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

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    INTRAUTERINE DEVICE REMOVER

    FDA 510(k)
    FDA Class 1 ·Obstetrics/Gynecology

    Sirius Femoral Stem, Size 30A

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SMARTSCREW II, MODELS 232010, 232012, 232014, 232016, 232018, 232020

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·June 1, 2014

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·November 21, 2012

    HX2 TEMPERATURE MANAGEMENT SYSTEM

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DWC·August 27, 2010