POSTERIOR AUGMENT TRIAL REVISION FEMUR – SIZE 2+, 5mm

No Certificate FoundLegacy device

Snapshot 2026-11-02 · Link to EUDAMED

UDI-DI 00841690121909Basic UDI-DI B-00841690121909

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Class IIa · MDD (legacy) · OMNIlife science, Inc.

Identification

Model: Apex Knee Instruments
EMDN: L0999
Issuing agency: GS1
Device status: active
Sterile: No
Implantable: No
Measuring function: No
Reusable surgical: Yes

Manufacturer

OMNIlife science, Inc.

SRN US-MF-000015882

US · Raynham

manufacturer

Authorised representative: CORIN FRANCE SAS (FR-AR-000001192)

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Canonical device page: /device/posterior-augment-trial-revision-femur-size-2-5mm-1909 · UDI page: /udi/00841690121909

All devices from OMNIlife science, Inc.