
Biological Evaluation Of Medical Devices - Part 7: Ethylene Oxide Sterilization Residuals
出版:Swiss Standards

专家解读视频
Specifies allowable limits for residual ethylene oxide (EO) and ethylene chlorohydrin (ECH) individual EO-sterilized medical devices, procedures for the measurement of EO and ECH, and methods for determining compliance so that devices may be released.
NBN EN ISO 10993-7:2008 - Identical
NS EN ISO 10993-7:2008 - Identical
ONORM EN ISO 10993-7:2009 - Identical
ISO 10993-7 : 2008(R2016) - Identical
EN ISO 10993-7:2008 - Identical
NBN EN ISO 10993-7:1996 - Identical
UNI EN ISO 10993-7:1997 - Identical
NS EN ISO 10993-7 Ed. 1 (1995) - Identical
UNE EN ISO 10993-7:1996 - Identical
ONORM EN ISO 10993-7:2010 - Identical
UNE EN ISO 10993-7:2009 - Identical
UNI EN ISO 10993-7:2009 - Identical
DIN EN ISO 10993-7 (2009-02) - Identical
SS EN ISO 10993-7 Ed. 2 (2008) - Identical
NEN EN ISO 10993-7:2008 - Identical
NF EN ISO 10993-7:2008 - Identical
BS EN ISO 10993-7:2008 - Identical
I.S. EN ISO 10993-7:2008 - Identical
ISO 10993-7:2008 - Identical
DIN EN ISO 10993-7 (1995-11) - Identical
ONORM EN ISO 10993-7:1996 - Identical