Millet Innovation

- The conformity of the devices, in accordance with the quality management system under which the devices are manufactured, before a device is released; - The technical documentation and the EU declaration of conformity, - The post-market surveillance obligations complied with in accordance with Article 10(10); - The reporting obligations referred to in Articles 87 to 91; - Clinical investigations in line with the statement referred to in Section 4.1 of Chapter II of Annex XV.

- The conformity of the devices, in accordance with the quality management system under which the devices are manufactured, before a device is released; - The technical documentation and the EU declaration of conformity, - The post-market surveillance obligations complied with in accordance with Article 10(10); - The reporting obligations referred to in Articles 87 to 91; - Clinical investigations in line with the statement referred to in Section 4.1 of Chapter II of Annex XV.