Hangzhou Primecare Medical Co.,Ltd.

1.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; 2.The technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; 3.The post-market surveillance obligations are complied with in accordance with MDR Article10(10); 4.The reporting obligations referred to in MDR Articles 87 to 91 are fulfilled;