Plasmapheresis refers to the treatment of a medical condition in which there is a leakage or escape of some of the blood’s nutrients, usually arterial or venous, into the space between the skin and muscle layers. Plasmapheresis is usually used in a medical emergency where the patient’s entire blood system may be compromised or injured. The plasmapheresis processes used in emergency medicine are particularly complex because they involve the use of an invasive process to remove large volumes of blood from the body without causing any damage to the internal organs. Plasmapheresis can also be used in the ICU to facilitate the transfer of a patient’s own platelets to replace those lost in the event of a disaster such as a heart attack or stroke. Plasmapheresis devices are typically composed of a pump and a cannula.
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Major Company Profiles Covered in This Report: Asahi Kasei Corporation., Terumo Corporation, Baxter International Inc., B. Braun Melsungen AG, Kawasumi Laboratories Inc., Kaneka Corporation, Haemonetics Corporation, Shanghai Dahua Medical Apparatus Co., Ltd., Infomed SA, and Fresenius SE & Co. KGaA
Increasing global per capita income and growing spending on healthcare infrastructure are significantly propelling the growth of the plasmapheresis device market. Improving health care infrastructure and government reimbursement policies across developed as well as developing regions is again propelling the growth of the market. Increasing adoption of plasmapheresis in the treatment of rare diseases such as thrombotic thrombocytopenic purpura (TTP), Goodpasture’s syndrome, Guillain-Barré syndrome, and Wegener’s Granulomatosis is also contributing to the growth of the market. An increasing number of clinics and hospitals around the globe is another key factor fostering the growth of the plasmapheresis device market.
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North America is projected to dominate the global plasmapheresis device market and this is accredited to the continuous launch of innovative products in the market. For instance, in July 2019, Baxter International Inc. announced 510(k) clearance of the PrisMax system and integrated TherMax blood warmer, the company’s next-generation platform for continuous renal replacement therapy (CRRT) and therapeutic plasma exchange (TPE). PrisMax system offers innovative technology to help simplify therapy delivery.
In April 2020, Terumo BCT, Inc. and Marker Therapeutics AG announced that the U.S. Food and Drug Administration (FDA) has issued Emergency Use Authorization (EUA) for the use of Terumo BCT’s Spectra Optia® Apheresis System combined with Marker Therapeutics’ D2000 Adsorption Cartridge to treat patients 18 years of age or older with confirmed Coronavirus Disease 2019 (COVID-19)
In January 2019, Fresenius Medical Care, the provider of dialysis products and services announced the launch of its 4008A dialysis machine, which was specially designed to meet the needs of emerging markets
In July 2017, Haemonetics Corporation has received FDA 510(k) clearance for its NexSys PCS™ plasmapheresis system.
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