- Reprocessing of Varicose Vein Ablation Catheter Continues to Gain Customers
- Excellent Record of Safety and Reliability
- Reprocessing Lowers Costs and Reduces Medical Waste for U.S. Vein Clinics
MINNEAPOLIS, Aug. 17, 2015 (GLOBE NEWSWIRE) -- Vascular Solutions, Inc. (Nasdaq:VASC) today announced that more than 100,000 ClosureFAST catheters have been successfully reprocessed by its partner, Northeast Scientific, Inc. (NES), since Vascular Solutions launched its reprocessing service for the popular vein ablation catheters in January 2012.
“We are now in the fourth year on the market with our reprocessing service for the ClosureFAST vein ablation catheter, and with the achievement of another milestone in the number of successfully reprocessed catheters, we continue to demonstrate an excellent record of safety and reliability,” said Howard Root, Chief Executive Officer of Vascular Solutions. “The benefits of a well-executed reprocessing program are clear, and as a result Vascular Solutions continues to add vein clinic customers that are motivated to reduce costs and cut medical waste while serving the needs of their patients.”
Reprocessing of the ClosureFAST catheter is a service offered exclusively by Vascular Solutions in collaboration with NES. To date, more than 660 U.S. vein practices have contracted with Vascular Solutions to have their ClosureFAST catheters reprocessed by NES.
“Our reprocessing partner, NES, has done an excellent job of meeting physicians’ demands for a reliable system of reprocessing ClosureFAST catheters,” Mr. Root said. “We are very pleased with the results of our ClosureFAST reprocessing program and we look forward to ongoing success with this service.”
The ClosureFAST radiofrequency ablation catheter, which is manufactured and marketed by Medtronic, is the most popular product used for performing endovenous therapy for the treatment of varicose veins in the U.S. Vascular Solutions is offering the reprocessing service under contract with NES, an established third-party reprocessor of medical devices. NES received 510(k) clearance from the U.S. Food and Drug Administration on November 30, 2011 for reprocessing the ClosureFAST catheter.
Craig Allmendinger, Chief Executive Officer of NES, commented: “We are proud of our achievements with the ClosureFAST reprocessing service. Since the program was launched in January of 2012 in collaboration with Vascular Solutions, we have demonstrated the highest standards of performance within the industry. We are pleased that a growing number of physicians are embracing the opportunities for reprocessing, making reprocessing one of the fastest-growing segments within the medical device industry.”
Vascular Solutions markets and sells the ClosureFAST reprocessing service to hospitals and clinics in the United States through Vascular Solutions’ 100-person direct sales force. Subscribers to the service send their used ClosureFAST catheters directly to NES for reprocessing. NES’s validated reprocessing system for ClosureFAST involves multiple stages, including decontamination, cleaning, drying, packaging, labeling, sterilization, and biological quarantine testing. As part of the process, each catheter is subjected to function testing and undergoes multiple inspections to ensure that quality standards are met.
In addition to supporting its Vari-Lase® laser ablation product line and offering the ClosureFAST reprocessing service, Vascular Solutions offers a full range of accessory products that are needed to perform both RF- and laser-based procedures. The company provides procedure packs that are designed for either RF or laser procedures, micro-introducers and 7F micro-HV kits, 0.018” and 0.025” guidewires,18G echogenic needles for percutaneous entry, and the Auto-Fill® Syringe for administering tumescent anesthesia. Vascular Solutions also sells a line of disposable vein hooks for use in phlebectomy procedures and the Veinsite® system used to visualize veins beneath the skin surface.
About Northeast Scientific
Northeast Scientific, Inc. (NES), a privately-held company headquartered in Waterbury, Connecticut, is registered with the U.S. Food and Drug Administration as a reprocessor of single-use medical devices. Founded in 2005, NES received its first 510(k) clearance in 2007. NES’s facility was designed specifically to reprocess single-use devices. The process employs a high capacity reverse osmosis deionized water system for cleaning, and only environmentally safe detergents are used. NES performs all sterilization in-house using 100% ethylene oxide systems that limit waste and ensure sterility. Functional testing of each reprocessed device and heat-seal packaging is carried out in NES’s Class 10,000 clean room.
For more information about NES, visit the company’s website at www.mdreprocess.com.
About Vascular Solutions
Vascular Solutions, Inc. is an innovative medical device company that focuses on developing unique clinical solutions for coronary and peripheral vascular procedures. The company has launched more than 100 products that are sold to interventional cardiologists, interventional radiologists, electrophysiologists, and vein specialists through the company’s 100-employee direct U.S. sales force and international independent distributor network covering 60 countries.
The information in this press release contains forward-looking statements that involve risks and uncertainties. Our actual results could differ materially from those anticipated in these forward-looking statements. Important factors that may cause such differences include those discussed in our Annual Report on Form 10-K for the year ended December 31, 2014 and other recent filings with the Securities and Exchange Commission. The risks and uncertainties include, without limitation, risks associated with the need for adoption of our new products, lack of sustained profitability, exposure to intellectual property claims, significant variability in quarterly results, exposure to possible product liability claims, the development of new products by others, doing business in international markets, the availability of third party reimbursement, and actions by the FDA.
ClosureFast is a registered trademark of Covidien LP (a subsidiary of Medtronic plc). Reprocessing of ClosureFast catheters is performed by NEScientific and is not affiliated in any way with Covidien, Covidien LP, VNUS Medical Technologies, Inc., Tyco Healthcare Group, LP, or Medtronic plc.
For further information, connect to www.vasc.com.