EU declaration of conformity

2341
(Document No. / Številka poročila)
(Year, Month (yyyy/mm) in which the CE mark is affixed / Leto namstitve
CE znaka)
2019/05
EU DECLARATION OF CONFORMITY
(Izjava o skladnosti)
We, PHILIPS CONSUMER LIFESTYLE B.V.
(Company name / Ime)
Philips Consumer Lifestyle B.V.
TUSSENDIEPEN 4, 9206 AD DRACHTEN, THE NETHERLANDS
(address / Naslov)
declare under our responsibility that the product(s):
(S polno odgovornostjo izjavljamo)
Philips
(brand name, Ime znamke)
AC3033,AC3036,AC3039,AC3055,AC3059,AC3854,AC3858,AC4236
(Type version or model, Tip, verzija ali model)
Air Purifier
(product description, Opis proizvoda)
to which this declaration relates is in conformity with the following harmonized standards:
(Na katerega se nanaša ta izjava je skladen z naslednjimi harmoniziranimi standardi)
following the provisions of :
(V skladu z naslednjimi odločbami)
EN 60335-1:2012+A11:2014+A13:2017
EN 60335-2-65:2003+A1:2008+A11:2012
EN 62233:2008
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
EN 50581:2012
EN 62311:2008
ETSI EN 301 489-1 V2.2.1, ETSI EN 301 489-17 V3.2.0, ETSI EN 300 328 V2.1.1
2011/65/EU
2014/53/EU
And are produced under a quality scheme at least in conformity with ISO 9001 or CENELEC Permanent Documents
(In so proizvedeni v skladu s shemo kakovosti najmanj v skladu z ISO 9001 ali CENELEC stalnimi dokumenti)
Only for Medical Devices produced under a quality scheme at least in conformity with EN13485:
The Notified Body:
performed:
(Priglašeno organ)
(Name and number/ Ime in številka)
(Izvršeno)
(description of intervention / Opis ukrepa )
and issued the certificate:
(Izdaja certifikat)
(certificate number / Številka certifikata)
(place,date / Kraj, datum)
06-Jun-19
(signature, name and function / Podpis, Ime in funkcija)
Remarks:
A.Speelman, CL Compliance Manager
Drachten,