The MHRA public access registration database (PARD) website allows you to find:
Registered manufacturers
Registered Medical Device type by Global Medical Device Nomenclature (GMDN®)*
Registration of medical devices with the MHRA (the UK Competent Authority) does not represent any form of accreditation, certification, approval or endorsement by the MHRA. Therefore, it is not permitted to make any claims to this effect, including the use of any MHRA logos in any marketing materials, on device packaging, in the instructions for use, on laboratory tickets/dockets, or in any other documentation.
Where device status is displayed as 'Conformity Assessment Certificate Expired', existing medical device stock already placed on the UK market (including stock in UK warehouses) prior to the expiry of the conformity assessment certificate can remain on the UK market. However, devices (including new stock) with expired conformity assessment certificates cannot be registered or placed on the UK market.
*GMDN® is a registered trademark of The GMDN Agency. All rights reserved. See Frequently Asked Question (FAQ) 'What is GMDN®?' for further information on use of GMDN®
Frequently Asked Questions (FAQ)