The definition of medical device under this regulation is any instrument, apparatus, tool, machine, appliance, implant, material, or other similar or related item used alone or in combination with each other, including accessories and software necessary for its proper application as proposed by the manufacturer for use on human beings, intended for the diagnosis, prevention, monitoring, treatment, and alleviation of disease, injury, or disability. They are also used in research, replacement or modification of the anatomy, physiological processes, and the control of conception.
The teleconsultation guide aims to provide clear and timely information to the population on aspects related to COVID-19. It does not address how care should be provided using ICTs.