- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Jun 1, 2026
693811931296J216941617121850693811931296J2STNET0080(01)16941617121850
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.
R01030201ENDOTRACHEAL TUBES, CUFFED, NOT REINFORCED7 warnings recorded — scroll inside the panel to see all entries.
CW011CW010CW009CW001CW007CW032CW136No certificate specifically references this device's Basic UDI-DI.
Primary placement in Italy; available across 3 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Still on market | |
| Germany | Still on market | |
| France | Still on market |
CN-MF-000013924No 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.