Public Access Database for Medical Device Registration

Registration does not represent any form of accreditation, certification or approval by the UK Competent Authority(MHRA)
Where a conformity assessment certificate is listed as expired, existing products already placed on the market prior to the expiry may not be affected by this expiry and can continue to be used. This expiry stops new products being placed on the market until there is a new certificate of conformity

Manufacturer's By Name

By Device

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Manufacturer's Devices - Bayteks Teknik Tekstil Sanayi ve Ticaret Anonim irketi

Address:

Organize Sanayi Bölgesi 19 Nolu Cadde

No:9 Merkez

Kilis

79000

Turkey

Authorised Representative/ UK Responsible Person
Name: Advena Ltd
Address:

Pure Offices Plato Close

Warwick

CV34 6WE

England United Kingdom

Code/Term Type

Patient surgical drape single-use Patient surgical drape single-use Class I

Surgical apron single-use Surgical apron single-use Class I

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

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Code/Term		Type
Patient surgical drape single-use	Patient surgical drape single-use	Class I
Surgical apron single-use	Surgical apron single-use	Class I