Registration number (WIID)Project No.TitleStatus
75596EN ISO 10993-1:2025Biological evaluation of medical devices - Part 1: Requirements and general principles for the evaluation of biological safety within a risk management process (ISO 10993-1:2025)Standarts spēkā
60721LVS EN ISO 10993-1:2021Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2018, including corrected version 2018-11)Standarts spēkā
65727LVS EN ISO 10993-4:2018Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2017)Standarts spēkā
33857LVS EN ISO 10993-7:2009 /AC:2010Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals - Technical Corrigendum 1 (ISO 10993-7:2008/Cor 1:2009)Standarts spēkā
60725LVS EN ISO 10993-18:2020Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020)Standarts spēkā
68925EN ISO 10993-23:2021Biological evaluation of medical devices - Part 23: Tests for irritation (ISO 10993-23:2021)Standarts spēkā
65480EN ISO 22442-1:2020Medical devices utilizing animal tissues and their derivatives - Part 1: Application of risk management (ISO/DIS 22442-1:2018)Standarts spēkā
60133LVS EN ISO 10993-11:2018Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2017)Standarts spēkā
74131LVS EN ISO 10993-18:2020/A1:2023Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process - Amendment 1: Determination of the uncertainty factor (ISO 10993-18:2020/Amd 1:2022)Standarts spēkā
74131EN ISO 10993-18:2020/A1:2023Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process - Amendment 1: Determination of the uncertainty factor (ISO 10993-18:2020/Amd 1:2022)Standarts spēkā
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