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- Date of registration
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EUDAMED last updated this device on Mar 20, 2026
B-08033717011764IT-MF-000009298No 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 Netherlands; available across 6 countries total.
| Country | On market since | Until |
|---|---|---|
| NetherlandsPrimary placement | Jan 1, 2028 | |
| Germany | Jan 1, 2028 | |
| Spain | Jan 1, 2028 | |
| France | Jan 1, 2028 | |
| Croatia | Jan 1, 2028 | |
| Italy | Jan 1, 2028 |
European Medical Device Nomenclature — the EU product classification assigned to this device.
R060101COLD NEBULISATION SYSTEMS