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

Back to MHRA

Manufacturer's Devices - Qualimed Innovative Medizinprodukte GmbH

Address:

Boschstraße 16

Winsen

21423

Germany

Authorised Representative/ UK Responsible Person
Name: Emergo Consulting (UK) Limited
Address:

Compass House Vision Park Histon c/o Cr360 – UL International

Cambridge

CB24 9BZ

England United Kingdom

Code/Term Type

Vascular guide-catheter single-use Vascular guide-catheter single-use Class IIa

Peripheral artery stent bare-metal Peripheral artery stent bare-metal Class IIb

Peripheral angioplasty balloon catheter basic Peripheral angioplasty balloon catheter basic Class IIa

Thrombectomy suction catheter Thrombectomy suction catheter Conformity Assessment Certificate Expired Class III

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

© 2011 Crown Copyright. To contact us about this website, use our feedback form.

Code/Term		Type
Vascular guide-catheter single-use	Vascular guide-catheter single-use	Class IIa
Peripheral artery stent bare-metal	Peripheral artery stent bare-metal	Class IIb
Peripheral angioplasty balloon catheter basic	Peripheral angioplasty balloon catheter basic	Class IIa
Thrombectomy suction catheter	Thrombectomy suction catheter Conformity Assessment Certificate Expired	Class III