Friability Tester LTFT-T2010

Introduction

Friability Tester is a benchtop tablet friability tester with single path, and synchronously running two drums. The number of turns and rotating speed of friability tester is in accordance with international standards, to enable convenient dispensing, modifications and operations. For research and quality purpose, high accuracy is achieved by testing speed and circle number in this friability tester.

This pharmaceutical machinery is designed to meet the rigorous requirements of modern laboratory operations, ensuring high precision, reliability, and ease of use for various experimental applications.

Applications

Used to detect friability, abrasion of non-coated tablets, coated tablets, capsules, mechanical stability, and collision resistance across pharmaceutical, medicine, and cosmetics for quality and research purpose.

Specifications

Number of cylinder	2
Rotating speed of cylinders	25 rpm
Rotating accuracy	± 1 rpm
Counting mode	Adopted with countdown, 100 turns can be set arbitrarily
Inner diameter of cylinder	286 mm
Cylinder depth	39 mm
Sliding height	156 mm
Power Consumption	20 W
Power supply	220 V, 50 Hz
Dimension	370 × 300 × 340 mm
Packaging Dimension	420 × 410 × 500 mm
Net Weight	7.7 kg
Gross Weight	11.5 kg

Features

High quality hyaline acryl drums

Microprocessor controlled operations

Fixed speed and rotation of the drums

Present or real data is displayed on screen

Auto stop on completion of experiment

Auto test, auto diagnose, auto alarm functions

User-friendly operations

FAQs

1. What are the key factors to consider when selecting this pharmaceutical machinery for laboratory use?

When selecting this pharmaceutical machinery, key factors include: 1) The instrument's precision and accuracy to meet experimental requirements; 2) Compatibility with the types of samples and applications you will be working with; 3) Ease of use and maintenance requirements; 4) Safety features to protect operators and samples; 5) Calibration and certification requirements; 6) Cost-effectiveness and long-term reliability; 7) Technical support and service availability from the supplier. Evaluating these factors ensures that the instrument meets your laboratory's specific needs.

2. How often should this pharmaceutical machinery be calibrated to ensure accurate results?

It is recommended to calibrate this pharmaceutical machinery at least once every 6-12 months under normal usage conditions. More frequent calibration (every 3-6 months) may be necessary if: 1) The instrument is used continuously for extended periods; 2) It is exposed to harsh environmental conditions (temperature fluctuations, humidity, dust); 3) It is used for critical applications requiring high precision; 4) The instrument has been moved or subjected to physical shock; 5) Calibration checks indicate significant deviations from standard values. Always follow the manufacturer's calibration guidelines.

3. What are the common maintenance procedures required for this pharmaceutical machinery?

Common maintenance procedures include: 1) Regular cleaning of the instrument's exterior and sample contact surfaces to prevent contamination and ensure proper operation; 2) Inspection of moving parts (if applicable) for wear and lubrication as recommended by the manufacturer; 3) Replacement of consumable parts (filters, bulbs, reagents) according to usage guidelines; 4) Verification of performance parameters (temperature, pressure, voltage) regularly; 5) Storage of the instrument in a clean, dry environment when not in use; 6) Keeping a maintenance log to track service activities and identify potential issues early; 7) Following the manufacturer's specific maintenance schedule for optimal performance and longevity.

4. Can this pharmaceutical machinery be used with different types of samples, and are there any compatibility considerations?

Yes, this pharmaceutical machinery can be used with a variety of sample types, but compatibility considerations are important: 1) Check if the instrument's materials are compatible with the chemical composition of your samples (avoid corrosive or reactive substances that may damage the instrument); 2) Ensure that the sample volume and concentration are within the instrument's recommended range; 3) For biological samples, consider sterility requirements and potential cross-contamination risks; 4) For volatile or hazardous samples, ensure proper ventilation and safety precautions are in place; 5) Consult the manufacturer's documentation for specific sample compatibility guidelines, and perform compatibility tests with new sample types before regular use.

5. What should be done if the pharmaceutical machinery malfunctions or produces inconsistent results?

If malfunctions or inconsistent results occur: 1) First, check the instrument's user manual for troubleshooting guidelines specific to the issue; 2) Verify that the instrument is properly calibrated and within its calibration period; 3) Inspect for obvious issues such as loose connections, damaged parts, or incorrect settings; 4) Clean the instrument thoroughly to remove any contamination that may affect results; 5) Repeat the experiment with a known standard sample to determine if the issue is with the instrument or the sample; 6) If the problem persists, discontinue use of the instrument to prevent further damage or inaccurate results; 7) Contact technical support or a qualified service technician for diagnosis and repair, providing details of the issue and any troubleshooting steps already performed.