BEUDAMED
    17 results · 23ms · Sources: EU EUDAMED, US FDA

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    LapBox Tissue Containment Removal System

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

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517629814·CoRoent Ant TLIF Ti, 12x11x36mm 15°

    BD BBL™ Hektoen Enteric Agar

    FDA UDI
    BECTON, DICKINSON AND COMPANY·10382902213656·BD BBL™ Hektoen Enteric Agar

    CAPTURE-R READY INDICATOR CELLS

    FDA Adverse Event
    Malfunction ·IMMUCOR·Product code KSZ·June 3, 2009

    True 3D Viewer

    FDA 510(k)
    FDA Class 2 ·Radiology

    THERMOFORMED MOUTHGUARDS

    FDA 510(k)
    FDA Unclassified ·Unknown

    FRESTYLE

    FDA Adverse Event
    Malfunction ·THERASENSE, INC.·Product code LFR·May 30, 2005

    BD BBL¿ HEKTOEN ENTERIC AGAR

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code JSI·July 21, 2021

    ENDOPATH** ETS COMPACT

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·August 24, 2011

    UNKNOWN_RECONSTRUCTIVE_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·November 3, 2014

    4000CMS

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·July 1, 2013

    BD BACTEC¿ MGIT¿ MYCOBACTERIA GROWTH INDICATOR TUBES

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code MDB·June 9, 2025

    BD BBL¿ HEKTOEN ENTERIC AGAR

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code JSI·July 15, 2021

    BX2 Needle Guide, Part Number 644-094, tool for performing needle-guided (or catheter) procedures with the use of diagnostic ultrasound transducers

    FDA Enforcement
    Class II ·Ongoing·Civco Medical Instruments Co. Inc.·June 11, 2025

    BD BBL¿ HEKTOEN ENTERIC AGAR

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code JSI·June 18, 2021

    BD BBL¿ HEKTOEN ENTERIC AGAR

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code JSI·July 6, 2021

    BD BBL¿ HEKTOEN ENTERIC AGAR

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code JSI·July 14, 2021