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 - Intensiv Medical Products IMPROMEDIFORM GmbH

Address:

Gielster Stück 11

Lüdenscheid

58513

Germany

Authorised Representative/ UK Responsible Person
Name: Medical Device Management Ltd
Address:

31 Braintree Business Park Blackwell Drive

Braintree

Essex CM7 2PU

England United Kingdom

Code/Term Type

Electric infusion pump administration set single-use Electric infusion pump administration set single-use Class I

Blood transfer set Blood transfer set Class IIa

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

Intravenous administration bag/bottle Intravenous administration bag/bottle 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
Electric infusion pump administration set single-use	Electric infusion pump administration set single-use	Class I
Blood transfer set	Blood transfer set	Class IIa
Basic intravenous administration set noninvasive	Basic intravenous administration set noninvasive	Class IIa
Intravenous administration bag/bottle	Intravenous administration bag/bottle	Class IIa