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

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    Ulthera System

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

    SignaLoc Screw

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215116729·

    OLYMPUS EMPOWER H65

    FDA Adverse Event
    Malfunction ·QUANTA SYSTEM S.P.A.·Product code GEX·May 19, 2022

    AESCULAP IMPLANT SYSTEMS S4 SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CHOLESTEROL OXIDASE JASE, AND GLYCEROL INASE TRIGLYCERIDES, MODEL NA

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    COVIDIEN

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH, INC.·Product code KNT·July 24, 2024

    COVIDIEN

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH, INC.·Product code KNT·July 24, 2024

    KANGAROO

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC·Product code KNT·January 28, 2026

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·April 26, 2022

    ACCESS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MALTA·Product code LHI·July 27, 2011

    DIMENSION XPAND W HM

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JGS·June 20, 2013

    2250051-2008-00337

    FDA Adverse Event
    Malfunction ·Product code KSZ·July 18, 2008