Platelet Incubator LPTI-T2011

Introduction

Platelet Incubator maintains a stable temperature range of 20 to 24 °C, ensuring optimal storage conditions for platelet preservation. Prevents ice build-up, ensuring consistent temperature, optimal storage conditions, and maintenance-free operation. It uses forced air cooling to ensure stable temperature and uniform airflow. Our Platelet Incubator stores and preserves platelets with precise temperature control and gentle agitation.

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 is used in medical and laboratory settings to preserve platelets under stable conditions. It maintains an ideal environment to ensure platelet quality before transfusion.

Specifications

Temperature	20℃ to 24℃
Ambient Temperature	10℃ to 32℃
Cooling Method	Forced air cooling
Noise	53 db
Temperature Controller	Microprocessor
Sensor
Refrigerant	R134a
Power Failure Backup	72 H
Drawer Quantity	7 layers
Platelet Bag Quantity	14 layers
Oscillation Frequency	60±5 e/min
Oscillation Amplitude	50±10 mm
Shipping	0.5
Current	1.3 A
Power	2700 W
Power Consumption	197 W
Power Supply	220V 50Hz / 110V 60Hz
Internal Dimension (W×D×H)	427 × 360 × 467 mm
External Dimension (W×D×H)	522 × 600 × 1056 mm
Packaging Dimensions (W×D×H)	590 × 710 × 1200 mm
Net Weight	68 kg
Gross Weight	90 kg

Features

Integrated quiet agitation system

Real-time data printing

Extended power failure backup

Reliable five-alarm system

Mobile lockable caster wheels

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.