FQD-A9600 Fully Automated Gene Analysis System

Delivers end-to-end unattended automation from raw sample tubes to PCR results, providing efficient, safe, and intelligent nucleic acid testing solutions for hospital laboratories, third-party medical testing centers, disease control agencies, and research labs.

FQD-A9600

Core Features

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End-to-End Automation

Achieves full-process automation from sample tube to PCR result. Operators simply load samples; all remaining steps are completed automatically.

High Throughput

Supports 1–96 samples per batch, over 2,200 samples in 24 hours. The first round takes only 2 hours.

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Safety Certified

Class III Medical Device Registration Certificate issued by the National Medical Products Administration.

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Pipeline Detection

Rolling detection mode: each round after the first 2-hour takes just 1 hour.

Integrated Workflow

Completes cap opening, scanning, transfer, extraction, PCR setup, sealing, and detection for 96 samples in a single operation.

Clinically Qualified

Full-scenario clinical application qualifications, validated against national metrology technical specifications.

Application Areas

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Hospital Laboratories

Routine and emergency nucleic acid testing for clinical departments.

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Medical Testing Facilities

Large-scale screening services for third-party medical laboratories.

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Centers for Disease Control and Prevention

Infectious disease surveillance and public health emergency response.

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Research Institutions

High-throughput nucleic acid extraction solutions for universities and research institutes.

Technical Specifications

AttributeDescription
Product ModelFQD-A9600
Product NameFully Automated Gene Analysis System
Sample Capacity1-96 samples per batch
24h ThroughputOver 2,200 samples
First Round Time2 hours
Subsequent Rounds1 hour per round
Automation StepsCap opening, scanning, transfer, extraction, PCR setup, sealing, detection
CertificationNMPA Class III Medical Device Registration

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