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

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    CAREMIBRAIN

    FDA 510(k)
    FDA Class 2 ·Radiology

    DTE

    FDA UDI
    Guilin Woodpecker Medical Instrument Co., Ltd.·06944843657769·Dental X-Ray Device

    Responsive Arthroscopy Interference Screw System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SHORT INTRODUCER SHEATH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BD VACUTAINER® SST¿ II ADVANCE PLUS BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·April 6, 2026

    BD VACUTAINER® SST¿ II ADVANCE PLUS BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·April 6, 2026

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·November 13, 2008

    DEXTRUS 4136

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVZ·August 19, 2011

    TECNIS 1 MULTIFOCAL

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code MFK·July 18, 2013