(a) Checking the conformity of the devices, in accordance with the quality management system under which the devices are manufactured, before releasing the device;
(b) The technical documentation and the EU declaration of conformity are drawn up and kept up-to-date;
(c) Compiling the post-market surveillance obligations in accordance with Article 10(10);
(d) Fulfilling the reporting obligations in line with Articles 87 to 91.