BEUDAMED
    3 results · 101ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    AU 4000 U-ARM

    FDA Adverse Event
    Injury ·KONICA MINOLTA HEALTHCARE AMERICAS, INC.·Product code KPR·October 1, 2018

    SU-4000U-ARM

    FDA Adverse Event
    Malfunction ·KONICA MINOLTA HEALTHCARE AMERICAS INC.·Product code KPR·November 2, 2018

    CS-7

    FDA Adverse Event
    Malfunction ·KONICA MINOLTA HEALTHCARE AMERICAS, INC.·Product code MQB·May 2, 2018