BEUDAMED
    13 results · 51ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    FLEX FOCUS 800 SYSTEM

    FDA Adverse Event
    Malfunction ·BK MEDICAL APS·Product code IYN·December 20, 2017

    IP57 ULTRASOUND PROBE

    FDA Adverse Event
    Malfunction ·BK MEDICAL APS·Product code ITX·October 25, 2017

    LAPAROSCOPIC BK PROBE L12C4F

    FDA Adverse Event
    Injury ·BK MEDICAL APS·Product code ITX·August 2, 2023

    ENDOCAVITY BIPLANE TRANSDUCER

    FDA Adverse Event
    Malfunction ·BK MEDICAL APS·Product code ITX·November 24, 2020

    ENDOCAVITY BIPLANE TRANSDUCER

    FDA Adverse Event
    Malfunction ·BK MEDICAL APS·Product code ITX·December 7, 2020

    BKSPECTO ULTRASOUND SYSTEM

    FDA Adverse Event
    Malfunction ·BK MEDICAL APS·Product code ITX·September 29, 2022

    LAPAROSCOPIC BK PROBE L12C4F

    FDA Adverse Event
    Malfunction ·BK MEDICAL APS·Product code ITX·December 12, 2022

    ULTRASOUND SCANNER FLEX FOCUS

    FDA Adverse Event
    Malfunction ·BK MEDICAL APS·Product code IYN·May 29, 2025

    ULTRASOUND SCANNER FLEX FOCUS

    FDA Adverse Event
    Malfunction ·BK MEDICAL APS·Product code IYN·March 25, 2026

    BK ULTRASOUND DEVICE

    FDA Adverse Event
    Malfunction ·BK MEDICAL APS·Product code ITX·February 24, 2025

    LAPAROSCOPIC BK PROBE L12C4F

    FDA Adverse Event
    Injury ·BK MEDICAL APS (PART OF GE HEALTHCARE)·Product code ITX·July 18, 2023

    ULTRASOUND SCANNER SYSTEM 2300

    FDA Adverse Event
    Malfunction ·BK MEDICAL APS (PART OF GE HEALTHCARE)·Product code IYN·August 23, 2024

    TRIDENT 10° X3 INSERT 36MM ID

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·September 26, 2014