Reporting adverse incidents: inferior vena cava filter (IVC)
For manufacturers reporting adverse incidents with IVC filters under the vigilance system.
Documents
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Guidance on how to report adverse incidents with IVCs. To be read in conjunction with the guidelines on a medical devices vigilance system MEDDEV 2.12/1.
Last updated 30 December 2020 + show all updates
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This page has been updated due to the end of the transition period.
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First published.