Dvot Multiplex Test Kit for Respiratory Antigens 9in1 (Professional Use)

The Dvot Multiplex Test Kit for Respiratory Antigens 9in1 is a comprehensive lateral flow immunoassay for the simultaneous qualitative detection of nine major respiratory pathogens in a single test cassette. Designed for professional use in medical practices, clinics, emergency departments, and laboratories, this CE-certified point-of-care diagnostic tool enables rapid differential diagnosis of respiratory infections without requiring laboratory equipment. Buy the Dvot 9in1 multiplex test today for reliable, fast, and resource-efficient respiratory pathogen screening.

Highlights & Benefits

• 9-in-1 Multi-Pathogen Detection: Simultaneously identifies SARS-CoV-2, Influenza A, Influenza B, RSV, Parainfluenza 1–3, Human Metapneumovirus (hMPV), Adenovirus, and Mycoplasma pneumoniae from a single sample.
• Rapid Results: Lateral flow immunoassay with clear line indication delivers actionable results within the specified incubation time—no waiting for lab processing.
• Ready-to-Use Kit: Pre-filled extraction buffer, sterile swabs, and test cassettes included. No additional reagents or equipment required.
• Flexible Sample Types: Compatible with both nasal and nasopharyngeal swabs, allowing clinicians to choose the most appropriate collection method.
• Cost & Time Efficient: One multiplex test replaces up to nine individual tests, significantly reducing costs, time, and consumable waste.
• Built-In Quality Control: Integrated control line confirms sufficient sample volume and validates correct test procedure for every test run.
• CE Certified: Meets European regulatory standards for in vitro diagnostic medical devices.

Who Should Use the Dvot 9in1 Test?

• General Practitioners & Urgent Care: Differential diagnosis of acute respiratory symptoms during cold, flu, and RSV season without sending samples to external labs.
• Emergency Departments: Rapid triage of respiratory infections to prioritize isolation measures and further diagnostic workup.
• Pediatric Clinics: Broad coverage of common childhood respiratory pathogens including RSV, Adenovirus, Parainfluenza, and Mycoplasma pneumoniae.
• Care Facilities & Nursing Homes: Outbreak investigation and cluster analysis when multiple pathogens may be circulating simultaneously.
• Occupational Health Services: Rapid point-of-care screening to support return-to-work decisions and infection control protocols.
• Laboratories & Reference Centers: First-line screening tool before confirmatory PCR testing.

Detected Pathogens

The Dvot 9in1 Multiplex Test covers the most clinically relevant respiratory pathogens in a single cassette:

• SARS-CoV-2 (COVID-19)
• Influenza A
• Influenza B
• RSV (Respiratory Syncytial Virus)
• Parainfluenza Virus Type 1
• Parainfluenza Virus Type 2
• Parainfluenza Virus Type 3
• Human Metapneumovirus (hMPV)
• Adenovirus
• Mycoplasma pneumoniae

How to Use

Test procedure follows the manufacturer's instructions for professional use:

Step 1: Sample Collection
Collect a nasal or nasopharyngeal swab using the sterile swab provided in the kit. Follow standard clinical swabbing protocols for optimal sample quality.

Step 2: Sample Extraction
Insert the swab into the pre-filled extraction buffer tube and rotate vigorously to ensure thorough sample release. Remove and discard the swab according to biosafety guidelines.

Step 3: Apply to Cassette
Dispense the required number of drops from the extraction tube into the sample well of the test cassette.

Step 4: Read Results
After the specified incubation time, interpret results by reading test and control lines. The control line (C) must appear for a valid test. Any visible test line indicates a positive result for the corresponding pathogen.

Package Contents

• 1 × Dvot 9in1 Multiplex Test Cassette (individually sealed)
• 1 × Sterile Swab
• 1 × Pre-filled Extraction Buffer Tube
• 1 × Instructions for Use (IFU)

Available Variants

• Dvot Multiplex Test Kit for Respiratory Antigens 9in1 (Professional Use) – single test

Notes

• For in vitro diagnostic purposes and professional use only
• Store according to manufacturer specifications (2–30°C)
• Do not use if packaging is damaged or the test has expired
• Test results should be evaluated in clinical context; confirm with PCR or other laboratory methods if needed
• Dispose of used test materials according to local biosafety regulations
• This product complies with European in vitro diagnostic regulations