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TrackSense Pro 無線數據記錄儀
8 bar壓力感測器
8 Bar 壓力感測器的壓力範圍為 20 mBar 至8 Bar Absolute，測量精度為 ± 0.25% 滿量程。它可用於食品、製藥和醫療行業，適用於蒸煮滅菌、蒸氣滅菌、烤箱、環境室等應用。
高品質無線TrackSense Pro 數據記錄器由高強度不銹鋼製成，並提供高端技術，可在不同的熱過程中進行穩定和高精度的測量。
TrackSense Pro 數據記錄器系列配備可互換感測器選項，可解鎖多個測量參數：
✓ Temperature
✓ Pressure
✓ Conductivity
✓ Relative Humidity
✓ Vacuum
✓ 蒸氣滲透
數據記錄器可以輕鬆地被多讀取站啟動和讀取，並透過無線通訊與天空模組結合獲取即時數據。
| Sensors with this logger configuration: | 8BAR壓力感測器 | Logger with this sensor configuration: | 還有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: | Piezoresistive | Working temperature: | -20 to +150°C |
| Sensor element: | Strain gauge | Surface material: | 316 Liter Stainless Steel |
| Measurement accuracy: | ± 0.25% Full Scale | Diameter of the logger: | 25毫米 |
| Recorder length: | 44毫米 | ||
| With battery weight: | 48克 | ||
| Memory capacity: | 120,000 data points / 120,000 sample values | ||
| Minimum sampling rate: | 0.33秒 | ||
| 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秒/24小時 | ||
| 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
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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.
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.
