• BS EN ISO 11138-2:2017

    Current The latest, up-to-date edition.

    Sterilization of health care products. Biological indicators Biological indicators for ethylene oxide sterilization processes

    Available format(s):  Hardcopy, PDF

    Language(s):  English

    Published date:  30-04-2017

    Publisher:  British Standards Institution

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    Table of Contents - (Show below) - (Hide below)

    Foreword
    Introduction
    1 Scope
    2 Normative references
    3 Terms and definitions
    4 General requirements
    5 Test organism
    6 Suspension
    7 Carrier and primary packaging
    8 Inoculated carriers and biological indicators
    9 Population and resistance
    Annex A (normative) - Method for determination of
            resistance to ethylene oxide sterilization
    Annex B (informative) - Rationale for the inclusion
            of a second minimum D value specification
            as a result of changes to the test gas used
            to evaluate resistance and deletion of the
            requirement for a minimum D value at
            30 degrees C
    Bibliography

    Abstract - (Show below) - (Hide below)

    Describes requirements for test organisms, suspensions, inoculated carriers, biological indicators and test methods intended for use in assessing the performance of sterilizers and sterilization processes employing ethylene oxide gas as the sterilizing agent, either as pure ethylene oxide gas or mixtures of this gas with diluent gases, at sterilizing temperatures within the range of 29 degrees C to 65 degrees C.

    Scope - (Show below) - (Hide below)

    This document specifies requirements for test organisms, suspensions, inoculated carriers, biological indicators and test methods intended for use in assessing the performance of sterilizers and sterilization processes employing ethylene oxide gas as the sterilizing agent, either as pure ethylene oxide gas or mixtures of this gas with diluent gases, at sterilizing temperatures within the range of 29°C to 65°C.

    NOTE1 Requirements for validation and control of ethylene oxide sterilization processes are provided by ISO11135 and ISO14937 .

    NOTE2 National or regional regulations can provide requirements for work place safety.

    General Product Information - (Show below) - (Hide below)

    Committee CH/198
    Development Note Supersedes BS EN 866-2, BS EN 866-8 & 04/30078099 DC (08/2006) Supersedes 15/30321505 DC. (04/2017)
    Document Type Standard
    Publisher British Standards Institution
    Status Current
    Supersedes

    Standards Referencing This Book - (Show below) - (Hide below)

    ISO 11135:2014 Sterilization of health-care products Ethylene oxide Requirements for the development, validation and routine control of a sterilization process for medical devices
    ISO 14937:2009 Sterilization of health care products General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices
    ISO 18472:2006 Sterilization of health care products Biological and chemical indicators Test equipment
    ISO 11138-1:2017 Sterilization of health care products — Biological indicators — Part 1: General requirements
    ISO 14161:2009 Sterilization of health care products Biological indicators Guidance for the selection, use and interpretation of results
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