- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on May 28, 2026
6970966660030DYRespiratory Tract Humidifiers for Medical Use is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Gentec (Shanghai) Corporation. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
069709666644836970966660030DY7300R(01)06970966664483
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.
R060202OXYGEN ADMINISTRATION HUMIDIFICATION SYSTEMSNo certificate specifically references this device's Basic UDI-DI.
Primary placement in France; available across 5 countries total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | Still on market | |
| Germany | Still on market | |
| Spain | Still on market | |
| Italy | Still on market | |
| Portugal | Still on market |
CN-MF-000012841No 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.6970966660010DSOn the market"Medical Flow Meter For Terminal Units of Medical Gas Pipe System "6970966660010DSOn the marketHigh Flow Nasal Cannula6970966660020DVOn the marketHigh Flow Nasal Cannula6970966660020DVOn the marketHigh Flow Nasal Cannula6970966660020DVOn the market