BEUDAMED
    6 results · 20ms · 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 ×

    4874946

    FDA Adverse Event
    Malfunction ·June 26, 2015

    MENTOR MEMORYGEL XTRA BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·December 9, 2025

    TDX/TDXFLX CANNABINOIDS REAGENT

    FDA Adverse Event
    Injury ·ABBOTT HEALTH PRODUCTS, INC.·Product code LDJ·November 8, 2006

    HEARTSTART ONSITE

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 25, 2014

    AED10

    FDA Adverse Event
    Malfunction ·WELCH ALLYN PROTOCOL, INC.·Product code MKJ·October 13, 2010

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 16, 2012