BEUDAMED
    7 results · 24ms · 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 ×

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·January 15, 2011

    MEDTRONIC IPG

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVZ·July 17, 2019

    MEDTRONIC IPG

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVZ·July 17, 2019

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 19, 2013

    PALMAZ GENESIS OPTA PRO

    FDA Adverse Event
    Injury ·CORDIS EUROPA, N.V.·Product code FGE·March 8, 2011

    AXSYM DIGOXIN III

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS INTERNATIONAL, LTD.·Product code KXT·May 11, 2007

    SPECTRA OPTIA

    FDA Adverse Event
    Death ·TERUMO BCT·Product code LKN·January 7, 2026