BEUDAMED
    9 results · 35ms · Sources: EU EUDAMED, US FDA

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    Irregular Rhythm Notification Feature

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LOADPRO™ Intraoperative Rod Strain Sensor

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MISEQDX UNIVERSAL KIT 1.0

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    ECHOTIP INSIGHT PORTOSYSTEMIC PRESSURE GRADIENT MEASUREMENT SYSTEM

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code QIJ·July 28, 2023

    ECHOTIP INSIGHT PORTOSYSTEMIC PRESSURE GRADIENT MEASUREMENT SYSTEM

    FDA Adverse Event
    Malfunction ·COOK MEDICAL IRELAND·Product code QIJ·July 11, 2024

    DUETTE MULTI-BAND MUCOSECTOMY DEVICE

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code KNS·October 24, 2023

    ECHOTIP INSIGHT PORTOSYSTEMIC PRESSURE GRADIENT

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code QIJ·January 27, 2022

    ECHOTIP INSIGHT PORTOSYSTEMIC PRESSURE GRADIENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code QIJ·November 3, 2021

    ECHOTIP INSIGHT PORTOSYSTEMIC PRESSURE GRADIENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code QIJ·May 27, 2024