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BSI - BS EN ISO 10993-3

Biological evaluation of medical devices Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity

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Organization: BSI
Publication Date: 31 October 2014
Status: active
Page Count: 48
ICS Code (Biological evaluation of medical devices): 11.100.20

Document History

BS EN ISO 10993-3
October 31, 2014
Biological evaluation of medical devices Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity
A description is not available for this item.
BS EN ISO 10993-3
June 30, 2009
Biological evaluation of medical devices Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity
A description is not available for this item.
BS EN ISO 10993-3
October 31, 2003
Biological evaluation of medical devices Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity
A description is not available for this item.
BS EN ISO 10993-3
October 31, 2003
Biological evaluation of medical devices Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity
A description is not available for this item.

References

This document references:
BS EN ISO 10993-12 - Biological evaluation of medical devices Part 12: Sample preparation and reference materials
Published by BSI on October 31, 2012
A description is not available for this item.
This document references:
BS EN ISO 10993-1 - Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process
Published by BSI on December 31, 2020
A description is not available for this item.
This document references:
ISO 10993-12 FRENCH - Évaluation biologique des dispositifs médicaux — Partie 12: Préparation des échantillons et matériaux de référence
Published by ISO on January 1, 2021
A description is not available for this item.
This document references:
ISO 10993-6 - Biological evaluation of medical devices - Part 6: Tests for local effects after implantation
Published by ISO on December 1, 2016
This part of ISO 10993 specifies test methods for the assessment of the local effects after implantation of biomaterials intended for use in medical devices. This part of ISO 10993 applies to...
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 10993-12 - Biological evaluation of medical devices - Part 12: Sample preparation and reference materials
Published by ISO on January 1, 2021
This document specifies requirements and gives guidance on the procedures in the preparation of samples and the selection of reference materials for medical device testing primarily in biological...
This document references:
ISO 10993-6 FRENCH - Évaluation biologique des dispositifs médicaux - Partie 6: Essais concernant les effets locaux après implantation
Published by ISO on December 1, 2016
A description is not available for this item.
This document references:
BS EN ISO 10993-12 - Biological evaluation of medical devices Part 12: Sample preparation and reference materials
Published by BSI on October 31, 2012
A description is not available for this item.
This document references:
BS EN ISO 10993-1 - Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process
Published by BSI on December 31, 2020
A description is not available for this item.
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