MSB Medical (Wuhan) 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;