BEUDAMED
    3 results · 17ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    HEARTSINE SAMARITAN 300P AND PAD PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES, LTD·Product code MKJ·January 23, 2013

    GLENOID, PE WITH PEG, LARGE

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·December 20, 2010

    STAPLE, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 14, 2014