United Orthopedic Corporation

Ensuring 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

1. Ensuring the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; 2. Ensuring the post-market surveillance obligations are complied with in accordance appropriate regulatory； 3. Ensuring the reporting obligations referred to appropriate regulatory.