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 - KLAS MEDIKAL CIHAZLAR SANAYI MÜMESSILLIK IÇ VE DI TIC LTD.TI

Address:

RAMAZANOLU MAHALLES YILDIRIM SOKAK NO: 1 PENDK

STANBUL

34906

Turkey

Authorised Representative/ UK Responsible Person
Name: Anser Medical Ltd
Address:

11 Whiteshot Way

Saffron Walden

Essex CB102AN

United Kingdom

Code/Term Type

Surgical anti-adhesion material implantable bioabsorbable non-medicated Surgical anti-adhesion material implantable bioabsorbable non-medicated Class III

Patient surgical drape single-use Patient surgical drape single-use Class III

Neurosurgical sponge Neurosurgical sponge Class III

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
Surgical anti-adhesion material implantable bioabsorbable non-medicated	Surgical anti-adhesion material implantable bioabsorbable non-medicated	Class III
Patient surgical drape single-use	Patient surgical drape single-use	Class III
Neurosurgical sponge	Neurosurgical sponge	Class III