Guidance

Reporting adverse incidents: inferior vena cava filter (IVC)

For manufacturers reporting adverse incidents with IVC filters under the vigilance system.

From:
Medicines and Healthcare products Regulatory Agency
Published
2 January 2014
Last updated
30 December 2020 鈥� See all updates

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Details

Guidance on how to report adverse incidents with IVCs. To be read in conjunction with the guidelines on a medical devices vigilance system .

Updates to this page

Published 2 January 2014
Last updated 30 December 2020 show all updates

  1. This page has been updated due to the end of the transition period.

  2. First published.

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