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

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    ELECTRO-CAUTERY KNIFE CLEANER 6000 1

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704283822·

    GIVEN DIAGNOSTIC SYSTEM

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

    MagView BIOMAGNETOMETER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    MEGA NEEDLE DRIVER INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·June 5, 2014

    EON PATIENT PROGRAMMER

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·November 12, 2012

    SPRINTER LEGEND RX BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code LOX·September 29, 2010

    Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.

    FDA Enforcement
    Class II ·Terminated·STERILMED, INC.·December 16, 2015