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EUDAMED last updated this device on May 21, 2026
B-KR-FT3-02300JZINNODX FT3 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 Spain. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
D-KR-FT3-02300JZB-KR-FT3-02300JZKR-FT3-02300D-KR-FT3-02300JZ
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.
European Medical Device Nomenclature — the EU product classification assigned to this device.
W01020401FREE TRIIODOTHYRONINENo certificate specifically references this device's Basic UDI-DI.
Primary placement in Spain; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| SpainPrimary placement | Still on market |
CN-MF-000041071Certificate health across this manufacturer's portfolio.
V13 108673 0002Issued