BEUDAMED
    22 results · 17ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    CONCHAPAK OXYGEN DILUTER

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    Triad

    FDA UDI
    Nuvasive, Inc.·00887517265043·Triad Cervical Rasp, 11x11x11mm

    Washbon

    FDA UDI
    ORMCO CORPORATION·00889989043723·UPPER LEFT FIRST MOLAR WASHBON BAND SIZE 11

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690189886·pin puller

    PECTUS BLU (TM)

    FDA UDI
    BIOMET MICROFIXATION, INC·00888233028783·

    Device, Vascular, For Promoting Embolization

    FDA Pre-Market Approval
    FDA Class 2 ·MINI BALLOON

    REAGENT, TRIGLYCERIDES

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Pulmonx Chartis Tablet Console

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Device, Vascular, For Promoting Embolization

    FDA Pre-Market Approval
    FDA Class 2 ·MINI BALLOON

    Device, Vascular, For Promoting Embolization

    FDA Pre-Market Approval
    FDA Class 2 ·MINI BALLOON

    Device, Vascular, For Promoting Embolization

    FDA Pre-Market Approval
    FDA Class 2 ·MINI BALLOON

    Device, Vascular, For Promoting Embolization

    FDA Pre-Market Approval
    FDA Class 2 ·MINI BALLOON

    Device, Vascular, For Promoting Embolization

    FDA Pre-Market Approval
    FDA Class 2 ·MINI BALLOON

    Device, Vascular, For Promoting Embolization

    FDA Pre-Market Approval
    FDA Class 2 ·MINI BALLOON

    Device, Vascular, For Promoting Embolization

    FDA Pre-Market Approval
    FDA Class 2 ·MINI BALLOON

    Device, Vascular, For Promoting Embolization

    FDA Pre-Market Approval
    FDA Class 2 ·MINI-BALLOON DETACHABLE BALLOON SYSTEM

    Device, Vascular, For Promoting Embolization

    FDA Pre-Market Approval
    FDA Class 2 ·MINI BALLOON

    EYEVAN7285

    FDA UDI
    EYEVAN INC.·04571445047746·

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 6, 2014

    COGNIS

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·October 10, 2012