BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    A8 INTEGR8™ Porous Pedicle Screws

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CARDIOFAX CE, MODEL PEA-1110K

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Visi Mobile Monitoring System, Visi Mobile Chest Sensor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·November 2, 2023

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·November 11, 2014

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·September 11, 2011

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·July 23, 2013