitted
for testing/evaluation.
Assessment of compliance of the product with
the requirements relating to Directive 1999/5/EC
was performed by ACB, Inc.(Notified Body No.15
88) and assessment of compliance of the product
with the requirements relating to Directive 2011/65
/EU was performed by Intertek Testing Services Ltd.,
Shanghai LAB and Directive 2009/125/EC was
performed by Shenzhen Huatongwei International
Inspection Co., Ltd.The assessments were based
on the following regulations and standards:
Requirement: Health and safety
Standard:
EN 50360:2001/A1:2012;
EN 50566:2013;
EN 62311:2008;
EN 62209-1:2006;
EN 62209-2:2010;
EN 62479-2010;
EN 50332-1:2000;
EN 50332-2:2003;
EN 60950-1:2006+A11:2009+A1:2010+A12:2011;
Requirement: EMC
Standard:
EN 301 489-1 V1.9.2;
EN 301 489-3 V1.4.1;
EN 301 489-7 V1.3.1;
EN 301 489-17 V2.2.1;
EN 301 489-24 V1.5.1;
EN 55013:2001/A1:2003/A2:2006;
EN 55020:2007/A11:2011
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