BEUDAMED
    9 results · 22ms · Sources: EU EUDAMED, US FDA

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    CHALLENGE 4010 ONE CHANNEL WIDE PULSE STIMULATOR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    LEVEEN PERITINEO-VENOUS SHUNT

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    SAXON ULTRA THIN

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    UNKNOWN SCREW

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·July 2, 2019

    UNKNOWN SCREW

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·September 6, 2019

    ELLIS RIGHT TRIFLANGE SZ 25

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·September 6, 2019

    LAMITRODE 44 LEAD, 60CM LENGTH

    FDA Adverse Event
    Malfunction ·ADVANCED NEUROMODULATION SYSTEMS·Product code LGW·October 28, 2010

    INGENIO

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 1, 2014

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·November 30, 2012