BEUDAMED
    15 results · 61ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    YELLOPORT ELITE

    FDA Adverse Event
    Malfunction ·SURGICAL INNOVATIONS LTD·Product code GCJ·March 3, 2022

    LOGI

    FDA Adverse Event
    Malfunction ·SURGICAL INNOVATIONS LTD·Product code GEI·May 5, 2022

    LOGICUT SCISSOR

    FDA Adverse Event
    Malfunction ·SURGICAL INNOVATIONS LTD·Product code GEI·October 29, 2018

    YELLOPORT PLUS

    FDA Adverse Event
    Malfunction ·SURGICAL INNOVATIONS LTD·Product code GCJ·October 21, 2020

    YELLOPORT PLUS

    FDA Adverse Event
    Malfunction ·SURGICAL INNOVATIONS LTD·Product code GCJ·October 1, 2020

    YELLOPORT PLUS

    FDA Adverse Event
    Malfunction ·SURGICAL INNOVATIONS LTD·Product code GCJ·October 8, 2020

    YELLOPORT ELITE

    FDA Adverse Event
    Malfunction ·SURGICAL INNOVATIONS LTD·Product code GCJ·November 1, 2021

    YELLOPORT PLUS

    FDA Adverse Event
    Malfunction ·SURGICAL INNOVATIONS LTD·Product code GCJ·July 23, 2018

    LOGIC

    FDA Adverse Event
    Malfunction ·SURGICAL INNOVATIONS LTD·Product code GEI·January 4, 2019

    LOGICUT

    FDA Adverse Event
    Injury ·SURGICAL INNOVATIONS LTD·Product code GEI·February 12, 2020

    PRETZELFLEX 3MM DEVICE

    FDA Adverse Event
    Malfunction ·SURGICAL INNOVATIONS LTD·Product code GCJ·January 20, 2015

    YELLOPORT PLUS

    FDA Adverse Event
    Malfunction ·SURGICAL INNOVATIONS LTD·Product code GCJ·January 17, 2022

    YELLOPORT ELITE

    FDA Adverse Event
    Malfunction ·SURGICAL INNOVATIONS LTD·Product code GCJ·January 17, 2022

    AMPLATZER SEPTAL OCCLUDER

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code MLV·September 29, 2021

    AMPLATZER CRIBRIFORM OCCLUDER

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code MLV·September 29, 2021