Register medical devices to place on the market

Information

Type

Guidance

Regulated products

Medical Devices

Topics

Health And Social Care

Published

December 31, 2020

Last updated

August 2, 2024

Description

How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland

Organization

Country / Region

United Kingdom

License

Open Government Licence 2.0 (United Kingdom)

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