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

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    SNAP EEG MONITOR

    FDA 510(k)
    FDA Class 2 ·Neurology

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·H65820202181·Channels PT NiTi Rotary SAMPLE

    Safco TruCheck

    FDA UDI
    SAFCO DENTAL SUPPLY CO.·D72310202183·TruCheck 5-1/4 x 7-1/2 pouches, 200/box

    Asnis

    FDA UDI
    Stryker GmbH·07613154631476·CANNULATED SCREW

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694000253·2.0mm x 18mm Locking Screw

    NITRILE EXAM GLOVE, POWDER-FREE, COLOR BLUE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    VISTAKON (HEFILCON C) CONTACT LENSES

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    BD PHOENIX PMIC110

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·October 19, 2021

    BD PHOENIX¿ M50 AUTOMATED MICROBIOLOGY SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·August 23, 2021

    BD PHOENIX PANEL PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·November 10, 2023

    BD PHOENIX PANEL PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·November 10, 2023

    MEDIAL ROTATION KNEE

    FDA Adverse Event
    Injury ·MATORTHO LIMITED·Product code JWH·January 22, 2016

    MEDIAL ROATION KNEE

    FDA Adverse Event
    Malfunction ·MATORTHO LIMITED·Product code JWH·January 22, 2016

    BD PHOENIX¿ PMIC/ID-106

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·September 2, 2025

    BD PHOENIX¿ PMIC/ID-106

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·September 2, 2025

    BD PHOENIX¿ PMIC/ID-106

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·April 15, 2024

    BD PHOENIX¿ PMIC/ID-106

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·October 23, 2024

    BD PHOENIX¿ PMIC/ID-106

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·November 26, 2024

    BD PHOENIX¿ PMIC/ID-106

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·November 26, 2024

    MEDIAL ROATION KNEE

    FDA Adverse Event
    Injury ·MATORHTO LIMITED·Product code JWH·January 22, 2016