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

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    SILVERSTEIN MICROWICK

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    MaXcess

    FDA UDI
    Nuvasive, Inc.·00887517200747·MaXcess-C Blade, 70mm Lateral Serrated

    BD L-CATH SINGLE AND DUAL LUMENT CATHETERS, MIDLINE CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CureOs TCP

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HDI 5000 ULTRASOUND STANDARD SYSTEM

    FDA Adverse Event
    Malfunction ·PHILIPS ULTRASOUND, INC.·Product code IYO·March 30, 2012

    EPIC SELF-EXPANDING NITINOL STENT WITH DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code FGE·March 6, 2013

    CAPSURE SENSE

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·August 8, 2014

    SCREW-IN

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011