Guangdong Kindly Medical Device Group Co.,Ltd.

1. Before the device is released, check the compliance and consistency of the device according to the requirements of the quality management system; 2. Technical documents and EU Declaration of Conformity are formulated and kept up to date; 3. Comply with post-listing supervision obligations; 4. Perform medical device reporting obligations; 5. Issue the statement mentioned in Section 4.1 of Chapter II of Annex XV for devices that are undergoing clinical trials。

1. Before the device is released, check the compliance and consistency of the device according to the requirements of the quality management system; 2. Technical documents and EU Declaration of Conformity are formulated and kept up to date; 3. Comply with post-listing supervision obligations; 4. Perform medical device reporting obligations;