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 (ISO 11137-1:2006, including Amd 1:2013)
active, Most Current
| Organization: | TSE |
| Publication Date: | 23 October 2015 |
| Status: | active |
| ICS Code (Sterilization and disinfection in general): | 11.080.01 |
scope:
This part of ISO 11137 specifies requirements for thedevelopment, validation and routine control of a radiationsterilizati
Document History
TS EN ISO 11137-1
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...
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
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