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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    FST CATH-UD CATHETER

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

    AXILLOBIFEMORAL GORE-TEX VASCULAR GRAFT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CANNULA, SUCTION UTERINE

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·November 12, 2010

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·January 9, 2013

    FINELINE II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code DTB·July 1, 2014