Declaration of Conformity

EDC EN-SER:
2220
(Document No. / Dokument br.)
(Year, Month (yyyy/mm) in which the CE mark is affixed / Godina kada je
dodeljena CE oznaka)
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 )
BRI858;BRI860; BRI861; BRI862; BRI863; BRI864
(Type version or model, Verzija tipa ili model)
Intense Pulse Light Hair removal device
(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 50581:2012
EN 60335-2-8:2015 +A1:2016
EN 60335-1:2012 +A11:2014 +A13:2017
EN 62233:2008
EN 55011:2009 +A1:2010
EN 55014-1:2006 +A1:2009, EN 55014-2:2015
EN 61000-3-2:2014, EN 61000-3-3:2013
EN 50564:2011
EN 50563:2011
2014/35/EU
2014/30/EU
2011/65/EU
2009/125/EC (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)
09-Jan-19
(signature, name and function)
Remarks:
A.Speelman, CL Compliance Manager
Drachten,