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§ LATIN AMERICA
ANMAT
ANMAT — Argentina Medical Device Regulatory Authority
Argentina
ANMAT is the national regulatory authority responsible for medical device oversight in Argentina. It manages device registration, market surveillance, and adverse event reporting within the Latin America regulatory framework.
DEVICE CLASSES
Class I, II, III, IV
APPROVAL PATHWAY
ANMAT registration
KEY REGULATORY FUNCTIONS
- ▸Device registration
- ▸Market surveillance
- ▸Adverse event reporting
- ▸Import/export control
OFFICIAL WEBSITE
https://www.argentina.gob.ar/anmat →MedFlux monitors ANMAT regulatory changes, safety alerts, and market signals in real time — so your team never misses a critical update.
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