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Premium Model

Filter Integrity Tester V8.0

Advanced automated filter integrity testing system with audit trail, Linux OS, and 10-inch touchscreen — CE Certified

Product Introduction

Hexa Pharma Chem brings you the Filter Integrity Tester V8.0, powered by Beijing Neuronbc technology established in 2004. With thousands of pharmaceutical enterprise customers globally, the V8.0 model features a complete system upgrade with enhanced audit trail functionality to meet the latest regulatory requirements for data integrity.

The V8.0 represents the pinnacle of filter integrity testing technology, combining precision engineering, reliable Linux-based operation, and an intuitive 10-inch color touchscreen interface. We believe our commitment to quality products and dedicated service makes us your trusted partner for pharmaceutical quality assurance.

Product Features

  • Multiple filter integrity test methods supported
  • Optimized Linux operating system for maximum reliability
  • Optimized test operation with shortened test time
  • 10-inch true-color touch screen with friendly HMI
  • Offline/online testing with high-precision pressure sensors
  • Automatic self-test function with real-time fault reporting
  • Ultrafiltration system integrity testing capability
  • Scientific user management with password login & electronic signatures
  • Built-in comprehensive audit trail for data integrity
  • 1000 pre-stored programs for multiple filter types & conditions
  • Diffusion flow-pressure curve display with 3-curve visualization
  • Optimized air intake control for speed and stability
  • Expandable data communication with wireless support
  • Test records and audit trails queryable and exportable
  • Built-in thermal printer (no particle/ink contamination)
  • Bilingual interface — Chinese & English, freely switchable
  • Multiple pressure units (mbar, kPa, psi, kgf/cm²)
  • 1000 user accounts with 4-level customizable authority management
  • Tests up to 12-core 20-inch filter cartridges
  • Rich data interfaces — RS232, USB standard
  • Independent R&D team for custom solutions & technical support
  • CE Certified for quality and safety compliance

Application Areas

Pharmaceutical Industry Medical Device Industry Food & Beverage Industry Environmental Protection

Technical Parameters

Power Supply 100–240 VAC, 50Hz, 120W
Operation Pressure 100 – 10000 mbar (150 psi)
Operating Conditions Ambient: +5℃ ~ +40℃; Relative Humidity: 10–80%
Dimensions (mm) 292 × 480 × 115 (H1) × 190 (H2)
Test Functions Basic Bubble Point, Manual Bubble Point, Extensive Bubble Point, Pressure Hold Test, Diffusion Flow Test, Water Intrusion Test, Ultrafiltration Membrane Test
Test Accuracy Upstream Volume: ±4%; Bubble Point: ±50 mbar; Diffusion Flow: ±4%; Water Immersion: ±0.01 ml
Test Scope BP: 100–8000 mbar | DF: 1–900 ml/min | WI: 0.01–100 ml/min
Applied Range Symmetric & asymmetric membranes, needle filters, capsule filters, flat filters, cartridge filters (within 12 cores & 20 inches), ultrafiltration membrane packages/columns, various irregular filters
Audit Trail Exportable & irreversible audit trail records
Authority Management Username & Password login, 4 Authority Grades
Pre-stored Programs 1000 sets
Audit Trail Storage ≥5 years storage capacity
Anti-backflow Device Customizable (liquid)
User Accounts 1000 sets
Operating System Linux System
Dust & Splash Level IP54 Rated
Print Function Built-in thermal printer, PC controllable, subject selectable
Historical Records 300,000 sets records storage
Records Export USB disk export support (including test curves)
Display Screen High-definition 10-inch color touch screen
Work Mode Online / Offline
Applicable Environment Above D level cleanroom
Weight 10.7 KG

Product Content — Applied Range

  • Disc Membrane: Φ25mm – Φ300mm
  • Standard Cartridge: 2.5″ – 40″
  • Capsule & Mini Cartridge
  • Air Filter Test: 2.5″ – 40″

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