Επεξεργασία προϊόντων υγειονομικής περίθαλψης - Πληροφορίες που πρέπει να παρέχονται από τον κατασκευαστή ιατροτεχνολογικών προϊόντων για την επεξεργασία ιατροτεχνολογικών προϊόντων

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.