BEUDAMED
    6 results · 25ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    HUMAPEN UNKNOWN DEVICE

    FDA Adverse Event
    Injury ·ELI LILLY AND COMPANY·Product code NSC·April 30, 2014

    ENDURANT II STENT GRAFT SYSTEM

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code MIH·October 10, 2012

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·June 12, 2007

    COMPREHENSIVE REVERSE SHOULDER GLENOSPHERE STD 36MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PAO·November 2, 2017

    E1 44-36 STD HMRL BRNG

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PAO·November 2, 2017

    COMPREHENSIVE REVERSE SHOULDER SYSTEM

    FDA Adverse Event
    Injury ·BIOMET·Product code KWS·September 20, 2017