The Tosoh G8 HPLC Analyzer, provided by Tosoh Corporation
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Package Size: EA
Diamond Diagnostics presents the refurbished Tosoh G8, an HbA1c analyzer available in a benchtop configuration, manufactured by Tosoh Corporation. With the capacity to process up to 37 tests per hour and featuring a load-up capacity of 90 samples, this analyzer is designed for efficient and accurate analysis of glycated hemoglobin levels. Equipped with advanced technology, the Tosoh G8 delivers comprehensive insights into HbA1c levels, crucial for monitoring diabetes management. Its precision and reliability make it an indispensable tool in healthcare settings, providing valuable information for diagnosing and managing diabetes. Whether in hospital laboratories, clinics, or research facilities, the Tosoh G8 plays a crucial role in patient care by facilitating timely and accurate diagnostic results. By furnishing healthcare professionals with actionable data, it enables informed decision-making and personalized treatment strategies, ultimately contributing to improved patient outcomes and overall wellness. From routine screenings to specialized diagnostics, the Tosoh G8 stands as a trusted ally in the pursuit of better healthcare, offering consistent performance and dependable results in HbA1c testing.
Manufacturer: | Tosoh Corporation |
Series: | G8 |
Maximum Throughput: | 37 tests/hour |
Sample Cycle Time: | 96 (sec) |
Sample Size Min: | 4000 μL |
Configuration: | Bench Top |
Height: | 49 cm (19 in) |
Width: | 53 cm (21 in) |
Depth: | 52 cm (20 in) |
Weight: | 34 kg (75 lb) |
Power Supply: | 110V-220V |
Point Of Care: | No |
All units sold by Diamond Diagnostics or units qualified by Diamond Diagnostics are eligible for Field Service coverage. Service plans are the best way to maximize your instrument investment and avoid the high costs associated with instrument failure. Our plans are designed to support optimum instrument performance, ensure reproducible results and minimize down-time. Our service plans provide a timely response from our dedicated engineers who are certified on an ongoing basis to ensure top-notch results, even in the most complex laboratory environments.
: Included
: Chargeable
: None
* Contact for more details
For the laboratory looking to manage manufacture recommended preventative maintenance (PM) schedules for instrumentation at a fixed cost. The PM Service Plan will increase the reliability and reduce the risk and costs of unplanned maintenance and equipment downtime. Our plans are scheduled and planned around your specific instrument and operational needs.
For the laboratory looking to maximize the life of their instrumentation while effectively managing repair costs. The Depot Repair is a per diem plan designed for any size instrument needing major repair, complete rebuild or recycling.
For the laboratory looking to maximize the life of their instrumentation while effectively managing repair costs. Annual Depot Repair is an annual based plan designed for small to mid-sized instruments needing maintenance or repairs and can be easily shipped by your local carrier to our Depot Service Facility in Holliston, MA.
For the laboratory employing qualified service professionals, the Virtual Plan may be a suitable choice to replace or supplement Field Services. The Virtual plan offers its customers support by email and telephone, within business hours with communication directly with Clinical Engineering staff specialized in the model of instrumentation that the laboratory is utilizing. The Virtual Plan is annual.
Corporate Headquarters (USA)
Diamond Diagnostics Inc.
333 Fiske Street
Holliston, MA 01746-2048
Tel: +1 (508) 429-0450
Distribution Center (EU)
Diamond Diagnostics Kft.
1044 Budapest, Hungary
Óradna Street 6
Tel: +36 (1) 787 2222
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ISO 13485:2016 (EU)
Diamond Diagnostics Inc. is registered with the United States Food and Drug Administration as an Initial Importer Manufacturer and Contract Manufacturer. Establishment registration and device listing can be found under ID: 3003030793.
Diamond has been registered with the Food and Drug Administration since 2001 and regulated by its cGMP system requirements.
All products manufactured by Diamond carry the necessary FDA clearance and comply to the European Union IVD Directive. Every department and function in our company is standardized, controlled and routinely audited.
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