Synflate Vertebral Balloon Small Medium Large
by Synthes GmbH
Ref 03.804.702S, 03.804.700S, 03.804.701SModel Synflate Vertebral Balloon
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number7611819a00286JW | Date11 Jul 2025 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Synflate Vertebral Balloon Small Medium Large
- Model / Reference
- Synflate Vertebral Balloon, 03.804.702S, 03.804.700S, 03.804.701S
- Primary DI / UDI-DI
- 07611819525405, 07611819525382, 07611819525399
- Basic UDI-DI
- 7611819a00286JW
- EMDN Code
- K010301 Spinal percutaneous plastic devices with balloon
- Device Class
- Class IIa
- EU market of registration
- Belgium
Manufacturer details
- EUDAMED SRN
- CH-MF-000013345
- Authorised representative
- DePuy Ireland UC IE-AR-000009328
Other devices from Synthes GmbH
Properties
Other properties (12)
- 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