Dirigeants et représentants réglementaires de Implai Sp. z o.o.
MARTYNIAK Marcin
ensuring that 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; that the technical documentation and the EU declaration of conformity
are drawn up and kept up-to-date; that the post-market surveillance obligations are complied; that other obligations of medical devices law are fulfilled.