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 - Trulife Limited

Address:

39 East Davis Street

Trenton Ontario

K8V 4K8

Canada

Authorised Representative/ UK Responsible Person
Name: MDSS-UK RP LIMITED
Address:

6 Wilmslow Road Rusholme

Manchester

M14 5TP

England United Kingdom

Code/Term Type

Stump sock Stump sock 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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