BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SONICFILL COMPOSITE

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·September 23, 2013

    SONICFILL COMPOSITE

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·September 23, 2013

    SONICFILL COMPOSITE

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·September 23, 2013

    SONICFILL COMPOSITE

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·September 23, 2013

    SONICFILL COMPOSITE

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·September 23, 2013

    FUJIFILM 600 SERIES ENDOSCOPE EC-600WM

    FDA Adverse Event
    Malfunction ·FUJIFILM CORPORATION·Product code FDF·January 22, 2025

    GEMSTAR PUMP 220V SP

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·March 7, 2014

    MEGASUTURECUT NEEDLE DRIVER

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·November 14, 2012

    MYOCARDIAL LEAD

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·June 10, 2015