Philips BDP2180/12 User Manual Declaraţie De Conformitate Bdp2180 12 Doc Aen
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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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