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

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    EUROMI

    FDA Adverse Event
    Malfunction ·EUROMI·Product code GEA·March 29, 2023

    EUROMI REUSABLE CANNULA

    FDA Adverse Event
    Injury ·EUROMI SA·Product code GEA·June 23, 2023

    EUROMI REUSABLE CANNULA

    FDA Adverse Event
    Malfunction ·EUROMI SA·Product code GEA·June 27, 2023

    CANNULA

    FDA Adverse Event
    Malfunction ·EUROMI SA·Product code GEA·April 17, 2023

    CANULE VITERBO 3*250 MM TUNGSTÈNE

    FDA Adverse Event
    Malfunction ·EUROMI SA·Product code GEA·April 14, 2023

    CANNULA

    FDA Adverse Event
    Malfunction ·EUROMI SA·Product code GEA·April 17, 2023

    REBELO 5*350 TITANIUM

    FDA Adverse Event
    Malfunction ·EUROMI SA·Product code GEA·June 28, 2023

    EVAMATIC

    FDA Adverse Event
    Injury ·EUROMI SA·Product code QPB·June 28, 2023

    CANNULAS

    FDA Adverse Event
    Malfunction ·EUROMI SA·Product code GEA·November 8, 2024

    EURO-MED

    FDA Adverse Event
    Injury ·COOPERSURGICAL, INC.·Product code EME·August 5, 2003

    EURO-MED

    FDA Adverse Event
    Injury ·COOPERSURGICAL, INC.·Product code EME·February 18, 2003

    EURO-MED

    FDA Adverse Event
    Injury ·COOPERSURGICAL, INC.·Product code KNW·March 29, 2007

    EURO-MED

    FDA Adverse Event
    Injury ·COOPERSURGICAL, INC.·Product code KNW·March 29, 2007

    EURO-MED

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code KNW·October 3, 2007

    EURO-MED

    FDA Adverse Event
    Injury ·COOPERSURGICAL, INC.·Product code EME·November 1, 2007

    EURO-MED

    FDA Adverse Event
    Injury ·COOPERSURGICAL, INC.·Product code KNW·September 4, 2009

    EURO-MED

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code KNW·July 12, 2007

    EURO-MED

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code KNW·April 2, 2008

    HL20 INTEGRATED PERFUSION SYSTEM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTQ·August 1, 2016

    HL20 INTEGRATED PERFUSION SYSTEM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTQ·January 14, 2016