BEUDAMED
    7 results · 34ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    A/R SCREW DRILL

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code HTW·January 30, 2024

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·May 22, 2014

    ACCU-CHEK D-TRONPLUS

    FDA Adverse Event
    Malfunction ·ROCHE INSULIN DELIVERY SYSTEMS, INC.·Product code LZG·October 8, 2010

    ACCESS

    FDA Adverse Event
    Malfunction ·BIEFFE MEDITAL MANUFACTURING S.A.R.L. TUNIS·Product code FPA·December 13, 2012

    NEEDLE 18X1-1/2 RB

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMI·October 16, 2020

    NEEDLE 20GA 1IN

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·October 9, 2020

    NEEDLE 20GA 1IN

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·October 15, 2020