Guidance

Reporting adverse incidents: intraocular lenses

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

Document

Adverse incidents with intraocular lenses

This file may not be suitable for users of assistive technology. Request an accessible format.

If you use assistive technology (such as a screen reader) and need a version of this document in a more accessible format, please email webupdates@mhra.gsi.gov.uk. Please tell us what format you need. It will help us if you say what assistive technology you use.

Details

Guidance on how to report adverse incidents with intraocular lenses. You need to read this alongside the European Commission’s guidelines on the vigilance system for medical devices.

Published 1 June 2009