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 - Clearstream Technologies Ltd.

Address:

Moyne Upper

Enniscorthy

Wexford Y21 Y9T0

Ireland

Authorised Representative/ UK Responsible Person
Name: Cordis Medical UK Limited
Address:

Suite 402 Chadwick House Birchwood Park

Warrington

WA3 6AE

England United Kingdom

Code/Term Type

Peripheral angioplasty balloon catheter basic Peripheral angioplasty balloon catheter basic 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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