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

专家解读视频
This part of ISO 17665 specifies requirements for the development, validation and routine control of a moist heat sterilization process for medical devices.
SANS 17665-1 : 1ED 2007(R2013) - Identical
AAMI ISO 17665-1 : 2006 : R2013 - Identical
SS-EN ISO 17665-1 : 2006 - Identical
DS EN ISO 17665-1 : 2006 - Identical
GOST R ISO 17665-1 : 2016 - Identical
NBR ISO 17665-1 : 2010 - Identical
PN EN ISO 17665-1 : 2008 - Identical
CSA Z17665-1:2009(R2019) - Identical
AAMI ISO 17665-1 : 2006 - Identical
AAMI ISO 17665-1 : 2006 - Identical
SAC GB 18278.1 : 2015 - Identical