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ISO 10993-11

Biological evaluation of medical devices Part 11: Tests for systemic toxicity

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Organization: ISO
Publication Date: 15 August 2006
Status: inactive
Page Count: 34
ICS Code (Biological evaluation of medical devices): 11.100.20
scope:

This part of ISO 10993 specifies requirements and gives guidance on procedures to be followed in the evaluation of the potential for medical device materials to cause adverse systemic reactions.

Document History

September 1, 2017
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity
This document specifies requirements and gives guidance on procedures to be followed in the evaluation of the potential for medical device materials to cause adverse systemic reactions.
ISO 10993-11
August 15, 2006
Biological evaluation of medical devices Part 11: Tests for systemic toxicity
This part of ISO 10993 specifies requirements and gives guidance on procedures to be followed in the evaluation of the potential for medical device materials to cause adverse systemic reactions.
January 1, 1993
Biological Evaluation of Medical Devices - Part 11: Tests for Systemic Toxicity; (CEN EN ISO 10993-11: 1995)
This part of ISO 10993 specifies methodologies for the evaluation of the systemic toxicity potential of medical devices which release constituents into the body. In addition, it includes pyrogenicity...

References

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