ISO 17665:2024Published

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

Stérilisation des produits de santé — Chaleur humide — Exigences pour le développement, la validation et le contrôle de routine d’un procédé de stérilisation des dispositifs médicaux

Abstract / scope

This document provides requirements for the development, validation and routine control of moist heat sterilization processes for medical devices. It also contains guidance which is intended to explain the requirements set forth in the normative sections. The guidance given is intended to promote good practice related to moist heat sterilization processes according to this document. The application within industrial and health care settings is considered.

Life cycle

Amendments & corrigenda

ISO 17665:2024/AWI Amd 1Under developmentSterilization of health care products — Moist heat — Requirements for the development, validation and routine control of a sterilization process for medical devices — Amendment 1International Standard · ISO/TC 198

Replaces

ISO 17665-1:2006WithdrawnSterilization of health care products — Moist heat — Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devicesInternational Standard · Published 17 Aug 2006 · ISO/TC 198ISO/TS 17665-2:2009WithdrawnSterilization of health care products — Moist heat — Part 2: Guidance on the application of ISO 17665-1Technical Specification · Published 5 Jan 2009 · ISO/TC 198ISO/TS 17665-3:2013WithdrawnSterilization of health care products — Moist heat — Part 3: Guidance on the designation of a medical device to a product family and processing category for steam sterilizationTechnical Specification · Published 12 Apr 2013 · ISO/TC 198