BEUDAMED
    4 results · 26ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    RAPIDPOINT 500

    FDA Adverse Event
    Death ·SIEMENS HEALTHCARE DIAGNOSTICS·Product code KQO·May 15, 2014

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC., USA·Product code LFR·October 30, 2007

    CONSULTA CRT-P

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code NVZ·October 31, 2012

    REVERSE SHOULDER SYSTEM 04.01.0172 GLENOSPHERE 36XØ27

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·December 6, 2023