Medical Nitric Oxide Detector Market by Technology (Chemiluminescence, Electrochemical, Optical), Portability (Benchtop, Portable), Distribution Channel, Application, End User - Global Forecast 2026-2032
Description
The Medical Nitric Oxide Detector Market was valued at USD 150.35 million in 2025 and is projected to grow to USD 172.46 million in 2026, with a CAGR of 9.59%, reaching USD 285.60 million by 2032.
Introduction to clinical-grade nitric oxide detection and its role in modern healthcare diagnostics, monitoring, and translational research applications
Nitric oxide detection has evolved from a niche laboratory capability into a clinical and translational asset that informs diagnostics, therapeutic monitoring, and research workflows. Devices that reliably quantify exhaled or ambient nitric oxide support decision-making across respiratory medicine, anesthesia management, and investigational studies probing inflammatory biology. Clinicians and researchers increasingly demand instruments that marry analytical performance with workflow compatibility, enabling point-of-care use, bedside monitoring, and integration with electronic health records.
Against this backdrop, commercial and development teams face a dual imperative: preserve analytical fidelity while improving accessibility and ease of use. Advances in sensor technology, miniaturization, and data analytics are enabling a new generation of instruments that reduce user burden and broaden applicability. At the same time, regulatory expectations and clinical validation pathways continue to shape product design and adoption timelines. Understanding these technical, clinical, and regulatory forces provides a foundation for strategic planning and targeted investment in nitric oxide detection capabilities.
Transformative shifts reshaping nitric oxide detection devices, from sensor miniaturization to AI-enabled signal interpretation across clinical workflows
The landscape for nitric oxide detection is being transformed by converging technological and clinical trends that redefine device value propositions. Sensor miniaturization and low-power electronics have made portable platforms more viable, while improvements in selective chemistry and signal processing have narrowed the performance gap between benchtop standards and compact instruments. At the same time, artificial intelligence and advanced signal deconvolution techniques enable real-time interpretation of noisy physiological signals, supporting clinical decision workflows rather than simply producing raw measurements.
Clinically, there is a rising emphasis on personalized and longitudinal monitoring. Physicians are looking for tools that allow repeated assessments in clinic or home settings, complementing episodic spirometry and imaging. Regulatory authorities are also clarifying expectations for software as a medical device, which in turn accelerates investment in validated analytics and post-market surveillance. As a result, suppliers that combine robust sensor hardware with clear validation narratives and interoperable software stacks will find differentiated adoption pathways. Moreover, cross-sector partnerships between device makers, software vendors, and clinical research organizations are becoming increasingly important to bridge evidence gaps and hasten clinical utility.
Cumulative effects of United States tariff adjustments in 2025 on medical sensor supply chains, component sourcing, and cross-border manufacturing strategies
Policy shifts in tariff regimes and cross-border trade can have pronounced downstream effects on the production and distribution of medical sensors and diagnostic subsystems. When tariffs affect electronic components, specialty gases, or precision-machined parts, manufacturers face higher landed costs and may need to re-evaluate supplier portfolios and assembly footprints. The cumulative impact often manifests as lengthened procurement cycles, renegotiation of supplier terms, or the relocation of certain manufacturing stages to tariff-favored jurisdictions.
In response, procurement and product teams typically pursue a mix of mitigation strategies. These include qualifying alternative suppliers with compatible quality systems, redesigning assemblies to reduce reliance on tariff-exposed components, and leveraging longer-term contracts to stabilize input costs. Additionally, companies reconsider inventory strategies to buffer short-term cost shocks while exploring nearshoring for key subassemblies to reduce exposure. For clinical customers and distributors, these supply-side dynamics can translate into longer lead times and changed commercial terms, which demands transparent communication and coordinated planning across stakeholders to preserve service levels and clinical continuity.
Key segmentation insights revealing how technology, application, end user, portability, and distribution dynamics drive clinical nitric oxide detector adoption
A nuanced segmentation perspective illuminates the heterogeneity of demand and the technical trade-offs that define product strategies. Based on technology, devices are differentiated by chemiluminescence, electrochemical, optical, and paramagnetic measurement principles, each offering distinct strengths in sensitivity, response time, maintenance needs, and cost structure. Based on application, end uses span anesthesia monitoring, diagnostics, research, and respiratory care, with each application imposing unique accuracy, calibration, and integration requirements. Based on end user, deployment scenarios include clinics, home healthcare, hospitals, and research institutes, and each setting drives different expectations for usability, serviceability, and connectivity.
Portability is another critical axis: bench‑top systems emphasize analytical performance and multi-parameter integration, while portable units are designed for cart-mounted or handheld use and prioritize rapid setup, battery life, and simplified calibration. Finally, distribution channel dynamics matter: direct sales allow for clinical training and tailored integration, distributors can extend geographic reach and after-sales support, and online channels, including e-commerce and manufacturer platforms, lower the barrier to entry for smaller buyers and enable streamlined reorder processes. Taken together, these segmentation lenses reveal that successful commercialization requires aligning sensor technology, user experience, and channel strategy to specific clinical workflows and procurement behaviors.
Regional dynamics and adoption trends across the Americas, Europe Middle East & Africa, and Asia-Pacific that shape device deployment and clinical uptake
Regional factors significantly influence adoption pathways and commercialization approaches for nitric oxide detectors. In the Americas, healthcare systems tend to emphasize evidence-based reimbursement and large integrated hospital networks, which creates demand for validated clinical-grade instruments and consolidated service agreements. Suppliers typically focus on establishing strong clinical partnerships and building local service infrastructure to meet stringent uptime and quality expectations.
In Europe, Middle East & Africa, regulatory heterogeneity and a mixture of public and private healthcare procurement require flexible market strategies. Companies must navigate CE marking pathways, regional procurement consortia, and diverse payment models while tailoring training and support programs to varying resource levels. In Asia-Pacific, rapid adoption in urban centers is driven by strong research investment and growing demand for point-of-care diagnostics, while cost sensitivity and distribution complexity in some markets necessitate scalable manufacturing and adaptive commercialization approaches. Across all regions, local clinical evidence generation, distributor relationships, and clear regulatory pathways remain decisive factors for sustained device uptake.
Competitive and collaborative company insights outlining strategic positioning, product portfolios, partnerships, and innovation pathways in nitric oxide detection
Competitive dynamics in the nitric oxide detection landscape are characterized by a mix of established medical device manufacturers, specialist sensor suppliers, agile startups, and integrators that combine hardware with software-driven analytics. Established firms often leverage extensive clinical networks, regulatory experience, and scale manufacturing to maintain leadership in high-performance benchtop systems. In contrast, sensor specialists and startups tend to drive innovation around miniaturized transducers, novel chemistries, and low-cost manufacturing techniques that enable portable solutions and new use cases.
Partnership models and vertical integration strategies are increasingly common. Alliances between component OEMs and clinical system integrators accelerate time-to-market by aligning component roadmaps with end-user documentation and support systems. At the same time, companies that invest in modular platforms and open interoperability are better positioned to capitalize on hospital IT strategies and device consolidation efforts. Intellectual property in sensor chemistry, calibration algorithms, and signal processing provides defensibility, while service models and clinical support offerings create recurring revenue opportunities and strengthen customer retention.
Actionable strategic recommendations for industry leaders to optimize product design, supply resilience, regulatory positioning, and go-to-market acceleration
Companies seeking durable advantage should pursue coordinated strategies across product design, supply chain resilience, regulatory engagement, and commercial outreach. Invest in platform architectures that allow sensor modules and analytics to be upgraded independently, which preserves hardware lifecycles while enabling continuous software innovation. Concurrently, design for manufacturability and supplier diversification reduces exposure to component-specific tariff effects and strengthens production continuity.
On the regulatory and clinical evidence front, prioritize early and iterative engagement with regulatory bodies and frontline clinicians to align validation studies with intended use cases. For commercial deployment, tailor channel strategies to the target end user: direct clinical partnerships and hospital training programs work well for high-acuity deployments, whereas robust distributor relationships and online channels facilitate wide geographic reach and smaller-volume buyers. Finally, incorporate service, calibration, and software subscription models to create stable post-sale revenue and deepen customer relationships, which accelerates adoption and improves lifetime value.
Robust research methodology and evidence synthesis explaining primary interviews, secondary data triangulation, technology validation, and quality assurance
The research approach combined primary engagement with key stakeholders and rigorous secondary evidence synthesis to ensure analytical robustness. Primary research included structured interviews with clinicians, procurement leaders, R&D engineers, and manufacturing partners to capture practical constraints, desired performance benchmarks, and unmet clinical needs. Secondary research synthesized regulatory guidance, standards documents, peer-reviewed literature on nitric oxide physiology and measurement methods, and supplier specifications to validate technical assumptions and contextualize clinical requirements.
Data were triangulated through cross-validation of interview insights, device datasheets, and independent technical reports. Technology validation emphasized side-by-side comparisons of sensor principles, calibration regimes, maintenance burdens, and interoperability characteristics. Quality assurance processes included review by subject-matter experts in respiratory diagnostics and medical device regulation, and all findings were stress-tested against alternative scenarios for supply disruption and policy shifts. This multi-layered methodology supports confident interpretation of trends and strategic recommendations.
Conclusive synthesis that distills implications for clinicians, device manufacturers, payers, and researchers to advance nitric oxide detection utility and accessibility
The consolidated findings point to a maturing field where technical innovation, regulatory clarity, and pragmatic commercialization converge to expand clinical utility. High-performance benchtop instruments remain essential for reference laboratories and complex clinical workflows, while advancements in portable sensors and analytics are opening pathways for expanded point-of-care and home-based monitoring. Supply chain resilience and adaptable distribution strategies will determine which suppliers can reliably meet clinical demand in diverse geographies, particularly under changing trade policies.
For stakeholders across the value chain, the implication is clear: invest in validated sensor platforms that support modular upgrades, prioritize clinical partnerships that generate meaningful evidence, and align commercial models with customer procurement realities. By doing so, organizations can accelerate adoption, improve patient monitoring capabilities, and realize long-term service relationships that underpin sustainable growth in nitric oxide detection applications.
Note: PDF & Excel + Online Access - 1 Year
Introduction to clinical-grade nitric oxide detection and its role in modern healthcare diagnostics, monitoring, and translational research applications
Nitric oxide detection has evolved from a niche laboratory capability into a clinical and translational asset that informs diagnostics, therapeutic monitoring, and research workflows. Devices that reliably quantify exhaled or ambient nitric oxide support decision-making across respiratory medicine, anesthesia management, and investigational studies probing inflammatory biology. Clinicians and researchers increasingly demand instruments that marry analytical performance with workflow compatibility, enabling point-of-care use, bedside monitoring, and integration with electronic health records.
Against this backdrop, commercial and development teams face a dual imperative: preserve analytical fidelity while improving accessibility and ease of use. Advances in sensor technology, miniaturization, and data analytics are enabling a new generation of instruments that reduce user burden and broaden applicability. At the same time, regulatory expectations and clinical validation pathways continue to shape product design and adoption timelines. Understanding these technical, clinical, and regulatory forces provides a foundation for strategic planning and targeted investment in nitric oxide detection capabilities.
Transformative shifts reshaping nitric oxide detection devices, from sensor miniaturization to AI-enabled signal interpretation across clinical workflows
The landscape for nitric oxide detection is being transformed by converging technological and clinical trends that redefine device value propositions. Sensor miniaturization and low-power electronics have made portable platforms more viable, while improvements in selective chemistry and signal processing have narrowed the performance gap between benchtop standards and compact instruments. At the same time, artificial intelligence and advanced signal deconvolution techniques enable real-time interpretation of noisy physiological signals, supporting clinical decision workflows rather than simply producing raw measurements.
Clinically, there is a rising emphasis on personalized and longitudinal monitoring. Physicians are looking for tools that allow repeated assessments in clinic or home settings, complementing episodic spirometry and imaging. Regulatory authorities are also clarifying expectations for software as a medical device, which in turn accelerates investment in validated analytics and post-market surveillance. As a result, suppliers that combine robust sensor hardware with clear validation narratives and interoperable software stacks will find differentiated adoption pathways. Moreover, cross-sector partnerships between device makers, software vendors, and clinical research organizations are becoming increasingly important to bridge evidence gaps and hasten clinical utility.
Cumulative effects of United States tariff adjustments in 2025 on medical sensor supply chains, component sourcing, and cross-border manufacturing strategies
Policy shifts in tariff regimes and cross-border trade can have pronounced downstream effects on the production and distribution of medical sensors and diagnostic subsystems. When tariffs affect electronic components, specialty gases, or precision-machined parts, manufacturers face higher landed costs and may need to re-evaluate supplier portfolios and assembly footprints. The cumulative impact often manifests as lengthened procurement cycles, renegotiation of supplier terms, or the relocation of certain manufacturing stages to tariff-favored jurisdictions.
In response, procurement and product teams typically pursue a mix of mitigation strategies. These include qualifying alternative suppliers with compatible quality systems, redesigning assemblies to reduce reliance on tariff-exposed components, and leveraging longer-term contracts to stabilize input costs. Additionally, companies reconsider inventory strategies to buffer short-term cost shocks while exploring nearshoring for key subassemblies to reduce exposure. For clinical customers and distributors, these supply-side dynamics can translate into longer lead times and changed commercial terms, which demands transparent communication and coordinated planning across stakeholders to preserve service levels and clinical continuity.
Key segmentation insights revealing how technology, application, end user, portability, and distribution dynamics drive clinical nitric oxide detector adoption
A nuanced segmentation perspective illuminates the heterogeneity of demand and the technical trade-offs that define product strategies. Based on technology, devices are differentiated by chemiluminescence, electrochemical, optical, and paramagnetic measurement principles, each offering distinct strengths in sensitivity, response time, maintenance needs, and cost structure. Based on application, end uses span anesthesia monitoring, diagnostics, research, and respiratory care, with each application imposing unique accuracy, calibration, and integration requirements. Based on end user, deployment scenarios include clinics, home healthcare, hospitals, and research institutes, and each setting drives different expectations for usability, serviceability, and connectivity.
Portability is another critical axis: bench‑top systems emphasize analytical performance and multi-parameter integration, while portable units are designed for cart-mounted or handheld use and prioritize rapid setup, battery life, and simplified calibration. Finally, distribution channel dynamics matter: direct sales allow for clinical training and tailored integration, distributors can extend geographic reach and after-sales support, and online channels, including e-commerce and manufacturer platforms, lower the barrier to entry for smaller buyers and enable streamlined reorder processes. Taken together, these segmentation lenses reveal that successful commercialization requires aligning sensor technology, user experience, and channel strategy to specific clinical workflows and procurement behaviors.
Regional dynamics and adoption trends across the Americas, Europe Middle East & Africa, and Asia-Pacific that shape device deployment and clinical uptake
Regional factors significantly influence adoption pathways and commercialization approaches for nitric oxide detectors. In the Americas, healthcare systems tend to emphasize evidence-based reimbursement and large integrated hospital networks, which creates demand for validated clinical-grade instruments and consolidated service agreements. Suppliers typically focus on establishing strong clinical partnerships and building local service infrastructure to meet stringent uptime and quality expectations.
In Europe, Middle East & Africa, regulatory heterogeneity and a mixture of public and private healthcare procurement require flexible market strategies. Companies must navigate CE marking pathways, regional procurement consortia, and diverse payment models while tailoring training and support programs to varying resource levels. In Asia-Pacific, rapid adoption in urban centers is driven by strong research investment and growing demand for point-of-care diagnostics, while cost sensitivity and distribution complexity in some markets necessitate scalable manufacturing and adaptive commercialization approaches. Across all regions, local clinical evidence generation, distributor relationships, and clear regulatory pathways remain decisive factors for sustained device uptake.
Competitive and collaborative company insights outlining strategic positioning, product portfolios, partnerships, and innovation pathways in nitric oxide detection
Competitive dynamics in the nitric oxide detection landscape are characterized by a mix of established medical device manufacturers, specialist sensor suppliers, agile startups, and integrators that combine hardware with software-driven analytics. Established firms often leverage extensive clinical networks, regulatory experience, and scale manufacturing to maintain leadership in high-performance benchtop systems. In contrast, sensor specialists and startups tend to drive innovation around miniaturized transducers, novel chemistries, and low-cost manufacturing techniques that enable portable solutions and new use cases.
Partnership models and vertical integration strategies are increasingly common. Alliances between component OEMs and clinical system integrators accelerate time-to-market by aligning component roadmaps with end-user documentation and support systems. At the same time, companies that invest in modular platforms and open interoperability are better positioned to capitalize on hospital IT strategies and device consolidation efforts. Intellectual property in sensor chemistry, calibration algorithms, and signal processing provides defensibility, while service models and clinical support offerings create recurring revenue opportunities and strengthen customer retention.
Actionable strategic recommendations for industry leaders to optimize product design, supply resilience, regulatory positioning, and go-to-market acceleration
Companies seeking durable advantage should pursue coordinated strategies across product design, supply chain resilience, regulatory engagement, and commercial outreach. Invest in platform architectures that allow sensor modules and analytics to be upgraded independently, which preserves hardware lifecycles while enabling continuous software innovation. Concurrently, design for manufacturability and supplier diversification reduces exposure to component-specific tariff effects and strengthens production continuity.
On the regulatory and clinical evidence front, prioritize early and iterative engagement with regulatory bodies and frontline clinicians to align validation studies with intended use cases. For commercial deployment, tailor channel strategies to the target end user: direct clinical partnerships and hospital training programs work well for high-acuity deployments, whereas robust distributor relationships and online channels facilitate wide geographic reach and smaller-volume buyers. Finally, incorporate service, calibration, and software subscription models to create stable post-sale revenue and deepen customer relationships, which accelerates adoption and improves lifetime value.
Robust research methodology and evidence synthesis explaining primary interviews, secondary data triangulation, technology validation, and quality assurance
The research approach combined primary engagement with key stakeholders and rigorous secondary evidence synthesis to ensure analytical robustness. Primary research included structured interviews with clinicians, procurement leaders, R&D engineers, and manufacturing partners to capture practical constraints, desired performance benchmarks, and unmet clinical needs. Secondary research synthesized regulatory guidance, standards documents, peer-reviewed literature on nitric oxide physiology and measurement methods, and supplier specifications to validate technical assumptions and contextualize clinical requirements.
Data were triangulated through cross-validation of interview insights, device datasheets, and independent technical reports. Technology validation emphasized side-by-side comparisons of sensor principles, calibration regimes, maintenance burdens, and interoperability characteristics. Quality assurance processes included review by subject-matter experts in respiratory diagnostics and medical device regulation, and all findings were stress-tested against alternative scenarios for supply disruption and policy shifts. This multi-layered methodology supports confident interpretation of trends and strategic recommendations.
Conclusive synthesis that distills implications for clinicians, device manufacturers, payers, and researchers to advance nitric oxide detection utility and accessibility
The consolidated findings point to a maturing field where technical innovation, regulatory clarity, and pragmatic commercialization converge to expand clinical utility. High-performance benchtop instruments remain essential for reference laboratories and complex clinical workflows, while advancements in portable sensors and analytics are opening pathways for expanded point-of-care and home-based monitoring. Supply chain resilience and adaptable distribution strategies will determine which suppliers can reliably meet clinical demand in diverse geographies, particularly under changing trade policies.
For stakeholders across the value chain, the implication is clear: invest in validated sensor platforms that support modular upgrades, prioritize clinical partnerships that generate meaningful evidence, and align commercial models with customer procurement realities. By doing so, organizations can accelerate adoption, improve patient monitoring capabilities, and realize long-term service relationships that underpin sustainable growth in nitric oxide detection applications.
Note: PDF & Excel + Online Access - 1 Year
Table of Contents
196 Pages
- 1. Preface
- 1.1. Objectives of the Study
- 1.2. Market Definition
- 1.3. Market Segmentation & Coverage
- 1.4. Years Considered for the Study
- 1.5. Currency Considered for the Study
- 1.6. Language Considered for the Study
- 1.7. Key Stakeholders
- 2. Research Methodology
- 2.1. Introduction
- 2.2. Research Design
- 2.2.1. Primary Research
- 2.2.2. Secondary Research
- 2.3. Research Framework
- 2.3.1. Qualitative Analysis
- 2.3.2. Quantitative Analysis
- 2.4. Market Size Estimation
- 2.4.1. Top-Down Approach
- 2.4.2. Bottom-Up Approach
- 2.5. Data Triangulation
- 2.6. Research Outcomes
- 2.7. Research Assumptions
- 2.8. Research Limitations
- 3. Executive Summary
- 3.1. Introduction
- 3.2. CXO Perspective
- 3.3. Market Size & Growth Trends
- 3.4. Market Share Analysis, 2025
- 3.5. FPNV Positioning Matrix, 2025
- 3.6. New Revenue Opportunities
- 3.7. Next-Generation Business Models
- 3.8. Industry Roadmap
- 4. Market Overview
- 4.1. Introduction
- 4.2. Industry Ecosystem & Value Chain Analysis
- 4.2.1. Supply-Side Analysis
- 4.2.2. Demand-Side Analysis
- 4.2.3. Stakeholder Analysis
- 4.3. Porter’s Five Forces Analysis
- 4.4. PESTLE Analysis
- 4.5. Market Outlook
- 4.5.1. Near-Term Market Outlook (0–2 Years)
- 4.5.2. Medium-Term Market Outlook (3–5 Years)
- 4.5.3. Long-Term Market Outlook (5–10 Years)
- 4.6. Go-to-Market Strategy
- 5. Market Insights
- 5.1. Consumer Insights & End-User Perspective
- 5.2. Consumer Experience Benchmarking
- 5.3. Opportunity Mapping
- 5.4. Distribution Channel Analysis
- 5.5. Pricing Trend Analysis
- 5.6. Regulatory Compliance & Standards Framework
- 5.7. ESG & Sustainability Analysis
- 5.8. Disruption & Risk Scenarios
- 5.9. Return on Investment & Cost-Benefit Analysis
- 6. Cumulative Impact of United States Tariffs 2025
- 7. Cumulative Impact of Artificial Intelligence 2025
- 8. Medical Nitric Oxide Detector Market, by Technology
- 8.1. Chemiluminescence
- 8.2. Electrochemical
- 8.3. Optical
- 8.4. Paramagnetic
- 9. Medical Nitric Oxide Detector Market, by Portability
- 9.1. Benchtop
- 9.2. Portable
- 9.2.1. Cart Mounted
- 9.2.2. Handheld
- 10. Medical Nitric Oxide Detector Market, by Distribution Channel
- 10.1. Direct Sales
- 10.2. Distributors
- 10.3. Online
- 10.3.1. E-Commerce
- 10.3.2. Manufacturer Platforms
- 11. Medical Nitric Oxide Detector Market, by Application
- 11.1. Anesthesia Monitoring
- 11.2. Diagnostics
- 11.3. Research
- 11.4. Respiratory Care
- 12. Medical Nitric Oxide Detector Market, by End User
- 12.1. Clinics
- 12.2. Home Healthcare
- 12.3. Hospitals
- 12.4. Research Institutes
- 13. Medical Nitric Oxide Detector 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 Nitric Oxide Detector Market, by Group
- 14.1. ASEAN
- 14.2. GCC
- 14.3. European Union
- 14.4. BRICS
- 14.5. G7
- 14.6. NATO
- 15. Medical Nitric Oxide Detector 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. United States Medical Nitric Oxide Detector Market
- 17. China Medical Nitric Oxide Detector Market
- 18. Competitive Landscape
- 18.1. Market Concentration Analysis, 2025
- 18.1.1. Concentration Ratio (CR)
- 18.1.2. Herfindahl Hirschman Index (HHI)
- 18.2. Recent Developments & Impact Analysis, 2025
- 18.3. Product Portfolio Analysis, 2025
- 18.4. Benchmarking Analysis, 2025
- 18.5. Aeroqual Ltd.
- 18.6. Air Liquide S.A.
- 18.7. Alphasense Ltd.
- 18.8. Amphenol Corporation
- 18.9. Analog Devices, Inc.
- 18.10. Bellerophon Therapeutics, Inc.
- 18.11. Beyond Air, Inc.
- 18.12. Circassia Pharmaceuticals plc
- 18.13. Eco Physics AG
- 18.14. GE HealthCare
- 18.15. Hamilton Medical AG
- 18.16. Honeywell International Inc.
- 18.17. Koninklijke Philips N.V.
- 18.18. Linde plc
- 18.19. Mallinckrodt Pharmaceuticals
- 18.20. Medtronic plc
- 18.21. Nu-Med Plus, Inc.
- 18.22. Sensirion AG
- 18.23. TE Connectivity Ltd.
- 18.24. Thermo Fisher Scientific Inc.
- 18.25. Vero Biotech LLC
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