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|Medtronic Begins Distribution of i-port Advance® Injection Port Device for People with Diabetes|
Distribution Rights Broaden Medtronic's Diabetes Management Solutions to Include Injection Therapy Assistance
MINNEAPOLIS - February 13, 2014 - Medtronic, Inc. (NYSE:MDT) has begun distribution of i-port Advance® as part of a continued focus to provide meaningful therapy management solutions for people with diabetes. i-port Advance can be used for people on insulin injection therapy who want to administer insulin conveniently while eliminating the need to puncture the skin with each dose of medication. i-port Advance injection port is cleared by the FDA and indicated for patients who administer multiple daily subcutaneous injections of physician prescribed medications, including insulin.
i-port Advance provides a safe, effective, and easy way for people with diabetes to administer insulin, especially those on injection therapy who have needle-related bruising and scarring, pain and discomfort, or who experience anxiety from injecting their diabetes medications. i-port stands for injection port and it is a three-day-wear device that people with diabetes inject into instead of injecting directly into the skin. Because the device may remain in place for up to 72 hours, i-port Advance accommodates multiple drug injections without the discomfort of additional needle sticks.
"Adding i-port Advance to our diabetes solutions portfolio puts us in a stronger position to support a broader group of people with diabetes - including those currently on injection therapy - with tools to help simplify diabetes management routines," said Jeff Hubauer, vice president and general manager of insulin delivery for the Diabetes business of Medtronic.
Benefits of i-port Advance include:
Medtronic acquired important assets from Patton Medical and is now the exclusive distributor of i-port Advance. The device is now available for sale in the U.S., with expansion to additional global markets planned to take place over the next several months. The device is both FDA-cleared and CE (Conformité Européenne)-marked.
Healthcare professionals and people with diabetes interested in learning more about the product should contact Medtronic's customer center at 800.646.4633 or online at www.i-port.com.
About the Diabetes Business at Medtronic
Any forward-looking statements are subject to risks and uncertainties such as those described in Medtronic's periodic reports on file with the Securities and Exchange Commission. Actual results may differ materially from anticipated results.
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 IPA Wear Trial. Patton Medical 2011. PTN: 0909.2. Data on File.