BEUDAMED
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    Filters FDA Adverse Event × Regulation: Us FDA × Clear all

    PERCUTANEOUS SHEATH INTRODUCER SET

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES PR·Product code DQY·April 24, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 1, 2012

    MINI-CAP, DISCONNECT W/PVP-1SOLUTION

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·July 27, 2010