Abstract
PreviewISO 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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Status: PublishedPublication date: 2017-09
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Edition: 3Number of pages: 29
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- ICS :
- 11.100.20 Biological evaluation of medical devices
Buy this standard
en
Format | Language | |
---|---|---|
std 1 145 | PDF + ePub | |
std 2 145 | Paper |
- CHF145
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/AWI 10993-11
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