BEUDAMED
    8 results · 29ms · Sources: EU EUDAMED, US FDA

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    Shadow Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Oticon

    FDA UDI
    Sbo Hearing A/S·05714464055050·OTICON PLAY PX 1 MINIRITE R C044

    BD LUER-LOK¿ DISPOSABLE SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·April 23, 2018

    Meridian Anterior Plate System, Regatta Lateral Plate System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    QUANTA LITE GP210 ELISA

    FDA 510(k)
    FDA Class 2 ·Immunology

    BED, HOSPITAL

    FDA Adverse Event
    Other ·JOERNS HEALTHCARE, INC.·Product code FNJ·November 10, 2008

    OLYMPUS HF RESECTION ELECTRODE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code FAS·August 5, 2011

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·July 17, 2013