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Homepage>UNE standards>UNE EN ISO 11135:2015/A1:2020 Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices - Amendment 1: Revision of Annex E, Single batch release (ISO 11135:2014/Amd 1:2018)
in stockReleased: 2020-07-22
UNE EN ISO 11135:2015/A1:2020 Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices - Amendment 1: Revision of Annex E, Single batch release (ISO 11135:2014/Amd 1:2018)

UNE EN ISO 11135:2015/A1:2020

Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices - Amendment 1: Revision of Annex E, Single batch release (ISO 11135:2014/Amd 1:2018)

Esterilización de productos para asistencia sanitaria. Óxido de etileno. Requisitos para el desarrollo, la validación y el control de rutina de un proceso de esterilización para productos sanitarios. Modificación 1: Revisión del Anexo E, Liberación de un único lote. (ISO 11135:2014/Amd 1:2018).

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Standard number:UNE EN ISO 11135:2015/A1:2020
Pages:23
Released:2020-07-22
DESCRIPTION
This standard UNE EN ISO 11135:2015/A1:2020 Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices - Amendment 1: Revision of Annex E, Single batch release (ISO 11135:2014/Amd 1:2018) is classified in these ICS categories:
  • 11.080.01
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