Disintegration tester LDIT-T2010

Introduction

Disintegration tester is adopted with high-precision digital electronic sensor, ensures quality precision and accuracy of the water bath temperature without need for calibration. Equipped with one set of basket to conduct disintegration experiments. The default setting for lifting time of the basket is 15 mins, can manually set the other time value as per the experimental need.

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 for detection of rate of disintegration of solids such as tablets, capsules, pills in required /set (prescriptive) conditions at pharmaceutical industry.

Specifications

Number of basket lifting set	1 set
Lifting frequency of the basket	30 to 32/ min
Lifting distance of basket	55 ± 1 mm
Minimum spacing from screen to bottom of beaker	25 ± 2 mm
Mesh size	2 mm (as per standard configuration )
Automatic time range	5 to 120 min
Work noise	< 60 dB
Temperature prefabrication range	Room Temperature to 50°C, display resolution: 0.1 °C
Temperature control accuracy	± 0.3°C
Time prefabrication range	1 to 900 min
Time control accuracy	0.5 min
Accuracy of temperature control	37 ± 0.5°C
Dimension (L × W × H)	260 × 300 × 440 mm
Power supply	220 V/50 Hz
Total power	600 W
Gross Weight	15 kg

Features

1 set of basket with 6 tubes

Microprocessor controlled automation system

Even °C temperature maintenance in water bath

Transparent organic glass for water bath

Increase and decrease splash proof buttons

Automatic system for controlling temperature, time, frequency

Alternative display for the preset and real time data

Auto-diagnose, auto-alarm system for over-temperature

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.