ISO 11138-1 PDF

ISO 11138-1 PDF

Summary: Specifies general requirements for production, labelling, test methods and performance characteristics of biological indicators. BS EN ISO specifies general requirements for production, labelling, test methods and performance characteristics of biological. Published in March , the ISO documents have undergone an update. ISO Sterilization of healthcare products – Biological indicators.

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This is the first part of a five part standard the ISO series on the sterilization of health care products and biological indicators.

It specifies general requirements for production, labelling, test 111138-1 and performance characteristics of biological indicators, including inoculated carriers and suspensions, and their components, to be used in the validation and routine monitoring of sterilization processes.

ISO 11138-1, Part 2

It also specifies basic and common requirements that are applicable to all parts of ISO Requirements for biological indicators for particular specified processes are provided in the relevant parts of ISO If no specific subsequent part is provided, this document applies. This document does not apply to microbiological test 1138-1 for processes that rely on physical removal of microorganisms, e.

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This document, however, can contain elements relevant to such microbiological test systems. This standard is a full technical revision of the version, which makes the following amendments:.

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ISO Sterilization of Health Care Products – Biological Indicators | Biological Indicators

Click to learn more. Overview Product Details What is this standard about? The other parts of the standard are: Biological indicators for ethylene oxide sterilization processes Part 3: Biological indicators for moist heat sterilization processes Part 4: Biological indicators for dry heat sterilization processes Part 5: Biological indicators iao low-temperature steam and formaldehyde sterilization processes Who is this standard for?

Sterilization equipment manufacturers Sterilization service providers Infection control professionals Other professionals responsible for sterilization Why should you use this standard?

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National or regional regulations can apply. This standard is a full technical revision of the version, which makes the following amendments: Your basket is empty.

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ANSI/AAMI/ISO (PDF)

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Accept and continue Learn more about the cookies we use and how to change your settings. Labelling processPackaging, Culture containers, Culture techniques, Microbiological analysis, Biological analysis and testing, Medical equipment, Sterilizers, Microorganisms, Bioassay, Sterilization hygienePerformance testing.