BEUDAMED
    11 results · 58ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PROFLOR 25MM HERNIA MESH

    FDA Adverse Event
    Injury ·INSIGHTRA MEDICAL INC.·Product code FTL·December 10, 2018

    ULTRA IABP BALLOON CATHETER KIT

    FDA Adverse Event
    Malfunction ·INSIGHTRA MEDICAL, INC.·Product code DSP·July 1, 2009

    ULTRA IABP CATHETER KIT

    FDA Adverse Event
    Malfunction ·INSIGHTRA MEDICAL, INC.·Product code DSP·September 1, 2016

    ULTRA IABP

    FDA Adverse Event
    Injury ·INSIGHTRA MEDICAL, INC.·Product code DSP·October 13, 2023

    ULTRA IAB CATHETER KIT

    FDA Adverse Event
    Malfunction ·INSIGHTRA MEDICAL, INC.·Product code DSP·June 8, 2015

    ULTRA IAB CATHETER KIT

    FDA Adverse Event
    Malfunction ·INSIGHTRA MEDICAL, INC.·Product code DSP·June 8, 2015

    ULTRA IAB CATHETER KIT

    FDA Adverse Event
    Malfunction ·INSIGHTRA MEDICAL, INC.·Product code DSP·June 8, 2015

    ULTRA IAB CATHETER KIT

    FDA Adverse Event
    Malfunction ·INSIGHTRA MEDICAL, INC.·Product code DSP·June 8, 2015

    ULTRA IAB CATHETER KIT

    FDA Adverse Event
    Malfunction ·INSIGHTRA MEDICAL, INC.·Product code DSP·June 8, 2015

    ULTRA IAB CATHETER KIT

    FDA Adverse Event
    Malfunction ·INSIGHTRA MEDICAL, INC.·Product code DSP·June 8, 2015

    ULTRA IAB CATHETER

    FDA Adverse Event
    Death ·INSIGHTRA MEDICAL, INC.·Product code DSP·December 19, 2019