BEUDAMED
    294 results · 18ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 3 ×

    Stimulator, Ultrasound And Muscle, For Use Other Than Applying Therapeutic Deep

    FDA Pre-Market Approval
    FDA Class 3 ·SONIC ACCELERATED FRACTURE HEALING SYSTEM MODEL 2A

    Stimulator, Ultrasound And Muscle, For Use Other Than Applying Therapeutic Deep

    FDA Pre-Market Approval
    FDA Class 3 ·EXOGEN 2000+(TM) SONIC ACCELERATED FRACTURE HEALING SYSTEM (SAFHS(R))

    Stimulator, Ultrasound And Muscle, For Use Other Than Applying Therapeutic Deep

    FDA Pre-Market Approval
    FDA Class 3 ·EXOGEN ULTRASOUND BONE HEALING SYSTEM

    Stimulator, Ultrasound And Muscle, For Use Other Than Applying Therapeutic Deep

    FDA Pre-Market Approval
    FDA Class 3 ·EXOGEN 4000+

    Stimulator, Ultrasound And Muscle, For Use Other Than Applying Therapeutic Deep

    FDA Pre-Market Approval
    FDA Class 3 ·EXOGEN ULTRASOUND BONE HEALING SYSTEM

    Stimulator, Ultrasound And Muscle, For Use Other Than Applying Therapeutic Deep

    FDA Pre-Market Approval
    FDA Class 3 ·EXOGEN 2000+ BONE HEALING SYSTEM

    Stimulator, Ultrasound And Muscle, For Use Other Than Applying Therapeutic Deep

    FDA Pre-Market Approval
    FDA Class 3 ·EXOGEN 4000+ BONE HEALING SYSTEM

    Stimulator, Ultrasound And Muscle, For Use Other Than Applying Therapeutic Deep

    FDA Pre-Market Approval
    FDA Class 3 ·SONIC ACCELERATED FRACTURE HEALING SYSTEM (SAFHS) MODEL 2000, EXOGEN 2000

    Stimulator, Ultrasound And Muscle, For Use Other Than Applying Therapeutic Deep

    FDA Pre-Market Approval
    FDA Class 3 ·SONIC ACCELERATED FRACTURE HEALING SYSTEM/EXOGEN 3000 (TM)

    Stimulator, Ultrasound And Muscle, For Use Other Than Applying Therapeutic Deep

    FDA Pre-Market Approval
    FDA Class 3 ·EXOGEN 2000+ AND EXOGEN 3000

    Stimulator, Ultrasound And Muscle, For Use Other Than Applying Therapeutic Deep

    FDA Pre-Market Approval
    FDA Class 3 ·SONIC ACCELERATED FRACTURE HEALING SYSTEM MODEL 2000

    Stimulator, Ultrasound And Muscle, For Use Other Than Applying Therapeutic Deep

    FDA Pre-Market Approval
    FDA Class 3 ·SONIC ACCELERATED FRACTURE HEALING SYSTEM MODEL 2000

    Kit, Dna Detection, Human Papillomavirus

    FDA Pre-Market Approval
    FDA Class 3 ·digene Hybrid Capture 2 (HC2) HPV DNA Test and digene Hybrid Capture 2 (HC2) High Risk

    Kit, Dna Detection, Human Papillomavirus

    FDA Pre-Market Approval
    FDA Class 3 ·DML 3000 Microplate Luminometer, 5000-00031, digene® HC2 High-Risk HPV DNA Test (I plate), 5199-1220, digene® HC2 High-R