The outpatient electromedical For health care professionals.

The high frequencies of Maximum for

Physiotherapists - Nurses - Pain therapists.

Maximum ambulatoriale

Maximum®: What is it and how does it work?

The Maximum®, designed specifically for outpatient use, is inspired by the ProNexibus Plus®.

It is an electro-medical device developed for the treatment of musculoskeletal problems such as low back pain, arthritis and local inflammatory states.

Maximum® is dedicated to healthcare professionals working in the field of physical therapy and rehabilitation such as physical therapists, nurses, and physicians who do not need to work at the patient’s home.

Maximum® emits high frequencies at 4 or 8 MHz combined with a maximum power of 80 watts. In addition, the intuitive graphical interface allows the operator to modulate therapy easily.
Thanks to the handy handpieces, all body districts of the patient can be treated in comfort and simplicity.

Safe and practical device for the surgery

  • Unlike tecar therapy devices, Maximum® does not require conductive creams or gels for application.
  • It can be used on hair.
  • It can be used on prosthetic wearers such as Kirschner wires, orthopedic prostheses, etc.
  • Therapy is modulable during treatment.
  • It does not require time-consuming mechanical work on the part of the operator.
  • The mobile trolley (purchased separately) is not bulky and allows easy repositioning of the instrument after use.

See the following pages for a description of the beneficial effects that can be achieved by using Maximum®.

ProNexibus Plus - benessere

Device not yet placed on the market, soon to be released

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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.