BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Xcess Guiding Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FETAL MATERNAL MONITOR MODEL F9 EXPRESS AND EXPRESS

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

    HUMIDAIRE 2I

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 11, 2025

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE·Product code KDJ·June 20, 2013

    ADJ. X.CONN.SMALL 40-50MM

    FDA Adverse Event
    Malfunction ·INTEGRA, MEDINA·Product code KWP·July 7, 2011

    PRECISION XTRA / OPTIUM

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC., USA·Product code NBW·September 22, 2008

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code NIQ·January 11, 2007

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code NIQ·January 11, 2007