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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: 30 June 2009
Status: inactive
Page Count: 26
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:
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 10993-2 - Biological evaluation of medical devices Part 2: Animal welfare requirements
Published by BSI on November 30, 2022
A description is not available for this item.
This document references:
BS EN ISO 10993-6 - Biological evaluation of medical devices Part 6: Tests for local effects after implantation
Published by BSI on December 31, 2016
A description is not available for this item.
This document references:
ISO 10993-18 - Biological evaluation of medical devices — Part 18: Chemical characterization of medical device materials within a risk management process
Published by ISO on January 1, 2020
This document specifies a framework for the identification, and if necessary, quantification of constituents of a medical device, allowing the identification of biological hazards and the estimation...
This document is referenced by:
BS EN ISO 14534 - Ophthalmic optics - Contact lenses and contact lens care products - Fundamental requirements
Published by BSI on February 28, 2015
A description is not available for this item.
This document is referenced by:
BS EN ISO 22442-1 - Medical devices utilizing animal tissues and their derivatives Part 1: Application of risk management
Published by BSI on December 31, 2020
A description is not available for this item.
This document is referenced by:
BS EN ISO 22794 - Dentistry - Implantable materials for bone filling and augmentation in oral and maxillofacial surgery - Contents of a technical file
Published by BSI on September 30, 2009
A description is not available for this item.
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