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

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    Filters Status: Injury ×

    NUCLETRON PLATO

    FDA Adverse Event
    Injury ·NUCLETRON CORP. NUCLETRON B.V.·Product code MUJ·April 21, 2005

    FLEXITRON HDR

    FDA Adverse Event
    Injury ·NUCLETRON B.V.·Product code JAQ·September 27, 2024

    GENEVA

    FDA Adverse Event
    Injury ·NUCLETRON B.V.·Product code JAQ·October 9, 2025

    ONCENTRA MASTERPLAN VER. 3.1 SP1 AND SP2

    FDA Adverse Event
    Injury ·NUCLETRON B.V.·Product code MUJ·November 20, 2008

    ONCENTRA BRACHY

    FDA Adverse Event
    Injury ·NUCLETRON B.V.·Product code JAQ·October 12, 2021

    MICROSELECTRON DIGITAL

    FDA Adverse Event
    Injury ·NUCLETRON B.V.·Product code JAQ·January 16, 2026

    PROGUIDE NEEDLES

    FDA Adverse Event
    Injury ·NUCLETRON B.V.·Product code JAQ·February 4, 2026

    PROGUIDE NEEDLE SET

    FDA Adverse Event
    Injury ·NUCLETRON B.V.·Product code JAQ·September 26, 2019

    ELEKTA RING CT / MR APPLICATOR SET: 6 CM, 45 DEGREE TANDEM

    FDA Adverse Event
    Injury ·ELEKTA / NUCLETRON B.V.·Product code JAQ·September 12, 2022