EU Declaration of Conformity

EDC EN-SER:
2578
(Document No. / Dokument br.)
(Year, Month (yyyy/mm) in which the CE mark is affixed / Godina kada je
dodeljena CE oznaka)
2020/07
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 )
BRL130, BRL140, adapter HQ850, HQ8505
BRL160, BRL170, BRL180, adapter HQ8505
(Type version or model, Verzija tipa ili model)
Ladyshaver, adapter(s)
(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 +A14:2019 +A1:2019 +A2:2019
EN 60335-2-8: 2015 + A1:2016
EN 62233:2008
EN 61558-1:2005 A1:2009, EN 61558-2-16:2009 A1:2013
EN 55014-1: 2017
EN 55014-2: 2015
EN 61000-3-2: 2014, EN 61000-3-3: 2013
EN 50564:2011
EN 50581:2012
EN 50563:2011
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-Aug-20
(signature, name and function)
Remarks:
A.Speelman, CL Compliance Manager
Drachten,