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