BEUDAMED
    9 results · 22ms · Sources: EU EUDAMED, US FDA

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    JEIL BONE FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    CT LUCIA

    FDA UDI
    CARL ZEISS MEDITEC PRODUCTION, LLC·00843045100904·3-piece, monofocal, hydrophobic, acrylic, intra...

    MEDIVISION I-VIEW PERSONAL VIDEO DISPLAY

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

    NEUROGRAPH EVOKED POTENTIAL SYSTEMS (EPS), MODEL EPS-1

    FDA 510(k)
    FDA Class 2 ·Neurology

    STIMQ PERIPHERAL NERVE STIMULATOR (PNS) SYSTEM

    FDA Adverse Event
    Injury ·STIMWAVE TECHNOLOGIES INC.·Product code GZF·December 20, 2018

    HEARTSTREAM FR2

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·March 14, 2013

    CONTAK RENEWAL

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·April 12, 2011

    RIATA ST OPTIM ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·May 27, 2008

    STIMQ PERIPHERAL NERVE STIMULATOR (PNS) SYSTEM

    FDA Adverse Event
    Injury ·STIMWAVE TECHNOLOGIES INC.·Product code GZF·April 1, 2019