V1.1 Full-Automatic Filter Integrity Tester Integtest

Send Inquiry

Request To Call Back

V1.1 Full-Automatic Filter Integrity Tester Integtest

Get a Price/Quote

V1.1 Full-Automatic Filter Integrity Tester Integtest Specification

Humidity
80% RH (non-condensing)

Specimen Size
Compatible with standard filter cartridges and capsules

Max Height
35 cm

Response Time
<2 seconds

Number of Specimens
Single or multiple

Mounting Type
Bench-top

Gas Pressure
0.20.8 MPa (Clean and dry compressed air)

Automation Grade
Fully Automatic

Temperature
5~40C (41~104F)

Equipment Type
Filter Integrity Tester

Application
Integrity testing of membrane filters in pharmaceuticals, food & beverage, biological and laboratories

Display Type
Touchscreen LCD

Power Supply
AC 220V 10%, 50/60Hz

Interface Type
USB, Ethernet

Operating Voltage
220V AC

Resolution
0.1 mbar

Measuring Range
06000 millibar

Features
Automated testing, built-in printer, data storage, password protection, self-diagnostics

Port Size
1/4 NPT Standard

Test Range
06000 mbar

Frequency
50/60 Hz

Accuracy
0.5% FS

Usage
Filter integrity (bubble point, diffusion, water intrusion tests)

Capacity
One filter element per cycle

Machine Weight
12 kg

Test Speed
Up to 60 tests/hour

Test Stroke
Customizable

Control Mode
Full-automatic, Microcomputer Control

Alarm
Automatic alarm for failure or completion

Compliance
Meets GMP/GLP requirements

Data Storage
20,000+ test records

Dimensions (LxWxH)
41 x 32 x 35 cm

Communication
RS232/RS485 supported

Printer
Inbuilt thermal printer for direct report printing

Calibration
Automatic and manual calibration modes

Operating Language
Multilingual support

Noise Level
<60 dB(A)

Enclosure Material
304 Stainless Steel

Safety
Overpressure protection; password access system

About V1.1 Full-Automatic Filter Integrity Tester Integtest

Main features

Display of test data and curves in real time, monitoring the whole process of testing.
Provides automatic printing set function, the user can operate more simple and convenient.
Water Based test (WH) for Hydrophobic Filter: using purified water as test liquid instead of IPA and Ethanol, thus it can avoid trace quantity of ethanol or IPA contamination when testing filters.
The instrument can store 500 history record and curve.

Applied range

Disc Membrane:25mm-300mm;
Standard Cartridge:2.5- 40
Capsule & Mini Catridge
Air filter test :2.5- 40

Streamlined Testing with Full Automation

Experience seamless filter integrity analysis with the V1.1 tester's fully automated operation and microcomputer control. With customizable test parameters, users can perform bubble point, diffusion, or water intrusion tests effortlessly, ensuring accuracy and repeatability for stringent laboratory and industrial requirements.

Efficient Data Management and Easy Reporting

Store over 20,000 test records directly in the device for effortless traceability, while the integrated thermal printer provides instant hardcopy reports. Convenient data export options through USB and Ethernet interfaces support secure transfer and review, crucial for audit trails and regulatory compliance.

Safety and Compliance at the Forefront

The V1.1 tester incorporates advanced safety features like overpressure protection, password-access security, and an automatic alarm for test failures or completion. Designed to comply with GMP and GLP standards, it helps users maintain high-quality standards and regulatory adherence in diverse operational environments.

FAQ's of V1.1 Full-Automatic Filter Integrity Tester Integtest:

Q: How does the V1.1 Full-Automatic Filter Integrity Tester ensure safety during operation?

A: The tester features overpressure protection and a secure password access system to prevent unauthorized use. It also includes automatic alarms that notify users upon test failure or completion, supporting safe and controlled operation throughout the process.

Q: What types of tests can I perform with this filter integrity tester?

A: The V1.1 tester is capable of conducting bubble point, diffusion, and water intrusion tests, making it suitable for various membrane filter integrity applications in pharmaceutical, food, beverage, and laboratory environments.

Q: When should calibration be performed and how is it managed?

A: Calibration can be scheduled routinely or as required, with both automatic and manual calibration modes available. This flexibility ensures the tester maintains precise measurement accuracy while complying with regulatory requirements.

Q: Where can I use the V1.1 Filter Integrity Tester?

A: This equipment is ideal for bench-top use in controlled environments such as pharmaceutical facilities, food and beverage processing plants, biological laboratories, and research institutions within the temperature range of 5 to 40C.

Q: What is the process for printing and storing test reports?

A: After each test, results are immediately printable via the inbuilt thermal printer. Additionally, the instrument can store over 20,000 test records internally, with data export possible through USB or Ethernet for comprehensive documentation and traceability.

Q: How does full automation benefit daily operations with this tester?

A: Full automation allows operators to perform up to 60 tests per hour with minimal intervention, reducing manual workload and human error. This leads to higher efficiency and consistent, reliable integrity testing.

Q: What makes the V1.1 suitable for compliance with GMP/GLP standards?

A: The tester's comprehensive data storage, self-diagnostics, traceable reporting, and robust security features ensure all procedures meet GMP/GLP requirements for quality assurance and regulatory inspections.

Tell us about your requirement