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 - Veryan Medical Ltd

Address:

Block 5 Parkmore East Business Park

Parkmore Co. Galway

Galway

H91 V0TX

Ireland

Authorised Representative/ UK Responsible Person
Name: Veryan Medical Ltd
Address:

9400 Garsington Road Oxford Business Park

Oxford

OX4 2HN

England United Kingdom

Code/Term Type

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

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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