Numero verde: 800-456220

Controlled High Frequencies

Aninnovativedevice, practical ed effective

ProNexibus Plus® is designed for

Physiotherapists - Rehabilitators - 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 tissues and overcome the resistance offered by the body and cell membranes.

The high frequencies, overcoming the barriers they encounter on their way, reach directly deep into the injured cells and activate immediately the processes of cellular healing.

Thebeneficial effectsofProNexibus Plus® high-frequencies are:

  • Antalgic
  • Antiedemigenous
  • Anti-inflammatory
  • Pro-Regenerative
Effetto Antiinfiammatorio


Effetto Antalgico


Effetto Antiedemigeno


ProNexibus Plus - Effetto Prorigenerativo


Benefits of ProNexibus Plus®

  • Immediate results on all musculoskeletal conditions.
  • It does not require conductive creams or gels, unlike tecartherapy devices.
  • Can be used over hair (atlas, pubis, chest).
  • It can be used over prosthetic materials (plates, osteosynthesis media).
  • No mechanical work is needed on the part of the operator.
  • Lightweight and easy to carry.
ProNexibus Plus - benessere

Contact us to purchase our high-frequency 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.