- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Jan 12, 2026
8030413FTN06N8401016FD2NMD is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Mediberg S.r.l. Unipersonale. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
080304131130448030413FTN06N8401016FD2NMD(01)08030413113044
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
European Medical Device Nomenclature — the EU product classification assigned to this device.
A060399FLUID COLLECTION BAGS AND SYSTEMS - OTHERNo certificate specifically references this device's Basic UDI-DI.
Primary placement in Italy; available across 1 country total.
Placed on the market in Italy; per-country availability dates not published.
IT-MF-000012712No 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.