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EUDAMED last updated this device on May 12, 2026
694831892a004MBKBQP-23-12-15-18 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 Croatia. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
06948318987818694831892a004MBKBQP-23-12-15-18(01)06948318987818
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.
G03050101DIGESTIVE ENDOSCOPY, RETRIEVAL BALLOON DEVICESNo certificate specifically references this device's Basic UDI-DI.
Primary placement in Croatia; available across 11 countries total.
| Country | On market since | Until |
|---|---|---|
| CroatiaPrimary placement | Still on market | |
| Austria | Still on market | |
| Bulgaria | Still on market | |
| Cyprus | Still on market | |
| Czechia | Still on market | |
| Germany | Still on market | |
| Estonia | Still on market | |
| EL | Still on market | |
| Italy | Still on market | |
| Poland | Still on market | |
| Portugal | Still on market |
CN-MF-000009964Certificate health across this manufacturer's portfolio.
G26 086239 0022IssuedG15 086239 0021Issued