
BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 7: ETHYLENE OXIDE STERILIZATION RESIDUALS
出版:International Organization for Standardization

专家解读视频
Describes allowable limits for residual ethylene oxide (EO) and ethylene chlorohydrin (ECH) in individual EO-sterilized medical devices, procedures for the measurement of EO and ECH, and methods for determining compliance so that devices may be released.
NBR ISO 10993-7 : 2005 - Identical
SAC GB/T 16886.7 : 2001 - Identical
SS-EN ISO 10993-7:2008 - Identical
PN-EN ISO 10993-7: 2009 - Identical
GOST ISO 10993-7 : 2011 - Identical
AAMI ISO 10993-7 : 2008 : R2012 - Identical
CSA ISO 10993-7 : 1998 - Identical
NEN-EN-ISO 10993-7 : 2008 - Identical
DS/EN ISO 10993-7:2008 - Identical
AAMI ISO 10993-7 : 2008 - Identical
SN EN ISO 10993-7 : 2008 - Identical
AAMI TIR19 : 1998 - Identical
GOST R ISO 10993-7 : 2009 - Identical
AAMI ISO 10993-7 : 2008 - Identical
NBN EN ISO 10993-7 : 2008 COR 2009 - Identical
EN ISO 10993-7 : 2008 COR 2009 - Identical
DS/EN ISO 10993-7:2008 - Identical
NS EN ISO 10993-7 : 2008 AC 2009 - Identical
AAMI ISO 10993-7 : 2008 - Identical
GOST R ISO 10993-7 : 2009 - Identical
I.S. EN ISO 10993-7:2008 - Identical
PN-EN ISO 10993-7: 2009 - Identical
SS-EN ISO 10993-7:2008 - Identical
GOST ISO 10993-7 : 2011 - Identical
NF EN ISO 10993-7 : 2008 - Identical
UNI EN ISO 10993-7 : 2009 - Identical
DIN EN ISO 10993-7 : 2009 - Identical
UNE EN ISO 10993-7 : 2009 - Identical
NEN-EN-ISO 10993-7 : 2008 - Identical
SN EN ISO 10993-7 : 2008 - Identical