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 - Infumed GmbH

Address:

Industriestraße 45-47a

Friedeburg

26446

Germany

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

2 The Drift

Thurston

Suffolk IP31 3RT

United Kingdom

Code/Term Type

Radiographic procedure tubing Radiographic procedure tubing Class IIa

Basic intravenous administration set noninvasive Basic intravenous administration set noninvasive Class IIa

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
Radiographic procedure tubing	Radiographic procedure tubing	Class IIa
Basic intravenous administration set noninvasive	Basic intravenous administration set noninvasive	Class IIa