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ISO 20857:2010Published

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

Stérilisation des produits de santé — Chaleur sèche — Exigences pour l'élaboration, la validation et le contrôle de routine d'un processus de stérilisation pour dispositifs médicaux

Abstract / scope

ISO 20857:2010 specifies requirements for the development, validation and routine control of a dry heat sterilization process for medical devices.

Although ISO 20857:2010 primarily addresses dry heat sterilization, it also specifies requirements and provides guidance in relation to depyrogenation processes using dry heat.