This document outlines the requirements for type examination of medical devices according to the Medical Devices Regulation 2017/745. It discusses the process by which a manufacturer applies to a notified body for type examination, including submitting technical documentation and a sample of the device. It also describes the notified body's assessment process, including examining documentation, reviewing clinical evidence, and testing devices. The notified body issues an EU type examination certificate if the device fulfills the regulation's requirements. Requirements are also provided for changes to the device type and record keeping.