Enraf-Academy Introduction Note

  • Users of Enraf-Nonius treatment devices must be trained in how to use the system properly and have the appropriate skills.
  • Any treatment instructions regarding treatment location, duration and strength require medical knowledge and should only be given by authorised doctors, therapists and health professionals. It is imperative that these instructions are followed.
  • Before using Enraf-Nonius equipment, read, understand and practice the instructions for use. Know the limitations and hazards associated with using the device. Also observe the precautionary and operational decals placed on the unit.

Treatment Couches

Enraf-Nonius' Leading examination- and treatment couches at close range

Electrotherapy

Enraf-Nonius electrotherapy: Dutch quality, innovation and design

Rehabilitation and Medical Fitness

Enraf-Nonius equipment for Rehabilitation and Medical Fitness

Distribution

Enraf-Nonius global sales and support. Find you local representative here!

Enraf-Nonius Projects (ENP)

The specialist in turn-key medical solutions, not only realizes hospital- and rehabilitation projects but also offers procurement and project management.

Indications:

  • Radial and ulnar epicondylitis
  • Calcific tendonitis of the shoulder / shoulder problems
  • Status post muscular injuries
  • Chronic patellar tendonitis
    Jumper's knee
  • Achillodynia
  • Plantar fasciitis
  • Heel spurs
  • Myofascial trigger point treatment e.g. neck
  • Myofascial trigger point treatment e.g. back, muscular back pain
  • Bursitis Trochanterica
  • Periostitis / shin splints (status post strain)

Contraindications:

  • vascular diseases present in or near the treatment area
  • local infections in the treatment area
  • around malignant or benign tumours
  • directly on cartilage surfaces or near the small facet joints of the spinal column
  • directly over implanted electronic devices such as pacemakers, analgesic pumps, etc.
  • in areas, in which mechanical energy in the form of vibrations may lead to tissue damage such as metal implants after a fracture

In general we advise against treatment

  • if blood clotting disorders are present or the patient is receiving treatment that results in a change in the blood clotting behaviour
  • during pregnancy
  • on patients with neurological diseases resulting in impairment of the vasomotor function in the treatment area
  • over air-filled cavities such as treatment on the thoracic spine, etc.
  • on children, particularly around the epiphyseal plates

Care is required for patients

  • with impaired sensibility
  • with severe autonomic disorders
  • under the influence of drugs and/or alcohol as circulatory stresses and inadequate treatment responses cannot be excluded.

 

Instruction for Use Please consult the Instructions for Use for more information on indications and contra-indications and for warnings and recommendations.

These indications and contra-indications originated from the Endopuls 811 User Manual 1650751-41


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