Shahab Surgical Industries

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 Article 10(10); 4- the reporting obligations referred to in Articles 87 to 91 are fulfilled;