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BSI - BS EN ISO 10993-10

Biological evaluation of medical devices Part 10: Tests for irritation and delayed-type hypersensitivity

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Organization: BSI
Publication Date: 8 October 2002
Status: inactive
Page Count: 62
ICS Code (Laboratory medicine): 11.100

Document History

BS EN ISO 10993-10
February 28, 2023
Biological evaluation of medical devices Part 10: Tests for skin sensitization
A description is not available for this item.
BS EN ISO 10993-10
February 28, 2014
Biological evaluation of medical devices Part 10: Tests for irritation and skin sensitization
A description is not available for this item.
BS EN ISO 10993-10
October 31, 2010
Biological evaluation of medical devices Part 10: Tests for irritation and skin sensitization
A description is not available for this item.
BS EN ISO 10993-10
February 28, 2010
Biological evaluation of medical devices Part 10: Tests for irritation and delayed-type hypersensitivity
A description is not available for this item.
BS EN ISO 10993-10
October 8, 2002
Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity
A description is not available for this item.
BS EN ISO 10993-10
October 8, 2002
Biological evaluation of medical devices Part 10: Tests for irritation and delayed-type hypersensitivity
A description is not available for this item.
BS EN ISO 10993-10
October 8, 2002
Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity
A description is not available for this item.
BS EN ISO 10993-10
May 15, 1996
Biological Evaluation of Medical Devices Part 10: Tests for Irritation and Sensitization
A description is not available for this item.
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References

This document references:
EN ISO 10993-1 - Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process
Published by CEN on December 1, 2020
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:
EN ISO 10993-14 - Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics
Published by CEN on April 1, 2009
This part of ISO 10993 specifies two methods of obtaining solutions of degradation products from ceramics (including glasses) for the purposes of quantification. It also gives guidance on the...
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 10993-14 - Biological Evaluation of Medical Devices - Part 14: Identification and Quantification of Degradation Products from Ceramics
Published by ISO on November 15, 2001
This part of ISO 10993 specifies two methods of obtaining solutions of degradation products from ceramics (including glasses) for the purposes of quantification. It also gives guidance on 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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