Registration number (WIID)Project No.TitleStatus
67095EN ISO 10993-12:2021Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO/DIS 10993-12:2019)Standarts spēkā
9493LVS EN ISO 10993-7:2009Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2008)Standarts spēkā
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
65481EN ISO 22442-2:2020Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling (ISO 22442-2:2020)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
75885EN ISO 10993-7:2026Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2026)Standarts spēkā
80820EN ISO 10993-5:2009/A11:2025Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicityStandarts spēkā
22089EN ISO 10993-5:2009Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009)Standarts spēkā
78993EN ISO 10993-23:2021/A1:2025Biological evaluation of medical devices - Part 23: Tests for irritation - Amendment 1: Additional in vitro reconstructed human epidermis models (ISO 10993-23:2021/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
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