

Compact Benchtop Chemiluminescence Immunoassay Analyzer
小型台式化学发光免疫分析仪
- SKU CLI-0004
- CLIA Analyzers
- 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 | 20–60 tests/h |
|---|---|
| Menu size | 10–40 assays |
| Reagent format | Single-test or small-batch cartridges |
| First-result time | 15–25 min |
| Sample volume | 30–150 µL per test |
| Reagent storage | Cooled carousel at 4–10 °C for 10–20 cartridges |
By Lab Manufacturers China Technical TeamLast reviewed Standards: ISO 15189, CLSI EP05, CLSI EP15
What is the Compact Benchtop Chemiluminescence Immunoassay Analyzer?
This compact analyzer brings chemiluminescence detection to small laboratories, running a limited menu at 20 to 60 tests per hour with the same principle and traceability as larger platforms. It suits clinics, satellite laboratories and specialized clinics with a focused test menu.
What is the Compact Benchtop Chemiluminescence Immunoassay Analyzer?
This compact analyzer brings chemiluminescence detection to small laboratories, running a limited menu at 20 to 60 tests per hour with the same principle and traceability as larger platforms. It suits clinics, satellite laboratories and specialized clinics with a focused test menu.
Overview
The instrument keeps the essential elements of a chemiluminescence system in a smaller package: a reagent carousel with a few cooled positions, a single reaction path, magnetic separation and a photomultiplier detector. Menu sizes are typically ten to forty assays, chosen to cover a clinical focus such as thyroid function, fertility, diabetes or cardiac markers. Reagent cartridges are often single-test or small-batch, which simplifies inventory but raises cost per test compared with bulk reagents. First-result time is similar to larger analyzers, often fifteen to twenty-five minutes, because the reaction chemistry sets the timing. Calibration stability, control requirements and traceability are the same as for a full platform, so the laboratory still needs the same quality management discipline.
How does it work?
In chemiluminescence immunoassay the label is a molecule, often an acridinium ester or a luminol derivative, that emits light when triggered by an oxidant or a catalyst. Capture antibody or antigen is immobilised on magnetic particles, a well or a tube. After sample binding and washing, the labelled detection reagent forms a sandwich or competes with the analyte, and a trigger solution initiates the light-emitting reaction. A photomultiplier tube measures the light flash, which is integrated over a fixed interval, and the signal is converted into concentration using a calibration curve, usually a four-parameter logistic or a master curve with a lot-specific adjustment. Because light emission is measured against a dark background rather than as a difference between two absorbance values, chemiluminescence gives a wider dynamic range and better sensitivity than chromogenic enzyme immunoassay, and magnetic separation simplifies washing and automation.
What are the key features?
- Compact footprint with a single reaction path
- Ten to forty single-test or small-batch reagent cartridges
- Cooled reagent carousel with onboard lot tracking
- First result in fifteen to twenty-five minutes
- Same calibration and quality control discipline as larger platforms
- Barcode sample identification with LIS interface
What are the technical specifications?
A typical compact benchtop chemiluminescence immunoassay analyzer configuration offers throughput of 20–60 tests/h, menu size of 10–40 assays, reagent format of Single-test or small-batch cartridges, first-result time of 15–25 min, sample volume of 30–150 µL per test and reagent storage of Cooled carousel at 4–10 °C for 10–20 cartridges. 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 Compact Benchtop Chemiluminescence Immunoassay Analyzer is used in clinic thyroid and fertility testing, diabetes and cardiac marker testing in small hospitals, satellite laboratories of a larger network and specialized outpatient clinics. Across the wider CLIA Analyzers class, laboratories also deploy it for hormone and fertility testing, cardiac marker measurement in emergency care and tumour marker monitoring.
Which standards and certifications apply?
Relevant standards and methods include ISO 15189, CLSI EP05, CLSI EP15, CLSI EP17, CLSI I/LA20, 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 analyzer on a stable bench with controlled temperature and humidity, a grounded power supply and space for reagent and waste containers. Verify performance at installation with precision, linearity and method comparison studies for every assay you will report, following CLSI EP05, EP15 and EP17 where detection limits are relevant. Establish calibration and control intervals per assay and document the curve validity period. Daily work includes checking reagent volumes and waste, running controls and reviewing the calibration status; trigger solutions and wash buffers must be prepared or replaced as specified because deteriorated solutions cause erratic light signals. Replace tubing, syringes and photodetector-related parts on schedule, and treat all samples, controls and liquid waste as biohazardous.
How do I select the right Compact Benchtop Chemiluminescence Immunoassay Analyzer?
Choose a compact analyzer when the menu can be limited to a defined clinical focus and daily volume is below about one hundred tests, or when a satellite site needs the sensitivity of chemiluminescence. In the RFQ compare cost per test with bulk-reagent platforms, confirm the registration of each assay, and check the shelf life and storage conditions of the cartridges.
How does it compare with other CLIA Analyzers variants?
Select a CLIA analyzer from the assay menu first, because registration of each test with the platform is the decisive constraint, then size throughput from daily and peak-hour demand plus about thirty percent headroom. Check the first-result time for emergency markers such as troponin and beta-hCG, since several platforms need twenty to thirty minutes. Compare sensitivity and linear range for the analytes that matter to your clinical service, the sample volume per test, and the calibration stability, which determines how often curves must be rebuilt. Decide between magnetic bead, coated tube and microplate formats according to menu size and acceptable hands-on time. Confirm onboard reagent capacity, refrigeration, STAT access, carryover control, LIS interface, and the availability of calibrators, controls and service support locally.
Full specifications
| Throughput | 20–60 tests/h |
|---|---|
| Menu size | 10–40 assays |
| Reagent format | Single-test or small-batch cartridges |
| First-result time | 15–25 min |
| Sample volume | 30–150 µL per test |
| Reagent storage | Cooled carousel at 4–10 °C for 10–20 cartridges |
| Data storage | 20,000 patient results |
| Footprint | 0.5–0.8 m² on a bench |
| Interfaces | LAN with HL7 or ASTM, USB |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Clinic thyroid and fertility testing
- Diabetes and cardiac marker testing in small hospitals
- Satellite laboratories of a larger network
- Specialized outpatient clinics
Key features
- Compact footprint with a single reaction path
- Ten to forty single-test or small-batch reagent cartridges
- Cooled reagent carousel with onboard lot tracking
- First result in fifteen to twenty-five minutes
- Same calibration and quality control discipline as larger platforms
- Barcode sample identification with LIS interface
Frequently asked questions about Compact Benchtop Chemiluminescence Immunoassay Analyzer
Usually yes, because single-test or small-batch cartridges carry more packaging and handling cost than bulk reagents. The trade-off is lower capital cost, smaller footprint and simpler inventory, which may be appropriate when volumes are low or when the site is remote.
Only within the assays registered for that platform and accepted by its software. Laboratories should check the full registered menu rather than only the tests they need today, because a platform that cannot add an assay later may force a second instrument purchase.
Most cartridges are stored at 2 to 8 degrees Celsius and have a defined onboard life once loaded, often two to four weeks. Cartridges must not be frozen, and the laboratory should rotate stock so that the oldest lot is loaded first and expiry dates are respected.
It can be for a clinic or specialized service with a defined menu and moderate volume, provided a backup arrangement exists for urgent results. Laboratories needing a wide menu, high throughput or continuous random access should choose a full-size platform instead.
Chemiluminescence measures light emission against a dark background, giving a wider measuring range and lower detection limits than the absorbance difference measured in ELISA. It also automates more easily because magnetic separation replaces repeated plate washing, though reagent and instrument costs are usually higher.
Most assays use a stored master curve with a lot-specific calibration that remains valid for two to four weeks, with a full curve required at each new reagent lot or after major maintenance. Daily control results confirm that the calibration remains acceptable, and any shift triggers recalibration before reporting.
At extremely high analyte concentrations both capture and detection antibodies become saturated and the signal falls, which can produce a falsely low result. Most analyzers detect this by diluting and re-measuring samples above a defined concentration or by comparing the reaction rate with expected curve behaviour.
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