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

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    CYPRESS MEDICAL PRODUCTS CATHETER (INSERTION) TRAY/WITH OUT CATHETER

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

    BASE

    FDA UDI
    Nuvasive, Inc.·00887517700292·BASE Guide, Single I

    Sierra

    FDA UDI
    Seaspine Orthopedics Corporation·10889981094225·CrossBar Driver

    TRILLIUM BIOPUMP PLUS, MODEL BPX80T

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Arrow Pressure Injectable Jugular Axillo-subclavian Central Catheter (JACC) with Sustain Technology

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CROSSBAR DRIVER

    FDA Adverse Event
    Malfunction ·SEASPINE, INC.·Product code KWP·March 6, 2014

    UNK ZIMMER HIP

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code JDI·December 7, 2010

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·February 8, 2013

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code IOR·July 22, 2014