Identity
- Trade Name
- Proteza kości oczodołu EUDAMED
- Device Name
- Codubix OCZODÓŁ 3D EUDAMED
- Model / Reference
- MP EUDAMEDMA-272-COKO-SPM EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05900516853532 EUDAMED
- Basic UDI-DI
- B-05900516853532 EUDAMED
- EMDN Code
- P900403 NON-RESORBABLE FILLING AND RECONSTRUCTION DEVICES EUDAMED
Classification
- Device Class
- Class IIb EUDAMED
- Market of Registration
- Poland EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
Yes
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Proteza kości oczodołu by Tricomed S.a. — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-05900516853532 | Class IIb | Active |
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Manufacturer
- Manufacturer
- Tricomed S.a.
- EUDAMED SRN
- PL-MF-000002483
Sources (1)
- EUDAMED a05b0b1c-5f91-4406-9083-a5ff981f0ad8 61 fields · synced Jun 17, 2026