For medical devices that are approved for registration or filing for the first time, the registrant shall complete the previous year's regular product risk assessment report within 60 days after every 1 year.
For medical devices approved for registration or filing for the first time, the registrar shall complete the periodic risk assessment report of the previous year's product within 60 days after each year.
For the medical devices approved for registration or filing for the first time, the registrant shall complete the periodic risk assessment report of the previous year within 60 days after each year.<br>