I don't know what class of medical device you are applying for.
Class I, Class II and Class III correspond to municipal, provincial and State Food and Drug Administration respectively.
The application for registration is divided into two steps
1, formal review (10 working days with a response)
2, substantive review (review of qualified persons within 10 working days to issue a certificate of registration)
Procedure:
Enterprises to submit the application information - (formal review) meets the requirements to issue a grant of registration - (substantive review) meets the requirements. A written decision to grant registration, and then within 10 working days to issue a certificate of registration.
Suggest you can look at the "Medical Device Registration Management Measures", there you can see what you need.
Hope it can help you. Thank you!