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

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    MODIFICATION OF TISSUE DILATOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SWAN GANZ CATHETER PLACEMENT KIT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SonoSite iViz Ultrasound System

    FDA 510(k)
    FDA Class 2 ·Radiology

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code NIQ·December 7, 2012

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·January 23, 2014

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·June 23, 2015