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

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    CROSSVENT-4 VENTILATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    GAMBRO PRISMAFLEX HF1000 AND HF1400 SETS

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

    G3 Active Plate Large Fragment System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PRISMAFLEX SETS (HF)

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE CORPORATION·Product code KDI·May 22, 2023

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 5, 2013

    BRIGHTVIEW XCT IMAGING SYSTEMS

    FDA Adverse Event
    PHILIPS MEDICAL SYSTEMS (CLEVELAND), INC.·Product code KPS·November 19, 2010

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 17, 2014

    INFUSOMAT SPACE PUMP IV SET

    FDA Adverse Event
    Malfunction ·B. BRAUN DOMINICAN REPUBLIC·Product code FPA·November 17, 2009