BEUDAMED
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    REPROCESSED HARMONIC SHEAR

    FDA 510(k)
    FDA Unclassified ·Unknown

    Bernafon

    FDA UDI
    Bernafon AG·05711584050996·CA3 ITCD, WL R BE CARISTA 3

    WAVEWRITER ALPHA 16

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·December 24, 2024

    OWL CANNULAE

    FDA 510(k)
    FDA Class 2 ·Neurology

    NATURAL COMFORT BATTERY/ELECTRIC BREAST PUMP

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

    BELT CLIP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OYC·October 1, 2014

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FPO·May 1, 2013

    MESH - VENTRALEX

    FDA Adverse Event
    Injury ·DAVOL INC·Product code FTL·June 10, 2011