BEUDAMED
    6 results · 17ms · Sources: EU EUDAMED, US FDA

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    OUTPUT DIGITAL DISPLAY MODULE, MODEL 401

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    inui In-Home Urine Analysis Test System

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    DISH, STERILE DISPOSABLE POLYSTYRENE

    FDA 510(k)

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 3, 2014

    SEE H-10

    FDA Adverse Event
    Injury ·STAAR SURGICAL COMPANY·Product code HQL·October 10, 2012

    COAGUCHEK S SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JPA·September 12, 2007