BEUDAMED
    3 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PENUMBRA SYSTEM REPERFUSION CATHETER 054

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code NRY·January 11, 2013

    NONE

    FDA Adverse Event
    Malfunction ·OGDEN MANUFACTURING·Product code FJI·November 3, 2010

    SELF CENT HIP 53X28 BLU

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.-1818910·Product code KWY·July 3, 2014