Officers and regulatory representatives of 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.
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Device catalog for Santec Medicalprodukte GmbH
No devices registered for this manufacturer.
Certificate health for Santec Medicalprodukte GmbH