Dirigeants et représentants réglementaires de Medtronic, Inc.
2 contacts identifiés
SCHLEIS Carrie
a) Ensuring conformity of the devices is appropriately checked before a device is released
b) Ensuring the post-market surveillance (PMS) obligations in accordance with EU MDR Article 10(10) are complied with
c) Ensuring the reporting obligations for Vigilance and Field Safety Corrective Action Reporting per EU MDR Articles 87 to 91 are fulfilled
d) Ensuring that the statement in accordance with EU MDR Annex XV Chapter II Section 4.1 is issued for investigational devices
Masqué
GUZZETTA Rita
Ensuring the technical documentation and the EU Declaration of Conformity (DOC) are drawn up and kept up-to-date