BEUDAMED
    10 results · 24ms · Sources: EU EUDAMED, US FDA

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    pORTAL Steerable Hydrophilic Guidewire and pORTAL EXT Extension Wire

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EMG SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    PACSMATE, MODEL MMD-4300C/MMD-4300CX

    FDA 510(k)
    FDA Class 2 ·Radiology

    AESCULAP SURGICAL INSTRUMENTS

    FDA Adverse Event
    Injury ·CHRISTOPH MIETHKE GMBH & CO. KG·Product code JXG·November 27, 2019

    AESCULAP SURGICAL INSTRUMENTS

    FDA Adverse Event
    Injury ·CHRISTOPH MIETHKE GMBH & CO. KG·Product code JXG·November 27, 2019

    AZUR VASCULAR PLUG 8

    FDA Adverse Event
    Injury ·MICROVENTION, INC.·Product code KRD·March 29, 2022

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·October 22, 2014

    PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·August 4, 2011

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code FSA·June 26, 2013

    22 G X 1.00 IN. BD INSYTE¿ AUTOGUARD¿ SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·October 30, 2017