ANVISA vs ANSM: Medical Device Regulatory Comparison
Compare the medical device registration pathways, classification, and regulatory requirements of ANVISA (Brazil) vs ANSM (France).
ANVISA
Agência Nacional de Vigilância Sanitária (Brazil)
Brazil
ANVISA regulates medical devices in Brazil using a four-class risk-based system. Brazil is an MDSAP participating country. ANVISA requires a Brazilian Registration Holder (BRH) for foreign manufacture…
Class I, II, III, IV
ANVISA cadastro (Class I-II) / registro (Class III-IV)
- ▸Device registration (cadastro/registro)
- ▸Brazilian Registration Holder requirement
- ▸MDSAP participation
- ▸GMP (INMETRO) certification
- ▸ANVISA Technical Opinion
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 regulat…
EU MDR classes
ANSM registration
- ▸Device registration
- ▸Market surveillance
- ▸Adverse event reporting
- ▸Import/export control
MedFlux monitors both ANVISA and ANSM in real time — every regulatory change, safety alert, and market signal delivered in under 90 seconds.
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