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: 15 January 2025 — See all updates

Documents

Device-specific vigilance guidance: intraocular lenses

HTML

Details

Guidance for manufacturers on reporting adverse incidents involving intraocular lenses under the vigilance system.

To be read in conjunction with the guidelines on post market surveillance.

Published 1 June 2009
Last updated 15 January 2025 + show all updates

1. 15 January 2025

   Updated to reflect the laying of The Medical Devices (Post-market Surveillance requirements) (Amendment) Regulations 2024.

2. 30 December 2020

   Updated due to the end of the transition period.

3. 1 June 2009

   First published.