BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA,INC.·Product code LWP·June 10, 2014

    CONCERTO CRT-D DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code NIK·October 12, 2010

    GOBED II

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·November 9, 2012

    COMP RVS TRAY CO 44MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·March 14, 2019

    E1 44-41 STD +3 HMRL BRG

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PAO·March 14, 2019

    COMP RVSR SHLDR GLNSP +3 41MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PHX·March 14, 2019

    HERBERT PM COMPR RVS HA BP

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HSD·March 14, 2019

    VERSA-DIAL/COMP TI STD TAPER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBF·March 14, 2019