BEUDAMED
    18 results · 42ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    BLOOD PRESSURE MONITOR

    FDA Adverse Event
    Malfunction ·VISICU, INC·Product code DXN·November 18, 2016

    ECARECOORDINATOR

    FDA Adverse Event
    Malfunction ·VISICU, INC·Product code DRG·October 13, 2016

    ECARECOORDINATOR

    FDA Adverse Event
    Malfunction ·VISICU, INC.·Product code DRG·July 2, 2015

    TELEHEALTH CENTER PRODUCT LICENSE

    FDA Adverse Event
    Death ·VISICU, INC.·Product code MSX·September 2, 2021

    ECARECOORDINATOR

    FDA Adverse Event
    Malfunction ·VISICU, INC·Product code DRG·October 14, 2016

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·VISICU, INC.·Product code MNT·October 31, 2024

    ECARECOMPANION

    FDA Adverse Event
    Injury ·VISICU, INC - DUP·Product code DXN·February 21, 2017

    ECARECOORDINATOR

    FDA Adverse Event
    Malfunction ·VISICU, INC - DUP·Product code DRG·January 19, 2017

    ECARECOMPANION

    FDA Adverse Event
    Malfunction ·VISICU, INC - DUP·Product code DXN·February 21, 2017

    ECARECOORDINATOR

    FDA Adverse Event
    Malfunction ·VISICU, INC - DUP·Product code DRG·February 22, 2017

    ECARECOMPANION

    FDA Adverse Event
    Injury ·VISICU, INC - DUP·Product code DXN·August 2, 2017

    SAMSUNG

    FDA Adverse Event
    Malfunction ·VISICU, INC - DUP·Product code MSX·January 22, 2020

    ECARECOMPANION

    FDA Adverse Event
    Injury ·VISICU, INC - DUP·Product code DRG·February 19, 2020

    ECAREMANAGER SYSTEM

    FDA Adverse Event
    Death ·VISICU, INC - DUP·Product code MSX·May 15, 2018

    PHILIPS TELEHEALTH SYSTEM

    FDA Adverse Event
    Death ·VISICU, INC - DUP·Product code DRG·April 13, 2017

    TELEHEALTH CENTER PRODUCT LICENSE

    FDA Adverse Event
    Death ·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code MSX·November 5, 2024

    TELEHEALTH CENTER PRODUCT LICENSE

    FDA Adverse Event
    Death ·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code MSX·August 28, 2024

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·February 16, 2026