NEN-EN-ISO 14937
Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices
inactive
| Organization: | NEN |
| Publication Date: | 5 February 2001 |
| Status: | inactive |
| Page Count: | 50 |
| ICS Code (Sterilization and disinfection in general): | 11.080.01 |
scope:
Specifies general requirements for the characterization of a sterilizing agent, and for the development, validation and routine control of a sterilization process for medical devices.
Document History
October 1, 2009
Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices
This International Standard specifies general requirements for the characterization of a sterilizing agent and for the development, validation and routine monitoring and control of a sterilization...
December 1, 2007
Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process
This International Standard specifies general requirements for the characterization of a sterilizing agent and for the development, validation and routine monitoring and control of a sterilization...
May 1, 2007
Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices
A description is not available for this item.
NEN-EN-ISO 14937
February 5, 2001
Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices
Specifies general requirements for the characterization of a sterilizing agent, and for the development, validation and routine control of a sterilization process for medical devices.
May 1, 1999
Sterilization of health care products - General criteria for characterization of a sterilizing agent and development, validation and routine control of a sterilization process
Specifies general requirements for the characterization of a sterilizing agent, and for the development, validation and routine control of a sterilization process for medical devices.