ISO 11135-1 PDF

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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Why should you use this standard? We use cookies to make our website easier to use and to better understand your needs. Requirements for the 11135- validation and routine control of a sterilization process for medical devices.

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You may find similar items within these categories by selecting from the choices below:. Requirements for the development, validation and routine control of a sterilization process for medical devices Status: Sterilization of health-care products. It also adds additional information. It tackles the need for quality systems, staff training and proper safety measures and covers the following points: You may experience issues viewing this site in Internet Explorer 9, 10 or Find Similar Items This product falls into the following categories.

Anyone responsible for sterilizing medical devices in both industrial and health care settings. Accept and continue Learn more about the cookies we use and how to change your settings.

BS EN ISO 11135:2014

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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Overview Product Details What is this standard about? It describes requirements that, if met, will provide an ethylene oxide sterilization process with appropriate microbiocidal activity intended to sterilize medical devices.

This website is best viewed with browser version of sio to Microsoft Internet Explorer 8 or Firefox 3. Your basket is empty. Who is this standard for?

It tackles the need for quality systems, staff training and proper ieo measures and covers the following points:. This international standard sets out how to ensure that medical devices are sterilized effectively using an ethylene oxide sterilization process.

Symbols to be used with medical device labels, labelling and information to be supplied General requirements. The faster, easier way to work with standards.