BEUDAMED
    12 results · 25ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    QDOT MICRO

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code OAE·May 27, 2026

    QDOT MICRO

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code OAE·April 28, 2026

    QDOT MICRO

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code OAE·May 19, 2026

    NGEN RF GENERATOR

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code OAE·December 16, 2025

    NGEN RF GENERATOR, JAPAN

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code LPB·April 21, 2023

    QDOT MICRO

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code OAE·March 6, 2026

    QDOT MICRO

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code OAE·February 6, 2026

    SPINAL SET 25GA 3-1/2IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code MIA·December 27, 2023

    1.0MM TI CABLE WITH CRIMP DOUBLE LEAD 470MM-STERILE

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code JDQ·December 18, 2015

    CE 2 ML PATIENT CONTROL MODULE SINGLE PACK 6/CARTON

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP.·Product code MEA·October 21, 2008

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·June 27, 2013

    ENDO GIA UNIVERSAL 12MM SINGLE USE INST

    FDA Adverse Event
    Injury ·UNITED STATES SURGICAL A·Product code GDW·August 2, 2011