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The Brazil hemostats market was valued at USD 230.13 Million in 2025 driven by the rising surgical volumes across the region. It is expected to grow at a CAGR of 5.80% during the forecast period of 2026-2035 and attain a market value of USD 404.42 Million by 2035. Brazil relies on both domestic production and foreign suppliers for medical devices.
Multinational companies have targeted Brazil as a priority market in Latin America, expanding distribution networks and offering localized training for surgical staff to support product adoption. There's growing interest in absorbable hemostats, especially those based on collagen and oxidized cellulose, as these products are easier to use and often reduce operating time. Additionally, the country's robust public health system, led by the Brazilian Unified Health System (SUS), supports wide access to surgical care, boosting demand for hemostatic agents.
Compound Annual Growth Rate
5.8%
Value in USD Million
2026-2035
Hemostats are widely used in Brazil to control bleeding during surgeries and traumatic injuries, ensuring a clear surgical field and reducing complications. Their use is rising due to increased surgical procedures, a growing elderly population, and a high prevalence of chronic diseases like diabetes and cardiovascular conditions, which require frequent surgical intervention and effective bleeding management. The Brazil hemostats market is expected to grow at a CAGR of 5.80% during the forecast period of 2026-2035 across the region.
Technological Innovation and Surgical Demand Driving Brazil Hemostats Market
The rising prevalence of cardiovascular diseases and the growing number of surgical interventions in Brazil are driving the demand for effective bleeding control solutions. The market is further supported by advancements in hemostatic technologies, enhancing surgical outcomes. Continuous innovation in product development is improving patient safety and treatment efficacy, thereby encouraging the adoption of healthcare facilities. These factors collectively position the market for robust growth throughout the forecast period, meeting increasing clinical needs and improving procedural success rates.
Baxter launched the HEMOPATCH Sealing Hemostat with room-temperature storage in European markets. The product is an evolution of HEMOPATCH that allows storage at room temperature, simplifying handling and eliminating the need for refrigerated storage. Baxter positioned the development for use during surgery, where HEMOPATCH provides haemostatic control and sealing. The change is relevant to hospitals because easier storage can simplify operating-room logistics and product preparation. Baxter officially announced the European availability on 10 April 2025, making this a verified market-player product development.
Cresilon received U.S. FDA clearance for TRAUMAGEL, a flowable haemostatic gel intended for temporary external use to control moderate-to-severe bleeding. The product is supplied in a syringe and is designed to conform to different wound geometries while achieving rapid bleeding control. Cresilon is commercialising the plant-based haemostatic technology for emergency medical services, trauma hospitals, military and law-enforcement applications. The development adds a gel-based product format to the haemostat competitive landscape alongside conventional dressings, sponges and powders.
Ethicon, part of Johnson & Johnson MedTech, announced CE Mark approval for the ETHIZIA Hemostatic Sealing Patch. The product was cleared as an adjunctive haemostat for controlling disruptive bleeding on internal organs, excluding cardiovascular and neurological applications. ETHIZIA uses a synthetic polymer technology developed by GATT Technologies, which Johnson & Johnson had acquired in 2022. Ethicon stated that the product would initially launch in EMEA, followed by planned expansion into other regions, including Latin America, subject to regulatory approvals.
Flowable hemostatic gels are gaining prominence as an individual class in which the product has to mold itself according to the wound that is irregularly shaped instead of being dependent on a fixed sponge or patch form. The TRAUMAGEL by Cresilon is a plant-derived polysaccharide gel available in a 30 ml syringe and is ready to use directly on external bleeding points without any preparation process. The FDA 510(k) clearance for Cresilon was acquired in August 2024, and the product came into the market in January 2025. The technology creates a mechanical barrier at the wound and is intended for moderate-to-severe external bleeding. This format is particularly relevant to trauma and emergency applications where rapid, direct application is important.
Another trend related to product development is the removal of the need for refrigeration of certain absorbable haemostatic agents. In April 2025, Baxter launched a non-refrigerated version of the HEMOPATCH Sealing Hemostat in Europe. It is still a ready-to-use absorbable collagen pad designed for use in tissue sealing, dura sealing, and hemostasis, but the new storage format enables hospitals to store it right in the operating room without refrigerated storage. Baxter states that the change resulted from collaboration with surgeons and was intended to improve immediate availability during procedures. Such storage simplification can be particularly valuable for hospitals managing operating-room inventory across multiple surgical specialties.
The development of patches has gone beyond merely controlling blood loss into haemostatic patches that also seal tissues. ETHIZIA Hemostatic Sealing Patch by Ethicon utilizes activated polymer technology incorporated into a gelatin-based patch that can be controlled through stuffing, rolling, separating, cutting, and shaping it according to the needs of the surgical site. According to the clinical trial performed by Johnson & Johnson MedTech, ETHIZIA Hemostatic Sealing Patch attained haemostasis in 80% of patients in 30 seconds. This patch can be applied in both open and minimally invasive surgery and in organs for specific sites of bleeding. This creates a more versatile product category for surgeons dealing with difficult-to-control bleeding.
Haemostatic powders are evolving as procedure specific delivery devices, especially for gastrointestinal endoscopic procedures. Nexpowder Endoscopic Hemostasis System from Medtronic uses a powder that serves as an adhesive for difficult and active non-variceal bleeding in GI tract. Delivery device of this system is made in such a way that it avoids catheter occlusion and powder scatter without requiring any carbon dioxide or extra air compressor. The powder also changes into an adhesive gel when exposed to moisture, allowing it to interact with the bleeding site. This type of specialised endoscopic haemostat expands powder-based products beyond general surgical application and supports their use in gastroenterology, where conventional clipping or thermal methods may be difficult to apply.
The commercialization of plant-based polymers for haemostatic purposes instead of animal-based material is another factor resulting in market growth. According to Cresilon, TRAUMAGEL consists of plant-based polysaccharide materials and is not based on any animal product. When applied directly to the wound, the gel sticks to the wound and provides a physical barrier allowing the clot formation process. This approach is relevant to the haemostat landscape as material origin can become an important consideration for hospitals and clinicians when selecting products for different surgical and emergency applications.
The market report offers a detailed analysis of the market based on the following segments:
Market Breakup by Type
Market Breakup by Formulation
Market Breakup by Application
Market Breakup by Indication
Market Breakup by End User
Cardiovascular and Cardiothoracic to Lead the Segmentation by Application
The cardiovascular and cardiothoracic segment is poised to hold the largest market share due to the high prevalence of cardiovascular diseases requiring surgical interventions. Rising cases of heart disease and related complications drive demand for effective bleeding control during complex surgeries. Additionally, technological advancements in cardiovascular procedures and increased healthcare infrastructure investments support market growth. This segment’s critical need for reliable hemostatic agents positions it as the dominant application area during the forecast period.
The key features of the market report comprise patent analysis, funding and investment analysis, and strategic initiatives by the leading players. The major companies in the market are as follows:
Johnson & Johnson Services Inc., headquartered in New Brunswick, New Jersey, was established in 1886. It offers a broad portfolio of medical devices, pharmaceuticals, and consumer health products. In the hemostats market, Johnson & Johnson provides advanced surgical hemostatic agents and wound care solutions, driving innovation and improving patient outcomes globally.
Baxter International, founded in 1931 and based in Deerfield, Illinois, specializes in medical devices, pharmaceuticals, and biotechnology. Its portfolio includes hemostatic products, infusion therapies, and surgical care solutions, focusing on improving treatment efficacy and patient safety in hospitals and clinics worldwide.
Pfizer Inc., established in 1849 and headquartered in New York City, is a global pharmaceutical leader. It offers a wide range of medicines and vaccines, including innovative therapies for bleeding control and surgical applications, contributing significantly to advancements in the hemostats and surgical care market.
B. Braun SE, founded in 1839 and based in Melsungen, Germany, is a leading medical device and pharmaceutical company. It provides hemostatic agents, surgical instruments, and infusion therapies, focusing on enhancing surgical outcomes and patient safety across global healthcare settings.
*Please note that this is only a partial list; the complete list of key players is available in the full report. Additionally, the list of key players can be customized to better suit your needs.*
Other key players in the market include Becton, Dickinson and Company (BD), Medtronic plc, and Stryker Corporation.
*While we strive to always give you current and accurate information, the numbers depicted on the website are indicative and may differ from the actual numbers in the main report. At Expert Market Research, we aim to bring you the latest insights and trends in the market. Using our analyses and forecasts, stakeholders can understand the market dynamics, navigate challenges, and capitalize on opportunities to make data-driven strategic decisions.*
Explore our key highlights of the report and gain a concise overview of key findings, trends, and actionable insights that will empower your strategic decisions.
| REPORT FEATURES | DETAILS |
| Base Year | 2025 |
| Historical Period | 2019-2025 |
| Forecast Period | 2026-2035 |
| Scope of the Report |
Historical and Forecast Trends, Industry Drivers and Constraints, Historical and Forecast Market Analysis by Segment:
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| Breakup by Type |
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| Breakup by Formulation |
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| Breakup by Application |
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| Breakup by Indication |
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| Breakup by End User |
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| Market Dynamics |
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| Supplier Landscape |
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| Companies Covered |
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