September, 2014 : iMRS/Omnium1 PEMF Therapy Devices have passed all necessary audits and received the Certificate DIN ISO 13485 with the supplementary CMDCAS-Certificate for the Canadian regulatory authority.
Effective immediately the iMRS is a registered and approved class II medical device within Health Canada. As far as we can assess at this time the iMRS is the only PEMF-System of its kind for home use that has this rating. With this certificate from Health Canada all competitive PEMF systems on the market, that do not have this certificate are illegal and can no longer be sold without a classification by Health Canada.
Effective immediately the iMRS is a registered and approved class II medical device within Health Canada. As far as we can assess at this time the iMRS is the only PEMF-System of its kind for home use that has this rating. With this certificate from Health Canada all competitive PEMF systems on the market, that do not have this certificate are illegal and can no longer be sold without a classification by Health Canada.
