BEUDAMED
    7 results · 27ms · Sources: EU EUDAMED, US FDA

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    ULTRACLONE ECL-01-900 CELL LINE

    FDA 510(k)
    FDA Class 1 ·Hematology

    GUIDANT MICROWAVE ABLATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    THIOGLYCOLLATE MEDIUM W/OUT INDICATOR

    FDA 510(k)
    FDA Class 1 ·Microbiology

    BD BBL¿ HEMO (HAEMOPHILUS) ID QUAD (WITH GROWTH FACTORS)

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code JSI·February 24, 2022

    HARMONIC FOCUS* CURVED SHEARS, TORQUE WRENCH AND GRIP ASSIST

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·May 30, 2014

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·October 19, 2012

    ARCHITECT C16000 SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code JJE·September 22, 2010