Sartorius Sartocheck 3 Plus Filter Integrity Tester

• Ensuring sterility in pharmaceutical manufacturing processes.
• Validating filter integrity in biopharmaceutical production.
• Quality control for sterile filtration in laboratories.
• Testing membrane filters used in food and beverage processing.
• Compliance with regulatory standards for sterile product manufacturing.

Typical testing range

For this class of equipment, it typically handles filters from 0.1 to 10 square metres.

Power supply

Commonly found on units of this type, it operates on 100-240 V, single-phase, 47-63 Hz.

Test types

Includes Diffusion, Bubble Point, Combined Diffusion and Bubble Point, Water Intrusion, Water Flow, Pressure Drop, and Multipoint Diffusion tests.

Data storage

Typically stores up to 60 programs internally, expandable to 240 with a memory card.

Construction materials

Units of this type commonly feature stainless steel construction for chemical compatibility and ease of cleaning.

Connectivity

Often includes ports for printer output for cGMP-compliant paper reports.

• What is the primary function of a filter integrity tester?

  Its primary function is to verify the integrity of membrane filter systems, ensuring they are free from defects and capable of performing their intended filtration task effectively, particularly in sterile applications.

• Why is filter integrity testing important in pharmaceutical manufacturing?

• Can this unit test different types of filters?

• What kind of maintenance does a filter integrity tester require?

• Does this equipment generate reports for regulatory compliance?

Laboratory filtration systems are valued for reliability and durability, making them suitable for used purchase when sourced carefully. Buyers typically prioritise checking membrane and filter condition, as replacement costs can be significant. Industry sentiment favours systems from established manufacturers known for consistent performance. Common strengths include robust construction, compatibility with various applications, and availability of spare parts. When assessing used units, verifying maintenance history and operational specifications remains essential for ensuring continued performance in biotech and pharmaceutical environments.

General overview for this equipment type