BEUDAMED
    9 results · 49ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    EDAP PROSTATRON

    FDA Adverse Event
    Malfunction ·EDAP TECHNOMED, INC.·Product code MEQ·September 29, 2000

    PROSTATRON

    FDA Adverse Event
    Injury ·EDAP TECHNOMED, INC.·Product code MEQ·April 7, 2000

    TUMT & PROSTATRON

    FDA Adverse Event
    Injury ·EDAP TECHNOMED, INC.·Product code MEQ·December 28, 2000

    PROSTATRON

    FDA Adverse Event
    Injury ·EDAP TECHNOMED, INC.·Product code MEQ·March 22, 2000

    TECHNOMED

    FDA Adverse Event
    Malfunction ·EDAP TECHNOMED, INC.·Product code MEQ·October 6, 1999

    PROSTATRON

    FDA Adverse Event
    Injury ·EDAP TECHNOMED, INC.·Product code MEQ·May 2, 2001

    PROSTATRON

    FDA Adverse Event
    Other ·EDAP TECHNOMED, INC.·Product code MEQ·December 29, 1998

    FOCAL ONE HIFU SYSTEM

    FDA Adverse Event
    Injury ·EDAP TECHNOMED INC.·Product code PLP·March 5, 2026

    PROSTATRON - TUMT

    FDA Adverse Event
    Injury ·EDAP TECHNOMED INC.·Product code MEQ·February 4, 1999