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 - M.A. Med Alliance SA

Address:

Rue de Rive 5

Nyon

1260

Switzerland

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

C/O Ids + Co 38 Beansburn

Kilmarnock

Ayrshire KA3 1RL

Scotland United Kingdom

Code/Term Type

Peripheral angioplasty balloon catheter drug-coated Peripheral angioplasty balloon catheter drug-coated Class III

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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