BEUDAMED
    3 results · 28ms · 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 ×

    CONSULTA CRT-D

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code NIK·June 10, 2014

    CONSULTA

    FDA Adverse Event
    Malfunction ·MEDTRONIC S.A.·Product code NIK·October 12, 2010

    PULSE-GENERATOR, PACEMAKER, EXTERNAL

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code DTE·December 10, 2012