
Biological Evaluation Of Medical Devices - Part 13: Identification And Quantification Of Degradation Products From Polymeric Medical Devices
出版:Standardiserings-Kommissionen I Sverige

专家解读视频
Describes general requirements for the design of tests in a simulated environment for identifying and quantifying degradation products from finished polymeric medical devices ready for clinical use.
NBN EN ISO 10993-13:2010 - Identical
NEN EN ISO 10993-13:2010 - Identical
BS EN ISO 10993-13:2010 - Identical
NS EN ISO 10993-13:2010 - Identical
ONORM EN ISO 10993-13:2010 - Identical
SN EN ISO 10993-13:2010 - Identical
DIN EN ISO 10993-13 (2010-11) - Identical
UNE EN ISO 10993-13:2010 - Identical
ONORM EN ISO 10993-13:2009 - Identical
I.S. EN ISO 10993-13:2010 - Identical
UNI EN ISO 10993-13:2010 - Identical
NF EN ISO 10993-13:2010 - Identical
BS EN ISO 10993-13:2009 - Identical
NS EN ISO 10993-13:2009 - Identical
DIN EN ISO 10993-13 (2009-08) - Identical
UNE EN ISO 10993-13:2009 - Identical
SN EN ISO 10993-13:2009 - Identical
EN ISO 10993-13:2010 - Identical