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

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    ARK Methotrexate Assay

    FDA 510(k)
    FDA Unclassified ·Unknown

    3M™ Unitek™

    FDA UDI
    3M UNITEK CORPORATION·00652221046130·Unitek(TM) Molar Band General Purpose Wide Hard...

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172973530·

    FINESSE ULTRA BREAST BIOPSY SYSTEM DRIVER (BLUE, PINK)

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

    INQU

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DEPTH ELECTRODE

    FDA Adverse Event
    Malfunction ·AD-TECH MEDICAL INSTRUMENT CORP.·Product code GZL·December 14, 2021

    SUBDURAL ELECTRODES, DEPTH ELECTRODES, AND ANCHOR BOLTS

    FDA Adverse Event
    Injury ·AD-TECH MEDICAL INSTRUMENT CORP.·Product code GZL·June 14, 2019

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·October 10, 2014

    M2A-MAGNUM PF CUP 60ODX54ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 11, 2013

    PFC SIG RPF CEM FEM SZ 4 LT

    FDA Adverse Event
    Injury ·DEPUY WARSAW·Product code NJL·July 8, 2011