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EUDAMED last updated this device on May 25, 2026
805572853SPLINT03G2IT-MF-000032551805572853SPLINT03G2On the marketATTELLE CAPITONNÉE ALUMOUSSE PRÉFORMÉE SS 160805572853SPLINT03G2On the marketATTELLE CAPITONNÉE ALUMOUSSE PRÉFORMÉE SS 270805572853SPLINT03G2On the marketATTELLE CAPITONNÉE ALUMOUSSE SA 100100805572853SPLINT03G2On the marketATTELLE CAPITONNÉE ALUMOUSSE SA 4040805572853SPLINT03G2On the marketNo 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.Primary placement in France; available across 1 country total.
Placed on the market in France; per-country availability dates not published.
European Medical Device Nomenclature — the EU product classification assigned to this device.
M030505ZIMMER SPLINTS