EU Declaration of Conformity

160
(Document No. / Ziņojums Nr)
(Year, Month (yyyy/mm) in which the CE mark is affixed / Gads kurā CE
zīme ieviesta)
2013/08
EUROPEAN DECLARATION OF CONFORMITY
(EC deklarācija atbilstība)
We, PHILIPS CONSUMER LIFESTYLE B.V.
(Company name / vārds)
Philips Consumer Lifestyle B.V.
TUSSENDIEPEN 4, 9206 AD DRACHTEN, THE NETHERLANDS
(address / adrese)
declare under our responsibility that the product(s)
(deklarēt zem vai atbildība ka, elektronisks produkts)
Philips
(brand name, fabrikas marka vārds)
RQ1250, RQ1251, RQ1252, RQ1253, RQ1254, RQ1257, RQ1258, RQ1260,
RQ1261, RQ1265, RQ1270, RQ1273, RQ1275, RQ1280, RQ1284,
RQ1285,RQ1286, RQ1290, RQ1295, RQ1296
(Type version or model, Tips, versija vai modelis)
Shaver
(product description, produkta apraksts)
to which this declaration relates is in conformity with the following harmonized standards:
(Kam ši deklarācija atbilst ir apliecināt ar sekojošiem saskaņotiem standartiem)
following the provisions of :
(Sekojot noteikumiem)
EN 60335-1: 2002 A11:2004 A1:2004 A12:2006 A2:2006 A1:2004 A13:2008 A14:2010 A15:2011
EN 60335-2-8: 2003 A1:2005 A2:2008
EN 62233: 2008
EN55014-1: 2006 A1:2009 A2:2011
EN61000-3-2: 2006 A1:2009 A2:2009, EN61000-3-3: 2008
EN55014-2: 1997 A1:2001 A2:2008
EN50564:2011
EN50581:2012
2006/95/EC
2004/108/EC
2009/125/EC
2011/65/EU
EC/1275/2008
EC/278/2009
And are produced under a quality scheme at least in conformity with ISO 9001 or CENELEC Permanent Documents
(Tiek ražots zem kvalitātes sistēma kas ir apstiprināta ar ISO 9001 vai CENELEC pastāvošiem dokumentiem )
Only for Medical Devices and R&TTE products:
The Notified Body:
performed:
(Reģistrēta galvenā daļa)
(Name and number/ vārds un numurs)
(paveikts)
(description of intervention / intervencijas apraksts)
and issued the certificate:
(Un izveido sertifikātu)
(certificate number / sertifikāta numurs)
(place,date / vieta, datums)
30-aug-13
(signature, name and function / parskts, vārds un amatpienākums)
Remarks:
A.Speelman, CL Compliance Manager
Drachten,