BEUDAMED
    14 results · 61ms · Sources: EU EUDAMED, US FDA

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    LCC - PEEK 5 DEGREES MEDIUM SPACER - 10MM X 20MM X 8MM

    FDA Adverse Event
    Malfunction ·ALPHATEC SPINE INC·Product code MQP·February 12, 2015

    KYPHX INFLATABLE BONE TAMP

    FDA Adverse Event
    Injury ·MEDTRONIC SPINE LLC·Product code HRX·September 24, 2010

    DEVICE FOR SPINAL SURGERY FOR 1180 (EU)

    FDA Adverse Event
    Injury ·HOLGER ULLRICH·Product code FWZ·July 13, 2018

    LUCEA 50

    FDA Adverse Event
    Injury ·MAQUET SAS·Product code FSY·January 26, 2018

    NEXUS® BONESCALPEL® 25MM BLUNT BLADE AND IRRIGATION TUBING KIT

    FDA Adverse Event
    Malfunction ·MISONIX, INC.·Product code LFL·September 4, 2024

    2953769-2011-00016

    FDA Adverse Event
    Malfunction ·MEDTRONIC SPINE LLC·Product code NDN·February 14, 2011

    X-STOP IPD SYSTEM

    FDA Adverse Event
    Other ·MEDTRONIC SPINE LLC.·Product code NQO·August 26, 2009

    ARTIFICIAL CERVICAL DISC

    FDA Adverse Event
    Injury ·SPINAL KINETICS LLC·Product code MJO·June 30, 2020

    OT ULTRA EASY

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code NBW·August 30, 2010

    MW5080740

    FDA Adverse Event
    Injury ·October 22, 2018

    NEXUS® BONESCALPEL® 20MM, BLUNT BLADE + IRRIGATION TUBING KIT

    FDA Adverse Event
    Malfunction ·MISONIX, INC.·Product code LFL·October 25, 2024

    NEXUS® STANDARD HANDPIECE

    FDA Adverse Event
    Injury ·MISONIX, INC.·Product code LFL·July 18, 2023

    NEXUS® BONESCALPEL® 20MM, UNI-LATERAL SERRATED BLADE + IRRIGATION TUBING KIT

    FDA Adverse Event
    Malfunction ·MISONIX, INC.·Product code LFL·November 6, 2024

    NEXUS® BONESCALPEL® MIS 10 MM BLADE AND SHEATH + IRRIGATION TUBING KIT

    FDA Adverse Event
    Malfunction ·MISONIX, INC.·Product code LFL·November 6, 2024