BEUDAMED
    5 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    POLARIS ULTRA

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FAD·June 27, 2019

    FRESENIUS 2008K

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KDI·April 25, 2014

    LEAD MODEL UNKNOWN

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·October 31, 2012

    TRIDENT 0X3 INSERT 32 MM ID

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code LPH·August 12, 2010

    INTRFX ADV - LG 30MM INSERTER

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code LXH·January 10, 2022