Blood Collection System for Test Tube Labeing for Hospital Lis

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Blood Collection System for Test Tube Labeing for Hospital Lis

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Product Description

📊 Basic Information

Certification

CE, FDA, EEC, MSDS, ISO13485

Group

Adult and Kids

Usage

Hospital Blood Collection

Transport Package

Wooden Box

Specification

480*480*520mm

Origin

China

HS Code

84729090

Capacity

100 Set/Month

💡 Intelligent Blood Collection Management System

The intelligent blood collection management system is a new blood collection management mode which is widely used in the medical industry in recent years. It has innovated the original blood collection mode, transforming crowded queuing and manual nurse checks into a simplified, efficient, and accurate automated workflow. This system eliminates manual tube selection, labeling, and sorting, optimizing the entire process for both medical staff and patients.

System Overview:

The system consists of four integrated subsystems: queuing, test tube automatic labeling, test tube delivery, and test tube sorting. It is designed for hospital outpatient clinics, physical examination centers, and high-concentration blood collection areas.

✅ Key Advantages

✔ Modular design allowing subsystems to be used separately or combined.

✔ Parallel functioning at blood collection windows for independent labeling.

✔ High-speed sorting capacity: 3100 pcs/hr with ≥ 16 categories.

✔ Rapid processing: Single device labeling speed ≤ 4s / pc.

✔ Continuous operation: Add test tubes at any time without downtime.

🔄 Operational Workflow

Patient takes a queueing number via card swipe.
Patient waits in the designated area for their number.
Nurse calls the patient to the window.
System performs automatic tube selection, printing, and labeling.
Completed tubes are placed on a conveyor belt.
Sorting system identifies and categorizes tubes via barcode scanning.

📍 Queuing & Display System

Realizes seamless interfacing with hospital LIS, managing patient information and doctor orders. It features high-definition LCD displays, intelligent voice prompts, and self-service report printing.

Component	Key Parameters
Queuing Device	22 inch infrared multi-touch screen; thermal printer
Dimensions	1500 x 520 x 310 (mm)
Waiting Room Screen	70 inch HD LCD (optional sizes available)
Window LED	Single line 8-word high definition display

🏷️ Automatic Labeling System

Dimensions	480mm × 480 mm × 520mm
Weight	32KG
Tank Capacity	240 test tubes total (8 tanks x 30 pcs)
Tube Sizes	Diameter: 12-13mm, Length: 50-100mm
Edge Searching	Automatic detection to ensure window visibility
Processing Speed	≤ 4s / pc
Data Interfaces	LIS, HIS

🚚 Tube Delivery & Sorting

Parameter	Details
Delivery Speed	≥ 18m / min
Sorting Speed	≥ 3100 pcs / hr
Sorting Categories	≥ 16 kinds (expandable)
Tank Capacity	≥ 350 pcs
Barcode Formats	Code39, Code128, EAN128, Codabar, etc.
Applicable Tubes	Diameter: 10-16mm, Length: 50-130mm

❓ Frequently Asked Questions

Can the system be integrated with existing Hospital Information Systems?

Yes, the system is designed for seamless interfacing with hospital LIS and HIS protocols to ensure smooth data transfer and patient traceability.

How fast does the tube labeling process take?

The single device processing speed is extremely fast, taking ≤ 4 seconds per test tube, which helps hospitals meet peak blood collection demands.

What happens if a barcode cannot be recognized during sorting?

The system features an alarm prompt and a separate storage function specifically for unrecognized barcodes to ensure they are handled correctly.

Is the system modular?

Yes, the four subsystems (queuing, labeling, delivery, and sorting) adopt a modular design and can be used individually or combined as a complete system.

What types of test tubes are compatible with the automatic labeler?

The labeler accommodates standard test tubes with diameters of 12-13 mm and lengths between 50-100 mm. The sorting system supports even wider ranges.

Note: The information and recommendations related to the application and end-use of the products are given in good faith based on current knowledge and experience when properly stored, handled, and applied under normal conditions. Users are requested to ensure they possess the latest documentation for accurate implementation.