BEUDAMED
    28 results · 62ms · Sources: EU EUDAMED, US FDA

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    UF-100I SYSTEM MODULE

    FDA Adverse Event
    Other ·DATA INNOVATIONS, INC.·Product code KQO·February 6, 2013

    INSTRUMENT MANAGER SOFTWARE

    FDA Adverse Event
    Malfunction ·DATA INNOVATIONS, INC.·Product code JQP·January 7, 2013

    UF100I SYSTEM MODULE

    FDA Adverse Event
    Other ·DATA INNOVATIONS, INC.·Product code JQP·April 22, 2013

    INSTRUMENT MANAGER SOFTWARE

    FDA Adverse Event
    Malfunction ·DATA INNOVATIONS, INC.·Product code JQP·September 13, 2007

    INSTRUMENT MANAGER SOFTWARE

    FDA Adverse Event
    Malfunction ·DATA INNOVATIONS, INC.·Product code JQP·February 20, 2009

    INSTRUMENT MANAGER SOFTWARE

    FDA Adverse Event
    Malfunction ·DATA INNOVATIONS, INC.·Product code JQP·August 16, 2006

    INSTRUMENT MANAGER SOFTWARE

    FDA Adverse Event
    Malfunction ·DATA INNOVATIONS, INC.·Product code JQP·December 17, 2013

    SHOWER CHAIR

    FDA Adverse Event
    Malfunction ·INNOVATIVE PRODUCTS·September 15, 1993

    COULTER FC500 FLOW CYTOMETER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·November 15, 2011

    INSTRUMENT MANAGER SOFTWARE

    FDA Adverse Event
    Malfunction ·DATA INNOVATIONS LLC·Product code JQP·July 8, 2019

    JRESULTNET USING PROVUE DRIVER V1.5.3 OR LOWER

    FDA Adverse Event
    Malfunction ·DATA INNOVATIONS LLC·Product code JQP·August 22, 2014

    FC 500 WITH UPS

    FDA Adverse Event
    Other ·BECKMAN COULTER, INC.·Product code LXG·August 16, 2007

    TOSOH HLC-723G8 ANALYZER G8

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·March 23, 2018

    FC 500 WITH CXP SOFTWARE

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code LXG·November 21, 2007

    UNK_SMART TOUCH UNIDIRECTIONAL

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code LPB·October 7, 2022

    TOSOH HLC-723G8 ANALYZER G8

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·March 14, 2018

    PROLENE POLYPROPYLENE MESH UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·July 16, 2024

    ALLERGAN CUP (GORTEX)

    FDA Adverse Event
    Malfunction ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code LPN·September 23, 2020

    A1A-360

    FDA Adverse Event
    Malfunction ·TOSOH BIOSCIENCE, INC.·Product code KHO·March 30, 2018

    TOSOH HLC-723G8 ANALYZER G8

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·March 23, 2018