BEUDAMED
    16 results · 64ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    UNKNOWN MIC KEY

    FDA Adverse Event
    Injury ·AVANOS MEDICAL INC.·Product code KNT·December 17, 2021

    LIBERATOR 45

    FDA Adverse Event
    Injury ·CAIRE INC.·Product code BYJ·April 25, 2018

    STROLLER

    FDA Adverse Event
    Injury ·CAIRE INC.·Product code BYJ·April 25, 2018

    UNKNOWN ON-Q ELASTOMERIC PUMP

    FDA Adverse Event
    Injury ·AVANOS MEDICAL INC.·Product code MEB·March 30, 2021

    MIC GASTROSTOMY FEEDING TUBE WITH ENFIT CONNECTORS - 14 FR

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code KNT·November 21, 2024

    PRESET PCA PUMP

    FDA Adverse Event
    Injury ·SUMMIT MEDICAL PRODUCTS, INC.·Product code FRN·June 8, 2022

    ON-Q PAIN RELIEF SYSTEM WITH SELECT-A-FLOW, 400 ML, 2-14 ML/HR

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL, INC.·Product code MEB·August 13, 2020

    NTG LIGHT THERAPY ACNE MASK USA

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON CONSUMER INC·Product code OLP·June 28, 2019

    AIA-360

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·March 26, 2018

    NTG LIGHT THERAPY ACNE MASK USA

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON CONSUMER INC·Product code OLP·June 28, 2019

    CORTRAK ENTERAL ACCESS SYSTEM

    FDA Adverse Event
    Injury ·AVANOS MEDICAL INC.·Product code KNT·July 9, 2025

    LIGHTSHEER XC

    FDA Adverse Event
    Injury ·LUMENIS LTD·Product code GEX·April 28, 2022

    PULSE GEN MODEL 1000

    FDA Adverse Event
    Injury ·LIVANOVA USA, INC.·Product code LYJ·October 25, 2024

    AIA-600II

    FDA Adverse Event
    Malfunction ·TOSOH BIOSCIENCE·Product code KHO·February 13, 2018

    PULSE GEN MODEL 104

    FDA Adverse Event
    Injury ·LIVANOVA USA, INC.·Product code LYJ·March 26, 2025

    CLEARDETECT COVID-19

    FDA Adverse Event
    Malfunction ·MAXIM BIOMEDICAL, INC.·Product code QKP·August 22, 2022