High Performance Liquid Chromatography HbA1c Test Analyzer IFCC NGSP
HbA1c Analyzer LD-560 Fully Automaic HbA1c Testing Analyzer HPLC System For Hemoglobin Testing
Intended Use
- The Fully Automated HbA1c Analyzer is used in conjunction with suitable reagents for the quantitative detection of glycosylated hemoglobin (HbA1c) in human blood.
- This analyzer is a fully automated instrument used to analyze glycosylated hemoglobin. It has the characteristics of small sample amount and simple operation. It is suitable for the detection of glycosylated hemoglobin in medical institutions.
- The analyzer consists of an auto sample injection module, a liquid chromatography separation module, a colorimetric detection and control module, a barcode scanning module, and a display printing module.
Specifications
| Name |
Fully Automated HbA1c Analyzer |
| Model | LD-560 |
| Method | HPLC(High Performance Liquid Chromatography) |
| Parameters | HbA1c, HbF, HbA1a, HbA1b, HbA0; HbA2 (optional) |
| Test Speed | 90 seconds per test |
| Wavelength | 420nm |
| Sample Type | Whole Blood, Pre-diluted blood |
| Autoloader Capacity | 20 tubes |
| Precision | CV<2% |
| Column Capacity | 3000 tests |
| Working Condition | Temperature: 15-30℃ |
| Net weight | 28kg |
| Storage environment: Temperature | -20℃~55℃ |
| Humidity | 10%~93% |
Principle
Using high performance liquid chromatography (HPLC), the stationary phase used is a weakly acidic cation exchanger. Glycosylation of hemoglobin will result in the loss of cations on the surface of hemoglobin without being charged, and non-glycosylated hemoglobin has a positive charge.
Feature
- Information Input
- Sample Dispense
- Automatic Detection
- Result Output
- Easy Operation
- Fast Testing Speed
Advantage
- HPLC Method
- Full Automation
- Smart System
- Best Quality And Performance
- Most Cost-effective
Performance Parameters
-
Reporting unit: Glycosylated hemoglobin (HbA1c) is reported in NGSP (%) and IFCC units (mmol/mol).
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Accuracy: The accuracy is tested with reference materials as samples, and the relative deviation of the test results should be within ±5%.
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Stability Within 8 hours after the analyzer is turned on and stabilized, the same normal sample is tested, and the relative deviation of the test results is not more than ±3.0%.
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Carrying pollution: The carrying pollution rate of the analyzer should not be greater than 2.0%.
Certificated
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