- Role
- Country
- Date of registration
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EUDAMED last updated this device on Jul 12, 2023
803371701NEB6204244IT-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 Italy; available across 18 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Jan 1, 2023 | Jan 1, 2028 |
| Belgium | Still on market | |
| Bulgaria | Jan 1, 2023 | Jan 1, 2028 |
| Czechia | Jan 1, 2023 | Jan 1, 2028 |
| Germany | Jan 1, 2023 | Jan 1, 2028 |
| EL | Jan 1, 2023 | Jan 1, 2028 |
| Spain | Jan 1, 2023 | Jan 1, 2028 |
| France | Jan 1, 2023 | Jan 1, 2028 |
| Croatia | Jan 1, 2023 | Jan 1, 2028 |
| Hungary | Jan 1, 2023 | Jan 1, 2028 |
| Latvia | Jan 1, 2023 | Jan 1, 2028 |
| Poland | Jan 1, 2023 | Jan 1, 2028 |
| Portugal | Jan 1, 2023 | Jan 1, 2028 |
| Romania | Jan 1, 2023 | Jan 1, 2028 |
| Slovenia | Jan 1, 2023 | Jan 1, 2028 |
| Slovakia | Jan 1, 2023 | Jan 1, 2028 |
| Türkiye | Jan 1, 2023 | Jan 1, 2028 |
| XI | Jan 1, 2023 | Jan 1, 2028 |
European Medical Device Nomenclature — the EU product classification assigned to this device.
R060101COLD NEBULISATION SYSTEMS