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EUDAMED last updated this device on Jun 3, 2026
693811931296J2LET0090 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Henan Tuoren Medical Device Co., Ltd. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
16941617121058693811931296J2LET0090(01)16941617121058
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.
R01030201ENDOTRACHEAL TUBES, CUFFED, NOT REINFORCED7 warnings recorded — scroll inside the panel to see all entries.
CW011CW010CW007CW032CW001CW009CW136No certificate specifically references this device's Basic UDI-DI.
Primary placement in France; available across 3 countries total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | Still on market | |
| Germany | Still on market | |
| Italy | Still on market |
CN-MF-000013924No 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.