BEUDAMED
    5 results · 23ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    V18 CONTROL WIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORP·Product code DQX·March 16, 2007

    V18 CONTROL WIRE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DQX·May 23, 2007

    AVAULTA PLUS BIOSYNTHETIC SUPPORT SYSTEM - POSTERIOR

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (COVINGTON)·Product code FTL·January 28, 2013

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·February 1, 2014

    8800

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD·Product code JAA·November 24, 2010