BEUDAMED
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    Filters FDA Adverse Event ×

    KLEENSPEC 590 SERIES DISP VAGINAL SPECULA

    FDA Adverse Event
    Malfunction ·WELCH ALLYN·Product code HIB·March 13, 2013

    HEARTSINE SAMARITAN 300P AND PAD PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES, LTD·Product code MKJ·July 7, 2014

    HYLAMER NEUT 52OD X 28ID

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWY·May 8, 2008