- Role
- Country
- Date of registration
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EUDAMED last updated this device on Oct 25, 2023
8710103BM781JYNL-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 11 countries total.
| Country | On market since | Until |
|---|---|---|
| AustriaPrimary placement | Jul 8, 2021 | Dec 31, 9999 |
| Belgium | Jul 8, 2021 | Dec 31, 9999 |
| Czechia | Jul 8, 2021 | Dec 31, 9999 |
| Spain | Jul 8, 2021 | Dec 31, 9999 |
| France | Jul 8, 2021 | Dec 31, 9999 |
| Hungary | Jul 8, 2021 | Dec 31, 9999 |
| Italy | Jul 8, 2021 | Dec 31, 9999 |
| Netherlands | Jul 8, 2021 | Dec 31, 9999 |
| Poland | Jul 8, 2021 | Dec 31, 9999 |
| Portugal | Jul 8, 2021 | Dec 31, 9999 |
| Slovakia | Jul 8, 2021 | Dec 31, 9999 |
European Medical Device Nomenclature — the EU product classification assigned to this device.
U1003PUERPERIUM DEVICES