AR Baltic Medical UAB

That the conformity of the devices is appropriately checked, in accordance with the QMS under which the devices are manufactured, before a device is released; that the technical documentation and the EU declaration of conformity are drawn up, the post-market surveillance are complied in accordance with Article 10 and the reporting obligations in Articles 87 to 91 are fulfilled; For investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued.