Philips M888 User Manual

137

(Document No.)

(Year, Month (yyyy/mm) in which the CE mark is affixed )

2013/08

EUROPEAN DECLARATION OF CONFORMITY

We, PHILIPS CONSUMER LIFESTYLE B.V.

(Company name)

Philips Consumer Lifestyle B.V.

TUSSENDIEPEN 4, 9206 AD DRACHTEN, THE NETHERLANDS

(address)

declare under our responsibility that the product(s):

Philips

(brand name)

M888

(Type version or model)

DECT Phone

(product description)

to which this declaration relates is in conformity with the following harmonized standards:

following the provisions of :

EN 60950-1:2006+A11:2009+A1:2010+A12:2011
EN 301 489-1 V1.9.2:2011
EN 301 489-6 V1.3.1:2008
EN 301 406 V2.1.1:2009
EN 50360:2001
EN 50385:2002

1999/5/EC
2006/95/EC
2004/108/EC
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

Only for Medical Devices and R&TTE products:

The Notified Body:

BABT / 0168

performed:

Notified Body Opinion

(Name and number)

and issued the certificate:

NC17388

(certificate number)

(place,date)

14-aug-13

(signature, name and function)

Remarks:

A.Speelman, CL Compliance Manager

Drachten,

137

(Document No. /Bericht Nr. )

(Year, Month (yyyy/mm) in which the CE mark is affixed /Jahr der CE
Zeichenerteilung )

2013/08

EUROPEAN DECLARATION OF CONFORMITY

(EG - Konformitätserklärung)

We, PHILIPS CONSUMER LIFESTYLE B.V.

(Company name / Name)

Philips Consumer Lifestyle B.V.

TUSSENDIEPEN 4, 9206 AD DRACHTEN, THE NETHERLANDS

(address / Anschrift)

declare under our responsibility that the product(s)

erklären als Verantwortliche, daß folgende(s) elektrische(n) Produkt(e)

Philips

(brand name, Markenname)

M888

(Type version or model, Typenbezeichnung oder Modell )

DECT Phone

(product description, Produktbezeichnung)

to which this declaration relates is in conformity with the following harmonized standards:

(auf die sich diese Konformitätserklärung bezieht, allen nachstehenden hamonisierten Normen entspricht.)

following the provisions of :

(Entsprechend den Bestimmungen der)

EN 60950-1:2006+A11:2009+A1:2010+A12:2011
EN 301 489-1 V1.9.2:2011
EN 301 489-6 V1.3.1:2008
EN 301 406 V2.1.1:2009
EN 50360:2001
EN 50385:2002

1999/5/EC
2006/95/EC
2004/108/EC
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

(und die gemäß eines Qualitätsystems produziert werden, dass mindestens der ISO 9001 oder CENELEC Permanent Documents entspricht)

Only for Medical Devices and R&TTE products:

The Notified Body:

BABT / 0168

performed:

Notified Body Opinion

(benannte Stelle)

(Name and number/ Name und Kennnummer )

(ausgeführt)

(description of intervention / Beschreibung des Verfahrens)

and issued the certificate:

NC17388

(und stellen das Zertifikat)

(certificate number / Zertifikatnummer)

(place,date / Ort, Datum )

14-aug-13

(signature, name and function / Unterschrift, Name und Funktion des Unterzeichners )

Remarks:

A.Speelman, CL Compliance Manager

Drachten,

137

(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)

2013/08

EUROPEAN DECLARATION OF CONFORMITY

(DECLARATION DE CONFORMITE CE)

We, PHILIPS CONSUMER LIFESTYLE B.V.

(Company name / Nom de l’entreprise)

Philips Consumer Lifestyle B.V.

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

(brand name, nom de la marque)

M888

(Type version or model, référence ou modèle)

DECT Phone

(product description, description du produit)

to which this declaration relates is in conformity with the following harmonized standards:

(auquel cette déclaration se rapporte, est conforme aux normes harmonisées suivantes)

following the provisions of :

(conformément aux exigences essentielles et autres dispositions pertinentes de:)

EN 60950-1:2006+A11:2009+A1:2010+A12:2011
EN 301 489-1 V1.9.2:2011
EN 301 489-6 V1.3.1:2008
EN 301 406 V2.1.1:2009
EN 50360:2001
EN 50385:2002

1999/5/EC
2006/95/EC
2004/108/EC
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

(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:

BABT / 0168

performed:

Notified Body Opinion

(L’Organisme Notifié)

(Name and number/ nom et numéro)

(a effectué)

(description of intervention / description de ’intervention)

and issued the certificate:

NC17388

(et a délivré le certificat)

(certificate number / numéro du certificat)

(place,date / lieu, date)

14-aug-13

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

Remarks:

A.Speelman, CL Compliance Manager

Drachten,

137

(Document No. / Documentnummer)

(Year, Month (yyyy/mm) in which the CE mark is affixed / Jaar, maand
waarin de CE markering is uitgegeven)

2013/08

EUROPEAN DECLARATION OF CONFORMITY

(Europeese Conformiteitsverklaring)

We, PHILIPS CONSUMER LIFESTYLE B.V.

(Company name / Bedrijfsnaam)

Philips Consumer Lifestyle B.V.

TUSSENDIEPEN 4, 9206 AD DRACHTEN, THE NETHERLANDS

(address / adres)

declare under our responsibility that the product(s)

(verklaren dat onder onze verantwoordelijkheid de product(en))

Philips

(brand name, merknaam)

M888

(Type version or model, typenummer of model)

DECT Phone

(product description, productbeschrijving)

to which this declaration relates is in conformity with the following harmonized standards:

(waar deze verklaring betrekking op heeft voldoen aan de volgende geharmoniseerde standaarden)

following the provisions of :

(volgens de voorwaarden van:)

EN 60950-1:2006+A11:2009+A1:2010+A12:2011
EN 301 489-1 V1.9.2:2011
EN 301 489-6 V1.3.1:2008
EN 301 406 V2.1.1:2009
EN 50360:2001
EN 50385:2002

1999/5/EC
2006/95/EC
2004/108/EC
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

(En worden geproduceerd volgens een kwaliteitsprogramma wat minimaal overeenkomt met ISO9001 of de CENELEC permanente documenten)

Only for Medical Devices and R&TTE products:

The Notified Body:

BABT / 0168

performed:

Notified Body Opinion

(Notified Body)

(Name and number/ Naam en nummer)

(heeft uitgevoerd)

(description of intervention / uitgevoerd testprotocol)

and issued the certificate:

NC17388

(en heeft een certificaat uitgegeven)
(certificate number / nummer van het certificaat)

(place,date / plaats, datum)

14-aug-13

(signature, name and function / handtekening, naam en functie)

Remarks:

A.Speelman, CL Compliance Manager

Drachten,

137

(Document No. / Číslo zprávy)

(Year, Month (yyyy/mm) in which the CE mark is affixed / Rok udělění

známky CE)

2013/08

EUROPEAN DECLARATION OF CONFORMITY

(Prohlášení o shodě v EU)

We, PHILIPS CONSUMER LIFESTYLE B.V.

(Company name / Jméno)

Philips Consumer Lifestyle B.V.

TUSSENDIEPEN 4, 9206 AD DRACHTEN, THE NETHERLANDS

(address / adresa)

declare under our responsibility that the product(s)

(Prohlašujeme na svou odpovědnost, že elektrický výrobek)

Philips

(brand name, značka)

M888

(Type version or model, Typ verze nebo model)

DECT Phone

(product description, popis výrobku)

to which this declaration relates is in conformity with the following harmonized standards:

(na nějž se toto prohlášení vztahuje, je ve shodě s následujícími harmonizovanými normami:)

following the provisions of :

(Následovaných ustanoveními Směrnic:)

EN 60950-1:2006+A11:2009+A1:2010+A12:2011
EN 301 489-1 V1.9.2:2011
EN 301 489-6 V1.3.1:2008
EN 301 406 V2.1.1:2009
EN 50360:2001
EN 50385:2002

1999/5/EC
2006/95/EC
2004/108/EC
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

(A jsou vyráběny v systému řízení kvality minimálně ve shodě s ISO 9001 nebo)

Only for Medical Devices and R&TTE products:

The Notified Body:

BABT / 0168

performed:

Notified Body Opinion

(Kompetentní orgán)

(Name and number/ Název a číslo)

(provedl)

(description of intervention / popis operace)

and issued the certificate:

NC17388

(a vydal certifikát,)

(certificate number / číslo certifikátu)

(place,date / místo, datum)

14-aug-13

(signature, name and function / podpis, jméno a funkce)

Remarks:

A.Speelman, CL Compliance Manager

Drachten,

137

(Document No. / Rapportnummer)

(Year, Month (yyyy/mm) in which the CE mark is affixed / Årstal for
påhæftning af CE-mærkningen)

2013/08

EUROPEAN DECLARATION OF CONFORMITY

(EU KONFORMITETSERKLÆRING)

We, PHILIPS CONSUMER LIFESTYLE B.V.

(Company name / Virksomhedens navn)

Philips Consumer Lifestyle B.V.

TUSSENDIEPEN 4, 9206 AD DRACHTEN, THE NETHERLANDS

(address / adresse)

declare under our responsibility that the product(s)

(Erklærer i henhold til vores ansvar, at de(t) elektriske produkt(er))

Philips

(brand name, navn på varemærke)

M888

(Type version or model, type eller model)

DECT Phone

(product description, produktbeskrivelse)

to which this declaration relates is in conformity with the following harmonized standards:

(til hvilke(t) denne erklæring relaterer sig, er i konformitet med følgende harmoniserede standarder)

following the provisions of :

(Opfylder de ufravigelige krav og øvrige forskrifter i)

EN 60950-1:2006+A11:2009+A1:2010+A12:2011
EN 301 489-1 V1.9.2:2011
EN 301 489-6 V1.3.1:2008
EN 301 406 V2.1.1:2009
EN 50360:2001
EN 50385:2002

1999/5/EC
2006/95/EC
2004/108/EC
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

(Og er produceret i en kvalitet, der, som minimum, opfylder kravene i ISO 9001-standarden eller CENELEC's permanente dokumenter)

Only for Medical Devices and R&TTE products:

The Notified Body:

BABT / 0168

performed:

Notified Body Opinion

(Det Notificerede Organ)

(Name and number/ Navn og nummer)

(har gennemført)

(description of intervention / beskrivelse af intervention)

and issued the certificate:

NC17388

(og udstedt erklæringen)

(certificate number / erklæringsnummer)

(place,date / sted, dato)

14-aug-13

(signature, name and function / Signatur, navn og titel)

Remarks:

A.Speelman, CL Compliance Manager

Drachten,

137

(Document No. / Documento nº.)

(Year, Month (yyyy/mm) in which the CE mark is affixed / Año en el que
se incluye el marcado CE))

2013/08

EUROPEAN DECLARATION OF CONFORMITY

(EU DECLARACIÓN CE DE CONFORMIDAD)

We, PHILIPS CONSUMER LIFESTYLE B.V.

(Company name / Nombre compaña )

Philips Consumer Lifestyle B.V.

TUSSENDIEPEN 4, 9206 AD DRACHTEN, THE NETHERLANDS

(address / dirección )

declare under our responsibility that the product(s):

(Declaramos bajo nuestra propia responsabilidad que el (los) producto(s):

Philips

(brand name, nombre de la marca)

M888

(Type version or model, Referencia o modelo)

DECT Phone

(product description, descripción del producto )

to which this declaration relates is in conformity with the following harmonized standards:

(Al que hace referencia esta declaración cumple con las siguientes normas armonizadas)

following the provisions of :

(Siguiendo las disposiciones relativas a:)

EN 60950-1:2006+A11:2009+A1:2010+A12:2011
EN 301 489-1 V1.9.2:2011
EN 301 489-6 V1.3.1:2008
EN 301 406 V2.1.1:2009
EN 50360:2001
EN 50385:2002

1999/5/EC
2006/95/EC
2004/108/EC
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

(Y se fabrican conforme a una calidad al menos conforme a la norma ISO 9001 o a los Documentos Permanentes CENELEC)

Only for Medical Devices and R&TTE products:

The Notified Body:

BABT / 0168

performed:

Notified Body Opinion

(El organismo notificado)

(Name and number/ Nombre y número)

(realizador)

(description of intervention / descripción de la intervención)

and issued the certificate:

NC17388

(Y expidió el certificado)

(certificate number / número de certificado)

(place,date / lugar, fecha)

14-aug-13

(signature, name and function / firma, nombre y cargo )

Remarks:

A.Speelman, CL Compliance Manager

Drachten,