BEUDAMED
    8 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    GORE DRYSEAL FLEX INTRODUCER SHEATH

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code DYB·October 19, 2020

    GORE® DRYSEAL FLEX INTRODUCER SHEATH

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DYB·October 6, 2016

    530G INSULIN PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·November 18, 2014

    EON MINI 16 - CHANNEL RECHARGEABLE IPG

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·August 25, 2011

    TENDRIL ST

    FDA Adverse Event
    Death ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·August 1, 2013

    GORE® DRYSEAL FLEX INTRODUCER SHEATH

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code DYB·May 30, 2023

    ZIMMON BILIARY STENT SET

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·February 18, 2021

    VERSAONE

    FDA Adverse Event
    Malfunction ·DAVIS & GECK CARIBE LTD·Product code GCJ·March 24, 2025