Registration number (WIID)Project No.TitleStatus
67095LVS EN ISO 10993-12:2021Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2021)Standarts spēkā
65481EN ISO 22442-2:2020Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling (ISO/DIS 22442-2:2018)Standarts spēkā
67767LVS EN ISO 10993-17:2023Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents (ISO 10993-17:2023)Standarts spēkā
80820EN ISO 10993-5:2009/A11:2025Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicityStandarts spēkā
33857EN ISO 10993-7:2008/AC:2009Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals - Technical Corrigendum 1 (ISO 10993-7:2008/Cor 1:2009)Standarts spēkā
68925EN ISO 10993-23:2021Biological evaluation of medical devices - Part 23: Tests for irritation (ISO/DIS 10993-23:2019)Standarts spēkā
62983EN ISO 14155:2020Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)Standarts spēkā
80820LVS EN ISO 10993-5:2009/A11:2025Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicityStandarts spēkā
27051LVS EN ISO 10993-13:2010Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:2010)Standarts spēkā
60133EN ISO 10993-11:2018Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO/DIS 10993-11:2015)Standarts spēkā
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