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.
Ensuring Safe IV Bag PerformanceThis instrument subjects IV bags and tubing to rigorous stress, burst, leakage, and tensile tests, guaranteeing their reliability in critical healthcare settings. By using automated and customizable procedures, it assesses the material compatibility, durability, and integrity of medical-grade and composite polymer IV bags in accordance with global regulatory standards. Its advanced technology and multiple-language support enhance user experience and test reliability.
Comprehensive Data Management & CalibrationOperators benefit from extensive data storage-32GB internal and USB external-facilitating robust data logging and reporting. Export functions, user-level access controls, and microcomputer automation provide secure and reliable record-keeping. Internal and manual calibration routines ensure testing accuracy, supported by built-in diagnostic error detection that alerts users to potential issues instantly.
Versatile Automated Testing PlatformIdeal for routine safety and compliance checks, this bench-top instrument accommodates up to six different IV bag specimens of various sizes simultaneously. Its adjustable speed, wide measuring range, automated features, and comprehensive accessory kit (tubing clamps, leak detectors, adapters) streamline the testing process, saving time while upholding strict quality control standards for healthcare products.
FAQ's of Laboratory Instrument for Rigorous Testing Ensuring IV Bag Safety:
Q: How does the instrument ensure IV bag safety during testing?
A: The instrument subjects each IV bag to a suite of standardized tests-including tensile, burst, hold, and leakage protocols-to detect any structural vulnerabilities. These tests are performed in compliance with international standards such as ISO 8536 and USP <661>, ensuring comprehensive safety verification for medical-grade and composite polymer IV bags.
Q: What is the process for performing a test with this instrument?
A: Place up to six IV bag specimens using the included adapters for varying sizes. Set test parameters via the touch LCD panel, select the desired test mode (burst, tensile, leakage, or hold), and initiate the fully automated testing sequence. Results are displayed immediately and stored for export or review.
Q: Where can operators access stored testing data and generate reports?
A: Test data is securely stored on the instrument's 32GB internal memory and can be exported via USB or Ethernet. The software provides data logging and reporting features, making it easy to review results on the instrument or transfer them for regulatory compliance and record-keeping.
Q: What are the calibration and diagnostic capabilities of the system?
A: The instrument features both internal automatic and manual calibration routines to maintain precise performance. It also includes a built-in diagnostic mode that detects errors and provides real-time notifications via audible and visual alerts, supporting continuous reliable operation.
Q: When would remote monitoring be utilized, and how is it set up?
A: Remote monitoring is useful for real-time supervision, data integration, and troubleshooting, particularly in networked lab environments or for off-site quality assurance. Simply connect the instrument to your network via the Ethernet port to enable online monitoring and integration with other systems.
Q: How does using this equipment benefit routine IV bag quality testing?
A: The instrument automates complex testing sequences, provides rapid and accurate results (0.5% accuracy), and enables comprehensive documentation. It streamlines compliance with stringent healthcare safety standards, minimizes operator workload, and helps prevent defective IV bags from reaching clinical settings.
Q: What environmental and operational conditions does the instrument support?
A: It is RoHS compliant, emits low volatile organic compounds (VOCs), and operates within a 10C-40C temperature range with 20%-80% humidity. This makes it suitable for most laboratory and manufacturing environments, while environmental protections ensure both safety and compliance.