![ONORM EN ISO 11135:2020 - Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014 + Amd 1:2018) (consolidated version) ONORM EN ISO 11135:2020 - Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014 + Amd 1:2018) (consolidated version)](https://webstore.ansi.org/cover-pages/small/ON/ONORM+EN+ISO+11135_2020.jpg)
ONORM EN ISO 11135:2020 - Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014 + Amd 1:2018) (consolidated version)
![ANSI/AAMI/ISO 11135:1994 - Medical devices-Validation and routine control of ethylene oxide sterilization, 3ed ANSI/AAMI/ISO 11135:1994 - Medical devices-Validation and routine control of ethylene oxide sterilization, 3ed](https://webstore.ansi.org/cover-pages/small/AAMI/ANSI+AAMI+ISO+11135-1994.jpg)
ANSI/AAMI/ISO 11135:1994 - Medical devices-Validation and routine control of ethylene oxide sterilization, 3ed
![ISO 11135-1:2007 - Sterilization of health care products — Ethylene oxide — Part 1: Requirements for ISO 11135-1:2007 - Sterilization of health care products — Ethylene oxide — Part 1: Requirements for](https://cdn.standards.iteh.ai/images/43185/2146a4ad815941c6b326e7f601729bdf/page1.jpg)
ISO 11135-1:2007 - Sterilization of health care products — Ethylene oxide — Part 1: Requirements for
![ONORM EN ISO 11135:2015 - Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014) (Austrian Standard) ONORM EN ISO 11135:2015 - Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014) (Austrian Standard)](https://webstore.ansi.org/cover-pages/small/ON/ONORM+EN+ISO+11135_2015.jpg)
ONORM EN ISO 11135:2015 - Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014) (Austrian Standard)
![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: International Organization for Standardization: 9789267107011 ... 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: International Organization for Standardization: 9789267107011 ...](https://m.media-amazon.com/images/I/41fZNiUL1UL._AC_UF1000,1000_QL80_.jpg)
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: International Organization for Standardization: 9789267107011 ...
![ISO 11135 Etilen Oksit - Tıbbi Cihazlar için Bir Sterilizasyon İşleminin Geliştirilmesi için Gereklilikler ISO 11135 Etilen Oksit - Tıbbi Cihazlar için Bir Sterilizasyon İşleminin Geliştirilmesi için Gereklilikler](https://laboratuar.com/images/iso-11135-etilen-oksit---tibbi-cihazlar-icin-bir-sterilizasyon-isleminin-gelistirilmesi-icin-gereklilikler.jpg)
ISO 11135 Etilen Oksit - Tıbbi Cihazlar için Bir Sterilizasyon İşleminin Geliştirilmesi için Gereklilikler
![ISO 11135-1:2007 - Sterilization of health care products - Ethylene oxide - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices ISO 11135-1:2007 - Sterilization of health care products - Ethylene oxide - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices](https://webstore.ansi.org/cover-pages/small/ISO/ISO+11135-1-2007.jpg)
ISO 11135-1:2007 - Sterilization of health care products - Ethylene oxide - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
Medical device software and sterilization professionals - We are proud to announce the CPD accreditation of our online course regarding validation of sterilization according to EN ISO 11135. This is important for
ISO 11135:2014 - Understanding the changes | Take a look at our recent webinar in which Jenni Tranter and Richard Cowman discuss the changes to ISO 11135:2014. Please share to anyone who
![ANSI/AAMI/ISO 11135:2014/A1:2018; 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 ANSI/AAMI/ISO 11135:2014/A1:2018; 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](https://array.aami.org/cms/asset/831978d4-9e3b-45f4-8260-9486a46e89b6/9781570207457.cover.png)