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The ReFlow Ventricular System is FDA cleared and CE Marked for use by a qualified clinician to facilitate a safe, noninvasive retrograde fluid flush when ventriculoperitoneal shunt flow is restricted or blocked. The ReFlow System Mini is under development and not available for sale. The ReFlow System is a prescription device sold by or on the order of a physician.
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Anuncia Inc. is not affiliated with or an official partner of MD&DI, Fast Company, and The FDA.