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