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

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    Filters FDA Adverse Event ×

    BOOMERANG PEEK FUSION DEVICE

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code MQP·January 14, 2011

    60-00302-01 PEDI 1/P 60/CA

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code MKJ·August 13, 2019

    HT70 VENTILATOR

    FDA Adverse Event
    Injury ·NEWPORT MEDICAL INSTRUMENTS·Product code CBK·March 27, 2013

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC·Product code GJS·March 21, 2011

    UNK DEPUY HIP LINER

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWB·April 16, 2008

    ALINITY I PROCESSING MODULE

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code JJE·May 10, 2021