BEUDAMED
    3 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    INSIGNIA

    FDA Adverse Event
    Injury ·GUIDANT CLONMEL IRELAND·Product code NVZ·October 5, 2010

    ASPHERE M SPEC 12/14 40 +1.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code JDI·November 30, 2012

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·June 6, 2014