BEUDAMED
    9 results · 18ms · Sources: EU EUDAMED, US FDA

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    REDI-DISC HEMOGLOBIN GEL TUBE KIT

    FDA 510(k)
    FDA Class 2 ·Hematology

    WALLSTENT ENDOPROSTHESIS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code JCT·January 15, 2025

    TransEnterix Senhance Surgical System

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    COOLTOUCH MODELS LC215 AND COOLLIPO

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

    WALLSTENT ENDOPROSTHESIS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MAF·December 22, 2025

    WALLSTENT ENDOPROSTHESIS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MAF·December 1, 2025

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 3, 2014

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·October 10, 2012

    COAGUCHEK S SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JPA·September 21, 2007