Packaging Liquid Leak Tester MFT-1000

Product Introduction

Hexa Pharma Chem presents the Packaging Liquid Leak Tester MFT-1000, an automated sealing integrity testing system for pharmaceutical packaging. The MFT-1000 adopts an autonomous optimization Linux system with a robotic arm for automated operation, providing vacuum pressure and pressure decay difference detection with high accuracy and efficiency.

Designed to prevent moisture, oxygen, and microorganisms from contaminating products, the MFT-1000 complies with USP 1207, ASTM F2338, and FDA standards. With a 10-inch touchscreen, built-in printer, 300,000+ history records, and comprehensive audit trail functionality, it's the ideal choice for high-throughput pharmaceutical packaging integrity testing.

Compatible Packaging Types

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
• Autonomous optimization Linux operating system
• Semi-automatic detection with robotic arm — suitable for small batch & multi-variety testing
• Non-destructive testing — high accuracy, repeatability, sensitivity
• Vacuum pressure & pressure decay difference detection
• Leak rate automatically converted into defect aperture (μm)
• Database storage of test results for easy quality management
• 10-inch touch-type man-machine interface — simple and quick operation
• Automatic flow rate testing and aperture size change throughout process
• Automatic leak flow calibration function
• Equipped with standard leak bottles (third-party certified)
• Four-level user authority management meets FDA 21 CFR Part 11
• Built-in printer with ≥300,000 history record storage
• Ethernet, USB, RS485 interfaces for comprehensive connectivity

Application Areas

Technical Parameters

Advantage Functions & Services

• Linux OS — autonomous optimization Linux system for reliable performance
• Automatic flow rate testing — tests flow rate and changes aperture size throughout process
• Automatic leak flow calibration — built-in calibration for consistent accuracy
• Standard leaks included — equipped with standard leak bottles with third-party certification
• FDA 21 CFR Part 11 — four-level user authority management with audit trail
• Split design — test chamber above host, customizable for different product types
• Supporting services — positive bottle/mould 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