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 - Shanghai MicroPort Endovascular MedTech (Group) Co. Ltd

Address:

Building 1 3399 Kangxin Road

Shanghai

201318

China

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

4 Trident Park

Didcot

Oxfordshire OX11 7HJ

England United Kingdom

Code/Term Type

Descending thoracic aorta endovascular stent-graft Descending thoracic aorta endovascular stent-graft Class III

Abdominal aorta endovascular stent-graft Abdominal aorta endovascular stent-graft Class III

Peripheral angioplasty balloon catheter drug-coated Peripheral angioplasty balloon catheter drug-coated Class III

Peripheral angioplasty balloon catheter basic Peripheral angioplasty balloon catheter basic Class III

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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Code/Term		Type
Descending thoracic aorta endovascular stent-graft	Descending thoracic aorta endovascular stent-graft	Class III
Abdominal aorta endovascular stent-graft	Abdominal aorta endovascular stent-graft	Class III
Peripheral angioplasty balloon catheter drug-coated	Peripheral angioplasty balloon catheter drug-coated	Class III
Peripheral angioplasty balloon catheter basic	Peripheral angioplasty balloon catheter basic	Class III
Peripheral angioplasty balloon catheter basic	Peripheral angioplasty balloon catheter basic	Class III