- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on May 9, 2026
69239801ND1CBNHBerman Airway 80mm is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by GaleMed (Xiamen) Co., Ltd.. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0692398010201169239801ND1CBNHAW0053(01)06923980102011
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 TUBESNo certificate specifically references this device's Basic UDI-DI.
Primary placement in Germany; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Still on market |
CN-MF-000020627Certificate health across this manufacturer's portfolio.
HZ 2058519-1Issued