BEUDAMED
    18 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    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

    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

    9616026-2006-00252

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

    9616026-2006-00245

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

    9616026-2006-00253

    FDA Adverse Event
    Other ·Product code FII·June 21, 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

    FLEXTEND II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·April 8, 2013

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code CBK·August 12, 2014

    FLEXTEND

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVN·April 6, 2011

    PRISMAFLEX SETS (M & ST)

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

    ULTRA 2 CUTTING BALLOON

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code LOX·August 4, 2010