MED-Announcement by CFDA on Matters Relating to the Record of Medical Device Operation

MED-(English Version) Notice of National Medical Products Administration on the Pilot Use of Electronic Registration Certificate of Medical devices

MED-(Chinese version) Announcement on Carrying out Designated Examination Work for Registration of Medical Devices

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?