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Philips Consumer Lifestyle B.V.
HK-1304- BDP2100,BDP2180

2013/01

.................................................................

..............................................................................................
(Year, Month (yyyy/mm) in which the CE mark is affixed /
Année/mois (aaaa/mm) au cours de laquelle le marquage
CE a été apposé)

(Document No. / Numéro du document)

EUROPEAN DECLARATION OF CONFORMITY
(DECLARATION DE CONFORMITE CE)

We / Nous, PHILIPS CONSUMER LIFESTYLE B.V.
(Company name / Nom de l’entreprise)

TUSSENDIEPEN 4, 9206 AD DRACHTEN, THE NETHERLANDS
(address / adresse)

declare under our responsibility that the product(s):
(déclarons sous notre propre responsabilité que le(s) produit(s))

PHILIPS

BDP2100/12,/05,/51; BDP2180/12,/05,/51

.............................................................................

...........................................................................

(brand name, nom de la marque)

(Type version or model, référence ou modèle)

Blu-Ray Disc/DVD Player
.............................................................................
(product description, description du produit)

to which this declaration relates is in confirmity with the following harmonized standards:
(auquel cette déclaration se rapporte, est conforme aux normes harmonisées suivantes)

(title, number and date of issue of the standard / titre, numéro et date de parution de la norme)

EN60065:2002+A1:2006+A11:2008+A2:2010+A12:2011
EN55013:2001+A1:2003+A2:2006
EN55020:2007+A11:2011
EN55022:2010
EN55024:2010
EN61000-3-2:2006+A1:2009+A2:2009
EN61000-3-3:2008
EN50564:2011
EN62311:2008

following the provisions of :
(conformément aux exigences essentielles et autres dispositions pertinentes de:)

2006/95/EC (Low Voltage Directive)
2004/108/EC (EMC Directive)
2011/65/EU (RoHS Directive)
2009/125/EC (Eco Design) - EC/1275/2008
And are produced under a quality scheme at least in conformity with ISO 9001 or CENELEC Permanent Documents
(Et sont fabriqués conformément à une qualité au moins conforme à la norme ISO 9001 ou aux Documents Permanents CENELEC)

Only for Medical Devices and R&TTE products:

The Notified Body:
(L’Organisme Notifié)

..................................................
(Name and number/ nom et numéro)

and issued the certificate:
(et a délivré le certificat)

performed:
(a effectué)

........................................................................
(description of intervention / description de ’intervention)

............................................................
(certificate number / numéro du certificat)

Remarks:

Drachten, Netherlands, Jan. 24, 2013

A.Speelman, CL Compliance Manager

.........................................................

.........................................................

(place,date / lieu, date)

(signature, name and function / signature, nom et fonction)

Philips Consumer Lifestyle B.V.

template AMB 544-9056



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