BEUDAMED
    13 results · 19ms · Sources: EU EUDAMED, US FDA

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    MODIFIED CUSHION-FLEX(TM)

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    NA

    FDA UDI
    Smith & Nephew, Inc.·03596010269751·VACUUM TUBE W/SUCTION BYPASS

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690189626·6+ FEMUR / 7 TIBIA TRIALS INSTRUMENT PAN

    FORZA

    FDA UDI
    Orthofix US LLC·18257200076932·9MM STRAIGHT IMPLANT REMOVER

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690189619·AK3 6+ Femur/7 Tibia Instrument pan insert

    FILTERSET 0.22, I.V. PUMP

    FDA 510(k)
    FDA Class 2 ·General Hospital

    HOVEROUND TEKNIQUE FWD MK4 POWER WHEELCHAIR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    NIM-ECLIPSE® CONTROLLER

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC·Product code GWF·December 9, 2014

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·February 7, 2014

    TERUMO CDI 101 MONITOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTY·October 22, 2010

    ATLAS II PLUS HF

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·December 28, 2012

    BD ALARIS¿ EXTENSION SET

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·November 24, 2021

    UNSPECIFIED BD INFUSION SET

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·December 22, 2022