BEUDAMED
    13 results · 38ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 8, 2014

    6800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 17, 2012

    9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·August 11, 2010

    HEALON DUET

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code LZP·December 19, 2013

    HEALON DUET

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code LZP·December 19, 2013

    AIRSEAL

    FDA Adverse Event
    Malfunction ·CONMED·Product code HIF·December 17, 2025

    AIRSEAL IFS, 110V

    FDA Adverse Event
    Injury ·W.O.M. WORLD OF MEDICINE GMBH·Product code HIF·October 20, 2020

    AIRSEAL IFS, 110V

    FDA Adverse Event
    Injury ·W.O.M. WORLD OF MEDICINE GMBH·Product code HIF·August 23, 2023

    AIRSEAL IFS, 110V

    FDA Adverse Event
    Malfunction ·W.O.M. WORLD OF MEDICINE GMBH·Product code HIF·June 19, 2024

    AIRSEAL IFS, 110V

    FDA Adverse Event
    Death ·W.O.M. WORLD OF MEDICINE GMBH·Product code HIF·February 27, 2023

    AIRSEAL

    FDA Adverse Event
    Injury ·W.O.M. WORLD OF MEDICINE GMBH·Product code HIF·June 12, 2025

    AIRSEAL

    FDA Adverse Event
    Malfunction ·CONMED·Product code HIF·March 10, 2026

    HEALON DUET

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code LZP·December 17, 2013