System Comparisons

Understanding System Comparisons Questions - book a Consultation with Bionic Health today

Swiss Bionic Solutions, the developer and manufacturer of the iMRS-Systems is the only company worldwide which fulfills all country requirements for supplying PEMF-devices for home use. PEMF system comparisons should be based on the factors of:

  • Device safety, registration and regulatory compliance
  • User safety
  • Functional impact of the PEMF on the user
  • Pricing
  • Application Options and functionality of the device
  • Time tested data research to guide the user for optimal performance
  • Company backed Research & Development
  • Company history, mission & vision for future improvements

System comparisons worldwide

In the USA the iMRS-series is registered and regulated with the FDA. In Canada the iMRS is a 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 complimentary and alternative field (CAM-section) and never makes any false claims. As a reputable organization 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.

FDA registered-regulated Bionic Health Today Health Canada Bionic Health Today mdc-certification-iso_13458 mdc-certification-93_42_EEC





iMRS System Details (READ MORE)


To compare Swiss Bionic Solutions PEMF Systems to other systems being marketed today please request details through the “Book a Consultation” form. We will be happy to answer all your questions.

Bionic Health Today PEMF Systems System Comparisons


Read about PEMF – How PEMF Works to understand how PEMF systems vary in their use of the four parameters of waveform (signal shape), field strength, frequency and resonance and how results will vary according to these parameters.



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The iMRS® Systems are listed and regulated by the FDA and by Health Canada. However, these systems are not intended to diagnose, cure, treat, mitigate or prevent any particular disease.