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SFS-EN ISO 10993-18:2020:en – Biological evaluation of medical devices. Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020)
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SFS-EN ISO 10993-6:2016:en – Biological evaluation of medical devices. Part 6: Tests for local effects after implantation (ISO 10993-6:2016)
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SFS-EN ISO 10993-14:en – Biological evaluation of medical devices. Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001)
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SFS-EN ISO 10993-13:en – Biological evaluation of medical devices. Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:2010)
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SFS-EN ISO 10939:2017:en – Ophthalmic instruments. Slit-lamp microscopes (ISO 10939:2017)
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SFS-EN ISO 10993-7:en – Biological evaluation of medical devices. Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2008)
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SFS-EN ISO 10993-4:2017:en – Biological evaluation of medical devices. Part 4: Selection of tests for interactions with blood (ISO 10993-4:2017)
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SFS-EN ISO 10993-3:en – Biological evaluation of medical devices. Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:2014)
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SFS-EN ISO 10944:en – Ophthalmic instruments. Synoptophores (ISO 10944:2009)
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SFS-EN ISO 10940:en – Ophthalmic instruments. Fundus cameras (ISO 10940:2009)
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