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 - Hemoteq AG

Address:

Adenauerstrasse 15

Würselen

52146

Germany

Authorised Representative/ UK Responsible Person
Name: Boston Scientific Limited
Address:

100 New Bridge Street

London

EC4V 6JA

England United Kingdom

Code/Term Type

Peripheral angioplasty balloon catheter basic Peripheral angioplasty balloon catheter basic 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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