Integrity tester HTY-FT100
for filterslaboratoryfor the pharmaceutical industry

Integrity tester - HTY-FT100 - Tailin - for filters / laboratory / for the pharmaceutical industry
Integrity tester - HTY-FT100 - Tailin - for filters / laboratory / for the pharmaceutical industry
Integrity tester - HTY-FT100 - Tailin - for filters / laboratory / for the pharmaceutical industry - image - 2
Integrity tester - HTY-FT100 - Tailin - for filters / laboratory / for the pharmaceutical industry - image - 3
Integrity tester - HTY-FT100 - Tailin - for filters / laboratory / for the pharmaceutical industry - image - 4
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Characteristics

Tested parameter
integrity
Applications
laboratory, for the pharmaceutical industry, for filters, for radiopharmacy
Configuration
desk, modular
Other characteristics
digital, with touchscreen, waterproof, with built-in printer
Weight

12 kg
(26.5 lb)

Width

33 cm
(13 in)

Height

26.5 cm
(10.4 in)

Description

Product overview
A non-destructive filter integrity tester for verification of filter cartridges and membranes in pharmaceutical, biotechnology and sterile manufacturing environments. Intended for pre- and post-use quality control of sterilizing-grade and process filters to support aseptic production workflows.

Key features
  • Versatile test modes: Bubble Point, Forward Flow, Water Intrusion, Combined Forward Flow & Bubble Point, and Pressure Hold to cover standard integrity protocols.
  • High measurement precision: high-resolution sensors and prediction algorithms deliver reliable results while reducing test time.
  • Operator interface: 10-inch color touchscreen with Windows OS, one-click testing and multitasking capability for lab and production use.
  • Flexible connectivity: optional needle or thermal printer; supports OPC-UA and Modbus TCP for automation and LIMS integration.
  • Data integrity: 4-level user access control, GMP-compliant audit trail, dual-level approval, e-signature support and data encryption.
  • Industrial design: IP54 protection, modular hardware architecture and redundant safety mechanisms for process environments.


Regulatory compliance
Provides test methods recommended by EU GMP Annex 1, US FDA guidance on aseptic processing and PDA Technical Report 26. Suitable for pre- and post-filtration integrity checks required in sterile drug manufacture and related regulated processes.

Applications
  • Disposable filtration systems (PUPSIT)
  • Radiopharmaceutical production
  • Pharmaceutical liquid preparation systems
  • Freeze dryer intake pressure recovery systems


Technical specifications
  • Model: HTY-FT100
  • Weight: 12 kg
  • Dimensions: 420 mm × 330 mm × 265 mm
  • Input voltage: 100–240 VAC, 50/60 Hz
  • Input power: 125 W; Fuse <5 A
  • Operating temperature: 5–50 °C; Storage: -10–60 °C
  • Ambient humidity: ≤85% RH (non-condensing)
  • Test modes & ranges: Forward Flow 0.01–1000 mL/min; Water Intrusion 0.01–100 mL/min; Bubble Point 400–8000 mbar; Pressure Hold 100–8000 mbar
  • Sensitivity: Forward Flow 0.01 mL/min; Water Intrusion 0.01 mL/min; Bubble Point 50 mbar; Pressure Hold 1 mbar
  • Protection rating: IP54
  • User interface: 10-inch color touchscreen, Windows OS
  • Data & communication: 4-level user access, GMP audit trail, OPC-UA and Modbus TCP, dual-level approval and e-signature support

Catalogs

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Exhibitions

Meet this supplier at the following exhibition(s):

Bio Asia-Taiwan
Bio Asia-Taiwan

16-19 Jul 2026 Taipei (Taiwan Region)

  • More information
    ISPE Singapore Conference &amp; Exhibition
    ISPE Singapore Conference &amp; Exhibition

    19-21 Aug 2026 Singapore (Singapore)

  • More information
    *Prices are pre-tax. They exclude delivery charges and customs duties and do not include additional charges for installation or activation options. Prices are indicative only and may vary by country, with changes to the cost of raw materials and exchange rates.