Officers and regulatory representatives of Vital Pro Kft.
LEVAUX Philippe Daniel Alfred
The conformity of the devices is appropriately checked; 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 in accordance with Article 10(10); The reporting obligations referred to in Articles 87 to 91 are fulfilled; In the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued.