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STN EN ISO 10993-12 (856510)
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Biological evaluation of medical devices — Part 12: Sample preparation and reference materials
Standard published on 1.9.2021
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STN EN ISO 10993-12:2021/A1 (856510)
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Biological evaluation of medical devices — Part 12: Sample preparation and reference materials
Change published on 1.2.2026
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STN EN ISO 10993-13 (856510)
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Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:2010)
Standard published on 1.11.2010
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STN EN ISO 10993-14 (856510)
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Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001)
Standard published on 1.8.2009
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STN EN ISO 10993-15 (856510)
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Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2019)
Standard published on 1.8.2023
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STN EN ISO 10993-16 (856510)
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Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2017)
Standard published on 1.6.2018
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STN EN ISO 10993-17 (856510)
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Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents (ISO 10993-17:2023)
Standard published on 1.3.2024
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STN EN ISO 10993-17:2024/A1 (856510)
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Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents (ISO 10993-17: 2023/Amd 1: 2025)
Change published on 1.4.2026
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STN EN ISO 10993-18 (856510)
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Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020)
Standard published on 1.9.2020
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STN EN ISO 10993-18:2020/A1 (856510)
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Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020)
Change published on 1.10.2023
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