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EUDAMED last updated this device on Nov 28, 2025
B-08059340930043IT-MF-000024333No 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.1 warning recorded — scroll inside the panel to see all entries.
CW010Primary placement in Italy; available across 6 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Dec 1, 2021 | Still on market |
| Belgium | Dec 1, 2021 | Still on market |
| Germany | Dec 1, 2021 | Still on market |
| Spain | Dec 1, 2021 | Still on market |
| France | Dec 1, 2021 | Still on market |
| Croatia | Dec 1, 2021 | Still on market |
(01)08059340930043
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z12040203DERMAL REGENERATION EQUIPMENT