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11.100.20 Biological evaluation of medical devices
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BS EN ISO 10993-1:2025
Biological evaluation of medical devices Requirements and general principles for the evaluation of biological safety within a risk management process
Biological evaluation of medical devices Requirements and general principles for the evaluation of biological safety within a risk management process
Released: 2026-01-09
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319.34 USD
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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
Released: 2010-10-31
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BS EN ISO 14155:2026
Clinical investigation of medical devices for human subjects. Good clinical practice
Clinical investigation of medical devices for human subjects. Good clinical practice
Released: 2026-04-22
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BS EN ISO 10993-17:2023+A1:2025
Biological evaluation of medical devices Toxicological risk assessment of medical device constituents
Biological evaluation of medical devices Toxicological risk assessment of medical device constituents
Released: 2026-01-26
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BS EN ISO 10993-6:2026
Biological evaluation of medical devices Tests for local effects after implantation
Biological evaluation of medical devices Tests for local effects after implantation
Released: 2026-05-20
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BS EN ISO 10993-3:2026
Biological evaluation of medical devices Evaluation of genotoxicity, carcinogenicity, reproductive toxicity and developmental toxicity
Biological evaluation of medical devices Evaluation of genotoxicity, carcinogenicity, reproductive toxicity and developmental toxicity
Released: 2026-10-08
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BS EN ISO 10993-9:2021
Biological evaluation of medical devices Framework for identification and quantification of potential degradation products
Biological evaluation of medical devices Framework for identification and quantification of potential degradation products
Released: 2022-05-19
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BS ISO 17593:2022
Clinical laboratory testing and in vitro medical devices. Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy
Clinical laboratory testing and in vitro medical devices. Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy
Released: 2022-03-15
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