Multi Channel Pipette Market by Product Type (Electronic Multi Channel Pipettes, Manual Multi Channel Pipettes), Channel Configuration (Eight Channel, Twelve Channel), Volume Range, End User - Global Forecast 2026-2032
Description
The Multi Channel Pipette Market was valued at USD 1.15 billion in 2025 and is projected to grow to USD 1.21 billion in 2026, with a CAGR of 5.09%, reaching USD 1.64 billion by 2032.
Introduction framing the strategic role of multi-channel pipettes in modern laboratories, outlining innovation drivers, workflow benefits and adoption dynamics
Multi-channel pipettes have moved from a niche tool to a central enabler of throughput, reproducibility, and ergonomic safety in contemporary laboratory workflows. Modern laboratory operations increasingly prioritize methods that reduce manual variability, support parallel processing, and enable consistent sample handling across assay plates. As a result, procurement teams and lab managers evaluate multi-channel pipettes not only for throughput but also for integration with automation platforms, user comfort, and lifecycle serviceability.
In parallel, product innovation has diversified the choices available to end users: electronic devices offer programmable steps and force reduction while manual variants emphasize low cost, simplicity, and field robustness. This bifurcation has encouraged laboratories to adopt mixed-device strategies that match task complexity and budgetary constraints. Consequently, stakeholders now balance instrument capability with training requirements, ergonomic outcomes, and long-term maintenance considerations when selecting pipetting solutions.
Transformative shifts reshaping the multi-channel pipette landscape driven by automation, digital integration, ergonomic design, and changing laboratory practices
The multi-channel pipette landscape is undergoing rapid transformation as laboratories pursue greater automation, digital traceability, and user-centric design. Automation initiatives have elevated expectations for device interoperability and standardized plate handling, prompting manufacturers to prioritize electronic control systems, battery longevity, and programmable protocols. Concurrently, digital integration - including data logging and device connectivity - has emerged as a differentiator that supports audit readiness and reproducible workflows.
Beyond technology, ergonomic design has taken center stage to address repetitive strain and to improve operator consistency. This shift has shortened product development cycles as suppliers iterate on materials, grip ergonomics, and weight distribution. Moreover, evolving end-user requirements across academic, clinical, and industrial laboratories are driving specialized product variants. Taken together, these dynamics encourage a market environment where innovation pace, regulatory alignment, and user training converge to determine which solutions gain traction within different institutional settings.
Anticipating the cumulative implications of United States tariffs in 2025 on supply chains, manufacturing decisions, and procurement strategies
Policy shifts and trade actions in major economies can materially affect procurement strategies and supply chain configurations for laboratory equipment, and the United States tariff changes slated for 2025 are likely to drive a range of operational responses across manufacturers, distributors, and end users. In the short term, purchasing teams will reassess sourcing options to minimize cost exposure and delivery uncertainty, favoring suppliers with resilient logistics, local inventory, or diversified manufacturing footprints. At the same time, manufacturers reliant on cross-border components will evaluate component sourcing, tariff classifications, and potential nearshoring to reduce vulnerability to tariff swings.
In addition, distributors and service providers will adjust contractual terms and inventory positioning to maintain service levels while absorbing or passing through incremental costs. Over time, procurement frameworks may increasingly emphasize total cost of ownership, service responsiveness, and supplier risk metrics rather than unit price alone. Consequently, laboratories and corporate procurement functions should prepare for lengthened supplier qualification cycles and heightened focus on contractual protections, while vendors will need to demonstrate transparent supply chain practices and flexible fulfillment models.
Key segmentation insights revealing how product type variations, channel configurations, volume ranges, and end-user categories shape applications and selection
Segmentation analysis reveals distinct value propositions and user behavior across product types, channel configurations, volume ranges, and end-user categories. Considering product type, the market divides between electronic multi-channel pipettes, which are further differentiated into battery replaceable and rechargeable variants, and manual multi-channel pipettes that are available as fixed tip or interchangeable tip designs. Each option addresses different operational priorities: electronic models prioritize repeatability and programmable protocols, while manual alternatives emphasize simplicity and lower acquisition cost.
Channel configuration also guides selection, with eight-channel and twelve-channel devices catering to different plate formats and throughput requirements. Volume range segmentation further refines suitability: high volume applications concentrate on ranges such as 200–500 µL and 500–1000 µL, medium volume tasks typically fall within 10–100 µL and 100–200 µL bands, and low volume assays most often require precision in the 0.1–2 µL and 2–10 µL windows. End-user categories shape procurement and deployment decisions as well; academic and research institutes tend to favor flexibility and cost-effectiveness, clinical diagnostics emphasize traceability and regulatory conformity with subsegments like histology and in vitro diagnostics, food and beverage laboratories focus on quality control and R&D use cases, and pharmaceutical and biotechnology organizations require rigorous performance across biotechnology and pharmaceutical applications. Taken together, these segmentation factors influence not only product selection but also supplier relationships, validation strategies, and post-sale support models.
Key regional insights explaining demand drivers, supply chain nuances and regulatory impacts across the Americas, Europe, Middle East & Africa and Asia-Pacific
Regional dynamics materially influence procurement patterns, supplier strategies, and regulatory compliance for multi-channel pipettes. In the Americas, demand drivers emphasize rapid adoption of automation, strong service networks, and a preference for devices that support high-throughput screening and clinical workflows. Consequently, suppliers with established distribution channels and responsive after-sales support tend to find favorable adoption conditions in this region.
In Europe, Middle East & Africa, regulatory alignment and interoperability are paramount, with laboratories often prioritizing devices that meet strict documentation and traceability requirements. Fragmented regulatory landscapes in the region encourage suppliers to offer robust compliance support and localized technical assistance. Meanwhile, in Asia-Pacific, growth is driven by expanding research infrastructure, increasing R&D investments, and a mix of cost-sensitive and early-adopter segments. Here, suppliers that can combine scalable manufacturing, competitive pricing, and rapid localization of service tend to perform well. Across all regions, logistics resilience, spare parts availability, and training resources remain critical differentiators that influence both initial purchase decisions and long-term loyalty.
Key company-level insights highlighting competitive strategies, product innovation, partnerships, and service differentiation among leading manufacturers
Company-level dynamics reflect a mix of product innovation, channel strategy, and service model differentiation. Leading manufacturers compete not only on device accuracy and ergonomic design but also on the depth of their service offerings, warranty terms, and the availability of consumables and validated accessories. Strategic partnerships and OEM arrangements enable some suppliers to extend their market reach while maintaining focus on core competencies such as electronics, software integration, or precision manufacturing.
Furthermore, competitive positioning increasingly hinges on lifecycle support, including calibration services, training programs, and digital tools that enhance traceability. As a result, commercial success depends on demonstrating measurable improvements in workflow efficiency and operator well-being. In this environment, companies that invest in modular product platforms, robust service networks, and data-driven customer engagement are better positioned to secure long-term contracts with research institutions, clinical labs, and industrial R&D departments.
Actionable recommendations for industry leaders to optimize procurement, accelerate adoption of advanced pipetting solutions, and strengthen R&D focus
Industry leaders should pursue pragmatic steps to optimize procurement and accelerate adoption while maintaining operational resilience. First, align purchasing criteria to prioritize total cost of ownership and service reliability rather than short-term price considerations; by doing so, organizations mitigate supply disruptions and reduce long-term operational risk. Second, pilot mixed-device deployments that combine electronic and manual multi-channel pipettes to balance throughput, cost, and training requirements; iterative pilots allow teams to build internal best practices and capture real-world performance data.
Third, strengthen supplier relationships by negotiating flexible inventory and fulfillment terms that account for potential tariff or logistics volatility. Fourth, invest in operator training and standardized protocols to maximize the reproducibility benefits of advanced pipetting solutions; this reduces user-related variability and increases return on equipment investments. Finally, integrate device data into laboratory information systems where possible to enhance traceability and to support compliance documentation. Collectively, these measures help organizations capture efficiency gains while preserving agility in the face of changing regulatory and supply conditions.
Research methodology describing data sources, qualitative and quantitative approaches and stakeholder engagement used to ensure robust and objective analysis
The research methodology combined structured qualitative inquiry with targeted quantitative validation to ensure findings reflect operational realities. Primary inputs included in-depth interviews with procurement managers, laboratory directors, product engineers, and service leads, supplemented by technical evaluations of device specifications and usability factors. These engagements helped to identify the drivers of device selection, service expectations, and the practical constraints that influence adoption across different laboratory types.
In addition, secondary research synthesized regulatory guidance, standards documentation, and supply chain literature to contextualize vendor practices and logistics considerations. Findings were triangulated through comparative analysis across end-user segments and regions to expose consistent patterns and to highlight areas of divergence. Throughout the process, iterative validation sessions with industry stakeholders refined the conclusions and ensured the recommendations remain actionable for both operational teams and executive decision-makers.
Conclusion summarizing strategic takeaways on technology adoption, procurement considerations, segmentation implications and regional priorities for stakeholders
The analysis converges on several strategic takeaways that should guide stakeholder action: prioritize device interoperability and data capture to support reproducibility, balance electronic and manual device investments according to task specificity, and reinforce supplier relationships to reduce exposure to trade and logistics disruptions. Segmentation nuances-spanning product type, channel configuration, volume range, and end-user requirements-underscore the need for tailored procurement and deployment strategies rather than one-size-fits-all purchasing.
Regional considerations further refine these priorities; suppliers must adapt their service and compliance models to meet local requirements, while end users should evaluate total cost, support responsiveness, and training availability when choosing solutions. Ultimately, organizations that align product selection with operational processes and that invest in training and supplier resilience will realize the greatest improvements in throughput, data integrity, and operator safety.
Note: PDF & Excel + Online Access - 1 Year
Introduction framing the strategic role of multi-channel pipettes in modern laboratories, outlining innovation drivers, workflow benefits and adoption dynamics
Multi-channel pipettes have moved from a niche tool to a central enabler of throughput, reproducibility, and ergonomic safety in contemporary laboratory workflows. Modern laboratory operations increasingly prioritize methods that reduce manual variability, support parallel processing, and enable consistent sample handling across assay plates. As a result, procurement teams and lab managers evaluate multi-channel pipettes not only for throughput but also for integration with automation platforms, user comfort, and lifecycle serviceability.
In parallel, product innovation has diversified the choices available to end users: electronic devices offer programmable steps and force reduction while manual variants emphasize low cost, simplicity, and field robustness. This bifurcation has encouraged laboratories to adopt mixed-device strategies that match task complexity and budgetary constraints. Consequently, stakeholders now balance instrument capability with training requirements, ergonomic outcomes, and long-term maintenance considerations when selecting pipetting solutions.
Transformative shifts reshaping the multi-channel pipette landscape driven by automation, digital integration, ergonomic design, and changing laboratory practices
The multi-channel pipette landscape is undergoing rapid transformation as laboratories pursue greater automation, digital traceability, and user-centric design. Automation initiatives have elevated expectations for device interoperability and standardized plate handling, prompting manufacturers to prioritize electronic control systems, battery longevity, and programmable protocols. Concurrently, digital integration - including data logging and device connectivity - has emerged as a differentiator that supports audit readiness and reproducible workflows.
Beyond technology, ergonomic design has taken center stage to address repetitive strain and to improve operator consistency. This shift has shortened product development cycles as suppliers iterate on materials, grip ergonomics, and weight distribution. Moreover, evolving end-user requirements across academic, clinical, and industrial laboratories are driving specialized product variants. Taken together, these dynamics encourage a market environment where innovation pace, regulatory alignment, and user training converge to determine which solutions gain traction within different institutional settings.
Anticipating the cumulative implications of United States tariffs in 2025 on supply chains, manufacturing decisions, and procurement strategies
Policy shifts and trade actions in major economies can materially affect procurement strategies and supply chain configurations for laboratory equipment, and the United States tariff changes slated for 2025 are likely to drive a range of operational responses across manufacturers, distributors, and end users. In the short term, purchasing teams will reassess sourcing options to minimize cost exposure and delivery uncertainty, favoring suppliers with resilient logistics, local inventory, or diversified manufacturing footprints. At the same time, manufacturers reliant on cross-border components will evaluate component sourcing, tariff classifications, and potential nearshoring to reduce vulnerability to tariff swings.
In addition, distributors and service providers will adjust contractual terms and inventory positioning to maintain service levels while absorbing or passing through incremental costs. Over time, procurement frameworks may increasingly emphasize total cost of ownership, service responsiveness, and supplier risk metrics rather than unit price alone. Consequently, laboratories and corporate procurement functions should prepare for lengthened supplier qualification cycles and heightened focus on contractual protections, while vendors will need to demonstrate transparent supply chain practices and flexible fulfillment models.
Key segmentation insights revealing how product type variations, channel configurations, volume ranges, and end-user categories shape applications and selection
Segmentation analysis reveals distinct value propositions and user behavior across product types, channel configurations, volume ranges, and end-user categories. Considering product type, the market divides between electronic multi-channel pipettes, which are further differentiated into battery replaceable and rechargeable variants, and manual multi-channel pipettes that are available as fixed tip or interchangeable tip designs. Each option addresses different operational priorities: electronic models prioritize repeatability and programmable protocols, while manual alternatives emphasize simplicity and lower acquisition cost.
Channel configuration also guides selection, with eight-channel and twelve-channel devices catering to different plate formats and throughput requirements. Volume range segmentation further refines suitability: high volume applications concentrate on ranges such as 200–500 µL and 500–1000 µL, medium volume tasks typically fall within 10–100 µL and 100–200 µL bands, and low volume assays most often require precision in the 0.1–2 µL and 2–10 µL windows. End-user categories shape procurement and deployment decisions as well; academic and research institutes tend to favor flexibility and cost-effectiveness, clinical diagnostics emphasize traceability and regulatory conformity with subsegments like histology and in vitro diagnostics, food and beverage laboratories focus on quality control and R&D use cases, and pharmaceutical and biotechnology organizations require rigorous performance across biotechnology and pharmaceutical applications. Taken together, these segmentation factors influence not only product selection but also supplier relationships, validation strategies, and post-sale support models.
Key regional insights explaining demand drivers, supply chain nuances and regulatory impacts across the Americas, Europe, Middle East & Africa and Asia-Pacific
Regional dynamics materially influence procurement patterns, supplier strategies, and regulatory compliance for multi-channel pipettes. In the Americas, demand drivers emphasize rapid adoption of automation, strong service networks, and a preference for devices that support high-throughput screening and clinical workflows. Consequently, suppliers with established distribution channels and responsive after-sales support tend to find favorable adoption conditions in this region.
In Europe, Middle East & Africa, regulatory alignment and interoperability are paramount, with laboratories often prioritizing devices that meet strict documentation and traceability requirements. Fragmented regulatory landscapes in the region encourage suppliers to offer robust compliance support and localized technical assistance. Meanwhile, in Asia-Pacific, growth is driven by expanding research infrastructure, increasing R&D investments, and a mix of cost-sensitive and early-adopter segments. Here, suppliers that can combine scalable manufacturing, competitive pricing, and rapid localization of service tend to perform well. Across all regions, logistics resilience, spare parts availability, and training resources remain critical differentiators that influence both initial purchase decisions and long-term loyalty.
Key company-level insights highlighting competitive strategies, product innovation, partnerships, and service differentiation among leading manufacturers
Company-level dynamics reflect a mix of product innovation, channel strategy, and service model differentiation. Leading manufacturers compete not only on device accuracy and ergonomic design but also on the depth of their service offerings, warranty terms, and the availability of consumables and validated accessories. Strategic partnerships and OEM arrangements enable some suppliers to extend their market reach while maintaining focus on core competencies such as electronics, software integration, or precision manufacturing.
Furthermore, competitive positioning increasingly hinges on lifecycle support, including calibration services, training programs, and digital tools that enhance traceability. As a result, commercial success depends on demonstrating measurable improvements in workflow efficiency and operator well-being. In this environment, companies that invest in modular product platforms, robust service networks, and data-driven customer engagement are better positioned to secure long-term contracts with research institutions, clinical labs, and industrial R&D departments.
Actionable recommendations for industry leaders to optimize procurement, accelerate adoption of advanced pipetting solutions, and strengthen R&D focus
Industry leaders should pursue pragmatic steps to optimize procurement and accelerate adoption while maintaining operational resilience. First, align purchasing criteria to prioritize total cost of ownership and service reliability rather than short-term price considerations; by doing so, organizations mitigate supply disruptions and reduce long-term operational risk. Second, pilot mixed-device deployments that combine electronic and manual multi-channel pipettes to balance throughput, cost, and training requirements; iterative pilots allow teams to build internal best practices and capture real-world performance data.
Third, strengthen supplier relationships by negotiating flexible inventory and fulfillment terms that account for potential tariff or logistics volatility. Fourth, invest in operator training and standardized protocols to maximize the reproducibility benefits of advanced pipetting solutions; this reduces user-related variability and increases return on equipment investments. Finally, integrate device data into laboratory information systems where possible to enhance traceability and to support compliance documentation. Collectively, these measures help organizations capture efficiency gains while preserving agility in the face of changing regulatory and supply conditions.
Research methodology describing data sources, qualitative and quantitative approaches and stakeholder engagement used to ensure robust and objective analysis
The research methodology combined structured qualitative inquiry with targeted quantitative validation to ensure findings reflect operational realities. Primary inputs included in-depth interviews with procurement managers, laboratory directors, product engineers, and service leads, supplemented by technical evaluations of device specifications and usability factors. These engagements helped to identify the drivers of device selection, service expectations, and the practical constraints that influence adoption across different laboratory types.
In addition, secondary research synthesized regulatory guidance, standards documentation, and supply chain literature to contextualize vendor practices and logistics considerations. Findings were triangulated through comparative analysis across end-user segments and regions to expose consistent patterns and to highlight areas of divergence. Throughout the process, iterative validation sessions with industry stakeholders refined the conclusions and ensured the recommendations remain actionable for both operational teams and executive decision-makers.
Conclusion summarizing strategic takeaways on technology adoption, procurement considerations, segmentation implications and regional priorities for stakeholders
The analysis converges on several strategic takeaways that should guide stakeholder action: prioritize device interoperability and data capture to support reproducibility, balance electronic and manual device investments according to task specificity, and reinforce supplier relationships to reduce exposure to trade and logistics disruptions. Segmentation nuances-spanning product type, channel configuration, volume range, and end-user requirements-underscore the need for tailored procurement and deployment strategies rather than one-size-fits-all purchasing.
Regional considerations further refine these priorities; suppliers must adapt their service and compliance models to meet local requirements, while end users should evaluate total cost, support responsiveness, and training availability when choosing solutions. Ultimately, organizations that align product selection with operational processes and that invest in training and supplier resilience will realize the greatest improvements in throughput, data integrity, and operator safety.
Note: PDF & Excel + Online Access - 1 Year
Table of Contents
192 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. Multi Channel Pipette Market, by Product Type
- 8.1. Electronic Multi Channel Pipettes
- 8.1.1. Battery Replaceable
- 8.1.2. Rechargeable
- 8.2. Manual Multi Channel Pipettes
- 8.2.1. Fixed Tip
- 8.2.2. Interchangeable Tip
- 9. Multi Channel Pipette Market, by Channel Configuration
- 9.1. Eight Channel
- 9.2. Twelve Channel
- 10. Multi Channel Pipette Market, by Volume Range
- 10.1. High Volume
- 10.1.1. 200-500 µL
- 10.1.2. 500-1000 µL
- 10.2. Low Volume
- 10.2.1. 0.1-2 µL
- 10.2.2. 2-10 µL
- 10.3. Medium Volume
- 10.3.1. 10-100 µL
- 10.3.2. 100-200 µL
- 11. Multi Channel Pipette Market, by End User
- 11.1. Academic & Research Institutes
- 11.2. Clinical Diagnostics
- 11.2.1. Histology
- 11.2.2. In Vitro Diagnostics
- 11.3. Food & Beverage
- 11.3.1. Quality Control
- 11.3.2. R&D
- 11.4. Pharmaceutical & Biotechnology
- 11.4.1. Biotechnology
- 11.4.2. Pharmaceutical
- 12. Multi Channel Pipette Market, by Region
- 12.1. Americas
- 12.1.1. North America
- 12.1.2. Latin America
- 12.2. Europe, Middle East & Africa
- 12.2.1. Europe
- 12.2.2. Middle East
- 12.2.3. Africa
- 12.3. Asia-Pacific
- 13. Multi Channel Pipette Market, by Group
- 13.1. ASEAN
- 13.2. GCC
- 13.3. European Union
- 13.4. BRICS
- 13.5. G7
- 13.6. NATO
- 14. Multi Channel Pipette Market, by Country
- 14.1. United States
- 14.2. Canada
- 14.3. Mexico
- 14.4. Brazil
- 14.5. United Kingdom
- 14.6. Germany
- 14.7. France
- 14.8. Russia
- 14.9. Italy
- 14.10. Spain
- 14.11. China
- 14.12. India
- 14.13. Japan
- 14.14. Australia
- 14.15. South Korea
- 15. United States Multi Channel Pipette Market
- 16. China Multi Channel Pipette Market
- 17. Competitive Landscape
- 17.1. Market Concentration Analysis, 2025
- 17.1.1. Concentration Ratio (CR)
- 17.1.2. Herfindahl Hirschman Index (HHI)
- 17.2. Recent Developments & Impact Analysis, 2025
- 17.3. Product Portfolio Analysis, 2025
- 17.4. Benchmarking Analysis, 2025
- 17.5. Agilent Technologies, Inc.
- 17.6. Axygen Scientific, Inc.
- 17.7. Beckman Coulter, Inc.
- 17.8. Benchmark Scientific, Inc.
- 17.9. Biohit Oyj
- 17.10. Biotix Laboratories Pvt. Ltd.
- 17.11. Bio‑Rad Laboratories, Inc.
- 17.12. BrandTech Scientific, Inc.
- 17.13. Corning Incorporated
- 17.14. Danaher Corporation
- 17.15. DLAB Global Co., Ltd.
- 17.16. Eppendorf SE
- 17.17. Gilson, Inc.
- 17.18. Greiner Bio‑One International GmbH
- 17.19. Hangzhou Zixin Scientific Instrument Co., Ltd.
- 17.20. Hirschmann Laborgeräte GmbH & Co. KG
- 17.21. Integra Biosciences AG
- 17.22. Labnet International, Inc.
- 17.23. Mettler‑Toledo International Inc.
- 17.24. NEST Biotechnology Co., Ltd.
- 17.25. Nichiryo Co., Ltd.
- 17.26. Sartorius AG
- 17.27. Scilogex, LLC
- 17.28. Shenzhen Lifescience Instruments Co., Ltd.
- 17.29. Socorex Isba SA
- 17.30. The Hamilton Company
- 17.31. Thermo Fisher Scientific, Inc.
- 17.32. TOMY Company, Ltd.
- 17.33. TZERO LLC
- 17.34. Wuhan Inno Instruments Co., Ltd.
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