BEUDAMED
    13 results · 14ms · Sources: EU EUDAMED, US FDA

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    Resectoscope, Working Element

    FDA classification
    FDA Class 2 ·Resectoscope, Working Element

    L-Leucyl B-Naphthylamide, Leucine Aminopeptidase

    FDA classification
    FDA Class 1 ·L-Leucyl B-Naphthylamide, Leucine Aminopeptidase

    Thyroglobulin, Antigen, Antiserum, Control

    FDA classification
    FDA Class 2 ·Thyroglobulin, Antigen, Antiserum, Control

    Fc, Antigen, Antiserum, Control

    FDA classification
    FDA Class 1 ·Fc, Antigen, Antiserum, Control

    Auxiliary Power Supply (Ac Or Dc) For Low-Energy Dc-Defibrillator

    FDA classification
    FDA Class 2 ·Auxiliary Power Supply (Ac Or Dc) For Low-Energy Dc-Defibrillator

    Fc, Fitc, Antigen, Antiserum, Control

    FDA classification
    FDA Class 1 ·Fc, Fitc, Antigen, Antiserum, Control

    Fc, Rhodamine, Antigen, Antiserum, Control

    FDA classification
    FDA Class 1 ·Fc, Rhodamine, Antigen, Antiserum, Control

    Dc-Defibrillator, Low-Energy, (Including Paddles)

    FDA classification
    FDA Class 2 ·Dc-Defibrillator, Low-Energy, (Including Paddles)

    Dc-Defibrillator, High Energy, (Including Paddles)

    FDA classification
    FDA Class 3 ·Dc-Defibrillator, High Energy, (Including Paddles)

    Igg (Fc Fragment Specific), Antigen, Antiserum, Control

    FDA classification
    FDA Class 1 ·Igg (Fc Fragment Specific), Antigen, Antiserum, Control

    Instrument, Surgical, Orthopedic, Dc-Powered Motor And Accessory/Attachment

    FDA classification
    FDA Class 1 ·Instrument, Surgical, Orthopedic, Dc-Powered Motor And Accessory/Attachment

    Auxiliary Power Supply (Acor Dc) For External Transcutaneous Cardiac Pacemaker

    FDA classification
    FDA Class 2 ·Auxiliary Power Supply (Acor Dc) For External Transcutaneous Cardiac Pacemaker

    Modified Version Of Another Manufacturer’S Fda-Authorized Test Within Scope Described In Preamble To Ldt Final Rule

    FDA classification
    FDA Not Classified ·Modified Version Of Another Manufacturer’S Fda-Authorized Test Within Scope Described In Preamble To Ldt Final Rule