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.
General information
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Status: Under developmentStage: Close of comment period [30.60]
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Edition: 4
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Technical Committee :ISO/TC 194
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Life cycle
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Previously
PublishedISO 10993-11:2017
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Now
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