BEUDAMED
    7 results · 35ms · Sources: EU EUDAMED, US FDA

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    MODIFICATION TO: ARTHREX V-TAK

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HEARTSTREAM XL DEFIBIBRILLATOR/MONITOR, MODEL M4735A, HEARTSTREAM XLT DEFIBRILLATOR/MONITOR.MODEL M2500B

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    ROD TO ROD CROSS BRACES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AMPLATZER CRIBRIFORM OCCLUDER

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL CATD·Product code MLV·October 8, 2019

    VALVE, O.P.S. BULK, N-S

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTL·March 14, 2013

    ENRHYTHM DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code DXY·April 12, 2011

    TENDRIL SDX

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·May 27, 2008