BEUDAMED
    10 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    OPTISENSE LEAD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.·Product code NVN·December 26, 2018

    GLIDEWIRE GT

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·March 30, 2026

    PULSE GEN MODEL 105

    FDA Adverse Event
    Death ·CYBERONICS, INC.·Product code LYJ·February 11, 2013

    TENDRIL SDX

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·January 10, 2011

    ANIMAS INSULIN CARTRIDGE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 24, 2014

    GLIDEWIRE GT

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·May 29, 2026

    TITANIUM HEXALOBE SET SCREW, 8.5MM

    FDA Adverse Event
    Malfunction ·ALPHATEC SPINE INC·Product code KWP·July 23, 2013

    RADIFOCUS GLIDEWIRE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·November 26, 2025

    TERUMO RADIFOCUS GUIDE WIRE

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·July 3, 2025

    GLIDEWIRE GT

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·February 21, 2018