BEUDAMED
    12 results · 36ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    PULSE GEN MODEL 101

    FDA Adverse Event
    Injury ·CYBERONICS INC·Product code LYJ·February 21, 2013

    HEARTSTART MRX - EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·January 20, 2011

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·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