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EUDAMED last updated this device on May 26, 2026
697209192FDT09GC50410002 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Bonree Medical Co., Ltd.. Placed on the EU market in Poland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
06972091923305697209192FDT09GC50410002(01)06972091923305
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.
G020299GASTROINTESTINAL FEEDING/ASPIRATION TUBES - OTHER3 warnings recorded — scroll inside the panel to see all entries.
CW011CW009CW007No certificate specifically references this device's Basic UDI-DI.
Primary placement in Poland; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| PolandPrimary placement | Jan 1, 2020 | Dec 31, 2040 |
CN-MF-000017844No 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.