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.
|Published (Last):||23 March 2010|
|PDF File Size:||11.22 Mb|
|ePub File Size:||12.92 Mb|
|Price:||Free* [*Free Regsitration Required]|
July Replaced By: Learn more about the cookies we use and how to change your settings.
CEN ISO/TS 11135-2:2008/AC:2009
Search all products by. Find Similar Items This product falls into the following categories.
You may find similar items within these categories by selecting from the choices below:. Guidance on the application of ISO Status: Click to learn more. Your basket is empty. Take the smart route to manage medical device compliance.
The faster, easier way to work with standards. Ethylene oxide Requirements for development, validation and routine control of a sterilization process for medical devices.
CEN ISO/TS /AC – Estonian Centre for Standardisation
You may experience issues viewing this site in Internet Explorer 9, 10 or Please download Chrome or Firefox or view our jso tips. This website is best viewed with browser version of up to Microsoft Internet Explorer 8 or Firefox 3.
Sterilization of health care products. Guidance on the application of ISO Medical equipment, Sterilization hygieneEthylene oxide, Hygiene, Medical instruments, Sterile equipment, Performance, Performance testing, Quality control, Maintenance, Acceptance approvalVerification, Microbiological analysis, Instructions for use, Ieo, Sterilizers, Management.
Leitfaden zur Anwendung von ISO