Platelet Incubator Agitator LPIA-T2011

Introduction

Platelet Incubator Agitator operates at a temperature of 22℃ and features a 10 layer storage system, accommodating 30 to 60 bags of samples. It offers an oscillation frequency of 60 cycles/min ensuring optimal mixing conditions for platelet storage. It utilizes an air-cooling method to regulate temperature and maintain the functionality of platelets. Our incubator is integrated with an display for navigating various parameters.

This medical 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

Platelet Incubator Agitator is widely used in blood banks, hospitals, research laboratories, and clinical settings.

Specifications

Temperature	22℃
Environmental Temperature	5 to 35 ℃
Temperature Controller	Digital signal detection, Microprocessor
Cooling Method	Air cooling
Oscillation Frequency	60 ± 5cycles /min
Oscillation Amplitude	50 mm
Storage Area and Layers	600 × 410 × 540 mm 10 layers
Blood Bags	30 to 60
Refrigerant	R134a
Oscillation Modes	continuous back and forth from left to right, horizontal oscillation
Display
Alarm Temperature	24℃, abnormal shutdown power failure alarm
Alarm Functions	Ultra-high/low temperatureMotor fault
Refrigeration Power	300W
Heating Power	200W
Dimension (W × D × H)	720 × 600 × 1070 mm
Package Dimension (W × D × H)	790 × 780 × 1200 mm
Weight	85kg

Features

Microprocessor controlled unit

Multiple alarm functions

Variable oscillation modes

R134A refrigerant

Equipped with casters with lock

FAQs

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

When selecting this medical 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 medical equipment be calibrated to ensure accurate results?

It is recommended to calibrate this medical 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 medical 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 medical equipment be used with different types of samples, and are there any compatibility considerations?

Yes, this medical 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 medical 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.