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BS EN ISO 10993-5:2009+A11:2025
Biological evaluation of medical devices Tests for in vitro cytotoxicity
Biological evaluation of medical devices Tests for in vitro cytotoxicity
Vydáno: 2025-03-17
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BS EN ISO 10993-3 Biological evaluation of medical devices Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity
BS EN ISO 10993-3 Biological evaluation of medical devices Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity
Vydáno: 2025-04-04
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BS EN ISO 10993-1:2020
Biological evaluation of medical devices Evaluation and testing within a risk management process
Biological evaluation of medical devices Evaluation and testing within a risk management process
Vydáno: 2020-12-16
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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 10993-13:2010
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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BS EN ISO 18812:2003
Health informatics. Clinical analyser interfaces to laboratory information systems. Use profiles
Health informatics. Clinical analyser interfaces to laboratory information systems. Use profiles
Vydáno: 2003-06-24
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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 10993-6:2016 - 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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