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

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    Reherniation Reduction Device

    FDA Pre-Market Approval
    FDA Class 3 ·BARRICAID ANULAR CLOSURE DEVICE (ACD)

    Reherniation Reduction Device

    FDA Pre-Market Approval
    FDA Class 3 ·Barricaid® Annular Closure Device

    Reherniation Reduction Device

    FDA Pre-Market Approval
    FDA Class 3 ·Barricaid® Annular Closure Device

    Reherniation Reduction Device

    FDA Pre-Market Approval
    FDA Class 3 ·Barricaid Anular Closure Device

    Reherniation Reduction Device

    FDA Pre-Market Approval
    FDA Class 3 ·Barricaid® Annular Closure Device

    Reherniation Reduction Device

    FDA Pre-Market Approval
    FDA Class 3 ·Barricaid® Annular Closure Device - Model Number BAR-A8-8MM (2730815-A&), Barricaid® Annular Closure Device - Model Numb

    Reherniation Reduction Device

    FDA Pre-Market Approval
    FDA Class 3 ·Barricaid® Annular Closure Device

    Reherniation Reduction Device

    FDA Pre-Market Approval
    FDA Class 3 ·Barricaid® Annular Closure Device

    Reherniation Reduction Device

    FDA Pre-Market Approval
    FDA Class 3 ·Barricaid Anular Closure Device (ACD)

    Reherniation Reduction Device

    FDA Pre-Market Approval
    FDA Class 3 ·Barricaid Annular Closure Device

    Reherniation Reduction Device

    FDA Pre-Market Approval
    FDA Class 3 ·Barricaid Annular Closure Device

    Reherniation Reduction Device

    FDA Pre-Market Approval
    FDA Class 3 ·Barricaid Anular Closure Device

    Vincent

    FDA UDI
    MEDTRONIC XOMED, INC.·00763000036829·PROSTHESIS 1160050 TI PART VINCENT HA

    NA

    FDA UDI
    MEDTRONIC XOMED, INC.·00885074371177·PROSTHESIS 1160050 TI PART VINCENT HA

    Potassium Test

    FDA UDI
    STANBIO LABORATORY, L.P.·00657498000984·Quantitative Turbidimetric Determination of Pot...

    RaPET® s-LE

    FDA UDI
    STANBIO LABORATORY, L.P.·00657498001288·Latex Agglutination Slide Test for the Detectio...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694048026·2.8mm x 300mm Unthreaded Guide Wire

    Canaveral®

    FDA UDI
    FLOSPINE LLC·B183121600500·6.0mm Straight Rod, Ti Alloy 50mm

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528108345·2.8 mm x 300 mm Smooth Guide Wire, Sterile, 2 Pk

    SERFAS 90-S Electrosurgical Probe

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