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Liner PE
EUDAMEDClass III (EU MDR)
Ref BO76.1806.000.00Model Liner PE Standard D.32 H
Identity
- Device Name
- Liner PE EUDAMED
- Model / Reference
- Liner PE Standard D.32 H EUDAMEDBO76.1806.000.00 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08050507911189 EUDAMED
- Basic UDI-DI
- B-08050507911189 EUDAMED
- Direct Marketing DI
- 08050507911189 EUDAMED
- EMDN Code
- P090803040101 STANDARD POLYETHYLENE HIP PROSTHESES INSERTS 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
Liner PE 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-08050507911189 | Class III | Active |
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Manufacturer
- Manufacturer
- Lincotek Bologna S.r.l
- EUDAMED SRN
- IT-MF-000033944
Sources (1)
- EUDAMED ac74fb2d-0abb-46cb-a98f-486d45fd9b8e 61 fields · synced Jun 20, 2026