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TrackSense Pro X-內部溫度傳感器
TrackSense Pro X Wireless Data Logger
Internal Temperature Sensor
內部溫度傳感器的溫度範圍為 -80 至 +150 °C，具有無與倫比的 ± 0.05 °C（範圍 -25 至 +150 °C）精度。它可用於食品和制藥行業的各種應用，尤其適用於空間有限和/或需要最大限度保護傳感器的應用。
The TrackSense Pro X data logger series is equipped with an interchangeable sensor option that unlocks multiple measurement parameters:
✓ Temperature
✓ Pressure
✓ Conductivity
✓ Relative Humidity
✓ Vacuum
✓ Vapor penetration
數據記錄器可以很容易地被多讀取站激活和讀取，並通過無線通信與天空模塊結合獲取實時數據。
| Sensors with this logger configuration: | Internal Temperature Sensor | Recorders with this sensor configuration: | PRO X 3G |
|---|---|---|---|
| Temperature measurement range: | -80 to +150°C | Working temperature: | -80 to +150°C |
| Measurement Principle: | Resistance | Operational pressure: | 0.001 mBar to 10 Bar ABS |
| Sensor element: | Pt1000 | Surface material: | 316 Liter Stainless Steel |
| Diameter: | Not applicable | Diameter of the logger: | 25mm |
| Length: | Not applicable | Recorder length: | 44mm |
| Measurement point from the tip position: | Not applicable | With battery weight: | 48g |
| Precision: | Memory capacity: | 120,000 data points / 120,000 sample values | |
| -80 to -50°C: | ± 0.3 °C | Minimum sampling rate: | 1s |
| -50 to -40°C: | ± 0.2 °C | Maximum sampling rate: | 24h |
| -40 to -25°C: | ± 0.1 °C | Maximum startup delay: | 14 days |
| -25 to +150°C: | ± 0.05 °C | Benan: | Ex II1GD Ex ia IIC T3 Ga, -50 °C ≤ Tamb ≤ +105 °C |
| Sensor response time: | Time accuracy: | ±5s/24h | |
| T-63%: | 11 s | Battery: | TSP Standard Battery |
| T-90%: | 42 s | 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
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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.
cold store
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.
