BEUDAMED
    29 results · 21ms · Sources: EU EUDAMED, US FDA

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    ANGIOCATH PERIPHERAL VENOUS CATHETER

    FDA Adverse Event
    Other ·BECTON DICKINSON INFUSION THERAPY SYSTEMS·Product code FOZ·March 30, 2006

    INVERNESS EAR PIERCING SYSTEM

    FDA Adverse Event
    Other ·INVERNESS CORPORATION·Product code JYS·November 15, 2007

    AFFINITY 3

    FDA Adverse Event
    Other ·HILL-ROM RITTER·Product code KNC·June 8, 2006

    INVERNESS EAR PIERCING SYSTEM

    FDA Adverse Event
    Other ·INVERNESS CORP.·Product code JYS·May 22, 2007

    ACRYSOF

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD./ HUNTINGTON·Product code HQL·March 26, 2008

    CD 3700 SL

    FDA Adverse Event
    Other ·ABBOTT LABORATORIES DIV/ CELLDYN·Product code JJE·October 11, 2006

    UNICEL DXL 800 ACCESS IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Other ·BECKMAN COULTER, INC.·Product code JJE·November 20, 2006

    VASCULIGHT

    FDA Adverse Event
    Other ·LUMENIS LTD·Product code GEX·March 9, 2007

    VASCULIGHT

    FDA Adverse Event
    Other ·LUMENIS LTD·Product code GEX·March 9, 2007

    ACRYSOF RESTOR

    FDA Adverse Event
    Other ·ALCON LABORATORIES, INC./HUNTINGTON·Product code HQL·October 20, 2006

    ACRYSOF RESTOR

    FDA Adverse Event
    Other ·ALCON LABORATORIES, INC./HUNTINGTON·Product code HQL·October 20, 2006

    VASCULIGHT HR

    FDA Adverse Event
    Other ·LUMENIS, LTD.·Product code GEX·May 9, 2007

    LIGHTSHEER (ALL MODELS)

    FDA Adverse Event
    Other ·LUMENIS, INC.·Product code GEX·April 3, 2007

    LUMENIS 1

    FDA Adverse Event
    Other ·LUMENIS LTD·Product code GEX·May 9, 2007

    LUMENIS ONE

    FDA Adverse Event
    Other ·LUMENIS·Product code GEX·March 15, 2007

    LUMENIS

    FDA Adverse Event
    Other ·LUMENIS·Product code GEX·March 15, 2007

    OLYMPUS EVIS EXERA COLONOVIDEOSCOPE

    FDA Adverse Event
    Other ·OLYMPUS MEDICAL SYSTEM CORP·Product code FDF·July 2, 2012

    VASCULIGHT ELITE

    FDA Adverse Event
    Other ·LUMENIS·Product code GEX·March 13, 2007

    VASULIGHT SR

    FDA Adverse Event
    Other ·LUMENIS·Product code GEX·March 15, 2007

    LIGHTSHEER

    FDA Adverse Event
    Other ·LUMENIS·Product code GEX·June 29, 2006