BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    VENT TUBE FORCEPS

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM-NITROFURANTOIN GRAM POSITIVE

    FDA 510(k)
    FDA Class 2 ·Microbiology

    KEELER SLIT LAMP H-SERIES

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    BRYAN DUMON SILICONE STENT

    FDA Adverse Event
    Malfunction ·LYMOL MEDICAL CORPORATION·Product code NWA·October 28, 2019

    ACCESS

    FDA Adverse Event
    Malfunction ·BIEFFE MEDITAL MANUFACTURING S.A.R.L. TUNIS·Product code FPA·May 25, 2014

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code FTL·November 14, 2012

    CONCERTO II CRT-D

    FDA Adverse Event
    Malfunction ·IPG MFG SWITZERLAND·Product code NIK·June 10, 2015

    BD PHOENIX¿ PMIC-108

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·July 25, 2024

    BD PHOENIX¿ PMIC-108

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·July 19, 2024