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The HIV 1/2 Ab Rapid Test Cassette (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay with a double antigen system for the qualitative detection of antibodies to HIV-1 and/or HIV-2 in whole blood, serum or plasma. It is intended to be used as a screening test and as an aid in the diagnosis of infection with HIV. Any reactive specimen with the HIV 1/2 Ab Rapid Test Cassette must be confirmed with alternative testing method(s).

Name: Novel Coronavirus (SARS-Cov-2) Antigen Rapid test Cassette (saliva). Quality: Applicable Standarts: EN ISO 13485:2016; EN ISO 15223-1:2016; EN ISO 14971:2012; EN ISO 13612:2002; EN ISO 17511:2003; EN ISO 18113-1:2011; EN ISO 23640:2015. Tests meets the provisions of the Directive 98/79/EC of the European Parliament and of the Council on In-Vitro Diagnostic Medical Devices Origin: China, manufacturer HANGZHOU REALY TECH CO, LTD. Quantity: 100 000 Cassettes per week. 1 pallet Cassettes; Packing: 5 test kits/ inner box, 500 tests/carton, Gross weight per carton: 9.2 KGS; Delivery terms: FCA Vilnius, Lithuania (EU) (Incoterms 2010); The price includes customs duties and transport, VAT 0%;

Name: Novel Coronavirus (SARS-Cov-2) Antigen Rapid test Cassette (swab). Quality: Applicable Standarts: EN ISO 13485:2016; EN ISO 15223-1:2016; EN ISO 14971:2012; EN ISO 13612:2002; EN ISO 17511:2003; EN ISO 18113-1:2011; EN ISO 18113-1:2011; EN ISO 23640:2015. Tests meets the provisions of the Directive 98/79/EC of the European Parliament and of the Council on In-Vitro Diagnostic Medical Devices Origin: China, manufacturer HANGZHOU REALY TECH CO, LTD. Quantity: 100 000 Cassettes per week.; Packing: 5 test kits/ inner box, 500 tests/carton, Gross weight per carton: 9.2 KGS; Delivery terms: FCA Vilnius, Lithuania (EU) (Incoterms 2010) The price includes customs duties and transport, VAT 0%;

Dear Sir/Madam If you are someone who appreciated high quality,high cost-effective rapid test cassette, then I've got some helpful information with you. I am the sales manager of Avioq Bio-tech Co., Ltd. We are mainly engaged in the R&D, production, sales and services of in-vitro diagnose (IVD) reagents in biomedical field. We help many start-ups and well-known brands grow and expand business in their market.Let me know if you are interested on taking a look at our lastest catalogue. Email:

HBsAg Rapid Test Cassette Uncut Sheet Specimen :WB/S/P Size :300*60mm One-Step HBsAg Rapid Test is to detect the Hepatitis B Virus Surface Antigen in serum, plasma or whole blood. Analytical sensitivity : 1ng/ml of HBsAg Sensitivity :100% , Specificity : 100% Specimen : Serum , Plasma or Whole Blood Reading Time : 10 min

We have on stock in Romania CLUNGENE COVID-19 Antigen Rapid Test Cassette 20 pcs/box and CLUNGENE COVID-19 Antigen Rapid Test Individual, 1 pcs/pack. For more info, please contact us. .

The IgM rapid Test Cassette (Serum/Plasma) is a lateral flow chromatographic immunoassay for the qualitative detection of IgM antibodies in human serum to Rheumatoid Factor (RF) antigen. It is intended to be used as ascreening test and as an aid in the diagnosis of rheumatoid arthritis. Any reactive specimen with the RF IgM Rapid Test Cassette must be confirmed with alternative testing method(s) and clinical findings.

Cheap Drug Metabolites Rapid Test Accu-Tell® Multi-line Drug Cassette (Urine) is a rapid chromatographic immunoassay for the qualitative detection of multiple drugs and drug metabolites in urine at the cut-off concentrations. TEST PROCEDURE of Saliva Rapid Test Cassette Allow the test, urine specimen, and/or controls to reach room temperature (15-30 ºC) prior to testing. 1. Bring the pouch to room temperature before opening it. Remove the test cassette from the sealed pouch and use it within one hour. 2. Place the test cassette on a clean and level surface. Hold the dropper vertically and transfer 3 full drops of urine (approx. 120 �¼L) to the specimen well (S) of the test cassette, and then start the timer. Avoid trapping air bubbles in the specimen well (S). See the illustration below. 3. Wait for the colored line(s) to appear. Read results at 5 minutes. Do not interpret the result after 10 minutes.   LIMITATIONS 1. ACCU-TELL ®  Multi-line Drug Cassette (Urine) provides only a qualitative, preliminary analytical result. A secondary analytical method must be used to obtain a confirmed result. Gas chromatography/mass spectrometry (GC/MS) is the preferred confirmatory method. 2. There is a possibility that technical or procedural errors, as well as interfering substances in the urine specimen may cause erroneous results. 3. Adulterants, such as bleach and/or alum, in urine specimens may produce erroneous results regardless of the analytical method used. If adulteration is suspected, the test should be repeated with another urine specimen. 4. A positive result does not indicate level or intoxication, administration route or concentration in urine. 5. A negative result may not necessarily indicate drug-free urine. Negative results can be obtained when drug is present but below the cut-off level of the test. 6. This test does not distinguish between drugs of abuse and certain medications. 7. A positive test result may be obtained from certain foods or food supplements.  We are Saliva Test Manufacturer. Note: The above information is for reference use only. Please refer to the product insert provided with the products before use.

- CE Certificate - MOQ: 30,000 units

COVID-19 One step rapid test device Within 10 minutes you will have the test result. Very accurate and simple operation. Please contact me for the video to see how easy it can be. With CE certificate. One box can take 25 samples

Name Testing kit for New coronavirus (2019-nCOV) IgG/IgM antibody Rapid Test WB/S/P Specifications 25 tests Introduce This kit uses the colloidal gold immunochromatographic principle to qualitatively detect novel coronavirus igg/igm antibodies in human serum, plasma, or whole blood. the sample to be tested was added to the sample hole of the test paper, and then added 2 drops of sample diluent. the igg/igm antibody in the sample combined with the recombinant new coronavirus antigen labeled with the colloidal gold on the binding pad formed complex. under the action of chromatography, it diffused forward along the nitrocellulose membrane (nc membrane). the nitrocellulose membrane was fixed with two detection lines (g line, m line) and one quality control line (c line). the g line was fixed with anti-human igg antibody for the detection of new coronavirus igg antibody; the m line was fixed with anti-human igm antibody for the detection of new coronavirus igm antibody; and the c line had quality control for the detection of the new coronavirus ig antibody. If the sample contains a new coronavirus IgG antibody, then the antibody binds to the recombinant new coronavirus antigen labeled with colloidal gold, diffuses forward, and then binds to the anti-human IgG antibody fixed on the NC membrane detection line (G line). if the sample contains a novel coronavirus igm antibody, then the antibody binds to the recombinant new coronavirus antigen labeled with colloidal gold, diffuses forward, and then binds to the anti-human igm antibody fixed on the nc membrane detection line (m line). The darker the color of the colloidal gold accumulated on the detection line, the higher the concentration of the new coronavirus antibody in the sample. To monitor the effectiveness of the test card, set up a quality control line (line C), whether there is a detection line (line T), quality control line (line C) should be color, otherwise the test results are judged invalid. Storage Stored at 4 to 30c and valid for 18 months. After the aluminum foil bag is unsealed, please use it as soon as possible. Sample 1. It is suitable for human serum, plasma and whole blood samples. 2. The samples should be used as soon as possible; if they cannot be used immediately, the serum / plasma samples should be kept at 2-8C for 5 days and -20C for long-term preservation; the whole blood samples should be placed at 2-8C to avoid hemolysis; 3.The sample contains a large amount of lipids, hemolysis or turbidity, do not use, so as not to affect the judgment of the results.

The test cassette is a solid phase immunochromatographic assay for the rapid, qualitative and differential detection of IgG and IgM antibodies to 2019 Novel Coronavirus in human whole blood, serum or plasma.

I am the manufacturer of COVID-19 RAPID TEST in China. The ACtest COVID-19 IgG/IgM Rapid Test is a lateral flow immunoassay for the simultaneous detection and differentiation of IgG and IgM anti-nCoV-19 virus in human whole blood, serum or plasma. It is intended to be used by the professionals as a screening test and as an aid in the diagnosis of infection with nCoV-19 viruses. The product has obtained the CE certification and is on the list of government export permits. And has been exported to Thailand, the Philippines, Germany, Italy, Ecuador, South Africa and other countries.

We are a manufacturer of SARSCoV2 RAPID TEST CASSETTE in China. We can provide customers following SARSCoV2 rapid testing products that have obtained the CE or other certifications. And has been exported to Thailand, the Philippines, Germany, Italy, Ecuador, South Africa and other countries. SARSCoV2 IgG/IgM Rapid Test Cassette SARSCoV2 Antigen Rapid Test (nasopharyngeal swab) SARSCoV2 Antigen Rapid Test (Saliva) SARSCoV2 and Influenza A+B Antigen Combo Rapid Test SARSCoV2 Neutralizing Antibody Test Kit

One Step Fecal Occult Blood (FOB) Rapid Test Cassette (Feces) Cat. No.: RH0301T INTENDED USE The One-Step Fecal Occult Blood (FOB) Diagnostic Kit is a qualitative detection of human occult blood in feces forself-testing. PRINCIPLE The One-Step Fecal Occult Blood (FOB) Diagnostic Kit is an immunochromatographic sandwich method, which employ two specific monoclonal antibodies to selectively identify hemoglobin in test samples. The result is very specific, and easier to interpret than those of guaiac-based test. The sensitivity is very high with the ability to detect 200ng/ml hemoglobin in feces. In addition, the accuracy of the test is not affected by interfering substances, and dietary restriction is not necessary. STORAGE The kits should be stored at temperature 4-30�°C, the sealed pouch for the duration of the shelf life (24 months). Do the test in 1 hour after open the pouch. WARNING AND PRECAUTIONS 1. For in vitro diagnostic use only. 2. Do not use kit beyond the expiration date. 3. Patient specimens may contain infectious agents and should be handled as though capable of transmitting disease. Wear disposable gloves throughout the specimen collection and assay procedures. 4. The test device should not be reused. REAGENTS AND MATERIALS PROVIDED 1. One pouched cassette with desiccant. 2. One operating Instruction MATERIALS REQUIRED BUT NOT PROVIDED 1. Clock or Timer SPECIMEN COLLECTION AND PREPARATION 1. Collect stool sample by using the sample collection device provided. 2. Unscrew the top of the sample collection device, take out the sample collection stick, and collect the sample by dipping the stick into 3 different places of the stool sample. 3. Put the sample collection stick back in the sample collection device and screw together tightly. 4. If the sample cannot be tested on the day of collection, store the stool sample at 4C. Bring the specimen to room temperature before testing. ASSAY PROCEDURE 1. Remove the test device from foil pouch by tearing along the notch. 2. Specimen collection. Please see also SAMPLE COLLECTION AND PREPARATION 3. Shake the sample collection device several times. 4. Holding the sample collection device upright, carefully unscrew the tip of collection device. 5. Squeeze 2-3 drops of the sample solution on the test sample pad. 6. Read the test results in 5 minutes. INTERPRETATION OF RESULTS Negative: Only one colored band appears on the control region (C). No colored band in the test region (T). Positive: In addition to the control band (C), a distinct colored band also appears in the test region (T). Invalid: If no bands appear, or a test band appears without a control band, the test should be repeated using a new test device.

PRoduct Name : Sars cov 2 (covid 19) igg/igm rapid test cassette Product Description : The ACtest COVID-19 IgG/IgM Rapid Test is a lateral flow immunoassay for the simultaneous detection and differentiation of IgG antinCoV-19 virus and IgM anti-nCoV-19 virus in human whole blood, serum or plasma. It is intended to be used by professionals as a screening test and as an aid in the diagnosis of infection with nCoV-19 viruses. The product has obtained the CE certification and is on the list of government export permits. And has been exported to Thailand, the Philippines, Germany, Italy, Ecuador, South Africa and other countries. Price of product ( USD price or FOB price) : USD 3.5- USD 5 per test Product origin : Hangzhouï¼?Zhejiangï¼?China Key Specifications/Special Features : " Place of OriginHangzhouï¼?Zhejiangï¼?China Port Of Loading Shanghai Payment Term T/T Delivery Time Shipment within 7 working " Minimum Order Size and Packaging details Packing 40test/box, 25box/carton ,Minimum Order Quantity 1000test

The CK-MB Rapid Test Cassette (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay for the qualitative detection of human CK-MB in whole blood, serum or plasma as an aid in the diagnosis of myocardial infarction (MI).

INTENDED USE The HCV Gold Rapid Screen Test (RST) is a Chromatographic immunoassay (CIA) for direct qualitative detection of antibodies to Hepatitis C type virus (HCV) in human serum/ plasma and whole blood. PRINCIPLE HCV RST is a chromatographic immunoassay (CIA) for the detection of antibodies to HCV in human serum/plasma and whole blood. HCV recombinant antigens are precoated onto membrane as a capture reagent on the test region. During the test, specimen is allowed to react with the colloidal gold particles, which have been labeled with HCV recombinant antigens. If antibodies to HCV present, a pink colored band will develop on the membrane in proportion to the amount of HCV antibodies present in the specimen .Absence of this pink colored band in the test region suggests a negative result. To serve as a procedural control, a purple colored band in the control region will always appear regardless the presence of antibodies to HCV. REAGENTS AND MATERIALS PROVIDED 1. One pouched cassette with desiccant. 2. Blood diluent in a dropper bottle, stored at 4-30°C. 3. One piece of operating instruction. WARNING AND PRECAUTIONS 1. For in vitro diagnostic uses only. 2. All patient samples should be treated as if capable of transmitting diseases. 3. Do not interchange reagents from different lots or use test kit beyond expiration date. 4. Icteric, lipemic, hemolysed, heat treated and contaminated sera may cause erroneous results. STORAGE The kits should be stored at temperature 4-30°C, the sealed pouch for the duration of the shelf life (24 months).