Registration number (WIID)Project No.TitleStatus
75596LVS EN 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)Atcelts
35184LVS EN ISO 10993-1:2010 /AC:2010Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process - Technical Corrigendum 1 (ISO 10993-1:2009/Cor 1:2010)Atcelts
27092LVS EN ISO 10993-1:2010Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2009)Atcelts
32005LVS EN ISO 10993-1:2009Biological evaluation of medical devices - Part 1: Evaluation and testing (ISO 10993-1:2003)Atcelts
22598LVS EN ISO 10993-1:2003Biological evaluation of medical devices - Part 1: Evaluation and testingAtcelts
9492LVS EN ISO 10993-1:2000Biological evaluation of medical devices - Part 1: Evalution and testingAtcelts
60133LVS EN ISO 10993-11:2018Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2017)Standarts spēkā
32007LVS EN ISO 10993-11:2009Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006)Atcelts
21797LVS EN ISO 10993-11:2006Biological evaluation of medical devices - Part 11: Tests for systemic toxicityAtcelts
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