Healthcare Temperature Monitoring Devices Market by Device Type (Fixed, Portable, Wearable), Monitoring Mode (Continuous, Intermittent), Application - Global Forecast 2025-2032
Description
The Healthcare Temperature Monitoring Devices Market was valued at USD 5.70 billion in 2024 and is projected to grow to USD 6.01 billion in 2025, with a CAGR of 6.03%, reaching USD 9.11 billion by 2032.
How modern sensor innovation, connectivity, and clinical workflow integration are redefining temperature monitoring as a strategic element of patient surveillance
Temperature monitoring devices are increasingly central to modern healthcare delivery, driven by the convergence of sensor innovation, connectivity, and evolving care models. Advances in infrared sensing, thermistor probes, compact handheld scanners, and wearable patches and smart-watch platforms have broadened how clinicians and caregivers capture core vitals across inpatient, ambulatory, and home settings. As a result, device design now prioritizes integration with clinical workflows, seamless interoperability with electronic health records, and regulatory pathways that balance safety with rapid adoption.
Beyond hardware, software ecosystems that enable continuous telemetry, intelligent alerts, and analytics-led trend detection are reshaping clinician expectations. Consequently, procurement bodies and clinical leaders now evaluate solutions not only on accuracy and reliability but also on cybersecurity posture, data governance, and the clarity of evidence for clinical impact. The combination of hardware evolution and digital enablement establishes temperature monitoring as a strategic element of patient surveillance systems rather than a standalone measurement instrument. This introduction sets the context for deeper discussion on market shifts, regulatory headwinds, segmentation dynamics, and regional variations that follow.
Technological miniaturization, continuous monitoring adoption, and regulatory focus on cybersecurity are reshaping procurement and product strategies across care settings
The landscape for temperature monitoring devices has shifted substantially as technological advances intersect with changing care pathways. Miniaturization of sensors and improvements in low-power wireless communications have accelerated the transition from episodic to continuous monitoring, enabling earlier detection of clinical deterioration and more flexible care delivery outside traditional settings. In parallel, tighter integration with health IT enables automated escalation workflows and richer trend analysis, which in turn raises the bar for device interoperability and data standards compliance.
Regulatory emphasis on cybersecurity and post-market surveillance has also changed procurement risk profiles. Manufacturers must now demonstrate robust software lifecycle management and incident response capabilities alongside device accuracy. Meanwhile, clinical practice is evolving: telehealth expansion and decentralized care models have increased demand for portable and wearable solutions that support remote monitoring and home-based recovery pathways. Taken together, these transformative shifts are incentivizing vendors to develop platform-level offerings that combine validated sensing hardware with analytics and service models to drive adoption and sustain clinical trust.
Tariff-driven supply chain recalibrations and total landed cost focus prompting manufacturers to diversify sourcing and invest in regional production capabilities
New tariff measures implemented in 2025 have introduced additional considerations for supply chain resilience and cost pass-through for temperature monitoring device manufacturers and healthcare buyers. Import duties on certain electronic components and finished medical devices have incentivized reassessment of supplier geographies and nearshoring options. In response, some manufacturers have accelerated dual-sourcing of critical components and increased inventory buffers to mitigate delivery risk, while others have explored local assembly or contract manufacturing partnerships to reduce tariff exposure.
The tariffs have also elevated the importance of total landed cost analysis in procurement decisions. Healthcare systems and distributors are evaluating not only unit price but also logistics, customs clearance reliability, and maintenance support capabilities when selecting vendors. Consequently, value propositions that emphasize predictable service levels, local spares provisioning, and straightforward warranty terms gain comparative advantage. Over time, these dynamics are likely to influence strategic supplier consolidation and encourage investments in regional manufacturing footprints that reduce exposure to import duty volatility.
Segmentation-driven product, validation, and go-to-market strategies that align device capabilities with clinical workflows and care setting requirements
A refined look at device segmentation reveals distinct adoption drivers and validation requirements across device types, monitoring modes, and clinical applications. Based on device type, fixed solutions-which include variants built on infrared sensors and thermistor probes-remain valued in critical care and high-throughput settings where continuous reliability and integration with central monitoring systems are paramount. Portable devices, encompassing handheld thermometers and thermal scanners, answer the need for rapid triage, outpatient screening, and point-of-care assessment because their form factors and user workflows prioritize speed and ease of use. Wearable devices such as skin-applied patches and smart watches unlock continuous, ambulatory monitoring that supports remote care, early warning systems, and longitudinal trend analysis; these wearables demand robust battery life, skin compatibility, and clinically validated algorithms to ensure trust outside controlled environments.
Based on monitoring mode, continuous monitoring solutions deliver granular trend data and enable early detection of deterioration, but they also introduce greater requirements for data handling, alarm management, and clinician workflow integration. Intermittent monitoring remains essential where episodic checks suffice or where resource constraints mandate simpler approaches; these devices typically emphasize measurement accuracy, ease of sanitation, and speed of measurement. Based on application, general ward usage prioritizes rapid interoperability with nursing workflows and centralized charting; home healthcare emphasizes patient comfort, remote clinician visibility, and secure consumer-grade connectivity; intensive care units require the highest accuracy and redundancy, with adult ICU and pediatric ICU settings imposing distinct physiological ranges, sensor placement considerations, and regulatory testing expectations. Understanding how these segments interact informs product development priorities, clinical validation strategies, and go-to-market approaches that align device capabilities with real-world use cases.
How regional regulatory diversity, procurement models, and healthcare maturity influence device adoption across Americas, Europe Middle East and Africa, and Asia-Pacific
Regional dynamics shape adoption pathways and product requirements in meaningful ways. In the Americas, heterogeneous healthcare reimbursement environments and advanced hospital networks create pockets of rapid uptake for innovative monitoring platforms, while rural and community settings drive demand for cost-effective, portable solutions that support telehealth and remote patient management. Regulatory frameworks emphasize safety and clinical evidence, and large private and public procurement customers often require extensive post-market support and clear warranty terms.
In Europe, Middle East & Africa, fragmentation across regulatory regimes and procurement models leads manufacturers to prioritize CE marking and region-specific clinical validation. European markets frequently emphasize interoperability with national patient data infrastructures and strong cybersecurity controls, whereas markets in the Middle East and Africa balance investment in high-acuity hospital systems with growing demand for scalable remote monitoring to expand access. Vendors that can offer adaptable service models and staged deployment plans tend to gain traction across this diverse region.
In Asia-Pacific, a mix of highly advanced urban centers and rapidly developing healthcare systems creates simultaneous demand for cutting-edge continuous monitoring and affordable portable devices. Local manufacturing hubs and regional supply chains play an important role, and policy initiatives in several markets have accelerated digital health adoption. Success in this region often depends on demonstrating localized clinical validation, competitive total cost of ownership, and partnerships with regional distributors or health system integrators.
Competitive advantage driven by platform integration, demonstrated clinical impact, localized service networks, and regulatory rigor across the supplier landscape
Competitive dynamics in the temperature monitoring device space increasingly center on the ability to deliver platform-level value, demonstrated clinical outcomes, and dependable service networks. Leading firms are investing in end-to-end propositions that bundle validated sensing hardware with software for trend analytics, alarm optimization, and clinician workflow integration. Partnerships with electronic health record providers and telehealth platforms serve as force multipliers, enabling smoother integration into day-to-day clinical operations and reducing adoption friction.
At the same time, smaller innovators frequently differentiate through focused clinical applications, such as pediatric-specific algorithms, ultra-low-power wearables for prolonged ambulatory monitoring, or ruggedized portable devices for field deployment. Service differentiation-rapid technical support, local spare parts provisioning, and training programs for nursing staff-remains a pivotal competitive lever. Finally, regulatory and quality assurance investments function as market access enablers, where clear documentation of clinical performance, robust cybersecurity practices, and post-market surveillance plans can be decisive in institutional procurement decisions.
Action plan for leaders to reduce supply risk, accelerate platform integration, and monetize analytics while strengthening clinical trust and regulatory compliance
Industry leaders should prioritize actions that balance short-term resilience with long-term platform differentiation. First, strengthen supply chain elasticity by qualifying multiple suppliers for critical electronic components and evaluating regional assembly options to minimize tariff exposure and logistics risk. Parallel to this, invest in modular product architectures that enable common hardware platforms to support fixed, portable, and wearable variants, thereby lowering development cost and accelerating regulatory submission timelines.
Next, double down on interoperability and clinical workflow integration by building validated interfaces to major electronic health record systems and by co-developing alerting logic with frontline clinicians. This will reduce alarm fatigue and increase clinician trust. Additionally, commit resources to cybersecurity and post-market surveillance programs; transparent reporting of vulnerability management and field performance will become a procurement differentiator. Finally, adopt flexible commercial models that combine device sales with subscription-based analytics and service packages, enabling predictable revenue streams for vendors and clearer total cost of ownership for buyers. Executing these priorities will position companies to capture demand across both acute and decentralized care settings.
Rigorous mixed-methods research combining stakeholder interviews, technical validation reviews, and standards analysis to ensure convergent evidence and practical insights
This report synthesizes findings from a mixed-methods research approach that combines primary stakeholder interviews, targeted device bench testing reviews, and secondary literature synthesis. Primary engagement included structured discussions with clinicians, procurement officers, biomedical engineers, and device manufacturers to surface practical adoption barriers and validation needs. Where available, bench testing reports and peer-reviewed clinical studies were analyzed to corroborate accuracy claims across device types and to identify performance differentials in real-world settings.
Secondary research encompassed regulatory guidance documents, standards for device interoperability and cybersecurity, and publicly available product manuals and white papers to establish product feature baselines. The research team applied qualitative coding to interview transcripts and cross-validated emergent themes against documented regulatory trends and recent supply chain events. Care was taken to avoid overreliance on any single information source; triangulation was used to ensure that conclusions reflect convergent evidence from multiple stakeholder perspectives and technical assessments.
Synthesis of technological, regulatory, and operational drivers indicating that integrated, validated platforms will define future success in patient surveillance
Temperature monitoring devices are evolving from isolated measurement tools into integrated components of patient surveillance ecosystems, driven by sensor advances, digital enablement, and shifting care delivery models. The combined pressures of regulatory expectations around cybersecurity, supply chain disruptions that increase the emphasis on sourcing strategy, and clinical demand for continuous, interoperable solutions are reshaping both product roadmaps and procurement criteria. Vendors that can demonstrate clinical validity, data security, and dependable post-sale service will tend to outcompete those relying solely on incremental hardware improvements.
Looking ahead, the market is likely to favor modular platforms capable of addressing diverse clinical settings-from high-acuity intensive care units with stringent accuracy requirements to home healthcare environments where comfort and connectivity matter most. Strategic investments in regional manufacturing, validated integration with health IT systems, and analytics that reduce clinician burden will be decisive. For healthcare leaders, the imperative is to treat temperature monitoring as part of a broader surveillance strategy that emphasizes outcomes, workflow alignment, and operational resilience.
Please Note: PDF & Excel + Online Access - 1 Year
How modern sensor innovation, connectivity, and clinical workflow integration are redefining temperature monitoring as a strategic element of patient surveillance
Temperature monitoring devices are increasingly central to modern healthcare delivery, driven by the convergence of sensor innovation, connectivity, and evolving care models. Advances in infrared sensing, thermistor probes, compact handheld scanners, and wearable patches and smart-watch platforms have broadened how clinicians and caregivers capture core vitals across inpatient, ambulatory, and home settings. As a result, device design now prioritizes integration with clinical workflows, seamless interoperability with electronic health records, and regulatory pathways that balance safety with rapid adoption.
Beyond hardware, software ecosystems that enable continuous telemetry, intelligent alerts, and analytics-led trend detection are reshaping clinician expectations. Consequently, procurement bodies and clinical leaders now evaluate solutions not only on accuracy and reliability but also on cybersecurity posture, data governance, and the clarity of evidence for clinical impact. The combination of hardware evolution and digital enablement establishes temperature monitoring as a strategic element of patient surveillance systems rather than a standalone measurement instrument. This introduction sets the context for deeper discussion on market shifts, regulatory headwinds, segmentation dynamics, and regional variations that follow.
Technological miniaturization, continuous monitoring adoption, and regulatory focus on cybersecurity are reshaping procurement and product strategies across care settings
The landscape for temperature monitoring devices has shifted substantially as technological advances intersect with changing care pathways. Miniaturization of sensors and improvements in low-power wireless communications have accelerated the transition from episodic to continuous monitoring, enabling earlier detection of clinical deterioration and more flexible care delivery outside traditional settings. In parallel, tighter integration with health IT enables automated escalation workflows and richer trend analysis, which in turn raises the bar for device interoperability and data standards compliance.
Regulatory emphasis on cybersecurity and post-market surveillance has also changed procurement risk profiles. Manufacturers must now demonstrate robust software lifecycle management and incident response capabilities alongside device accuracy. Meanwhile, clinical practice is evolving: telehealth expansion and decentralized care models have increased demand for portable and wearable solutions that support remote monitoring and home-based recovery pathways. Taken together, these transformative shifts are incentivizing vendors to develop platform-level offerings that combine validated sensing hardware with analytics and service models to drive adoption and sustain clinical trust.
Tariff-driven supply chain recalibrations and total landed cost focus prompting manufacturers to diversify sourcing and invest in regional production capabilities
New tariff measures implemented in 2025 have introduced additional considerations for supply chain resilience and cost pass-through for temperature monitoring device manufacturers and healthcare buyers. Import duties on certain electronic components and finished medical devices have incentivized reassessment of supplier geographies and nearshoring options. In response, some manufacturers have accelerated dual-sourcing of critical components and increased inventory buffers to mitigate delivery risk, while others have explored local assembly or contract manufacturing partnerships to reduce tariff exposure.
The tariffs have also elevated the importance of total landed cost analysis in procurement decisions. Healthcare systems and distributors are evaluating not only unit price but also logistics, customs clearance reliability, and maintenance support capabilities when selecting vendors. Consequently, value propositions that emphasize predictable service levels, local spares provisioning, and straightforward warranty terms gain comparative advantage. Over time, these dynamics are likely to influence strategic supplier consolidation and encourage investments in regional manufacturing footprints that reduce exposure to import duty volatility.
Segmentation-driven product, validation, and go-to-market strategies that align device capabilities with clinical workflows and care setting requirements
A refined look at device segmentation reveals distinct adoption drivers and validation requirements across device types, monitoring modes, and clinical applications. Based on device type, fixed solutions-which include variants built on infrared sensors and thermistor probes-remain valued in critical care and high-throughput settings where continuous reliability and integration with central monitoring systems are paramount. Portable devices, encompassing handheld thermometers and thermal scanners, answer the need for rapid triage, outpatient screening, and point-of-care assessment because their form factors and user workflows prioritize speed and ease of use. Wearable devices such as skin-applied patches and smart watches unlock continuous, ambulatory monitoring that supports remote care, early warning systems, and longitudinal trend analysis; these wearables demand robust battery life, skin compatibility, and clinically validated algorithms to ensure trust outside controlled environments.
Based on monitoring mode, continuous monitoring solutions deliver granular trend data and enable early detection of deterioration, but they also introduce greater requirements for data handling, alarm management, and clinician workflow integration. Intermittent monitoring remains essential where episodic checks suffice or where resource constraints mandate simpler approaches; these devices typically emphasize measurement accuracy, ease of sanitation, and speed of measurement. Based on application, general ward usage prioritizes rapid interoperability with nursing workflows and centralized charting; home healthcare emphasizes patient comfort, remote clinician visibility, and secure consumer-grade connectivity; intensive care units require the highest accuracy and redundancy, with adult ICU and pediatric ICU settings imposing distinct physiological ranges, sensor placement considerations, and regulatory testing expectations. Understanding how these segments interact informs product development priorities, clinical validation strategies, and go-to-market approaches that align device capabilities with real-world use cases.
How regional regulatory diversity, procurement models, and healthcare maturity influence device adoption across Americas, Europe Middle East and Africa, and Asia-Pacific
Regional dynamics shape adoption pathways and product requirements in meaningful ways. In the Americas, heterogeneous healthcare reimbursement environments and advanced hospital networks create pockets of rapid uptake for innovative monitoring platforms, while rural and community settings drive demand for cost-effective, portable solutions that support telehealth and remote patient management. Regulatory frameworks emphasize safety and clinical evidence, and large private and public procurement customers often require extensive post-market support and clear warranty terms.
In Europe, Middle East & Africa, fragmentation across regulatory regimes and procurement models leads manufacturers to prioritize CE marking and region-specific clinical validation. European markets frequently emphasize interoperability with national patient data infrastructures and strong cybersecurity controls, whereas markets in the Middle East and Africa balance investment in high-acuity hospital systems with growing demand for scalable remote monitoring to expand access. Vendors that can offer adaptable service models and staged deployment plans tend to gain traction across this diverse region.
In Asia-Pacific, a mix of highly advanced urban centers and rapidly developing healthcare systems creates simultaneous demand for cutting-edge continuous monitoring and affordable portable devices. Local manufacturing hubs and regional supply chains play an important role, and policy initiatives in several markets have accelerated digital health adoption. Success in this region often depends on demonstrating localized clinical validation, competitive total cost of ownership, and partnerships with regional distributors or health system integrators.
Competitive advantage driven by platform integration, demonstrated clinical impact, localized service networks, and regulatory rigor across the supplier landscape
Competitive dynamics in the temperature monitoring device space increasingly center on the ability to deliver platform-level value, demonstrated clinical outcomes, and dependable service networks. Leading firms are investing in end-to-end propositions that bundle validated sensing hardware with software for trend analytics, alarm optimization, and clinician workflow integration. Partnerships with electronic health record providers and telehealth platforms serve as force multipliers, enabling smoother integration into day-to-day clinical operations and reducing adoption friction.
At the same time, smaller innovators frequently differentiate through focused clinical applications, such as pediatric-specific algorithms, ultra-low-power wearables for prolonged ambulatory monitoring, or ruggedized portable devices for field deployment. Service differentiation-rapid technical support, local spare parts provisioning, and training programs for nursing staff-remains a pivotal competitive lever. Finally, regulatory and quality assurance investments function as market access enablers, where clear documentation of clinical performance, robust cybersecurity practices, and post-market surveillance plans can be decisive in institutional procurement decisions.
Action plan for leaders to reduce supply risk, accelerate platform integration, and monetize analytics while strengthening clinical trust and regulatory compliance
Industry leaders should prioritize actions that balance short-term resilience with long-term platform differentiation. First, strengthen supply chain elasticity by qualifying multiple suppliers for critical electronic components and evaluating regional assembly options to minimize tariff exposure and logistics risk. Parallel to this, invest in modular product architectures that enable common hardware platforms to support fixed, portable, and wearable variants, thereby lowering development cost and accelerating regulatory submission timelines.
Next, double down on interoperability and clinical workflow integration by building validated interfaces to major electronic health record systems and by co-developing alerting logic with frontline clinicians. This will reduce alarm fatigue and increase clinician trust. Additionally, commit resources to cybersecurity and post-market surveillance programs; transparent reporting of vulnerability management and field performance will become a procurement differentiator. Finally, adopt flexible commercial models that combine device sales with subscription-based analytics and service packages, enabling predictable revenue streams for vendors and clearer total cost of ownership for buyers. Executing these priorities will position companies to capture demand across both acute and decentralized care settings.
Rigorous mixed-methods research combining stakeholder interviews, technical validation reviews, and standards analysis to ensure convergent evidence and practical insights
This report synthesizes findings from a mixed-methods research approach that combines primary stakeholder interviews, targeted device bench testing reviews, and secondary literature synthesis. Primary engagement included structured discussions with clinicians, procurement officers, biomedical engineers, and device manufacturers to surface practical adoption barriers and validation needs. Where available, bench testing reports and peer-reviewed clinical studies were analyzed to corroborate accuracy claims across device types and to identify performance differentials in real-world settings.
Secondary research encompassed regulatory guidance documents, standards for device interoperability and cybersecurity, and publicly available product manuals and white papers to establish product feature baselines. The research team applied qualitative coding to interview transcripts and cross-validated emergent themes against documented regulatory trends and recent supply chain events. Care was taken to avoid overreliance on any single information source; triangulation was used to ensure that conclusions reflect convergent evidence from multiple stakeholder perspectives and technical assessments.
Synthesis of technological, regulatory, and operational drivers indicating that integrated, validated platforms will define future success in patient surveillance
Temperature monitoring devices are evolving from isolated measurement tools into integrated components of patient surveillance ecosystems, driven by sensor advances, digital enablement, and shifting care delivery models. The combined pressures of regulatory expectations around cybersecurity, supply chain disruptions that increase the emphasis on sourcing strategy, and clinical demand for continuous, interoperable solutions are reshaping both product roadmaps and procurement criteria. Vendors that can demonstrate clinical validity, data security, and dependable post-sale service will tend to outcompete those relying solely on incremental hardware improvements.
Looking ahead, the market is likely to favor modular platforms capable of addressing diverse clinical settings-from high-acuity intensive care units with stringent accuracy requirements to home healthcare environments where comfort and connectivity matter most. Strategic investments in regional manufacturing, validated integration with health IT systems, and analytics that reduce clinician burden will be decisive. For healthcare leaders, the imperative is to treat temperature monitoring as part of a broader surveillance strategy that emphasizes outcomes, workflow alignment, and operational resilience.
Please Note: PDF & Excel + Online Access - 1 Year
Table of Contents
183 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. Adoption of wearable continuous temperature sensors integrated with telehealth solutions for remote patient monitoring
- 5.2. Integration of infrared thermography and AI algorithms for rapid fever screening in public healthcare settings
- 5.3. Emergence of multi-parameter IoT platforms combining temperature and vital signs for comprehensive chronic disease management
- 5.4. FDA and CE regulatory clearances driving commercialization of novel non-contact medical grade thermometers in clinical use
- 5.5. Use of blockchain-enabled temperature data logging to ensure tamper-proof tracking of cold chain pharmaceuticals and vaccines
- 5.6. Development of sensor-embedded smart patches for real-time continuous monitoring of neonatal hypothermia risks in preterm infants
- 5.7. Implementation of predictive analytics models within hospital temperature monitoring systems to forecast patient deterioration risks
- 5.8. Rising demand for sustainable disposable probe materials in single-use temperature monitoring devices to reduce clinical waste
- 5.9. Expansion of remote patient monitoring programs with multi-zone skin temperature sensors for home-based infection control management
- 6. Cumulative Impact of United States Tariffs 2025
- 7. Cumulative Impact of Artificial Intelligence 2025
- 8. Healthcare Temperature Monitoring Devices Market, by Device Type
- 8.1. Fixed
- 8.1.1. Infrared Sensor
- 8.1.2. Thermistor Probe
- 8.2. Portable
- 8.2.1. Handheld Thermometer
- 8.2.2. Thermal Scanner
- 8.3. Wearable
- 8.3.1. Patch
- 8.3.2. Smart Watch
- 9. Healthcare Temperature Monitoring Devices Market, by Monitoring Mode
- 9.1. Continuous
- 9.2. Intermittent
- 10. Healthcare Temperature Monitoring Devices Market, by Application
- 10.1. General Ward
- 10.2. Home Healthcare
- 10.3. Intensive Care Unit
- 10.3.1. Adult ICU
- 10.3.2. Pediatric ICU
- 11. Healthcare Temperature Monitoring Devices Market, by Region
- 11.1. Americas
- 11.1.1. North America
- 11.1.2. Latin America
- 11.2. Europe, Middle East & Africa
- 11.2.1. Europe
- 11.2.2. Middle East
- 11.2.3. Africa
- 11.3. Asia-Pacific
- 12. Healthcare Temperature Monitoring Devices Market, by Group
- 12.1. ASEAN
- 12.2. GCC
- 12.3. European Union
- 12.4. BRICS
- 12.5. G7
- 12.6. NATO
- 13. Healthcare Temperature Monitoring Devices Market, by Country
- 13.1. United States
- 13.2. Canada
- 13.3. Mexico
- 13.4. Brazil
- 13.5. United Kingdom
- 13.6. Germany
- 13.7. France
- 13.8. Russia
- 13.9. Italy
- 13.10. Spain
- 13.11. China
- 13.12. India
- 13.13. Japan
- 13.14. Australia
- 13.15. South Korea
- 14. Competitive Landscape
- 14.1. Market Share Analysis, 2024
- 14.2. FPNV Positioning Matrix, 2024
- 14.3. Competitive Analysis
- 14.3.1. 3M Company
- 14.3.2. American Diagnostic Corporation
- 14.3.3. Becton, Dickinson and Company
- 14.3.4. Braun GmbH
- 14.3.5. Briggs Healthcare
- 14.3.6. Cadi Scientific
- 14.3.7. Cardinal Health, Inc.
- 14.3.8. Drägerwerk AG & Co. KGaA
- 14.3.9. EarlySense Ltd.
- 14.3.10. Exergen Corporation
- 14.3.11. GE Healthcare
- 14.3.12. Gentherm Incorporated
- 14.3.13. Hicks Thermometers India Limited
- 14.3.14. Hill‑Rom Holdings, Inc.
- 14.3.15. Kaz USA, Inc.
- 14.3.16. Koninklijke Philips N.V.
- 14.3.17. Masimo Corporation
- 14.3.18. Medtronic plc
- 14.3.19. Microlife Corporation
- 14.3.20. Omron Healthcare, Inc.
- 14.3.21. Sensitech, Inc.
- 14.3.22. Stryker Corporation
- 14.3.23. Terumo Corporation
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