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 - Ascyrus Medical GmbH

Address:

Bethmannstrasse 8

Frankfurt

60311

Germany

Authorised Representative/ UK Responsible Person
Name: CryoLife Europa Ltd.
Address:

Bramley House The Guildway Old Portsmouth Road

Old Portsmouth Road Guildford

Guildford

-- Please select - GU3 1LR

England United Kingdom

Code/Term Type

Bare-metal aortic stent Bare-metal aortic stent 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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