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.
Status: PublishedPublication date: 2017-09
Edition: 3Number of pages: 29
Technical Committee: ISO/TC 194 Biological and clinical evaluation of medical devices
- ICS :
- 11.100.20 Biological evaluation of medical devices
This standard contributes to the following Sustainable Development Goal:
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A standard is reviewed every 5 years
Stage: 90.92 (To be revised)
Will be replaced byUnder development
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