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

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    Filters FDA Adverse Event ×

    ZIPWIRE HYDROPHILIC GUIDEWIRE

    FDA Adverse Event
    Injury ·LAKE REGION MFG., INC.·Product code DQX·May 27, 2015

    HEMOSPLIT XK LONG-TRM HEMODIALYSIS CATHETER 16F STANDARD

    FDA Adverse Event
    Injury ·BARD EYNOSA S.A DE C.V·Product code MSD·May 22, 2015

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON LABORATORIES IRELAND LTD·Product code HQL·April 3, 2013

    FLEXTEND

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·April 5, 2011

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code NIQ·May 7, 2008

    DAVINCI XI

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·November 13, 2020

    EVOLUT FX DCS

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code NPT·July 29, 2025

    DAVINCI XI

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·December 28, 2023