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PD ISO/TR 15499:2016
Biological evaluation of medical devices. Guidance on the conduct of biological evaluation within a risk management process
Biological evaluation of medical devices. Guidance on the conduct of biological evaluation within a risk management process
Vydáno: 2017-01-31
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BS EN ISO 10993-6:2016 - TC
Tracked Changes. Biological evaluation of medical devices Tests for local effects after implantation
Tracked Changes. Biological evaluation of medical devices Tests for local effects after implantation
Vydáno: 2020-02-24
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BS EN ISO 10993-13:2010
Biological evaluation of medical devices Identification and quantification of degradation products from polymeric medical devices
Biological evaluation of medical devices Identification and quantification of degradation products from polymeric medical devices
Vydáno: 2010-10-31
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PD ISO/TR 10993-22:2017
Biological evaluation of medical devices Guidance on nanomaterials
Biological evaluation of medical devices Guidance on nanomaterials
Vydáno: 2017-07-19
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BS EN ISO 10993-3:2014
Biological evaluation of medical devices Tests for genotoxicity, carcinogenicity and reproductive toxicity
Biological evaluation of medical devices Tests for genotoxicity, carcinogenicity and reproductive toxicity
Vydáno: 2014-10-31
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BS EN ISO 10993-14:2009
Biological evaluation of medical devices Identification and quantification of degradation products from ceramics
Biological evaluation of medical devices Identification and quantification of degradation products from ceramics
Vydáno: 2009-06-30
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PD ISO/TS 16782:2016
Clinical laboratory testing. Criteria for acceptable lots of dehydrated Mueller-Hinton agar and broth for antimicrobial susceptibility testing
Clinical laboratory testing. Criteria for acceptable lots of dehydrated Mueller-Hinton agar and broth for antimicrobial susceptibility testing
Vydáno: 2016-11-30
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