Abstract 

ISO 10993-11:2006 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  • Status :  Withdrawn
    Publication date : 2006-08
  • Edition : 2
    Number of pages : 26
  • Technical Committee
    :
    ISO/TC 194
    Biological and clinical evaluation of medical devices
  • ICS :
    11.100.20
    Biological evaluation of medical devices

Life cycle

A standard is reviewed every 5 years



Revisions / Corrigenda

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