The medical device must first be registered on the electronic system of the Control
Department of Medical Devices and Supplies at the Directorate General of Pharmacy and
Drug Control.Moreover, the
medical device will be tested so that it meets safety and security requirements according to
the World Health Organization to ensure the safety of patients and device operators.It is provided by the manufacturer to support and assist the device users in its safe and
appropriate use.Warning: Statement that alerts users about a situation that, if not avoided,