BEUDAMED
    5 results · 19ms · 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 ×

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·September 14, 2016

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·December 30, 2013

    BIPOL LEAD MODEL 300

    FDA Adverse Event
    Malfunction ·CYBERONICS INC·Product code LYJ·February 21, 2013

    MARATHON MICRO CATHETER

    FDA Adverse Event
    Malfunction ·EV3 NEUROVASCULAR·Product code KRA·January 28, 2011

    ESSURE

    FDA Adverse Event
    Injury ·BAYER·Product code HHS·July 28, 2014