- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Aug 8, 2022
87193275323DSA1000GJNL-MF-000010964No 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 11 countries total.
| Country | On market since | Until |
|---|---|---|
| NetherlandsPrimary placement | Aug 8, 2022 | Jan 1, 2040 |
| Austria | Aug 8, 2022 | Jan 1, 2040 |
| Belgium | Aug 8, 2022 | Jan 1, 2040 |
| Germany | Aug 8, 2022 | Jan 1, 2040 |
| Spain | Aug 8, 2022 | Jan 1, 2040 |
| France | Aug 8, 2022 | Jan 1, 2040 |
| Ireland | Aug 8, 2022 | Jan 1, 2040 |
| Luxembourg | Aug 8, 2022 | Jan 1, 2040 |
| Portugal | Aug 8, 2022 | Jan 1, 2040 |
| Sweden | Aug 8, 2022 | Jan 1, 2040 |
| XI | Aug 8, 2022 | Jan 1, 2040 |
European Medical Device Nomenclature — the EU product classification assigned to this device.
V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER