UK Registration Deadline: Mid-Risk Devices

1 September 2021

Class IIb Non-implantable, Class IIa medical devices and Annex II, List B and Self-test IVDs 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

Date: 1 September 2021
Event Tags:Registration, UK Responsible Person (UKRP), UKCA Marking

Other

Legislation: UK MDR 2002 (as amended)
Region: United Kingdom

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