BEUDAMED
    33 results · 37ms · Sources: EU EUDAMED, US FDA

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    UNKNOWN ENDOFLIP CATHETER

    FDA Adverse Event
    Injury ·CROSPON LTD·Product code FFX·June 30, 2021

    ENDOFLIP

    FDA Adverse Event
    Injury ·CROSPON LTD·Product code FFX·April 27, 2022

    ESOFLIP

    FDA Adverse Event
    Injury ·CROSPON LTD·Product code PID·September 8, 2021

    ESOFLIP

    FDA Adverse Event
    Injury ·CROSPON LTD·Product code PIE·June 25, 2019

    UNKNOWN ENDOFLIP CATHETER

    FDA Adverse Event
    Malfunction ·CROSPON LTD·Product code FFX·June 18, 2019

    ESOFLIP

    FDA Adverse Event
    Injury ·CROSPON LTD·Product code PIE·April 12, 2019

    ESOFLIP

    FDA Adverse Event
    Malfunction ·CROSPON LTD·Product code PIE·April 9, 2019

    ENDOFLIP

    FDA Adverse Event
    Malfunction ·CROSPON LTD·Product code FFX·May 8, 2019

    ENDOFLIP

    FDA Adverse Event
    Malfunction ·CROSPON LTD·Product code FFX·April 4, 2019

    ENDOFLIP

    FDA Adverse Event
    Malfunction ·CROSPON LTD·Product code FFX·May 27, 2026

    ENDOFLIP

    FDA Adverse Event
    Malfunction ·CROSPON LTD·Product code FFX·May 27, 2026

    UNKNOWN ENDOFLIP CATHETER

    FDA Adverse Event
    Injury ·CROSPON LTD·Product code FFX·March 27, 2024

    ENDOFLIP

    FDA Adverse Event
    Malfunction ·CROSPON LTD·Product code FFX·May 27, 2026

    ENDOFLIP

    FDA Adverse Event
    Malfunction ·CROSPON LTD·Product code FFX·May 27, 2026

    ENDOFLIP

    FDA Adverse Event
    Malfunction ·CROSPON LTD·Product code FFX·May 27, 2026

    ENDOFLIP

    FDA Adverse Event
    Malfunction ·CROSPON LTD·Product code FFX·May 27, 2026

    ESOFLIP

    FDA Adverse Event
    Injury ·CROSPON LTD·Product code PIE·March 26, 2019

    ENDOFLIP

    FDA Adverse Event
    Injury ·CROSPON LTD·Product code FFX·March 4, 2019

    ESOFLIP

    FDA Adverse Event
    Injury ·CROSPON LTD·Product code PIE·February 26, 2019

    ESOFLIP

    FDA Adverse Event
    Death ·CROSPON LTD·Product code PIE·March 11, 2019