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Abstract Preview

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.


General information

  • Status :  Published
    Publication date : 2017-09
  • Edition : 3
    Number of pages : 29
  • Technical Committee
    :
    ISO/TC 194
    Biological and clinical evaluation of medical devices
  • ICS :
    11.100.20
    Biological evaluation of medical devices

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A standard is reviewed every 5 years



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