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 - Corvia Medical Inc.

Address:

1 Highwood Drive Suite 300

Tewksbury

MA 01876 01876

United States

Authorised Representative/ UK Responsible Person
Name: ICON (LR) Limited
Address:

Concept House 6 Stoneycroft Rise

Chandlers Ford Eastleigh

Hampshire

SO53 3LD

England United Kingdom

Code/Term Type

Interatrial shunt Interatrial shunt 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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