Guidance

Reporting adverse incidents: intraocular lenses

For manufacturers reporting adverse incidents with intraocular lenses under the vigilance system.

From:
Medicines and Healthcare products Regulatory Agency
Published
1 June 2009
Last updated
30 December 2020 — See all updates

Documents

Adverse incidents with intraocular lenses

PDF, 82.1 KB, 3 pages

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Details

Guidance on how to report adverse incidents with intraocular lenses. To be read in conjunction with the guidelines on a medical devices vigilance system MEDDEV 2.12/1.

Published 1 June 2009
Last updated 30 December 2020 + show all updates

  1. Updated due to the end of the transition period.

  2. First published.

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