- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Oct 25, 2023
8710103BM780JWNL-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 Netherlands; available across 10 countries total.
| Country | On market since | Until |
|---|---|---|
| NetherlandsPrimary placement | Still on market | |
| Austria | Still on market | |
| Belgium | Apr 21, 2021 | Dec 31, 9999 |
| Czechia | Apr 21, 2021 | Dec 31, 9999 |
| Spain | Apr 21, 2021 | Dec 31, 9999 |
| France | Apr 21, 2021 | Dec 31, 9999 |
| Hungary | Apr 21, 2021 | Dec 31, 9999 |
| Poland | Apr 21, 2021 | Dec 31, 9999 |
| Portugal | Apr 21, 2021 | Dec 31, 9999 |
| Slovakia | Apr 21, 2021 | Dec 31, 9999 |
European Medical Device Nomenclature — the EU product classification assigned to this device.
U1003PUERPERIUM DEVICES