BEUDAMED
    5 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SCREWDRIVER SHAFT, COMPRESSION T2 TIBIA 3.5 MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code HXX·July 27, 2012

    ALLURA XPER FD20

    FDA Adverse Event
    Injury ·PHILIPS HEALTHCARE·Product code OWB·December 16, 2019

    PLM A+ SPANISH DEVIC

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·May 15, 2014

    ATLAS PLUS VR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·November 10, 2010

    KOPANS MODIFIED BREAST LESION LOCALIZATION NEEDLE

    FDA Adverse Event
    Malfunction ·COOK, INC.·Product code DWO·November 20, 2012