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Philips Consumer Lifestyle B.V.
Philips Consumer Lifestyle B.V. template AMB 544-9056
HK-1315-HMP7100# Year 2013
........................................................ ...........................................................................
(Document No. / Numéro du document) (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)
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
..........................................................
HMP7100#/05, /12, /58
(“#” can be A-W consist of different cabinet colour)
................................................................................
(brand name, nom de la marque) (Type version or model, référence ou modèle)
Home Media 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)
EN 60065:2002+A1(2006)+A11(2008)+A12(2011)
EN 55013:2001+A1(2003)+A2(2006)
EN 55020:2007+A11(2011)
EN 55022:2010
EN 55024:2010
EN301489-1 V1.9.2 (2011)
EN301489-17 V2.1.1 (2009)
EN300328 V1.7.1 (2006)
EN 61000-3-2:2006 + A1(2009)+A2(2009)
EN 61000-3-3:2008
EN50564:2011
EN62479:2010
EN50581:2012
following the provisions of :
(conformément aux exigences essentielles et autres dispositions pertinentes de:)
2006/95/EC (Low Voltage Directive)
1999/5/EC (R&TTE 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:
Dekra Certification B.V.
PHOENIX TESTLAB GmbH (0700)
..................................................
CB test
R&TTE test
........................................................................
(L’Organisme Notifié)
(Name and number/ nom et numéro)
a effectué)
(description of intervention / description de ’intervention)
and issued the certificate:
NL-26369 13-111539
............................................................
(et a délivré le certificat)
(certificate number / numéro du certificat)
Drachten, Netherlands, April 15, 2013 A.Speelman, CL Compliance Manager
.........................................................
.........................................................
(place,date / lieu, date)
(signature, name and function / signature, nom et fonction)
2


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