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Suzhou Sujing Automation Equipment corporation limited
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Laboratory Liquid Electronic Particle Counter FDA 21 CFR Part 11

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Laboratory Liquid Electronic Particle Counter FDA 21 CFR Part 11

Brand Name : SUJING

Model Number : LE100

Place of Origin : China

MOQ : 1

Price : Negotiable

Payment Terms : T/T

Supply Ability : 800/per month

Delivery Time : 5 work days

Packaging Details : Wooden Case

Name : Liquid Particle Counter Compliant With FDA 21 CFR Part 11 In Lab

Particle size channel : 24

Display : 7inch LCD color touch screen

Sample stirring method : Magnetic stirring (adjustable)

Data output : RS232 port, USB, built-in printer

Warranty time : 1 Year

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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 parametersliquid particle counter
Particle size range2-100 μm
Particle size channel24
Maximum detection concentration10000 particles/ml
Accuracy±10%
RepeatabilityRSD<2% (particles>1000 per ml, 5ml sample)
Resolution<10% (U.S.P, ISO 21501)
Syringe specifications1ml, 5ml, 10ml*, 25ml
Sampling speed20 ml/min*
Sample volume accuracy±1%
Minimum sampling volume0.2ml**
Sensor material316 stainless steel, quartz glass, PTFE, NBR
Power supplyAC 100~240V, 50/60HZ
Mixing methodMagnetic stirrer (speed adjustable)
Data outputRS232 port; USB; built-in thermal printer
Display output7 inch LCD color touch screen
Size320(L)×309(W)×394(H) mm
Weight11.0 kg
Operating environmentTemperature 10-40 ℃; RH 0 ~ 95% non-condensing
Software systemLE-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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