Salt Lake City, UT, January 19, 2009 -- JTECH Medical, a medical device company developing innovative, next-generation therapeutic and evaluation products, announces the receipt of ISO 13485 and ISO 9001 certification for its manufacturing facility.

Being certified to ISO 13485 and ISO 9001 in our manufacturing facility gives further assurance to customers and partners that we are able to satisfy their most stringent quality, reliability, efficiency and cost-effectiveness requirements. This certification provides an internal manufacturing platform as we advance our products worldwide.

To receive this certification is a significant milestone for the team to achieve. This accomplishment allows us to move closer to our goal of providing the highest quality therapeutic and evaluation products.

The ISO 13485:2003 standard, published by the International Organization for Standardization, is an international reference for facility management requirements. The ISO 13485 standard provides a tried and tested framework for taking a systematic approach to managing an organization's processes so that it consistently turns out products that satisfy customer expectations and can assure regulatory authorities that JTECH Medical is manufacturing products using a quality management system in its facility.

About the ISO 13485 Certification

The ISO 13485:2003 standard is an international reference standard for the evaluation of quality management systems for the medical industry. The standard refers to an organization's structure for managing its processes or activities that transform inputs of resources into a product or service to meet customized objectives, such as satisfying customer quality requirements. Companies' compliance to ISO standards are certified by third-party audit and registration organizations, such as Orion Registrar, Inc. For more information about Orion Registrar Inc., visit http://www.orion4value.com.