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 - Acrostak AG

Address:

Stegackerstrasse 14

Winterthur

8409

Switzerland

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

55-66 Frederick Street

Edinburgh EH2 1LS

EH2 1LS

Scotland United Kingdom

Code/Term Type

Coronary angioplasty balloon catheter perfusing Coronary angioplasty balloon catheter perfusing Class III

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

Vascular guide-catheter single-use Vascular guide-catheter single-use 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
Coronary angioplasty balloon catheter perfusing	Coronary angioplasty balloon catheter perfusing	Class III
Peripheral angioplasty balloon catheter basic	Peripheral angioplasty balloon catheter basic	Class IIa
Vascular guide-catheter single-use	Vascular guide-catheter single-use	Class IIa