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

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    Filters FDA Adverse Event ×

    COMPREHENSIVE MD HYBRID GLENOID BASE 4MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·October 18, 2018

    COMPREHENSIVE VERSA-DIAL/COMP TI STD TAPER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HSD·October 18, 2018

    COMPREHENSIVE MINI HUMERAL STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·October 18, 2018

    COMPREHENSIVE VERSA-DIAL 50X24X52 HUMERAL HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HSD·October 18, 2018

    COMPREHENSIVE PT HYBRID GLENOID POST REGENEREX

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·October 18, 2018

    MD HYBRID GLENOID BASE 4MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·October 2, 2017

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 14, 2014

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·October 12, 2012

    MAMMOTOME** EX PROBE AND VACUUM SET

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code KNW·August 10, 2010

    STERIS SYSTEM 1E

    FDA Adverse Event
    STERIS CORPORATION - HOPKINS·Product code MED·August 23, 2013