LD-100 PPOCT HbA1c Auto Hematology Analyzer Machine 220mm*150mm*120mm

HbA1c Analyzer LD-100 (PPOCT) Fully Automatic HbA1c Testing Analyzer One Step Operation Analyzer

Intended Use

• It is one of the Labnovation HbA1c Testing Analyzer
• Intended for the content determination of hemoglobin A1c (HbA1c) in human whole blood.
• Testing with 4μL sample,fast testing speed within 3min
• Color touch screen easy to click and read the results
• Protable and convience,suitable for the detection of HbA1c in medical units at all levels.

Specifications

Basic Parameters

• Blood collection volume: The sampling volume of whole blood should not be less than 4μl.
• Sample volume: 4μl full-blood.
• Analytical wave-length: 510nm and 580nm.

Analysis Interface

Click the Analysis button on the main interface to enter the sample detection program. For details, see 5.3 Sample Detection

PRINCIPLE

• Uses the (borate affinity) fluorescent immunoturbidimetry
• Push a mixture containing a fluorescent borate conjugate into an integrated test cup and mix to dissolve sufficiently.
• The blood samples in the sample collector are then pushed into the buffer and mixed to release the hemoglobin from the red blood cells.
• The total concentration of hemoglobin depends on the initial reduced fluorescence signal.
• Fluorescent borate conjugates bind to glycosylated hemoglobin, and glycosylated hemoglobin is determined by detecting the decrease of fluorescent active ingredients.
• The percentage of glycosylated hemoglobin in total hemoglobin can be determined.

Feature

• Simple Operation Step, One-Step Testing Process
• Protable, Light and Small,Easy to carry
• Working environment: Standard
• Battery Integrated
• Operating mode: Continuous
• High Accuracy
• RFID For Batch Management
• Color Touch Screen
• One Analyzer For HbA1c Testing

Reliable

Use Step

• Place cartridge in analyzer
• Push bead into reagents
• Insert sample into cartridge

Performance Indicators

• Accuracy: tested with the reference material as samples, and the relative deviation of the determination results of the analyzer should be within the range of ±8%.
• Precision: Samples with a concentration of 4.0%-6.5% are detected, and the sample coefficient of variation (CV) of the test results is within 3%.
• Linearity:In the range of 4%-16% of HbA1c, the linear correlation coefficient r of the test results should be no less than 0.9900.
• Stability:Within 8 hours after the instrument is turned on and stable, the same normal sample is tested, and the relative deviation of the test results is not more than ±3%.
• Permission: The authority is the first-level authority, and the login authority is the first-level authority.

Certificated