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
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Status: WithdrawnPublication date: 2006-08Stage: Withdrawal of International Standard [95.99]
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Edition: 2Number of pages: 26
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Technical Committee :ISO/TC 194ICS :11.100.20
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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