BEUDAMED
    1,106 results · 29ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    Sepsis ImmunoScore

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Software Device To Aid In The Prediction Or Diagnosis Of Sepsis

    FDA classification
    FDA Class 2 ·Software Device To Aid In The Prediction Or Diagnosis Of Sepsis

    ASK-300

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ASK System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK INTERBODY FUSION SYSTEM

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK INTERBODY FUSION SYSTEM

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK INTERBODY FUSION SYSTEM

    AccuPoint Electrode

    FDA 510(k)
    FDA Class 2 ·Neurology

    Synvitro Hyadase

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK/PROXIMITY(TM) INTERBODY FUSION SYSTEM

    TOTIM Patient Cushion Immobilization System

    FDA 510(k)
    FDA Class 2 ·Radiology

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK/C VISTA CERVICAL INTERBODY FUSION DEVICE

    BAK-ON SP PORCELAIN ALLOY

    FDA 510(k)
    FDA Class 2 ·Dental

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK/CERVICAL (BAK/C) INTERBODY FUSION SYSTEM

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK/CERVICAL (BAK/C) INTERBODY FUSION SYSTEM

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK INTERBODY FUSION SYSTEM

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK/L INTERBODY FUSION SYSTEM

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK/CERVICAL (BAK/C) (R) INTERBODY FUSION SYSTEM

    VALLEYLAB MICROWAVE ABLATION GENERATOR

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

    FORCETRIAD ELECTROSURGICAL GENERATOR; LIGASURE INSTRUMENTS

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