Abstract
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.
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General information
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Status: PublishedPublication date: 2017-09Stage: International Standard to be revised [90.92]
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Edition: 3Number of pages: 29
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Technical Committee :ISO/TC 194ICS :11.100.20
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Life cycle
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Previously
WithdrawnISO 10993-11:2006
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Now
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Will be replaced by
Under developmentISO/CD 10993-11
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