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

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    ROSA ONE Spine application

    FDA 510(k)
    FDA Class 2 ·Neurology

    Bernafon

    FDA UDI
    Bernafon AG·05711584081440·CAPTO 9 MNR FW 1.0

    LENSTEC LC INJECTION SYSTEM

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    NUBIC AND RABEA DEVICES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·June 11, 2013

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·July 28, 2011

    MINI TREK CORONARY DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code LOX·October 17, 2014