1. Clinical application data: the effect and safety of medical devices in the actual application of post-market need to be clinically verified over a long period of time. Through the collection and analysis of a large amount of clinical data, the risk points and the use of medical devices in the actual application of the effect can be found, so as to assess the risk.
2. Medical malpractice reports: Medical devices may cause medical malpractice if they are used improperly or have quality problems. Through the collection and analysis of medical incident reports, we can understand the possible safety risks of medical devices.
3. Production quality control data: Quality control is a very important part of the production process of medical devices. Through the collection and analysis of production quality control data, you can understand the possible risk points in the production process of medical devices, so as to control and improve their quality.
4. Industry regulatory data: Medical device industry regulators will collect and analyze relevant data, including medical device registration data, production license data, business license data, etc., from which they can find possible risk points, so as to regulate and control medical devices.
5. User feedback data: During the use of medical devices, users will provide feedback on their effectiveness and safety. Through the collection and analysis of user feedback data, we can understand the effect and safety of medical devices in actual use, so as to assess and improve the risk.