BEUDAMED
    3 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    HEAD EPOCA Ø50 H18.75 SST

    FDA Adverse Event
    Injury ·SYNTHES SELZACH·Product code KWT·June 12, 2014

    MICROSENSOR VENTRICULAR CATHETER KIT

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC.·Product code GWM·October 11, 2010

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION·Product code DRM·November 13, 2012