
This product is intended for the in vitro qualitative detection of 12 respiratory pathogen nucleic acids in human throat swab and sputum samples, including:
Categor | Pathogens |
Atypical pathogen | Mycoplasma pneumoniae, Chlamydia pneumoniae |
Respiratory viruses | Influenza A virus (H1N1, H3N2, H5N1, H7N9), Influenza B virus, Parainfluenza virus (types 1–4), Adenovirus, Respiratory syncytial virus (RSV), Rhinovirus, Human metapneumovirus (hMPV) |
Regulatory Status: CE Mark certified (EU),ISO 13485 certified
Main clinical applications:
1.Comprehensive and accurate pathogenicity monitoring
2.Early diagnosis of respiratory infectious diseases
3.Rational use of medication, to avoid the abuse of antibiotics
4.Reduce the burden on patients and save medical resources
Applicable Instruments:
ABI 7500, SLAN-96S, Tianlong Gentier 96E, and other four-channel real-time PCR instruments.
1. Innovative MPA Technology
Patented Multiplex Probe Amplification (MPA) delivers high sensitivity and high specificity.
2. Single-Tube Multiplex Detection
Simultaneous detection of 10 viruses and 2 atypical pathogens (Mycoplasma pneumoniae, Chlamydia pneumoniae) in one tube.
3. Comprehensive Pathogen Coverage
Provides comprehensive detection coverage of clinically significant respiratory pathogens commonly found in outpatient, emergency, and hospitalized patients, enabling effective surveillance and early diagnosis of acute respiratory tract infections.
4. Universal Platform Compatibility
Compatible with any standard four-channel real-time PCR instrument. Closed-tube system minimizes contamination risk and ensures operator safety.
5. High-Throughput & Smart Workflow
Supports high-throughput testing for batch processing. Automated software interpretation eliminates subjective judgment.

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