BEUDAMED
    9 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 ×

    O2asis Personal Oxygen Humidifier

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690198222·AK3 PS Insert Trial Size 4, 11mm

    9.3MHZ MICROVASCULAR PROBE

    FDA UDI
    PARKS MEDICAL ELECTRONICS, INC.·00816787021578·

    EDWARD VENT CATHETERS EDWARD VENT CATHETERS WITH DURAFLO COATING DISPERSION AORTIC PERFUSION CANNULA

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    IDEAL IQ SOFTWARE OPTION

    FDA 510(k)
    FDA Class 2 ·Radiology

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 23, 2025

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·October 7, 2008

    VASOVIEW HEMOPRO

    FDA Adverse Event
    Injury ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·June 21, 2013

    NEXGEN LCCK FEMORAL COMPONENT

    FDA Adverse Event
    Malfunction ·ZIMMER INC·Product code JWH·July 13, 2011