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TheStreet Open House

Haemonetics Provides Update On Hemerus Medical, LLC Acquisition

BRAINTREE, Mass., Sept. 17, 2012 /PRNewswire/ -- Haemonetics Corporation (NYSE: HAE) today provided an update on the status of its previously announced agreement to acquire Hemerus Medical, LLC ("Hemerus"), a Minnesota-based company that develops innovative technologies for the collection of whole blood and for the processing and storage of blood components.  Hemerus' US New Drug Application and EU Medical Device Directive technical file for the SOLX ® whole blood collection system had been submitted to the FDA and TUV SUD notified body, respectively.

(Logo: http://photos.prnewswire.com/prnh/20120206/NE47232LOGO )

Today the Company announced that it has learned that Hemerus has received a request from the FDA for resubmission of their application with additional information.  As a result, the timing of the closing of the acquisition, which is contingent upon receipt of FDA approval, is still pending and now is expected to occur early in fiscal 2014.  In addition, the Company has also learned that Hemerus has received CE Marking ( Conformite Europeenne) in the European Union to market SOLX with the world's first 56-day red blood cell storage indication.  

Haemonetics' plans include delivery of its first whole blood automation software package, an automated whole blood collection device and continued development of acquired Pall whole blood products.  We believe SOLX remains an important part of the strategy for rapid market adoption of the whole blood product suite.  The FDA request for resubmission has minimal effect on our pipeline development since the inclusion of the SOLX solution in these products was contemplated for fiscal 2014 and beyond. 

Brian Concannon, President and CEO, stated: "The addition of Hemerus' SOLX collection system is intended to complement the portfolio of whole blood collection, filtration and processing product lines we recently acquired from Pall Corporation.  We will proceed with the Haemonetics and Pall elements of that offering while the FDA examination process for the SOLX solution continues.  We are pleased that CE Marking has been granted which gives credibility to the value of this new science."

Haemonetics paid $1 million cash in its first fiscal 2013 quarter and, upon receipt of the aforementioned FDA approvals for the product, will pay the remainder of the $27 million purchase price for Hemerus Medical.  Additionally, Haemonetics has agreed to pay a royalty of up to $14 million on future sales of SOLX-based products. 

Haemonetics is a global healthcare company dedicated to providing innovative blood management solutions for our customers.  Together, our devices and consumables, information technology platforms, and consulting services deliver a suite of business solutions to help our customers improve clinical outcomes and reduce the cost of healthcare for blood collectors, hospitals, and patients around the world.  Our technologies address important medical markets: blood and plasma component collection, the surgical suite, and hospital transfusion services.  To learn more about Haemonetics, visit our web site at http://www.haemonetics.com.             

This release contains forward-looking statements that are not historical facts. Haemonetics has identified some of these forward-looking statements with words like "will," "expect," "intend," "believe," "may," "could," "would," "might," "possible," "plan," "anticipate," or "continue," the negative of these words, other terms of similar meaning or the use of future dates.  Forward-looking statements in this release include without limitation statements regarding the expected timing of the completion of the transaction and statements regarding the effect of the transaction on Haemonetics' business and competitive position, statements regarding future innovation and statements regarding Haemonetics' future financial performance and financial condition. Information set forth in this press release is current as of today and the Company undertakes no duty or obligation to update this information.

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