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 - R&D Systems Inc.

Address:

614 McKinley Place N.E

Minneapolis

Minnesota 55413

United States

Authorised Representative/ UK Responsible Person
Name: Bio-Techne Ltd
Address:

19 Barton Lane Abingdon Science Park

Abingdon

Oxfordshire OX14 3NB

England United Kingdom

Code/Term Type

Erythropoietin (EPO) IVD kit chemiluminescent immunoassay Erythropoietin (EPO) IVD kit chemiluminescent immunoassay 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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