Xuzhou Yongkang Electronic Science Technology Co., Ltd.

1. Responsible for developing and maintaining the latest status of technical documents and EU conformity declarations; 2.According to Article 10 (10) of MDR, compliance with post market supervision obligations. 3. Fulfill the reporting obligations for medical devices as described in MDR clauses 87 to 91 4. For devices used in clinical trials, the statement mentioned in Section 4.1 of Chapter 2 of Annex XV of the MDR terms should be issued

Before releasing the device, the conformity and consistency of the device should be checked according to the requirements of the quality management system

1. Responsible for developing and maintaining the latest status of technical documents and EU conformity declarations; 2.According to Article 10 (10) of MDR, compliance with post market supervision obligations. 3. Fulfill the reporting obligations for medical devices as described in MDR clauses 87 to 91 4. For devices used in clinical trials, the statement mentioned in Section 4.1 of Chapter 2 of Annex XV of the MDR terms should be issued