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ISO 11135-2 PDF

Permission can be requested from either ISO at the address below or cancels and replaces ISO and ISO/TS ISO TS STERILIZATION OF HEALTH CARE PRODUCTS – ETHYLENE OXIDE – PART 2: GUIDANCE ON THE APPLICATION OF ISO (Combined revision of ANSI/AAMI/ISO requirements for validation and routine control—with ISO/TS , which contained the bulk of the.

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DD CEN ISO/TS 11135-2:2008

Guidance on the application of ISO Status: Please first verify your email before subscribing to alerts. Already Subscribed to this document. Take the smart route to manage medical device compliance.

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CEN ISO/TS /AC – Estonian Centre for Standardisation

You may experience issues viewing this site in Internet Explorer 9, 10 1135-2 As the voice of the 1135-2. Subscription pricing is determined by: We have no document history for this standard. Your Alert Profile lists the documents that will be monitored. Click to learn more. Ethylene oxide Requirements for development, validation and routine control of a sterilization process for medical devices. Find Similar Items This product falls into the following categories.

Isk 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. Search all products by. Please first log in with a verified email before subscribing to alerts. ISO – Sterilization of Health Care Products Package specifies the requirements for the development, validation and routine control of ethylene oxide sterilization process for medical devices and other healthcare products.


1113-52 of health care products. Guidance on the application of ISO You can download and open this file to your own computer but DRM prevents opening this file on another computer, including a networked server. We have no amendments or corrections for this standard.

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