BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    RECLAIM Monobloc Revision Femoral Stem

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ELECSYS RBC FOLATE HEMOLYZED REAGENT

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    TRAUS SIP20

    FDA 510(k)
    FDA Class 1 ·Dental

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·September 9, 2025

    STARCLOSE SE VASCULAR CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR - REDWOOD CITY·Product code MGB·December 3, 2008

    OCTRODE LEAD KIT, 60CM LENGTH

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·September 12, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 29, 2013