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 20 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 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 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.
Swiss Bionic Solutions, the developer and manufacturer of the MRS- and iMRS-Systems, fulfills all legally required standards for product safety and compliance for the distribution of PEMF devices for home use within the designated countries. In USA the MRS- and iMRS-series are registered and regulated with the FDA. In Canada, the iMRS-series is certified by Health Canada.
In Europe the MRS- and 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 USA, Canada and Australia.
Oxford Medical Instruments Ltd (OMI) is a UK-based multinational corporation specializing in all-natural + drug free medical devices, wellness and fitness equipment. We design, manufacture, and distribute each of our products to wholesalers and directly to consumers.
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 + Manufactured in Europe
For over 15 years, Oxford Medical Instruments Ltd. (OMI) has been helping people regain balance with the natural world. Operations began in Europe, but have expanded as global interest in all-natural therapies continues to grow. Most recently, OMI expanded our operations to cover North America.
Highest Quality Standards
We never compromise. Our products are of the highest quality + clinically tested for safety. All of our products meet the highest US FDA and EU CE standards.
Research is foundational to OMI. We are constantly evaluating new findings and market trends to ensure that OMI products are at the cutting-edge of medical technology.