Officers and regulatory representatives of curasan develops, produces and markets biomaterials and medical devices for bone and tissue regeneration.
MANIG Steffi
According to Art. 15 MDR (EU), (3) resposible for:
a) Conformity of medical devices in accordance with the QMS
b) The technical documentation and the EU DoC.
c) PMS Obligation in accordance with article 10
d) Reporting obligations (Articles 87 to 91)
e) in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued.
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Device catalog for curasan develops, produces and markets biomaterials and medical devices for bone and tissue regeneration.
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Certificate health for curasan develops, produces and markets biomaterials and medical devices for bone and tissue regeneration.
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