Registration number (WIID)Project No.TitleStatus
32000LVS EN ISO 10993-14:2009Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001)Standarts spēkā
78994EN ISO 10993-17:2023/A1:2025Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents - Amendment 1 (ISO 10993-17:2023/Amd 1:2025)Standarts spēkā
67095LVS EN ISO 10993-12:2021Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2021)Standarts spēkā
60722LVS EN ISO 10993-9:2021Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:2019)Standarts spēkā
67095EN ISO 10993-12:2021Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO/DIS 10993-12:2019)Standarts spēkā
27051EN ISO 10993-13:2010Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO/DIS 10993-13:2008)Standarts spēkā
22089LVS EN ISO 10993-5:2009Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009)Standarts spēkā
38319LVS EN ISO 10993-6:2017Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2016)Standarts spēkā
60723LVS EN ISO 10993-15:2023Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2019)Standarts spēkā
67187LVS EN ISO 10993-10:2023Biological evaluation of medical devices - Part 10: Tests for skin sensitization (ISO 10993-10:2021)Standarts spēkā
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