
STERILIZATION OF HEALTH CARE PRODUCTS - RADIATION - PART 1: REQUIREMENTS FOR DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES
出版:International Organization for Standardization

专家解读视频
Describes requirements for the development, validation and routine control of a radiation sterilization process for medical devices.
BS EN ISO 11137-1 : 2015 - Identical
SS-EN ISO 11137-1:2015 - Identical
I.S. EN ISO 11137-1:2015&A2:2019 - Identical
PN EN ISO 11137-1 : 2015 - Identical
DS EN ISO 11137-1 : 2015 - Identical
AAMI ISO 11137-1 : 2006 - Identical
AAMI ISO 11137-1 : 2006 - Identical
GOST ISO 11137-1 : 2011 - Identical
UNI EN ISO 11137-1 : 2015 - Identical
SANS 11137-1 : 1ED 2007(R2013) - Identical
AS/NZS ISO 11137.1:2006 (R2017) - Identical
AAMI ISO 11137-1 : 2006 : R2010 - Identical
GOST R ISO 11137-1 : 2008 - Identical
I.S. EN ISO 11137-1:2015 - Identical
CSA Z11137-1A : 2016(R2016) - Identical
AAMI ISO 11137-1 : 2006 : INC : AMD 1 : 2013 : R201000 - Identical