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Certification of TheraCell


The device is subject to EC-guidelines 93/42/EWG. TheraCell® is a licensed medical product (class II a) with the identification CE 0483. So far, no side effects of the device TheraCell® have been reported.

Since March 6th 2009 TheraCell® is also licenced for Canada.


EC-Certificate Canadian Licence
MDC-Zertifikat-Theracell-en-small Kanada-Zertifikat-Theracell-small