Salt Lake City, UT, August 12, 2010 -- JTECH Medical, a medical device company developing innovative, next-generation therapeutic and evaluation products, announces that it has received certification to ISO 13485:2003 by Intertek Testing Services NA Ltd., a Health Canada recognized registrar.  JTECH received certification to ISO 13485:2003 and ISO 9001 in 2008 but sought to expand opportunities for users and patients in Canada which required certification by a Health Canada recognized registrar. JTECH also applied for, and received, a Device Establishment License to distribute our products throughout Canada.

Commenting on the announcement, Len Smith, President of JTECH Medical, said, "Achieving CMDCAS certification is a further endorsement of JTECH's manufacturing capabilities and approach to quality system management. This has enabled us to move forward with the registration and commercialization of our products in Canada.  We plan to aggressively promote and market our products in Canada immediately."

In addition to ISO 13485:2003, JTECH Medical also renewed its ISO 9001:2008 certification demonstrating that JTECH Medical is continually looking to improve our quality management system in order to meet our clients' and regulatory agencies' expectations. The transition to the 2008 version of the standard was first completed in 2009.

ISO 13485:2003 CMDCAS Certificate
ISO 9001:2008 Certificate
Canadian Medical Device Establishment License