ISO/DIS 11135 : 60.00 (2014)被替代
STERILIZATION OF HEALTH-CARE PRODUCTS - ETHYLENE OXIDE - 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
Gives requirements for the development, validation and routine control of an ethylene oxide sterilization process for medical devices in both the industrial and health care facility settings, and it acknowledges the similarities and differences between the two applications.
11/30244091 DC : 0 - Identical
NF EN ISO 11135 : 2012 PR - Identical
11/30244091 DC : 0 - Identical
PREN ISO 11135 : DRAFT 2011 - Identical
04/30048118 DC : DRAFT MAY 2004 - Identical
