Covid antigen rapid test kit made in Turkey seller : manufactory company minimum order : 10,000 pcs Licensed in Europe and UK 1 box 25 pcs T/T
[Intended Usage] This kit is used for the in vitro qualitative detection of suspected cases of pneumonia caused by New Coronavirus infection, patients with suspected clusters, other patients who need to be diagnosed or differentially diagnosed with the New Coronavirus infection, and nasopharyngeal swabs, oropharyngeal swabs, and bronchoalveolar lavage fluid samples of patients with mutation beads for the New Coronavirus ORF1ab and N gene, S gene N501Y mutation and S gene E484K mutation sites. [Storage Conditions & Validity] 1. The kit should be stored frozen at -20 and protected from light; the expiration date is 6 months; the production date and expiration date are shown in the outer packaging box. 2. Avoid repeated freezing and thawing of the kit and the number of freezing and thawing shall not exceed 7 times. 3. After opening, the bottles should be stored at -20 and protected from light. The number of bottles opening times should not exceed 7 times, which will not affect the use within the validity period. [Applicable Instruments] 1. This kit has been validated on ABI7500 quantitative fluorescence PCR instrument. 2. For other models not listed, relevant experiments have not been performed or completed for this kit. If users need to use this type of instrument platform to carry out the detection of this reagent, please contact our Technical Department at for relevant support. NB: The other devices can include quantitative fluorescence PCR platforms with FAM, VIC, ROX and Cy5 channels. [Sample Requirements] 1. Nasopharyngeal swabs, oropharyngeal swabs and other methods are used to obtain samples, and it is recommended to use commercial virus sampling kits for sample collection devices. [Test Results Interpretation] 1. Negative and positive controls should be tested in each experiment and the test result can be determined only when the controls meet the quality control requirements. 2. When FAM, VIC and ROX channels are positive, Cy5 channel result may be negative due to the system competition. 3. When the internal standard result is negative, if the FAM, VIC and ROX signals of the test sample are also negative, the test result of the sample is invalid, and the cause should be found and eliminated, and the experiment repeated for this sample. [Product Performance Index] 1. Precision: The coefficient of variation Intra-batch / Inter-batch, Intra-day / Inter-day among different operators shall not be higher than 5.0%. 2. Coincidence rate of negative positive controls: The coincidence rate of positive controls and negative controls is 100%. 3. Minimum detection limit: The minimum detection limit of this kit is 500 copies/mL. [CE Mark Registration No.]: RPS/499/2021. [EC REP.]: CMC MEDICAL DEVICES & DRUGS S.L. C/ Horacio Lengo n18, C.P 29006, Milaga, Spain.
INTENDED USE For qualitative detection and differentiation of IgM and IgG antibodies to SARS-CoV-2 in serum, plasma (EDTA, sodium citrate and lithium heparin) or fingerstick whole blood, venous whole blood specimens from patients suspected of COVID-19 infection. FEATURES Coated with carefully selected specific Nucleocapsid and Spike protein antigen. Detection for IgM and IgG antibodies simultaneously. Simple operation, easy result interpreted. Rapid test within 15 minutes. RESULTS INTERPRETATION Positive: 1. The presence of 3 red lines (T1, T2 and C) within the reaction window, no matter which band appears first, indicates presence of both SARS-CoV-2 IgM and IgG antibodies. 2. The presence of 2 red lines (T1 and C) within the reaction window, no matter which band appears first, indicates presence of SARS-CoV-2 IgM antibody. 3. The presence of 2 red lines (T2 and C) within the reaction window, no matter which band appears first, indicates presence of SARS-CoV-2 IgG antibody. Negative: 1. The presence of line (control line) only within the reaction window indicates that no SARS-CoV-2 antibodies are detected. The results is negative. Invalid: 1. If the control(C) line is not displayed in 10-15 min, regardless of whether T1 and/or T2 line is present, the test result is invalid. It is recommended that the specimen should be re-tested. 2. The test result is invalid after 15 min. CLINICAL PERFORMANCE - Positive Percent Agreement (PPA) = 91.07% (153/168) (95% CI: 85.70%-94.92%). - Negative Percent Agreement (NPA) = 95.37% (103/108) (95% CI: 89.53%-98.48%). - Overall Rates of Agreement (ORA) = 92.75% [(153+103)/ (168+108)] (95% CI: 89.03%-95.52%). [Product Name]: SARS-CoV-2 IgM/IgG Duo Test [Product Code]: Cat# FP-319 [Sample Type]: Whole blood /Plasma/Serum [Sample Volume]: 20L /10L/10L [Detection Method]: Colloidal Gold [Reaction Time]: 10-15min [Packing Size]: 1T x 20 cassettes per box + Sample diluent 1 vial x 5mL. [Storage Condition]: 2oC ~ 30oC [Shelf Life]: 12 months [CE Mark Registration No.]: RPS/499/2021.
Covid Ab IgG/IgM Ab Whole blood test device Covid Antigen Ag swab rapid test card Covid Antigen Ag saliva rapid test card
Rapid Antigen and Antibody test kit covid 19 Manufacturer: Shenzhen Lvshiyuan Biotechnology Co., Ltd / Green Spring Brand The time required: 15 -20 minutes Detect the virus 3 days after the infection Accuracy: High Specificity: High Cost Saving : Low cost
SARS-CoV-2 Antigen Test Kit CRDLIGHT 25 pcs/ box 5 pcs/ box
Medical Sterile Cotton Swab to collect specimen of corona virus VTM (Viral Transport medium) to deliver the specimen samples to testing place
COVID-19 antigen rapid test Simple Accurate Safe 1 PU * (25 pieces) specificity 99.0%, sensitivity 97.3%, overall accuracy 98.1% From 4 PUs : one FFP2 mask per test free of charge * PU = Packing unit; 1 PU = 25 pieces; Offer valid while supplies last. For bulk orders of 1000 or more, please contact us
COVID-19 antibody test 1 PU * (25 pieces) from 4 PUs : one FFP2 mask per test free of charge * PU = packaging unit; 1 PU = 25 pieces; Offer valid while supplies last. PU = Packing unit; 1 PU = 25 pieces; Offer valid while supplies last. For bulk orders of 1000 or more, please contact us
Covid 19 detection kit, famous for efficient detection of Covid 19/coronaVirus made in south korea
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 Sensitivity 98.56% Sensitivity 99.03% Accuracy 98.84% 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.
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)
The CareStart COVID-19 Antigen Test is a lateral flow immunochromatographic assay for the detection of extracted nucleocapsid protein antigens specific to SARS-CoV-2 in swab specimens directly collected from symptomatic individuals who are suspected of COVID-19 by their healthcare providers. Kit Includes 20 Test Devices 20 Assay Buffer 20 Extraction Vials and Caps 20 Specimen Collection Swabs 1 Positive and 1 Negative Control Swabs 1 Instructions for Use
We supply: COVID-19 tests Tests: COVID-19 IgM COVID-19 IgG COVID-19 Antigen Rapid Test COVID-19 A+B.
Standard Q Covid 19 Ag is a rapid chromatographic immunoassay for the qualitative detection of antigens specific to SARS-CoV-2 in swab samples collected from a human nasopharynx. Fast results within 15~30 mins Easy to useSpecimen : Nasopharyngeal swab All necessary reagents provided & no equipment needed
We offer antigenic tests saliva and nasal. Product free of EU customs clearance. Shipment according to quantities averages 2-3weeks.
