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 - InspireMD Ltd.

Address:

4 Menorat Hamaor street

Tel Aviv

6744832

Israel

Authorised Representative/ UK Responsible Person
Name: Obelis UK Ltd
Address:

Sandford Gate East Point Business Park

Oxford

OX4 6LB

England United Kingdom

Code/Term Type

Mesh-sleeve carotid artery stent Mesh-sleeve carotid artery 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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