- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Mar 24, 2025
B-MS01347PVIT-MF-000010738No 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.2 warnings recorded — scroll inside the panel to see all entries.
CW010CW009Primary placement in Italy; available across 16 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Still on market | |
| Bulgaria | Still on market | |
| Cyprus | Still on market | |
| Czechia | Still on market | |
| EL | Still on market | |
| Spain | Still on market | |
| France | Still on market | |
| Hungary | Still on market | |
| Ireland | Still on market | |
| Lithuania | Still on market | |
| Latvia | Still on market | |
| Poland | Still on market | |
| Romania | Still on market | |
| Slovenia | Still on market | |
| Slovakia | Still on market | |
| Türkiye | Still on market |
European Medical Device Nomenclature — the EU product classification assigned to this device.
W0104080207MYCOPLASMA / UREAPLASMA - (INCL. COMBINED ID-AST)