BEUDAMED
    13 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SS COMPRESSION HIP SCREW LAG SCREW

    FDA Adverse Event
    Injury ·BIOMET TRAUMA·Product code KTT·September 19, 2016

    FENESTRATED BIPOLAR FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·February 21, 2013

    LIFEPAK 12 DEFIBRILLATOR/MONITOR SERIES

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·January 20, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·August 1, 2014

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·April 26, 2018

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI, INC.·Product code EGS·May 12, 2015

    NSK

    FDA Adverse Event
    Malfunction ·NAKANISHI INC.·Product code EGS·October 9, 2025

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·December 19, 2016

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·March 1, 2018

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·January 15, 2018

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·June 6, 2018

    DA-800C5L

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·May 2, 2016

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·April 26, 2018