BS-EN-ISO-11135 › Historical Revision Information
Sterilization of health-care products. Ethylene oxide. Requirements for the development, validation and routine control of a sterilization process for medical devices
Document Center Inc. is an authorized dealer of BSI standards.
The following bibliographic material is provided to assist you with your purchasing decision:
The following bibliographic material is provided to assist you with your purchasing decision:
Sterilization of health-care products. Ethylene oxide. Requirements for the development, validation and routine control of a sterilization process for medical devices
Keywords
Verification;Medical instruments;Quality control;Microbiological analysis;Performance;Sterile equipment;Instructions for use;Sterilizers;Personnel;Sterilization (hygiene);Acceptance (approval);Hygiene;Medical equipment;Maintenance;Performance testing;Management;Ethylene oxide
To find similar documents by classification:
This document comes with our free Notification Service, good for the life of the document.
This document is available in either Paper or PDF format.
Document Number
BS-EN-ISO-11135
Revision Level
2014/A1 EDITION CORRIGENDUM 1
Status
Current
Publication Date
Jan. 15, 2020
Replaces
BS EN ISO 11135-1:2007;DD CEN ISO/TS 11135-2:2008
Page Count
102
ISBN
9780539127089
International Equivalent
EN ISO 11135:2014/A1:2019;ISO 11135:2014/Amd.1:2018;ISO 11135:2014/Amd 1:2018
Committee Number
CH/198