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TrackSense Pro-壓力和剛性溫度傳感器

Pressure and Rigid Temperature Sensors

The combined pressure and rigid temperature sensor has a pressure range of 15 mBar to 6 Bar absolute with an accuracy of ±0.25% full scale and a temperature range of -20 to +150 °C with a measurement accuracy of ± 0.05 °C . It can be used in a variety of applications in the food, pharmaceutical and medical industries.

 

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

 

The TrackSense Pro DataCORDER series is equipped with an interchangeable sensor option that unlocks multiple measurement parameters:

 

✓ Temperature

✓ Pressure

✓ Conductivity

✓ Relative Humidity

✓ Vacuum

✓ Vapor penetration

 

The DataCORDER can be easily activated and read by multiple readout stations and combined with the Sky Module via wireless communication to obtain real-time data.

Sensors with this logger configuration:壓力和剛性溫度感測器Logger with this sensor configuration:LAN 3G
Pressure measurement range:15 mBar to 6 Bar ABS (0 to 6 Bar)
(+140 °C calibration)
Operational pressure:0.001 mBar to 10 Bar ABS
Measurement Principle:Pressure Resistance/ResistanceWorking temperature:-20 to +150°C
Sensor element:Strain gauge / Pt1000Surface material:316 Liter Stainless Steel
Precision:± 0.25% Full ScaleDiameter of the logger:25mm
Temperature measurement range:-20 to +150 °C (calibrated to 0 to +140 °C)Recorder length:44mm
Temperature accuracy: With battery weight:48g
0 to +140°C:± 0.05 °CMemory capacity:120,000 data points/40,000 sample values
Temperature response time: Minimum sampling rate:1s
T-63%:0.8 sMaximum sampling rate:24h
T-90%:1.7 sMaximum startup delay:14 days
  Benan:Ex II1GD Ex ia IIC T3 Ga, -50 °C ≤ Tamb ≤ +105 °C
  Time accuracy:±5s/24h
  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

Washing Machine Sterilizer

Sterilizers are used in medical and pharmaceutical applications to prepare items for future autoclaving (e.g. surgical instruments for removing residues such as blood and proteins) or sterilizing (semi-sterilizing) items for later use.

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.

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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