We are supplying FDA's EUA approved Covid 19 Test Kit to the US. Our COVID-19 Detection Kit is a real-time PCR based in-vitro diagnostic product intended for detection of the novel coronavirus SARS-CoV-2 (COVID-19) RNA in sputum, bronchoalveolar lavage, oropharyngeal or nasopharyngeal smears collected from patients with suspect viral infection The kit is composed of Internal Positive Control (IPC), to monitor appropriate performance of amplification and detection of the kit. Accurate detection of the viral RNA is confirmed parallelly by using Positive and Negative controls which are composed in the kit
The test is a rapid colloidal gold immunochromatographic assay for the in vitro qualitative detection of the novel coronavirus(SARS-CoV-2), the influenza A virus (FluA) and the influenza B(FluB) antigen in human nasopharyngeal swab, oropharyngeal swab, nasal swab, and saliva samples from individuals suspected of respiratory viral infection.
25tests*40box/ctn professional antigen test kit by nasal swab carton size : PEI BFARM CE certificate 53.5*50*34CM GW:16KG
We Supple Grade A medical examination Disposable Covid-19 test kit and Syringes with affordable prices in major international market free to contact us for more Quotation.
The iNSTAXPLOR 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. SALIENT FEATURES -Best suited for early detection of COVID â?? 19 infection from the onset of symptoms -Point-of-care test / On the spot test -Quick results in 15 to 30 mins -ICMR validated and approved -No Equipment required - All Material provided in the Kit to perform the test -Recommended for administration by qualified healthcare workers -Storage at Room Temperature (2-30C). -Shelf life: 24 months
RAPID ANTIBODY/Finger Prick 10 to 15 Minute Results An antibody test is also known as a serology test looks for the presence of antibodies, which are specific proteins made in response to infections. It is effective at detecting the recent past SARS-CoV2 infection. This test can detect the body's IgM Antibody response in as little as 7 days (IgG in 14 days) from infection with CDC validated 100% specificity and 100% sensitivity. The highest accuracy serological test on the market FDA EUA Approved Manufactured by one of the leaders in lateral flow technology Results in 10-15 minutes FINGER PRICK NO LAB RESULTS REQUIRED
A blood test measures the amount of antibodies your body's defences have produced if you have been exposed to the virus.
Due to contractual obligations to the federal government, Current suppliers have increased costs and limited production of all point of care tests without notice. We have great news! To shield our customers from excessive price increases as well as provide immediate availability, we have secured multiple FDA EUA rapid antigen test kit options. These tests have similar and/or better accuracy along with individual buffer bottles. We are currently able to provide three options: Clarity-Sienna, Indicaid and Celltrion DiaTrust kits. We work directly with the distributor and can supply by the pallet or case with pricing as low as $6.00 per kit.
Types of Transport Systems Suitable for Test of COVID-19 The formula contains special ingredients to maintain and store viruses for a longer time. It helps viruses to maintain its viability. Flocked Swab Suitable for Sample Collection of Different Types of Virus Specimens Flocked swab can uptake and release sample into liquid medium better than rayon swab. Room Temperature Storage up to 96 Hours Good Virus vitality and infectivity after stored under room temperature 96 hours
Specimen Collection: Nasal, Saliva Packing: 1 test / 25 Tests Accurancy: >93% Specificy: 99% Warranty: 2 year Certificate: CE, ISO13485,BfArM,BASG,MDA,Thai FDA
CAT No : RK055-25. STANDARD Q COVID-19 Ag is a rapid Immunochromatographic assay for the qualitative detection of specific antigens to SARS-CoV-2 present in human nasopharynx. Qualitatively detects specific antigens to SARS-CoV-2 present in Human Nasopharynx. The test should be used as an aid in early diagnosis of symptomatic cases in healthcare setting having ILI. Validated by ICMR & AIIMS Sensitivity of 84.38 % & Specificity of 100% Sample Type- Human Nasopharyngeal swab (No other sample recommended) Results in 15-30 mins
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.
Direct to the seller side Covid-19 Rapid Antibody, Antigen Test Kits Covid-19 Vaccine -> Currently actively working with many govt bodies experiencing Massive success. after my own dd & NCNDA, will link you up directly to the sell side. this is as close as you can get to the end seller for this sort of commodity. Contact me for more information. There are however, a very high demand and I experience high volumes of enquiries daily and i do not wish to waste anyone time. Looking for a sincere long term working relationship/partnership. so any circumventing, funny business will not be tolerated.
* NEW* Covid-19 ANTIGEN RAPID TEST KIT *NEW * with CE Mark EU APPROVED | Collodial Gold Method | 15 Minutes Rapid Covid-19 Rapid Antigen Test Kit | Collodial Gold Method Accurate: 96.1% sensitivity, 96.67% specificity compared with PCR FAST: only 15 minutes required EASY-TO-USE: no special requirements Room temperature storage MOQ 2000 units (25pcs) per unit MAX 300.000 units PER DAY Payment terms 100% TT in Advance Lead time 7 days Global delivery Results
Antigen test kits Allocation Available 10 Million pcs/month MOQ : 2.5M Pcs $5.80 including (CIF Via AIR) SOP: ICPO/POF Commercial Invoice/SPA/POP SBLC AWB/SGS/Delivery SBLC Released
The CorDx COVID-19 Ag Test is a lateral flow immunoassay device intended for the qualitative detection of nucleocapsid protein antigen from the SARS-CoV-2 virus. View File Non-prescription home use for the qualitative detection of nucleocapsid protein antigen from the SARS-CoV-2 virus with self-collected anterior nasal (nares) swab samples from individuals aged 14 years or older or adult collected anterior nasal (nares) swab samples from individuals aged 2 years or older. This test is authorized for individuals with symptoms of COVID-19 within the first 7 days of symptom onset when tested at least twice over three days with at least 48 hours between tests, and for individuals without symptoms or other epidemiological reasons to suspect COVID-19, when tested at least three times over five days with at least 48 hours between tests.
The CorDx COVID-19 Ag Test is a lateral flow immunoassay device intended for the qualitative detection of nucleocapsid protein antigen from the SARS-CoV-2 virus. View File Non-prescription home use for the qualitative detection of nucleocapsid protein antigen from the SARS-CoV-2 virus with self-collected anterior nasal (nares) swab samples from individuals aged 14 years or older or adult collected anterior nasal (nares) swab samples from individuals aged 2 years or older. This test is authorized for individuals with symptoms of COVID-19 within the first 7 days of symptom onset when tested at least twice over three days with at least 48 hours between tests, and for individuals without symptoms or other epidemiological reasons to suspect COVID-19, when tested at least three times over five days with at least 48 hours between tests.
1. Generic Name: Novel Coronavirus COVID-19 IgG Antigen Test Kit 2. Brand Name: NIL 3. Notified Category: Other than above substances intended for qualitative determination of COVID-19 infection 4. Class of Medical Device: Class D 5. Shelf life :15 months 6. Sterile/Non-Sterile: Non-Sterilized 7. Contains Drugs: No 8. Medical Device Grouping Category: IVD-Kit 9. Grouping Description: Intended for qualitative determination of COVID-19 infection 10. Intended Use: The Novel Coronavirus COVID-19 IgG Kit is intended for the qualitative detection of human anti-COVID- 19 IgG antibody in human serum/plasma. Any reactive specimen with the Novel Coronavirus COVID-19 IgG Kit must be confirmed with alternative testing method(s). 11. Product Description: Assay controls and 1:10 diluted human serum samples are added to the microtiter wells of a microplate that was coated with COVID-19 recombinant full length recombinant protein. After the first incubation period, the unbound protein matrix is removed with a subsequent washing step. A horseradish peroxidase (HRP) labeled polyclonal goat anti-human IgG tracer antibody is added to each well. After an incubation period, an immunocomplex of "COVID-19 recombinant antigen-human anti-COVID-19 IgG antibody - HRP labeled anti human IgG tracer antibody" is formed if there is specific Coronavirus IgG antibody present in the tested specimen. The unbound tracer antibody is removed by the subsequent washing step. HRP-Labeled tracer antibody bound to the well is then incubated with a substrate solution in a timed reaction and then measured in a spectrophotometric microplate reader. The enzymatic activity of the tracer antibody bound to the anti-COVID-19 IgG on the wall of the microtiter well is proportional to the amount of the anti-COVID-19 IgG antibody level in the tested specimen. SALIENT FEATURES: â?¢ Recombinant COVID-19 Spike subunit Protein coated on Microwell Plate â?¢ HRP Conjugated Polyvalent Anti-Human IgG â?¢ Assay Time: 80 mins (30mins+30 Mins+20mins) â?¢ Strip Format Microwell Plate â?¢ Ready to use Substrate and Controls â?¢ Only 20 pL of human serum is required for measurement in duplicate. â?¢ Works on any open ELISA system â?¢ Assay procedure is easy to automate OUR TEST: â?¢ Principle: Indirect ELISA â?¢ The normal healthy patients with samples collected prior to the COVID-19 outbreak [December 3, 2019] (n = 150) and RT-PCR confirmed positive patients in after the second week of the onset of the disease (n = 32). The Positive sample evaluation was done at external Approved Lab. The results are as follows: â?¢ Diagnostic sensitivity is 100% (>98%) â?¢ Diagnostic specificity is 98.67% (>97%) â?¢ PPV: 94.12�°/0 â?¢ NPV: 100% Please contact us for more information and product details.
Covid 19 Rapid Antigen Test Kits Brand: Healgen Scientific Antigen Protein Swab Rapid Test 96% Accurate 15 Minute Response
Boson Antigen Test Kits OTC 1M 2M 5M 10M 50M 100M
