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

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    Filters FDA Adverse Event ×

    AMPLATZER DUCT OCCLUDER

    FDA Adverse Event
    Injury ·AGA MEDICAL CORPORATION·Product code MAE·June 7, 2018

    HUDSON AQUAPAK 340 SW, 340 ML W/040 ADAPTOR

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code BTT·June 5, 2014

    ENDURANT ABDOMINAL STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·February 8, 2013

    IKARIA

    FDA Adverse Event
    Malfunction ·IKARIA·Product code MRN·December 28, 2010