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EUDAMED last updated this device on Jun 5, 2026
694831892a003M9GW-SS3526S-U is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Anrei Medical (HZ) Co., Ltd.. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
06948318932337694831892a003M9GW-SS3526S-U(01)06948318932337
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.