Dear members of Elsmar,
Does anybody know which regulation/registration are applicable to medical device intended to be exported to Mexico?
Namely, my team planning to do shipment there, one device just for demonstration purposes (not for sale) so I someone is able to give me instructions/guidelines or links to COFEPRIS it will be appreciated, since I am not sure are registration requirements applicable to all medical devices or only to ones intended to be sold.
Thanks in advance.
Does anybody know which regulation/registration are applicable to medical device intended to be exported to Mexico?
Namely, my team planning to do shipment there, one device just for demonstration purposes (not for sale) so I someone is able to give me instructions/guidelines or links to COFEPRIS it will be appreciated, since I am not sure are registration requirements applicable to all medical devices or only to ones intended to be sold.
Thanks in advance.