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

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    Filters FDA Adverse Event ×

    DELTA CER FEM HD 28/0MM T1

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·January 31, 2024

    CURLIN INFUSION IV PUMP

    FDA Adverse Event
    Malfunction ·MOOG MEDICAL DEVICES GROUP·Product code FRN·April 2, 2014

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·January 29, 2013

    LIFEPAK 12 DEFIBRILLATOR/MONITOR SERIES

    FDA Adverse Event
    Death ·PHYSIO-CONTROL, INC.·Product code MKJ·December 16, 2010