Both COVID-19 and influenza A/B viruses (Flu A/B) can cause acute respiratory infections, and people are generally susceptible. These three viruses are highly contagious, spread quickly, have a short incubation period, and have a high incidence. Symptoms of COVID-19 and influenza may look similar; the main symptoms include fever, dry cough, fatigue, etc. With this combination test, healthcare workers can provide an accurate diagnosis to patients and treat them with the appropriate measures.
Feature
Results ready in 15 minutes
Accurate diagnostic tool for active infection
Easy to administer and read results
Affordable, no need for instrument, highly portable
Enable testing on a massive scale
For healthcare workers use only
To help stop the spread of COVID-19, Singclean Medical has developed COVID-19 Antigen Test Kits saliva swab which is a solid phase immunochromatographic assay for the rapid, qualitative detection of antigen from COVID-19 in human saliva swab specimen. The test provides only a preliminary test result. Therefore, any reactive specimen with the COVID-19 Antigen Test kit (Colloidal Gold) must be confirmed with alternative testing method (s) and clinical findings.
Advantage:
Quick: results ready in 15 minutes
Affordable: no need for instrument
Accurate diagnostic tool for active infection
Easy to administer and read results
Enable testing on a massive scale
Non-invasive: more comfortable than nasopharyngeal swab
Warnings
1. Use fresh samples whenever possible.
2. Positive results do not rule out bacterial infection or co-infection with other viruses.
3. A negative result can occur if the quantity of the COVID-19 antigen present in the specimen is below the detection limits of the assay, or failed to collect the COVID-19 antigen.
4. Negative results do not rule out infection with COVID-19 and should not be used as the final or sole basis for treatment or patient management decisions. Negative results should be considered in the context of a patientâ??s recent exposures, history and the presence of clinical signs and symptoms consistent with COVID-19. For a more accurate test result, repeat the tests or confirmed with other testing methods and clinical findings is recommended
CE Approved Covid-19 IgG/IgM Antibody Blood Test Kit can be used as an initial screening for qualitative and differential detection. Throughout testing the antibody of IgG and IgM immunoglobulins in human serum, plasma or blood, the test kit can show the result in a short time.
Relative sensitivity 96.00%(192/200)
Relative specificity 98.29%(806/820)
Accuracy 97.84% (998/1020)
Advantages
Fast detection: 10 minutes to interpret the result;
Easy to operate: no complex equipment required during test;
Sensitive: the product has a higher sensitivity than PCR Nucleic Acid
Global Network
Singclean@COVID-19 lgG/gM Test Kit has been sold to more than 50 countries in the worid, like Brazil, Chie,Polandï¼?spain, Bolivia, Greece, Lihuania, Ecuador, Ukraine and Turkey.
Precaution
It is worth noting that the result of Covid-19 IgG/IgM antibody blood test should not be used as the only evidence of Coronavirus diagnosis. Professional doctors and clinical findings are necessary if the result of antibody test is positive. Besides, the test kit should be operated by professionals only. Use by individuals may cause deviation in test results.
Limitation
False negative and false positive could happen. If the antibody is lower than the detection level, especially in the 7 days of the onset of symptoms, a positive patient may also be diagnosed as negative.
Dr. Guard is space sterilization and deodorant using pure chlorine dioxide.
[Dr. Guard]
* Sterilization test against COVID-19 showed a high result of 99.99% effectiveness
* Registered as a disinfectant for general disinfection in the Central Defense Countermeasures Headquarters of Korean government
* Corona 19 self-disinfecting environment approved product
* Completed safety check test and the only product certified by the Ministry of Environment
* Registered with the FDA. Safety verification completed in WHO.
* With proven technical skills, Dr. Guard has been recognized for its effectiveness in removing germs and odors.
* Obtained certifications from honorable global health institutions such as CE, FDA, PFDA and KEMENKES
[ClO2 Chlorine Dioxide]
* Chlorine Dioxide (ClO2) is a World Health Organization (WHO) recognized safety class A-1 safety material.
As a sanitary disinfectant already in Korea under the Drinking Water Management Act of 1999. It is soluble in chlorine dioxide. This is because there is no problem even when used for drinking water.
* The fatal drawback is that it is difficult to commercialize because it vaporizes quickly and is not easy to manufacture in gaseous form. However, since the sterilizing and deodorizing power is strong, manufacturers have added additional additives (sulfur, surfactant, etc.) for long-term storage.
* So, to make pure chlorine dioxide, special and difficult differentiated technology is required. Dr. Guard is a pure chlorine dioxide product made by a purely Korean technology by an honest company.
[Germs that can be sterilized by Dr. guard]
COROPNA-19 virus, N1N1, Pneumococcus, Dermatophyte, Norovirus, Pseudomonas aeruginosa, Fungi, Salmonella typhi, Staphyococcus aureus, Legionella
[Applications of Dr. Guard]
Using pure silicon dioxide chlorine sterilizing and deodorizing agent, we use the best technology in producing Dr. Guard for variety of purposes.
Bedroom, Bathroom, Refrigerator, Kitchen
No alcohol, No cancerous agents, No preservatives
Air purification, Antivirul action
[How to use Dr. Guard]
The stick contains main solution�?� and an ample (secondary solution)
1. Bend central part of the stick.
2. Once the ample inside the stick cracks, shake it enough to mix the power with the solution well.
3. As it turns yellow, the active ingredients are released to the surface of the stick.
4. After 3~4 weeks of usage, dispose stick into normal trash bag once solution inside turns transparent.
CE Approved Singclean COVID-19Test Kit (Colloidal Gold Method) is a solid phase immunochromatographic assay for the rapid,qualitative detection of antigen from COVID-19 in human nasal swab specimen.This test provides only a preliminarytest result. Therefore, any reactive specimen with the COVID-19 Test Kit (Colloidal Gold Method) must be confimed with alternative testing method(s) and clinical findings.
This rapid antigen test kit is the second test kit developed by Singclean Medical for COVID-19 testing on the basis of Colloidal Gold Method after Singclean COVID-19 lgG/IgM Test Kit, an antibody test, was launched globally in March.
Advantage
Results ready in 15 minutes
Accurate diagnostic tool for active infection
Easy to administer and read results
Affordable, no need for instrument, highly portable
Enable testing on a massive scale
For healthcare workers use only
Warnings
1. This test is not for at home testing, and should only be operated by healthcare workers.
2. Optimal assay performance requires strict adherence to the assay procedure described in this insert sheet. Inadequate or inappropriate sample collection, storage, and transport may cause false test results.
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Strengths of antigen rapid test: FAST & EASY
(Compared with PCR test)
People could RAPIDLY & EASILY be tested as a prerequisite to school attendance, work, or travel.
FAST
--PCR test - the swab test looks for viral RNA - may take days to perform.
--Antigen test might take only 15-30 minutes to complete.
EASY
--PCR test swabs must be sent to laboratory to be performed by experienced technicians, it requires expensive and specialized equipment and can take days to get result.
-- Antigen test can be run in an office or at home in about 15-30 minutes. The sampling process is FAST & EASY and requires very little expertise. Similar tests are done routinely in clinics for influenza all the time.
Korean made Gmate COVID-19 Saliva Antigen Test Kit is a rapid chromatographic immunoassay for the qualitative detection of specific antigens to SARS-CoV-2 present in human saliva specimens. This test is an aid to early diagnosis of SARS-CoV-2 infection in patients with clinical symptoms with SARS-CoV-2 infection.
â?¢ 90.9% Sensitivity, 100% Specificity
â?¢ Made in Korea
â?¢ Easy to Use
â?¢ Currently the only imported brand approved and fully registered with governments and medical / health agencies for professional and home use.
Provides initial screening result only
Disclaimer: Reactive specimens must be confirmed with alternative testing method(s)
For in vitro qualitative detection of SARS-CoV-2 nucleocapsid antigen in nasal (NS) swab specimens directly from individuals who are suspected of COVID-19 by their healthcare provider within the first 5 days after onset of symptoms.
This test is only provided for use by clinical laboratories or to healthcare workers for point-of-care testing, not for at-home testing.
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2, or 2019-nCoV) is an enveloped non-segmented positive-sense RNA virus. It is the cause of coronavirus disease (COVID-19), which is contagious in humans. SARS-CoV-2 has several structural proteins including spike (S), envelope (E), membrane (M), and nucleocapsid (N).
The antigen is generally detectable in upper respiratory samples during the acute phase of infection. Positive results indicate the presence of viral antigens, but the clinical correlation with patient history and other diagnostic information is necessary to determine infection status.
Positive results do not rule out a bacterial infection or co-infection with other viruses. The agent detected may not be the definite cause of disease.
Negative results should be treated as presumptive, which do not rule out SARS-CoV-2 infection and should not be used as the sole basis for treatment or patient management decisions, including infection control decisions. Negative results should be considered in the context of a patient's recent exposures, history, and the presence of clinical signs and symptoms consistent with COVID-19, and confirmed with a molecular assay, if necessary, for patient management.
For in vitro diagnostic use only. For professional use only .
Lateral flow assay
No equipment required
Rapid results within 10 minutes
Minimally invasive specimen collection (nasopharyngeal swabs)
POC setting (i.e. in patient care settings) by medical professionals
Detects SARS-CoV-2 nucleocapsid protein antigen with ultra high performance
Identify acute infection wit 88.4% sensitive and 100% specificity
20 test/box
20 test devices
20 assay buffer
20 extraction vials and caps
20 specifimen collection swabs
1 positive and 1 negative control swabs
1 instructions for use
Contents:
Lancet, Pipette, Silica Gel, Alcohol Swab, Test cassette
Number of Kits in a Box:
15 tests
Storage Condition:
Room Temperature
Shipping Type:
Shipping storage condition Room temperature
Analysis Time:
15 Min <
In short:
In the IgG or IgM test line area, it reacts with locally bound anti-human IgG or IgM, respectively and forms a colored line. If sample does not contain any COVID-19 antibodies, a colored line showing a negative result will not appear in any of the Test Line Areas. As a positive check for the correct performance of the tape's procedure and operation, a colored line should always be appearing in the Control Line Area. If Control Line area is empty, then the test is invalid.
Type:
FAMEX SARS-CoV-2 Saliva Antigen Rapid Test Kit
Technical:
Rapid Antigen Test Kit
Specimen Types:
Sputum
Claim:
Sensitivity .4 Specifity ,3
Contents:
Pipette, Test Cassette, Specimen Tube, Medical Waste Bag, Silica Gel
Storage:
2 C -30 C
Shipment Type:
2 C -3 C
Analysis Time:
15 Minutes
Shortly :
This kit is used for the qualitative detection of SARS-CoV-2 antigen in vitro environment. It is a lateral flow sandwich assay designed for the qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 directly in saliva.Packaging, package leaflet and manual customized for various markets.
Type:
FAMEX SARS-CoV-2 NASOPHARYNGEAL AG RAPID TEST KIT
Technical:
Rapid Antigen Test Kit
Specimen Types:
Nasopharyngeal Swab
Claim:
Sensitivity .7- Specifity .06
Contents:
Swab, Test Cassette, Specimen Tube, Medical Waste Bag,Silica Gel
Storage:
2C - 30 C
Shipment Type:
2 C- 30 C
Analysis Time:
15 Minutes
Shortly:
This kit is a rapid chromatographic immunoassay for the
qualitative detection of SARS-CoV-2 Nucleocapsid Protein in Nasopharyngeal Swab
as an aid in the scientific research of primary and secondary COVID- 19 infections.Packaging, package leaflet and manual customized for various markets.
Contents:
Swab, Test Cassette, Specimen Tube, Medical Waste Bag,Silica Gel
Number of Test:
Disposable
Storage:
2C 30 C
Shipment Type:
2�°C â?? 30�°C
Analysis Time:
15 Minutes
Shortly:
This kit is a rapid chromatographic immunoassay for the
qualitative detection of SARS-CoV-2 Nucleocapsid Protein in nasal swab
as an aid in the scientific research of primary and secondary COVID- 19 infections.Packaging, package leaflet and manual customized for various markets.
1. Nasopharynx swab specimen, non-invasive
2. Very simple to use
3. Convenient, no devices required
4. Rapid, results within 20 minutes
5. Cost-efficient
6:Listed on German BfArm ,got approval by PEI
Clinical report from local CDC
Sensitivity is 97.14%, Specificity is 100%, total accuracy rate is 99.68%.
