BEUDAMED
    14 results · 23ms · 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

    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

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·April 8, 2013

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·August 27, 2014

    PRISMAFLEX SETS (M & ST)

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