

High-Throughput Automated Urinalysis System
高通量全自动尿液分析系统
- SKU AUS-0005
- Automated Urinalysis Systems
- CE (to be confirmed)
- ISO 13485 manufacturing (to be confirmed)
- NMPA class II registration (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Throughput | 200–400 samples/h combined |
|---|---|
| Sample positions | 100–200 with continuous loading |
| Strip capacity | Up to 400 strips onboard |
| Sediment method | Flow cytometry or flow imaging |
| Chemical parameters | 10–14 parameters per sample |
| Quality control | Per-line controls with cross-line comparison |
By Lab Manufacturers China Technical TeamLast reviewed Standards: ISO 15189, CLSI GP16, CLSI EP05
What is the High-Throughput Automated Urinalysis System?
A high-throughput urinalysis system processes 200 to 400 samples per hour with parallel chemistry and sediment lines and continuous loading. It suits large hospital and reference laboratories that report urinalysis in volumes comparable to other routine disciplines.
What is the High-Throughput Automated Urinalysis System?
A high-throughput urinalysis system processes 200 to 400 samples per hour with parallel chemistry and sediment lines and continuous loading. It suits large hospital and reference laboratories that report urinalysis in volumes comparable to other routine disciplines.
Overview
The configuration uses independent lines for strip chemistry and sediment analysis, each with its own loading, so throughput is not limited by the slower module. Continuous sample loading, large reagent and strip capacities, and automated waste handling allow long unattended periods. The software balances work between lines, applies review rules and manages quality control across the system, and the combined report is generated per sample with full traceability of strip and reagent lots. Because high throughput concentrates work on one platform, downtime has a wide impact, so laboratories should plan redundancy, keep critical consumables in stock and define how flagged and abnormal samples are handled when the system is unavailable.
How does it work?
The platform links two analytical modules through one sample and one worklist. The chemistry module dips a reagent strip, reads the pads by reflectance photometry at defined wavelengths, applies colour and ascorbate compensation and reports semiquantitative categories. The sediment module either uses flow cytometry with a nucleic acid stain and scatter signals to classify particles by size, granularity and fluorescence, or images a sediment chamber or centrifuged slide and classifies particles by pattern recognition. The software merges both result sets into one report, applies review rules such as reflex microscopy for flagged samples, and transmits results to the laboratory information system. Sample barcode reading, mixing before aspiration and automatic washing between samples reduce operator handling and improve traceability, while quality control records and reagent lot tracking support accreditation.
What are the key features?
- Independent chemistry and sediment lines operating in parallel
- Continuous sample loading with large reagent capacities
- Throughput of 200 to 400 samples per hour
- Automated waste handling for unattended operation
- Cross-line workload balancing with consistent review rules
- Full traceability of strip and reagent lots per report
What are the technical specifications?
A typical high-throughput automated urinalysis system configuration offers throughput of 200–400 samples/h combined, sample positions of 100–200 with continuous loading, strip capacity of Up to 400 strips onboard, sediment method of Flow cytometry or flow imaging, chemical parameters of 10–14 parameters per sample and quality control of Per-line controls with cross-line comparison. 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 High-Throughput Automated Urinalysis System is used in large hospital routine urinalysis, reference laboratory urinalysis services, screening programmes with high sample numbers and consolidated multi-site urinalysis testing. Across the wider Automated Urinalysis Systems class, laboratories also deploy it for hospital routine urinalysis with combined reporting, nephrology and urology outpatient testing and emergency department urine screening.
Which standards and certifications apply?
Relevant standards and methods include ISO 15189, CLSI GP16, CLSI EP05, CLSI AUTO10, CLSI POCT04, IEC 61010-1 and IEC 61010-2-101. Certification candidates for this model are CE, ISO 13485 manufacturing and NMPA class II registration; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Install the system on a level bench with controlled temperature, stable power and enough space for reagent and waste containers, and verify each module separately before validating the combined workflow with a set of normal and abnormal samples compared against manual microscopy. Define the review rules and test them before go-live, since rule errors affect which results are released automatically. Daily work includes running chemistry control strips and sediment control material, checking reagent and strip status and inspecting the flow cell or imaging chamber for deposits. Wash solutions, cuvettes and flow cells require scheduled cleaning, and results flagged by the system should be reviewed according to documented criteria. Treat all urine samples and waste as potentially infectious.
How do I select the right High-Throughput Automated Urinalysis System?
Specify a high-throughput system when daily urinalysis volume exceeds about one thousand samples or when several smaller analyzers currently run in parallel. In the RFQ confirm throughput on a realistic mix of normal and abnormal samples, capacity for strips and reagents per shift, and the redundancy plan for consumables and service.
How does it compare with other Automated Urinalysis Systems variants?
Choose an automated urinalysis system when sediment results are required routinely and the daily sample number exceeds a few hundred, or when manual microscopy cannot keep up with the workload. Compare systems by which sediment technology is used, the particle classes reported, whether a microscope image is available for review, and the review rules offered. Check the chemistry parameters, cross-contamination control between samples, barcode handling and the combined report format. Confirm the throughput on a realistic mixture of normal and abnormal samples, since flagged samples take longer, and the sample volume needed for both modules. Verify LIS integration and the traceability features, and plan a downtime procedure because a single platform carries both chemistry and sediment reporting.
Full specifications
| Throughput | 200–400 samples/h combined |
|---|---|
| Sample positions | 100–200 with continuous loading |
| Strip capacity | Up to 400 strips onboard |
| Sediment method | Flow cytometry or flow imaging |
| Chemical parameters | 10–14 parameters per sample |
| Quality control | Per-line controls with cross-line comparison |
| Waste handling | Automatic drain or large waste container |
| Footprint | 2.5–4.0 m² including service access |
| Interfaces | LAN with HL7 or ASTM and optional track connection |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Large hospital routine urinalysis
- Reference laboratory urinalysis services
- Screening programmes with high sample numbers
- Consolidated multi-site urinalysis testing
Key features
- Independent chemistry and sediment lines operating in parallel
- Continuous sample loading with large reagent capacities
- Throughput of 200 to 400 samples per hour
- Automated waste handling for unattended operation
- Cross-line workload balancing with consistent review rules
- Full traceability of strip and reagent lots per report
Frequently asked questions about High-Throughput Automated Urinalysis System
Abnormal samples often need more images or additional rule evaluation and may be held for review, so effective throughput on a clinical population is lower than the maximum figure. Ask for throughput measured on a sample mix typical of your clinical setting.
Stock should cover the supplier lead time plus a safety margin, with particular attention to strips, sheath fluid and controls, which have limited shelf lives. Laboratories should monitor consumption weekly and rotate stock so that short-dated items are used first.
A backup plan should include a smaller urinalysis analyzer for urgent samples, a service contract with committed response times and a manual procedure for reviewing and reporting results during downtime. The plan should be documented and tested periodically.
It can process the same sample types as smaller instruments, but pediatric urine volumes are often lower than the combined requirement, so such samples may need to be reserved for chemistry or run on a manual sediment chamber. Confirm the minimum volume per module before selecting.
Chemistry parameters such as glucose, protein, blood, leukocyte esterase, nitrite, ketones, bilirubin, urobilinogen, pH and specific gravity, together with sediment counts for red cells, white cells, epithelial cells, casts, crystals, bacteria and yeast, usually with semiquantitative categories.
It reduces manual microscopy substantially but does not eliminate it. Guidelines expect microscopical confirmation when the automated result is abnormal, when the clinical picture suggests a discrepancy, or when the sediment includes particles the system cannot classify, so a microscope and trained staff remain necessary.
Rules are usually based on chemistry flags such as positive blood, protein or leukocyte esterase, on sediment counts above defined limits, and on clinical requests for specific patients. Each rule should be documented, tested against known samples and reviewed after any software update.
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带流动成像沉渣模块的全自动尿液分析仪
- CE (to be confirmed)
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