Officers and regulatory representatives of Diversey Europe Operations B.V.
CALISKAN Gokhan
Among additional duties, the main responsibilities are the one mentioned on Article 15 of the EU MDR 2017/745:
- Conformity of the product device to the Medical Device Regulation and Quality Management System
- Conformity of the Technical Documentation and EU Declaration of conformity
- Compliance with Post-Market Surveillance (PMS) following Article 10(10)
- Compliance with the Vigilance Reporting obligations (Article 87 to 91)
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BAARS Edwin
Among additional duties, the main responsibilities are the one mentioned on Article 15 of the EU MDR 2017/745:
- Conformity of the product device to the Medical Device Regulation and Quality Management System
- Conformity of the Technical Documentation and EU Declaration of conformity
- Compliance with Post-Market Surveillance (PMS) following Article 10(10)
- Compliance with the Vigilance Reporting obligations (Article 87 to 91)
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Device catalog for Diversey Europe Operations B.V.
No devices registered for this manufacturer.
Certificate health for Diversey Europe Operations B.V.