BEUDAMED
    12 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Niti-S Biliary Slim M Stent

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

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111318764·METZENBAUM SCISS DEL STR 7"

    IQ FLEX M

    FDA Adverse Event
    Malfunction ·FIRST SOURCE INC.·Product code IZL·May 29, 2024

    PCCS GRAFT DELIVERY SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Cefaly Dual Enhanced with RFID - OTC, Cefaly Dual Enhanced with RFID - Rx, Cefaly Dual Connected - OTC, Cefaly Dual Connected - Rx

    FDA 510(k)
    FDA Class 2 ·Neurology

    Widex

    FDA UDI
    Widex A/S·05706069809930·Widex EVOKE E-FS (Cappuccino brown ) 220, Telec...

    LOCATOR ABUTMENT

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code DZE·October 20, 2022

    TALENT CAPTIVIA

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code MIH·November 3, 2014

    GORE PRECLUDER DURA SUBSTITUTE

    FDA Adverse Event
    Injury ·W. L. GORE ASSOCIATES INC.·Product code GXQ·July 2, 2013

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·November 12, 2015

    CEFALY

    FDA Adverse Event
    Injury ·CEFALY TECHNOLOGY·Product code PCC·March 9, 2026

    CEFALY

    FDA Adverse Event
    Injury ·CEFALY TECHNOLOGY·Product code PCC·March 9, 2026