Plasma Thawing System LPTSM-T2010

Introduction

Plasma Thawing System is designed to accommodate 200ml/250ml plasma in up to 12 bags or 600ml in 6 bags, ensuring efficient and scalable thawing. Its dual temperature display allows for real-time monitoring of both set and actual thermal conditions. Features built-in audible alarm that alerts users to any heat deviations or signals completion of process. The digital touch panel simplifies parameter adjustments, enhancing user convenience and operational ease. Additionally, the energy-efficient motor helps reduce power consumption while maintaining optimal thawing performance. 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

Our Plasma Thawing System automates and streamlines the process of thawing plasma, ensuring rapid and precise temperature control for reliable results in medical research, clinical diagnostics, and blood storage.

Specifications

Thawing Mode	Five modes available
Max. Plasma Capacity	200ml/250ml at 12 bags; 600ml at 6 bags
Pump Capacity	60L/min or 30L/min
Temperature Range & Precision	Room temperature to 41°C / ± 0.1°C
Vibration Frequency	30r/min
Thawing Time	Completion of a full load of bags within 30 min.
Time Function	1 to 99 min
QC Data Traceability	Dynamically tests and saves core water tank temperature data
Water Temperature Monitoring	Analyzes temperature difference between upper and lower probes for accuracy
Display	Microcomputer touch screen with real-time Temp./Time curve display
Data Records and Storage	Up to 2000 sets of data
Power Consumption	2000W
Pump Supply	220V ± 10% / 50Hz
Product Dimensions (L×W×H)	730 × 450 × 370 mm
Packaging Dimensions (L×W×H)	940 × 640 × 620 mm
Net Weight	45kg
Packaging Weight	72Kg

Features

Adjustable thawing time settings

Easy-to-clean interior chamber

Optimized for plasma preservation

Advanced thermal circulation system

Portable and lightweight design

Analyzes plasma feedback data

User-friendly Intelligent Operation System

Barcode scanning and entry data

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.