- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Feb 7, 2024
8710103BM782K2NL-MF-000001693No 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 Austria; available across 14 countries total.
| Country | On market since | Until |
|---|---|---|
| AustriaPrimary placement | Apr 21, 2021 | Dec 31, 9999 |
| Belgium | Still on market | |
| Czechia | Still on market | |
| Spain | Still on market | |
| France | Still on market | |
| Hungary | Still on market | |
| Netherlands | Still on market | |
| Poland | Still on market | |
| Portugal | Still on market | |
| Slovakia | Still on market | |
| Germany | Apr 21, 2021 | Dec 31, 9999 |
| EL | Dec 31, 9999 | Dec 31, 9999 |
| Ireland | Apr 21, 2021 | Dec 31, 9999 |
| Italy | Apr 21, 2021 | Dec 31, 9999 |
European Medical Device Nomenclature — the EU product classification assigned to this device.
U1003PUERPERIUM DEVICES