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 - Medical Service GmbH

Address:

Medical Service GmbH Luisenstrasse 8

75378 Bad Liebenzell/ Unterhaugstett Germany

Bad Liebenzell/ Unterhaugstett

75378

Germany

Authorised Representative/ UK Responsible Person
Name: TFX Group Ltd (T/A Teleflex Medical UK)
Address:

Grosvenor House Horseshoe Crescent

Old Town Beaconsfield

Buckinghamshire HP9 1LJ

England United Kingdom

Code/Term Type

Single-administration urethral drainage catheter Single-administration urethral drainage catheter Class III

Stoma drainage catheter Stoma drainage catheter Class III

Stoma drainage catheter Stoma drainage catheter Class I

Stoma drainage catheter Stoma drainage catheter 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
Single-administration urethral drainage catheter	Single-administration urethral drainage catheter	Class III
Stoma drainage catheter	Stoma drainage catheter	Class III
Stoma drainage catheter	Stoma drainage catheter	Class I
Stoma drainage catheter	Stoma drainage catheter	Class I