The medical device registration certificate comes with some of the "medical device registration form" and some of the "medical device product manufacturing approval form" What is the difference?

1: Medical Device Registration Form (SFDA also known as "Medical Device Manufacturing Approval Form") is used to register the basic information of the medical device product, which includes: such as the name of the product, the manufacturer, the production address, product specifications, product composition, product expectations, use, precautions or contraindications, other necessary information, and so on. Use, precautions or contraindications, other necessary information.

2: It should be used in conjunction with the medical device product registration certificate to be effective.