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 - ALN S.A.R.L.

Address:

589 Chemin du Niel

Bormes les Mimosas

83230

France

Authorised Representative/ UK Responsible Person
Name: Qserve Group UK Ltd.
Address:

49 Greek Street

London

W1D 4EG

England United Kingdom

Code/Term Type

Vena cava filter extraction/repositioning kit Vena cava filter extraction/repositioning kit Class III

Vena cava filter temporary/permanent Vena cava filter temporary/permanent 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
Vena cava filter extraction/repositioning kit	Vena cava filter extraction/repositioning kit	Class III
Vena cava filter temporary/permanent	Vena cava filter temporary/permanent	Class III