- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Mar 24, 2026
B-08053172971946IT-MF-000039031No 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 Italy; available across 1 country total.
Placed on the market in Italy; per-country availability dates not published.
European Medical Device Nomenclature — the EU product classification assigned to this device.
W0103020502FIBRINOGEN DEGRADATION PRODUCTS