EU declaration of conformity

EDC EN-SER:
1830
(Document No. / Dokument br.)
(Year, Month (yyyy/mm) in which the CE mark is affixed / Godina kada
je dodeljena CE oznaka)
2017/12
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):)
(brand name, naziv robne marke )
AC3829/xx
xx: 00 to 99. indicating indicating graphic, packaging, shipping
method/destination, marketing/retail changes, or the combination of non-
electrical attachments and/or filters packaged with the units which will not
(Type version or model, Verzija tipa ili model)
Air purifier and humidifier
(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
EN 60335-2-98:2003+A1:2005+A2:2008, EN 60335-2-65:2003+A1:2008+A11:2012
EN62233:2008 ( EMF)
EN 55014-1:2006+A1:2009+A2:2011, EN 55014-2:1997+A1:2001+A2:2008
EN 61000-3-2:2014, EN 61000-3-3:2013
EN50581:2012
ETSI EN 300328 V1.9.1(2015), ETSI EN 301489-1 V1.9.2(2011), ETSI EN 301489-17 V2.2.1(2012)
2014/35/EU
2014/53/EU
2014/30/EU
2011/65/EU
2002/96/EC
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)
19-dec-17
(signature, name and function)
Remarks:
A.Speelman, CL Compliance Manager
Drachten,