BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    MAGELLAN NEEDLE 25 G 1 INCH

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FMI·November 8, 2018

    MAGELLAN

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FMI·December 17, 2018

    INRATIO2

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC·Product code GJS·August 1, 2011

    SAFETY NEEDLE 25 X 1

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FMI·December 4, 2018

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·May 20, 2014

    ARTICULEZE M HEAD 36MM +8.5

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code JDI·November 7, 2012

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·UNKNOWN MANUFACTURING FACILITY·Product code KDJ·August 31, 2010

    SAFETY NEEDLE 25 X 1

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FMI·December 11, 2018

    SAFETY NEEDLE 25 X 1

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FMI·December 11, 2018

    SAFETY NEEDLE 25 G X 1"

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FMI·December 3, 2018

    SAFETY NEEDLE 25 G X 1"

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FMI·January 17, 2019