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 - VLVbio AB

Address:

Hästholmsvägen 32

Västra Finnbodavägen Nacka

Nacka

Stockholms Län 131 30

Sweden

Authorised Representative/ UK Responsible Person
Name: Eurobio Scientific UK Ltd
Address:

Eclipse House Curtis Road

Dorking

Surrey RH4 1EJ

England United Kingdom

Code/Term Type

Cytokeratin IVD kit enzyme immunoassay (EIA) Cytokeratin 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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