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EUDAMED last updated this device on May 25, 2026
69569370HOMED00005ZCJLQ-004 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Shenzhen Homed Medical Device Co., Ltd.. Placed on the EU market in Türkiye. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0695693700127369569370HOMED00005ZC06956937001273(01)06956937001273
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.
R060101COLD NEBULISATION SYSTEMSNo certificate specifically references this device's Basic UDI-DI.
Primary placement in Türkiye; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| TürkiyePrimary placement | Still on market |
CN-MF-000016463No 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.