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Aortic Perfusion Cannula Research: with a compound annual growth rate (CAGR) of 6.3% in the next few years

10-24-2025 11:31 AM CET | Advertising, Media Consulting, Marketing Research

Press release from: QY Research Inc.

Aortic Perfusion Cannula Research: with a compound annual

QY Research Inc. (Global Market Report Research Publisher) announces the release of 2025 latest report "Aortic Perfusion Cannula- Global Market Share and Ranking, Overall Sales and Demand Forecast 2025-2031". Based on current situation and impact historical analysis (2020-2024) and forecast calculations (2025-2031), this report provides a comprehensive analysis of the global Aortic Perfusion Cannula market, including market size, share, demand, industry development status, and forecasts for the next few years.

The global market for Aortic Perfusion Cannula was estimated to be worth US$ 355 million in 2024 and is forecast to a readjusted size of US$ 628 million by 2031 with a CAGR of 7.7% during the forecast period 2025-2031.

【Get a free sample PDF of this report (Including Full TOC, List of Tables & Figures, Chart)】
https://www.qyresearch.com/reports/4348600/aortic-perfusion-cannula

Aortic Perfusion Cannula Market Summary

According to the latest report "Global Aortic Perfusion Cannula Market Report 2025-2031" by the QYResearch research team, the global market size is expected to reach US$ 1.206 billion in 2031, with a compound annual growth rate (CAGR) of 6.3% in the next few years.

An aortic perfusion cannula is a critical medical device used to establish a connection between the aorta and the cardiopulmonary bypass machine during extracorporeal circulation surgery, primarily for maintaining systemic blood circulation during cardiac arrest. This cannula delivers oxygenated blood to the patient's entire body through an aortic insertion port, ensuring tissue oxygenation and metabolic needs. Its structure typically consists of a tube, connector, guide tip, and fixture. The tube is typically made of medical-grade silicone, polyurethane, or polytetrafluoroethylene, offering excellent flexibility, torsion resistance, and biocompatibility. Depending on the intended use and surgical procedure, it can be categorized into adult and pediatric types, with side ports, and with pressure monitoring. This product requires high flow capacity and a low-resistance design to minimize blood damage and ensure stable perfusion pressure. It is an essential core component in cardiac surgery and extracorporeal circulation equipment systems.

The aortic perfusion cannula market is a typical technology-driven specialty medical market, whose development is highly dependent on the global growth in cardiac surgery volume and technological advancements. Key drivers of this market growth include the increase in cardiac surgery procedures driven by an aging global population and the widespread adoption of minimally invasive cardiac surgery techniques. These factors, in turn, place higher demands on cannula morphology, flexibility, and fluid dynamics, driving product upgrades. However, the market also faces significant challenges, including continued pricing pressure from global payers and the potential substitution of traditional open-chest surgery by advancements in interventional cardiac technologies (such as transcatheter aortic valve replacement (TAVR)). Looking ahead, the aortic perfusion cannula market will continue to evolve towards safer and more efficient procedures. Innovative products that minimize blood trauma, optimize hemodynamics, and enhance intraoperative visualization (such as improved ultrasound imaging) will be key to maintaining a competitive advantage.

The main drivers of aortic perfusion cannula growth are as follows:

1. The increasing prevalence of cardiovascular disease drives increased surgical demand.

The core driver of the aortic perfusion cannula market is the continued rise in the global incidence of cardiovascular disease. The number of surgeries such as heart bypass surgery, valve replacement, and congenital heart disease repair is increasing year by year. Especially against the backdrop of a rapidly aging population, the number of patients with atherosclerosis, coronary artery disease, and heart failure is rising. According to the World Health Organization, cardiovascular disease causes approximately 18 million deaths worldwide each year, accounting for one-third of all deaths. This trend directly drives sustained demand for key consumables such as extracorporeal circulation devices and aortic perfusion cannulas.

II. Advances in Medical Technology Promote Product Upgrades

With the advancement of minimally invasive and precision surgical techniques, aortic perfusion cannulas are gradually evolving towards high performance, small outer diameters, low resistance, and monitorability. Minimally invasive cardiac surgery and robotic-assisted surgery require cannulas with increased flexibility and precision, as well as high-pressure resistance and anti-twisting properties. In recent years, smart cannulas with integrated pressure monitoring and temperature control sensors have entered clinical use, significantly improving safety and perfusion efficiency, further expanding the market. 3. Increased medical investment in emerging markets is driving demand.

In Asia Pacific, Latin America, and the Middle East, medical infrastructure development and government health spending have grown significantly. In particular, countries like China, India, and Brazil are accelerating the localization and upgrading of cardiovascular surgical equipment. The rapid growth of cardiac centers in these regions has created a new market for aortic perfusion cannula manufacturers. Furthermore, increased medical insurance coverage and policies to localize the production of mid- to high-end consumables are also driving market penetration for this product.

4. High-performance materials and standardized regulations are driving industry upgrades.

Aortic perfusion cannulas place extremely high demands on material safety and biocompatibility. As national drug regulatory agencies in Europe, the United States, and China tighten medical device standards, manufacturers are adopting high-end materials such as medical-grade silicone, polyurethane (PU), and polytetrafluoroethylene (PTFE) to meet stringent clinical performance verification requirements. This not only improves product stability and lifespan but also drives the global market toward high-tech, high-value-added technologies, creating a long-term growth engine centered on material innovation and quality standards.

This report profiles key players of Aortic Perfusion Cannula such as MERA、Cardinal Health、EUROSETS、ANDOCOR、Medtronic、LivaNova PLC、Edwards Lifesciences Corporation、Getinge、Nipro、SurgiKart India、Terumo Cardiovascular、Braile Biomédica、Weigao Group、VITALCOR. In 2023, the global top five Aortic Perfusion Cannula players account for 73% of market share in terms of revenue.

Aortic perfusion cannulas, critical, high-value consumables used in cardiac surgery, have an industry chain that combines the common characteristics of the medical device industry with its own high standards and regulatory oversight.

Upstream Industry Chain: Raw Materials, Components, and Core Technologies

The upstream industry chain for aortic perfusion cannulas primarily includes various materials, core components, and related equipment used in manufacturing and R&D. The technical level and quality of this process directly determine the performance and safety of the final product. Medical-grade polymer materials, such as medical PVC, silicone rubber, polyurethane, and TPE, are central to the manufacture of the cannula itself. These materials must exhibit excellent biocompatibility, flexibility, collapse resistance, and adequate blood compatibility. To ensure clear positioning during surgery, cannulas typically require radiopaque markers, which rely on contrast materials such as tungsten wire, barium sulfate, or bismuth compounds. Furthermore, auxiliary components such as suture rings and connectors on the cannulas require specialized silicone or plastics. The upstream manufacturing process also includes the design and manufacture of precision injection molding machines, extruders, and molds. The precision of the mold directly impacts the smoothness of the cannula wall and the flow path design. Finally, sterilization equipment (such as ethylene oxide autoclaves and electron beam irradiation equipment) and packaging materials (such as blister packs and Tyvek lids) are also essential steps before a product leaves the factory.

Midstream of the Industry Chain: R&D, Production, Quality Control, and Regulatory Registration

The midstream is the core value chain, encompassing product design and development, production and manufacturing, quality control, and market access. Companies conduct fluid dynamics design based on surgeons' clinical needs, optimizing the cannula's opening shape and wall curvature to maximize blood flow efficiency and minimize shear forces, thereby reducing blood trauma and the risk of hemolysis. Prototyping and rigorous testing (including fluid dynamics bench testing and animal experiments) are key steps before product finalization. The production process, conducted in a highly cleanroom, involves multiple processes, including precision extrusion, assembly, vulcanization, and coating, placing extremely high demands on process stability and the production environment. Quality control is implemented throughout the entire process, from incoming raw material inspection to online monitoring on the production line and comprehensive performance testing of finished products (such as flow testing, pressure resistance, and biocompatibility testing), all in compliance with Good Manufacturing Practices for Medical Devices. Furthermore, companies must invest significant resources in regulatory registration, such as submitting a 510(k) application to the US FDA or applying for a medical device registration certificate from the National Medical Products Administration in China. This process is time-consuming and costly. Brand building, marketing, and establishing partnerships with hospitals and distributors are also core business activities for midstream companies.

Downstream of the Industry Chain: Distribution, Clinical Applications, and the End Market

The downstream of the industry chain connects end users, primarily including distribution logistics, medical institutions, and payers. Products reach hospitals primarily through two channels: first, through large medical device distributors (such as Cardinal Health, although it also produces its own brand), which have extensive logistics networks responsible for distributing products to hospitals at all levels; second, through direct academic promotion and sales to large cardiac centers through companies' in-house marketing teams. The end application scenario is the primary operating room in a hospital's cardiovascular surgery department, where cardiac surgeons and perfusionists are users. Physician usage habits, brand trust, and immediate product availability are crucial. Therefore, providing comprehensive technical training, on-site clinical support, and emergency stocking services are key to maintaining customer relationships. Ultimately, product costs are covered by national medical insurance, commercial insurance, or out-of-pocket payments. In different countries, medical insurance catalogs and payment policies have a decisive influence on product pricing and penetration. End-market demand is directly driven by an aging population, the incidence of cardiovascular disease, and the increasing popularity of minimally invasive cardiac surgery.

Industry Chain Support System: Regulation, R&D, and Standards

The operation of the entire industry chain relies on a strong support system. Government regulatory agencies (such as the US FDA, China's National Medical Products Administration, and Europe's European Medical Equipment Manufacturers) serve as the "gatekeepers" of the industry chain, establishing regulations and standards that ensure product safety and effectiveness. Academic research institutions and universities are the source of cutting-edge technology and basic research, fueling industry innovation. Industry standards organizations (such as ISO and ASTM International) are responsible for developing unified international standards for medical device materials, performance testing, and sterilization validation, ensuring product compatibility and consistent quality. This support system, closely interacting with upstream, midstream, and downstream sectors, together forms a solid foundation for the continued development and iteration of the aortic perfusion cannula industry. The competitive landscape of the aortic perfusion cannula market primarily exhibits the following characteristics:

International Market Landscape:

Globally, the aortic perfusion cannula market is dominated by a handful of large medical device groups, resulting in a competitive landscape characterized by high technological barriers and significant product concentration. European and American companies dominate the high-end market. Leveraging robust R&D systems and extensive clinical data accumulation, some companies offer high-end aortic cannulas with pressure monitoring, flow optimization, and improved biocompatibility, which are widely used in major cardiac surgery hospitals and heart centers. Furthermore, some Japanese and European manufacturers, leveraging their strengths in supporting equipment for extracorporeal circulation, maintain a stable market share in the Asia-Pacific and European markets.

Domestic Market Landscape:

The competitive landscape in the Chinese market is relatively fragmented, with local companies making significant progress in the mid-range and domestic substitution sectors. By incorporating imported materials and improving perfusion tubing design, these companies have achieved a balance between cost control and product performance, gradually gaining entry into the centralized procurement catalogs of tertiary hospitals and cardiac surgery departments. Furthermore, domestic companies are actively pursuing overseas certifications (such as FDA and CE) to enhance their international market recognition. Overall, the global aortic perfusion cannula market exhibits a dual structure characterized by international high-end monopoly and regional expansion of domestic substitution. The high-end market is dominated by European, American, and Japanese companies, with technological barriers concentrated in areas such as perfusion fluid dynamics design, material purity control, and blood compatibility verification. Meanwhile, Chinese, Indian, and South Korean companies are rapidly emerging in the mid- and low-end markets, leveraging pricing advantages and policy support to accelerate domestic substitution. Future competition will shift from single-product performance to systematic extracorporeal circulation solutions and monitorable smart cannulae, leading to further market concentration.

The report provides a detailed analysis of the market size, growth potential, and key trends for each segment. Through detailed analysis, industry players can identify profit opportunities, develop strategies for specific customer segments, and allocate resources effectively.

The Aortic Perfusion Cannula market is segmented as below:
By Company
Medtronic
Edwards Lifesciences
Terumo
LivaNova
CARDINAL HEALTH
Medical Materials, Inc.
MERA
Andocor
Nipro Medical
Braile Biomédica
Prymax Healthcare LLP
Weigao Group
Chalice Medical
Senko Medical
MicroPort

Segment by Type
Polyvinyl Chloride
Polyethylene
Stainless Steel
Others

Segment by Application
Adults
Children

Each chapter of the report provides detailed information for readers to further understand the Aortic Perfusion Cannula market:

Chapter 1: Introduces the report scope of the Aortic Perfusion Cannula report, global total market size (valve, volume and price). This chapter also provides the market dynamics, latest developments of the market, the driving factors and restrictive factors of the market, the challenges and risks faced by manufacturers in the industry, and the analysis of relevant policies in the industry. (2020-2031)
Chapter 2: Detailed analysis of Aortic Perfusion Cannula manufacturers competitive landscape, price, sales and revenue market share, latest development plan, merger, and acquisition information, etc. (2020-2025)
Chapter 3: Provides the analysis of various Aortic Perfusion Cannula market segments by Type, covering the market size and development potential of each market segment, to help readers find the blue ocean market in different market segments. (2020-2031)
Chapter 4: Provides the analysis of various market segments by Application, covering the market size and development potential of each market segment, to help readers find the blue ocean market in different downstream markets.(2020-2031)
Chapter 5: Sales, revenue of Aortic Perfusion Cannula in regional level. It provides a quantitative analysis of the market size and development potential of each region and introduces the market development, future development prospects, market space, and market size of each country in the world..(2020-2031)
Chapter 6: Sales, revenue of Aortic Perfusion Cannula in country level. It provides sigmate data by Type, and by Application for each country/region.(2020-2031)
Chapter 7: Provides profiles of key players, introducing the basic situation of the main companies in the market in detail, including product sales, revenue, price, gross margin, product introduction, recent development, etc. (2020-2025)
Chapter 8: Analysis of industrial chain, including the upstream and downstream of the industry.
Chapter 9: Conclusion.

Benefits of purchasing QYResearch report:

Competitive Analysis: QYResearch provides in-depth Aortic Perfusion Cannula competitive analysis, including information on key company profiles, new entrants, acquisitions, mergers, large market shear, opportunities, and challenges. These analyses provide clients with a comprehensive understanding of market conditions and competitive dynamics, enabling them to develop effective market strategies and maintain their competitive edge.

Industry Analysis: QYResearch provides Aortic Perfusion Cannula comprehensive industry data and trend analysis, including raw material analysis, market application analysis, product type analysis, market demand analysis, market supply analysis, downstream market analysis, and supply chain analysis.

and trend analysis. These analyses help clients understand the direction of industry development and make informed business decisions.

Market Size: QYResearch provides Aortic Perfusion Cannula market size analysis, including capacity, production, sales, production value, price, cost, and profit analysis. This data helps clients understand market size and development potential, and is an important reference for business development.

Other relevant reports of QYResearch:
Global Aortic Perfusion Cannula Market Research Report 2025
Global Aortic Perfusion Cannula Market Insights, Forecast to 2031
Global Aortic Perfusion Cannula Sales Market Report, Competitive Analysis and Regional Opportunities 2025-2031

About Us:
QYResearch founded in California, USA in 2007, which is a leading global market research and consulting company. Our primary business include market research reports, custom reports, commissioned research, IPO consultancy, business plans, etc. With over 18 years of experience and a dedicated research team, we are well placed to provide useful information and data for your business, and we have established offices in 7 countries (include United States, Germany, Switzerland, Japan, Korea, China and India) and business partners in over 30 countries. We have provided industrial information services to more than 60,000 companies in over the world.

Contact Us:
If you have any queries regarding this report or if you would like further information, please contact us:
QY Research Inc.
Add: 17890 Castleton Street Suite 369 City of Industry CA 91748 United States
EN: https://www.qyresearch.com
Email: global@qyresearch.com
Tel: 001-626-842-1666(US)
JP: https://www.qyresearch.co.jp

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