About Swiss Bionic Solutions

In the field of Pulsed Electromagnetic Field (PEMF) technology, numerous systems for home use have appeared on the market in the last 25 years. Some, like Swiss Bionic Solutions (manufacturer of the iMRS) were developed under the premise of providing evidence-based pulsed electromagnetic fields within a certain signal structure, frequency range and intensity.

Today there are many new companies entering the marketplace and confusion reigns. All kinds of medical claims are being made by some of the less reputable companies even though legal requirements in designated countries, particularly in the field of complementary and alternative medicine (CAM-section), have become very strict to protect the integrity and safety regulations of PEMF devices.

Swiss Bionic Solutions, the developer and manufacturer of the iMRS Systems, is the only company worldwide that fulfils all country requirements for supplying PEMF devices for home use. In the USA the iMRS series is registered with the FDA. In Canada, the iMRS is a registered Class II approved medical device. In Europe, the iMRS systems are certified as Class IIa-medical devices within the directive EEC 93/42. Furthermore, all systems have a basic CE-Certificate as well as a more advanced CB-Certificate, which guarantees electronic safety and electromagnetic compatibility in the majority of countries including USA, Canada and Australia. Swiss Bionic Solutions respects the legal requirements within the complementary and alternative field (CAM-section) and never makes any false claims. As a reputable organisation, Swiss Bionic Solutions proudly accepts its responsibility in protecting the powerful technology of PEMF's and to guarantee effective, reliable and safe applications with every use.


Certificates

Swiss Bionic Solutions, the developer and manufacturer of the iMRS-Systems, fulfils all legally required standards for product safety and compliance for the distribution of PEMF devices for home use within the designated countries. In the USA, the iMRS Systems are registered with the FDA. In Canada, the iMRS series is certified by Health Canada.

In Europe the iMRS systems are certified as Class IIa-medical devices within the directive EEC 93/42. Furthermore, all systems have a CE-Certificate as well as a more advanced CB-Certificate, which guarantees electronic safety and electromagnetic compatibility in the majority of countries including the USA, Canada and Australia.

With an expanding global reach, we work with clients across Europe, the Middle East, and now the U.S. and Canada to help others achieve optimal health and wellness. All of our products are developed and manufactured in Europe. Our American subsidiary handles distribution throughout the U.S, Canada and now Australia.

Designed in Switzerland + Manufactured in Germany