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EUDAMED last updated this device on May 26, 2026
69380010003QMFS920L (02) is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by FOSHAN DONGFANG MEDICAL EQUIPMENT MANUFACTORY LTD.. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0693800102440169380010003QMFS920L (02)(01)06938001024401
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.
Y120399WALKING DEVICES, ONE-HANDED OPERATION - OTHERNo certificate specifically references this device's Basic UDI-DI.
Primary placement in France; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | Still on market |
CN-MF-000036028No 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.