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- Date of registration
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EUDAMED last updated this device on May 20, 2026
B-KR-CA50-01100C28INNODX CA50 CMIA is an IVDD-legacy in vitro diagnostic registered in EUDAMED. It is classified as IVDD — General. Manufactured by Xiamen Innodx Biotech Co., Ltd.. Placed on the EU market in Belgium. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
D-KR-CA50-01100C28B-KR-CA50-01100C28KR-CA50-01100CD-KR-CA50-01100C28
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.
European Medical Device Nomenclature — the EU product classification assigned to this device.
W0102030104CANCER ANTIGEN 501 warning recorded — scroll inside the panel to see all entries.
CW011No certificate specifically references this device's Basic UDI-DI.
Primary placement in Belgium; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| BelgiumPrimary placement | Still on market |
CN-MF-000041071No 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.