TSE - TS 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: | TSE |
| Publication Date: | 12 October 2006 |
| Status: | inactive |
| ICS Code (Sterilization and disinfection in general): | 11.080.01 |
Document History
October 23, 2015
Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11137-1:2006, including Amd 1:2013)
This part of ISO 11137 specifies requirements for thedevelopment, validation and routine control of a radiationsterilization process for medical devices.
March 8, 2012
Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
Bu standard, tibbi cihazlar icin radyasyon ile sterilizasyonsurecinin gelistirilmesi, gecerli kilinmasi ve rutin kontrolunuicin gerekleri kapsar. Not -Bu standardin kapsami tibbi cihazlarlasinirli...
TS EN ISO 11137-1
October 12, 2006
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.