CMI has received CAN/CSA ISO 13485 certificate which is required by the Canadian medical device authorities from manufactures to be able to place their devices into the market in Canada.
CMI pursued the CAN/CSA ISO 13485 certificate as part of an ongoing commitment to achieve compliance with the regulatory requirements of the global medical community.
The certificate was issued by KEMA Quality who is a recognized registrar for the Canadian Medical Devices Conformity Assessment System (CMDCAS) as well as one of the leading Notified Bodies worldwide.

You can find all updated certificates here