DIN EN ISO 11135/A1
Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014/DAM 1:2017); German and English version EN ISO 11135:2014/prA1:2017
inactive
Organization: | DIN |
Publication Date: | 1 September 2017 |
Status: | inactive |
Page Count: | 15 |
ICS Code (Disinfectants and antiseptics): | 11.080.20 |
Document History

May 1, 2023
Sterilization of health care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO/DIS 11135:2023); German and English version prEN ISO 11135:2023
A description is not available for this item.

April 1, 2020
Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014 + Amd.1:2018) (includes Amendment :2019)
A description is not available for this item.

DIN EN ISO 11135/A1
September 1, 2017
Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014/DAM 1:2017); German and English version EN ISO 11135:2014/prA1:2017
A description is not available for this item.

October 1, 2014
Sterilization of health care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014)
Inclusions
This International Standard specifies requirements for the development, validation and routine control of an ethylene oxide sterilization process for medical devices in both the...