Guidance

Borderlines with medical devices and other products in Great Britain

Guidance on whether or not your product is a medical device.

From:
Medicines and Healthcare products Regulatory Agency
Published
19 January 2015
Last updated
8 April 2024 — See all updates

Documents

Borderlines with medical devices and other products in Great Britain

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Details

This document gives help in working out if your product is considered to be a medical device under UK legislation.

Updates to this page

Published 19 January 2015
Last updated 8 April 2024 + show all updates

  1. Updated 'Borderlines with medical devices and other products in Great Britain' guidance, as of March 2024.

  2. File 'updated in light of the extension of acceptance of CE marked devices on the GB market' updated in light of the extension of acceptance of CE marked devices on the GB market.

  3. Updates to 'Borderlines with medical devices and other products'.

  4. This has been updated due to the end of the Brexit transition period.

  5. First published.

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