POSTERIOR AUGMENT TRIAL REVISION FEMUR – SIZE 4+, 5mm

No Certificate FoundLegacy device

Snapshot 2026-11-02 · Link to EUDAMED

UDI-DI 00841690126584Basic UDI-DI B-00841690126584

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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)

Related UDI-DIs

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Canonical device page: /device/posterior-augment-trial-revision-femur-size-4-5mm-6584 · UDI page: /udi/00841690126584

All devices from OMNIlife science, Inc.