BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    THE CEN-SLIDE(TM) CENTRIFUGE TUBE

    FDA 510(k)
    FDA Class 1 ·Pathology

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867130043·AIMING GUIDE,LT, NARROW VOLAR DRP

    XYLOSE LYSINE DEOXYCHOLATE AGAR

    FDA 510(k)
    FDA Class 1 ·Microbiology

    PATHFINDER ELECTRODIAGNOSTIC SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    AIMING GUIDE,LT, NARROW VOLAR DRP

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MDM·June 26, 2025

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 24, 2014

    ACRYSOF RESTOR

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD./HUNTINGTON·Product code MFK·October 22, 2010

    KNIFE

    FDA Adverse Event
    Malfunction ·ALCON PRECISION DEVICE - SINKING SPRING·Product code HNN·December 7, 2012

    VASOVIEW HEMOPRO 2

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR LLC·Product code GEI·October 3, 2023