Packaging Liquid Leak Tester MFT-900

Product Introduction

Hexa Pharma Chem presents the Packaging Liquid Leak Tester MFT-900, designed for sealing integrity testing of pharmaceutical packaging to prevent moisture, oxygen, and microorganisms from contaminating products. The MFT-900 uses vacuum pressure difference detection technology for non-destructive testing with high accuracy, repeatability, and sensitivity.

The instrument complies with USP 1207, ASTM F2338, and FDA standards. It features a split design with the test chamber located above the host, and various test chambers can be provided according to different product types. The leak rate can be automatically converted into defect aperture in μm, with database storage of test results for easy quality management.

Compatible Packaging Types

The MFT-900 supports a comprehensive range of pharmaceutical packaging formats:

Spray Cans: Plunger spray cans, bag-lined spray cans, "energy jacket" spray cans, flexible tube spray cans.

Product Features

• Complies with USP 1207, ASTM F2338 and FDA standards
• Semi-automatic detection — suitable for small batch and multi-variety testing
• Non-destructive testing — high accuracy, repeatability, sensitivity
• Vacuum pressure difference detection technology
• Leak rate automatically converted into defect aperture (μm)
• Database storage of test results for easy quality management
• Touch-type man-machine interface — simple and quick operation
• Manual put-in/take-out after program selection
• Automatic flow rate testing and aperture size change throughout process
• Automatic leak rate calibration function
• Equipped with standard leaks (standard positive bottles, with third-party certification)
• Four-level user authority management meets FDA 21 CFR Part 11 requirements
• Split design — customizable test chambers for different product types
• ≥5 years audit trail storage with multiple event logs

Application Areas

Technical Parameters

Product Content & Services

• Automatic flow rate testing — automatically tests flow rate and changes aperture size during the whole process
• Automatic leak rate calibration — built-in calibration function for consistent accuracy
• Standard leaks included — equipped with standard positive bottles with third-party certification
• FDA 21 CFR Part 11 compliance — four-level user authority management with electronic signature
• Split design — test chamber above host, customizable for different product types
• Supporting services — positive bottle production, standard leak rate/annual leak verification, new sample mold customization, sample methodological parameter development & verification
• Customized test cavity — fully matched to customer's product for rapid and sensitive testing