BEUDAMED
    5 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    CANNULATED COCR STANDARD GLENOSPHERE 39MM

    FDA Adverse Event
    Injury ·TORNIER INC·Product code PHX·February 28, 2025

    SHOULDER ID PRM REV GLENOID 35MM POST CENTERED 25MM

    FDA Adverse Event
    Injury ·TORNIER INC·Product code PHX·February 28, 2025

    SARA 3000

    FDA Adverse Event
    Injury ·ARJOHUNTLEIGH POLSKA SP. ZO.O.·Product code FSA·March 12, 2013

    AED PLUS

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·February 7, 2011

    DEXTRUS 4136

    FDA Adverse Event
    Injury ·BIOTRONIK GMBH AND CO.·Product code DTB·February 25, 2008