Charder Electronic Co. Ltd.

1.Appropriately check the conformity of the devices, in accordance with our quality management system, before a device is released; 2.Draw up and keep up-to-date the technical documentation and the EU declaration of conformity; 3.Ensure and maintain the operation of post-market surveillance system; 4.Fulfill the reporting obligations referred to in Articles 87 to 91 5.in the case of investigational devices, ensure the statement referred to in Section 4.1 of Chapter II of Annex XV is issued.