NEN-EN-ISO 11137-1/A2
Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices - Amendment 2: Revision to 4.3.4 and 11.2
active, Most Current
| Organization: | NEN |
| Publication Date: | 1 November 2019 |
| Status: | active |
| Page Count: | 26 |
| ICS Code (Sterilization and disinfection in general): | 11.080.01 |
Document History
NEN-EN-ISO 11137-1/A2
November 1, 2019
Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices - Amendment 2: Revision to 4.3.4 and 11.2
A description is not available for this item.
June 1, 2015
Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
NEN-EN-ISO 11137-1 specifies requirements for the development, validation and routine control of a radiation sterilization process for medical devices.
July 1, 2013
Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
A description is not available for this item.
May 1, 2012
Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
A description is not available for this item.
May 1, 2006
Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
This part of ISO 11137 specifies requirements for the development, validation and routine control of a radiation sterilization process for medical devices.
May 1, 2004
Sterilization of health care products - Radiation - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices
This part of ISO 11137 specifies requirements for the development, validation and routine control of a radiation sterilization process for medical devices.