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ISO 15798 FRENCH

Implants ophtalmiques - Dispositifs ophtalmiques viscoélastiques

inactive
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Organization: ISO
Publication Date: 1 February 2010
Status: inactive
Page Count: 22
ICS Code (Ophthalmic equipment): 11.040.70

Document History

ISO 15798 FRENCH
May 1, 2017
Implants ophtalmiques - Dispositifs ophtalmiques viscoélastiques AMENDEMENT 1
A description is not available for this item.
ISO 15798 FRENCH
September 15, 2013
Implants ophtalmiques - Dispositifs ophtalmiques viscoélastiques
A description is not available for this item.
ISO 15798 FRENCH
February 1, 2010
Implants ophtalmiques - Dispositifs ophtalmiques viscoélastiques
A description is not available for this item.

References

This document references:
EN 1041 - Information supplied by the manufacturer of medical devices
Published by CEN on August 1, 2008
This European Standard specifies requirements for information to be supplied by a manufacturer for medical devices regulated by Council Directive 90/385/EEC relating to active implantable medical...
This document references:
EN 980 - Symbols for use in the labelling of medical devices
Published by CEN on May 1, 2008
This European Standard specifies symbols for use in the information supplied by the manufacturer with medical devices. The requirements of this European Standard are not intended to apply to symbols...
This document references:
ISO 10993-1 - Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process
Published by ISO on August 1, 2018
This document specifies: — the general principles governing the biological evaluation of medical devices within a risk management process; — the general categorization of medical devices based on the...
This document references:
ISO 10993-16 - Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables
Published by ISO on May 1, 2017
This document provides principles on designing and performing toxicokinetic studies relevant to medical devices. Annex A describes the considerations for inclusion of toxicokinetic studies in the...
This document references:
ISO 10993-2 - Biological evaluation of medical devices Part 2: Animal welfare requirements
Published by ISO on July 15, 2006
This part of ISO 10993 is aimed at those who commission, design and perform tests or evaluate data from animal tests undertaken to assess the biocompatibility of materials intended for use in medical...
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