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

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    Filters FDA Adverse Event ×

    PROPAQ MD DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code LDD·February 13, 2014

    GORE HELEX SEPTAL OCCLUDER

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MLV·June 3, 2009

    VANCOMYCIN ADD-VANTAGE 750 MG

    FDA Adverse Event
    Malfunction ·HOSPIRA·Product code KYX·December 3, 2012