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EUDAMED last updated this device on May 28, 2026
0175008/OPB-BEAD/D9OPB-BEAD-TEVO is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by rdgKompagne. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
087215932050240175008/OPB-BEAD/D9OPB-BEAD-TEVO(01)08721593205024
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.
Y122499WHEELCHAIRS ACCESSORIES - OTHERNo certificate specifically references this device's Basic UDI-DI.
Primary placement in Netherlands; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| NetherlandsPrimary placement | Still on market |
NL-MF-000041828No 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.