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BSI - BS EN ISO 15798

Ophthalmic implants - Ophthalmic viscosurgical devices

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Organization: BSI
Publication Date: 30 September 2013
Status: active
Page Count: 28
ICS Code (Ophthalmic equipment): 11.040.70

Document History

BS EN ISO 15798
July 31, 2022
Ophthalmic implants - Ophthalmic viscosurgical devices
A description is not available for this item.
BS EN ISO 15798
September 30, 2013
Ophthalmic implants - Ophthalmic viscosurgical devices
A description is not available for this item.
BS EN ISO 15798
September 30, 2013
Ophthalmic implants - Ophthalmic viscosurgical devices
A description is not available for this item.
BS EN ISO 15798
February 28, 2010
Ophthalmic implants - Ophthalmic viscosurgical devices
A description is not available for this item.
BS EN ISO 15798
August 15, 2001
Ophthalmic Implants - Ophthalmic Viscosurgical Devices
A description is not available for this item.
BS EN ISO 15798
August 15, 2001
Ophthalmic implants - Ophthalmic viscosurgical devices
A description is not available for this item.
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References

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 10993-16 FRENCH - Évaluation biologique des dispositifs médicaux - Partie 16: Conception des études toxicocinétiques des produits de dégradation et des substances relargables
Published by ISO on May 1, 2017
A description is not available for this item.
This document references:
ISO 10993-9 - Biological evaluation of medical devices — Part 9: Framework for identification and quantification of potential degradation products
Published by ISO on November 1, 2019
This document provides general principles for the systematic evaluation of the potential and observed degradation of medical devices through the design and performance of in vitro degradation...
This document references:
ISO 11137-3 - Sterilization of health care products - Radiation - Part 3: Guidance on dosimetric aspects of development, validation and routine control
Published by ISO on June 1, 2017
This document gives guidance on meeting the requirements in ISO 11137-1 and ISO 11137-2 and in ISO/TS 13004 relating to dosimetry and its use in development, validation and routine control of a...
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