Upgrading or Adding Equipment to your lab?
Upgrading or Adding Equipment to your lab?
Save up to 70% with refurbished equipment from Abbott, Alfa Wasserman, Beckman, Biomerieux, Biotechnia, Hitachi, Horiba ABX, IL, J&J, Radiometer, Randox, Roche, Siemens, Stago, Sysmex, Thermo and Tosoh.
Diamond is the only USA FDA registered, ISO Certified and Down-To-Frame® refurbisher of Chemistry, Immunology, Hematology, Caogulation and Blood Gas equipment. Inquire today for pricing and Details.
Every analyzer undergoes a systemized, rigorous and unique Down-To-Frame® Refurbishment process to rebuild each analyzer to its original specification and intended use.
Belonging to the original release of the Architect family of Chemistry and Immunoassay systems, the Abbott Architect c8000 is a reputable and high quality Japanese designed and manufactured Chemistry Analyzer testing over 80 assays with a maximum throughput of 1200 tests per hour. The system is partially an open reagent system allowing for use of alternative reagents on certain tests. Chemistry analyzers measure substances within bodily fluids to establish a pattern of abnormalities. The wide range of tests can be grouped under several categories such as electrolytes, enzymes, blood sugar, metabolites, thyroids, hormones, lipids, therapeutic drug monitoring, and drugs of abuse monitoring. This analysis can be conducted on blood (either whole, serum or plasma), urine, semen or cerebrospinal fluids Chemistry analysis begins with patient sample placed in separate capsules, test tubes, slides or sample cups that are transported on a conveyor with sample racks or in a carousel in a reagent tray. Specimens are sampled and then mixed automatically together with diluents and reagents in a reaction cuvette. The reagents are pulled from a reagent carousel, which is typically refrigerated to keep the reagents shelf life longer. The reactive cuvette is stored and processed in the Reaction carousel. The Reaction carousel holds the mixing station (which mixes samples and reagents) and wash station (which rinses the cuvettes). Dependent on the manufacturer, the cuvette is either made of glass or plastic, but must be optically clear so that light may pass through without any intervention from scratches or blemish. Chemistry analysis is calculated through the absorbance of the specific wavelengths as light is passed through the specimen. All chemistry analyzers possess a photometer (either filter photometer or spectrophotometer) that conducts the measurement of the light absorbance of the specimen, and results are calculated. Filter photometers use glass filters, on a rotating filter wheel, coated with colored material while spectrophotometers use prisms or gratings, to isolate these wavelengths from the scanner beam. In both cases, a lamp (typically halogen) is the light source. Spectrophotometry is a more commonly used method than Filter photometry, which is currently only used in J&J, Roche Cobas and Siemens Dimension systems. Spectraphometry is used in most other systems including Abbott, Beckman and Roche Hitachi systems. The process to attain the results from the absorbance tests are classified either as End Point or Kinetic. End point method incubates the reaction mixture for a predetermined amount of time to reach the end point, or equilibrium of the reaction. Kinetic method, as the reagents and the sample are mixed, the reaction is monitored, the rate of change in absorbance is then determined and related to analyte concentration. As such, Kinetic is a faster method than End Point.
|Private Labeled by:||Toshiba Medical|
|Private Label Source Model:||TO-C8000|
|Sample Types:||CSF, Plasma, Urine, Serum|
|Number of Assays:||81|
|Maximum Throughput:||1200 tests/hour|
|Sample Cycle Time:||562 (sec)|
|Sample Size Min:||1 μL|
|Sample Input Type:|
|Height:||122 cm (48 in)|
|Width:||201 cm (79 in)|
|Depth:||125 cm (49 in)|
|Weight:||646 kg (1421 lb)|
|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.
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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
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Diamond Diagnostics Kft.
1044 Budapest, Hungary
Óradna Street 6
Tel: +36 (1) 787 2222
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.
The names and logos of manufacturers, their instruments, and their products referred to herein may be protected by trademark or other law, and are used herein solely for purpose of reference. Products are available for international distribution only unless otherwise indicated. Diamond Diagnostics expressly disclaims any affiliation with products it does not manufacture, as well as sponsorship by other manufacturers. For current regulatory status on products within this website, please contact your sales representative. Prices and Information shown are for reference only and may change without notice. SmartLyte®, ProLyte®, CareLyte®, and Down-To-Frame® Refurbishing are Registered Trademarks of Diamond Diagnostics®.