Fully Automated Nucleic Acid Analysis System | Molecular POCT with Ultra-Multiplex qPCR

Model: GHM CQ-0404 Fully Automated Nucleic Acid Analysis System

Fully automated molecular POCT system with centrifugal microfluidic technology, 28-target ultra-multiplex qPCR, and "sample in, result out" workflow. Ideal for hospitals, ICUs, and labs.

The Global Healthcare Medical Fully Automated Nucleic Acid Analysis System is a groundbreaking molecular point-of-care testing (POCT) platform that redefines infectious disease diagnostics. By ingeniously integrating centrifugal microfluidic technology with real-time fluorescent PCR, this system delivers ultra-multiplex detection of up to 28 targets from a single sample in just 60–85 minutes.

Designed with a "sample in, result out" philosophy, the system automates the entire workflow—from nucleic acid extraction and purification through to amplification and detection—eliminating the need for a dedicated PCR laboratory or specially trained operators. Its fully enclosed cartridge design, combined with silica membrane-based purification and gold-standard qPCR, ensures exceptional accuracy while preventing cross-contamination.

With the capacity to process up to 4 samples per run and 24 samples per day, this system is engineered for high-throughput clinical environments. Whether deployed in hospital inpatient wards, intensive care units, emergency departments, or central laboratories, it delivers the speed, accuracy, and ease-of-use that modern molecular diagnostics demand.

This device is intended for professional use in clinical settings by trained healthcare professionals. Not a substitute for professional medical diagnosis.

Key Features

🧬 Ultra-Multiplex Detection Capability

The system leverages advanced centrifugal microfluidic technology to deliver unparalleled multiplexing power:

• Up to 28 targets per sample – Comprehensive pathogen detection from a single specimen

• 7 qPCR chambers + 4 fluorescence channels – Enables simultaneous detection of multiple pathogens in one run

• Broad pathogen panels – Upper respiratory, gastrointestinal, reproductive tract, meningitis, lower respiratory with antimicrobial resistance genes, blood culture, arboviral, and malaria panels available

⚡ Fully Automated "Sample In, Result Out" Workflow

Eliminates manual intervention and reduces the risk of human error:

• Automated nucleic acid extraction – Centrifugal force precisely controls the sequential release of lysis buffer, wash buffer, and elution buffer

• Integrated qPCR amplification – Proprietary lyophilized reagents pre-dispensed into microfluidic chips enable room-temperature storage and shipping

• End-to-end automation – From sample loading to result reporting, no PCR laboratory or professional operator required

• Minimal training – Intuitive touch-screen operation with less than 10 minutes of training needed

🛡️ Accuracy and Contamination Control

Engineered for clinical confidence:

• Silica membrane-based purification – Ensures high-purity nucleic acid extraction for reliable qPCR results

• Laser surface welding technology – Creates a fully sealed system that prevents amplicon contamination

• Gold-standard qPCR – Delivers the sensitivity and specificity that clinicians trust

• Built-in quality controls – Positive and negative controls included with each kit

📊 High Throughput for Busy Laboratories

Designed to meet the demands of high-volume clinical settings:

• 4 samples per run – Process multiple patients simultaneously

• Up to 24 samples per day – Maximizes laboratory efficiency

• 60–85 minutes total run time – Rapid time-to-result for critical clinical decisions

• CE certified – Meets rigorous European regulatory standards

🔬 Robust Engineering and Design

Built for reliability in demanding clinical environments:

• Instrument weight: 20 kg – Stable, benchtop design

• Dimensions: 580 × 350 × 305 mm – Compact footprint

• Temperature control accuracy: ≤0.5°C – Precise thermal cycling for optimal amplification

• Operating temperature: 15–30°C – Suitable for diverse laboratory conditions

• 4 fluorescence channels: FAM, CY5, ROX, VIC – Flexible dye selection for multiplex assays

📱 User-Friendly Interface and Connectivity

Streamlines workflow and data management:

• Intuitive touch-screen operation – Load, scan, click, and go

• Automatic LIS/HIS integration – Seamless connectivity with laboratory and hospital information systems

• Customizable report templates – Flexible reporting to meet institutional requirements

• Barcode scanning – Efficient sample and chip information tracking

Specifications

Available Test Panels

*Includes optional additional target

What's Included

• Fully Automated Nucleic Acid Analysis System Main Unit

• Power Cable

• Balance Chips (4 units)

• User Manual

• Calibration Certificate

Applications

The Fully Automated Nucleic Acid Analysis System is suitable for:

• Hospital Inpatient Wards – Rapid diagnosis of respiratory and bloodstream infections

• Intensive Care Units (ICU) – Critical care pathogen identification

• Emergency Departments – Fast turnaround for acute infectious disease presentations

• Clinical Laboratories – High-volume molecular diagnostic testing

• Infectious Disease Clinics – Comprehensive pathogen screening

• Public Health Laboratories – Outbreak surveillance and monitoring

Why Choose the Fully Automated Nucleic Acid Analysis System?

FAQ

Q: What is a fully automated nucleic acid analysis system?
A: This is a molecular point-of-care testing platform that automates the entire nucleic acid testing workflow—from extraction and purification to amplification and detection—using centrifugal microfluidic technology and real-time PCR.

Q: How many targets can be detected per sample?
A: The system can detect up to 28 targets from a single sample, making it one of the most highly multiplexed molecular diagnostic systems available.

Q: How many samples can be processed per run?
A: The system processes up to 4 samples per run, with a capacity of approximately 24 samples per day.

Q: How long does a test take?
A: Total run time is 60–85 minutes from sample loading to result reporting.

Q: Does the system require a dedicated PCR laboratory?
A: No. The fully enclosed cartridge design and automated workflow eliminate the need for a dedicated PCR laboratory or specially trained PCR operators.

Q: What sample types are supported?
A: The system supports various sample types depending on the test panel, including nasopharyngeal swabs, sputum, blood, stool, and other clinical specimens.

Q: What test panels are available?
A: Available CE-marked panels include Upper Respiratory Tract (26 targets), Reproductive Tract (10 targets), Gastrointestinal Tract (26 targets), Meningitis (19 targets), Lower Respiratory Tract with AMR genes (23 targets), Arboviral (8 targets), and Malaria (4 targets).

Q: Is the system CE marked?
A: Yes, the system and most test panels are CE certified for the European market.

Q: What is the weight and size of the instrument?
A: The instrument weighs 20 kg and measures 580 × 350 × 305 mm.

Q: What connectivity options are available?
A: The system integrates seamlessly with Laboratory Information Systems (LIS) and Hospital Information Systems (HIS) for automatic result upload.

Q: What is the delivery lead time?
A: The delivery lead time is approximately 10 working days.

Q: What is the warranty period?
A: The system comes with a 1‑year warranty.