ISO 17664:2017Withdrawn

Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices

Traitement de produits de soins de santé — Informations relatives au traitement des dispositifs médicaux à fournir par le fabricant du dispositif

This edition has been replaced by ISO 17664-1:2021.

Abstract / scope

ISO 17664:2017 specifies requirements for the information to be provided by the medical device manufacturer for the processing of a medical device that requires cleaning followed by disinfection and/or sterilization to ensure that the device is safe and effective for its intended use.

This includes information for processing prior to use or reuse of the medical device. The provisions of ISO 17664:2017 are applicable to medical devices that are intended for invasive or other direct or indirect patient contact.

Life cycle

Replaces

ISO 17664:2004WithdrawnSterilization of medical devices — Information to be provided by the manufacturer for the processing of resterilizable medical devicesInternational Standard · Published 25 Feb 2004 · ISO/TC 198

Replaced by

ISO 17664-1:2021PublishedProcessing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices — Part 1: Critical and semi-critical medical devicesInternational Standard · Published 6 Jul 2021 · ISO/TC 198