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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

inactive
Organization: NEN
Publication Date: 1 May 2006
Status: inactive
Page Count: 52
ICS Code (Sterilization and disinfection in general): 11.080.01
scope:

This part of ISO 11137 specifies requirements for the development, validation and routine control of a radiation sterilization process for medical devices.

Document History

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.
NEN-EN-ISO 11137-1
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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