
Biological Evaluation Of Medical Devices - Part 3: Tests For Genotoxicity, Carcinogenicity And Reproductive Toxicity (Iso 10993-3:2014)
出版:Belgian Standards

專家解讀視頻
Describes strategies for risk estimation, selection of hazard identification tests and risk management, with respect to the possibility of the following potentially irreversible biological effects arising as a result of exposure to medical devices: - genotoxicity - carcinogenicity, - reproductive and developmental toxicity.
Supersedes NBN EN 30993-3. (06/2007)
DIN EN ISO 10993-3 (2009-08) - Identical
UNE EN ISO 10993-3:2009 - Identical
I.S. EN ISO 10993-3:2014 - Identical
BS EN ISO 10993-3:2014 - Identical
NEN EN ISO 10993-3:2014 - Identical
SS EN ISO 10993-3 Ed. 3 (2014) - Identical
NF EN ISO 10993-3:2014 - Identical
NS EN ISO 10993-3:2014 - Identical
ONORM EN ISO 10993-3:2015 - Identical
SN EN ISO 10993-3:2014 - Identical
UNE EN ISO 10993-3:2015 - Identical