Registration number (WIID)Project No.TitleStatus
60721EN ISO 10993-1:2020Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO/DIS 10993-1:2017)Atcelts
35184EN ISO 10993-1:2009/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
27092EN ISO 10993-1:2009Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management system (ISO/FDIS 10993-1:2009)Atcelts
32005EN ISO 10993-1:2009Biological evaluation of medical devices - Part 1: Evaluation and testing (ISO 10993-1:2003)Atcelts
22598EN ISO 10993-1:2003Biological evaluation of medical devices - Part 1: Evaluation and testing (ISO 10993-1:2003)Atcelts
9492EN ISO 10993-1:1997Biological evaluation of medical devices - Part 1: Evaluation and testing (ISO 10993-1:1997)Atcelts
60133EN ISO 10993-11:2018Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO/DIS 10993-11:2015)Standarts spēkā
32007EN ISO 10993-11:2009Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006)Atcelts
21797EN ISO 10993-11:2006Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006)Atcelts
9478EN ISO 10993-11:1995Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:1993)Atcelts
Displaying 171-180 of 194 results.