BEUDAMED
    6 results · 26ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    2520274-2013-10510

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MNI·February 19, 2013

    ENDO STITCH 10MM SUTURING DEVICE

    FDA Adverse Event
    Injury ·UNITED STATES SURGICAL·Product code KOG·January 20, 2011

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·August 1, 2014

    COULTER ACT PAK REAGENT KIT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·September 24, 2014

    COULTER ACT PAK REAGENT KIT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·May 26, 2015

    COULTER ACT PAK REAGENT KIT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·May 5, 2015