# ISO 11135-1:2007 — Withdrawn and superseded ISO standards For ISO 11135-1:2007, item title is Sterilization of health care products — Ethylene oxide — Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices; status code is 9599; successor is ISO 11135:2014; withdrawn / published date is 2007-04-27, recorded from its source on 2026-08-05. - **Identifier:** ISO 11135-1:2007 _(verified: appears in the quote below)_ - **Item title:** Sterilization of health care products — Ethylene oxide — Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices _(verified: appears in the quote below)_ - **Status code:** 9599 _(verified: appears in the quote below)_ - **Successor:** ISO 11135:2014 - **Withdrawn / published date:** 2007-04-27 _(verified: appears in the quote below)_ ## What the source says > 43185,IS,,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","Stérilisation des produits de santé — Oxyde d'éthylène — Partie 1: Exigences de développement, de validation et de contrôle de routine d'un processus de stérilisation pour des dispositifs médicaux",2007-04-27,1,['11.080.01'],ISO/TC 198,9599,"[24811,19154]",[56137],"['en','fr','ru']",41,"

ISO 11135-1:2007 specifies requirements for the development, validation and routine control of an ethylene oxide sterilization process for medical devices.

Sterilization processes validated and ## Source - https://isopublicstorageprod.blob.core.windows.net/opendata/_latest/iso_deliverables_metadata/csv/iso_deliverables_metadata.csv Last verified: 2026-08-05. Review by: 2027-02-01. Part of [Withdrawn and superseded ISO standards](https://referencesource.org/iso-standard-supersessions/).