BEUDAMED
    7 results · 33ms · Sources: EU EUDAMED, US FDA

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    MODIFICATION TO BONE ANCHOR AND KIT (BAK)

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

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690197812·AK3 PS-C Insert Trial Size 3, 13mm

    HICOR

    FDA 510(k)
    FDA Class 2 ·Radiology

    DIGITAL CONDUCTANCE METER

    FDA 510(k)
    FDA Class 2 ·Neurology

    ASR ACETABULAR IMPLANT 56

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·March 8, 2013

    POLYURETHANE CONTRAST INJECTION LINE

    FDA Adverse Event
    Malfunction ·MERIT MEDICAL SYSTEMS, INC.·Product code DTR·January 14, 2011

    ANALYTICAL P MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·August 8, 2014