We design and develop innovative electromedical devices for healthcare needs
Who we are
We make electromedical devices, technologically advanced and made in Italy, to answer to healthcare related need.
We focus our efforts on continuously researching and developing our technology, and on the precision, the reliability and professionality with which, always, we deal with our customers
The patient is at the center of our project.
That’s why our aim is to to provide the professional with ready, simple and effective tools and responses in order to address immediately, concretely, and resolutely the patient’s problems.
Our greatest satisfaction is that we know that we can give real relief to those who suffer, thanks to our technology.
What we do
We work daily in close contact with highly qualified professionals, to continuously ameliorate our product, to make it most useful for the everyday clinical practice.
Our products are patented and built in Italy, are easy to use, light to carry and extremely safe. The EC certificate enlights the safety reliablity of our work.
That’s why we are proud of our patent, certification and our technology: the controlled high frequencies.
The ProNexibus Plus® and the Rinovacell®are developed specifically for:
Where we are
Largo Traiano, 4, 35036 Montegrotto Terme PD
049 891 1849
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.