BEUDAMED
    44 results · 25ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event × Regulation: Us FDA × Clear all

    VANGUARD DCM CR TIBIAL BEARING

    FDA Adverse Event
    Malfunction ·BIOMET, INC.·Product code JWH·May 20, 2008

    INSPIRE 8F M HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·May 5, 2020

    INSPIRE 8F M

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DTZ·January 3, 2024

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 18, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 22, 2013

    SYNCHRON® LX20 PRO ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·July 28, 2011

    ARCOM SERIES A STANDARD PATELLA

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 20, 2018

    INSPIRE 8F M

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA·Product code DTZ·January 4, 2024

    INSPIRE OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DTZ·March 12, 2026

    INSPIRE OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DTZ·March 12, 2026

    INSPIRE 8F

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA·Product code DTZ·November 5, 2025

    INSPIRE 8F

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA·Product code DTZ·November 5, 2025

    INSPIRE OXYGENATOR

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA·Product code DTZ·December 11, 2025

    INSPIRE 8F M HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·April 20, 2021

    INSPIRE 8F M HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·September 11, 2020

    INSPIRE 8F M HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·December 23, 2020

    INSPIRE 8F

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA SRL·Product code DTZ·July 24, 2025

    INSPIRE 8F M

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DTZ·June 7, 2023

    INSPIRE 8F M HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·August 5, 2022

    INSPIRE 8F M

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·December 6, 2022