BEUDAMED
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    imani i1

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772777624·LUMBAMED BASIC DORSAL STAYS WM SILVER V

    Zodiac Spinal Fixation System

    FDA UDI
    ALPHATEC SPINE, INC.·00844856068988·SS ROD 5.5MM DIA X 45CM - 90DEG LASERMARK

    SprintRay Standard Denture Base - Dark Meharry

    FDA UDI
    Sprintray, Inc.·00850039704260·SprintRay Standard Denture Base is a light-cura...

    ePatch 2.5, BTH

    FDA UDI
    BRAEMAR MANUFACTURING, LLC·B146EP2510·

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112489·BARRON VACUUM TREPHINE 7.25MM

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112472·BARRON VACUUM TREPHINE 7.0MM

    VICEROY Spinal System

    FDA UDI
    EOS BIOTEK,INC.·88000163011996·

    Viceroy

    FDA UDI
    DIOMEDICAL CO.,LTD.·08800039826266·Rod Pre-Bent 6.0 x 45mm

    VITEK GRAM POSITIVE SUSCEPTIBILITY (GPS) CARD FOR LINEZOLID

    FDA 510(k)
    FDA Class 2 ·Microbiology

    WATER PURIFICATION SYSTEM FOR HEMODIALYSIS

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

    BD SMARTSITE¿ VIALSHIELD CLOSED VIAL ACCESS DEVICE, 13 MM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code LHI·January 25, 2022

    BD SMARTSITE 13MM CLOSED VIAL ACCESS DEVICE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FPA·January 25, 2022

    BD SMARTSITE¿ VIALSHIELD CLOSED VIAL ACCESS DEVICE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FPA·January 25, 2022

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 29, 2025

    THERASPHERE

    FDA Adverse Event
    Injury ·BIOCOMPATIBLES UK LTD·Product code NAW·October 9, 2020

    EON MINI

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL - NEUROMODULATION·Product code LGW·June 27, 2013

    RELION CONFIRM BLOOD GLUCOSE SYSTEM

    FDA Adverse Event
    Injury ·ARKRAY, INC.·Product code NBW·August 11, 2011

    I-STAT CTNI CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE INC.·Product code MMI·September 23, 2008

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·August 5, 2024