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

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    3M™ Transbond™ Orthodontic Adhesive

    FDA 510(k)
    FDA Class 2 ·Dental

    M.U.S.T. PEDICLE SCREWS SYSTEM

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

    NO TOUCH+FOREHEAD NTF 3000 THERMOMETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    H-FLOW VALVE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    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

    SENSATION STANDARD OVAL SNARE

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

    PARIETEX UGYTEX PP POSTERIOR KIT X1

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION·Product code FTL·August 29, 2011

    GYNECARE TVT OBURATOR 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

    Luminos dRF with software VD10- A diagnostic imaging system for radiographic and fluoroscopic studies Model Number: 10094200

    FDA Enforcement
    Class II ·Ongoing·Siemens Medical Solutions USA, Inc·March 1, 2023