Neurovascular Insight V1.0
Ref AP-NVI-CT; AP-NVI-MR
Active
CE MDR 510(k)
Valid until
Not listed
FDA recalls
None foundTrust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number++EOLENEUROVASINSIGHTE7 +EOLENEUROVASIV1P00 | Date29 Apr 2026 | StatusActive |
| United States | FDA 510(k) 510(k) | NumberK243680 | Date25 Aug 2025 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Recalls
No FDA recalls found in the data synced 23 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- United States
- European Union
Specification
- Model / Reference
- AP-NVI-CT, AP-NVI-MR
- Primary DI / UDI-DI
- +EOLENEUROVASIV1P00
- Basic UDI-DI
- ++EOLENEUROVASINSIGHTE7
- EMDN Code
- Z11050182 Magnetic resonance (MR) systems - software accessories
- Device Class
- Class IIa
- Special Device Type
- Software
- EU market of registration
- France
Manufacturer details
- EUDAMED SRN
- FR-MF-000002403
Other devices from Olea Medical S.A.S.
Properties
Other properties (13)
- Sterile: No
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No