BEUDAMED
    9 results · 26ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    GLIDEWIRE GT

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

    SPRINT QUATTRO

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·February 11, 2013

    M2A-TAPER LINER SZ 41/32

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDL·July 24, 2014

    UNIFY CRT-D, DF-4 CONNECTOR

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

    GLIDEWIRE GT

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

    CONSTELLATION SURGICAL PROCEDURE PACK

    FDA Adverse Event
    Malfunction ·ALCON RESEARCH, LLC - HOUSTON·Product code LRO·November 21, 2025

    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