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EUDAMED last updated this device on Oct 9, 2024
B-05904326324015PL-MF-000007157B-05903728887043On the marketBone replacement composite FlexiOss®B-05903728887036On the marketBone replacement composite FlexiOss®B-05903728887005On the marketBone replacement composite FlexiOss®B-05903728887012On the marketBone replacement composite FlexiOss®B-05903728887029On 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.5 warnings recorded — scroll inside the panel to see all entries.
CW001CW007CW009CW010CW032Primary placement in Poland; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| PolandPrimary placement | May 13, 2021 | May 27, 2024 |
European Medical Device Nomenclature — the EU product classification assigned to this device.
P900403NON-RESORBABLE FILLING AND RECONSTRUCTION DEVICES