This section shall summarize the control measures and reasons taken by the regulatory authority or the registrant during the reporting period due to medical device risk issues, and attach relevant documents.
This section shall summarize the control measures and reasons taken by the regulatory authorities or registrars during the reporting period in response to medical device risk issues, and attach relevant documents.
This part shall summarize the control measures and reasons taken by the regulatory authorities or registrants due to medical device risk problems during the reporting period, and attach relevant documents.<br>