Container Closure Integrity Testing Solutions at Medical Technology Ireland

Container Closure Integrity Testing Solutions at Medical Technology Ireland Container Closure Integrity Testing Solutions at Medical Technology Ireland

Sepha will be exhibiting at Medical Technology Ireland this September demonstrating its newest CCIT and Leak Test solution, the Multi-Q on stand 106. The show that is known for showcasing innovative medical technology products and solutions fort the Irish medical device design and manufacturing industry will return to Galway Racecourse from 25 – 26 September 2019.

The Sepha Multi-Q is a multi-functional CCIT and Leak Test system that has been developed to work in combination with different test methods. Depending on the type and content of the packaging, the machine can utilize Vacuum Decay technology, Pressure Decay technology and a Flexible Membrane to test the integrity of a wide variety of packaging including vials, ampoules, pre-filled syringes, blow filled seals, bottles, sachets, bags, medical devices, trays and other flexible and rigid packaging.

The Sepha Multi-Q is compatible with:

  • Vacuum Decay
    The non-destructive, deterministic and quantitative vacuum decay technology utilizes the ASTM F2338-09 (2013), FDA approved test method to test vials, ampoules, bottles, pre-filled syringes, blow filled seals, medical devices and trays. The non-destructive, deterministic leak test device can identify leaks and channel leaks as low as 5µm and gives a pass/fail result in 10 seconds.
  • Pressure Decay
    The non-destructive, reliable and repeatable pressure decay test method is ideal for testing the integrity of lyophilized and liquid filled vials, ampoules, bottles and other containers. The device shows a pass/fail result in 10 seconds and can identify leaks and channel leaks as low as 5µm.
  • Flexible Membrane
    The non-destructive, tool-less leak detection device is designed to leak test flexible or semi-flexible packaging. Using hybrid membrane technology, the flexible head utilizes the ASTM F2338-09(2013), FDA approved Vacuum Decay test method to perform the leak test. Ideal for testing gross or micron holes in pouches, sachets and bags that contain tablets, capsules, powders or devices.
  • Vacuum Decay Bag Tester
    The non-destructive, deterministic, quantitative and calibrated leak test method has been developed to leak test empty plastic bags including IV, catheter and blood bags. It can detect micron as well as gross holes.
  • Ramp to Event
    Destructive, deterministic, quantitative test method using pressure/vacuum to ramp to an event. This method is used for component testing to detect weak welds, seals etc.
  • Ramp to Proof Pressure
    Non-destructive, deterministic, quantitative test method using pressure/vacuum to ramp to a target pressure
  • Occlusion
    Non-destructive, deterministic , quantitative test method using pressure drop/time. Typically used to test parts that must remain open to function correctly.

The Sepha Multi-Q includes software developed for manufacturers that need to comply with FDA 21 CFR Part 11. The software enables safe interaction between the machine, data reports and audit trails and protects reports from being edited or deleted.

To see a demo of the Sepha Multi-Q or discuss any of our other solutions including small blister packaging machines or deblistering solutions, visit us at Medical Technology Ireland, stand 106 on level 1.

We look forward to seeing you in Galway!

 

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