BEUDAMED
    6 results · 35ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    LINQ II™ Insertable Cardiac Monitor (ICM)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VSCAN WITH DUAL PROBE

    FDA 510(k)
    FDA Class 2 ·Radiology

    PTS PANELS LDL CHOLESTEROL TEST STRIPS

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    MINICAP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·September 9, 2011

    FORTIFY ASSURA DR, DF-4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·November 10, 2014

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OYC·July 22, 2013