Guidance
Reporting adverse incidents: joint replacement implants
For manufacturers reporting adverse incidents with joint replacement implants under the vigilance system.
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Guidance for manufacturers on reporting adverse incidents involving joint replacement implants under the vigilance system聽
To be read in conjunction with the guidelines on post-market surveillance.
Updates to this page
Published 1 June 2008
Last updated 15 January 2025
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Updated to reflect the laying of The Medical Devices (Post-market Surveillance requirements) (Amendment) Regulations 2024.
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This page has been updated due to the end of the transition period.
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First published.