BEUDAMED
    10 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Revolution CT, Revolution CT ES, Revolution Apex, Revolution CT with Apex edition

    FDA 510(k)
    FDA Class 2 ·Radiology

    PIONEER PLUS CATHETER, MODEL PLUS 120

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ALCON ULTRACHOPPER

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    FUJIFILM DUODENOSCOPE MODEL ED-580T

    FDA Adverse Event
    Injury ·FUJIFILM CORPORATION·Product code FDT·September 5, 2023

    FUJIFILM ENDOSCOPE

    FDA Adverse Event
    Malfunction ·FUJIFILM CORPORATION·Product code FDS·March 18, 2022

    FUJIFILM DUODENOSCOPE ED-580T

    FDA Adverse Event
    Injury ·FUJIFILM CORPORATION·Product code FDT·March 5, 2025

    TENDRIL ST

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, CRMD·Product code NVN·January 13, 2014

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·July 28, 2011

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 26, 2013

    BD¿ NEXIVA SINGLE PORT

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·March 21, 2019