BEUDAMED
    9 results · 18ms · 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 Status: Death ×

    HOVERMATT

    FDA Adverse Event
    Death ·Product code FRZ·December 22, 2014

    HOVERMATT

    FDA Adverse Event
    Death ·Product code FRZ·December 17, 2014

    HOVERMATT

    FDA Adverse Event
    Death ·D.T. DAVIS ENTERPRISES LTD.·Product code FRZ·December 22, 2014

    VIVAX MOBILITY SYSTEM (NOVA BED)

    FDA Adverse Event
    Death ·VIVAX MEDICAL CORP.·Product code FRZ·January 15, 1998

    1224873-1998-00001

    FDA Adverse Event
    Death ·Product code FRZ·January 15, 1998

    CODE ALERT

    FDA Adverse Event
    Death ·RF TECHNOLOGIES, INC.·Product code KMI·March 15, 2002

    SENSATEC

    FDA Adverse Event
    Death ·RF TECHNOLOGIES, INC·Product code KMI·February 7, 2007

    WONDERGUARD

    FDA Adverse Event
    Death ·RF TECHNOLOGIES, INC·Product code KMI·October 22, 2002

    STRETTA 8800 CATHETER AND ACCESSORIES KIT

    FDA Adverse Event
    Death ·MEDERI THERAPEUTICS / MEDERI RF LLC·Product code GEI·August 5, 2019