Sansure Biotech Inc.

Xiong Xiaoyan is responsible for whether devices are manufactured according to the requirements of the corresponding quality management system, carrying out post-market surveillance (PMS) and vigilance activities and reporting adverse events and field safety corrective actions in a timely manner in accordance with the requirements of the regulations.

Ren Xiaomei is responsible for signing the CE technical documents and the declaration of conformity, ensuring that the documents are kept up to date, responsible for properly checking the compliance of the device and regulations before the devices are released, and responsible for signing relevant declarations for devices that need to be used in clinical trials.