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ISO 10993-16:2010

Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables

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Publication date: 2010-02-15
Price: 68 vnd

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ISO 10993-16:2010 gives principles on how toxicokinetic studies relevant to medical devices should be designed and performed. Annex A describes the considerations for inclusion of toxicokinetic studies in the biological evaluation of medical devices.
Document identifier
ISO 10993-16:2010
Title
Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables
ISO Category
TC 194: Biological evaluation of medical devices
Publication date
2010-02-15
Status
Ineffective
International Relationship
BS EN ISO 10993-16:2010 * AAMI/ISO 10993-16:2010/(R)2014 * DIN EN ISO 10993-16
Cross references
Latest version
ISO 10993-16:2017
Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables
Document identifier ISO 10993-16:2017
Publication date 2017-05-01
Classification 11.100.20. Biological evaluation of medical devices, Medical microbiology, see 07.100.10
Status Effective
*
History of version
ISO 10993-16:2017*ISO 10993-16:2010 * ISO 10993-16:2017 * ISO 10993-16:2010 * ISO 10993-16:1997
Keywords
Classification
11.100.20. Biological evaluation of medical devices, Medical microbiology, see 07.100.10
Pages
Price 68 vnd

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