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 - Lionex GmbH

Address:

Salzdahlumer Str. 196

Gebäude 1A

38126 Braunschweig

Germany

Authorised Representative/ UK Responsible Person
Name: A. Menarini Diagnostics Ltd.
Address:

405 Wharfedale Road

Wokingham

Berkshire RG41 5RA

England United Kingdom

Code/Term Type

Interferon IVD kit enzyme immunoassay (EIA) Interferon IVD kit enzyme immunoassay (EIA) IVD General

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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