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Semi-Automated

Packaging Liquid Leak Tester MFT-1050

Cost-effective semi-automated vacuum pressure decay detection with Linux OS — same advanced principle as MFT-1000 without robotic arm. USP 1207, ASTM F2338 & FDA 21 CFR Part 11 compliant

Product Introduction

Hexa Pharma Chem presents the Packaging Liquid Leak Tester MFT-1050, a cost-effective semi-automated sealing integrity testing system for pharmaceutical packaging. The MFT-1050 uses the same advanced vacuum pressure and pressure decay difference detection principle as the MFT-1000, with the key difference being manual operation without an automatic robotic arm.

Designed to prevent moisture, oxygen, and microorganisms from contaminating products, the MFT-1050 complies with USP 1207, ASTM F2338, and FDA standards. It features a Linux operating system, 10-inch touchscreen, and all the core testing capabilities of the MFT-1000 at a more accessible price point for laboratories that don't require full automation.

MFT-1050 vs MFT-1000

Key Difference

The MFT-1050 shares the identical testing principle, Linux OS, vacuum pressure/pressure decay detection, 10-inch touchscreen, and all core specifications with the MFT-1000. The only difference is the absence of the automatic robotic arm, making the MFT-1050 a more cost-effective solution for laboratories that prefer manual sample handling while maintaining the same high-precision testing capabilities.

Compatible Packaging Types

Bottled
Bagged
Boxed
Ampoules
Vials
Cartridges
PFS
BFS / FFS

Features & Advantage Functions

  • Complies with USP 1207, ASTM F2338 and FDA standards
  • Autonomous optimization Linux operating system
  • Semi-automatic detection — 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
  • Split design with customizable test chambers

Technical Parameters

Differential Pressure Sensor ±2 kPa, error ≤0.5% F.S.
Differential Pressure Resolution 0.1 Pa
Test Pressure Sensor Error ≤±1% F.S.
Test Pressure Range -0.1~0.2 MPa / -0.1~0.7 MPa / -0.1~1.0 MPa (optional)
Minimum Detectable Aperture 2 μm (for IV bag minimum 5 μm)
Display 10-inch touch color screen
Power Supply AC 100V–240V, 50/60Hz, ≤200W
Audit Trail ≥5 years storage, multiple event logs, queryable by time
Authority Management Username & password login, 4-level authority, FDA 21 CFR Part 11
Print Function Built-in printer
History Records ≥300,000 storage
Data Backup USB disk export support
Interfaces Ethernet, USB, RS485 (optional)
Weight (Host) About 30 KG

Supporting Services

  • Customized test cavity — fully matched to customer's product for rapid and sensitive testing
  • Standard leaks included — equipped with standard leak bottles with third-party certification
  • 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

Cost-Effective Choice

Same

Performance

Identical specs as MFT-1000 · Manual operation · Lower investment

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