` VeriPac 465

PTI Packaging Technologies and Inspection

VeriPac 465

Performs leak detection based on the basic principles of physics & does not require the use of trace gasses or sample preparation to perform the test

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The VeriPac 465 performs leak detection based on the basic principles of physics and does not require the use of trace gasses or sample preparation to perform the test. The VeriPac 465 core technology is based on the ASTM vacuum decay leak test method (F2338) recognized by the FDA as a consensus standard for package integrity testing. This test method was developed using VeriPac leak test instruments. The VeriPac 465 combines technological innovation and practical adjustments to patented dual vacuum transducer technology, PERMA-VAC, to make it the most sensitive and versatile vacuum-based leak detection technology to date. Through the introduction of unique test cycles, pneumatic controls and processing algorithms, the VeriPac 465 is establishing itself as the foremost vacuum-based leak test for parenteral products.

The VeriPac 465 advances in high vacuum testing has redefined what is achievable with a vacuum-based leak detection technology. The next generation PERMA-VAC technology addresses vacuum leak detection at the very core of the physical test measurement, controlling the test system volume and maximizing the Signal-to-Noise Ratio (SNR) between good and defective samples. VeriPac 465 technology reduces the baseline measurement for good samples and amplifies the test result for defective samples. This technology is geared towards detecting leaks in the MALL range for parenteral packaging and can also be applied to flexible and semi flexible package formats.
 
The VeriPac 465 leak tester connects to a test chamber that is specially designed for the package or container. The package is placed inside the test chamber to which vacuum is applied. The dual transducer technology is used to monitor the test chamber for both the level of vacuum as well as the change in vacuum over a predetermined test time. The changes in absolute and differential vacuum indicate the presence of leaks and defects within the package. 

 • Non-destructive, non-subjective, no sample preparation

• Defect detection down to 0.005 ccm
• Highest level of sensitivity, repeatability and accuracy
• Results proven superior to dye ingress
• Deterministic, quantitative test method
• ASTM test method and FDA recognized standard

 



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