Dirigeants et représentants réglementaires de UAB SCIENCEFORBRAIN
OSAUSKAS Martynas
Before release, device conformity is appropriately verified per the quality management system under which they are manufactured. Technical documentation and the EU declaration of conformity are prepared and kept up-to-date. Post-market surveillance obligations are met per Article 10(10), and reporting duties under Articles 87–91 are fulfilled. For investigational devices, the statement in Section 4.1, Chapter II of Annex XV is duly issued.