Dirigeants et représentants réglementaires de SCI Health
BENDŽIUVIENĖ Vilma
Responsible for 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; the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; the post-market surveillance obligations are complied with requirements; the reporting fulfills the requirements.