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Global Industry Hub. (Aug, 2024). Resuscitative Endovascular Balloon Occlusion Of The Aorta Market Share & Forecast, 2024 - 2030 Global Industry Hub. Retrieved
Report ID: GIH 1003 | Aug 2024 | Format:
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Global Industry Hub. (Aug, 2024). Resuscitative Endovascular Balloon Occlusion Of The Aorta Market Share & Forecast, 2024 - 2030 Global Industry Hub. Retrieved
Resuscitative Endovascular Balloon Occlusion Of The Aorta Market size was valued at US$ 9.75 Mn in 2023, registering a CAGR of 19.8%% during the forecast period (2024-2030), and the market is projected to be worth US$ 34.7 Mn by 2030.
The report includes Vendor Assessment (Company Profiles, Market Positioning, Strategies, Recent Market Updates, Capabilities & Product Offerings / Mapping), Technology Assessment (Developments & Economic Impact), Partner & Customer Ecosystem (Product Services, Proposition & Key Features) Competitive Index & Regional Footprint by Global Industry Hub.
Resuscitative Endovascular Balloon Occlusion Of The Aorta Market Scope:
Report Coverage | Details |
---|---|
Base Year | 2023 |
Base Year Value | US$ 9.75 Mn |
Forecast Value | US$ 34.7 Mn |
CAGR | CAGR of 19.8%% |
Forecast Period | 2024-2030 |
Historical Data | 2019-2022 |
Largest Market | North America |
Fastest Growing Market | Europe |
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The Resuscitative Endovascular Balloon Occlusion Of The Aorta market is divided based on product, end user, application, and region. Each category has various sub-segments, and current trends in each segment help producers target specific customers effectively.
Important Features of the Report:
Reasons for buying this report:
End-use Outlook
Cardiac Arrest
Aortic Occlusion
Tactical Combat Casualty Care
Regional Outlook
North America
U.S.
Canada
Europe
Germany
UK
France
Italy
Spain
Asia Pacific
China
Japan
Key players in the industry are adopting growth strategies like partnerships, collaborations, mergers and acquisitions, and awareness programs to strengthen their market presence. The report also lists industry players for end users, facilitating communication between manufacturers and consumers.
In June 2024, Emergency Scientific, LLC successfully utilized its Landmark catheter for the first time in resuscitative endovascular occlusion of the aorta (REBOA). This innovative device, recently granted FDA 510(k) clearance, is designed for temporary occlusion of large vessels to manage emergency hemorrhage control.
In March 2024, Front Line Medical Technologies Inc. announced that it has received a NATO/National Stock Number (NSN) for its pioneering COBRA-OS (Control of Bleeding, Resuscitation, Arterial Occlusion System). This important milestone highlights the device's effectiveness and cost-efficiency in military medical contexts, where quick response and operational efficiency are crucial for saving lives.
In November 2022, Emergency Scientific received clearance from the United States Food and Drug Administration (FDA) to commercialize the Landmark REBOA Catheter system. This approval marks a significant advancement in the field of emergency medicine, particularly in the management of severe hemorrhaging.
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31 Aug 2024 This Report Contains the Latest Market Numbers, Statistics & Data Aavailable