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NEN-EN-ISO 11137-1

Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices

active, Most Current
Organization: NEN
Publication Date: 1 June 2015
Status: active
Page Count: 65
ICS Code (Sterilization and disinfection in general): 11.080.01
scope:

NEN-EN-ISO 11137-1 specifies requirements for the development, validation and routine control of a radiation sterilization process for medical devices.

Document History

NEN-EN-ISO 11137-1
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.

References

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