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 - Rossix AB

Address:

Taljegardsgatan 3B

Molndal

431 53

Sweden

Authorised Representative/ UK Responsible Person
Name: Quadratech Diagnostics Ltd
Address:

Suite 9-11 The Old Printworks 20 Wharf Road

Eastbourne

East Sussex BN21 3AW

England United Kingdom

Code/Term Type

Coagulation factor IX IVD kit chromogenic Coagulation factor IX IVD kit chromogenic 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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