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

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    Filters FDA Adverse Event ×

    HEARTMATE II LVAS

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·March 28, 2012

    MIDAS REX III MO3

    FDA Adverse Event
    Malfunction ·MEDTRONIC MIDAS REX·Product code HBB·March 18, 2002

    AUTO SUTURE MULTIFIRE ENDO GIA 30-3.5

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP.·Product code GCJ·June 28, 2000

    FUSA F80B (HF/PS/1.8/H)

    FDA Adverse Event
    Injury ·FRESENIUS·Product code KDI·August 24, 1998