Cough Monitoring Medical Solutions, S.A.

All PRRC responsibilities (Product Conformity, Technical Documentation, Post Market Surveillance, Reporting Obligations, Investigation Devices).

(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) of the MDR;