Medical Suction Devices Market by Product (Hand-Handled Devices, Wall-Mounted Devices), Vacuum Systems (AC-Powered Devices, Battery-Powered Devices, Dual-Powered Devices), Application, End User, Sales Channel - Global Forecast 2025-2032
Description
The Medical Suction Devices Market was valued at USD 1.26 billion in 2024 and is projected to grow to USD 1.32 billion in 2025, with a CAGR of 5.56%, reaching USD 1.94 billion by 2032.
A comprehensive orientation to how clinical priorities, technological advances, and regulatory emphasis are redefining expectations for medical suction device design and procurement
The medical suction device environment has evolved from a set of discrete clinical tools into an interconnected product category where clinical efficacy, ease of use, and supply resilience drive procurement decisions. Advances in battery chemistry, quieter pump mechanisms, and ergonomic hand-held designs have been complemented by renewed focus on infection prevention and single-patient-use disposables. Meanwhile, clinical settings ranging from acute hospitals to homecare increasingly demand devices that reconcile portability with reliable suction performance and regulatory compliance.
Against this backdrop, device designers and health systems are prioritizing interoperability, cleaning protocols, and training to reduce device-associated complications and streamline workflows. Regulatory scrutiny has shifted toward enhanced post-market surveillance and device labeling that clarifies intended setting and maintenance practices. Consequently, organizations moving from legacy procurement models to outcome-focused contracts are finding that product attributes such as battery endurance, ease of sterilization, and serviceability now influence purchasing decisions as much as nominal suction metrics. This introduction frames the subsequent analysis by highlighting how clinical imperatives and technological enablers are reshaping expectations for delivery, support, and continuous improvement across care settings.
How technological convergence, evolving care delivery models, and regulatory tightening are collectively transforming product design, procurement, and service expectations in suction devices
The landscape of medical suction devices is undergoing transformative shifts driven by converging forces in technology, care delivery, and supply chain strategy. Portable battery-powered and dual-powered systems have matured, enabling clinicians to extend high-quality suction capabilities beyond traditional hospital zones into ambulatory clinics, emergency response, and homecare. At the same time, the integration of quieter motors, improved filtration, and modular disposables has reduced device downtime and infection risk, prompting clinicians to re-evaluate standard operating protocols and equipment placement.
Concurrently, health systems are implementing procurement strategies that emphasize lifecycle cost, maintainability, and vendor service ecosystems. These shifts have prompted device manufacturers to adopt platform approaches that allow modular upgrades, remote diagnostics, and predictable aftermarket service offerings. In parallel, regulatory authorities are clarifying expectations for labeling, cleaning instructions, and post-market data collection, raising the bar for documentation and quality systems. Taken together, these dynamics are steering the industry toward devices that balance clinical performance with ease of use, cleaner infection-control profiles, and resilient supply relationships that accommodate rapid reconfiguration of clinical space and patient care models.
Observed supply chain adaptations and procurement responses following United States tariff changes in 2025 that have reshaped sourcing, inventory, and manufacturing strategies
The cumulative impact of tariffs introduced by the United States in 2025 has prompted tangible supply-chain and sourcing responses across the medical suction device value chain. Manufacturers and distributors have faced increased component and subassembly costs, which in turn elevated scrutiny on supplier contracts and encouraged strategic shifts toward alternative sourcing strategies. As a result, procurement teams have expanded qualification of secondary suppliers and revisited inventory strategies for critical components such as brushless motors, control electronics, and battery modules to preserve continuity of supply.
Moreover, the tariff environment has accelerated conversations about nearshoring and regional manufacturing investments, particularly for higher-value assemblies and devices destined for emergency care and home-use segments where rapid replenishment is critical. Manufacturers also intensified collaboration with logistics partners to optimize tariff classifications and leverage trade mitigation mechanisms where possible. Finally, purchasing organizations and hospital systems increasingly requested enhanced transparency on cost drivers, lead times, and contingency plans, prompting suppliers to enhance contractual flexibility and communicate more frequently about component lead times and substitution strategies. These cumulative responses reflect a practical industry adaptation to trade policy shifts while maintaining clinical availability across care settings.
Segment-driven strategic imperatives showing how product form factor, power architecture, clinical application, user setting, and sales channel collectively shape device design and commercialization
Insightful segmentation illuminates where innovation and adoption pressures are most acute across product, power system, clinical use, end-user environment, and distribution channel dimensions. Based on Product, market participants differentiate offerings between hand-handled devices that prioritize ergonomic controls and portability and wall-mounted devices that emphasize continuous availability and integration with facility infrastructure. Based on Vacuum Systems, product roadmaps and service strategies diverge among AC-powered devices favored for fixed locations, battery-powered devices engineered for mobility, dual-powered devices designed for operational flexibility, and manually operated devices retained for low-resource or backup applications.
Based on Application, clinical design and disposable configurations are tailored to airway clearing scenarios, research and diagnostics contexts, and surgical environments where suction requirements and sterility demands vary significantly. Based on End User, adoption patterns and procurement cycles reflect distinct needs among clinics that prioritize cost and space efficiency, homecare settings that require simplified maintenance and training, and hospitals that demand robust service agreements and regulatory documentation. Based on Sales Channel, manufacturers balance investments between offline distribution channels that support clinical demonstrations and integrated servicing and online channels that expand reach for smaller facilities and direct-to-consumer homecare purchases. These segmentation lenses reveal where engineering trade-offs, service models, and compliance priorities must be aligned to maximize clinical value and operational reliability.
Regional insights that illustrate how procurement, regulatory frameworks, and care delivery priorities differ across the Americas, Europe Middle East & Africa, and Asia-Pacific regions and drive strategic differentiation
Regional dynamics continue to inform product selection, regulatory timelines, and supply-chain priorities across the Americas, Europe, Middle East & Africa, and Asia-Pacific. In the Americas, providers emphasize rapid deployment, strong aftermarket service networks, and devices compatible with diverse emergency and outpatient care models, while procurement teams often require detailed device validation and service-level commitments. Meanwhile in Europe, Middle East & Africa, regulatory harmonization efforts and diverse reimbursement environments drive a need for localized compliance documentation and flexible distribution models, resulting in investments in regional regulatory affairs and multilingual service capabilities.
Across Asia-Pacific, rapid healthcare infrastructure expansion and growing homecare services have increased demand for portable, cost-efficient designs and scalable service offerings, prompting manufacturers to customize training materials, sterilization guidance, and spare-part availability for wide-ranging care settings. In response, device suppliers are differentiating by establishing regional maintenance hubs, adapting packaging and labeling to meet regulatory variants, and collaborating with local distributors to accelerate introduction into both urban and peri-urban care delivery contexts. These regional considerations collectively influence product configuration, warranty policies, and channel strategies that respond to diverse clinical practices and procurement expectations.
How leading device suppliers are shifting from transactional selling toward integrated solutions through service ecosystems, modular product roadmaps, and regulatory readiness initiatives
Key industry participants exhibit several consistent strategic behaviors that shape competitive dynamics and customer expectations. Companies are increasingly investing in service ecosystems that pair devices with training, preventative maintenance, and consumable supply plans to reduce clinical downtime and strengthen customer relationships. Product roadmaps emphasize modularity and upgrade pathways that allow legacy installations to benefit from newer control modules or battery packs without full system replacement, thereby addressing procurement preferences for lower lifecycle disruptions.
At the same time, vendors are refining go-to-market approaches by combining clinical education programs with digital resources that support rapid onboarding in clinics and homecare environments. Strategic collaborations with component specialists and healthcare providers are used to shorten design cycles and validate usability in real-world workflows. Several organizations also prioritize regulatory readiness by expanding post-market surveillance capabilities and strengthening complaint-handling systems. Collectively, these behaviors indicate a shift from selling standalone devices to delivering integrated clinical solutions that blend reliable hardware, service continuity, and documented compliance.
Actionable strategies for device makers and healthcare providers to secure competitive advantage through modular products, expanded services, regional sourcing, and strengthened regulatory practices
Industry leaders can take concrete actions to strengthen competitive position, improve clinical outcomes, and enhance supply resilience. First, align product development investments toward modular architectures that permit incremental upgrades to electronics and power modules, enabling longer equipment lifecycles and reduced capital replacement cycles. Second, expand service offerings to include predictive maintenance programs and remote diagnostics that minimize unplanned downtime and provide measurable benefits to institutional customers.
Third, invest in diversified supplier qualification and regional manufacturing or assembly capabilities to mitigate the effects of trade policy volatility and reduce lead-time variability. Fourth, prioritize clear labeling, simplified cleaning regimens, and clinician-focused training materials to accelerate adoption in homecare and low-resource settings. Fifth, develop channel strategies that balance offline clinical demonstration capacity with streamlined online fulfillment for smaller buyers. Finally, deepen regulatory and quality-system investments to meet heightened expectations for post-market surveillance and to support faster regulatory submissions across jurisdictions. Implementing these measures will help organizations deliver differentiated value while managing cost and compliance complexities in a constrained supply environment.
Rigorous mixed-methods research combining stakeholder interviews, technical reviews, regulatory scans, and supply-chain validation to produce actionable and verifiable insights on device performance and sourcing
The research underpinning this report relied on a mixed-methods approach combining primary stakeholder engagement and comprehensive secondary source analysis. Primary efforts included structured interviews with clinicians across acute, ambulatory, and homecare settings, in-depth conversations with procurement and biomedical engineering leaders, and consultative sessions with supply-chain and logistics experts to validate sourcing behaviors and tariff responses. Supplemental primary inputs involved device usability walkthroughs and service-level benchmarking with hospital and clinic maintenance teams to observe real-world performance and servicing constraints.
Secondary research encompassed regulatory review of product guidance and labeling requirements, patent landscape scans to identify incremental innovation trends, and technical literature appraisal of battery and vacuum-system developments. Data triangulation was applied throughout to corroborate claims and to reconcile divergent stakeholder perspectives. Quality controls included cross-validation of interview findings against published regulatory documents and independent engineering assessments of device performance characteristics. This methodology ensured a balanced, actionable analysis grounded in practitioner experience and documented technical progress.
Integrated conclusions stressing how product design, service models, and supply resilience together determine clinical adoption and long-term success in suction device portfolios
The trajectory of medical suction devices reflects a pragmatic convergence of clinical need, technological maturation, and supply-chain realism. Devices that successfully combine usability, infection-control features, and flexible power options are gaining traction in diverse care settings, while suppliers that couple hardware with robust service ecosystems are winning longer-term institutional commitments. The tariff-driven supply pressures introduced in 2025 have underscored the importance of supplier diversification, near-term inventory management, and regional manufacturing strategies, prompting both vendors and buyers to take more proactive risk-mitigation steps.
Looking ahead, organizations that adopt modular product strategies, invest in predictive maintenance and remote diagnostics, and tailor offerings to the nuanced requirements of hospitals, clinics, and homecare environments will be better positioned to meet evolving clinical workflows and purchaser expectations. Ultimately, sustained clinical adoption will depend on the industry’s ability to deliver demonstrable operational benefits, clear regulatory compliance, and dependable aftermarket support that together reduce total disruption and improve patient care continuity.
Note: PDF & Excel + Online Access - 1 Year
A comprehensive orientation to how clinical priorities, technological advances, and regulatory emphasis are redefining expectations for medical suction device design and procurement
The medical suction device environment has evolved from a set of discrete clinical tools into an interconnected product category where clinical efficacy, ease of use, and supply resilience drive procurement decisions. Advances in battery chemistry, quieter pump mechanisms, and ergonomic hand-held designs have been complemented by renewed focus on infection prevention and single-patient-use disposables. Meanwhile, clinical settings ranging from acute hospitals to homecare increasingly demand devices that reconcile portability with reliable suction performance and regulatory compliance.
Against this backdrop, device designers and health systems are prioritizing interoperability, cleaning protocols, and training to reduce device-associated complications and streamline workflows. Regulatory scrutiny has shifted toward enhanced post-market surveillance and device labeling that clarifies intended setting and maintenance practices. Consequently, organizations moving from legacy procurement models to outcome-focused contracts are finding that product attributes such as battery endurance, ease of sterilization, and serviceability now influence purchasing decisions as much as nominal suction metrics. This introduction frames the subsequent analysis by highlighting how clinical imperatives and technological enablers are reshaping expectations for delivery, support, and continuous improvement across care settings.
How technological convergence, evolving care delivery models, and regulatory tightening are collectively transforming product design, procurement, and service expectations in suction devices
The landscape of medical suction devices is undergoing transformative shifts driven by converging forces in technology, care delivery, and supply chain strategy. Portable battery-powered and dual-powered systems have matured, enabling clinicians to extend high-quality suction capabilities beyond traditional hospital zones into ambulatory clinics, emergency response, and homecare. At the same time, the integration of quieter motors, improved filtration, and modular disposables has reduced device downtime and infection risk, prompting clinicians to re-evaluate standard operating protocols and equipment placement.
Concurrently, health systems are implementing procurement strategies that emphasize lifecycle cost, maintainability, and vendor service ecosystems. These shifts have prompted device manufacturers to adopt platform approaches that allow modular upgrades, remote diagnostics, and predictable aftermarket service offerings. In parallel, regulatory authorities are clarifying expectations for labeling, cleaning instructions, and post-market data collection, raising the bar for documentation and quality systems. Taken together, these dynamics are steering the industry toward devices that balance clinical performance with ease of use, cleaner infection-control profiles, and resilient supply relationships that accommodate rapid reconfiguration of clinical space and patient care models.
Observed supply chain adaptations and procurement responses following United States tariff changes in 2025 that have reshaped sourcing, inventory, and manufacturing strategies
The cumulative impact of tariffs introduced by the United States in 2025 has prompted tangible supply-chain and sourcing responses across the medical suction device value chain. Manufacturers and distributors have faced increased component and subassembly costs, which in turn elevated scrutiny on supplier contracts and encouraged strategic shifts toward alternative sourcing strategies. As a result, procurement teams have expanded qualification of secondary suppliers and revisited inventory strategies for critical components such as brushless motors, control electronics, and battery modules to preserve continuity of supply.
Moreover, the tariff environment has accelerated conversations about nearshoring and regional manufacturing investments, particularly for higher-value assemblies and devices destined for emergency care and home-use segments where rapid replenishment is critical. Manufacturers also intensified collaboration with logistics partners to optimize tariff classifications and leverage trade mitigation mechanisms where possible. Finally, purchasing organizations and hospital systems increasingly requested enhanced transparency on cost drivers, lead times, and contingency plans, prompting suppliers to enhance contractual flexibility and communicate more frequently about component lead times and substitution strategies. These cumulative responses reflect a practical industry adaptation to trade policy shifts while maintaining clinical availability across care settings.
Segment-driven strategic imperatives showing how product form factor, power architecture, clinical application, user setting, and sales channel collectively shape device design and commercialization
Insightful segmentation illuminates where innovation and adoption pressures are most acute across product, power system, clinical use, end-user environment, and distribution channel dimensions. Based on Product, market participants differentiate offerings between hand-handled devices that prioritize ergonomic controls and portability and wall-mounted devices that emphasize continuous availability and integration with facility infrastructure. Based on Vacuum Systems, product roadmaps and service strategies diverge among AC-powered devices favored for fixed locations, battery-powered devices engineered for mobility, dual-powered devices designed for operational flexibility, and manually operated devices retained for low-resource or backup applications.
Based on Application, clinical design and disposable configurations are tailored to airway clearing scenarios, research and diagnostics contexts, and surgical environments where suction requirements and sterility demands vary significantly. Based on End User, adoption patterns and procurement cycles reflect distinct needs among clinics that prioritize cost and space efficiency, homecare settings that require simplified maintenance and training, and hospitals that demand robust service agreements and regulatory documentation. Based on Sales Channel, manufacturers balance investments between offline distribution channels that support clinical demonstrations and integrated servicing and online channels that expand reach for smaller facilities and direct-to-consumer homecare purchases. These segmentation lenses reveal where engineering trade-offs, service models, and compliance priorities must be aligned to maximize clinical value and operational reliability.
Regional insights that illustrate how procurement, regulatory frameworks, and care delivery priorities differ across the Americas, Europe Middle East & Africa, and Asia-Pacific regions and drive strategic differentiation
Regional dynamics continue to inform product selection, regulatory timelines, and supply-chain priorities across the Americas, Europe, Middle East & Africa, and Asia-Pacific. In the Americas, providers emphasize rapid deployment, strong aftermarket service networks, and devices compatible with diverse emergency and outpatient care models, while procurement teams often require detailed device validation and service-level commitments. Meanwhile in Europe, Middle East & Africa, regulatory harmonization efforts and diverse reimbursement environments drive a need for localized compliance documentation and flexible distribution models, resulting in investments in regional regulatory affairs and multilingual service capabilities.
Across Asia-Pacific, rapid healthcare infrastructure expansion and growing homecare services have increased demand for portable, cost-efficient designs and scalable service offerings, prompting manufacturers to customize training materials, sterilization guidance, and spare-part availability for wide-ranging care settings. In response, device suppliers are differentiating by establishing regional maintenance hubs, adapting packaging and labeling to meet regulatory variants, and collaborating with local distributors to accelerate introduction into both urban and peri-urban care delivery contexts. These regional considerations collectively influence product configuration, warranty policies, and channel strategies that respond to diverse clinical practices and procurement expectations.
How leading device suppliers are shifting from transactional selling toward integrated solutions through service ecosystems, modular product roadmaps, and regulatory readiness initiatives
Key industry participants exhibit several consistent strategic behaviors that shape competitive dynamics and customer expectations. Companies are increasingly investing in service ecosystems that pair devices with training, preventative maintenance, and consumable supply plans to reduce clinical downtime and strengthen customer relationships. Product roadmaps emphasize modularity and upgrade pathways that allow legacy installations to benefit from newer control modules or battery packs without full system replacement, thereby addressing procurement preferences for lower lifecycle disruptions.
At the same time, vendors are refining go-to-market approaches by combining clinical education programs with digital resources that support rapid onboarding in clinics and homecare environments. Strategic collaborations with component specialists and healthcare providers are used to shorten design cycles and validate usability in real-world workflows. Several organizations also prioritize regulatory readiness by expanding post-market surveillance capabilities and strengthening complaint-handling systems. Collectively, these behaviors indicate a shift from selling standalone devices to delivering integrated clinical solutions that blend reliable hardware, service continuity, and documented compliance.
Actionable strategies for device makers and healthcare providers to secure competitive advantage through modular products, expanded services, regional sourcing, and strengthened regulatory practices
Industry leaders can take concrete actions to strengthen competitive position, improve clinical outcomes, and enhance supply resilience. First, align product development investments toward modular architectures that permit incremental upgrades to electronics and power modules, enabling longer equipment lifecycles and reduced capital replacement cycles. Second, expand service offerings to include predictive maintenance programs and remote diagnostics that minimize unplanned downtime and provide measurable benefits to institutional customers.
Third, invest in diversified supplier qualification and regional manufacturing or assembly capabilities to mitigate the effects of trade policy volatility and reduce lead-time variability. Fourth, prioritize clear labeling, simplified cleaning regimens, and clinician-focused training materials to accelerate adoption in homecare and low-resource settings. Fifth, develop channel strategies that balance offline clinical demonstration capacity with streamlined online fulfillment for smaller buyers. Finally, deepen regulatory and quality-system investments to meet heightened expectations for post-market surveillance and to support faster regulatory submissions across jurisdictions. Implementing these measures will help organizations deliver differentiated value while managing cost and compliance complexities in a constrained supply environment.
Rigorous mixed-methods research combining stakeholder interviews, technical reviews, regulatory scans, and supply-chain validation to produce actionable and verifiable insights on device performance and sourcing
The research underpinning this report relied on a mixed-methods approach combining primary stakeholder engagement and comprehensive secondary source analysis. Primary efforts included structured interviews with clinicians across acute, ambulatory, and homecare settings, in-depth conversations with procurement and biomedical engineering leaders, and consultative sessions with supply-chain and logistics experts to validate sourcing behaviors and tariff responses. Supplemental primary inputs involved device usability walkthroughs and service-level benchmarking with hospital and clinic maintenance teams to observe real-world performance and servicing constraints.
Secondary research encompassed regulatory review of product guidance and labeling requirements, patent landscape scans to identify incremental innovation trends, and technical literature appraisal of battery and vacuum-system developments. Data triangulation was applied throughout to corroborate claims and to reconcile divergent stakeholder perspectives. Quality controls included cross-validation of interview findings against published regulatory documents and independent engineering assessments of device performance characteristics. This methodology ensured a balanced, actionable analysis grounded in practitioner experience and documented technical progress.
Integrated conclusions stressing how product design, service models, and supply resilience together determine clinical adoption and long-term success in suction device portfolios
The trajectory of medical suction devices reflects a pragmatic convergence of clinical need, technological maturation, and supply-chain realism. Devices that successfully combine usability, infection-control features, and flexible power options are gaining traction in diverse care settings, while suppliers that couple hardware with robust service ecosystems are winning longer-term institutional commitments. The tariff-driven supply pressures introduced in 2025 have underscored the importance of supplier diversification, near-term inventory management, and regional manufacturing strategies, prompting both vendors and buyers to take more proactive risk-mitigation steps.
Looking ahead, organizations that adopt modular product strategies, invest in predictive maintenance and remote diagnostics, and tailor offerings to the nuanced requirements of hospitals, clinics, and homecare environments will be better positioned to meet evolving clinical workflows and purchaser expectations. Ultimately, sustained clinical adoption will depend on the industry’s ability to deliver demonstrable operational benefits, clear regulatory compliance, and dependable aftermarket support that together reduce total disruption and improve patient care continuity.
Note: PDF & Excel + Online Access - 1 Year
Table of Contents
191 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. Increasing adoption of portable battery-powered suction units for emergency and home care settings
- 5.2. Integration of disposable closed system suction designs to reduce infection risks and cross-contamination
- 5.3. Development of smart suction devices with IoT connectivity for real-time procedural monitoring and analytics
- 5.4. Growth of minimally invasive surgical aspirator systems tailored for laparoscopic and robotic procedures
- 5.5. Rising demand for high vacuum surgical suction pumps offering low noise output and enhanced energy efficiency
- 5.6. Expansion of multifunctional suction applications in veterinary and dental markets driving product innovation
- 6. Cumulative Impact of United States Tariffs 2025
- 7. Cumulative Impact of Artificial Intelligence 2025
- 8. Medical Suction Devices Market, by Product
- 8.1. Hand-Handled Devices
- 8.2. Wall-Mounted Devices
- 9. Medical Suction Devices Market, by Vacuum Systems
- 9.1. AC-Powered Devices
- 9.2. Battery-Powered Devices
- 9.3. Dual-Powered Devices
- 9.4. Manually Operated Devices
- 10. Medical Suction Devices Market, by Application
- 10.1. Airway Clearing
- 10.2. Research & Diagnostics
- 10.3. Surgical
- 11. Medical Suction Devices Market, by End User
- 11.1. Clinics
- 11.2. Homecare
- 11.3. Hospital
- 12. Medical Suction Devices Market, by Sales Channel
- 12.1. Offline
- 12.2. Online
- 13. Medical Suction Devices 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 Suction Devices Market, by Group
- 14.1. ASEAN
- 14.2. GCC
- 14.3. European Union
- 14.4. BRICS
- 14.5. G7
- 14.6. NATO
- 15. Medical Suction Devices 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. Cardinal Health
- 16.3.2. Delex Pharma International, Inc.
- 16.3.3. Indoplas Philippines Inc.
- 16.3.4. Medela AG
- 16.3.5. Medtronic plc
- 16.3.6. Nareena Lifesciences Private Limited
- 16.3.7. Ohio Medical Corporation
- 16.3.8. Olympus Corporation
- 16.3.9. Panamed Philippines Inc.
- 16.3.10. Philips Healthcare
- 16.3.11. Siemens Healthineers
- 16.3.12. Stryker Corporation
- 16.3.13. The Getz Group of companies
- 16.3.14. TRANSMEDIC PHILIPPINES INC
- 16.3.15. Welch Allyn, Inc.
- 16.3.16. ZOLL Medical Corporation
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