
Biological Evaluation Of Medical Devices - Part 3: Tests For Genotoxicity, Carcinogenicity And Reproductive Toxicity
出版:Association Francaise de Normalisation

專家解讀視頻
Gives strategies for hazard identification and tests on medical devices for the following biological aspects: genotoxicity, carcinogenicity, and reproductive and developmental toxicity. Applicable for evaluation of a medical device whose potential for genotoxicity, carcinogenicity or reproductive toxicity has been identified. Also provides guidance on selection of tests.
Indice de classement: S99-501-3PR. PR NF EN ISO 10993-3 July 2000. (08/2004) Supersedes NF EN 30993-3. (10/2004) PR NF EN ISO 10993-3 March 2009. (03/2009)
NEN EN ISO 10993-3:2003 - Identical
SS EN ISO 10993-3 Ed. 1 (2004) - Identical
UNE EN ISO 10993-3:2004 - Identical
NS EN ISO 10993-3 Ed. 1 (2003) - Identical
UNI EN ISO 10993-3:2004 - Identical
I.S. EN ISO 10993-3:2003 - Identical
UNI EN ISO 10993-3:2009 - Identical
NBN EN ISO 10993-3:2009 - Identical
UNE EN ISO 10993-3:2009 - Identical
SS EN ISO 10993-3 Ed. 2 (2009) - Identical
NS EN ISO 10993-3:2009 - Identical
NEN EN ISO 10993-3:2009 - Identical
SN EN ISO 10993-3:2003 - Identical
BS EN ISO 10993-3:2003 - Identical
DIN EN ISO 10993-3 (2004-02) - Identical
NBN EN ISO 10993-3:2003 - Identical
ONORM EN ISO 10993-3:2004 - Identical
ISO 10993-3:2003 - Identical