Bruker manual PHILIPS CD1901B/21
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Manuell abstrakt: bruksanvisning PHILIPS CD1901B/21
Detaljerte instruksjoner for bruken står i bruksanvisningen.
[. . . ] 1:2009 EN 50360:2001 EN 50385:2002
following the provisions of :
(Entsprechend den Bestimmungen der)
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:
(benannte Stelle)
BABT / 0168
(Name and number/ Name und Kennnummer )
performed:
(ausgeführt) (description of intervention / Beschreibung des Verfahrens)
and issued the certificate:
(und stellen das Zertifikat)
NC 16322 / NC 16321
(certificate number / Zertifikatnummer)
Remarks:
Drachten, 16-aug-13
(place, date / Ort, Datum )
A. [. . . ] 1:2009 EN 50360:2001 EN 50385:2002
following the provisions of :
(conformément aux exigences essentielles et autres dispositions pertinentes de:)
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:
(L’Organisme Notifié)
BABT / 0168
(Name and number/ nom et numéro)
performed:
(a effectué) (description of intervention / description de ’intervention)
and issued the certificate:
(et a délivré le certificat)
NC 16322 / NC 16321
(certificate number / numéro du certificat)
Remarks:
Drachten, 16-aug-13
(place, date / lieu, date)
A. 1:2009 EN 50360:2001 EN 50385:2002
following the provisions of :
(volgens de voorwaarden van:)
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:
(Notified Body)
BABT / 0168
(Name and number/ Naam en nummer)
performed:
(heeft uitgevoerd) (description of intervention / uitgevoerd testprotocol)
and issued the certificate:
(en heeft een certificaat uitgegeven)
NC 16322 / NC 16321
(certificate number / nummer van het certificaat)
Remarks:
Drachten, 16-aug-13
(place, date / plaats, datum)
A. 1:2009 EN 50360:2001 EN 50385:2002
following the provisions of :
(Následovaných ustanoveními Směrnic:)
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:
(Kompetentní orgán)
BABT / 0168
(Name and number/ Název a číslo)
performed:
(provedl) (description of intervention / popis operace)
and issued the certificate:
(a vydal certifikát, )
NC 16322 / NC 16321
(certificate number / číslo certifikátu)
Remarks:
Drachten, 16-aug-13
(place, date / místo, datum)
A. (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))
CD191 / CD196
Philips
(brand name, navn på varemærke) (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)
EN 60950-1:2006+A11:2009+A1:2010+A12:2011 EN 301 489-1 V1. 1:2009 EN 50360:2001 EN 50385:2002
following the provisions of :
(În conformitate cu dispoziţiile directivelor)
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
(Şi sunt fabricate după o schemă de calitate conformă cel puţin cu standardul ISO 9001 sau Documentele Permanente CENELEC)
Only for Medical Devices and R&TTE products:
The Notified Body:
(Organismul notificat)
BABT / 0168
(Name and number/ Nume si număr)
performed:
(a efectuat) (description of intervention / descrierea intervenţiei)
and issued the certificate:
(Şi a emis certificatul)
NC 16322 / NC 16321
(certificate number / Numărul certificatului)
Remarks:
Drachten, 16-aug-13
(place, date / locul, data)
A. 1:2009 EN 50360:2001 EN 50385:2002
following the provisions of :
(В соответствие с положениями:)
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
(по крайней мере, в соответствии с ISO 9001 или)
Only for Medical Devices and R&TTE products:
The Notified Body:
BABT / 0168 NC 16322 / NC 16321
(certificate number / номер сертификата)
performed:
(проверил(а)) (description of intervention / описание проверки)
(Нотифицированный Орган) (Name and number/ Наз 1:2009 EN 50360:2001 EN 50385:2002
following the provisions of :
(V nadväznosti na ustanovenia)
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 sú vyrobené systémom kvality minimálne v súlade s normou ISO 9001 alebo CENELEC dokumentmi)
Only for Medical Devices and R&TTE products:
The Notified Body:
(Notifikovaný orgán)
BABT / 0168
(Name and number/ Názov a číslo)
performed:
(vykonal) (description of intervention / opis zásahu)
and issued the certificate:
(A vydal osvedčenie)
NC 16322 / NC 16321
(certificate number / číslo osvedčenia)
Remarks:
Drachten, 16-aug-13
(place, date / miesto, dátum)
A. 1:2009 EN 50360:2001 EN 50385:2002
following the provisions of :
(V skladu z naslednjimi odločbami)
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
(In so proizvedeni v skladu s shemo kakovosti najmanj v skladu z ISO 9001 ali CENELEC stalnimi dokumenti)
Only for Medical Devices and R&TTE products:
The Notified Body:
(Priglašeno organ)
BABT / 0168
(Name and number/ Ime in številka)
performed:
(Izvršeno) (description of intervention / Opis ukrepa )
and issued the certificate:
(Izdaja certifikat)
NC 16322 / NC 16321
(certificate number / Številka certifikata)
Remarks:
Drachten, 16-aug-13
(place, date / Kraj, datum)
A. 1:2009 EN 50360:2001 EN 50385:2002
following the provisions of :
(Yasal hükümler şu şekildedir:)
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 az ISO 9001 veya CENELEC Daimi Belgelerine uygun kalite şemasına binaen mevcut ürünlerdir)
Only for Medical Devices and R&TTE products:
The Notified Body:
(Yetkili Kurul)
BABT / 0168
(Name and number/ Isin ve numara)
performed:
(yerine getirmiştir) (description of intervention /müdahalenin tanımı )
and issued the certificate:
(sertifikayı düzenlemiştir)
NC 16322 / NC 16321
(certificate number / sertifika numarası)
Remarks:
Drachten, 16-aug-13
(place, date / Yer ve tarih )
A. [. . . ] 1:2009 EN 50360:2001 EN 50385:2002
following the provisions of :
(Yasal hükümler şu şekildedir:)
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 az ISO 9001 veya CENELEC Daimi Belgelerine uygun kalite şemasına binaen mevcut ürünlerdir)
Only for Medical Devices and R&TTE products:
The Notified Body:
(Yetkili Kurul)
BABT / 0168
(Name and number/ Isin ve numara)
performed:
(yerine getirmiştir) (description of intervention /müdahalenin tanımı )
and issued the certificate:
(sertifikayı düzenlemiştir)
NC 16322 / NC 16321
(certificate number / sertifika numarası)
Remarks:
Drachten, 16-aug-13
(place, date / Yer ve tarih )
A. [. . . ]
ANSVARSFRASKRIVELSE FOR NEDLASTING AV BRUKSANVISNING PHILIPS CD1901B/21
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Lastmanuals kan ikke på noen måte bli holdt ansvarlig for at det du leter etter ikke finnes, er ufullstendig, er i ett annet språk eller at produktet eller språket ikke tilsvarer det valgte produkt. Lastmanuals utfører ikke f.eks. Ikke oversettelses tjenester.
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