BEUDAMED
    8 results · 23ms · Sources: EU EUDAMED, US FDA

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    ELLAVI UBT

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    AMNISURE FETAL MEMBRANES RUPTURE TEST MODEL FMRT1

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    INTELLIVUE PATIENT MONITOR MX400; INTELLIVUE PATIENT MONITOR MX450

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 20, 2025

    LONG NAIL KIT R1.5, LEFT 10X260MM X 125

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·June 16, 2010

    TUBE, GASTROINTESTINAL (AND ACCESS)

    FDA Adverse Event
    Malfunction ·C. R. BARD INC. (BASD)·Product code KNT·November 6, 2008

    ENDEAVOR SPRINT RX CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·August 26, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 17, 2013