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DIN EN ISO 10993-3 rev
Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity
DIN EN ISO 10993-4 rev
Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood
DIN EN ISO 10993-4/A1
Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood - Amendment 1 (ISO 10993-4:2017/DAM 1:2024); German and English version EN ISO 10993-4:2017/prA1:2024
DIN EN ISO 10993-5/A11
Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009)
DIN EN ISO 10993-6
Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO/DIS 10993-6:2024); German and English version prEN ISO 10993-6:2024
DIN EN ISO 10993-7
Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO/DIS 10993-7:2024); German and English version prEN ISO 10993-7:2024
DIN EN ISO 10993-11 rev
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity
DIN EN ISO 10993-12/A1
Biological evaluation of medical devices - Part 12: Sample preparation and reference materials - AMENDMENT 1 (ISO 10993-12:2021/DAM 1:2024); German and English version EN ISO 10993-12:2021/prA1:2024
DIN EN ISO 10993-13 rev
Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices
DIN EN ISO 10993-14 rev
Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics
