ICS:11.100.20
Showing 28–36 of 48 results
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ISO 10993:2014 Biological evaluation of medical devices – Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity
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ISO 10993:2020 Biological evaluation of medical devices – Part 19: Physico-chemical, morphological and topographical characterization of materials
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ISO 10993:2019 Biological evaluation of medical devices – Part 9: Framework for identification and quantification of potential degradation products
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ISO 14155:2020 Clinical investigation of medical devices for human subjects – Good clinical practice
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ISO 10993:2020 Biological evaluation of medical devices – Part 18: Chemical characterization of medical device materials within a risk management process
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ISO 10993:2019 Biological evaluation of medical devices – Part 7: Ethylene oxide sterilization residuals – Amendment 1: Applicability of allowable limits for neonates and infants
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ISO 10993:2021 Biological evaluation of medical devices – Part 12: Sample preparation and reference materials
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ISO 10993-6:2026 Biological evaluation of medical devices — Part 6: Tests for local effects after implantation
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ISO 10993-17:2023/Amd 1:2025 Biological evaluation of medical devices — Part 17: Toxicological risk assessment of medical device constituents — Amendment 1
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