POSTERIOR AUGMENT TRIAL REVISION FEMUR – SIZE 1+, 10mm

No Certificate FoundLegacy device

Snapshot 2026-11-02 · Link to EUDAMED

UDI-DI 00841690123668Basic UDI-DI B-00841690123668

Scan an inventory CSV

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

No other UDI-DIs share this Basic UDI-DI in this snapshot.

All UDI-DIs in this Basic UDI-DI family

Canonical device page: /device/posterior-augment-trial-revision-femur-size-1-10mm-3668 · UDI page: /udi/00841690123668

All devices from OMNIlife science, Inc.