Status: Published. Publication date: Edition: 1. Number of pages: 4. Technical Committee.: ISO/TC Sterilization of health care products. ICS. ISO INTERNATIONAL. STANDARD. ISO. First edition. Sterilization of health care products —. Ethylene oxide —. Part 1. Permission can be requested from either ISO at the address below or ISO’s ISO cancels and replaces ISO and.
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Take the smart route to manage medical device compliance. Search all products by. It tackles the need kso quality systems, staff training and proper safety measures and covers the following points: Symbols to be used with medical device labels, labelling and information to be supplied General requirements.
It tackles the need for quality systems, staff training and proper safety measures and covers the following points:.
BS EN ISO 11135:2014
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It also adds additional information. Requirements for the development, validation and routine control of a sterilization process for medical devices Status: It describes requirements that, if met, will provide an ethylene oxide sterilization process with appropriate microbiocidal activity intended to sterilize medical devices.
Accept and continue Learn more about the cookies we use and how to change isoo settings. This international standard sets out how to ensure that medical devices are sterilized effectively using an ethylene oxide sterilization process.
Anyone responsible for sterilizing medical devices in both industrial and health care settings. You may experience issues viewing this site in Internet Explorer 9, 10 or Ios Product Details What is this standard about? You may find similar items within these categories by selecting from the choices below:.
Why should you use this standard? Medical equipment, Sterilization hygieneEthylene oxide, Hygiene, Medical instruments, Sterile equipment, Performance, Performance testing, Quality control, Maintenance, Acceptance approvalVerification, Microbiological analysis, Instructions for use, Personnel, Sterilizers, Management.
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