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

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    TriMed Threaded Intramedullary Nail System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    M.U.S.T. PEDICLE SCREWS SYSTEM

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

    BTL-9000; BTL-9000 RADIOFREQUENCY MODULE

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

    ESPRIT VENTILATOR, MODEL V1000

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    M.U.S.T. PEDICLE SCREW SYSTEM

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

    PECTUS SYSTEM ELONGATED PECTUS STABILIZER

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HRS·August 27, 2020

    M.U.S.T. PEDICLE SCREWS SYSTEM

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

    IMPLANTIUM

    FDA Adverse Event
    Injury ·DENTIUM USA·Product code DZE·August 29, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 7, 2014

    GYNECARE TVT RETROPUBIC SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·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