BEUDAMED
    10,000 results · 79ms · Sources: EU EUDAMED, US FDA

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    GPS Drill

    FDA UDI
    InnoBioSurg Co.,Ltd(IBS implant Co.,Ltd)·08800039381659·

    E500 VENTILATOR

    FDA Adverse Event
    Injury ·NEWPORT MEDICAL INSTRUMENTS, INC·Product code CBK·July 26, 2016

    Hemoglobin Variants System on Newborn Hemoglobin System with GDM and HbReview Software

    FDA 510(k)
    FDA Class 2 ·Hematology

    E500 VENTILATOR

    FDA Adverse Event
    Injury ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·January 17, 2013

    NEWPORT E500 VENTILATOR

    FDA Adverse Event
    Malfunction ·NEWPORT MEDICAL INSTRUMENTS·Product code CBK·May 11, 2004

    E500 VENTILATOR

    FDA Adverse Event
    Other ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·August 27, 2008

    VARIANTNBS WITH GDM 3.1 SOFTWARE

    FDA Adverse Event
    Malfunction ·BIO-RAD LABORATORIES·Product code GKA·October 15, 2013

    E500 VENTILATOR

    FDA Adverse Event
    Malfunction ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·April 1, 2008

    DEXCOM G6 CGM

    FDA Adverse Event
    Malfunction ·DEXCOM INC·Product code QBJ·March 30, 2021

    E360 VENTILATOR

    FDA Adverse Event
    Malfunction ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·October 30, 2008

    BD STERILE NEEDLE 0.23MM X 4MM 32G X 5/32"

    FDA Adverse Event
    Malfunction ·BD·Product code NSC·September 30, 2020

    TRUE TRACK GLUCOMETER

    FDA Adverse Event
    Injury ·NIPRO DIAGNOSTICS, INC. / TRIVIDIA HEALTH, INC.·Product code NBW·August 24, 2018

    ACRYSOF SINGLEPIECE IOL

    FDA Adverse Event
    Malfunction ·ALCON LABORATORIES IRELAND LTD.·Product code HQL·September 5, 2019

    LIFELINE

    FDA Adverse Event
    Malfunction ·DEFIBTECH, L.L.C.·Product code MKJ·August 2, 2024

    PEN NDL 32G 4MM 100BX 1200 USA

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·December 7, 2020

    TRUETRACK

    FDA Adverse Event
    Malfunction ·TRIVIDIA HEALTH, INC.·Product code NBW·October 5, 2018

    UNKNOWN STRATTICE

    FDA Adverse Event
    Injury ·LIFECELL·Product code FTM·May 17, 2018

    EVITA V300

    FDA Adverse Event
    Malfunction ·DRÄGERWERK AG & CO. KGAA·Product code CBK·January 22, 2026

    HAWKINS II BLN (BREAST LOCALIZATION NEEDLE)

    FDA Adverse Event
    Injury ·ARGON MEDICAL DEVICES INC.·Product code GDM·May 30, 2014

    HAWKINS II

    FDA Adverse Event
    Injury ·ARGON MEDICAL DEVICES·Product code GDM·May 12, 2014