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EUDAMED last updated this device on May 11, 2026
697061609RProbe360508TMLD R2 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Medlander Medical Technology Inc.. Placed on the EU market in Romania. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
06970616091980697061609RProbe360508TMLD R2(01)06970616091980
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.
Z12062485BIOFEEDBACK INSTRUMENTS - CONSUMABLES2 warnings recorded — scroll inside the panel to see all entries.
CW999CW999No certificate specifically references this device's Basic UDI-DI.
This device is not currently linked to any other device.
Primary placement in Romania; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| RomaniaPrimary placement | May 18, 2026 | Dec 31, 2026 |
CN-MF-000017801No 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.