Duplo
by Laboratorios Herbitas, S.L. 2 variants
Ref 6073.2, 6073.3
Duplo (6073.2) is a Class I device made by Laboratorios Herbitas, S.L., registered in EUDAMED on 6 Nov 2024 (Basic UDI-DI 84351355DUPLOQ9), active as of 22 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number84351355DUPLOQ9 | Date6 Nov 2024 | StatusActive |
Official records
- EUDAMED public site 84351355DUPLOQ9
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- Withdrawn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
- Talonera Duplo
- Model / reference
- 6073.2, 6073.3
- Primary DI / UDI-DI
- 08435135500439, 08435135500446
- Basic UDI-DI
- 84351355DUPLOQ9
- EMDN code
- Y061203 Orthoses, foot (including insoles and inserts)
- Device class
- Class I
- EU registration type
- Standard device
- EU market of registration
- Spain
Manufacturer details
- EUDAMED SRN
- ES-MF-000004599
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