BEUDAMED
    10 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    CARTIVA

    FDA Adverse Event
    Injury ·CARTIVA, INC·Product code PNW·July 21, 2020

    NA

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·May 5, 2026

    MICRA

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code PNJ·December 30, 2019

    VERCISE GENUS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC NEUROMODULATION·Product code NHL·February 9, 2024

    AUTOPULSE RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·May 20, 2013

    UNICEL® DXC 600I SYNCHRON® ACCESS® CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·July 5, 2011

    RSVR MMT-326A 10PK PRDGM 1.8ML 13L

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code FMF·August 27, 2008

    CARTIVA DEVICE 10MM T20-0329

    FDA Adverse Event
    Injury ·CARTIVA, INC·Product code PNW·April 23, 2021

    VERCISE GENUS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC NEUROMODULATION·Product code NHL·November 15, 2023

    MICRA

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code PNJ·December 27, 2019