BEUDAMED
    512 results · 68ms · Sources: EU EUDAMED, US FDA

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    HEARTSTART XL DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHILIPS NORTH AMERICA LLC·Product code MKJ·November 4, 2024

    BIG WHEELS WALKER KIT

    FDA Adverse Event
    Injury ·JOBAR INTERNATIONAL, INC·Product code ITJ·August 18, 2023

    BIG WHEELS WALKER KIT

    FDA Adverse Event
    Injury ·JOBAR INTERNATIONAL, INC·Product code ITJ·August 18, 2023

    V60 VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code MNT·February 9, 2016

    V200 VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC.·Product code CBK·August 20, 2014

    LIFEPAK CR PLUS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·December 16, 2010

    V60 VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code MNT·August 5, 2016

    V60 VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code MNT·May 5, 2016

    LIFEPAK CR PLUS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·August 5, 2010

    CARDIOSAVE RESCUE

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·August 30, 2021

    STRYKER INTERNAL DEFIBRILLATION PADDLES, LP20

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code LDD·May 21, 2025

    V200 VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code CBK·January 6, 2020

    CONSTELLATION VISION SYSTEM

    FDA Adverse Event
    Malfunction ·ALCON RESEARCH, LLC - IRVINE TECHNOLOGY CENTER·Product code HQC·July 12, 2019

    HANDLES AND CONNECTOR WITH DISCHARGE CONTROL FOR INTERNAL DEFIBRILLATION

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code LDD·December 18, 2013

    CARDIOSAVE HYBRID TYPE I (AU)

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·February 16, 2024

    CARDIOSAVE HYBRID TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE MAHWAH·Product code DSP·November 28, 2018

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNT·August 22, 2023

    INFINITI VISION SYSTEM

    FDA Adverse Event
    Malfunction ·ALCON RESEARCH, LTD. - IRVINE TECHNOLOGY CENTER·Product code HQC·September 20, 2016

    V60 VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code MNT·February 28, 2019

    LIFEPAK CR PLUS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·November 6, 2009