- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Jun 5, 2026
694831892a003M906948318932382694831892a003M9GW-SS3826G(01)06948318932382
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.
G0304010199ERCP CANNULAS, SINGLE-LUMEN - OTHERNo certificate specifically references this device's Basic UDI-DI.
Primary placement in Germany; available across 12 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Still on market | |
| Austria | Still on market | |
| Cyprus | Still on market | |
| Czechia | Still on market | |
| Estonia | Still on market | |
| EL | Still on market | |
| Spain | Still on market | |
| France | Still on market | |
| Croatia | Still on market | |
| Italy | Still on market | |
| Poland | Still on market | |
| Portugal | Still on market |
CN-MF-000009964No 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.