Femoral Head Ceramic

by Lincotek Bologna S.r.l 29 variants

Ref BO76.3107.000.00Model Femoral Head Ceramic Biolox®Delta D.32 L

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDD	NumberB-08050391091776 Basic UDI-DI 08050391091776UDI-DI	Date5 Dec 2025Registered	StatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name: Femoral Head Ceramic
Model / Reference: Femoral Head Ceramic Biolox®Delta D.32 L, BO76.3107.000.00

Primary DI / UDI-DI: 08050391091776
Basic UDI-DI: B-08050391091776
Direct Marketing DI: 08050391091776
EMDN Code: P090804050201 Ceramic femoral heads, total hip replacement

Device Class: Class III
EU market of registration: Italy

Manufacturer details

EUDAMED SRN: IT-MF-000033944

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Properties

Sterile
Implantable

Other properties (11)

Reusable: No
Contains Latex: No
Reprocessed: No
CMR Substance: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Endocrine Disruptor: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No