Rotary tablet compression machine LRTCM-T2010

Introduction

Rotary tablet compression machine is a cutting-edge single roller continuous automatic tablet compressor with 10 punch die stations. Designed with superior quality stainless steel for great durability and for protection against corrosion. Equipped with a safety sealing system and has an integrated dust proof system for the convenience of the user.

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

Rotary Tablet Compression Machine is widely used for pressing different types of various shapes tablets and plain tablets across pharmaceutical, chemical, and food industries.

Specifications

Punch Dies	10 stations
Maximum Tablet Size	18 mm
Maximum Tablet thickness	6 mm
Maximum Pressure	60 kn
Filling Depth	15 mm
Maximum rotary Speed	0 to 30 r/min
Maximum Production Capacity	18000 pcs/h
Power	2.2 kW
Dimension	620 × 480 ×1020 mm
Weight	310 Kg

Features

Maximum Tablet Size is 18 mm and maximum tablet thickness is 6 mm

Filling depth of 15 mm and maximum rotary speed of 0 to 30 r/min

Single Roller continuous automatic tablet pressing

Can compress different types of various shapes tablets and plain tablets

Stainless steel design for protection against corrosion

Safety sealing system for reliability of the device

Dust proof system for the convenience of the user

Isolated door with easier visualization of the experiment

No contact with experimental setup for observation, prevents cross contamination

Simple and quick removal of parts for easy maintenance

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.