BEUDAMED
    5 results · 27ms · 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 ×

    SIMON NITINOL FILTER

    FDA Adverse Event
    Injury ·NITINOL MEDICAL TECHNOLOGIES, INC.·Product code DTK·September 23, 1996

    X-SUIT NIR COVERED BILIARY METALLIC STENT

    FDA Adverse Event
    Malfunction ·MEDINOL LTD.·Product code FGE·December 27, 2017

    LEGACY 3 IMPLANT

    FDA Adverse Event
    Injury ·IMPLANT DIRECT SYBRON MANUFACTURING, LLC·Product code DZE·February 6, 2013

    FINELINE II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·January 6, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 22, 2014