Product Description
Parameters:
Channel setting | 16 channels, Thousands of particle sizes can be customized and the accuracy is 0.1 μ m |
Test range | 1-500 μ m (Segment sensor require) |
Count range | 0 ~ 99999 particles |
Sampling volume | 0.2ml-1000ml |
Accuracy | <±0.5%(0.2ml~1000ml) |
Syring size | 10ml、25ml |
Flow rate | 2~100ml/min, setting by self |
Counting accuracy | <setting value±5% |
Channel resolution | >95% |
Relative standard deviation | RSD<1.5%(standard particle≥1000 /ml) |
Maximum Concentration | 0~18000 /ml |
Mixing speed: | 0 ~ 2000 R / min, adjustable in spinning type |
Work temperature | 10~40℃ |
Power | AC220Ⅴ±10%;50Hz;<80W |
Data output | RS232 |
Dimension | 390*350*460(mm) |
Weight | 20KG |
Software | With audit trail ,can operate in PC |
Operation system | Windows 7, windows 10 |
Futures:
- NBC-36s particle detector can fully meet the design scheme of Chinese Pharmacopoeia (2020Edition) and the requirements of Pharmacopoeia of the United States, for the detection of insoluble particles in small volume injections. It can also be used for the detection of particles in large infusion and infusion equipment, the filtration effect of infusion terminal filter and other fields (such as petroleum, chemical industry, dye, food, etc.) of liquid particles testing.
- High performance imported laser light source and compensation circuit are adopted to ensure the test accuracy of colorless and colored samples, and the samples without electrolyte can be directly detected
- The imported high-pressure injection pump sampling system is adopted, which can be set according to the sample volume of the tested sample varieties, with high injection accuracy, meeting the detection requirements of high viscosity test articles, and not affected by geographical location and other factors, meeting the use requirements of different altitude areas.
- The injection slit and pipeline are made of imported 316L and PTFE materials, which can directly detect organic solvents, oil matrix and other special solutions.
- Different high-pressure injection systems can be replaced according to the demand of injection quantity.
- It is equipped with pharmacopoeia standard infusion test, and the test times can be set arbitrarily.
- There is a special test program for small volume injection (small injection), which can be injected according to the specifications of small injection, and automatically converted into the size and quantity of container particles after the test, which meets the requirements of Chinese Pharmacopoeia and international general requirements.
- It can detect the content of particles in anesthesia bag
- Detection of filtration rate of precision filter
- Detection of particulate pollution in GB8368-2005
- Detection of particulate pollution in GB8368-2018
- Detection of particle content of drug packaging materials
- Detection of particle content of drug packaging materials
- Full channel test (better than the calibration requirements for instruments in Pharmacopoeia)
- The screw type glass agitator is adopted, with uniform speed adjustable, and the mixing speed can be controlled at any time to ensure the uniformity of particles in the container. Improve data accuracy
- Color touch large screen operation: Chinese input, easy and fast operation, powerful function. Multi channel test data can be displayed at the same time.
Sample name storage function: the set sample name is automatically stored, which is convenient and quick to operate. It has automatic data processing and multiple printing modes to meet different printing needs. - It can be connected to the computer and has the function of data automatic transmission computer; it can be connected to the laboratory operation for management, and the special data analysis software is used for data storage and statistics
- Three level authority management
- 32 users operator management
- It has data view function, and can access historical data and operation behavior at any time
AI Product Description
*The following content is generated by AI and is for reference only.
The liquid particle counter is a sophisticated analytical instrument designed to detect, count, and size microscopic contaminants within fluid samples. Widely utilized across pharmaceutical manufacturing, biotechnology, semiconductor production, and precision engineering, its primary function is ensuring fluid purity by identifying particulate matter that could compromise product quality or system integrity. Unlike traditional visual inspection methods, this technology offers high sensitivity and automated analysis, capable of detecting particles as small as sub-micron levels in water for injection, buffers, solvents, and other critical liquids.
The device operates on principles such as light obscuration or laser scattering, where a fluid sample passes through a sensing zone illuminated by a focused light source. Particles interrupting the light beam generate electrical pulses proportional to their size, allowing the instrument to classify contaminants into specific size bins according to international standards like USP <788> or ISO 11171. This data is crucial for validating sterilization processes, monitoring filtration efficiency, and maintaining cleanroom environments.
Key operational precautions must be observed to ensure accuracy and equipment longevity. First, samples should be filtered or degassed if necessary to prevent air bubbles from interfering with detection, as bubbles can be misidentified as large particles. Second, the sampling line and flow cell must remain free of residues; regular cleaning with appropriate solvents prevents cross-contamination between batches. Third, operators must strictly adhere to calibration protocols using certified reference materials to maintain measurement traceability. Additionally, environmental factors such as temperature fluctuations and vibration can affect sensor stability, so the unit should be placed on a stable surface away from direct sunlight or drafts. Finally, proper waste disposal procedures are essential when handling hazardous or bio-contaminated fluids. By following these guidelines, laboratories can rely on consistent, reliable data to uphold rigorous quality control standards and safeguard patient safety or product performance.