BEUDAMED
    6 results · 25ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    CORDIS BIOPSY FORCEPS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PRESTODR 4143

    FDA 510(k)
    FDA Class 2 ·Radiology

    VERTEX ETCHANT

    FDA 510(k)
    FDA Class 2 ·Dental

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 9, 2014

    SCREW-IN

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 31, 2012

    PULSE GEN MODEL

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·February 29, 2008