Philips QG3380 User manual

Philips Consumer Lifestyle B.V.

1571	2016/09
(Document No.)	(Year, Month (yyyy/mm) in which the CE mark is affixed )
	EU DECLARATION OF CONFORMITY
	We, PHILIPS CONSUMER LIFESTYLE B.V.
	(Company name)
	TUSSENDIEPEN 4, 9206 AD DRACHTEN, THE NETHERLANDS
	(address)

declare under our responsibility that the product(s):

Philips

BT415, QG3360, QG3362, QG3370, QG3371, QG3378, QG3379, QG3380, QG3381, QG3382, QG3383, QG3385, QG3386, QG3387, QG3388, QG3389, QG3391, QG415,

HQ8505

(brand name)

(Type version or model)

Rechargeable Body groomer , Adapter

(product description)

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

EN60335-2-8:2003 + A1:2005 + A2:2008

EN60335-1:2002 A11:2004 A1:2004 A12:2006 A2:2006 A13:2008 A14:2010 A15:2011

EN61558-1:2005 A1:2009, EN61558-2-16:2009 A1:2013

EN62233:2008

EN55014-1:2006 + A1:2009 + A2:2011

EN61000-3-2:2014, EN61000-3-3:2013

EN55014-2:2015

EN50564:2011, EN50581:2012, EN50563:2011

following the provisions of :

2014/35/EU

2014/30/EU

2009/125/EC

EC/1275/2008 EC/278/2009, 2011/65/EU

And are produced under a quality scheme at least in conformity with ISO 9001 or CENELEC Permanent Documents

Only for Medical Devices produced under a quality scheme at least in conformity with EN13485:

The Notified Body:	performed:
	(Name and number)

and issued the certificate:

(certificate number)

Remarks:

Drachten, 04-mei-17	A.Speelman, CL Compliance Manager
(place,date)	(signature, name and function)

Philips Consumer Lifestyle B.V.

1571

(Document No. /Bericht Nr. )

2016/09

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

EU DECLARATION OF CONFORMITY

(EG - Konformitätserklärung)

We, PHILIPS CONSUMER LIFESTYLE B.V.

(Company name / Name)

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

BT415, QG3360, QG3362, QG3370, QG3371, QG3378, QG3379, QG3380, QG3381, QG3382, QG3383, QG3385, QG3386, QG3387, QG3388, QG3389, QG3391, QG415,

HQ8505

(brand name, Markenname)

(Type version or model, Typenbezeichnung oder Modell )

Rechargeable Body groomer , Adapter

(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.)

EN60335-2-8:2003 + A1:2005 + A2:2008

EN60335-1:2002 A11:2004 A1:2004 A12:2006 A2:2006 A13:2008 A14:2010 A15:2011

EN61558-1:2005 A1:2009, EN61558-2-16:2009 A1:2013

EN62233:2008

EN55014-1:2006 + A1:2009 + A2:2011

EN61000-3-2:2014, EN61000-3-3:2013

EN55014-2:2015

EN50564:2011, EN50581:2012, EN50563:2011

following the provisions of :

(Entsprechend den Bestimmungen der)

2014/35/EU

2014/30/EU

2009/125/EC

EC/1275/2008 EC/278/2009, 2011/65/EU

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 produced under a quality scheme at least in conformity with EN13485:

The Notified Body:

performed:

(benannte Stelle)

(Name and number/ Name und Kennnummer )

(ausgeführt)

(description of intervention / Beschreibung des Verfahrens)

and issued the certificate:

(und stellen das Zertifikat)

(certificate number / Zertifikatnummer)

Remarks:

Drachten, 04-mei-17	A.Speelman, CL Compliance Manager
(place,date / Ort, Datum )	(signature, name and function / Unterschrift, Name und Funktion des Unterzeichners )

Philips Consumer Lifestyle B.V.

1571

(Document No. / Numéro du document)

2016/09

(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)

EU DECLARATION OF CONFORMITY

(DECLARATION DE CONFORMITE CE)

We, 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

(brand name, nom de la marque)

BT415, QG3360, QG3362, QG3370, QG3371, QG3378, QG3379, QG3380, QG3381, QG3382, QG3383, QG3385, QG3386, QG3387, QG3388, QG3389, QG3391, QG415,

HQ8505

(Type version or model, référence ou modèle)

Rechargeable Body groomer , Adapter

(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)

EN60335-2-8:2003 + A1:2005 + A2:2008

EN60335-1:2002 A11:2004 A1:2004 A12:2006 A2:2006 A13:2008 A14:2010 A15:2011

EN61558-1:2005 A1:2009, EN61558-2-16:2009 A1:2013

EN62233:2008

EN55014-1:2006 + A1:2009 + A2:2011

EN61000-3-2:2014, EN61000-3-3:2013

EN55014-2:2015

EN50564:2011, EN50581:2012, EN50563:2011

following the provisions of :

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

2014/35/EU

2014/30/EU

2009/125/EC

EC/1275/2008 EC/278/2009, 2011/65/EU

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 produced under a quality scheme at least in conformity with EN13485:

The Notified Body:

performed:

(L’Organisme Notifié)

(Name and number/ nom et numéro)

(a effectué)

(description of intervention / description de ’intervention)

and issued the certificate:

(et a délivré le certificat)

(certificate number / numéro du certificat)

Remarks:

Drachten, 04-mei-17	A.Speelman, CL Compliance Manager
(place,date / lieu, date)	(signature, name and function / signature, nom et fonction)

Philips Consumer Lifestyle B.V.

1571

(Document No. / Documentnummer)

2016/09

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

EU DECLARATION OF CONFORMITY

(Europeese Conformiteitsverklaring)

We, PHILIPS CONSUMER LIFESTYLE B.V.

(Company name / Bedrijfsnaam)

TUSSENDIEPEN 4, 9206 AD DRACHTEN, THE NETHERLANDS

declare under our responsibility that the product(s)

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

Philips

(brand name, merknaam)

Rechargeable Body groomer , Adapter

(product description, productbeschrijving)

(address / adres)

BT415, QG3360, QG3362, QG3370, QG3371, QG3378, QG3379, QG3380, QG3381, QG3382, QG3383, QG3385, QG3386, QG3387, QG3388, QG3389, QG3391, QG415,

HQ8505

(Type version or model, typenummer of model)

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)

EN60335-2-8:2003 + A1:2005 + A2:2008

EN60335-1:2002 A11:2004 A1:2004 A12:2006 A2:2006 A13:2008 A14:2010 A15:2011

EN61558-1:2005 A1:2009, EN61558-2-16:2009 A1:2013

EN62233:2008

EN55014-1:2006 + A1:2009 + A2:2011

EN61000-3-2:2014, EN61000-3-3:2013

EN55014-2:2015

EN50564:2011, EN50581:2012, EN50563:2011

following the provisions of :

(volgens de voorwaarden van:)

2014/35/EU

2014/30/EU

2009/125/EC

EC/1275/2008 EC/278/2009, 2011/65/EU

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 produced under a quality scheme at least in conformity with EN13485:

The Notified Body:

performed:

(Notified Body)

(Name and number/ Naam en nummer)

(heeft uitgevoerd) (description of intervention / uitgevoerd testprotocol)

and issued the certificate:

(en heeft een certificaat uitgegeven)

(certificate number / nummer van het certificaat)

Remarks:

Drachten, 04-mei-17	A.Speelman, CL Compliance Manager
(place,date / plaats, datum)	(signature, name and function / handtekening, naam en functie)

Philips Consumer Lifestyle B.V.

1571

(Document No. / Číslo zprávy)

2016/09

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

EU DECLARATION OF CONFORMITY

(Prohlášení o shodě v EU)

We, PHILIPS CONSUMER LIFESTYLE B.V.

(Company name / Jméno)

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

BT415, QG3360, QG3362, QG3370, QG3371, QG3378, QG3379, QG3380, QG3381, QG3382, QG3383, QG3385, QG3386, QG3387, QG3388, QG3389, QG3391, QG415,

HQ8505

(brand name, značka)

(Type version or model, Typ verze nebo model)

Rechargeable Body groomer , Adapter

(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:)

EN60335-2-8:2003 + A1:2005 + A2:2008

EN60335-1:2002 A11:2004 A1:2004 A12:2006 A2:2006 A13:2008 A14:2010 A15:2011

EN61558-1:2005 A1:2009, EN61558-2-16:2009 A1:2013

EN62233:2008

EN55014-1:2006 + A1:2009 + A2:2011

EN61000-3-2:2014, EN61000-3-3:2013

EN55014-2:2015

EN50564:2011, EN50581:2012, EN50563:2011

following the provisions of :

(Následovaných ustanoveními Směrnic:)

2014/35/EU

2014/30/EU

2009/125/EC

EC/1275/2008 EC/278/2009, 2011/65/EU

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 produced under a quality scheme at least in conformity with EN13485:

The Notified Body:

performed:

(Kompetentní orgán)

(Name and number/ Název a číslo)

(provedl)

(description of intervention / popis operace)

and issued the certificate:

(a vydal certifikát,)

(certificate number / číslo certifikátu)

Remarks:

Drachten, 04-mei-17	A.Speelman, CL Compliance Manager
(place,date / místo, datum)	(signature, name and function / podpis, jméno a funkce)

Philips Consumer Lifestyle B.V.

1571

(Document No. / Rapportnummer)

2016/09

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

EU DECLARATION OF CONFORMITY

(EU KONFORMITETSERKLÆRING)

We, PHILIPS CONSUMER LIFESTYLE B.V.

(Company name / Virksomhedens navn)

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)

BT415, QG3360, QG3362, QG3370, QG3371, QG3378, QG3379, QG3380, QG3381, QG3382, QG3383, QG3385, QG3386, QG3387, QG3388, QG3389, QG3391, QG415,

HQ8505

(Type version or model, type eller model)

Rechargeable Body groomer , Adapter

(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)

EN60335-2-8:2003 + A1:2005 + A2:2008

EN60335-1:2002 A11:2004 A1:2004 A12:2006 A2:2006 A13:2008 A14:2010 A15:2011

EN61558-1:2005 A1:2009, EN61558-2-16:2009 A1:2013

EN62233:2008

EN55014-1:2006 + A1:2009 + A2:2011

EN61000-3-2:2014, EN61000-3-3:2013

EN55014-2:2015

EN50564:2011, EN50581:2012, EN50563:2011

following the provisions of :

(Opfylder de ufravigelige krav og øvrige forskrifter i)

2014/35/EU

2014/30/EU

2009/125/EC

EC/1275/2008 EC/278/2009, 2011/65/EU

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 produced under a quality scheme at least in conformity with EN13485:

The Notified Body:

performed:

(Det Notificerede Organ)

(Name and number/ Navn og nummer)

(har gennemført) (description of intervention / beskrivelse af intervention)

and issued the certificate:

(og udstedt erklæringen)

(certificate number / erklæringsnummer)

Remarks:

Drachten, 04-mei-17	A.Speelman, CL Compliance Manager
(place,date / sted, dato)	(signature, name and function / Signatur, navn og titel)

Philips Consumer Lifestyle B.V.

1571

(Document No. / Documento nº.)

2016/09

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

EU DECLARATION OF CONFORMITY

(EU DECLARACIÓN CE DE CONFORMIDAD)

We, PHILIPS CONSUMER LIFESTYLE B.V.

(Company name / Nombre compaña )

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

BT415, QG3360, QG3362, QG3370, QG3371, QG3378, QG3379, QG3380, QG3381, QG3382, QG3383, QG3385, QG3386, QG3387, QG3388, QG3389, QG3391, QG415,

HQ8505

(brand name, nombre de la marca)

(Type version or model, Referencia o modelo)

Rechargeable Body groomer , Adapter

(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)

EN60335-2-8:2003 + A1:2005 + A2:2008

EN60335-1:2002 A11:2004 A1:2004 A12:2006 A2:2006 A13:2008 A14:2010 A15:2011

EN61558-1:2005 A1:2009, EN61558-2-16:2009 A1:2013

EN62233:2008

EN55014-1:2006 + A1:2009 + A2:2011

EN61000-3-2:2014, EN61000-3-3:2013

EN55014-2:2015

EN50564:2011, EN50581:2012, EN50563:2011

following the provisions of :

(Siguiendo las disposiciones relativas a:)

2014/35/EU

2014/30/EU

2009/125/EC

EC/1275/2008 EC/278/2009, 2011/65/EU

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 produced under a quality scheme at least in conformity with EN13485:

The Notified Body:

performed:

(El organismo notificado)

(Name and number/ Nombre y número)

(realizador)

(description of intervention / descripción de la intervención)

and issued the certificate:

(Y expidió el certificado)

(certificate number / número de certificado)

Remarks:

Drachten, 04-mei-17	A.Speelman, CL Compliance Manager
(place,date / lugar, fecha)	(signature, name and function / firma, nombre y cargo )