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V6.5 Filter Integrity Tester Integtest

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V6.5 Filter Integrity Tester Integtest Specification

Frequency
50/60 Hz

Max Height
240 mm

Application
Integrity testing of hydrophilic and hydrophobic membrane filters

Test Range
0-6000 mL/min

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

Measuring Range
0-6000 mL/min (air flow)

Port Size
6 mm, 8 mm, 12 mm (customizable)

Mounting Type
Tabletop

Temperature
5C - 40C

Response Time
1 second

Humidity
85% RH (non-condensing)

Interface Type
USB, RS232, Ethernet

Gas Pressure
0.1-0.4 MPa (clean compressed air or nitrogen)

Resolution
0.01 mL/min

Specimen Size
Various (customizable adapters)

Accuracy
2% F.S.

Equipment Type
Automatic filter integrity tester

Automation Grade
Fully automatic

Features
Automatic data storage, printout, password protection, CFR21 compliance

Operating Voltage
AC 220V 10%, 50/60 Hz

Number of Specimens
Single filter or filter assembly

Display Type
7-inch Color Touchscreen Display

Usage
Laboratory integrity test, pharmaceutical QC

Machine Weight
9 kg

Test Speed
60 seconds per test

Control Mode
Touchscreen Interface

Compliance
CFR21 Part 11, GMP, GLP

Calibration
Automatic and manual

Dimensions
305 x 240 x 150 mm

Printing Capability
Built-in thermal printer

Noise Level
60 dB

Display Resolution
800 x 480 pixels

Language Support
English, Chinese (multilingual options)

Protection Level
IP21

Testing Methods
Bubble Point Test, Diffusion Test, Water Intrusion Test

Data Storage
Up to 100,000 test records

About V6.5 Filter Integrity Tester Integtest

Power Supply	100260 VAC, 50HZ, 120W
Operation Pressure	100-10000 mbar (145psi)
Unit	Mbar
Operation Condition	Ambient Temperature+5 ~ +40Relative Humidity10-80%
Dimension(mm)	400(Depth) 260(Width) 240(Height1)x220(Height2)
Function	Manual Bubble point TestBasic Bubble Point TestExtensive Bubble Point Test Pressure Holding TestDiffusion FLow TestWater Immersion TestUltrafitration Membrane Test
Test Accuracy	Net Volume Test 4%Bubble Point Test 50mbar Diffusion Flow Test 4% Water Immersion 0.01ml
Test Scope	BP100-8000mbar DF1-600ml/min WI0.01-100ml/min
Applied Range	Symmetric and asymmetric membrane test, syrine filters, capsule filters, plate filters, cartridge filters ;ultrafiltration membrane packages, ultrafiltration columns, various irregular filters
Audit Trial	Audit trail records can exportable and ireeversible
Authority Management	4 level User Name and Password to Login ,electronic signature to meet the FDA 21 CFR PART 11 requirements
Reservation Solution(programs)	120sets
Audit Trial (customization)	More subject logs
Print Function	Built-in printer
Applicable Environment	Above D level
Weight	8KG
Historical Record	More than 5000 sets unlimited sets records
Records Copy	Support USB disk to export include test curve
Display Screen	High definition 7 inch ,color touch screen;
Serial Connection	RS232/USB
Language	Chinese/English
Work Mode	Online/Offline
Dust and splash level	IP54
Signal output	4-20mA, RS485,12V Alarm output

Application Area:

Pharmaceutical industry
Medical device industry
Food and beverage industry
Environmental protection industry

Advanced Testing Technology

The V6.5 Filter Integrity Tester incorporates state-of-the-art automation and high-precision sensors to deliver reliable and reproducible results. With user-selectable testing methods-Bubble Point, Diffusion, and Water Intrusion-it caters to diverse filter applications. Customizable adapters make it versatile for a wide range of specimen sizes and assemblies.

User-Friendly and Secure Operation

Equipped with a 7-inch color touchscreen, the tester supports intuitive operations in English and Chinese. The device allows automatic data storage and password-protected access, ensuring compliance with strict industry regulations like CFR21 Part 11. Its thermal printer provides instant documentation of test outcomes.

Flexible and Efficient Integration

Compatible with USB, RS232, and Ethernet interfaces, the V6.5 Filter Integrity Tester integrates seamlessly into laboratory and pharmaceutical quality control systems. With rapid test speeds (60 seconds per test) and the capacity to handle up to 100,000 records, it is a powerful asset for busy QA/QC teams.

FAQ's of V6.5 Filter Integrity Tester Integtest:

Q: How does the V6.5 Filter Integrity Tester operate during filter testing?

A: The tester uses automated processes to perform Bubble Point, Diffusion, and Water Intrusion tests. The operator simply selects the desired method and test parameters via the touchscreen interface. The system then applies clean compressed air or nitrogen at precise pressures, measuring filter integrity within 60 seconds per test.

Q: What types of filters can be tested with this equipment?

A: The V6.5 is designed for both hydrophilic and hydrophobic membrane filters and accommodates single filters or filter assemblies. Customizable adapters allow testing of various specimen sizes, making it suitable for different brands and configurations.

Q: When should calibration of the tester be performed, and is it automatic?

A: The tester supports both automatic and manual calibration, ensuring ongoing accuracy. It's recommended to calibrate the device periodically as outlined in standard laboratory practices or before critical testing batches.

Q: Where is the data from filter integrity tests stored, and how can it be accessed?

A: Test data is automatically stored in the device, which holds up to 100,000 records. Data can be accessed and managed through the touchscreen interface, and transferred via USB, RS232, or Ethernet ports for further analysis or archiving.

Q: What processes ensure compliance with industry standards such as CFR21 Part 11 and GMP?

A: The V6.5 Filter Integrity Tester includes features like password protection, audit trail records, and controlled access settings. These functions, along with automatic data storage and secure printouts, ensure full compliance with CFR21 Part 11, GMP, and GLP guidelines.

Q: How do users benefit from the built-in thermal printer and large touchscreen display?

A: The integrated thermal printer delivers instant, legible test reports, supporting immediate documentation needs. The 7-inch color touchscreen enhances usability by allowing fast parameter input and clear viewing of test results in multiple languages.

Q: What makes the V6.5 suitable for use in Indian laboratories and pharmaceutical quality control environments?

A: Designed for tabletop use, the V6.5 operates on standard Indian power supplies (AC 220V 10%, 50/60 Hz), maintains low noise, and sustains performance in laboratory humidity and temperature conditions. Its integration capabilities and compliance with global standards make it an excellent choice for distributors, manufacturers, and service providers across India.

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