INVIMA vs Medsafe: Medical Device Regulatory Comparison
Compare the medical device registration pathways, classification, and regulatory requirements of INVIMA (Colombia) vs Medsafe (New Zealand).
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 Amer…
Class I, IIa, IIb, III
INVIMA registration
- ▸Device registration
- ▸Market surveillance
- ▸Adverse event reporting
- ▸Import/export control
Medsafe
Medsafe — New Zealand Medical Device Regulatory Authority
New Zealand
Medsafe is the national regulatory authority responsible for medical device oversight in New Zealand. It manages device registration, market surveillance, and adverse event reporting within the Asia-P…
Class I, IIa, IIb, III
Medsafe registration
- ▸Device registration
- ▸Market surveillance
- ▸Adverse event reporting
- ▸Import/export control
MedFlux monitors both INVIMA and Medsafe in real time — every regulatory change, safety alert, and market signal delivered in under 90 seconds.
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