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 - KOB GmbH

Address:

Lauterstr. 50

Wolfstein

67752

Germany

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

Pure Offices Plato Close

Warwick

CV34 6WE

England United Kingdom

Code/Term Type

Moist-cold pressure bandage Moist-cold pressure bandage Class I

Pressure bandage non-latex single-use Pressure bandage non-latex single-use Class I

Non-adhesive device retention bandage Non-adhesive device retention bandage Class I

Pressure bandage Hevea-latex single-use Pressure bandage Hevea-latex single-use Class I

Pressure bandage non-latex reusable Pressure bandage non-latex reusable 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
Moist-cold pressure bandage	Moist-cold pressure bandage	Class I
Pressure bandage non-latex single-use	Pressure bandage non-latex single-use	Class I
Non-adhesive device retention bandage	Non-adhesive device retention bandage	Class I
Pressure bandage Hevea-latex single-use	Pressure bandage Hevea-latex single-use	Class I
Pressure bandage non-latex reusable	Pressure bandage non-latex reusable	Class I