BEUDAMED
    19 results · 70ms · Sources: EU EUDAMED, US FDA

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    Ambu aScope 4 Cysto

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

    E-CARE INFRARED EAR THERMOMETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SPRINTER LEGEND 1.25MM RX AND SPRINTER LEGEND 1.25MM OTW BALLOON

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Femoral Fixation System

    FDA UDI
    Zimmer, Inc.·00889024036796·

    Versa-Fx®

    FDA UDI
    Zimmer, Inc.·00889024036871·

    Versa-Fx®

    FDA UDI
    Zimmer, Inc.·00889024036833·

    Versa-Fx®

    FDA UDI
    Zimmer, Inc.·00889024036857·

    Versa-Fx®

    FDA UDI
    Zimmer, Inc.·00889024036826·

    Versa-Fx®

    FDA UDI
    Zimmer, Inc.·00889024036864·

    Versa-Fx®

    FDA UDI
    Zimmer, Inc.·00889024036819·

    Versa-Fx®

    FDA UDI
    Zimmer, Inc.·00889024036888·

    Versa-Fx®

    FDA UDI
    Zimmer, Inc.·00889024036802·

    Versa-Fx®

    FDA UDI
    Zimmer, Inc.·00889024036840·

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code CBK·June 24, 2013

    ONE TOUCH ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code NBW·October 6, 2008

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·July 21, 2011

    INDIGO SYSTEM ASPIRATION CATHETER 7D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code QEW·December 10, 2024

    INDIGO SYSTEM ASPIRATION CATHETER 7D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code QEW·January 5, 2023

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·June 14, 2023