BEUDAMED
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    80 Beats Medical GmbH

    Manufacturer
    🇩🇪 Germany

    BEATS MEDICAL

    FDA registration
    BEATS MEDICAL·1 product·🇮🇪 Ireland

    EVOLUT PRO TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·February 19, 2024

    1600 SEMI AUTOMATIC DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORP.·Product code MKJ·December 18, 1998

    ENPULSE

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code DXY·June 10, 2010

    AZURE XT DR MRI SURESCAN

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code NVZ·July 20, 2020

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·February 12, 2016

    NELLCOR

    FDA Adverse Event
    Death ·MITG - GALWAY·Product code DQA·March 27, 2019

    SYNCARDIA FREEDOM DRIVER

    FDA Adverse Event
    Malfunction ·SYNCARDIA SYSTEMS, INC.·Product code LOZ·November 23, 2015

    PULSE GEN MODEL 102

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·August 1, 2008

    PATIENT INFORMATION CENTER IX

    FDA Adverse Event
    Injury ·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code MHX·October 7, 2025

    SPRINT QUATTRO SECURE MRI SURESCAN

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWS·January 14, 2022

    EMBLEM MRI S-ICD

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code LWS·December 15, 2025

    BODY GUARDIAN

    FDA Adverse Event
    Injury ·PREVENTICE SOLUTIONS·Product code DSI·August 28, 2016

    SYNVISC

    FDA Adverse Event
    Injury ·GENZYME CORPORATION(RIDGEFIELD)·Product code MOZ·June 10, 2021

    SYNVISC

    FDA Adverse Event
    Injury ·GENZYME CORPORATION(RIDGEFIELD)·Product code MOZ·February 1, 2021

    PERMANENT PACEMAKER ELECTRODE

    FDA Adverse Event
    Injury ·UNKNOWN·Product code DTB·August 12, 2023

    PULSE GEN MODEL 1000

    FDA Adverse Event
    Injury ·HOUSTON·Product code LYJ·May 22, 2026

    S2 CONTROL UNIT

    FDA Adverse Event
    Other ·SOMNUS MEDICAL TECHNOLOGIES, INC.·Product code GEI·May 15, 2000

    LUCAS 2

    FDA Adverse Event
    Death ·PHYSIO-CONTROL·Product code DRM·August 12, 2023