BEUDAMED
    12 results · 22ms · Sources: EU EUDAMED, US FDA

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    M.U.S.T. PEDICLE SCREWS SYSTEM

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

    M.U.S.T. Pedicle Screw System - Extension

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    M.U.S.T. PEDICLE SCREW SYSTEM

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

    M.U.S.T. PEDICLE SCREWS SYSTEM

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

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

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

    R&D GLU-LINE HEMATOLOGY CONTROL

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Millipede 088 Access Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AMPLATZER PFO OCCLUDER

    FDA Adverse Event
    Injury ·AGA MEDICAL CORPORATION·Product code MLV·October 5, 2018

    AMPLATZER PFO OCCLUDER

    FDA Adverse Event
    Injury ·AGA MEDICAL CORPORATION·Product code MLV·October 9, 2018

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code NIQ·November 4, 2008

    ABGII. FEMORAL STEM WITH HYDROXYAPATITE LEFT N 7

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS CORK·Product code MAY·August 29, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 18, 2013