It is not a medical device registration certificate, but a second-class and third-class product produced by a medical device manufacturer. The product registration certificate obtained after the registration of the product to be listed is the proof that a product can be listed. Class I products are produced and put on record by the Municipal Food and Drug Administration.
The record certificate is that the second-class medical device business enterprise can handle the license of a certain type of medical device in the Municipal Food and Drug Administration.