BEUDAMED
    14 results · 24ms · Sources: EU EUDAMED, US FDA

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    xeo+ Family

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    GEL-BEAD EMBOLIZATION SPHERES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VASCULAR SOLUTIONS VARI-LASE ENDOVENOUS LASER CONSOLE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    AGILE ESOPHAGEAL

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code ESW·December 26, 2024

    BD POSIFLUSH

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FOZ·January 12, 2026

    AGILE ESOPHAGEAL

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code ESW·December 26, 2024

    AGILE ESOPHAGEAL

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code ESW·February 20, 2025

    AGILE ESOPHAGEAL

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code ESW·February 14, 2025

    AGILE ESOPHAGEAL

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code ESW·January 30, 2025

    SOLITAIRE FR

    FDA Adverse Event
    Injury ·COVIDIEN·Product code NRY·November 6, 2014

    INFUSOMAT SPACE

    FDA Adverse Event
    Malfunction ·B. BRAUN·Product code FRN·August 23, 2011

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 18, 2013

    UNSPECIFIED BD VACUTAINER® SODIUM FLUORIDE/POTASSIUM OXALATE TUBES

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code JKA·October 15, 2025

    BD VACUTAINER® SODIUM FLUORIDE/POTASSIUM OXALATE 5MG/4MG

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·May 23, 2024