Abstract
ISO 10993-1:2009 describes:
- the general principles governing the biological evaluation of medical devices within a risk management process;
- the general categorization of devices based on the nature and duration of their contact with the body;
- the evaluation of existing relevant data from all sources;
- the identification of gaps in the available data set on the basis of a risk analysis;
- the identification of additional data sets necessary to analyse the biological safety of the medical device;
- the assessment of the biological safety of the medical device.
General information
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Status: WithdrawnPublication date: 2009-10Stage: Withdrawal of International Standard [95.99]
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Edition: 4Number of pages: 21
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Technical Committee :ISO/TC 194ICS :11.100.20
- RSS updates
Life cycle
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Previously
WithdrawnISO 10993-1:2003
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Now
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00
Preliminary
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10
Proposal
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20
Preparatory
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30
Committee
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40
Enquiry
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50
Approval
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60
Publication
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90
Review
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95
Withdrawal
Corrigenda
Correct the current edition; free; not included in the text of the existing standard.WithdrawnISO 10993-1:2009/Cor 1:2010
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00
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Revised by
PublishedISO 10993-1:2018