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 - PXD Limited

Address:

The Biosphere Draymans Way

Newcastle Upon Tyne

Newcastle Upon Tyne

England NE4 5BX

England United Kingdom

Authorised Representative/ UK Responsible Person
Name: Not Available

Address:

Code/Term Type

Clinical management support software Clinical management support software Class I

General specimen collection kit IVD home-use General specimen collection kit IVD home-use 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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Code/Term		Type
Clinical management support software	Clinical management support software	Class I
General specimen collection kit IVD home-use	General specimen collection kit IVD home-use	IVD General