Product Description
Featuresnote1
Batch Testing
- Equipped with fully-automatic gravity fed sample feeder, which is Labthinks latest scientific and technological achievement that can facilitate continuous testing of 20 to 120 samples.
- A & B dual-channel design can test samples of two different specifications simultaneously.
- The target vacuum degree can be set by the operator to meet testing requirements of different samples.
- Dual methods of vacuum decay and pressure decay provide the flexibility to accommodate various types of package samples.
Precise Data
- Advanced pressure detection technology, using world renowned components for data stability which is not affected by ambient environment.
- Advanced microflow automatic flow control technology that can accurately simulate different sizes of leakage holes without manual adjustment.
- Both the differential pressure transducer and flow meter are traceable to NIST.
- The system can achieve a higher test repeatability of 1um.
Intelligent Control
- 15.6" embedded touch tablet computer with Windows OS.
- New longitudinal interface layout, and easy to use graphic user interface.
- Automatic alarm, automatic capture, automatic collection of unqualified samples.
- The pressure curve is displayed in real time, and the test results are counted automatically.
- Leakage rates are calculated automatically.
- The system is equipped with various sensors as intelligent reminders for safer operation and control.
- Universal printer can be connected for test results output.
- The system features embedded with USB and network ports to facilitate the external access and data transmission of the system, which can be upgraded remotely
Security Compliance
- Verified by compensation and calibration methods.
- The leak tester meets GMP requirements for data traceability and meets the needs of the pharmaceutical industry.
- User operation permission is managed at multiple levels, and the permission content can be configured on demand.
- Electronic signature is designed according to the standard requirements of 21 CFR Part11.
Test Principle
The sample is placed in the sample feeder and automatically delivered into the test cell. The leak rate and other results can be calculated and obtained by analyzing pressure changes measured by the sensor.
Reference Standards
ASTM F2338, YY-T 0681.18, and USP<1207>
Applications
| Basic Applications |
Vials |
Various vial sealing test. |
| Extended Applications |
Ampoule |
Various ampoule bottle sealing tests. |
| Cartridge Bottles |
Various cartridge bottle sealing tests. |
| Injection bottles |
Various injection bottles sealing test. |
Technical Parameters
Table 1: Test Parameters Note2
| Parameter\Model |
C690H |
| Testing Range |
um(Reference aperture size USP1207) |
38great leakage |
| Detection Lower Limit |
um |
3 |
| Resolution |
um |
0.1 |
| Repeatability |
um |
1 |
| Pressure Range |
kPa |
-1000100 |
| Extended Functions |
21 CFR Part11 |
Optional |
| GMP computer system requirements |
Optional |
Table 2: Technical Specifications
| Testing Cell |
1 set for A group and 1 set for B group |
| Sample Feeder |
1 set for A group and 1 set for B group |
| Sample Size |
45 mm80mmNote3 |
| Sample Quantity |
20120 pieces |
| Gas Specifications |
Compressed Air (Gas source is provided by the user) |
| Gas Source Pressure |
40.6 PSI / 500 kPa |
| Port Size |
6 mm Polyurethane tube |
| Dimensions |
33.4 H x 19.6 W x 28.7 D (85cm 50cm 73cm) |
| Power |
120VAC10% 60Hz / 220VAC10% 50Hzselect one from the two |
| Net weight |
209Lbs (95kg) |
Product Configuration
| Standard Configuration |
Mainframe, embedded tablet computer, software, flow meter, European vacuum pump, 6 mm polyurethane tube |
| Customization |
Test cell and sample feeder of group A, test cell and sample feeder of group B, negative standard reference sample and positive standard reference sample designed according to sample specifications |
| Optional Parts |
GMP computer system requirements, 21 CFR Part11, air compressor, IQ/OQ/PQ documents |
Note 1: The described product characteristics are subject to the specific annotation of the "Technical Parameters" table.
Note 2: The parameters in the table are measured in the Labthink laboratory by professional operators according to the requirements and conditions of the relevant laboratory environmental standards.
Note 3: Group C test cell can be customized for samples beyond the "Sample Size", but the lower detection limit and test range will change according to the sample size, and the actual delivery shall prevail.
Advanced Integrity Testing for Vials and AmpoulesThis instrument allows laboratories to non-destructively assess the seal integrity of a variety of vials and ampoules, from 2 ml to 50 ml, without compromising the product inside. Utilizing vacuum or pressure differentials, it delivers rapid and traceable results, crucial for quality assurance in pharmaceutical and biotech industries.
User-Friendly Touch Panel and Programmable Test CyclesEquipped with an intuitive touch panel, the device supports easily programmable test cycles, ranging from 5 to 60 seconds. Operators benefit from digital LCD feedback, audio-visual alarms, and hassle-free data export via USB or SD card, streamlining record-keeping and batch documentation.
Certified Compliance and Reliable PerformanceMeeting stringent USP 1207 and GMP criteria, this benchtop system features stainless steel construction (304/316) and IP54 protection, ensuring consistent performance and safety. Digital calibration with a traceability certificate guarantees confidence in every measurement taken during regular or batch validation tests.
FAQs of Non-Destructive Testing Instrument for Vial Seal Integrity:
Q: How does this instrument ensure non-destructive vial seal integrity testing?
A: The instrument uses vacuum or pressure differential methods to evaluate seal integrity, allowing for accurate detection of leaks or weak seals without compromising or opening the vial. This preserves sample sterility and product usability.
Q: What vials or ampoules are compatible with this device?
A: It is suitable for testing a range of glass and plastic vials or sealed ampoules, with sizes from 2 ml up to 50 ml. The adjustable pedestal and customizable port size accommodate various specimen formats typically used in laboratories.
Q: When should calibration and traceability certification be carried out?
A: Calibration is recommended before initial use and at regular intervals as prescribed by your quality system or regulatory requirements. Each device is provided with a traceability certificate to ensure ongoing measurement accuracy.
Q: Where is this testing instrument typically installed and operated?
A: Designed for benchtop mounting, it fits laboratory environments in pharmaceutical manufacturing, quality control, or research settings. Front panel service access and compact dimensions support easy integration into existing laboratory workflows.
Q: What benefits does the programmable test cycle offer?
A: Programmable cycles (560 seconds) provide flexibility for different vial sizes and product types. This adaptability helps optimize test precision, minimize downtime, and support high-throughput quality assurance needs.
Q: How is test data recorded and exported for audits?
A: The system features robust data logging capabilities, storing results internally and enabling easy export to USB or SD cards. This supports regulatory compliance and simplifies documentation for audits and quality management.
Q: What are the key safety and compliance standards met by this product?
A: The instrument complies with USP 1207 and GMP guidelines, operates within an IP54-rated chassis for dust and splash resistance, and includes both audio and visual alert mechanisms to ensure operator safety and process reliability.