BEUDAMED
    6 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    M2A 38MMX52MM CUP

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·April 30, 2014

    8800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 5, 2012

    LIGACLIP MCA SMALL APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC (CINCINNATI)·Product code GDO·January 30, 2008

    CODMAN MALIS INTEGRATED TUBE SET UNITIZED PLUG

    FDA Adverse Event
    Malfunction ·CODMAN & SHURTLEFF, INC.·Product code GEI·November 15, 2017

    CODMAN MALIS INTEGRATED TUBE SET UNITIZED PLUG

    FDA Adverse Event
    Malfunction ·CODMAN & SHURTLEFF, INC.·Product code GEI·November 15, 2017

    MEDTRONIC LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DXY·August 21, 2020