BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    ACS® LD FB Knee 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

    EP-TRACER SYSTEM, EP-TRACER SYSTEM, EP-TRACER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    14HQ901G-B

    FDA 510(k)
    FDA Class 2 ·Radiology

    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

    WALLSTENT RX BILIARY ENDOPROSTHESIS

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

    EXETER V40 STEM 44MM NO 0

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

    SYSTEM 2000

    FDA Adverse Event
    Malfunction ·ARJO HOSPITAL EQUIMPENT, AB·Product code ILM·July 11, 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