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 - ARTHESYS

Address:

4 rue René Razel

Saclay

91400

France

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

Pure Offices Plato Close

Warwick

CV34 6WE

England United Kingdom

Code/Term Type

Thrombectomy suction catheter Thrombectomy suction catheter Class III

Haemostasis valve Haemostasis valve Class IIa

Peripheral angioplasty balloon catheter basic Peripheral angioplasty balloon catheter basic Class IIa

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
Thrombectomy suction catheter	Thrombectomy suction catheter	Class III
Haemostasis valve	Haemostasis valve	Class IIa
Peripheral angioplasty balloon catheter basic	Peripheral angioplasty balloon catheter basic	Class IIa