BEUDAMED
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    Filters FDA Adverse Event × Regulation: Us FDA × Clear all

    QUIKDRIVE BATTERY POWERED SCREWDRIVER MINI

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS FREIBURG·Product code LXH·November 12, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HLTHCARE CORP·Product code FRN·January 14, 2014

    TOTALCARE BARIATRIC PLUS BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·December 28, 2012