Medical Fluid Bags Market by Product Type (Blood Bags, Chemotherapy Bags, Parenteral Nutrition Bags), Material (Non PVC, PVC), Delivery Mode, Sterilization Method, End User - Global Forecast 2025-2032
Description
The Medical Fluid Bags Market was valued at USD 3.34 billion in 2024 and is projected to grow to USD 3.55 billion in 2025, with a CAGR of 6.83%, reaching USD 5.67 billion by 2032.
A comprehensive introduction framing clinical needs, material innovation, regulatory pressure, and supply chain dynamics that define the contemporary medical fluid bags environment
The landscape for medical fluid bags is shaped by converging clinical needs, regulatory scrutiny, and supply chain dynamics that demand informed strategic action. Advances in materials science, heightened focus on patient-centric care delivery, and an increasingly complex global logistics environment are transforming how providers, manufacturers, and distributors approach the design, procurement, and use of fluid containment systems. This introduction establishes the foundational context, clarifies the scope of inquiry, and outlines the thematic threads that run through the subsequent analysis.
Clinicians are placing a premium on reliability, sterility assurance, and ease of use, while procurement teams balance cost pressures against quality and compliance obligations. Simultaneously, manufacturers are innovating across polymer chemistry and manufacturing processes to address concerns about biocompatibility, chemical leachables, and waste management. These trends intersect with evolving regulatory expectations related to single-use devices and sterilization validation, prompting enterprises to rethink product portfolios and supplier relationships. By setting this context, the introduction frames the strategic imperatives that industry participants must address to thrive in an environment defined by rapid clinical change and constrained supply options.
How material breakthroughs, decentralizing care models, regulatory scrutiny, and sustainability mandates are reshaping product design, sourcing, and competitive positioning in the industry
The medical fluid bags sector is experiencing transformative shifts driven by technological innovation, changing care delivery models, and environmental and regulatory pressures. Technological advances include the adoption of alternative polymers and improved manufacturing controls that enhance barrier properties and reduce patient safety risks. In parallel, care delivery is decentralizing: infusion therapies are increasingly administered in outpatient ambulatory centers, clinics, and home care settings, which alters product design priorities toward portability, simplified connections, and compatibility with diverse pump systems. These converging forces are expanding the functional requirements placed on fluid bags and accelerating demand for differentiated features.
Regulatory focus on sterilization validation and medical device traceability is encouraging greater investment in sterilization method control and supply chain transparency. Environmentally driven procurement policies are prompting manufacturers to explore non-PVC materials and more sustainable packaging and disposal pathways. On the commercial side, consolidation among healthcare providers and strategic sourcing initiatives are reshaping supplier relationships, with larger buyers seeking integrated value propositions that combine product performance, regulatory reassurance, and predictable logistics. Taken together, these shifts are not incremental; they represent a recalibration of priorities that will define competitive positioning and product development roadmaps over the near to medium term.
Evaluating the cumulative operational and procurement consequences of recent tariff activity on supply continuity, sourcing strategy, and manufacturing investments within the industry
Recent tariff measures and trade policy adjustments by the United States have introduced new cost and operational considerations for manufacturers and suppliers of medical fluid bags that rely on global value chains. Tariffs on key inputs-particularly polymers, specialty additives, and certain medical components-have influenced procurement strategies by increasing the direct landed cost of imported materials and prompting firms to reassess the geographic distribution of their supply bases. In response, many enterprises have been compelled to explore alternative sourcing, nearshoring, and vertical integration to mitigate exposure to tariff volatility and to maintain continuity of supply for critical clinical products.
Operationally, tariff pressures have accelerated supply chain mapping efforts and forced more rigorous supplier qualification processes. Buyers are increasingly demanding visibility into upstream raw material origins and are incorporating tariff risk into contract terms and inventory policies. As a result, some manufacturers have prioritized investments in domestic production capacity or in long-term supplier agreements that provide tariff pass-through protections or hedging mechanisms. At the same time, tariff-driven cost increases can affect pricing negotiations with healthcare purchasers and may shift the calculus around product feature trade-offs. Overall, the cumulative impact of recent tariff activity has been to elevate strategic supply chain planning from a cost-containment exercise to a core element of commercial and manufacturing strategy.
Strategic segmentation insights that link product types, material choices, end-user settings, delivery mechanisms, and sterilization pathways to practical design and commercialization priorities
Segmentation provides the analytical lenses needed to align product development and commercialization strategies with clinical and procurement realities. When viewed through the prism of product type, distinctions among blood bags, chemotherapy bags, parenteral nutrition bags, and saline bags reveal divergent performance requirements, regulatory pathways, and user handling considerations that affect design choices, labeling, and clinician training. Material-focused segmentation between non-PVC and PVC options highlights trade-offs between flexibility, chemical compatibility, sterilization behavior, and end-of-life disposal practices, each of which carries implications for procurement criteria and clinician acceptance.
End-user segmentation across ambulatory centers, clinics, home care, and hospitals underscores how setting-specific workflows, staffing models, and infrastructure change the value proposition for different product formats. Delivery mode segmentation that contrasts gravity systems with pump-assisted administration-and further differentiates pumps into elastomeric, syringe, and volumetric pump types-illuminates compatibility needs, connection standards, and performance tolerances that designers must meet. Finally, sterilization method segmentation comparing ethylene oxide and gamma irradiation draws attention to material selection, validation requirements, and turnaround considerations for sterilized goods. Integrating these segmentation perspectives enables clearer prioritization of innovation investments and customer engagement strategies, and it supports targeted messaging that aligns product attributes with the operational realities of each buyer and care setting.
How regional regulatory regimes, procurement practices, and manufacturing footprints across the Americas, Europe Middle East & Africa, and Asia-Pacific shape product strategies and competitive advantage
Regional dynamics exert a powerful influence on procurement norms, regulatory expectations, and competitive intensity in the sector. In the Americas, buyers are driven by a combination of stringent quality requirements and a strong emphasis on supplier reliability and domestic production resilience, which has led to strategic sourcing shifts and investments in regional manufacturing capacity. Purchasing decisions are also shaped by payer structures and the balance between hospital and outpatient care, thereby affecting demand patterns for specific product types and delivery systems. Across Europe, Middle East & Africa, regulatory harmonization efforts and evolving environmental mandates are prompting suppliers to prioritize materials and sterilization processes that meet diverse jurisdictional requirements while minimizing logistical complexity.
Asia-Pacific exhibits pronounced heterogeneity, with leading markets investing heavily in domestic manufacturing capabilities, innovation in polymer processing, and scaling of contract manufacturing operations to serve both regional and global demand. At the same time, emerging markets in the region are characterized by rapid healthcare infrastructure development and growing adoption of outpatient and home-based infusion therapies, which creates opportunities for adaptable product formats and cost-competitive supply models. Transitioning between these regional conditions requires suppliers to balance standardized manufacturing platforms with the flexibility to meet local regulatory and clinical preferences, and successful regional strategies will hinge on nuanced market entry approaches and robust distribution partnerships.
Competitive landscape analysis highlighting how established manufacturers, niche innovators, and strategic partnerships are advancing material innovation, sterilization validation, and supply continuity
Competitive dynamics in the medical fluid bags space are defined by a mix of established global manufacturers, specialized regional producers, and emerging niche innovators. Leading firms differentiate through material science capabilities, validated sterilization pathways, and integrated supply chain solutions that guarantee product traceability and timely delivery. Newer entrants and smaller suppliers often compete on agility, offering rapid customization, localized support, and targeted product configurations that address specific clinical workflows or price-sensitive buyer segments. Both types of players are investing in quality systems and regulatory expertise to meet increasingly exacting standards for single-use medical devices.
Partnership patterns are also evolving: contract manufacturing and strategic alliances with logistics providers have become critical to ensuring sterilization coordination and cold-chain integrity where needed. Additionally, manufacturing investments focused on non-PVC alternatives and recyclable packaging have become areas of differentiation, especially for buyers with sustainability mandates. Across the competitive landscape, the ability to demonstrate validated sterilization processes, compatibility with a wide range of delivery systems, and reliable supply continuity remains the cornerstone of commercial credibility and market access.
Actionable recommendations for leaders to align product innovation, supply chain resilience, sterilization assurance, and go-to-market strategies with evolving clinical and regulatory imperatives
Industry leaders can convert insight into competitive advantage by aligning product roadmaps with clinician needs, regulatory trajectories, and resilient sourcing strategies. First, prioritize material and design investments that demonstrably improve patient safety and compatibility with prevalent delivery systems, while also assessing non-PVC alternatives to meet sustainability goals. Next, enhance supply chain resilience through diversified sourcing, nearshoring where feasible, and formalized supplier risk management that incorporates tariff exposure and logistics contingencies. These steps should be coupled with strengthened sterilization validation processes and documentation to reduce approval cycle friction across jurisdictions.
In parallel, develop go-to-market strategies that address the distinctive needs of ambulatory centers, clinics, hospitals, and home care settings, offering value propositions tailored to each environment’s workflow constraints and procurement preferences. Invest in partnerships with pump manufacturers and service providers to ensure seamless interoperability and to expand solution-level offerings that reduce procurement complexity for health systems. Finally, embed continuous regulatory surveillance and environmental compliance into product development cycles to ensure readiness for changing standards and buyer expectations, thereby protecting market access and reinforcing commercial credibility.
A rigorous mixed-methods research methodology combining primary stakeholder engagement, secondary technical review, and data triangulation to validate insights across product, material, and sterilization segments
This research approach integrates qualitative and quantitative techniques to produce robust, verifiable findings that inform strategic decision-making. Primary research included structured conversations with clinicians, procurement leaders, manufacturing executives, and sterilization specialists to capture operational realities, unmet needs, and product performance priorities. These insights were augmented by supplier interviews and site visits where feasible to validate manufacturing practices and sterilization controls. Secondary research encompassed a systematic review of regulatory guidance, industry standards, technical literature on polymer behavior and sterilization science, and trade data to understand supply chain exposures and material flows.
Data triangulation was applied to reconcile divergent inputs and to ensure conclusions rest on multiple independent evidence streams. Segmentation-specific analysis matched product characteristics to clinical workflows and procurement criteria across different care settings and sterilization pathways. Competitive profiling combined company-level capability assessments with observations on partnership structures and manufacturing footprints. Throughout, emphasis was placed on traceability, reproducibility of findings, and clear articulation of assumptions so that stakeholders can adapt the methodology to bespoke inquiries or deeper regional or technological investigations.
A concluding synthesis that ties material innovation, sterilization assurance, care delivery evolution, and supply chain resilience into an integrated strategic imperative for industry participants
The cumulative analysis points to an industry at an inflection point where material innovation, setting-specific product requirements, supply chain resilience, and sterilization assurance converge to redefine competitive advantage. Organizations that invest in validated non-PVC options, ensure compatibility across gravity and pump delivery modes, and develop robust sterilization pathways are better positioned to meet the dual demands of clinical performance and regulatory compliance. At the same time, tariff-induced sourcing challenges and regional regulatory heterogeneity underscore the importance of strategic supply chain planning and localized market approaches.
In conclusion, success in the sector will depend not only on product quality but also on the ability to anticipate regulatory shifts, align with evolving care delivery models, and provide demonstrable supply continuity. Companies that integrate these elements into coherent product and commercial strategies will be able to address provider needs more effectively and create sustainable differentiation in a market where clinical safety, operational efficiency, and environmental responsibility are increasingly inseparable.
Please Note: PDF & Excel + Online Access - 1 Year
A comprehensive introduction framing clinical needs, material innovation, regulatory pressure, and supply chain dynamics that define the contemporary medical fluid bags environment
The landscape for medical fluid bags is shaped by converging clinical needs, regulatory scrutiny, and supply chain dynamics that demand informed strategic action. Advances in materials science, heightened focus on patient-centric care delivery, and an increasingly complex global logistics environment are transforming how providers, manufacturers, and distributors approach the design, procurement, and use of fluid containment systems. This introduction establishes the foundational context, clarifies the scope of inquiry, and outlines the thematic threads that run through the subsequent analysis.
Clinicians are placing a premium on reliability, sterility assurance, and ease of use, while procurement teams balance cost pressures against quality and compliance obligations. Simultaneously, manufacturers are innovating across polymer chemistry and manufacturing processes to address concerns about biocompatibility, chemical leachables, and waste management. These trends intersect with evolving regulatory expectations related to single-use devices and sterilization validation, prompting enterprises to rethink product portfolios and supplier relationships. By setting this context, the introduction frames the strategic imperatives that industry participants must address to thrive in an environment defined by rapid clinical change and constrained supply options.
How material breakthroughs, decentralizing care models, regulatory scrutiny, and sustainability mandates are reshaping product design, sourcing, and competitive positioning in the industry
The medical fluid bags sector is experiencing transformative shifts driven by technological innovation, changing care delivery models, and environmental and regulatory pressures. Technological advances include the adoption of alternative polymers and improved manufacturing controls that enhance barrier properties and reduce patient safety risks. In parallel, care delivery is decentralizing: infusion therapies are increasingly administered in outpatient ambulatory centers, clinics, and home care settings, which alters product design priorities toward portability, simplified connections, and compatibility with diverse pump systems. These converging forces are expanding the functional requirements placed on fluid bags and accelerating demand for differentiated features.
Regulatory focus on sterilization validation and medical device traceability is encouraging greater investment in sterilization method control and supply chain transparency. Environmentally driven procurement policies are prompting manufacturers to explore non-PVC materials and more sustainable packaging and disposal pathways. On the commercial side, consolidation among healthcare providers and strategic sourcing initiatives are reshaping supplier relationships, with larger buyers seeking integrated value propositions that combine product performance, regulatory reassurance, and predictable logistics. Taken together, these shifts are not incremental; they represent a recalibration of priorities that will define competitive positioning and product development roadmaps over the near to medium term.
Evaluating the cumulative operational and procurement consequences of recent tariff activity on supply continuity, sourcing strategy, and manufacturing investments within the industry
Recent tariff measures and trade policy adjustments by the United States have introduced new cost and operational considerations for manufacturers and suppliers of medical fluid bags that rely on global value chains. Tariffs on key inputs-particularly polymers, specialty additives, and certain medical components-have influenced procurement strategies by increasing the direct landed cost of imported materials and prompting firms to reassess the geographic distribution of their supply bases. In response, many enterprises have been compelled to explore alternative sourcing, nearshoring, and vertical integration to mitigate exposure to tariff volatility and to maintain continuity of supply for critical clinical products.
Operationally, tariff pressures have accelerated supply chain mapping efforts and forced more rigorous supplier qualification processes. Buyers are increasingly demanding visibility into upstream raw material origins and are incorporating tariff risk into contract terms and inventory policies. As a result, some manufacturers have prioritized investments in domestic production capacity or in long-term supplier agreements that provide tariff pass-through protections or hedging mechanisms. At the same time, tariff-driven cost increases can affect pricing negotiations with healthcare purchasers and may shift the calculus around product feature trade-offs. Overall, the cumulative impact of recent tariff activity has been to elevate strategic supply chain planning from a cost-containment exercise to a core element of commercial and manufacturing strategy.
Strategic segmentation insights that link product types, material choices, end-user settings, delivery mechanisms, and sterilization pathways to practical design and commercialization priorities
Segmentation provides the analytical lenses needed to align product development and commercialization strategies with clinical and procurement realities. When viewed through the prism of product type, distinctions among blood bags, chemotherapy bags, parenteral nutrition bags, and saline bags reveal divergent performance requirements, regulatory pathways, and user handling considerations that affect design choices, labeling, and clinician training. Material-focused segmentation between non-PVC and PVC options highlights trade-offs between flexibility, chemical compatibility, sterilization behavior, and end-of-life disposal practices, each of which carries implications for procurement criteria and clinician acceptance.
End-user segmentation across ambulatory centers, clinics, home care, and hospitals underscores how setting-specific workflows, staffing models, and infrastructure change the value proposition for different product formats. Delivery mode segmentation that contrasts gravity systems with pump-assisted administration-and further differentiates pumps into elastomeric, syringe, and volumetric pump types-illuminates compatibility needs, connection standards, and performance tolerances that designers must meet. Finally, sterilization method segmentation comparing ethylene oxide and gamma irradiation draws attention to material selection, validation requirements, and turnaround considerations for sterilized goods. Integrating these segmentation perspectives enables clearer prioritization of innovation investments and customer engagement strategies, and it supports targeted messaging that aligns product attributes with the operational realities of each buyer and care setting.
How regional regulatory regimes, procurement practices, and manufacturing footprints across the Americas, Europe Middle East & Africa, and Asia-Pacific shape product strategies and competitive advantage
Regional dynamics exert a powerful influence on procurement norms, regulatory expectations, and competitive intensity in the sector. In the Americas, buyers are driven by a combination of stringent quality requirements and a strong emphasis on supplier reliability and domestic production resilience, which has led to strategic sourcing shifts and investments in regional manufacturing capacity. Purchasing decisions are also shaped by payer structures and the balance between hospital and outpatient care, thereby affecting demand patterns for specific product types and delivery systems. Across Europe, Middle East & Africa, regulatory harmonization efforts and evolving environmental mandates are prompting suppliers to prioritize materials and sterilization processes that meet diverse jurisdictional requirements while minimizing logistical complexity.
Asia-Pacific exhibits pronounced heterogeneity, with leading markets investing heavily in domestic manufacturing capabilities, innovation in polymer processing, and scaling of contract manufacturing operations to serve both regional and global demand. At the same time, emerging markets in the region are characterized by rapid healthcare infrastructure development and growing adoption of outpatient and home-based infusion therapies, which creates opportunities for adaptable product formats and cost-competitive supply models. Transitioning between these regional conditions requires suppliers to balance standardized manufacturing platforms with the flexibility to meet local regulatory and clinical preferences, and successful regional strategies will hinge on nuanced market entry approaches and robust distribution partnerships.
Competitive landscape analysis highlighting how established manufacturers, niche innovators, and strategic partnerships are advancing material innovation, sterilization validation, and supply continuity
Competitive dynamics in the medical fluid bags space are defined by a mix of established global manufacturers, specialized regional producers, and emerging niche innovators. Leading firms differentiate through material science capabilities, validated sterilization pathways, and integrated supply chain solutions that guarantee product traceability and timely delivery. Newer entrants and smaller suppliers often compete on agility, offering rapid customization, localized support, and targeted product configurations that address specific clinical workflows or price-sensitive buyer segments. Both types of players are investing in quality systems and regulatory expertise to meet increasingly exacting standards for single-use medical devices.
Partnership patterns are also evolving: contract manufacturing and strategic alliances with logistics providers have become critical to ensuring sterilization coordination and cold-chain integrity where needed. Additionally, manufacturing investments focused on non-PVC alternatives and recyclable packaging have become areas of differentiation, especially for buyers with sustainability mandates. Across the competitive landscape, the ability to demonstrate validated sterilization processes, compatibility with a wide range of delivery systems, and reliable supply continuity remains the cornerstone of commercial credibility and market access.
Actionable recommendations for leaders to align product innovation, supply chain resilience, sterilization assurance, and go-to-market strategies with evolving clinical and regulatory imperatives
Industry leaders can convert insight into competitive advantage by aligning product roadmaps with clinician needs, regulatory trajectories, and resilient sourcing strategies. First, prioritize material and design investments that demonstrably improve patient safety and compatibility with prevalent delivery systems, while also assessing non-PVC alternatives to meet sustainability goals. Next, enhance supply chain resilience through diversified sourcing, nearshoring where feasible, and formalized supplier risk management that incorporates tariff exposure and logistics contingencies. These steps should be coupled with strengthened sterilization validation processes and documentation to reduce approval cycle friction across jurisdictions.
In parallel, develop go-to-market strategies that address the distinctive needs of ambulatory centers, clinics, hospitals, and home care settings, offering value propositions tailored to each environment’s workflow constraints and procurement preferences. Invest in partnerships with pump manufacturers and service providers to ensure seamless interoperability and to expand solution-level offerings that reduce procurement complexity for health systems. Finally, embed continuous regulatory surveillance and environmental compliance into product development cycles to ensure readiness for changing standards and buyer expectations, thereby protecting market access and reinforcing commercial credibility.
A rigorous mixed-methods research methodology combining primary stakeholder engagement, secondary technical review, and data triangulation to validate insights across product, material, and sterilization segments
This research approach integrates qualitative and quantitative techniques to produce robust, verifiable findings that inform strategic decision-making. Primary research included structured conversations with clinicians, procurement leaders, manufacturing executives, and sterilization specialists to capture operational realities, unmet needs, and product performance priorities. These insights were augmented by supplier interviews and site visits where feasible to validate manufacturing practices and sterilization controls. Secondary research encompassed a systematic review of regulatory guidance, industry standards, technical literature on polymer behavior and sterilization science, and trade data to understand supply chain exposures and material flows.
Data triangulation was applied to reconcile divergent inputs and to ensure conclusions rest on multiple independent evidence streams. Segmentation-specific analysis matched product characteristics to clinical workflows and procurement criteria across different care settings and sterilization pathways. Competitive profiling combined company-level capability assessments with observations on partnership structures and manufacturing footprints. Throughout, emphasis was placed on traceability, reproducibility of findings, and clear articulation of assumptions so that stakeholders can adapt the methodology to bespoke inquiries or deeper regional or technological investigations.
A concluding synthesis that ties material innovation, sterilization assurance, care delivery evolution, and supply chain resilience into an integrated strategic imperative for industry participants
The cumulative analysis points to an industry at an inflection point where material innovation, setting-specific product requirements, supply chain resilience, and sterilization assurance converge to redefine competitive advantage. Organizations that invest in validated non-PVC options, ensure compatibility across gravity and pump delivery modes, and develop robust sterilization pathways are better positioned to meet the dual demands of clinical performance and regulatory compliance. At the same time, tariff-induced sourcing challenges and regional regulatory heterogeneity underscore the importance of strategic supply chain planning and localized market approaches.
In conclusion, success in the sector will depend not only on product quality but also on the ability to anticipate regulatory shifts, align with evolving care delivery models, and provide demonstrable supply continuity. Companies that integrate these elements into coherent product and commercial strategies will be able to address provider needs more effectively and create sustainable differentiation in a market where clinical safety, operational efficiency, and environmental responsibility are increasingly inseparable.
Please Note: PDF & Excel + Online Access - 1 Year
Table of Contents
189 Pages
- 1. Preface
- 1.1. Objectives of the Study
- 1.2. Market Segmentation & Coverage
- 1.3. Years Considered for the Study
- 1.4. Currency
- 1.5. Language
- 1.6. Stakeholders
- 2. Research Methodology
- 3. Executive Summary
- 4. Market Overview
- 5. Market Insights
- 5.1. Surge in home infusion therapy driving demand for lightweight portable fluid bags with integrated carrying solutions
- 5.2. Adoption of biodegradable polymer-based medical fluid bags to address regulatory and environmental concerns
- 5.3. Integration of smart sensors within fluid bags for real-time monitoring of infusion flow rate and temperature conditions
- 5.4. Development of multi-chamber parenteral nutrition bags to simplify complex nutritional therapy protocols in hospitals
- 5.5. Partnerships between medical bag manufacturers and telehealth platforms for remote infusion monitoring and data analytics
- 5.6. Implementation of anti-microbial surface coatings on fluid bags to prevent bacterial contamination during storage and transport
- 5.7. Shift towards closed system transfer devices integrated with fluid bags to minimize medication waste and exposure risks
- 5.8. Regulatory harmonization efforts influencing material selection and quality standards for medical fluid bag production across regions
- 5.9. Advancements in collapsible bag design to reduce medical waste volume and optimize hospital storage space and logistics
- 5.10. Deployment of AI-driven compounding automation stations for on-site preparation of personalized fluid bag therapies in hospitals
- 6. Cumulative Impact of United States Tariffs 2025
- 7. Cumulative Impact of Artificial Intelligence 2025
- 8. Medical Fluid Bags Market, by Product Type
- 8.1. Blood Bags
- 8.2. Chemotherapy Bags
- 8.3. Parenteral Nutrition Bags
- 8.4. Saline Bags
- 9. Medical Fluid Bags Market, by Material
- 9.1. Non PVC
- 9.2. PVC
- 10. Medical Fluid Bags Market, by Delivery Mode
- 10.1. Gravity
- 10.2. Pump
- 10.2.1. Elastomeric Pump
- 10.2.2. Syringe Pump
- 10.2.3. Volumetric Pump
- 11. Medical Fluid Bags Market, by Sterilization Method
- 11.1. Ethylene Oxide
- 11.2. Gamma
- 12. Medical Fluid Bags Market, by End User
- 12.1. Ambulatory Centers
- 12.2. Clinics
- 12.3. Home Care
- 12.4. Hospitals
- 13. Medical Fluid Bags Market, by Region
- 13.1. Americas
- 13.1.1. North America
- 13.1.2. Latin America
- 13.2. Europe, Middle East & Africa
- 13.2.1. Europe
- 13.2.2. Middle East
- 13.2.3. Africa
- 13.3. Asia-Pacific
- 14. Medical Fluid Bags Market, by Group
- 14.1. ASEAN
- 14.2. GCC
- 14.3. European Union
- 14.4. BRICS
- 14.5. G7
- 14.6. NATO
- 15. Medical Fluid Bags Market, by Country
- 15.1. United States
- 15.2. Canada
- 15.3. Mexico
- 15.4. Brazil
- 15.5. United Kingdom
- 15.6. Germany
- 15.7. France
- 15.8. Russia
- 15.9. Italy
- 15.10. Spain
- 15.11. China
- 15.12. India
- 15.13. Japan
- 15.14. Australia
- 15.15. South Korea
- 16. Competitive Landscape
- 16.1. Market Share Analysis, 2024
- 16.2. FPNV Positioning Matrix, 2024
- 16.3. Competitive Analysis
- 16.3.1. Becton, Dickinson and Company
- 16.3.2. Fresenius Kabi AG
- 16.3.3. Grifols, S.A.
- 16.3.4. ICU Medical, Inc.
- 16.3.5. Macopharma S.A.S.
- 16.3.6. Nipro Corporation
- 16.3.7. Pfizer Inc.
- 16.3.8. Poly Medicure Ltd.
- 16.3.9. Sichuan Kelun Pharmaceutical Co., Ltd.
- 16.3.10. SSY Group Limited
- 16.3.11. Terumo Corporation
- 16.3.12. Vetter Pharma-Fertigung GmbH & Co. KG
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