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EUDAMED last updated this device on Jul 12, 2023
803371701ASP44942ANIT-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 21 countries total.
| Country | On market since | Until |
|---|---|---|
| NetherlandsPrimary placement | Jun 1, 2023 | Jan 1, 2028 |
| Austria | Jun 1, 2023 | Jan 1, 2028 |
| Belgium | Jun 1, 2023 | Jan 1, 2028 |
| Cyprus | Jun 1, 2023 | Jan 1, 2028 |
| Czechia | Jun 1, 2023 | Jan 1, 2028 |
| Germany | Jun 1, 2023 | Jan 1, 2028 |
| Estonia | Jun 1, 2023 | Jan 1, 2028 |
| Spain | Jun 1, 2023 | Jan 1, 2028 |
| France | Jun 1, 2023 | Jan 1, 2028 |
| Croatia | Jun 1, 2023 | Jan 1, 2028 |
| Ireland | Jun 1, 2023 | Jan 1, 2028 |
| Iceland | Jun 1, 2023 | Jan 1, 2028 |
| Italy | Jun 1, 2023 | Jan 1, 2028 |
| Liechtenstein | Jun 1, 2023 | Jan 1, 2028 |
| Luxembourg | Jun 1, 2023 | Jan 1, 2028 |
| Malta | Jun 1, 2023 | Jan 1, 2028 |
| Norway | Jun 1, 2023 | Jan 1, 2028 |
| Poland | Jun 1, 2023 | Jan 1, 2028 |
| Portugal | Jun 1, 2023 | Jan 1, 2028 |
| Slovakia | Jun 1, 2023 | Jan 1, 2028 |
| XI | Jun 1, 2023 | Jan 1, 2028 |
European Medical Device Nomenclature — the EU product classification assigned to this device.
A060399FLUID COLLECTION BAGS AND SYSTEMS - OTHER