BEUDAMED
    13 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    YelloPort Elite Port Access System

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319721438·Sinus Suction Tube 5-3/4" (14.4cm) with bulbous...

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·December 31, 2014

    DANA REUSABLE BOWIE TEST PACK FOR DANA BOWIE DICK INDICATORS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    3.7MM/5.0MM DYNAMIC LOCKING SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 21, 2025

    MONOJECT

    FDA Adverse Event
    Malfunction ·JIANGSU CAINA MEDICAL CO., LTD·Product code PNR·April 14, 2024

    CARDINAL HEALTH

    FDA Adverse Event
    Malfunction ·JIANGSU CAINA MEDICAL CO., LTD.·Product code PNR·April 12, 2024

    CARDINAL

    FDA Adverse Event
    Malfunction ·JIANGSU CAINA MEDICAL CO., LTD.·Product code PNR·April 12, 2024

    BIPOLAR LEAD MODEL 300

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·October 6, 2008

    SM PLUS SBT/OVAL BALLOON DISSECTOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY USSC PUERTO RICO, INC.·Product code GCJ·June 13, 2013

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE·Product code KDJ·August 4, 2011

    CARDINAL HEALTH

    FDA Adverse Event
    Malfunction ·JIANGSU CAINA MEDICAL CO., LTD.·Product code PNR·April 12, 2024