Cellular Therapeutics
    bandoyog3@aol.com  (724-547-4898)

    additional info found at pemf4you.com

​Click on the individual links under each  symbol to view the certificates.

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.

Extensive investigating by Health Canada found that the iMRS system has 

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-Certificatewhich guarantees electronic safety and electromagnetic compatibility in the majority of countries including USA, Canada and Australia.

​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. No sales partner of Swiss Bionic Solutions is allowed to make any specific health claim aside from the legally authorized intent of use. MRS 2000+ designo®, SkinDream®, iMRS®, intelligent wellness® and Omnium1 - intelligent lifestyle® are registered trademarks of Swiss Bionic Solutions Holding GmbH.



"We crave for new sensations but soon become indifferent to them...

The wonders of yesterday are todays common occurrences."  
Nikola Tesla