COVID-19 Antigen Rapid Test

Gently insert the entire soft tip of the swab into one nostril about 2cm until you feel some resistance. Using medium pressure, slowly rub the swab in a circular motion around the inside wall of your nose 5 times for a total time of 15 seconds. Repeat the same process with the same swab in the other nostril.

The swab is soaked after sampling below the liquid level of the sample extraction buffer, twisted several times and pressed 5-6 times, the swab soaking time is at least 1 minute. The sampling tube is squeezed while the swab is removed. The collection tube is then sealed with the cap. The liquid in the tube is the post-treatment sample.

Place the test cassette and sample extraction buffer at room temperature for 15~30 minutes and bring to room temperature (10~30?). Open the aluminum foil pouch of the test cassette and place the test cassette on a flat surface. Add 4 drops of treated sample to the sample well of the test cassette (For chromatographic abnormalities, add an additional 1 to 2 drops of treated sample). Incubate at 10~30°C for 15 minutes.

Observe results after incubation at 10 to 30°C for 15 minutes. The result obtained after 30 minutes is invalid.

Your advantages:

• CE certified
• File number of the BfArM: AT1200/21
• Special approval for self-application
• Optimized testing process
• Nasal sampling
• High specificity of 96-100%
• High sensitivity of 93-99%
• Fast and reliable test results in just 15 minutes

Scope of delivery :

• SARS-CoV-2 antigen test cassette
• sample extraction buffer
• Disposable Virus Specimen Swab
• Garbage bags for contaminated waste

Important NOTE:

Please note that a negative result never completely rules out an infection, even when the test is performed on a person with no symptoms of the disease.

COVID-19 Ag rapid tests are in-vitro diagnostics and therefore medical devices. This means that the relevant legal regulations apply to their acquisition and use. 

Please read the instructions for use before using the test

Product details: Hotgen 1er Corona self-test, nasal swab – soft pack

Application:  Suitable for private individuals and laypersons

Packaging: The tests are individually wrapped and sealed

Omicron validated

Certification: CE 0123

It is officially certified CE goods.
In the past, a special approval from the BfArM was required for the lay tests in order to sell and use the products in Germany. This special approval was considered an interim solution until the regular CE certification and is now being replaced by this.

The way of testing remains unchanged with the updated certification.
You will receive your test result in 15 minutes with the usual reliability.

Application: By trained specialists

• Test type: 4in1 (saliva test, front nose swab, back nose and throat swab, mouth and throat swab
• CE certification: CE approved
• PEI Evaluation: Positive
• Sensitivity: 98.00%
• Specificity: 100.00%

It is officially certified CE goods.
In the past, a special approval from the BfArM was required for the lay tests in order to sell and use the products in Germany. This special approval was considered an interim solution until the regular CE certification and is now being replaced by this.

The way of testing remains unchanged with the updated certification.
You will receive your test result in about 15 minutes with the usual reliability.

Important NOTE:

Please note that a negative result never completely rules out an infection, even when the test is performed on a person with no symptoms of the disease.

COVID-19 Ag rapid tests are in-vitro diagnostics and therefore medical devices. This means that the relevant legal regulations apply to their acquisition and use. 

Please read the instructions for use before using the test

Application:  Suitable for private individuals and laypersons

for self-application is used for the detection of SARS-CoV-2 antigens

• Sensitivity: 98.04% – Specificity: 100%
• Fast and reliable test results in just 15 minutes

Fast and efficient detection of an infection with the Covid-19 within 15 minutes.

The production is intended for the qualitative detection of SARS-CoV-2 Antigen (Nucleocapsid protein) in Nasal sample from patients with suspected SARS-CoV-2 infection within the first 7 days after symptom onset in vitro.

The positive results indicate the existence of SARS-CoV-2 antigen. It should be further diagnosed by combining the patient‘s history and other diagnostic information ^[1]. The positive results do not exclude bacterial infection or other viral infection. Pathogens detected are not necessarily the main cause of disease symptoms.

The negative results do not exclude SARS-CoV-2 infection, and should not be the only basis for treatment or patient management decisions (including infection control decisions). Pay attention to the patient‘s recent contact history, medical history and the same signs and symptoms of COVID-19, if necessary, it is recommended to confirm these samples by PCR test for patient management.

SARS-CoV-2 Antigen Rapid Test (Colloidal Gold) is mainly suitable for use by laboratory personnel who have undergone professional guidance or training, in vitro diagnostic expertise, or related personnel who have undergone infection control or nursing training. It is also suitable Home self-testing by non-professionals