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

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    Filters FDA Classification ×

    Support, Breathing Tube

    FDA classification
    FDA Class 1 ·Support, Breathing Tube

    Device, Jaw Tracking, For Monitoring Jaw Positions

    FDA classification
    FDA Class 1 ·Device, Jaw Tracking, For Monitoring Jaw Positions

    Device, Jaw Repositioning

    FDA classification
    FDA Class 2 ·Device, Jaw Repositioning

    Light, Fiber Optic, Dental

    FDA classification
    FDA Class 1 ·Light, Fiber Optic, Dental

    Complement C5, Antigen, Antiserum, Control

    FDA classification
    FDA Class 2 ·Complement C5, Antigen, Antiserum, Control

    Device, Dental Sonography, For Monitoring Jaw Sounds

    FDA classification
    FDA Class 1 ·Device, Dental Sonography, For Monitoring Jaw Sounds

    Device, Jaw Tracking, For Diagnosis Of Tmj / Mpd Disorders

    FDA classification
    FDA Class 2 ·Device, Jaw Tracking, For Diagnosis Of Tmj / Mpd Disorders

    Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

    FDA classification
    FDA Class 2 ·Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

    Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

    FDA classification
    FDA Class 2 ·Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

    Ultrasound Imaging System For Acquiring Images At Home By Lay Users

    FDA classification
    FDA Class 2 ·Ultrasound Imaging System For Acquiring Images At Home By Lay Users

    Test For Detection Of Antibodies Associated With Syphilis Performed By Lay Users

    FDA classification
    FDA Class 2 ·Test For Detection Of Antibodies Associated With Syphilis Performed By Lay Users

    Test For Detection Of Microorganism(S) Causing Sexually Transmitted Infections Performed By Lay Users

    FDA classification
    FDA Class 2 ·Test For Detection Of Microorganism(S) Causing Sexually Transmitted Infections Performed By Lay Users

    Device For Home Collection And Transport Of Vaginal Specimens By Lay Users For Use In An Approved Hpv Molecular Assay

    FDA classification
    FDA Class 2 ·Device For Home Collection And Transport Of Vaginal Specimens By Lay Users For Use In An Approved Hpv Molecular Assay

    Assay To Measure Pct To Aid In The Risk Assessment Of Critically Ill Patients On Their First Day Of Icu Admission

    FDA classification
    FDA Class 2 ·Assay To Measure Pct To Aid In The Risk Assessment Of Critically Ill Patients On Their First Day Of Icu Admission