BEUDAMED
    3 results · 26ms · 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 ×

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 14, 2014

    BREAST IMPLANT EXPANDER/SMOOTH ROUND SPECTRUM SALINE

    FDA Adverse Event
    MENTOR CORP·Product code FWM·December 11, 2012

    PLM A+3 MEDNET WRLSS

    FDA Adverse Event
    Malfunction ·HOSPIRA, INC.·Product code FRN·September 20, 2010