BEUDAMED
    5 results · 17ms · 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 ×

    SPIROFLEX® ANGIOJET® THROMBECTOMY SET

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DXE·August 17, 2016

    TI PEDICLE HOOK/DUAL-OPENING SIDE

    FDA Adverse Event
    Malfunction ·SYNTHES·Product code KWP·February 8, 2013

    FIBER ONE

    FDA Adverse Event
    Malfunction ·AMS INNOVATION CENTER-SILICON VALLEY·Product code GEX·December 7, 2010

    CAPTURE-R SELECT

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSS·July 22, 2014

    NEXGEN MIS STEMMED TIBIAL COMPONENT

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code JWH·October 4, 2016