BEUDAMED
    22 results · 34ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    QUANTA SYSTEM S.P.A.

    FDA Adverse Event
    Malfunction ·QUANTA SYSTEM, S.P.A.·Product code GEX·July 10, 2015

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·October 7, 2021

    HAMILTON MEDICAL AG

    FDA Adverse Event
    Malfunction ·HAMILTON MEDICAL AG·Product code CBK·July 13, 2023

    HAMILTON MEDICAL AG

    FDA Adverse Event
    Malfunction ·HAMILTON MEDICAL AG·Product code CBK·July 13, 2023

    HAMILTON MEDICAL AG

    FDA Adverse Event
    Malfunction ·HAMILTON MEDICAL AG·Product code CBK·July 21, 2023

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code MEA·June 26, 2025

    25 G X 1 IN. BD ECLIPSE¿ NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FMI·January 19, 2016

    IFS

    FDA Adverse Event
    Malfunction ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code HNO·December 10, 2019

    COBAS 8000 ISE 900 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·February 5, 2025

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNT·October 28, 2025

    RESOLUTE ONYX RX

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code NIQ·April 24, 2020

    SORIN HEATER-COOLER SYSTEM 3T

    FDA Adverse Event
    Malfunction ·SORIN GROUP DEUTSCHLAND·Product code DWC·August 9, 2016

    RESOLUTE ONYX RX

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·April 24, 2020

    PORTICO TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code NPT·June 15, 2023

    PORTICO TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Death ·ABBOTT MEDICAL·Product code NPT·June 15, 2023

    COREVALVE TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·May 4, 2020

    EVOLUT R TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·May 4, 2020

    PYXIS ANESTHESIA SYSTEM ES

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·March 4, 2024

    SJM TRIFECTA VALVE

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code LWR·June 15, 2023

    CAPIOX FX OXYGENATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·February 8, 2017