BEUDAMED
    4 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    XENIUM LF

    FDA Adverse Event
    Malfunction ·NIPRO CORPORATION *USD*·Product code KDI·February 14, 2013

    CELL-DYN 1800 ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION·Product code GKZ·January 14, 2011

    OCTRODE

    FDA Adverse Event
    Injury ·ST JUDE MED - NEUROMODULATION·Product code GZB·July 18, 2014

    UNIVERSA FIRM URETERAL STENT SET

    FDA Adverse Event
    Injury ·COOK INC·Product code FAD·March 26, 2018