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

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    Filters Status: Malfunction ×

    9616026-2006-00240

    FDA Adverse Event
    Malfunction ·Product code FII·June 21, 2006

    9616026-2006-00244

    FDA Adverse Event
    Malfunction ·Product code FII·June 22, 2006

    ORTHOPEDIATRICS PEDIFRAG SYSTEM 3.5MM, 2.0MM DRILL BIT

    FDA Adverse Event
    Malfunction ·ORTHOPEDIATRICS·Product code HRS·July 22, 2016

    BD NEEDLE ECLIPSE 25X5/8

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·February 28, 2024

    BD NEEDLE ECLIPSE 25X5/8

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·February 28, 2024

    BD NEEDLE ECLIPSE 25X5/8

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·February 28, 2024

    BD NEEDLE ECLIPSE 25X5/8

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·February 28, 2024

    BD NEEDLE ECLIPSE 25X5/8

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·February 28, 2024

    9616026-2006-00239

    FDA Adverse Event
    Malfunction ·Product code FII·June 22, 2006

    9616026-2006-00222

    FDA Adverse Event
    Malfunction ·Product code FII·June 21, 2006

    PRISMAFLEX SYSTEM

    FDA Adverse Event
    Malfunction ·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006

    PRISMAFLEX SYSTEM

    FDA Adverse Event
    Malfunction ·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006

    PRISMAFLEX SYSTEM

    FDA Adverse Event
    Malfunction ·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006

    9616026-2006-00245

    FDA Adverse Event
    Malfunction ·Product code FII·June 22, 2006

    PRISMAFLEX SYSTEM

    FDA Adverse Event
    Malfunction ·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006

    9616026-2006-00221

    FDA Adverse Event
    Malfunction ·Product code FII·June 21, 2006

    PRISMAFLEX SETS (M)

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDI·May 13, 2024

    DIMENSION® CLINICAL CHEMISTRY SYSTEM

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC - BROOKFIELD·Product code JJE·March 8, 2011

    PRISMAFLEX SETS (M & ST)

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDI·March 28, 2023

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·August 23, 2024