BEUDAMED
    11 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    NM/CT 860

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS ISRAEL·Product code KPS·January 17, 2023

    OPTIMA NM/CT 640

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS ISRAEL·Product code KPS·January 17, 2023

    NM/CT 870

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS ISRAEL·Product code KPS·January 17, 2023

    NM/CT 870

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS ISRAEL·Product code KPS·January 17, 2023

    NM/CT 860

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS ISRAEL·Product code KPS·January 17, 2023

    NM/CT 830

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS ISRAEL·Product code KPS·January 17, 2023

    NM/CT 870

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS ISRAEL·Product code KPS·January 17, 2023

    NM/CT 850

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS ISRAEL·Product code KPS·January 17, 2023

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·December 10, 2018

    ERBE FLEXIBLE CRYOPROBE

    FDA Adverse Event
    Malfunction ·ERBE ELEKTROMEDIZIN GMBH·Product code GEH·May 12, 2026

    DIMENSION VISTA® CHEMISTRY 1 CALIBRATOR

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC - GLASGOW·Product code JIX·January 25, 2016