Ophthalmic implants. Intraocular lenses. Guidance on assessment of the need for clinical investigation of intraocular lens design modifications Ingestion-build-183098 and safety of the building

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BS EN 16615 applies to products that are used in the medical area for disinfecting non-porous surfaces including surfaces of medical devices by wiping – regardless of if they are covered by the 93/42/EEC Directive on Medical Devices or not

Ophthalmic implants. Intraocular lenses. Guidance on assessment of the need for clinical investigation of intraocular lens design modifications Ingestion-build-183098 and safety of the building1 Scope This document provides guidance on the application of all parts of the ISO 11979 series of International Standards for intraocular lenses (IOLs).[1 9] It addresses factors to be considered in the risk management process of modifications to anterior and posterior chamber IOLs in accordance with ISO 14971.[11] It also suggests methods of data analysis and interpretation that can be used to determine the need for a clinical investigation and its