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
Performance testing;Sterile equipment;Performance;Sterilizers;Instructions for use;Management;Microbiological analysis;Medical equipment;Ethylene oxide;Sterilization (hygiene);Acceptance (approval);Quality control;Personnel;Verification;Medical instruments;Maintenance;Hygiene
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 11135:2014
Revision Level
2014 EDITION
Status
Superseded
Publication Date
Jan. 31, 2015
Page Count
94
ISBN
9780580892219
International Equivalent
ISO 11135:2014;EN ISO 11135:2014
Committee Number
CH/198