BEUDAMED
    3 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·April 17, 2014

    EXTERNAL PULSE GENERATOR

    FDA Adverse Event
    Injury ·MEDTRONIC MILACA INC.·Product code DTE·October 31, 2012

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·August 17, 2010