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Hemanext Submits Hemanext ONE System to FDA For U.S. Marketing Authorization

Hemanext, HemanextInvF, News, Press Release

Innovative Blood Processing and Storage System Received CE Mark Certification for Sale in European Markets Last Year LEXINGTON, Mass., January 5, 2022, PR NEWSWIRE – Hemanext Inc., a leading innovator in blood processing and storage technology, announced that it...

Recent Posts

  • Hemanext signs agreement with Hemara Bio, a healthcare distributor in the U.A.E., to provide hospitals and clinicians across the GCC Region with Hemanext ONE® system
  • Hemanext Inc. Announces New HCPCS Code for “Red Blood Cells, Leukocytes Reduced, Oxygen/Carbon Dioxide Reduced, Each Unit.”
  • Hemanext Inc. Announces Completion of Post-Market Cancer and Burn Safety Study
  • AABB Science Innovation Forum Nov 2023
  • Hemanext Inc. Announces a Significant Milestone with FDA Marketing Authorization for Hemanext ONE®

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This website may contain information on products or uses of those products that are not authorized in all countries or regions. Hemanext ONE has been granted marketing authorization for commercial distribution via the De Novo process by the U.S. Food & Drug Administration. In Europe Hemanext ONE is CE marked which allows the medical device to be placed in the market in the EEA. Illustrations are artist's representations only and should not be considered as engineering drawings or photographs. Hemanext, Hemanext ONE, and the logos are registered trademarks of Hemanext, Inc. © 2023 Hemanext, Inc. All rights reserved.
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