VesselIQ Xpress
by GE Medical Systems SCS 4 variants
Ref 5854373
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 | Number8406821BUG00083HA 00195278301222 | Date16 May 2022 | StatusActive |
| United States | FDA 510(k) 510(k) | NumberK200626 | Date16 Feb 2021 | 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- Withdrawn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
- 5854373
- Primary DI / UDI-DI
- 00195278301222
- Basic UDI-DI
- 8406821BUG00083HA
- Direct Marketing DI
- 00195278301222
- EMDN Code
- Z11030192, Z11030692
- Device Class
- Class IIa
- Special Device Type
- Software
- EU market of registration
- France
Manufacturer details
- EUDAMED SRN
- FR-MF-000000687
Other devices from GE Medical Systems SCS
Properties
Other properties (12)
- 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
- Incorporates Medicinal Product: No