BEUDAMED
    10 results · 18ms · Sources: EU EUDAMED, US FDA

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    HEOMDIALYSIS SINGLE PATIENT SYSTEM (SPS) MODEL 650

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

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613062026·Diamond Rasp, Curved, Medium Grit, Overall Leng...

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613061999·Diamond Rasp, Straight, Medium Grit, Overall Le...

    URIC ACID REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code KNK·April 15, 2011

    IMPELLA 5.0 CATHETER FAMILY

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Contour 24

    FDA 510(k)
    FDA Class 2 ·Radiology

    SPEEDBAND SUPERVIEW SUPER 7, MODELS 4204

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code MND·October 26, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP.·Product code FRN·February 7, 2014

    HEARTWARE® VENTRICULAR ASSIST SYSTEM

    FDA Adverse Event
    Injury ·HEARTWARE, INC·Product code DSQ·December 21, 2012

    BD INSYTE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA.·Product code FOZ·August 26, 2024