NF EN ISO 11138-2
Sterilization of health care products - Biological indicators - Part 2 : biological indicators for ethylene oxide sterilization processes
ISO 11138-2:2006 provides specific 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.
ISO 11138-2:2006 provides specific 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.
Le présent document spécifie les exigences pour les porte-germes inoculés et les indicateurs biologiques utilisés pour l'évaluation de la performance des stérilisateurs et des procédés de stérilisation employant de l'oxyde d'éthylène gazeux comme agent de stérilisation.
Le présent document spécifie les exigences des indicateurs biologiques utilisés pour l'évaluation de la performance des stérilisateurs à l'oxyde d'éthylène.
ISO 11138-2:2006 provides specific 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.
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