Declaration of Conformity

2220
(Document No. / Pranešimo Nr.)
(Year, Month (yyyy/mm) in which the CE mark is affixed / Metai, kada CE
patvirtino)
EU DECLARATION OF CONFORMITY
(EC ATITIKTIES DEKLARACIJA)
We, PHILIPS CONSUMER LIFESTYLE B.V.
(Company name / Pavadinimas)
Philips Consumer Lifestyle B.V.
TUSSENDIEPEN 4, 9206 AD DRACHTEN, THE NETHERLANDS
(address / adresas)
declare under our responsibility that the product(s):
(Deklaruojame, kad elektronikos gaminys (-iai):)
Philips
(brand name, firmos ženklo pavadinimas )
BRI858;BRI860; BRI861; BRI862; BRI863; BRI864
(Type version or model, Tipas arba modelis)
Intense Pulse Light Hair removal device
(product description, gaminio aprašymas)
to which this declaration relates is in conformity with the following harmonized standards:
(Pagal šią deklaraciją atitinka toliau nurodytus standartus:)
following the provisions of :
(Atitinka tokias nuostatas:)
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
(Pagaminta atitinkant visus kokybės reikalavimus pagal ISO 9001 ar CENELEC nuolatinius dokumentus)
Only for Medical Devices produced under a quality scheme at least in conformity with EN13485:
The Notified Body:
performed:
(Informuota įstaiga)
(Name and number/ Pavadinimas ir numeris)
(atlikta)
(description of intervention / intervencijos aprašymas)
and issued the certificate:
(Sertifikatas išleistas)
(certificate number / sertifikato numeris)
(place,date / vieta, data)
09-Jan-19
(signature, name and function / parašas, vardas, pavardė ir pareigos)
Remarks:
A.Speelman, CL Compliance Manager
Drachten,