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EUDAMED last updated this device on Jul 11, 2024
++M483L0909Z3FLEXION HEMI SPACER H11 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by groupe lépine. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
+M483GNANW1750++M483L0909Z3GNANW175+M483GNANW1750
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.
European Medical Device Nomenclature — the EU product classification assigned to this device.
L090999ORTHOPAEDIC SURGERY CUTTING INSTRUMENTS, REUSABLE - OTHERNo certificate specifically references this device's Basic UDI-DI.
Primary placement in France; available across 1 country total.
Placed on the market in France; per-country availability dates not published.
FR-MF-000001182No certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.