BEUDAMED
    33 results · 26ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    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
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LPB·April 25, 2023

    MAESTRO FOOT SWITCH

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OAD·September 6, 2018

    MAESTRO 4000 CONTROLLER

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

    MAESTRO 4000 CONTROLLER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LPB·November 3, 2023

    MAESTRO 4000 CONTROLLER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OAD·September 7, 2023

    MAESTRO 4000 POD, 100W

    FDA Adverse Event
    Malfunction ·STELLARTECH RESEARCH CORPORATION·Product code LPB·August 17, 2023

    MAESTRO 4000 CONTROLLER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LPB·October 2, 2023

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Product code NPZ·March 27, 2013

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Product code NPM·March 28, 2013

    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