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§ EUROPE
ANSM
ANSM — France Medical Device Regulatory Authority
France
ANSM is the national regulatory authority responsible for medical device oversight in France. It manages device registration, market surveillance, and adverse event reporting within the Europe regulatory framework.
DEVICE CLASSES
EU MDR classes
APPROVAL PATHWAY
ANSM registration
KEY REGULATORY FUNCTIONS
- ▸Device registration
- ▸Market surveillance
- ▸Adverse event reporting
- ▸Import/export control
OFFICIAL WEBSITE
https://ansm.sante.fr →MedFlux monitors ANSM regulatory changes, safety alerts, and market signals in real time — so your team never misses a critical update.
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