MOUNT PLEASANT, SC--(Marketwire - September 09, 2009) - Revolutions Medical Corporation (“Revolutions Medical” or the “Company”) (OTCBB: RMCP), producers of the Rev Vac safety syringe, today announced that it has completed a significant redesign of its flagship Rev Vac syringe, reducing the product’s part count by nearly 30% and clearing the remaining economic hurdles to mass production and commercial launch. The Rev Vac safety syringe is already FDA approved.
“In this simple but bold redesign we not only made the final strides toward a market-ready product but have ensured a cost benchmark that will be difficult to compete with as well,” stated Revolutions Medical CEO Ron Wheet. “By reducing the Rev Vac’s part count we have accomplished two vital goals: 1) fewer parts simplifies the manufacturing process, slicing our upfront capital required and 2) the Rev Vac syringe performs even better than it did previously, and we have further reduced the variability of this already dependable product. This redesign places the Rev Vac safety syringe in a highly desirable competitive position, and the benefits of this design improvement will extend to our entire product line of safety syringes.
“This final milestone puts us firmly on pace to achieve our intended Q4 ’09 mass market launch.”
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About Revolutions Medical Corporation (www.revolutionsmedical.com)
Revolution Medical’s products include the Rev Vac safety syringe (FDA Approved), safety blood drawing device and safety IV catheter. Revolutions Medical also provides software solutions and proprietary tools that are compatible with standard MRIs and standard PACS. The software includes sorting of images, color, 3D and automatic segmentation of images.
FORWARD-LOOKING STATEMENTS
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