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 - The Phoenix Partnership (Leeds) Ltd

Address:

T P P Headquarters 129 Low Lane Horsforth

Leeds

West Yorkshire LS18 5PX

United Kingdom

Authorised Representative/ UK Responsible Person
Name:
Address:

Code/Term Type

Standalone Software Class I

Clinical management support software Class I

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
Standalone Software		Class I
Clinical management support software		Class I