Name: | Liquid Particle Counter Compliant With FDA 21 CFR Part 11 In Lab | Particle Size Channel: | 24 |
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Display: | 7inch LCD Color Touch Screen | Sample Stirring Method: | Magnetic Stirring (adjustable) |
Data Output: | RS232 Port, USB, Built-in Printer | Warranty Time: | 1 Year |
High Light: | RS232 Electronic Particle Counter,LE100 Electronic Particle Counter,FDA Electronic Particle Counter |
Liquid Particle Counter Compliant With FDA 21 CFR Part 11 In Lab
This liquid particle counter complies with USP <788>, USP <789> and other standards.
Technical parameters | liquid particle counter |
Particle size range | 2-100 μm |
Particle size channel | 24 |
Maximum detection concentration | 10000 particles/ml |
Accuracy | ±10% |
Repeatability | RSD<2% (particles>1000 per ml, 5ml sample) |
Resolution | <10% (U.S.P, ISO 21501) |
Syringe specifications | 1ml, 5ml, 10ml*, 25ml |
Sampling speed | 20 ml/min* |
Sample volume accuracy | ±1% |
Minimum sampling volume | 0.2ml** |
Sensor material | 316 stainless steel, quartz glass, PTFE, NBR |
Power supply | AC 100~240V, 50/60HZ |
Mixing method | Magnetic stirrer (speed adjustable) |
Data output | RS232 port; USB; built-in thermal printer |
Display output | 7 inch LCD color touch screen |
Size | 320(L)×309(W)×394(H) mm |
Weight | 11.0 kg |
Operating environment | Temperature 10-40 ℃; RH 0 ~ 95% non-condensing |
Software system | LE-Assistant (optional) |
* Standard configuration ** Under 1ml syringe specifications the minimum sampling volume is 0.2ml, under the standard configuration, the minimum sampling volume is 0.4ml |
Features of liquid particle counter
Built-in USP testing standards
Precision syringe sampling device, accurate sampling volume, stable speed
Built-in calibration curve, in line with calibration requirements of ISO-21501
Intelligent automatic detection and automatic calibration function, instrument performance judgment and calibration
Use of magnetic stirring, stirring speed adjustable
USB interface direct export data, paperless electronic print report
Powerful application software development support. Easy to connect to the laboratory information management system etc.
The LE-Assistant software implements PC control and provides professional data processing
Compliant with FDA 21 CFR part 11 "Electronic Records and Signatures" and user rating management
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