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About This Item

 

Full Description

BS EN ISO 10993-11:2009 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.



Cross References:
ISO 10993-1
ISO 10993-2
ISO 10993-12
ASTM F619-03
SN 119800:1990
93/42/EEC
90/385/EEC


All current amendments available at time of purchase are included with the purchase of this document.
 

Document History

  1. BS EN ISO 10993-11:2018


    Biological evaluation of medical devices - Tests for systemic toxicity

    • Most Recent
  2. BS EN ISO 10993-11:2018


    Biological evaluation of medical devices - Tests for systemic toxicity

    • Historical Version
  3. BS EN ISO 10993-11:2009

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    Biological evaluation of medical devices-Tests for systemic toxicity

    • Historical Version
  4. BS EN ISO 10993-11:2006


    Biological evaluation of medical devices-Tests for systemic toxicity

    • Historical Version
  5. BS EN ISO 10993-11:1996


    Biological evaluation of medical devices-Tests for systemic toxicity

    • Historical Version
  6. BS 5736-5:1982


    Evaluation of medical devices for biological hazards-Method of test for systemic toxicity; assessment of pyrogenicity in rabbits of extracts from medical devices

    • Historical Version
  7. BS 5736-3:1981


    Evaluation of medical devices for biological hazards-Method of test for systemic toxicity; assessment of acute toxicity of extracts from medical devices

    • Historical Version