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.