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InspireMD Completes First Phase of Manufacturing Upgrade and Partners with HealthLink for Global Logistics and Distribution Services
Date:8/26/2013

evice industry.  We look forward to working with InspireMD as the Company prepares for increased demand for its MGuard™ stent technology throughout Europe."   

About Stenting and MGuard™ EPS

Standard stents were not engineered for heart attack patients. They were designed for treating stable angina patients whose occlusion is different from that of an occlusion in a heart attack patient.

In acute heart attack patients, the plaque or thrombus is unstable and often breaks up as the stent is implanted causing downstream blockages (some of which can be fatal) in a significant portion of heart attack patients.

The MGuard EPS is integrated with a precisely engineered micro net mesh that prevents the unstable arterial plaque and thrombus (clots) that caused the heart attack blockage from breaking off.

While offering superior performance relative to standard stents in STEMI patients with regard to ST segment resolution, the MGuard EPS requires no change in current physician practice – an important factor in promoting acceptance and general use in time-critical emergency settings.

About InspireMD, Inc.

InspireMD seeks to utilize its proprietary MGuard technology to make its products the industry standard for embolic protection stents and to provide a superior solution to the key clinical issues of current stenting in patients with a high risk of distal embolization, no reflow and major adverse cardiac events.

InspireMD intends to pursue applications of this technology in coronary, carotid and peripheral artery procedures.  InspireMD's common stock is quoted on the NYSE MKT under the ticker symbol NSPR.

MGuard EPS is CE Mark approved. It is not approved for sale in the U.S. by the FDA at this time.

Forward-looking Statements:

This press release contains "forward-looking statements." Such statements may be preceded by the words "int
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SOURCE InspireMD, Inc.
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Related medicine technology :

1. InspireMDs MGuard Embolic Protection Stent (EPS) Shows Lower Mortality Rate in STEMI Patients at Six Months Compared to Control Group
2. InspireMD Reports Financial Results For Period Ended March 31, 2013
3. InspireMD Receives Approval From US Food and Drug Administration to Begin US Regulatory Trial
4. InspireMD Closes $25 Million Underwritten Public Offering
5. InspireMD Announces Pricing of Underwritten Public Offering of Common Stock and Listing on NYSE MKT
6. InspireMD Receives CE Mark Approval for Carotid Embolic Protection Stent
7. InspireMD Files Amended Registration Statement for Proposed Public Offering of Common Stock
8. InspireMD Reports Results for Period Ended Dec. 31, 2012
9. InspireMD to Discuss MGuard(TM) and the MASTER Randomized Trial Results at the ICI 2012 Meeting
10. Positive Results of InspireMDs MASTER Trial to be Published on November 6 in Journal of American College of Cardiology
11. InspireMD Reports Results For Period Ending Sept. 30, 2012
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