BEUDAMED
    10 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    VARIPULSE¿ BI-DIRECTIONAL CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code QZI·May 21, 2026

    TRUPULSE¿ GENERATOR

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code QZI·December 1, 2025

    TRUPULSE¿ GENERATOR

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code QZI·April 21, 2026

    SIGMA CRVD XLK INS 5 8MM

    FDA Adverse Event
    Injury ·DEPUY-CORK, A DIVISION OF DEPUY ORTHOPAEDICS·Product code JWH·November 19, 2008

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 8, 2011

    ENERGEN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 22, 2013

    UNKNOWN EGIA TRI STAPLE

    FDA Adverse Event
    Malfunction ·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·March 23, 2023

    UNKNOWN EGIA TRI STAPLE

    FDA Adverse Event
    Malfunction ·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·April 19, 2023

    DVR PEG SMOOTH 2.0MM X 26MM

    FDA Adverse Event
    Malfunction ·BIOMET TRAUMA·Product code LXT·July 7, 2017

    DVR PEG SMOOTH 2.0MM X 18MM

    FDA Adverse Event
    Malfunction ·BIOMET TRAUMA·Product code LXT·July 7, 2017