BEUDAMED
    11 results · 26ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    KRD DEVICE, EMBOLIZATION, VASCULAR

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRD·September 19, 2019

    LS LF MB EXT SET CLAVE LSC T

    FDA Adverse Event
    Malfunction ·HOSPIRA, LTD·Product code FPA·May 7, 2013

    ACCU-CHEK VOICEMATE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·August 13, 2008

    VITEK® 2 AST-ST01 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code LON·October 24, 2017

    RETRACTA DETACHABLE EMBOLIZATION COIL

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRD·September 17, 2018

    RETRACTA DETACHABLE EMBOLIZATION COIL

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRD·September 17, 2018

    RETRACTA DETACHABLE EMBOLIZATION COIL

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRD·January 2, 2020

    RETRACTA DETACHABLE EMBOLIZATION COIL

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRD·January 2, 2020

    RETRACTA DETACHABLE EMBOLIZATION COIL

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRD·March 11, 2020

    RETRACTA DETACHABLE EMBOLIZATION COIL

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRD·July 31, 2019

    RETRACTA DETACHABLE EMBOLIZATION COIL

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRD·February 3, 2020