TriE Medical, Inc. Receives ISO 13485 Certification

Morrisville, NC—TriE Medical, Inc, a privately held medical device development
company located near the Research Triangle Park, is proud to announce that the
organization has received ISO 13485 certification for its Quality Management System.
TriE's scope of registration includes contract design, development, engineering and
contract manufacturing services related to mechanical, electrical and software related
needs of the medical device industry. TriE has followed a detailed quality management
system for years, however we made the corporate decision to obtain certification for our
quality system as it was important to our customers and employees. ISO 13485
certification is an important milestone and attests to the quality of TriE's design and
documentation services.

"I am pleased to announce our ISO 13485 certification, it is a true testament of TriE's
dedication to the highly regulated medical device industry and the importance of quality
throughout the total product life cycle.."---John Popow, President

About TriE Medical, Inc.

TriE Medical is a medical device and development firm with extensive expertise in
therapeutic ultrasound, infusion pumps, respiratory devices, gas delivery systems, drug
delivery systems, biomedical monitoring devices, invitro diagnostic devices, and
cardiovascular devices. TriE works with our clients to develop medical devices along any
stage in the design process while maintaining documentation to meet FDA approvals.
TriE’s clients range in size from start-up, mid-size, to multinational companies.