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BSI - BS EN ISO 10993-12

Biological evaluation of medical devices Part 12: Sample preparation and reference materials

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Organization: BSI
Publication Date: 31 October 2012
Status: active
Page Count: 34
ICS Code (Biological evaluation of medical devices): 11.100.20

Document History

BS EN ISO 10993-12
June 30, 2021
Biological evaluation of medical devices Part 12: Sample preparation and reference materials
A description is not available for this item.
BS EN ISO 10993-12
October 31, 2012
Biological evaluation of medical devices Part 12: Sample preparation and reference materials
A description is not available for this item.
BS EN ISO 10993-12
July 31, 2009
Biological evaluation of medical devices Part 12: Sample preparation and reference materials
A description is not available for this item.
BS EN ISO 10993-12
December 31, 2007
Biological evaluation of medical devices - Part 12: Sample preparation and reference materials
A description is not available for this item.
BS EN ISO 10993-12
December 8, 2004
Biological evaluation of medical devices Part 12: Sample preparation and reference materials
A description is not available for this item.
BS EN ISO 10993-12
February 15, 1997
Biological Evaluation of Medical Devices Part 12: Sample Preparation and Reference Materials
A description is not available for this item.
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References

This document references:
BS EN ISO 10993-10 - Biological evaluation of medical devices Part 10: Tests for skin sensitization
Published by BSI on February 28, 2023
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 10993-5 - Biological evaluation of medical devices Part 5: Tests for in vitro cytotoxicity
Published by BSI on July 31, 2009
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 10993-10 - Biological evaluation of medical devices Part 10: Tests for skin sensitization
Published by BSI on February 28, 2023
A description is not available for this item.
This document references:
BS EN ISO 10993-3 - Biological evaluation of medical devices Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity
Published by BSI on October 31, 2014
A description is not available for this item.
This document references:
BS EN ISO 10993-5 - Biological evaluation of medical devices Part 5: Tests for in vitro cytotoxicity
Published by BSI on July 31, 2009
A description is not available for this item.
This document references:
ISO GUIDE 30 - Reference materials — Selected terms and definitions AMENDMENT 1: Revisions of definitions for reference material and certified reference material
Published by ISO on September 4, 2019
A description is not available for this item.
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 ISO 11350 - Water quality - Determination of the genotoxicity of water and waste water - Salmonella/microsome fluctuation test (Ames fluctuation test)
Published by BSI on August 31, 2012
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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