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Standard

Packaging Liquid Leak Tester MFT-600

Standard vacuum pressure difference detection with different valve configuration — same trusted principle as MFT-900. USP 1207, ASTM F2338 & FDA 21 CFR Part 11 compliant for pharmaceutical packaging integrity

Product Introduction

Hexa Pharma Chem presents the Packaging Liquid Leak Tester MFT-600, a standard vacuum pressure difference detection system for pharmaceutical packaging integrity testing. The MFT-600 uses the same trusted testing principle as the MFT-900, with the difference being a different valve configuration.

Designed to prevent moisture, oxygen, and microorganisms from contaminating products, the MFT-600 complies with USP 1207, ASTM F2338, and FDA standards. With its 10-inch touchscreen, built-in printer, and comprehensive audit trail functionality, it delivers reliable semi-automatic detection suitable for small batch and multi-variety testing at a standard price point.

MFT-600 vs MFT-900

Key Difference

The MFT-600 shares the identical testing principle, vacuum pressure difference detection, 10-inch touchscreen, and core testing capabilities with the MFT-900. The only difference is the valve configuration, making the MFT-600 a standard alternative for laboratories that don't require the specific valve setup of the MFT-900 while maintaining the same high-precision testing performance.

Compatible Packaging Types

Bottled
Bagged
Boxed
Ampoules
Vials
Cartridges
PFS
BFS / FFS

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

Features & Advantage Functions

  • Complies with USP 1207, ASTM F2338 and FDA standards
  • Semi-automatic detection — suitable for small batch & 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
  • 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 positive bottles (third-party certified)
  • Four-level user authority management meets FDA 21 CFR Part 11
  • Built-in printer with audit trail function
  • Split design with customizable test chambers
  • Different valve configuration from MFT-900

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 ≤5 years 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 positive 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

Standard Alternative

Same

Principle

Identical testing as MFT-900 · Different valve setup · Proven reliability

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