← Back to catalogue
Figulla Flex II UNI Occluder Procedure Pack
EUDAMEDClass III (EU MDR)
Ref 16UNI17P
Identity
- Trade Name
- Figulla Flex II UNI Occluder Procedure Pack EUDAMED
- Device Name
- Figulla Flex II UNI Occluder Procedure Pack EUDAMED
- Model / Reference
- 16UNI17P EUDAMED
Identifiers
- Primary DI / UDI-DI
- 07340175600005 EUDAMED
- Basic UDI-DI
- 73401756UNIIIPPWR EUDAMED
- EMDN Code
- P07040302 CARDIAC OCCLUDERS, ATRIAL SEPTAL DEFECTS EUDAMED
Classification
- Device Class
- Class III EUDAMED
- Medical Purpose
- The Figulla Flex II UNI Occluder is a permanent cardiac implant intended to close defects of type multi-fenestrated atrial septal defects. EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Figulla Flex II UNI Occluder Procedure Pack by Occlutech International AB — Class III — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 73401756UNIIIPPWR | Class III | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Occlutech International AB
- EUDAMED SRN
- SE-PR-000017759
Sources (1)
- EUDAMED 78164e35-fb27-47ee-a5e8-2860ac89da74 61 fields · synced Jun 18, 2026