Single Punch Tablet Press Machine LSTP-T2011

Introduction

Single Punch Tablet Press Machine comes with 50 KN Maximum pressure and offers 20 mm maximum diameter. Features a small desktop type press for motive and continual sheeting. It can also be hand-operated. Only one pair of punching die can be erected on this press. Both filling depth of material and thickness of tablet are adjustable. Designed with high precision of filling, low noise, low consumption, of material, and it works smoothly. The maximum consumption of lab material is just 200 g. Tablets of different granular materials are pressed under pressure for use in research and quality preparations across pharmaceutical, food, chemical industry, cosmetic industry etc.

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

Single Punch Tablet Press Machine is used in pharmaceutical, chemical, food, hospital, science research institution also used in manufacturing, production of small amount of different kinds of tablet, sugar piece, calcium tablet and tablet of abnormal shape.

Specifications

Maximum pressure	50 KN
Maximum diameter Tablet	20 mm
Maximum depth of filling	12 mm
Maximum thickness of tablet	6 mm
Production capacity	4000 PC/h
Dies	1 set of round shape dies
Motor power	750 W
Motor speed	1400 rpm
Dimension	650 × 440 × 650 mm
Net weight	125 kg

Features

Designed with single punch structure is rational and small

Offers high amount of pressure to reduce weight variations between tablets while maintaining a low noise level at the same time

Adopts flexible, lightweight tablet press that is utilized for compacting granulated and powdered materials into tablets

It is desktop type press for motive and control sheeting

Minimum consumption of lab material is 200 g

Adjustable thickness of the tablet

Easy to use and maintain

It is used for development of tablets and small batch production

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.