Flowstar V Filter Integrity Test Instrument

The product has been designed to be used in a cleanroom environment with validation in accordance with current GAMP® technological control and quality risk management features, including data integrity controls and the use of electronic records and signatures, mean that it operates in full compliance with the FDA’s 21 CFR Part 11.

The Volume Dosing measurement principle means that actual flow rates are recorded, negating the need to rely upon internal parameters or algorithms to convert pressure measurements into flow rates.

All surfaces that come into contact with test gases are manufactured from FDA-listed materials.

The human-machine interface is large, intuitive and easy to adjust, improving user experience. LED strips along the side of the machine indicate test status, providing feedback to operators at a distance.