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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CEN ISO/TS 11135-2:2008/AC:2009

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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. Isi Alert Profile lists the documents that will be monitored.

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CEN ISO/TS /AC – Estonian Centre for Standardisation

Already Subscribed to this document. Ethylene oxide Requirements for development, validation and routine control of a sterilization process for medical devices. You can download and open this file to your own computer but DRM prevents opening this file on another computer, including a networked server.

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DD CEN ISO/TS 11135-2:2008

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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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