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

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    Filters FDA Adverse Event ×

    SONICFILL COMPOSITE

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·August 13, 2014

    SONICFILL COMPOSITE

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·August 13, 2014

    SONICFILL COMPOSITE

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·August 13, 2014

    SONICFILL COMPOSITE

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·August 13, 2014

    SONICFILL COMPOSITE

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·August 13, 2014

    SONICFILL COMPOSITE

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·August 13, 2014

    SONICFILL COMPOSITE

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·August 13, 2014

    BD ULTRA-FINE INSULIN SYRINGE

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·October 7, 2020

    SYRINGE 1ML 31GA 6MM 10 BAG 500 SLA

    FDA Adverse Event
    Injury ·BD MEDICAL - DIABETES CARE·Product code FMF·January 20, 2021

    A5 ANESTHESIA SYSTEM

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC.·Product code BSZ·April 30, 2013

    RIATA ST ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL INC., CRMD·Product code NVY·January 13, 2014

    JETSTREAM G3

    FDA Adverse Event
    Injury ·PATHWAY MEDICAL TECHNOLOGIES, INC.·Product code MCW·April 28, 2011

    HU CD38 BV510 HIT2 50TST

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code MVU·December 22, 2020