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Nephros Engages Joseph S. Cervia, M.D. as Strategic Consultant
Date:11/21/2011

ent with STERIS Corp. (NYSE: STE) related to its ultrafiltration technology.

Nephros has contracted with the Office of Naval Research to develop an advanced water purification system for military field use. Nephros's proprietary dual stage cold sterilization ultrafilter will form the basis of the portable system.

In response to a Request For Information (RFI) from the U.S. Army, Nephros submitted its UF-40 ultrafilter for consideration as part of the standard issue hydration pack for soldiers in the field.  Nephros has been informed by the U.S. Army Public Health Command that its UF-40 filter has been validated to meet the military's NSF P248 standard for emergency military operations as a microbiological water purifier.  Nephros believes that its UF-40 filter is the only stand-alone filter to date to have met the performance criteria of the NSF P248 standard without secondary disinfection steps.  The Army has not to date issued a Request For Proposal (RFP), and Nephros has no information regarding when or if an RFP applicable to the UF-40 ultrafilter may be put forth by the U.S. Army.

About Nephros, Inc.

Nephros, Inc., headquartered in River Edge, New Jersey, is a medical device company developing and marketing filtration products for therapeutic applications, infection control, and water purification.

The Nephros hemodiafiltration (HDF) system is designed to improve the quality of life for the End-Stage Renal Disease (ESRD) patient while addressing the critical financial and clinical needs of the care provider. ESRD is a disease state characterized by the irreversible loss of kidney function. The Nephros HDF system removes a range of harmful substances more effectively, and with greater capacity, than existing ESRD treatment methods, particularly with respect to substances known collectively as "middle molecules." These molecule
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SOURCE Nephros, Inc.
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1. Nephros Reports Third Quarter 2011 Financial Results
2. Nephros Receives Initial FDA Response to 510(k) Application for Hemodiafiltration System
3. Nephros Reports Second Quarter 2011 Financial Results
4. Nephros Files 510(k) Application for Hemodiafiltration System
5. Nephros Receives 510k Approval to Market Additional Ultrafiltration Products
6. Nephros Reports First Quarter 2011 Financial Results
7. Nephros Receives Approval to Market Dual Stage Ultrafilters in Canada
8. Nephros Reports 2010 Fourth Quarter and Full Year Financial Results
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