Drug Stability Test Chamber LDST-T2011

Introduction

Drug Stability Test Chamber maintains a stable temperature and humidity condition by means of a highly advanced touch-screen controller and comes with a large display showing temperature and humidity parameters.

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

Applications

Drug Stability Test Chamber are used for a variety of applications like pharmaceutical and medical products package testing, stability and shelf-life testing.

Specifications

Volume	250 L
Temperature Range	0 - 65 °C
Temperature Fluctuation	± 0.5 °C
Temperature Control Precision	0.1 °C
Humidity Range	40 - 98 % RH
Internal Dimension	680 × 500 × 730 mm
Overall Dimension	880 × 1010 × 1740 mm
Power Supply	AC 380 V ± 10 % 50 ± 0.5 Hz

Features

Highly advanced temperature and humidity touch screen controller

7 inch HD color touch display

Real-time network monitoring and control functions

Sample shelves having adjustable height feature

Inner chamber made up of acid and corrosion resistant mirror finish SUS304 plate

High-quality door sealing strips and insulation materials for high performance

Shallow groove humidification method

Adopts automatic filling and standard water pump as water supply system

Water level automatic compensation and water shortage alarming system

PT100 platinum resistance thermometer as temperature sensor

Capacity to store around 1000 sections of programmes

Computer interface: Ethernet port

FAQs

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

When selecting this test equipment, 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 test equipment be calibrated to ensure accurate results?

It is recommended to calibrate this test equipment 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 test equipment?

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 test equipment be used with different types of samples, and are there any compatibility considerations?

Yes, this test equipment 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 test equipment 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.