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Friability Tester

Model NO. CS-1P

Quantity

Features：

Single-channel dual-barrel synchronous operation, with both timing and counting modes, and automatic stop.
High-precision servo stepper motor for precise speed control.
Touchscreen human-machine interface with password login support.
Automatic calculation of friability after weighing for convenient data processing.
Optional data printing function for efficient and intelligent operation.

Advantages:

Adopting dual-barrel synchronous operation with high precision, this Friability Tester equipped with Servo Motor Control and intuitive Touch Screen Control realizes automatic counting, timing stop and convenient friability calculation for pharmaceutical lab detection.

Specification：

Model	CS-1P
Cylinder Number	2
Cylinder Radius	286
Cylinder Depth	39mm
Tablet Fall Height	156mm
Rotating Speed	20-70rpm
Rotation Count	0~9999 turns
Consumption	40W
Power Supply	AC110/220V±10%, 50/60Hz
External Size(WDH)mm	370300340
Package Size(WDH)mm	440400525

Q1: What testing functions does this friability tester offer?

A: The device supports timing and counting modes, with automatic stop functionality, allowing flexible and precise testing based on different standards.

Q2: How accurate is the speed control?

A: It is equipped with a high-precision servo stepper motor, ensuring accurate and stable speed control for reliable test results.

Q3: Does the device support data management and security?

A: Yes. The touchscreen interface supports password login, enhancing data security and controlled access, especially in regulated environments.

Q4: Can the device automatically calculate friability results?

A:Yes. After weighing, the system can automatically calculate friability, simplifying data processing and reducing manual errors.

Q5: Is it possible to print test results?

A: Yes. An optional data printing function is available, allowing users to generate reports quickly for documentation and compliance purposes.

Applications

Pharmaceutical Industry：Essential for tablet friability testing, quality control, and formulation development.
Quality Control Laboratories (QC/QA)：Ensures compliance with pharmacopoeia standards (USP, EP, BP) for tablet strength and integrity.
Research & Development (R&D)：Supports drug formulation optimization and performance evaluation.
Contract Research Organizations (CROs)：Suitable for third-party testing and validation services.
Academic & Research Institutions：Used for pharmaceutical education and research studies.