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UDI Compass

ORIGIN® Knee Impaction Set XL

No Certificate FoundLegacy device

Snapshot 2026-10-31 · Link to EUDAMED

UDI-DI 07630013659839Basic UDI-DI B-07630013659839

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Class IIa · MDD (legacy) · Symbios Orthopédie S.A.

Identification

Model
—
Issuing agency
GS1
Device status
active
Sterile
Yes
Implantable
No
Measuring function
No
Reusable surgical
No

Manufacturer

Symbios Orthopédie S.A.

SRN CH-MF-000020168

CH · Yverdon-les-Bains

manufacturer

Authorised representative: Symbios France SAS (FR-AR-000017731)

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/origin-knee-impaction-set-xl-9839 · UDI page: /udi/07630013659839

All devices from Symbios Orthopédie S.A.