Adenovirus Rapid Test (1 pc/box)

Adenovirus Rapid Test (1 test/box)

The Adenovirus Rapid Test is a lateral flow immunoassay for the qualitative detection of adenovirus antigens in nasal/nasopharyngeal swab or nasal wash/aspirate specimens. Adenoviruses are a group of viruses that commonly affect the respiratory tract, causing flu-like symptoms, sore throat, pneumonia, or conjunctivitis. They can also lead to gastrointestinal infections, especially in children.

Adenoviruses are highly resistant and can survive for extended periods on surfaces and in the environment. Transmission typically occurs via respiratory droplets or contaminated surfaces. For professional use only

Specifications

Product name: Adenovirus Rapid Test Cassette

Sample type: Nasal/nasopharyngeal swab or nasal aspirate/wash

Format: Cassette

Packaging: 1 test/box

Manufacturer: Assure Tech. (Hangzhou) Co., Ltd., 3rd Floor, Building 4, No. 1418 Moganshan Road, Hangzhou, Zhejiang, China, Email: imd.assuretech@diareagent.com

EC REP: Lotus NL B.V., Koningin Julianaplein 10, 2595AA The Hague, Netherlands, Email: peter@lotusnl.com

Expiration date: 2026-11

Kit Contents

• 1 test cassette

• 1 extraction tube with buffer

• 1 sterile swab
  

• 1 user manual in English

Instructions for Use

Before testing, allow all components and samples to reach room temperature (15-30°C). Please follow the user manual carefully before proceeding.

Swab Specimen (Nasal/Nasopharyngeal)

1. Insert the swab into the extraction tube and mix thoroughly.

2. Squeeze the swab against the tube wall several times to release the sample.

3. Remove the swab while pressing it against the tube to retain liquid.

4. Close the tube and add 2 drops (approx. 100 μL) of the specimen into the sample well.

Nasal Wash/Aspirate Specimen

1. Mix sample well. Do not centrifuge.

2. Use a transfer pipette to add 300 μL to the extraction tube.

3. Follow the same procedure as above to apply the sample.

• Read results at 15 minutes.

• Do not interpret results after 30 minutes.

Result Interpretation

• Positive: Two lines appear (Control "C" and Test "T"). Any visible line in the "T" region, regardless of intensity, indicates a positive result.

• Negative: One line appears in the Control "C" region only.

• Invalid: No line in the Control region (C) – repeat the test with a new cassette.

Performance Characteristics

• Relative sensitivity: > 98.8% (93.5%–99.8%)

• Relative specificity: > 99.9% (97.1%–100.0%)

• Overall agreement: > 99.5% (97.4%–99.9%)

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