Sprystep Max
by Thuasne Deutschland GmbH 5 variants
Ref U0173460005002, U0173460305002, U0173460405002, U0173460205002, U0173460105002, U0173460205001
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number4035459DE0904D4N | Date8 Dec 2025 | StatusActive |
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Sprystep Max
- Model / Reference
- U0173460005002, U0173460305002, U0173460405002, U0173460205002, U0173460105002, U0173460205001
- Primary DI / UDI-DI
- 04035459401296, 04035459401357, 04035459401371, 04035459401333, 04035459401319, 04035459401326
- Basic UDI-DI
- 4035459DE0904D4N
- Direct Marketing DI
- 040354594012960403545940135704035459401371040354594013330403545940131904035459401326
- EMDN Code
- Y06120602 Energy return ankle-foot orthoses
- Device Class
- Class I
- EU market of registration
- France
Manufacturer details
- EUDAMED SRN
- DE-MF-000006210
Other devices from Thuasne Deutschland GmbH
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