BEUDAMED
    4 results · 29ms · Sources: EU EUDAMED, US FDA

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    NON-VENTED HIGH-VOLUME INLET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - ROUND LAKE·Product code LHI·July 24, 2019

    HEARTSINE SAMARITAN 300P AND PAD PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES, LTD·Product code MKJ·February 12, 2014

    ENDURANT II STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·October 23, 2012

    MAGIC 3TM FEMALE INTERMITTENT CATHETER

    FDA Adverse Event
    Malfunction ·ROCHESTER MEDICAL CORP.·Product code KOD·May 27, 2015