Customized Leak Detection Solutions

For your leak test project, you can choose from a wide range of test methods:

Dependable. Fast. Sensitive.
The ASM 2000 offers high helium pumping speed, an integrated automatic helium charging module, and optimized internal volumes. These features ensure high-performance measurements on helium-filled sealed containers and open sub-assemblies.

The ASM 2000 supports very high throughput, ensuring accuracy and reproducibility of measurement data while allowing ultra-fast cycle times.


Advanced software
The software features intuitive menus that are easy to navigate. User log-in is required to operate the equipment, with four access levels available: operator, advanced user, maintenance, and administrator.

Test recipes can be managed for each part format. At the end of the test sequence, results are clearly displayed, and PDF test and calibration certificates are automatically generated at batch closure.

Pharmaceutical industry: syringes, blisters, vials

Deterministic test method
With no operator intervention required, measurement data are completely objective. High accuracy measurements are achieved through a calibration-validation sequence using certified calibrated leaks.

Large detection range
Various detection methods can be combined to cover the entire detection range. Massive leak and fine leak tests are performed within a single test sequence, eliminating the need for additional gross leakage tests (e.g., blue dye ingress).

High sensitivity and high throughput
Combining high sensitivity tests with high throughput enables trend analysis to early identify manufacturing issues. In high sensitivity mode, optical emission spectroscopy (O.E.S) can detect 0.2 μm defect sizes on glass containers, corresponding to the sterility barrier defined as the Maximum Allowable Leakage Limit (MALL) in the USP4 <1207> guidelines.

Pharmaceutical industry: blisters, syringes and vials, intravenous therapy (IV) bags, plastic bottles

This module sets new benchmarks in delivering reliable data for testing container closure integrity at low temperatures. Customers benefit from real-time results of temperature and leak rate, optimizing your process without wasting cycle time.

The Dry Chiller Module is designed to prove that the container closure system maintains integrity at deep cold storage temperatures, either at -80°C (-112°F) or even lower. It ensures the quality of substances requiring cold storage conditions, particularly in medical and pharmaceutical environments.

Its flexibility ensures that the Dry Chiller Module can be integrated seamlessly into existing equipment.

Unmatched sensitivity for liquid products
When it comes to liquid products, the SpeedAir 3050 stands out as the most sensitive air-based technology available. You can rely on its results for their repeatability and reliability, significantly reducing the risk of false negatives and positives.

Global NDT on the container
Unlike alternative methods that focus on specific areas or access points, the SpeedAir 3050 provides a comprehensive global non-destructive testing (NDT) approach for your containers. It adheres to ASTM3 Standard F3287-17, demonstrating the ability to detect even the tiniest defects using an air-based technology.

Regulatory compliance assured
The SpeedAir 3050 is fully compliant with industry standards. It utilizes the USP4 <1207> recognized and deterministic Mass Extraction technology and operates with FDA5 21 CFR Part 115 compliant software, ensuring your testing processes meet the highest regulatory standards.

Pharmaceutical products: ampoules, autoinjectors, bottles, cartridges, flexible bags (IV bags, pouches, etc.), syringes, vials and more.