Wound Irrigation System Market by Technology (Reusable, Single Use), Product Type (Gravity Irrigation, Manual Syringe, Pressure Irrigation), Application, End User, Distribution Channel - Global Forecast 2025-2032
Description
The Wound Irrigation System Market was valued at USD 293.98 million in 2024 and is projected to grow to USD 310.59 million in 2025, with a CAGR of 5.97%, reaching USD 467.80 million by 2032.
Orienting leaders to how device design, clinical need, and procurement priorities intersect to redefine wound irrigation practices across care settings
The evolving complexity of wound care demands a focused examination of wound irrigation systems as a pivotal element of clinical protocols and care pathways. This analysis synthesizes contemporary product modalities, care settings, and stakeholder priorities to present a clear initial orientation for leaders evaluating technological options, clinical integration, and distribution strategies. It underscores how practitioners are balancing effectiveness, ease of use, and infection control considerations while institutions seek predictable supply chains and cost-efficient solutions.
Clinicians increasingly prioritize irrigation approaches that reduce biofilm burden and support debridement efficacy without introducing undue complexity into routine workflows. Consequently, procurement leaders and clinical champions must navigate performance trade-offs between reusable platforms and single-use disposables, while accounting for the practicalities of training, reprocessing, and bedside ergonomics. This section therefore serves as an entry point for stakeholders to appreciate the interplay between clinical outcomes, device design, and institutional imperatives prior to deeper strategic decision-making.
Decisive shifts in clinical priorities, device innovation, and procurement models are driving a new era of adoption and competitive differentiation in wound irrigation systems
The landscape for wound irrigation systems has shifted in ways that are reshaping clinical protocols, supply models, and product development priorities. Emerging clinical evidence and heightened emphasis on infection prevention have pushed clinicians toward methods that optimize contaminant removal while minimizing tissue trauma. As a result, there is rising interest in devices that deliver controlled pressure profiles and pulsed flow characteristics, which can enhance debridement efficiency and support downstream wound healing interventions.
Concurrently, health systems are recalibrating procurement strategies to emphasize single-use disposables in high-acuity areas to reduce cross-contamination risk, even as cost-containment pressures encourage consideration of reusable systems in lower-risk contexts. Device manufacturers are responding by accelerating modular designs and offering hybrid service models that blend reusable hardware with disposable interfaces. In parallel, regulatory agencies and standards bodies are clarifying sterilization and labeling expectations, prompting manufacturers to invest in compliance documentation and post-market surveillance capabilities. Taken together, these shifts are fostering a more nuanced competitive environment where clinical performance, operational compatibility, and regulatory readiness determine acceptance and scale.
How evolving tariff dynamics and customs-driven cost pressures are reshaping sourcing strategies, supplier risk-sharing, and procurement practices in the United States
Recent tariff adjustments across key trading lanes have introduced additional considerations for manufacturers, suppliers, and healthcare purchasers operating within the United States supply chain. Increased import duties and ancillary customs costs have elevated landed costs for certain device components and finished goods, prompting manufacturers to reassess sourcing, inventory strategies, and pricing approaches. In response, some suppliers are pursuing nearshoring or dual-sourcing strategies to mitigate exposure to tariff volatility and reduce transit lead times.
For healthcare providers and group purchasing organizations, the cumulative effect of tariff-related cost pressures has translated into a renewed focus on total cost of ownership and contract flexibility. Stakeholders are seeking cost transparency from vendors and exploring consignment or managed inventory models to smooth price impacts. From a strategic standpoint, tariff dynamics are accelerating conversations about vertical integration for critical components and encouraging innovation in local manufacturing capabilities. As these adaptations evolve, stakeholders should anticipate that procurement negotiations will increasingly include clauses that address customs-related adjustments and collaborative risk-sharing mechanisms.
A multi-dimensional segmentation framework revealing how technology choices, product modalities, clinical use cases, and channels define pathways to clinical uptake and commercial success
Deconstructing the market through a segmentation lens clarifies where clinical need and commercial opportunity intersect. Based on technology, offerings fall into reusable platforms that emphasize lifecycle cost and institutional reprocessing workflows, and single-use solutions that prioritize infection control, convenience, and rapid deployment at the bedside. Based on product type, the universe includes gravity irrigation devices valued for simplicity and low operational burden, manual syringes used for targeted irrigation in varied settings, pressure irrigation systems that offer consistent flow characteristics for deeper wound cleansing, and pulsatile irrigation technologies which deliver cyclic flow patterns; within pulsatile irrigation, distinctions matter between battery-operated systems that afford portability and consistent pulse generation versus manual-powered devices that emphasize low capital requirements and simplicity.
Further segmentation by application reveals divergent clinical requirements: chronic wound treatment scenarios demand gentle but thorough biofilm management compatible with ongoing wound bed preparation; emergency care usage prioritizes rapid, reliable evacuation of debris and contaminants under time pressure; and surgical applications require precision and compatibility with sterile workflows. End-user segmentation highlights differentiated procurement and workflow considerations across ambulatory surgery centers that value throughput and predictable consumable use, home care contexts that emphasize user-friendly, safe single-use formats, hospitals that balance scale with sterilization capacity, and specialty clinics that seek tailored clinical performance. Finally, distribution channel segmentation recognizes distinct purchasing behaviors and service expectations across hospital pharmacies that manage institutional contracts, online sales channels that offer convenience and direct-to-provider access, and retail pharmacies that serve outpatient and home care needs. Together, these segment perspectives enable targeted product development and go-to-market strategies that align clinical performance attributes with channel-specific expectations.
How distinct regional regulatory landscapes, procurement norms, and clinical workflows influence adoption patterns and commercial approaches across global markets
Regional dynamics are shaping product development priorities, regulatory strategies, and commercial approaches in meaningful ways. In the Americas, health systems emphasize infection prevention and value-based procurement, with demand concentrated around solutions that can demonstrate compatibility with bundled care pathways and institutional sterilization capabilities. Because reimbursement and institutional procurement frameworks vary by submarket, vendors often adopt differentiated commercial models that combine direct hospital engagement with distribution partnerships.
Across Europe, the Middle East & Africa, regulatory alignment and a focus on standardized clinical guidelines drive adoption of systems that meet stringent device safety and labeling requirements, while local procurement practices and variable infrastructure in parts of the region necessitate adaptable service and training models. In the Asia-Pacific region, rapid adoption is influenced by growing surgical volumes, expanding ambulatory care infrastructure, and a strong emphasis on cost-competitive manufacturing. This evolution has encouraged international manufacturers to form local partnerships and invest in region-specific clinical evidence generation. Overall, geographic variation in procurement norms, clinician preferences, and regulatory environments requires vendors to adopt finely tuned regional strategies rather than a single global approach.
Competitive dynamics shaped by clinical validation, ergonomic design, service models, and digital enablement that determine long-term institutional adoption and growth
The competitive landscape is defined by a blend of established medical device firms, niche innovators, and emerging technology players that focus on differentiated irrigation performance and service models. Leading organizations are investing in clinical validation studies to demonstrate comparative advantages in tissue preservation and contaminant removal, while others concentrate on ergonomic design and user experience to improve bedside adoption rates. Manufacturers with integrated sterilization and KOL engagement strategies tend to achieve deeper institutional penetration, whereas specialty-focused entrants often target home care and outpatient clinic segments where ease of use and single-use convenience are critical.
Beyond product features, strategic differentiation arises from channel partnerships and service offerings. Companies that provide robust training programs, warranty and service support, and consumable supply guarantees secure stronger purchasing commitments from hospitals and ambulatory centers. Meanwhile, firms that excel in digital enablement-such as providing online ordering platforms, data-driven consumption analytics, and remote training modules-are better positioned to capture growing demand through non-traditional channels. In this environment, sustained investment in clinical evidence, regulatory compliance, and customer success functions determines the ability to expand into high-value care settings and retain long-term contracts.
Practical strategic moves for manufacturers and health system leaders to strengthen clinical credibility, diversify channels, and secure resilient supply chains
For industry leaders seeking to translate insight into influence, three pragmatic actions should be prioritized. First, align product development roadmaps with documented clinical performance needs by investing in evidence generation that articulates outcomes relevant to surgeons, wound care specialists, and emergency clinicians. This evidence base should include comparative usability studies and real-world safety data to support purchasing decisions and clinician training.
Second, optimize commercial models by creating flexible channel strategies that address the distinct requirements of hospitals, ambulatory centers, home care markets, and retail channels. This may involve pilot consignment agreements, bundled consumable contracts, or digital-first sales channels to reach decentralized buyers. Finally, de-risk supply and pricing exposure through diversified sourcing, nearshoring of critical components where feasible, and contractual mechanisms that share customs or tariff-related risks. Executing these actions in tandem will strengthen market positioning, reduce procurement friction, and accelerate clinical acceptance across care settings.
A rigorous mixed-methods research approach combining clinician interviews, regulatory review, device specification analysis, and scenario testing to underpin actionable insights
This research is informed by a triangulated methodology that combines primary stakeholder engagement, systematic literature review of peer-reviewed clinical studies and regulatory guidance, and structured synthesis of product specifications and patent landscapes. Primary inputs include interviews with clinicians, hospital procurement leaders, and device engineers to capture real-world performance considerations and adoption barriers. Secondary inputs encompass device labeling, regulatory filings, clinical trial registries, and white papers from professional societies to ensure alignment with current clinical standards and guidelines.
Data synthesis emphasizes cross-validation of claims against independent clinical evidence and operational feasibility assessments. Where possible, multiple data sources were used to corroborate technology performance characteristics and supply chain constraints. The methodology also incorporated scenario analysis to stress-test strategic options for manufacturers and purchasers under varying operational and regulatory conditions. Throughout, quality controls were applied to ensure transparency in assumptions and traceability of source material while maintaining confidentiality agreements with proprietary contributors.
A concise synthesis of how clinical performance, regional dynamics, and supply resilience collectively determine the trajectory of wound irrigation adoption and institutional uptake
In conclusion, wound irrigation systems occupy a pivotal role in contemporary wound management strategies, with adoption shaped by clinical performance, operational fit, and regional procurement nuances. Advances in pulsatile and pressure-controlled irrigation, coupled with evolving preferences for single-use versus reusable platforms, are redefining clinical workflows across hospitals, ambulatory centers, and home care environments. At the same time, tariff pressures and supply chain complexities are prompting manufacturers and purchasers to re-evaluate sourcing strategies and contract structures to safeguard service continuity.
Moving forward, successful stakeholders will be those that integrate rigorous clinical validation with adaptable commercial models and resilient supply chain designs. By aligning product development with frontline clinician needs and regional market dynamics, manufacturers can create compelling value propositions that support safer, more effective wound care delivery. Decision-makers should therefore prioritize evidence-led adoption, targeted channel strategies, and collaborative procurement frameworks to ensure sustainable deployment and continuous improvement in patient outcomes.
Please Note: PDF & Excel + Online Access - 1 Year
Orienting leaders to how device design, clinical need, and procurement priorities intersect to redefine wound irrigation practices across care settings
The evolving complexity of wound care demands a focused examination of wound irrigation systems as a pivotal element of clinical protocols and care pathways. This analysis synthesizes contemporary product modalities, care settings, and stakeholder priorities to present a clear initial orientation for leaders evaluating technological options, clinical integration, and distribution strategies. It underscores how practitioners are balancing effectiveness, ease of use, and infection control considerations while institutions seek predictable supply chains and cost-efficient solutions.
Clinicians increasingly prioritize irrigation approaches that reduce biofilm burden and support debridement efficacy without introducing undue complexity into routine workflows. Consequently, procurement leaders and clinical champions must navigate performance trade-offs between reusable platforms and single-use disposables, while accounting for the practicalities of training, reprocessing, and bedside ergonomics. This section therefore serves as an entry point for stakeholders to appreciate the interplay between clinical outcomes, device design, and institutional imperatives prior to deeper strategic decision-making.
Decisive shifts in clinical priorities, device innovation, and procurement models are driving a new era of adoption and competitive differentiation in wound irrigation systems
The landscape for wound irrigation systems has shifted in ways that are reshaping clinical protocols, supply models, and product development priorities. Emerging clinical evidence and heightened emphasis on infection prevention have pushed clinicians toward methods that optimize contaminant removal while minimizing tissue trauma. As a result, there is rising interest in devices that deliver controlled pressure profiles and pulsed flow characteristics, which can enhance debridement efficiency and support downstream wound healing interventions.
Concurrently, health systems are recalibrating procurement strategies to emphasize single-use disposables in high-acuity areas to reduce cross-contamination risk, even as cost-containment pressures encourage consideration of reusable systems in lower-risk contexts. Device manufacturers are responding by accelerating modular designs and offering hybrid service models that blend reusable hardware with disposable interfaces. In parallel, regulatory agencies and standards bodies are clarifying sterilization and labeling expectations, prompting manufacturers to invest in compliance documentation and post-market surveillance capabilities. Taken together, these shifts are fostering a more nuanced competitive environment where clinical performance, operational compatibility, and regulatory readiness determine acceptance and scale.
How evolving tariff dynamics and customs-driven cost pressures are reshaping sourcing strategies, supplier risk-sharing, and procurement practices in the United States
Recent tariff adjustments across key trading lanes have introduced additional considerations for manufacturers, suppliers, and healthcare purchasers operating within the United States supply chain. Increased import duties and ancillary customs costs have elevated landed costs for certain device components and finished goods, prompting manufacturers to reassess sourcing, inventory strategies, and pricing approaches. In response, some suppliers are pursuing nearshoring or dual-sourcing strategies to mitigate exposure to tariff volatility and reduce transit lead times.
For healthcare providers and group purchasing organizations, the cumulative effect of tariff-related cost pressures has translated into a renewed focus on total cost of ownership and contract flexibility. Stakeholders are seeking cost transparency from vendors and exploring consignment or managed inventory models to smooth price impacts. From a strategic standpoint, tariff dynamics are accelerating conversations about vertical integration for critical components and encouraging innovation in local manufacturing capabilities. As these adaptations evolve, stakeholders should anticipate that procurement negotiations will increasingly include clauses that address customs-related adjustments and collaborative risk-sharing mechanisms.
A multi-dimensional segmentation framework revealing how technology choices, product modalities, clinical use cases, and channels define pathways to clinical uptake and commercial success
Deconstructing the market through a segmentation lens clarifies where clinical need and commercial opportunity intersect. Based on technology, offerings fall into reusable platforms that emphasize lifecycle cost and institutional reprocessing workflows, and single-use solutions that prioritize infection control, convenience, and rapid deployment at the bedside. Based on product type, the universe includes gravity irrigation devices valued for simplicity and low operational burden, manual syringes used for targeted irrigation in varied settings, pressure irrigation systems that offer consistent flow characteristics for deeper wound cleansing, and pulsatile irrigation technologies which deliver cyclic flow patterns; within pulsatile irrigation, distinctions matter between battery-operated systems that afford portability and consistent pulse generation versus manual-powered devices that emphasize low capital requirements and simplicity.
Further segmentation by application reveals divergent clinical requirements: chronic wound treatment scenarios demand gentle but thorough biofilm management compatible with ongoing wound bed preparation; emergency care usage prioritizes rapid, reliable evacuation of debris and contaminants under time pressure; and surgical applications require precision and compatibility with sterile workflows. End-user segmentation highlights differentiated procurement and workflow considerations across ambulatory surgery centers that value throughput and predictable consumable use, home care contexts that emphasize user-friendly, safe single-use formats, hospitals that balance scale with sterilization capacity, and specialty clinics that seek tailored clinical performance. Finally, distribution channel segmentation recognizes distinct purchasing behaviors and service expectations across hospital pharmacies that manage institutional contracts, online sales channels that offer convenience and direct-to-provider access, and retail pharmacies that serve outpatient and home care needs. Together, these segment perspectives enable targeted product development and go-to-market strategies that align clinical performance attributes with channel-specific expectations.
How distinct regional regulatory landscapes, procurement norms, and clinical workflows influence adoption patterns and commercial approaches across global markets
Regional dynamics are shaping product development priorities, regulatory strategies, and commercial approaches in meaningful ways. In the Americas, health systems emphasize infection prevention and value-based procurement, with demand concentrated around solutions that can demonstrate compatibility with bundled care pathways and institutional sterilization capabilities. Because reimbursement and institutional procurement frameworks vary by submarket, vendors often adopt differentiated commercial models that combine direct hospital engagement with distribution partnerships.
Across Europe, the Middle East & Africa, regulatory alignment and a focus on standardized clinical guidelines drive adoption of systems that meet stringent device safety and labeling requirements, while local procurement practices and variable infrastructure in parts of the region necessitate adaptable service and training models. In the Asia-Pacific region, rapid adoption is influenced by growing surgical volumes, expanding ambulatory care infrastructure, and a strong emphasis on cost-competitive manufacturing. This evolution has encouraged international manufacturers to form local partnerships and invest in region-specific clinical evidence generation. Overall, geographic variation in procurement norms, clinician preferences, and regulatory environments requires vendors to adopt finely tuned regional strategies rather than a single global approach.
Competitive dynamics shaped by clinical validation, ergonomic design, service models, and digital enablement that determine long-term institutional adoption and growth
The competitive landscape is defined by a blend of established medical device firms, niche innovators, and emerging technology players that focus on differentiated irrigation performance and service models. Leading organizations are investing in clinical validation studies to demonstrate comparative advantages in tissue preservation and contaminant removal, while others concentrate on ergonomic design and user experience to improve bedside adoption rates. Manufacturers with integrated sterilization and KOL engagement strategies tend to achieve deeper institutional penetration, whereas specialty-focused entrants often target home care and outpatient clinic segments where ease of use and single-use convenience are critical.
Beyond product features, strategic differentiation arises from channel partnerships and service offerings. Companies that provide robust training programs, warranty and service support, and consumable supply guarantees secure stronger purchasing commitments from hospitals and ambulatory centers. Meanwhile, firms that excel in digital enablement-such as providing online ordering platforms, data-driven consumption analytics, and remote training modules-are better positioned to capture growing demand through non-traditional channels. In this environment, sustained investment in clinical evidence, regulatory compliance, and customer success functions determines the ability to expand into high-value care settings and retain long-term contracts.
Practical strategic moves for manufacturers and health system leaders to strengthen clinical credibility, diversify channels, and secure resilient supply chains
For industry leaders seeking to translate insight into influence, three pragmatic actions should be prioritized. First, align product development roadmaps with documented clinical performance needs by investing in evidence generation that articulates outcomes relevant to surgeons, wound care specialists, and emergency clinicians. This evidence base should include comparative usability studies and real-world safety data to support purchasing decisions and clinician training.
Second, optimize commercial models by creating flexible channel strategies that address the distinct requirements of hospitals, ambulatory centers, home care markets, and retail channels. This may involve pilot consignment agreements, bundled consumable contracts, or digital-first sales channels to reach decentralized buyers. Finally, de-risk supply and pricing exposure through diversified sourcing, nearshoring of critical components where feasible, and contractual mechanisms that share customs or tariff-related risks. Executing these actions in tandem will strengthen market positioning, reduce procurement friction, and accelerate clinical acceptance across care settings.
A rigorous mixed-methods research approach combining clinician interviews, regulatory review, device specification analysis, and scenario testing to underpin actionable insights
This research is informed by a triangulated methodology that combines primary stakeholder engagement, systematic literature review of peer-reviewed clinical studies and regulatory guidance, and structured synthesis of product specifications and patent landscapes. Primary inputs include interviews with clinicians, hospital procurement leaders, and device engineers to capture real-world performance considerations and adoption barriers. Secondary inputs encompass device labeling, regulatory filings, clinical trial registries, and white papers from professional societies to ensure alignment with current clinical standards and guidelines.
Data synthesis emphasizes cross-validation of claims against independent clinical evidence and operational feasibility assessments. Where possible, multiple data sources were used to corroborate technology performance characteristics and supply chain constraints. The methodology also incorporated scenario analysis to stress-test strategic options for manufacturers and purchasers under varying operational and regulatory conditions. Throughout, quality controls were applied to ensure transparency in assumptions and traceability of source material while maintaining confidentiality agreements with proprietary contributors.
A concise synthesis of how clinical performance, regional dynamics, and supply resilience collectively determine the trajectory of wound irrigation adoption and institutional uptake
In conclusion, wound irrigation systems occupy a pivotal role in contemporary wound management strategies, with adoption shaped by clinical performance, operational fit, and regional procurement nuances. Advances in pulsatile and pressure-controlled irrigation, coupled with evolving preferences for single-use versus reusable platforms, are redefining clinical workflows across hospitals, ambulatory centers, and home care environments. At the same time, tariff pressures and supply chain complexities are prompting manufacturers and purchasers to re-evaluate sourcing strategies and contract structures to safeguard service continuity.
Moving forward, successful stakeholders will be those that integrate rigorous clinical validation with adaptable commercial models and resilient supply chain designs. By aligning product development with frontline clinician needs and regional market dynamics, manufacturers can create compelling value propositions that support safer, more effective wound care delivery. Decision-makers should therefore prioritize evidence-led adoption, targeted channel strategies, and collaborative procurement frameworks to ensure sustainable deployment and continuous improvement in patient outcomes.
Please Note: PDF & Excel + Online Access - 1 Year
Table of Contents
196 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. Growing adoption of portable wound irrigation systems with integrated pressure controls for home and remote care
- 5.2. Increased utilization of antimicrobial and antibiotic irrigation solutions to reduce infection rates in chronic wounds
- 5.3. Emergence of smart wound irrigation devices with sensor-driven flow regulation and digital connectivity for clinical data tracking
- 5.4. Development of single-use environmentally sustainable irrigation consumables to address hospital waste management challenges
- 5.5. Expansion of automated negative pressure wound irrigation systems for enhanced healing in complex and deep tissue injuries
- 5.6. Regulatory approval trends driving market entry of innovative high pressure pulsatile irrigation devices for surgical applications
- 5.7. Rising integration of telemedicine platforms with wound irrigation protocols enabling remote monitoring and virtual consultations
- 5.8. Adoption of 3D printed personalized irrigation nozzles tailored to wound geometry for precise fluid delivery
- 5.9. Shift toward low pressure constant flow irrigation systems to improve patient comfort and minimize tissue trauma
- 5.10. Research on bioactive wound irrigation formulations incorporating growth factors and anti-inflammatory agents for accelerated healing
- 6. Cumulative Impact of United States Tariffs 2025
- 7. Cumulative Impact of Artificial Intelligence 2025
- 8. Wound Irrigation System Market, by Technology
- 8.1. Reusable
- 8.2. Single Use
- 9. Wound Irrigation System Market, by Product Type
- 9.1. Gravity Irrigation
- 9.2. Manual Syringe
- 9.3. Pressure Irrigation
- 9.4. Pulsatile Irrigation
- 9.4.1. Battery Operated
- 9.4.2. Manual Powered
- 10. Wound Irrigation System Market, by Application
- 10.1. Chronic Wound Treatment
- 10.2. Emergency Care
- 10.3. Surgical
- 11. Wound Irrigation System Market, by End User
- 11.1. Ambulatory Surgery Centers
- 11.2. Home Care
- 11.3. Hospitals
- 11.4. Specialty Clinics
- 12. Wound Irrigation System Market, by Distribution Channel
- 12.1. Hospital Pharmacies
- 12.2. Online Sales
- 12.3. Retail Pharmacies
- 13. Wound Irrigation System 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. Wound Irrigation System Market, by Group
- 14.1. ASEAN
- 14.2. GCC
- 14.3. European Union
- 14.4. BRICS
- 14.5. G7
- 14.6. NATO
- 15. Wound Irrigation System 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. Stryker Corporation
- 16.3.3. Zimmer Biomet Holdings, Inc.
- 16.3.4. Smith & Nephew plc
- 16.3.5. Cardinal Health, Inc.
- 16.3.6. McKesson Corporation
- 16.3.7. Medline Industries, LP
- 16.3.8. B. Braun Melsungen AG
- 16.3.9. Mölnlycke Health Care AB
- 16.3.10. Integra LifeSciences Holdings Corporation
- 16.3.11. 3M Company
- 16.3.12. ConvaTec Group Plc
- 16.3.13. Coloplast Group
- 16.3.14. Hollister Incorporated
- 16.3.15. Irrimax Corporation
- 16.3.16. Centurion Medical Products Corporation
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