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About This Item

 

Full Description

ISO 10993-11:2017 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

  1. ISO 10993-11:2017

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

    • Most Recent
  2. ISO 10993-11:2006


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

    • Historical Version
  3. ISO 10993-11:1993


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

    • Historical Version