Carpatel - Tm/a
Ref CARPATELModel ATTELLE DE POIGNET
Carpatel - Tm/a is a Class I device made by Groupe Sober SAS, registered in EUDAMED on 24 Jul 2026 (Basic UDI-DI B-03760035447085), active as of 24 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-03760035447085 | Date24 Jul 2026 | StatusActive |
Official records
- EUDAMED public site B-03760035447085
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- Withdrawn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
- Trade name
- Carpatel - Tm/aCarpatel - Tl/aCarpatel - Ts/a
- Device name
- Carpatel
- Model / reference
- ATTELLE DE POIGNET, CARPATEL
- Primary DI / UDI-DI
- 03760035447085, 03760035447092, 03760035447061
- Basic UDI-DI
- B-03760035447085, B-03760035447092, B-03760035447061
- EMDN code
- Y060609 Wrist (forearm) 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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