BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SUPERION INDIRECT DECOMPRESSION SYSTEM

    FDA Adverse Event
    Injury ·VERTIFLEX INC.·Product code NQO·April 10, 2020

    SLIDE WHITE APEX SUPERIOR ADHESIVE

    FDA Adverse Event
    Injury ·Product code KEW·January 28, 2022

    PORTEX® CUFFED BLUE LINE ULTRA® TRACHEOSTOMY TUBE

    FDA Adverse Event
    Injury ·SMITHS MEDICAL ASD, INC.·Product code JOH·February 1, 2019

    SLIDE WHITE APEX SUPERIOR ADHESIVE

    FDA Adverse Event
    Malfunction ·LEICA BIOSYSTEMS·Product code KES·July 16, 2024

    TRACHEOSTOMY PVC - PORTEX TUBES BLUE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code BTO·October 13, 2022

    PORTEX BLUE LINE ULTRA TRACHEOSTOMY TUBE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL INTERNATIONAL, LTD.·Product code BTO·April 28, 2023

    TECNIS 1 MULTIFOCAL

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code MFK·October 22, 2012

    SPECTRUM INFUSION PUMP

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

    PULSE GEN MODEL UNK

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·August 11, 2010