BEUDAMED
    17 results · 45ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    AERIS BALLOON DILATION CATHETER

    FDA Adverse Event
    Malfunction ·BRYAN MEDICAL, INC.·Product code KTI·December 13, 2023

    TENAX

    FDA Adverse Event
    Malfunction ·BRYAN MEDICAL, INC·Product code BTR·July 29, 2024

    TENAX LASER SAFE ENDOTRACHEAL TUBE

    FDA Adverse Event
    Malfunction ·BRYAN MEDICAL INC.·Product code BTR·November 12, 2025

    TENAX ENDOTRACHEAL TUBE

    FDA Adverse Event
    Malfunction ·BRYAN MEDICAL INC.·Product code BTR·May 2, 2024

    TENAX

    FDA Adverse Event
    Malfunction ·BRYAN MEDICAL, INC.·Product code BTR·June 7, 2024

    TENAX LASER RESISTANT ENDOTRACHEAL TUBE

    FDA Adverse Event
    Malfunction ·BRYAN MEDICAL, INC.·Product code BTR·July 20, 2022

    TENAX LASER RESISTANT ENDOTRACHEAL TUBE

    FDA Adverse Event
    Malfunction ·BRYAN MEDICAL, INC.·Product code BTR·October 25, 2023

    AERIS

    FDA Adverse Event
    Malfunction ·BRYAN MEDICAL, INC·Product code EOQ·January 15, 2016

    AERIS BALLOON DILATION CATHETER 7MMX30MM

    FDA Adverse Event
    Malfunction ·BRYAN MEDICAL, INC·Product code KTI·May 6, 2026

    AERIS® BALLOON DILATION CATHETER

    FDA Adverse Event
    Malfunction ·BRYAN MEDICAL, INC·Product code EOQ·April 21, 2017

    AERIS BALLOON DILATION CATHETER

    FDA Adverse Event
    Malfunction ·BRYAN MEDICAL, INC.·Product code EOQ·October 26, 2023

    AERIS 6 MM X 30 MM LENGTH BALLOON DILATION CATHETER

    FDA Adverse Event
    Malfunction ·BRYAN MEDICAL, INC.·Product code EOQ·February 25, 2022

    INFUSOMAT SPACE

    FDA Adverse Event
    Malfunction ·B.BRAUN MELSUNGEN AG·Product code FRN·July 12, 2023

    SAF-T-CLIK

    FDA Adverse Event
    Malfunction ·RYAN MEDICAL, INC.·Product code FPA·March 2, 1994

    SHAMROCK SAFETY BLOOD COLLECTION SET

    FDA Adverse Event
    Malfunction ·RYAN MEDICAL, INC.·Product code JKA·December 26, 1995

    SHAMROCK SAFETY BLOOD COLLECTION SET

    FDA Adverse Event
    Malfunction ·RYAN MEDICAL, INC.·Product code JKA·March 7, 1997

    BRAUN

    FDA Adverse Event
    Malfunction ·B. BRUAN MEDICAL, INC.·Product code FPA·March 17, 2003