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Can anyone supply information on the requirements for registration of medical device in Nigeria?
We have a distributor that is saying a Class IIa UK made product does not require registration but the NAFDAC website says that all imported medical devices should be registered.
Any information would be greatly appreciated.

We have a distributor that is saying a Class IIa UK made product does not require registration but the NAFDAC website says that all imported medical devices should be registered.
Any information would be greatly appreciated.
