Expedium Verse Spine System
by Medos International SARL 200 variants
Ref 199725735SModel EXPEDIUM Verse System Bone Screw
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 | Number0705034a0017262 10705034440910 | Date17 Nov 2025 | StatusActive |
| United States | FDA 510(k) 510(k) | NumberK200245 | Date24 Apr 2020 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Recalls
No FDA recalls found in the data synced 24 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- United States
- European Union
Specification
- Device Name
- EXPEDIUM Verse Polyaxial Cannulated/Non-Cannulated screws
- Model / Reference
- EXPEDIUM Verse System Bone Screw, 199725735S
- Primary DI / UDI-DI
- 10705034440910
- Basic UDI-DI
- 0705034a0017262
- EMDN Code
- P09070302 Thoracolumbosacral fixation systems
- Device Class
- Class IIb
- EU market of registration
- Belgium
Manufacturer details
- EUDAMED SRN
- CH-MF-000014268
- Authorised representative
- DePuy Ireland UC IE-AR-000009328
Other devices from Medos International SARL
Properties
Other properties (10)
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No