BEUDAMED
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    Filters FDA Adverse Event ×

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD./HUNTINGTON·Product code MFK·November 6, 2009

    ACRYSOF RESTOR

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD./HUNTINGTON·Product code MFK·November 20, 2009

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code MFK·November 13, 2009

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON RESEARCH LTD.·Product code MFK·December 4, 2009

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code MFK·December 4, 2009

    ALINITY I PROCESSING MODULE

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code JJE·November 10, 2023

    ACRYSOF IQ TORIC

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code MJP·November 18, 2009

    ACRYSOF IQ TORIC

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code MJP·October 30, 2009

    ACRYSOF RESTOR

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD./HUNTINGTON·Product code MFK·November 20, 2009

    ACRYSOF RESTOR

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD./HUNTINGTON·Product code MFK·November 20, 2009

    UNK - IOL

    FDA Adverse Event
    Injury ·ALCON MANUFACTURING, LTD./ HUNTINGTON·Product code HQL·October 21, 2009

    UNK -- IOL

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·October 30, 2009

    ACRYSOF IQ TORIC

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD./ HUNTINGTON·Product code HQL·October 23, 2009

    ACRYSOF IQ TORIC

    FDA Adverse Event
    Other ·ALCON RESEARCH LTD/HUNTINGTON·Product code MJP·October 30, 2009

    ACRYSOF RESTOR

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code MFK·November 18, 2009

    ETHICON

    FDA Adverse Event
    Malfunction ·ASCENT·Product code GCJ·September 17, 2009

    TIMAX

    FDA Adverse Event
    Malfunction ·NSK TOCHIGI-KEN (JAPAN)·Product code EGS·October 15, 2009

    TIMAX

    FDA Adverse Event
    Injury ·NSK TOCHIGI-KEN (JAPAN)·Product code EGS·September 23, 2010

    *

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS·Product code LJT·July 28, 2010

    AZURION

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code OWB·April 3, 2026