Stabipoignet 3D
Ref STABIPOIGNET 3DModel ATTELLE POIGNET-MAIN
Stabipoignet 3D is a Class I device made by Groupe Sober SAS, registered in EUDAMED on 13 Jul 2026 (Basic UDI-DI B-03760035449249), active as of 25 Oct 2026.
Active
CE MDD
Valid until
No date given
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD | NumberB-03760035449249 | Date13 Jul 2026 | StatusActive |
Official records
- EUDAMED public site B-03760035449249
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- Withdrawn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/MDD Active
Specification
- Model / reference
- ATTELLE POIGNET-MAIN, STABIPOIGNET 3D
- Primary DI / UDI-DI
- 03760035449249, 03701459810079, 03701459801190, 03701459801183, 03760035449607, 03701459801152, 03760035449614, 03701459810086, 03701459801145, 03760035449232, 03701459801169, 03701459801176
- Basic UDI-DI
- B-03760035449249, B-03701459810079, B-03701459801190, B-03701459801183, B-03760035449607, B-03701459801152, B-03760035449614, B-03701459810086, B-03701459801145, B-03760035449232, B-03701459801169, B-03701459801176
- EMDN code
- Y060612 Wrist-hand orthoses
- Device class
- Class I
- System or procedure pack
- System which is a device in itself
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- France
Manufacturer details
- EUDAMED SRN
- FR-MF-000017818
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