BS EN ISO 11135. Sterilization of health-care products. Ethylene oxide. Requirements for the development, validation and routine control of a sterilization process for medical devices
Cross References: ISO 10012 ISO 10993-7 ISO 11138-1:2006 ISO 11138-2:2006 ISO 11140-1 ISO 11737-1 ISO 11737-2 ISO 13485:2003/CORR1:2009 ISO 14161:2009 ISO 9000:2005 ISO 9001 ISO 10993-1 ISO 11138-1:2006 ISO/TS 11139:2006 ISO 11607-1 ISO 11607-2 ISO 14001 ISO 14040 ISO 14937:2009 ISO 14971 ISO 15883-1 ISO 15883-2 ISO 15883-4 ISO/TS 15883-5 ISO/DIS 15883-6 ISO 17664 ISO 22442-1 ISO 22442-2 ISO 22442-3 ISO/IEC Guide 99:2007 ISO/IEC 90003 IEC 61010-1 IEC 61010-2-040 AAMI TIR15 AAMI TIR16 AAMI TIR28:2009 ANSI/AAMI ST41:1999 ANSI/AAMI ST67 AS/NZS 4187 2003 EN 1422:1997 EN 556-1
All current amendments available at time of purchase are included with the purchase of this document.
Sterilization of health-care products. Ethylene oxide. Requirements for the development, validation and routine control of a sterilization process for medical devices
BS EN ISO 11135. Sterilization of health-care products. Ethylene oxide. Requirements for the development, validation and routine control of a sterilization process for medical devices
