- Role
- Country
- Date of registration
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EUDAMED last updated this device on Jul 26, 2024
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 13 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Jul 5, 2024 | Jul 5, 2029 |
| Belgium | Jul 5, 2024 | Jul 5, 2029 |
| Germany | Jul 5, 2024 | Jul 5, 2029 |
| Spain | Jul 5, 2024 | Jul 5, 2029 |
| France | Jul 5, 2024 | Jul 5, 2029 |
| Latvia | Jul 5, 2024 | Jul 5, 2029 |
| Netherlands | Jul 5, 2024 | Jul 5, 2029 |
| Poland | Jul 5, 2024 | Jul 5, 2029 |
| Romania | Jul 5, 2024 | Jul 5, 2029 |
| Sweden | Jul 5, 2024 | Jul 5, 2029 |
| Slovenia | Jul 5, 2024 | Jul 5, 2029 |
| Slovakia | Jul 5, 2024 | Jul 5, 2029 |
| XI | Jul 5, 2024 | Jul 5, 2029 |
European Medical Device Nomenclature — the EU product classification assigned to this device.
R060101COLD NEBULISATION SYSTEMS