9-in-1 Antigen Rapid Test Kit for Respiratory Infections (1 pc/box)

9-in-1 Antigen Rapid Test Kit for Respiratory Infections (1 pc/box)

The new 9-in-1 Antigen Rapid Test Kit is an innovative diagnostic tool capable of detecting nine different respiratory infections quickly and reliably from a single sample! Acute respiratory infections are among the most common illnesses worldwide, with clinical symptoms ranging from common cold and pharyngitis to severe tracheitis and pneumonia. Young children, the elderly, and individuals with weakened immune systems are especially at risk, as these pathogens can lead to serious complications, particularly in the winter and spring seasons. For professional use only.

What does the test detect?

• COVID-19 (SARS-CoV-2): Primarily spreads via droplets, affects the upper and lower respiratory tracts, and may cause pneumonia in severe cases.

• Influenza A (Flu A) & Influenza B (Flu B): Infects the upper and lower respiratory tract, causing respiratory symptoms, fever, and muscle aches.

• Respiratory Syncytial Virus (RSV): A common pathogen in infants and the elderly; can lead to bronchiolitis or pneumonia.

• Adenovirus (ADV): Can cause a wide range of respiratory infections, including colds, sore throat, and more severe pneumonia.

• Mycoplasma pneumoniae (MP): An atypical bacterium that causes mild to moderate respiratory infections such as atypical pneumonia.

• Chlamydia pneumoniae (CP): Another atypical bacterium that can cause sore throat or pneumonia.

• Parainfluenza Virus 1/3 (PIV 1/3) & Parainfluenza Virus 2 (PIV 2): Often cause croup, bronchitis, and other respiratory infections.

Why choose this test?

• Fast results: Reliable diagnosis in a short time.

• Broad-spectrum detection: One test, nine pathogens.

• Easy to use: Suitable for both clinical and point-of-care settings.

• Accurate: Enables targeted treatment based on quick diagnosis.

Specifications

Product name: 9-in-1 Antigen Rapid Test Kit for Respiratory Infections

Sample type: Nasal swab (1.5 cm insertion depth)

Packaging: 1 pc/box

Format: Cassette

Manufacturer: Shenzhen Reagent Technology Co.,Ltd., 906–907, Yonghui Business Building, Xixiang Street, Bao'an District, Shenzhen, Guangdong, 518102, Kína, +86 755 2300 6611, reagen1@126.com

EC REP: CMC Medical Devices & Drugs S.L, C/Horacio Lengo No.18, 29006, Malaga, Spanyolország, +34 951214054, info@cmcmedicaldevices.com

Expiry date: 2027.03.19

Box Contents

• 1 test cassette

• 1 sterile swab

• 1 sample extraction buffer
  

• 1 instructions in English 

Test Procedure

Please read the instructions carefully before performing the test. Collect the sample as described in the manual. Let all materials (devices, reagents, samples, and/or controls) reach room temperature (15°C-30°C) before use.

After sample collection:

1. Remove the aluminum foil from the sample extraction tube.

2. Insert the swab containing the collected sample into the tube, ensure the buffer saturates the swab, rotate and press the swab 5 times, then remove and discard it.

3. Replace the cap on the extraction tube and close tightly. Shake gently for approx. 5 seconds to ensure thorough mixing.

4. Add 3 drops of the mixed solution into the sample well of the test cassette and start the timer.

5. Read the result after 10 minutes. Results are invalid after 20 minutes.

Performance

• Clinical Sensitivity: 96.20%

• Clinical Specificity: 98.90%

• Accuracy: 97.65%

Legal Notices

Professional Use

This product is an in vitro diagnostic (IVD) and intended exclusively for professional use by medical personnel. Use for self-testing is not permitted. The manufacturer/distributor accepts no liability for damages resulting from improper or unauthorized use.

Right of Withdrawal

In accordance with § 312g (2) No. 3 of the German Civil Code (BGB), there is no right of withdrawal for sealed goods which, for reasons of health protection or hygiene, are not suitable for return if their seal has been removed after delivery.

Disclaimer

The seller assumes no responsibility for compliance with legal regulations within the buyer’s procurement process. The seller’s responsibility is limited solely to the delivery of the ordered goods and the provision of information regarding their proper use.

Instructions