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UK Registration Deadline: Low-Risk Devices

1 January 2022

Class I medical devices, General IVDs and Custom-made Devices must be registered by this date.

The UK Responsible Person (UKRP) must complete the registration, if the manufacturer is established outside of the UK.

MHRA guidance to industry is available here. The British Healthcare Trades Association overview is available here.

Details

Other

Legislation
UK MDR 2002 (as amended)
Region
United Kingdom