Product Description
Product FeaturesNote1
Multiple Test Modes & Intelligent Statistics of Qualified Specimens
- Negative pressure method
- Multiple test modes including standard, multi-grade vacuum and methylthionine chloride mode
- Automatic test with traditional methylthionine chloride
- Vacuum degree, test time and infiltration time can be adjusted and test parameters can be saved automatically so that the tests with same test parameters can be started quickly
- Automatic constant pressure compensation ensures that the tests can be performed under preset vacuum conditions
- Real-time display of test curves, easy to observe the test results
- Automatic statistics of qualified specimens
- Main components and parts are supplied by well-known global manufacturers, with guaranteed performance
Brand New Patented Intelligent Touch Operating System
- Industrial grade touch screen, one-button operation, simplified operating interface, remote upgrade and maintenance
- Chinese and English operating interface
- Measurement unit conversion
- Automatic data storage and power failure memory to prevent data loss
- Storage up to 1200 test records (standard mode)
- Multiple-level user management and login with password
- Micro-printer and USB ports for data transmission (optional)
- The instrument conforms to the requirements of GMP (optional)
- Labthinks unique DataShiledTM System for data management and connecting with information system (optional)
Test Principle
Firstly submerge the specimen in the water in the vacuum chamber, and then evacuate the vacuum chamber to form differential pressure between the inside and outside of specimen. The seal property can be obtained by observing the steady progression of bubbles from the specimen or observing how the specimen expands and restores to its original shape after vacuum release.
Test StandardNote1
ASTM D3078, GB/T 15171
Applications
| Basic Applications |
- Glass Bottles, Pipes, Cans and Boxes
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- Plastic Bottles, Pipes, Cans and Boxes
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- Metal Bottles, Pipes, Cans and Boxes
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- Paper Plastic Composite Bags and Boxes
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| Extended Applications |
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Technical Specifications
| Specifications |
C660B |
| Vacuum Degree |
0 -90 KPa/ 0 -13 psi |
| Accuracy |
0.25% FS |
| Resolution |
0.1 KPa / 0.01 psi |
Vacuum Chamber Effective Sizes |
I270 mm x 210 mm (H) (standard) |
| I360 mm x 585 mm (H) (optional) |
| I460 mm x 330 mm (H) (optional) |
| Note: customization is available for other sizes |
| Gas Supply |
Air (outside of supply scope) |
| Gas Supply Pressure |
0.5 MPa 0.7 Mpa (73psi 101psi) |
| Instrument Dimension |
334 mm (L) x 230 mm (W) x 170 mm (H) |
| Power Supply |
220VAC10% 50Hz / 120VAC10% 60Hz |
| Net Weight |
Instrument: 6.5 kg Standard Vacuum Chamber: 9kg |
Configurations
- Standard Configurations
- Instrument, Standard Vacuum Chamber (I270 mm x 210 mm), I6 PU Tubing (1m)
- Optional Parts
- Micro Printer, Professional Software, Customized Vacuum Chamber, Air Compressor, GMP System, DataShieldTM Note3
- Note
- 1. The gas supply port of the instrument isI6 mm PU Tubing;
2. Customers need to prepare gas supply.
Note 1: The described test standard, applications and product features should be in line with Technical Specifications.
Note 2: The parameters in the table are measured by professional operators in Labthink laboratory under strictly controlled laboratory conditions.
Note 3: DataShieldTM provides safe and reliable data application support. Multiple Labthink instruments can share one single DataShieldTM system which can be configured as required.
Comprehensive Leakage DetectionThe system utilizes highly sensitive pressure and volume sensors to detect even the tiniest leaks in non-PVC infusion bags. The integration of compressed air or water as the test medium ensures reliable assessments, while an alarm system promptly alerts users to any detected issues, enhancing risk mitigation during quality checks.
Robust Strength TestingBurst and sealing strength tests evaluate the durability of bag materials and port-body seals. The equipment sustains pressures up to 300 kPa and applies repeated stress cycles, offering a holistic view of product robustness over time. These tests help manufacturers certify bag reliability in demanding medical scenarios.
Intuitive Operation and Data HandlingWith a user-friendly touchscreen and keypad interface, staff can easily navigate and configure tests. Automatic digital data logging streamlines record-keeping, while multiple connectivity options (USB, RS232, network) enable data export for analysis or compliance reporting. Factory and user calibration ensure maintained precision over repeated use.
FAQ's of Essential Quality Assurance Tests for Non-PVC Infusion Bags:
Q: How does the leakage test function identify minute leaks in non-PVC infusion bags?
A: The leakage test uses highly sensitive pressure, volume, and leakage sensors combined with compressed air or water. If even a tiny breach is present, these sensors detect fluctuations, and the system's integrated audio/visual alarms immediately notify the operator of any leaks detected.
Q: What strength tests are performed by the quality assurance system for infusion bags?
A: The device performs burst strength tests by incrementally increasing internal pressure until the bag's maximum capacity or failure is observed, and sealing strength tests are conducted on both the port and body seals to verify their integrity. This ensures each bag can withstand required operational stresses.
Q: When should routine calibration and maintenance be performed on the equipment?
A: Calibration is supported both at the factory level and by users in the field. Routine user calibration and minimal maintenance are recommended according to the operational guidelines to sustain accuracy and reliability, especially before critical or batch-testing runs.
Q: Where can the testing system be installed for maximum flexibility?
A: The equipment is designed for benchtop or floor-standing installation, making it suitable for various quality control labs or manufacturing environments. Its standard pedestal size fits commonly used setups, facilitating seamless integration into your existing workspace.
Q: What is the process for conducting a simultaneous multi-bag test?
A: Operators can load between one and five non-PVC infusion bags (up to 1000 mL each) into the testing chamber. Once the system is configured via the touchscreen or keypad, tests are automatically or manually initiated. Results for all specimens are digitally displayed and logged for review.
Q: How does using this equipment benefit quality assurance procedures?
A: The integrated test functions, automatic data logging, and compliance with ISO/USP standards guarantee precise, reproducible results while reducing manual errors and resource use. The audio/visual alarm system and emergency-stop safety features also protect operators and uphold manufacturing standards.
Q: What types of connectivity are available for exporting test data?
A: Test results and logs can be exported via USB, RS232, or network connections, enabling straightforward transfer for analysis, documentation, or compliance purposes, benefiting both manufacturers and third-party quality auditors.