SARS-CoV-2 Rapid Antigen Test Kit (Professional Use) - Vitrosens
Rapid Antigen Test Kit

RapidFor™ SARS-CoV-2 Rapid Antigen Test Kit (Professional Use - 3in1)

The RapidFor™ SARS-CoV-2 Rapid Antigen Test Kit (Professional Use) uses the colloidal label as a tool for SARS-CoV-2 antigen detection in the collected nasopharyngeal, nasal, oropharyngeal specimens.

Advantages

–  Easy to use and read
–  No extra lab equipment
–  Variant Detection [B.1.1.7 (Alpha), B.1.351 (Beta), E484K mutation,
B1.617.2 (Delta), P.1 (Gamma), C.37 (Lambda), B.1.1.529 (Omicron) ]
–  Early phase detection
–  Easy to store and transport

Box Content

– Test Cassette
– Swab
– Extraction Buffer
– User Manual

Specification

Intended use Detection of SARS-CoV-2 antigen
Storage 2-30℃ / 35.6-86℉
Specimen type Swab
Time to result 15 minutes
Shelf life 24 months
Sensitivity 97.3%
Specificity 99.05%
Accuracy 98.09%

Video

Certifications

Our test kits are prepared according to the following standards.
celogo
iso-13001-logo
iso-logo

Frequently Asked Questions

Would you like to learn about rapid diagnostic tests, COVID-19 and our products? Here are the frequently asked questions as your guide for your journey.
How accurate is RapidFor™ Rapid Antigen Test Kit?

Clinical performance of the kit varies depending on the type of specimen analyzed. With nasopharyngeal swabs, RapidFor™ Rapid Antigen Test Kit has demonstrated 97.3% sensitivity, 99.05% specificity, and 98.09% overall accuracy.

With nasal swabs, RapidFor™ Rapid Antigen Test Kit has demonstrated 97.05% sensitivity, 99.23% specificity, and 97.99% overall accuracy. With oropharyngeal swabs, RapidFor™ Rapid Antigen Test Kit has demonstrated 95.30% sensitivity, 100% specificity, and 97.19% overall accuracy. Moreover, no cross-reactivity or interference was observed with any of the substances and pathogens tested.

Can RapidFor™ Rapid Antigen Test Kit detect SARS-CoV-2 in the early stage of infection?

Yes, RapidFor™ Rapid Antigen Test Kit can successfully detect infections with SARS-CoV-2 as early as 3-7 days after viral exposure.

In which areas can RapidFor™ Rapid Antigen Test Kit be used?

RapidFor™ Rapid Antigen Test Kit is suitable for use in a wide range of areas including schools, workplaces, clinics, laboratories, airports, and hotels, along with various forms of care, congregate, and confinement facilities.

Can RapidFor™ Rapid Antigen Test Kit detect new variants of SARS-CoV-2?

Our examinations have shown that our test kits can detect current variants of SARS-CoV-2, including B.1.1.7 UK (Alpha), B.1.351 South Africa (Beta), E484K mutation, B1.617.2 India (Delta), P.1 Brazil (Gamma), C.37 (Lambda), and B.1.1.529 (Omicron) strains.

Which advantages does Rapid Antigen Test Kit offer over an RT-PCR test?

RapidFor™ Rapid Antigen Test Kit offers many unique benefits for public health. Unlike RT-PCR tests, RapidFor™ Rapid Antigen Test Kit can detect infections with SARS-CoV-2 in just a few minutes, which reduces turnaround time, ensures immediate isolation, prevents further transmission, and aids the initiation of optimal treatment.

Is sample collection with RapidFor™ Rapid Antigen Test Kit painful?

RapidFor™ Rapid Antigen Test Kit allows for safe, non-invasive, and pain-free sample collection with user-friendly nasal, nasopharyngeal, and oropharyngeal swabs. Please follow the instructions carefully in order to ensure maximum safety, comfort, and accuracy. While mild discomfort is possible during sample collection, make sure to stop the procedure and seek medical help if you experience any pain.

What should I pay attention to while performing RapidFor™ Rapid Antigen Test Kit?

Please read the instructions thoroughly before starting the procedure. The procedure should be concluded within 15 minutes after the test cassette is removed from the foil package. Please make sure to recap the buffer solution quickly after each use and utilize the sample as soon as possible. The sample should be used within 20 minutes at most, inactivation of samples is not recommended.

What should I do if I get a negative test result?

A negative test result with RapidFor™ Rapid Antigen Test Kit does not completely exclude an infection with SARS-CoV-2. Complementary testing with RT-PCR tests may be required to rule out the risk of an active infection.

What should I do if I get a positive test result?

A positive result with RapidFor™ Rapid Antigen Test Kit is indicative of active infection with SARS-CoV-2. Please go into quarantine and contact your healthcare provider. A confirmatory test by using an RT-PCR test may be necessary.

Is the test kit reusable?

No, RapidFor™ Rapid Antigen Test Kit is designed for one-time use only.

How should I dispose of the test kit after I use it?

After the process, all samples and materials should be placed in the aluminum foil and disposed of as biohazardous waste as soon as possible. Please refrain from using the recycling bin for disposal and make sure that animals and children are out of reach.

How and for how long can I store RapidFor™ Rapid Antigen Test Kit?

RapidFor™ Rapid Antigen Test Kit can be stored be between 2°C-30°C and within 40-60% of humidity in the sealed package until its expiration date. Please make sure to check the label on the packaging for the manufacturing and expiration dates. Do not store the kit below 2°C or use it after expired date.

Order Information

Product Ref. No Pack Size Pcs/ Carton Pcs/ Euro Palette Carton Size Euro Palette Size
RapidFor™ Rapid Antigen Test (3in1) VSCD02-5 1 Box / 5 Pc. 500 6000 71x54x36 80×120
RapidFor™ Rapid Antigen Test (3in1) VSCD02-25 1 Box / 25 Pcs. 1000 20000 58x45x43 100×120

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Vitrosens Biotechnology is a high-tech company in Turkey founded for the development, manufacture, and delivery of in vitro diagnostic devices (IVD) to the world.
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Vitrosens Biotechnology is a high-tech company in Turkey founded for the development, manufacture, and delivery of in vitro diagnostic devices (IVD) to the world.
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Follow USVITROSENS on Social Media
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Copyright by Vitrosens Biotechnology. All rights reserved.

Copyright by Vitrosens Biotechnology. All rights reserved.