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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It tackles the need for quality systems, staff training and proper safety measures and covers the following points: Requirements for the development, validation and routine control of a sterilization process for medical devices Status: Find Similar Items This product falls into the following categories.
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:. Sterilization of health-care products.
Isp faster, easier way to work with standards. Requirements for the development, validation and routine control of a sterilization process for medical devices.
Why should you use this standard?
ISO /Amd – Revision of Annex E, Single batch release
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BS EN ISO 11135:2014
This international standard sets out how to ensure that medical devices are sterilized effectively using an ethylene oxide sterilization process. You may find similar items within these categories 1113-51 selecting from the choices below:. Take the smart route to manage medical device compliance.
Overview Product Details What is this standard about? Anyone responsible for sterilizing medical devices in both industrial and health care settings. Symbols to be used with medical device labels, labelling and information to be supplied General requirements. It also adds additional information. Click to learn more.
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