ISO Sterilization of health care products—Biological indicators— Part 2: Biological indicators for ethylene oxide sterilization processes. American. Summary: Specifies requirements for test organisms, suspensions, inoculated carriers, biological indicators and test methods intended for use. ISO Sterilization of health care products —. Biological indicators —. Part 2: Third edition. Reference number. ISO (E).
|Published (Last):||28 October 2010|
|PDF File Size:||3.63 Mb|
|ePub File Size:||16.92 Mb|
|Price:||Free* [*Free Regsitration Required]|
Click to learn more. This document gives specific requirements for those biological indicators intended for use in ethylene oxide sterilization processes. Sterilization of health care products. 11318-2 following amendments have been made: Biological indicators for ethylene oxide sterilization processes Status: The intent is not to promote the use of biological indicators where such use is not advised, but rather to provide common requirements iwo the production of those biological indicators that are known to be in use today.
Accept and continue Learn more about the cookies we use and how to change your settings.
You may experience issues viewing this site in Internet Explorer 9, 10 or Biological indicators for dry heat sterilization processes Part 5: The faster, easier way to work with standards. General requirements Part 3: This standard is a full technical revision of the version.
Please download Chrome or Firefox or view our browser tips. This standard covers general requirements, test organism, suspension, carrier and primary packaging, inoculated carriers and biological indicators, and population and resistance.
Overview Product Details What is this standard about? Your basket is empty. Find Similar Items This product falls into the following categories. You may find similar items within these categories by selecting from the choices below:. Standards exist providing requirements for the validation and control of ethylene oxide sterilization see ISO and ISO Requirements of population and resistance clause 9 revised, e.
Part 1 specifies production, labelling, test methods and performance requirements for the manufacture of biological indicators, including inoculated carriers and suspensions intended for use in validation and monitoring of sterilization processes.
Association for the Advancement of Medical Instrumentation
Biological indicators for ethylene oxide sterilization processes. The following amendments have been made:. Sterilization equipment manufacturers Sterilization service providers Infection control professionals Other professionals responsible for sterilization Why should you use this standard? Organism-activity determination, Ethylene oxide, Microorganisms, Sterilization hygienePerformance testing, Biological analysis and testing, Sterilizers, Bioassay, Microbiological analysis, Medical equipment, Gas sterilizers.
This website is best viewed with browser version of up to Microsoft Internet Explorer 8 or Firefox 3. Biological indicators for moist heat sterilization processes Part 4: Learn more about the cookies we use and how to change your settings.
Biological indicators Biological indicators for moist heat sterilization processes. Biological indicators for low-temperature steam and formaldehyde sterilization processes Who is this standard for?
This is the second part of a five part standard the ISO series on the sterilization of health care products and biological indicators.
Take the smart route to manage medical device compliance. The other parts of the standard are: