BEUDAMED
    22 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    MEDTRONIC SURGICAL TISSUE VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code DYE·September 23, 2021

    MEDTRONIC SURGICAL TISSUE VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code DYE·August 9, 2021

    MEDTRONIC SURGICAL TISSUE VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code DYE·March 29, 2024

    MEDTRONIC SURGICAL TISSUE VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·August 10, 2023

    MEDTRONIC HALL PROSTHETIC HEART VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWQ·November 3, 2022

    MAESTRO 4000 CONTROLLER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code LPB·September 29, 2025

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 17, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 17, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 18, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 18, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 17, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 18, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 18, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 17, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 18, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 17, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 17, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 17, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 18, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 18, 2015