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Cup-G Trabecular
EUDAMEDClass III (EU MDR)
Ref BO76.2856.000.00Model Acetabular Cup-G D.50 F Trabecular CaP
Identity
- Device Name
- Cup-G Trabecular EUDAMED
- Model / Reference
- Acetabular Cup-G D.50 F Trabecular CaP EUDAMEDBO76.2856.000.00 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08050391090311 EUDAMED
- Basic UDI-DI
- B-08050391090311 EUDAMED
- Direct Marketing DI
- 08050391090311 EUDAMED
- EMDN Code
- P090803010201 PRIMARY IMPLANT UNCEMENTED METAL ACETABULAR CUPS EUDAMED
Classification
- Device Class
- Class III EUDAMED
- Market of Registration
- Italy EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
Yes
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Cup-G Trabecular by Lincotek Bologna S.r.l — Class III — 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-08050391090311 | Class III | Active |
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Manufacturer
- Manufacturer
- Lincotek Bologna S.r.l
- EUDAMED SRN
- IT-MF-000033944
Sources (1)
- EUDAMED a9e9365a-3495-4b75-9fc4-dd9ff29a42cd 61 fields · synced Jun 18, 2026