← Back to catalogue

Liner Ceramic

EUDAMED

Class III (EU MDR)

Ref BO76.1725.000.00Model Liner Ceramic D.32 D

by Lincotek Bologna S.r.l

Identity

Device Name
Liner Ceramic EUDAMED
Model / Reference
Liner Ceramic D.32 D EUDAMED
BO76.1725.000.00 EUDAMED

Identifiers

Primary DI / UDI-DI
08050507910373 EUDAMED
Basic UDI-DI
B-08050507910373 EUDAMED
Direct Marketing DI
08050507910373 EUDAMED
EMDN Code
P0908030402 HIP PROSTHESES CERAMIC ACETABULAR 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 Ceramic 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
IT-MF-000033944

Sources (1)

  • EUDAMED a0340805-ea8d-4ad5-9f25-e40939f0abd1 61 fields · synced Jun 18, 2026