Wuhan Vickor Medical Technology Co., Ltd

(a)the conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released; （b）the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; （c） the post-market surveillance obligations are complied with in accordance with Article 10(10); （d） the reporting obligations referred to in Articles 87 to 91 are fulfilled;