News
CSMG Technologies Comments on Importance of Live Tissue Connect Completing Key Onsite Audit; Milestone towards Achieving CE Mark Registration
Corpus Christi, TX, June 5, 2008 -- CSMG Technologies, Inc., (OTCBB: CTGI - News), a technology management company, announced that its Live Tissue Connect ("LTC") subsidiary completed the onsite audit portion of the CE Mark registration in accordance with the European Medical Device Directive - 93/42/EEC. LTC announced it has already received its ISO 13485:2003 certification for the design and manufacture of Bipolar Forceps Systems. This Quality Management System certificate was issued by BSI Management Systems, one of the world's leading certification bodies.
Donald S. Robbins, President and CEO of CSMG Technologies, said, "We are very pleased to have successfully completed the onsite audit last month. As we progress through this process towards achieving CE Mark in the Europe, the LTC team is currently researching marketing and sales channels."
Frank D'Amelio, President of LTC, stated, "Passing the onsite audit marks the second of three critical milestones towards achieving the CE Mark for LTC's Bipolar Sealing Forceps. The first step was the receipt of our ISO 13485:2003 Quality System Certification in March, 2008. The CE Mark is a requirement for the sale of medical devices in the European Union."
About Live Tissue Connect
LTC's surgical tissue bonding/welding device is a patented platform technology that bonds and reconnects human soft tissue through fusion, in contrast with conventional wound closing devices such as sutures, staples, sealant, or glues. LTC holds approximately 31 patents and pending patents in the U.S., Australia, Canada, European Union, Ukraine, and other countries.
For further information on CSMG Technologies and its various subsidiaries, please visit our website at www.csmgtechinternational.com.
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