Product details & mandatory information
The CLEARTEST® HIV 1.2 is a highly accurate rapid test for the qualitative detection of antibodies to human immunodeficiency virus (HIV) type 1 and type 2 in human whole blood, serum or plasma. This reliable diagnostic tool offers a quick and easy way to support HIV diagnosis and is specifically designed for professional in vitro diagnostics.
Key features
- Fast and reliable: The CLEARTEST® HIV 1.2 enables rapid diagnosis of HIV infection through the qualitative detection of HIV antibodies in various sample types.
- High accuracy: With a sensitivity and specificity of over 99.9 %, this test offers exceptionally precise results.
- Easy to use: The test is based on a chromatographic immunoassay that provides a clear and understandable interpretation of the results. In the presence of HIV antibodies, two coloured lines appear in the test area.
- Versatile sample type: The CLEARTEST® HIV 1.2 can be performed with whole blood (from venipuncture or finger prick), serum or plasma.
Field of application
The CLEARTEST® HIV 1.2 is used for the qualitative detection of antibodies against HIV type 1 and type 2. It supports healthcare professionals in the diagnosis of HIV infections and helps to enable early treatment.
Principle of the test
The test utilises recombinant HIV antigens coated on a membrane. During the test, the HIV antibodies in the sample react with these antigens. The results are indicated by the appearance of coloured lines, which indicate the presence or absence of HIV antibodies.
Manufacturer: Servoprax GmbH
Ideally suited for
- Hospitals
- Medical practices
- private individuals
- Inpatient and outpatient facilities
Advantages
- Quick and easy to perform.
- Highly accurate results.
- Safe and reliable to use.
Important notes
Use is recommended for healthcare professionals only
Notes on returns
For consumers, the right of cancellation does not apply to contracts for the delivery of sealed goods that are not suitable for return for reasons of health protection or hygiene if their seal has been removed after delivery.
Important notes
- Use by specialised personnel only: The test is intended exclusively for in-vitro diagnostics by trained personnel.
- Storage: The test should be stored at room temperature or refrigerated (2-30 °C) and is stable until the expiry date stated on the packaging. Do not freeze.
- Specimen handling: For accurate results, the test must be performed immediately after specimen collection. Samples should not be frozen and thawed repeatedly.
Instructions for use 
