BEUDAMED
    6 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    NIHON KOHDEN TEC-7531 CARDIOLIFE PORTABLE DEFIBRILLATOR AND ACCESSORIES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SMARTSPONGE SYSTEM

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Surefire Precision Infusion System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    8800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 4, 2013

    SECURA DR

    FDA Adverse Event
    Death ·MEDTRONIC MED REL, INC.·Product code LWS·January 27, 2011

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code LWS·July 31, 2014