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Cup-R Trabecular
EUDAMEDClass III (EU MDR)
Ref BO76.2828.000.00Model Acetabular Cup-R D.50 F Trabecular
Identity
- Device Name
- Cup-R Trabecular EUDAMED
- Model / Reference
- Acetabular Cup-R D.50 F Trabecular EUDAMEDBO76.2828.000.00 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08050391090175 EUDAMED
- Basic UDI-DI
- B-08050391090175 EUDAMED
- Direct Marketing DI
- 08050391090175 EUDAMED
- EMDN Code
- P0908030302 REVISION SURGERY UNCEMENTED 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-R 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-08050391090175 | Class III | Active |
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Manufacturer
- Manufacturer
- Lincotek Bologna S.r.l
- EUDAMED SRN
- IT-MF-000033944
Sources (1)
- EUDAMED d9f166ec-2d88-43ed-8d5d-ef8a814c0771 61 fields · synced Jun 18, 2026