BEUDAMED
    10 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: Malfunction ×

    FLOGARD

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 13, 2011

    XMAX MOTOR

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code ERL·June 11, 2013

    PROLIEVE THERMODILITATION KIT

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MEQ·September 12, 2008

    KANEKA PTCA CATHETER CO-R7 (IKAZUCHI ZERO)

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code LOX·April 14, 2022

    KANEKA PTCA CATHETER CO-R7 (IKAZUCHI ZERO)

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code LOX·December 21, 2020

    KANEKA PTCA CATHETER CO-R7 (IKAZUCHI ZERO)

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code LOX·April 13, 2022

    KANEKA PTCA CATHETER CO-R7 (IKAZUCHI ZERO)

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code LOX·October 29, 2021

    NEON PTCA BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code LOX·August 24, 2022

    KANEKA PTCA CATHETER ZINRAI

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code LOX·March 31, 2022

    HEARTMATE II LVAS IMPLANT KIT (WITH SEALED GRAFTS)

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·February 7, 2022