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EUDAMED last updated this device on May 22, 2026
B-80565185045704EOSP-20B is an MDD-legacy medical device registered in EUDAMED. It is classified as Class III. Manufactured by BIOTECK S.p.A.. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
D-80565185045704EB-80565185045704EOSP-20BD-80565185045704E
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.
European Medical Device Nomenclature — the EU product classification assigned to this device.
P900401BONE AND TENDON REPLACEMENT DEVICESP900402RESORBABLE FILLING AND RECONSTRUCTION DEVICES8 warnings recorded — scroll inside the panel to see all entries.
CW010CW267CW009CW001CW007CW032CW129CW161No certificate specifically references this device's Basic UDI-DI.
Primary placement in Italy; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Feb 15, 1999 | Dec 31, 2027 |
IT-MF-000011484No 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.EPT0477.MDD.19/3477.1