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

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    1st Glove Blue Nitrile Examination Gloves Powder Free

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MODIFICATION TO PYRAMID ANTERIOR PLATE FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DR Safety Syringe, Sterile Hypodermic needle for Single use

    FDA 510(k)
    FDA Class 2 ·General Hospital

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·November 11, 2021

    UNKNOWN PALMAZ STENT

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code FGE·February 22, 2018

    UNKNOWN PALMAZ STENT

    FDA Adverse Event
    Injury ·CORDIS CASHEL·Product code FGE·February 20, 2018

    UNKNOWN PALMAZ STENT

    FDA Adverse Event
    Injury ·CORDIS CASHEL·Product code FGE·February 20, 2018

    UNKNOWN PALMAZ STENT

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code FGE·February 22, 2018

    AERO STENT

    FDA Adverse Event
    Injury ·MERIT MEDICAL SYSTEMS INC.·Product code JCT·December 13, 2023

    COBAS E411 DISK SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·November 3, 2014

    APEX MONORAIL

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LOX·August 24, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 11, 2013

    UNKNOWN STRATA OR DELTA VALVES

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROSURGERY·Product code JXG·August 4, 2011

    ACRYSOF

    FDA Adverse Event
    Injury ·ALCON RESEARCH LTD. / HUNTINGTON·Product code HQL·July 26, 2012

    ACRYSOF

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD/HUNTINGTON·Product code HQL·July 26, 2012

    ACRYSOF

    FDA Adverse Event
    Injury ·ALCON RESEARCH LTD./HUNTINGTON·Product code HQL·July 26, 2012

    ACRYSOF

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD/HUNTINGTON·Product code HQL·July 26, 2012

    2.25MM PEDICLE PROBE

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC.·Product code HAW·March 6, 2026

    2.25MM PEDICLE PROBE

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC.·Product code HAW·August 25, 2025

    BD LUER-LOCK¿ SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON DE MEXICO·Product code FMF·March 14, 2023