- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Jun 12, 2026
69746292922ZU0697462929343069746292922ZU50000012(01)06974629293430
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.
R010102GUEDEL AIRWAY TUBES1 warning recorded — scroll inside the panel to see all entries.
CW010No certificate specifically references this device's Basic UDI-DI.
Primary placement in Belgium; available across 7 countries total.
| Country | On market since | Until |
|---|---|---|
| BelgiumPrimary placement | Still on market | |
| Cyprus | Still on market | |
| Ireland | Still on market | |
| Latvia | Still on market | |
| Malta | Still on market | |
| Netherlands | Still on market | |
| Slovenia | Still on market |
CN-MF-000008459No 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.