Dirigeants et représentants réglementaires de Santec Medicalprodukte GmbH
HINOJOSA Cesar
Review and approval of the conformity of the products in accordance to the QMS.
Creation and maintenance of the Technical Documentation and the documentation used for creation of the declaration of conformity.
Fulfillment of the obligations of post-market surveillance in accordance to Regulation (EU) 2017/745 Art. 10(10).
Organization and maintenance of the reporting structure for the fulfillment of the obligations in accordance to Regulation (EU) 2017/745 Art. 87 to 91.
Masqué
Catalogue des dispositifs de Santec Medicalprodukte GmbH
Aucun dispositif enregistré pour ce fabricant.
Santé des certificats de Santec Medicalprodukte GmbH