BEUDAMED
    7 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SCREWDRIVER SHAFT, COMPRESSION T2 TIBIA 3.5 MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code HXX·July 27, 2012

    ACCU-CHEK ® PERFORMA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·May 23, 2014

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Injury ·INSULET CORPORATION·Product code LZG·November 2, 2012

    SYMPHONY

    FDA Adverse Event
    Injury ·SORIN CRM·Product code NVZ·September 7, 2010

    USP II HUMERAL HEAD 44/17

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·December 7, 2020

    GLENOID, POLY WITH KEEL, SMALL

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·December 7, 2020

    UNIVERS II HUMERAL STEM 8MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·December 7, 2020