BEUDAMED
    7 results · 47ms · Sources: EU EUDAMED, US FDA

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    KONICA

    FDA Adverse Event
    Malfunction ·KONICA MINOLTA, INC.·Product code KPR·May 7, 2019

    RADIOLOGY XR7 FILM READER/ FILM RADIOGRAPHIC

    FDA Adverse Event
    Malfunction ·KONICA MINOLTA, INC.·Product code IWZ·May 25, 2018

    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

    ALL IONIZING RADIATION PRODUCTS

    FDA Adverse Event
    Malfunction ·KONICA MINOLTA MEDICAL IMAGING, INC.·Product code MQB·June 22, 2011

    CS-7

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

    RESIUS 190 XPRES

    FDA Adverse Event
    Malfunction ·KONICA-MINOLTA MEDICAL IMAGING USA, INC.·Product code IWZ·October 13, 2009