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Register as a manufacturer to sell medical devices from 1 January 2021

 

Published 7 December 2020
Last updated 7 December 2020 — see all updates
From:
Medicines and Healthcare products Regulatory Agency
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland from 1 January 2021

Contents

  1. Overview
  2. Who must register
  3. When you must register
  4. Information required when registering your devices with the MHRA
  5. Apply to register on the Device Online Registration System (DORS)
  6. Fees
  7. Making changes to your registration
  8. Public register of manufacturers
  9. Reference guides
  10. Contact

 

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