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 - Bentley InnoMed GmbH

Address:

Lotzenäcker 3

Hechingen

72379

Germany

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

Pure Offices Plato Close

Warwick

CV34 6WE

England United Kingdom

Code/Term Type

Iliac artery stent bare-metal Iliac artery stent bare-metal Class III

Bare-metal aortic stent Bare-metal aortic stent Class III

Mesh-sleeve coronary artery stent Mesh-sleeve coronary artery stent Class III

Peripheral artery stent bare-metal Peripheral artery stent bare-metal Class IIb

Iliofemoral vein stent Iliofemoral vein stent Class IIb

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
Iliac artery stent bare-metal	Iliac artery stent bare-metal	Class III
Bare-metal aortic stent	Bare-metal aortic stent	Class III
Mesh-sleeve coronary artery stent	Mesh-sleeve coronary artery stent	Class III
Peripheral artery stent bare-metal	Peripheral artery stent bare-metal	Class IIb
Iliofemoral vein stent	Iliofemoral vein stent	Class IIb