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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    Cellvizio I.V.E. with Confocal Miniprobes

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690198260·AK3 PS Insert Trial Size 4, 16mm

    TRILOGY 200 VENTILATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    NEXUS DRF DIGITAL X-RAY IMAGING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    TRILOGY 200

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC·Product code CBK·August 19, 2020

    CARDIOCHEK PLUS ANALYZER

    FDA Adverse Event
    Malfunction ·PTS DIAGNOSTICS·Product code CGA·June 16, 2025

    CARDIOCHEK PLUS ANALYZER

    FDA Adverse Event
    Malfunction ·PTS DIAGNOSTICS·Product code CGA·June 16, 2025

    CARDIOCHEK PLUS ANALYZER

    FDA Adverse Event
    Malfunction ·PTS DIAGNOSTICS·Product code CGA·October 22, 2025

    CARDIOCHEK PLUS ANALYZER

    FDA Adverse Event
    Malfunction ·PTS DIAGNOSTICS·Product code CGA·February 12, 2025

    PRECISION LINK

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC., USA·Product code NBW·October 7, 2008

    MULTI-LUMEN PI CVC KIT: 4-L 8.5 FR X 8IN

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC·Product code FOZ·July 13, 2011

    WALKING BOOT, BRACE

    FDA Adverse Event
    BLEDSOE COMPANY·Product code IQI·June 26, 2013

    CARDIOCHEK PLUS ANALYZERQ

    FDA Adverse Event
    Malfunction ·PTS DIAGNOSTICS·Product code CGA·August 18, 2022

    CARDIOCHEK PLUS ANALYZER

    FDA Adverse Event
    Malfunction ·PTS DIAGNOSTICS·Product code CGA·July 28, 2023

    CARDIOCHEK PLUS ANALYZER

    FDA Adverse Event
    Malfunction ·PTS DIAGNOSTICS·Product code CGA·May 24, 2024

    CARDIOCHEK PLUS ANALYZER

    FDA Adverse Event
    Malfunction ·PTS DIAGNOSTICS·Product code CGA·January 6, 2023

    CARDIOCHEK PLUS ANALYZER

    FDA Adverse Event
    Malfunction ·PTS DIAGNOSTICS·Product code CGA·January 11, 2024

    CARDIOCHEK PLUS ANALYZER

    FDA Adverse Event
    Malfunction ·PTS DIAGNOSTICS·Product code CGA·November 21, 2023

    CARDIOCHEK PLUS ANALYZER

    FDA Adverse Event
    Malfunction ·PTS DIAGNOSTICS·Product code CGA·June 14, 2024

    CARDIOCHEK PLUS ANALYZER

    FDA Adverse Event
    Malfunction ·PTS DIAGNOSTICS·Product code CGA·February 24, 2023