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 - Janssen Pharmaceutica NV

Address:

Turnhoutseweg 30

Beerse

2340 Beerse 2340

Belgium

Authorised Representative/ UK Responsible Person
Name: Johnson & Johnson Medical Ltd
Address:

Baird House 4 Lower Gilmore Bank

Edinburgh

EH3 9QP

Scotland United Kingdom

Code/Term Type

Blood test-based differential diagnosis interpretive software IVD Blood test-based differential diagnosis interpretive software IVD 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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