Competent authority
authority.competent-authority
Agence nationale de sécurité du médicament et des produits de santé (ANSM)
ANSM · structured requirements
🇫🇷 France medical device regulatory data
Explore the medical device requirements currently available for France, organized by topic and linked to official sources.
4 facts3 dimensions4 official sourceslatest verification 2026-08-13
Registration pathways
Which registration, notification, listing, reliance, or conformity route applies?
Market-access route or official registration surface
registration.market-access-route
- SubmissionSurface
EU MDR/IVDR and EUDAMED for covered Union-level obligations
- Caveat
Current French national declaration details require re-verification on a live ANSM source.
Reliance & recognition
Which foreign decisions or evidence can be reused, with what effect and conditions?
EU CE under MDR/IVDR — single market validity
reliance.reliance-edge-eu-ce-to-eea30-approval-eu-ce-mdr-ivdr-france
- Target
geo:fra
- SourceApproval
EU CE under MDR/IVDR
- EdgeType
Single Market Validity
- MarketAccessStrength
direct
- RegulatoryLayer
Product Marketing
- SameDeviceRequired
Yes
- LocalApplicationRequired
No
- TargetDecisionRetained
No
Conditions
- medical devices and IVDs subject to route-specific scope
- valid CE conformity route for the device
- country language, economic-operator, EUDAMED, and national vigilance obligations still apply
Türkiye CE under aligned MDR/IVDR — customs union free circulation
reliance.reliance-edge-turkiye-ce-to-eu27-approval-turkiye-ce-mdr-ivdr-france
- Target
geo:fra
- SourceApproval
Türkiye CE under aligned MDR/IVDR
- EdgeType
Customs Union Free Circulation
- MarketAccessStrength
Direct With Local Obligations
- RegulatoryLayer
Product Marketing
- LocalApplicationRequired
No
- TargetDecisionRetained
No
Conditions
- medical devices and IVDs subject to route-specific scope
- certificate duly issued by a Turkish notified body under aligned MDR/IVDR rules
Need to apply France's requirements to a product?
Confirm the current ANSM pathway, evidence, and local-role details for the actual device before filing.