MED-(English version) What considerations should be taken when replacing the biological test report of the applied product with the biological test report of the predicate devices marketed by the company?

MED-(Chinese Version) Announcement by CFDA on the Approval and Issuing of 40 Medical Device Sector Standards Including Biological Evaluation of Medical Devices Used in Dentistry - Part 7: Pulp and Dentine Usage Test

MED-(English Version) Interpretation of Rules for Unique Device Identification System

MED-(English Version) Adjustment of Approval Procedures for Part of Medical Devices