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TrackSense Pro-智能柔性溫度傳感器

智能柔性溫度傳感器

智能柔性溫度傳感器及其靈活的傳感器非常適合難以觸及的區域。它的溫度範圍為 -50 °C 至 +140 °C,精度為 ± 0.1 °C(在 -40 °C 至 +140 °C 範圍內)。它可以在各種行業中用於環境測試等應用。

 

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:智慧柔性溫度傳感器Recorders with this sensor configuration:LAN 3G
Temperature measurement range:-50 至+140°CWorking temperature:-50 至+140°C
Measurement Principle:ResistanceOperational pressure:0.001 mBar to 10 Bar ABS
Sensor element:Pt1000Surface material:316 Liter Stainless Steel
Diameter:1.8 mmDiameter of the logger:25mm
Length:100至1000 mm(1700 mm)Recorder length:44mm
Measurement point from the tip position:3 mmWith battery weight:48g
Precision: Memory capacity:120,000 data points / 120,000 sample values
-50 to -40°C:± 0.2 °CMinimum sampling rate:1s
-40 至+140°C:± 0.1 °CMaximum sampling rate:24h
Sensor response time: Maximum startup delay:14 days
T-63%:2.2 sBenan:Ex II1GD Ex ia IIC T3 Ga, -50 °C ≤ Tamb ≤ +105 °C
T-90%:4.3 sTime accuracy:±5s/24h
請注意:以上規格僅適用於標準產品版本——有關特殊解決方案的更多信息,請聯繫Ellab A/S。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.

冷酷

Refrigeration is used to prevent further biological activity, such as spoilage of food and medical products.儲存過程中的關鍵參數是溫度,但通常也會監測濕度以了解乾燥條件。

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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