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ISO/CD 11135

Sterilization of health-care products — Ethylene oxide — Requirements for the development, validation and routine control of a sterilization process for medical devices

General information

30.99     22 korr 2024

ISO

ISO/TC 198

International Standard

11.080.01  

Scope

ISO 11135:2014 specifies requirements for the development, validation and routine control of an ethylene oxide sterilization process for medical devices in both the industrial and health care facility settings, and it acknowledges the similarities and differences between the two applications.

Life cycle

PREVIOUSLY

Revises
ISO 11135:2014

Revises
ISO 11135:2014/Amd 1:2018

NOW

IN_DEVELOPMENT
ISO/CD 11135
30.99 CD approved for registration as DIS
22 korr 2024

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