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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ISO /Amd – Revision of Annex E, Single batch release

You may find similar items within these categories by selecting from the choices below:. Symbols to be used with medical device labels, labelling and information to be supplied General requirements.

Search all ido by. It tackles the need for quality systems, staff training and proper safety measures and covers the following points: Who is this standard for? Why should you use this standard? Worldwide Standards We can source any standard from anywhere in the world.

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BS EN ISO 11135:2014

Overview Product Details 11135-11 is this standard about? Please download Chrome or Firefox or view our browser tips. The faster, easier way to work with standards.

Click to learn more. It also adds additional information. 11135-1 Similar Items This product falls into the following categories. This website is best viewed with browser version of up to Microsoft Internet Explorer 8 or Firefox 3. Accept and continue Learn more about 11153-1 cookies we use and how to change your settings. Anyone responsible for sterilizing medical devices in both industrial and health care settings.

This international standard sets out how to ensure that medical devices are sterilized effectively using an ethylene oxide sterilization process.

You may experience issues viewing this site in Internet Explorer 9, 10 or Sterilization of health-care products. It describes requirements that, if met, will provide an ethylene oxide sterilization process with appropriate microbiocidal activity intended to sterilize medical devices. Your basket is empty.

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Take the smart route to manage medical device compliance. Learn more about the cookies we use and how to change your settings. Requirements for the development, validation and routine control of a sterilization process for medical devices. We use cookies to make our website easier to use and to better understand your needs. Requirements for the development, validation and routine control of a sterilization process for medical devices Status: 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.

It tackles the need for quality systems, staff training and proper safety measures and covers the following points:.