Numero verde: 800-456220

Controlled High Frequencies

An innovative, practical and effective device

ProNexibus Plus® is designed for

Physical therapists - Nurses - Pain therapists

ProNexibus Plus - Fisioterapia

What is it and how does it work?

The ProNexibus Plus® generates controlled high frequencies at 2, 4 and 8 MHz.

The emitted radio frequencies penetrate deep into the tissues and exceed the resistance offered by the body and cell membranes.

The high frequencies, overcoming the barriers they encounter in their path, reach directly deep into the damaged cells and immediately activate the cellular healing processes.

The beneficial effects of the high-frequency diathermy of the Pronexibus Plus® are:

  • Painkiller.
  • Antiedema.
  • Anti inflammatory.
  • Regenerative.
Effetto Antiinfiammatorio

Anti Inflammatory

Effetto Antalgico

Painkiller

Effetto Antiedemigeno

ANTI EDEMa

ProNexibus Plus - Effetto Prorigenerativo

Regenerative

Pros of ProNexibus Plus®

  • Immediate results on all musculoskeletal diseases.
  • It does not require creams or conductive gels.
  • It can be used over hairy areas(atlas, pubis, thorax).
  • It can be used on prosthetic materials (plaques, osteosynthesis media).
  • Mechanical work by the operator is not required.
  • Light and easy to carry.
ProNexibus Plus - benessere

Contact us for information on our patented high frequency capacitive diathermy devices

Are you a healthcare practitioner?

Access to the display of products and information material is reserved to operators in the sector in compliance with current legislation. FocusMed Srl requires to qualify as an operator of the sector to proceed with navigation.

Legislative Decree of 24 February 1997, No 46 Article 21

1. It is forbidden to advertise to the public devices that, according to provisions adopted by decree of the Minister of Health, may be sold only on prescription or may be used with the assistance of a doctor or other healthcare professional.
2. Advertising to the public of devices other than those referred to in paragraph 1 is subject to authorization by the Ministry of Health. On the requests for authorization expresses opinion the Commission of experts provided for by article 6, paragraph 3, of the legislative decree 30 December 1992, n. 541, which for this purpose is supplemented by a representative of the Department of the Ministry of Health responsible for medical devices and one of the Ministry of Industry, Commerce and Crafts.