Declaration of Conformity

EDC EN-SER:
2300
(Document No. / Dokument br.)
(Year, Month (yyyy/mm) in which the CE mark is affixed / Godina kada je
dodeljena CE oznaka)
2019/02
EU DECLARATION OF CONFORMITY
(EU DEKLARACIJA O USAGLAŠENOSTI)
We, PHILIPS CONSUMER LIFESTYLE B.V.
(Company name /Naziv privrednog društva )
Philips Consumer Lifestyle B.V.
TUSSENDIEPEN 4, 9206 AD DRACHTEN, THE NETHERLANDS
(address / adresa)
declare under our responsibility that the product(s):
(izjavljujemo pod punom odgovornošću da je(su) električni proizvod(i):)
Philips
(brand name, naziv robne marke )
XZ5800, SW5710, S6011, S5095, S5090, S5088, S5086, S5085, S5083,
S5081, S5076, S5075, S5074, S5073, S5072, S5071, S5070, HQ8505
(Type version or model, Verzija tipa ili model)
Shaver, adapter
(product description, opis proizvoda )
to which this declaration relates is in conformity with the following harmonized standards:
(na koji se ova deklaracija odnosi u skladu sa sledećim usaglašenim standardima:)
following the provisions of :
(U skladu sa odredbama)
EN 60335-1:2012 A11:2014 +A13:2017
EN 60335-2-8:2015 A1:2016
EN61558-1:2005 A1:2009, EN61558-2-16:2009 A1:2013
EN 62233:2008
EN55014-1:2017
EN61000-3-2:2014, EN61000-3-3:2013
EN55014-2:1997 A1:2001 A2:2008
EN50564:2011
EN50581:2012
EN50563:2011 A1:2013
2014/35/EU
2014/30/EU
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
(I da su proizvedeni prema šemi kvaliteta koja je najmanje u skladu sa ISO 9001 ili CENELEC stalnom dokumentacijom)
Only for Medical Devices produced under a quality scheme at least in conformity with EN13485:
The Notified Body:
performed:
(Ovlašćeno telo)
(Name and number/ Naziv i broj)
(izvršeno)
(description of intervention / opis intervencije)
and issued the certificate:
(i izdat sertifikat)
(certificate number / broj sertifikata)
(place,date / potpis, ime i funkcija)
18-Mar-19
(signature, name and function)
Remarks:
A.Speelman, CL Compliance Manager
Drachten,