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TrackSense Pro Wireless Data Logger

8 bar pressure sensor

8 Bar Pressure sensors are available in the following pressure ranges 20 mBar to 8 Bar AbsoluteThe measurement accuracy is ± 0.25% Full range. It can be used in the food, pharmaceutical, and medical industries for applications such as steam sterilization, vapor sterilization, ovens, environmental chambers, and more.

 

The high-quality wireless TrackSense Pro data logger is made of high-strength stainless steel and offers high-end technology for stable and highly accurate measurements in different thermal processes.

 

The TrackSense Pro data logger series comes with an interchangeable sensor option that unlocks multiple measurement parameters:

✓ Temperature
✓ Pressure
✓ Conductivity
✓ Relative Humidity
✓ Vacuum
✓ Vapor permeation

 

The datalogger can be easily activated and read by multiple reading stations and combined with a sky module via wireless communication to obtain real-time data.

Sensors with this logger configuration:8BAR Pressure SensorLogger with this sensor configuration:And 3G.
Pressure measurement range:20 mBar to 8 Bar ABS (0 to +140 °C calibration)Operational pressure:0.001 mBar to 10 Bar ABS
Measurement Principle:PiezoresistiveWorking temperature:-20 to +150°C
Sensor element:Strain gaugeSurface material:316 Liter Stainless Steel
Measurement accuracy:± 0.25% Full ScaleDiameter of the logger:25 mm
  Recorder length:44 mm
  With battery weight:48 grams
  Memory capacity:120,000 data points / 120,000 sample values
  Minimum sampling rate:0.33 seconds
  Maximum sampling rate:24 hours
  Maximum startup delay:14 days
  Benan:Ex II1GD Ex ia IIC T3 Ga, -50 °C ≤ Tamb ≤ +105 °C
  Time accuracy:±5 seconds/24 hours
  Battery:TSP Standard Battery
  Please note: If the equipment is to be used in an ATEX environment, the special conditions for safe use specified in section 17 of the ATEX Certificate must be taken into account.

Sensor Options

Key Benefits and Features

  • One Logger - Multiple Sensor Options
  • Conforms to 21 CFR Part 11
  • Real-time data of SKY module
  • User-friendly verification software
  • Works with E-Val Pro thermocouple system

Software

ValSuite software is the industry's leading verification and calibration software and is highly credited with countless reporting options, impeccable data integrity, user calibration options and data analysis capabilities.

 

The software is used to run all of ELLAB's hardware and can combine various measurement systems into a unified study. In addition to its wide range of features, ValSuite complies with FDA 21 CFR Part 11 and is designed according to the GAMP guidelines. In addition, the software automatically generates PDF reports with clear pass/fail indications and can be run on stand-alone PCs or networked computers.

✓ Complies with FDA 21 CFR Part 11
✓ safe and reliable
✓  Windows Security Options
✓ Compatible with Windows 10
✓ Available in multiple languages
✓ Suitable for various applications
✓ Multiple Reporting Options

  • One software platform for all Ellab devices
  • Combine TrackSense data logger and E-Val Pro wired thermocouple system in the same session
  • Automatic PDF report generation with clear pass/fail indication
  • Runs on standalone PC or network

Applications

Environmental Test Chamber

Environmental test chambers are suitable for a variety of applications: product shelf-life, stability and packaging testing, light and temperature assessment studies, electronic component aging, plant growth, and more.

They are characterized by precise control of parameters such as temperature and relative humidity.

Ethylene oxide sterilization

Ethylene oxide sterilization is a low temperature process used in the pharmaceutical and medical industries to reduce the level of infectious agents.This process is preferred for products that cannot withstand the high temperatures of typical autoclaves.Key parameters include temperature, humidity and pressure levels.

Hydrogen Peroxide

Hydrogen peroxide sterilization is a low-pressure, low-temperature, non-toxic process used in the pharmaceutical and medical industries to reduce the level of infectious agents. This process is preferred for products that cannot withstand the heat of a typical high-pressure sterilizer or have space for diffusion limitations, such as low-lumen medical equipment.

Key parameters include pressure/vacuum, transmitted RF energy, H2O2 concentration and temperature. Humidity can also be measured.

Steam sterilization

High-pressure sterilizers for the pharmaceutical and medical industries must meet established standards and specifications (EN 285 and ISO 17665) to ensure that their processes continue to provide safe and sterile results.

For this reason, autoclaves need to be identified and verified periodically to prove that they can sterilize within the qualified parameters.

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