NEN-EN-ISO 14160
Sterilization of medical devices - Validation and routine control of sterilization of single-use medical devices incorporating materials of animal origin by liquid chemical sterilants
inactive
| Organization: | NEN |
| Publication Date: | 1 August 1995 |
| Status: | inactive |
| ICS Code (Sterilization and disinfection in general): | 11.080.01 |
scope:
Specifies requirements for the development, validation, process control and monitoring of the sterilization of single-use medical devices comprising in whole or in part materials of animal origin using liquid chemical sterilants.
Document History
July 1, 2021
Sterilization of health care products - Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives - Requirements for characterization, development, validation and routine control of a sterilization process for medical devices
This document specifies requirements for the characterization of a liquid chemical sterilizing agent and for the development, validation, process control and monitoring of sterilization by liquid...
July 1, 2011
Sterilization of health care products - Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives - Requirements for characterization, development, validation and routine control of a sterilization process for medical devices
This International Standard specifies requirements for the characterization of a liquid chemical sterilizing agent and for the development, validation, process control and monitoring of sterilization...
May 1, 1998
Sterilization of single-use medical devices incorporating materials of animal origin - Validation and routine control of sterilization by liquid chemical sterilants
Specifies requirements for the development, validation, process control and monitoring of the sterilization of single-use medical devices comprising in whole or in part materials of animal origin...
NEN-EN-ISO 14160
August 1, 1995
Sterilization of medical devices - Validation and routine control of sterilization of single-use medical devices incorporating materials of animal origin by liquid chemical sterilants
Specifies requirements for the development, validation, process control and monitoring of the sterilization of single-use medical devices comprising in whole or in part materials of animal origin...