

Bench-Top Urine Chemistry Analyzer
台式尿液化学分析仪
- SKU USR-0004
- Urine Strip Readers
- 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
| Measured parameters | 10–14 parameters including microalbumin option |
|---|---|
| Throughput | 100–200 strips/h |
| Worklist | Barcode input with HL7 or ASTM interface |
| Quality control | Levey-Jennings charts per parameter and lot |
| Calibration | Reference strip verification with stored factory calibration |
| Data storage | 50,000 results with comments |
By Lab Manufacturers China Technical TeamLast reviewed Standards: ISO 15189, CLSI GP16, CLSI EP05
What is the Bench-Top Urine Chemistry Analyzer?
A bench-top urine chemistry analyzer combines strip reading with worklist management, result transmission and quality control records for a routine laboratory workflow. It suits medium-size laboratories that need traceable urine chemistry results linked to patient records.
What is the Bench-Top Urine Chemistry Analyzer?
A bench-top urine chemistry analyzer combines strip reading with worklist management, result transmission and quality control records for a routine laboratory workflow. It suits medium-size laboratories that need traceable urine chemistry results linked to patient records.
Overview
The instrument provides the optical reading system of a strip reader plus the data handling expected in a laboratory: barcode-driven worklists, two-way LIS communication, quality control storage with Levey-Jennings charts, and result comments for samples that are too coloured or dilute to interpret. Some models accept both urine strips and a limited number of other strip formats, and many can be connected to a sediment analyzer so that chemistry and microscopy reports appear together. Calibration uses the manufacturer's reference strip or a stored factory calibration that the laboratory verifies, and calibration status is recorded per strip lot. Bench-top analyzers are usually supplied with audit trail and user access control features that support accreditation requirements.
How does it work?
Each pad on a reagent strip contains reagents that change colour in proportion to the analyte concentration: glucose pads use a peroxidase-chromogen system, protein pads rely on the protein error of a pH indicator, blood pads detect the pseudoperoxidase activity of haemoglobin, leukocyte esterase cleaves an ester to release a diazonium-reactive compound, and nitrite is detected by diazotisation. The reader presses the strip against a light source and measures the light reflected from each pad with photodiodes or a camera at defined wavelengths, usually between 525 and 660 nanometres. A compensation pad or channel corrects for the intrinsic colour of the urine, and some instruments also compensate for ascorbic acid interference. The instrument converts reflectance into a category such as negative, trace, 1+, 2+, 3+ or a numeric value for pH and specific gravity.
What are the key features?
- Barcode-driven worklist with two-way LIS communication
- Quality control storage with Levey-Jennings charts
- Result comments for coloured, dilute or interfering samples
- Calibration status recorded per strip lot
- Connection to a sediment analyzer for combined reporting
- Audit trail and user access control for accreditation
What are the technical specifications?
A typical bench-top urine chemistry analyzer configuration offers measured parameters of 10–14 parameters including microalbumin option, throughput of 100–200 strips/h, worklist of Barcode input with HL7 or ASTM interface, quality control of Levey-Jennings charts per parameter and lot, calibration of Reference strip verification with stored factory calibration and data storage of 50,000 results with comments. 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 Bench-Top Urine Chemistry Analyzer is used in hospital laboratory routine urinalysis, combined chemistry and sediment reporting, outpatient laboratory workflows and screening programmes with full traceability. Across the wider Urine Strip Readers class, laboratories also deploy it for routine urine chemistry screening in clinics, antenatal and pre-employment health checks and diabetes and renal clinic monitoring.
Which standards and certifications apply?
Relevant standards and methods include ISO 15189, CLSI GP16, CLSI EP05, CLSI POCT04, ISO 18113-1, 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.
Read strips within the time stated in the instructions, because pad colour continues to develop and delays change results near category boundaries. Protect strips from moisture, heat and light, do not touch the pads and use them before expiry, since degraded strips give falsely negative results. Verify performance at installation with the manufacturer's calibration strip or reference panel, and run quality control material or a known urine sample each working day. Clean the reading window and strip carrier according to the manual, and check that the compensation channel is functioning, because a dirty window biases all reflectance readings. Treat urine as potentially infectious and decontaminate the strip carrier regularly.
How do I select the right Bench-Top Urine Chemistry Analyzer?
Specify this variant when urine chemistry results must be traceable to a worklist, when quality control records are required for accreditation, or when chemistry and sediment reporting should be combined. In the RFQ confirm the LIS interface protocol, quality control capabilities, strip lot handling and whether a sediment analyzer can be connected.
How does it compare with other Urine Strip Readers variants?
Decide first how many strips are read each day, because that determines whether a simple bench reader, an instrument with automatic strip feeding or a portable device is appropriate. Then check which parameters the reader measures and whether the report format matches what clinicians expect, especially if semiquantitative scales differ from other laboratories. Confirm the wavelengths and compensation features, since colour and ascorbate interference are the main sources of error, and check whether barcode or operator identification is supported for traceability. For portable and near-patient use, consider battery life, strip storage conditions and whether the device can transmit results. Confirm that the reagent strips specified for the reader are available locally and have an adequate shelf life.
Full specifications
| Measured parameters | 10–14 parameters including microalbumin option |
|---|---|
| Throughput | 100–200 strips/h |
| Worklist | Barcode input with HL7 or ASTM interface |
| Quality control | Levey-Jennings charts per parameter and lot |
| Calibration | Reference strip verification with stored factory calibration |
| Data storage | 50,000 results with comments |
| Audit trail | User login with change history |
| Interfaces | LAN with HL7 or ASTM, USB, RS-232 |
| Power supply | AC 100–240 V, 50/60 Hz |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Hospital laboratory routine urinalysis
- Combined chemistry and sediment reporting
- Outpatient laboratory workflows
- Screening programmes with full traceability
Key features
- Barcode-driven worklist with two-way LIS communication
- Quality control storage with Levey-Jennings charts
- Result comments for coloured, dilute or interfering samples
- Calibration status recorded per strip lot
- Connection to a sediment analyzer for combined reporting
- Audit trail and user access control for accreditation
Frequently asked questions about Bench-Top Urine Chemistry Analyzer
The instrument stores the factory calibration and requires verification with a reference strip when a new lot is loaded, recording the date, operator and result. Some laboratories also verify each new shipment, which is good practice where transport conditions vary.
Yes in many configurations: the chemistry analyzer and a sediment analyzer share a worklist, so results from both appear in one report. This reduces duplicate sample handling and makes the urinalysis report easier for clinicians to interpret.
It records user logins, result edits, calibration and quality control entries, and changes to comments, with timestamps. This supports investigation when a result is questioned and is commonly required during accreditation assessments of laboratory information handling.
Yes. Strip chemistry does not detect casts, crystals or dysmorphic red cells, and guidelines require sediment examination when clinically indicated. The bench-top chemistry analyzer complements, but does not replace, microscopy or a validated sediment analyzer.
A reader measures reflectance at defined wavelengths and compares it with stored calibration data, which removes some subjectivity in colour matching and prevents transcription errors when results are printed or transmitted. Visual reading is acceptable when the reader is unavailable, but requires trained staff and a printed colour chart.
Most measure glucose, protein, blood, leukocyte esterase, nitrite, ketones, bilirubin, urobilinogen, pH and specific gravity, and some add ascorbate, microalbumin, creatinine or calcium. The pad menu is determined by the strip used, so the reader must support the strips available in your market.
Strongly coloured urine changes the light reflected from every pad, which can shift several parameters in the same direction. Readers with a compensation pad or channel correct for this effect automatically, but very dark samples should be reported with a comment and the result verified by another method when clinically important.
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