

Floor-Standing Random-Access Analyzer
落地式随机存取分析仪
- SKU AUA-0002
- Automated Analyzers
- CE (to be confirmed)
- ISO 9001 manufacturing (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Type | Floor-standing random-access analyzer |
|---|---|
| Throughput | 400–2400 tests/h |
| Sample volume | 1–10 µL per test |
| Reagent volume | 50–200 µL per test |
| Onboard assays | 30–120 |
| Stat handling | Priority queue |
By Lab Manufacturers China Technical TeamLast reviewed Standards: IEC 61010-1 (safety requirements for electrical equipment), ISO 15189 (medical laboratories, quality and competence), ISO 17511 (traceability of calibrators and control materials)
What is the Floor-Standing Random-Access Analyzer?
A floor-standing random-access analyzer runs any test on any sample in any order at high throughput. It suits busy hospital and reference laboratories with mixed menus and urgent requests in a single integrated platform.
What is the Floor-Standing Random-Access Analyzer?
A floor-standing random-access analyzer runs any test on any sample in any order at high throughput. It suits busy hospital and reference laboratories with mixed menus and urgent requests in a single integrated platform.
Overview
The analyzer is a floor-standing unit with sample and reagent carousels, multiple reaction and detection channels, and integrated calibration and quality control. Throughput ranges from about 400 to 2400 tests per hour, and the system can run stat samples ahead of the queue while continuing routine work. Sample volumes of 1–10 µL and reagent volumes of 50–200 µL per test reduce consumption, and onboard reagent cooling maintains stability. Barcode-driven workflow, autodilution, reflex testing and autoverification reduce operator intervention, and bidirectional LIS connectivity reports results automatically. Consumables include cuvettes, probes and wash solutions, and waste is managed through sealed containers. The system needs a stable environment, a dedicated power supply and service access, and its complexity demands trained operators and documented maintenance.
How does it work?
An automated analyzer moves samples from an autosampler into reaction or detection positions, adds reagent, incubates and measures a signal, then calculates and reports results. Sample tubes are identified by barcode, and the software maps each tube to the requested test panel. Liquid handling draws sample and reagent with syringes or pumps, mixes them in cuvettes or wells, and holds them at a controlled temperature so the reaction proceeds consistently. Detection may be photometric, turbidimetric, ion-selective, fluorescent or luminescent depending on the assay. Random-access analyzers can run different tests on different samples in any order, while batch and continuous-flow systems process similar tests together. Onboard reagents are tracked with volume and expiry data, and results are reported to the laboratory information system with quality-control flags and calibration status.
What are the key features?
- Sample and reagent carousels
- Throughput 400–2400 tests per hour
- Stat sample priority
- Autodilution and reflex testing
- Autoverification with LIS reporting
- Onboard reagent cooling
What are the technical specifications?
A typical floor-standing random-access analyzer configuration offers type of Floor-standing random-access analyzer, throughput of 400–2400 tests/h, sample volume of 1–10 µL per test, reagent volume of 50–200 µL per test, onboard assays of 30–120 and stat handling of Priority queue. Values are indicative of the product class; the exact figures for each configuration are confirmed on the quotation and the calibration documents supplied with the instrument.
Which applications is it used for?
The Floor-Standing Random-Access Analyzer is used in hospital core laboratory, reference laboratory, emergency and stat testing and high-volume routine chemistry. Across the wider Automated Analyzers class, laboratories also deploy it for clinical routine chemistry, immunoassay and hormone testing and water and environmental analysis.
Which standards and certifications apply?
Relevant standards and methods include IEC 61010-1 (safety requirements for electrical equipment), ISO 15189 (medical laboratories, quality and competence), ISO 17511 (traceability of calibrators and control materials), EU IVDR (in vitro diagnostic medical devices), 21 CFR Part 11 (electronic records and signatures) and CLIA (clinical laboratory improvement requirements). Certification candidates for this model are CE and ISO 9001 manufacturing; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Install with adequate bench or floor space, power quality and drainage where required, and confirm room temperature stability because it affects reaction rates. Run quality control at the defined frequency and review results before releasing patient or sample results, and monitor calibration and reagent expiry. Perform daily, weekly and periodic maintenance as specified, including probe cleaning, cuvette checks and fluid replacement. Verify analyzer performance on installation, after major service and on a defined schedule, covering accuracy, precision, carry-over and linearity. Define autoverification rules carefully and review flagged results. Keep records of calibration, maintenance, quality control and software changes for audit, and train operators on error recovery and shutdown.
How do I select the right Floor-Standing Random-Access Analyzer?
Choose a floor-standing random-access system for high volume, mixed menus and urgent work. Confirm throughput, reagent capacity and connectivity. RFQ: peak workload, test menu, stat policy, redundancy and LIS interface. State the peak workload and stat expectations.
How does it compare with other Automated Analyzers variants?
Start from the test menu, the daily and peak sample numbers, and the turnaround time required. Random-access analyzers suit mixed test menus and urgent samples, while batch analyzers suit high volumes of a few tests. Confirm the analyzer offers the assays you need, either onboard or through open channels, and check reagent stability, onboard capacity and calibration frequency. Review the sample and reagent volume per test, since these drive running cost, and check the walk-away time for unattended operation. Consider connectivity to the LIMS, quality-control handling, and whether the instrument supports reflex testing and autoverification. Confirm maintenance intervals, service response and the availability of calibrators and controls, and verify traceability of calibrators to a reference standard.
Full specifications
| Type | Floor-standing random-access analyzer |
|---|---|
| Throughput | 400–2400 tests/h |
| Sample volume | 1–10 µL per test |
| Reagent volume | 50–200 µL per test |
| Onboard assays | 30–120 |
| Stat handling | Priority queue |
| Autodilution | Programmable |
| Reflex testing | Rule based |
| Reagent cooling | 2–10 °C |
| LIS interface | Bidirectional, host query |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Hospital core laboratory
- Reference laboratory
- Emergency and stat testing
- High-volume routine chemistry
Key features
- Sample and reagent carousels
- Throughput 400–2400 tests per hour
- Stat sample priority
- Autodilution and reflex testing
- Autoverification with LIS reporting
- Onboard reagent cooling
Frequently asked questions about Floor-Standing Random-Access Analyzer
A stat sample is inserted into the run queue and processed at the next available channel, ahead of routine samples but behind those already in progress. The software then reports the stat result first.
Consider whether assays can be moved to a second analyzer if one fails, and whether critical tests have a backup method. Downtime planning is as important as throughput planning in a core laboratory.
Onboard reagents degrade if they stay warm, so cooling to 2–10 °C extends the usable time on the analyzer. The software should track onboard age and expiry and warn before a reagent is no longer valid.
An instrument that automatically handles samples and reagents, performs reactions and detection, calculates results and reports them to the laboratory information system. It runs more tests with less manual work and better consistency.
When samples need a mixed test menu, urgent results or continuous loading. Random-access analyzers can run different tests on different samples in any order, whereas batch systems process similar tests together.
By accuracy, precision, linearity, carry-over and calibration checks using certified materials, at installation and on a defined schedule. Results are compared with acceptance criteria before the analyzer is used for reporting.
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