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

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    ART-Plan (v.2.2.0)

    FDA 510(k)
    FDA Class 2 ·Radiology

    M.U.S.T. PEDICLE SCREWS SYSTEM

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code NKB·November 10, 2025

    CONTOUR SE MICROSPHERES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Quantia IgE

    FDA 510(k)
    FDA Class 2 ·Immunology

    M.U.S.T. PEDICLE SCREW SYSTEM

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code NKB·January 13, 2026

    SYNCHRON® CK 2 X 400

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code CKA·May 10, 2011

    M.U.S.T. PEDICLE SCREWS SYSTEM

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code NKB·November 10, 2025

    ICON 20 HCG

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JHI·November 4, 2008

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code MDS·August 29, 2011

    FLOGARD

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 18, 2013

    M.U.S.T. SACRAL ILIAC SCREW AND PELVIC TRAUMA SYSTEM

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code OUR·October 16, 2024