This standard has been revised by ISO 10993-11:2017
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.
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Status: WithdrawnPublication date: 2006-08
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Edition: 2Number of pages: 26
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- ICS :
- 11.100.20 Biological evaluation of medical devices
Life cycle
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Previously
WithdrawnISO 10993-11:1993
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Now
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Revised by
PublishedISO 10993-11:2017
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