BEUDAMED
    6 results · 19ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    MAGNA-ROM 21 KNEE SYSTEEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SICKLE-CELL F TEST

    FDA 510(k)
    FDA Class 2 ·Hematology

    PowerFlow Implantable Apheresis IV Port

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Subcutaneous Implanted Apheresis Port

    FDA classification
    FDA Class 2 ·Subcutaneous Implanted Apheresis Port

    Assay, Fetal Hemoglobin

    FDA classification
    FDA Class 2 ·Assay, Fetal Hemoglobin

    Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

    FDA classification
    FDA Class 2 ·Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer