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Liner PE

EUDAMED

Class III (EU MDR)

Ref BO76.1742.000.00Model Liner PE Lipped D.28 F

by Lincotek Bologna S.r.l

Identity

Device Name
Liner PE EUDAMED
Model / Reference
Liner PE Lipped D.28 F EUDAMED
BO76.1742.000.00 EUDAMED

Identifiers

Primary DI / UDI-DI
08050507910540 EUDAMED
Basic UDI-DI
B-08050507910540 EUDAMED
Direct Marketing DI
08050507910540 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

Category: Non-constrained polyethylene acetabular liner

Liner PE by Lincotek Bologna S.r.l — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Non-constrained polyethylene acetabular liner.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
IT-MF-000033944

Sources (1)

  • EUDAMED 973b1d25-ce6b-406b-bc76-7cfdd9300a59 61 fields · synced Jun 18, 2026