Rapid Test Kit Nasal Swab Suppliers and Manufacturers

Product name: hCG One Step Pregnancy Test Kit,FSH One Step Menopause Rapid Test Kit ect. Specimen: Urine Format: Strip/cassette/midstream Specification: 25pcs, 40pcs, or customized MOQ: 10,000 pcs Accuracy: > 99% Storage: 4-30°C Valid for: 24 months

Multi-drug one step 2-15 drug test device (urine/saliva) 1.Product description 15.Png 20170120153542.Png Give a rapid diagnosis for reference to help in hospitals & clinics, rehabilitation centers, diseases control & prevention centers, military recruiting, high-risk group census, physical examination and some related special industries. Urine or saliva specimen to choose, easy specimen collection Instant result in 5 minutes Ce marked Valid for 24 months. Store at 2-30, 2.Features -choices: urine or saliva specimen for multi-drug test -test more than 2 drugs in one time, distinct c/t lines -customized sensitivity, printing color and packing -accurate, specific, quiet, stable, convenient -latest production -best seller in china domestic market, competitive quality and price -easy payment and shipment

General Information One-Step HBsAb Rapid Test is to detect the Hepatitis B Virus Surface Antibody in serum, plasma or whole blood. Analytical sensitivity : 10mIU/ml-30mIU/ml of Anti-HBs Sensitivity : 99.5%, Specificity : 99.8% Specimen : Serum , Plasma or Whole Blood Reading Time : 10 min

General Information 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

The Typhoid IgG/IgM Rapid Test is a lateral flow immunoassay for the simultaneous detection and differentiation of anti-Salmonella typhi (S. typhi)G and IgM in human serum or plasma. It is intended to be used as a screening test and as an aid in the diagnosis of infection with S. typhi. Any reactive specimen with the Typhoid IgG/IgM 2.0 Rapid Test must be confirmed with alternative testing method(s).

General Information One-Step HAV Rapid Test is immunochromatographic assay for the diagnosic of Hepatitis A and the detection of Antibodies to HAV. Sensitivity : 99.4.0% , Specificity : 99.5% Specimen : Serum, Plasma or Whole Blood Reading Time : 20 min

General Information The CRP Semi-Quantitative Rapid Test utilizes a combination of colloidal gold conjugate and anti-CRP antibodies to selectively detect CRP in human blood. Sensitivity:97% , Specificity:96.9% Specimen : Serum, Plasma or Whole Blood Reading Time : 10 -15min

The Cytomegalovirus Rapid Test is a rapid qualitative lateral flow test designed for the quantitive detection of Cytomegalovirus (CMV) in human serum/plasma samples. Cytomegalovirus is a herpes virus and a leading biological factor causing congenital abnormalities and complications among those who receive massive blood transfusions and immunosuppressive therapy. About half of the number of pregnant women who contract a primary infection, spread the disease to their fetus. When acquired in-utero, the infection may cause mental retardation, blindness, and/or deafness. Serological tests for detecting the presence of antibody to CMV can provide valuable information regarding the history of previous infection, diagnosis or active or recent infection, as well as in screening blood for transfusions in newborns and immuno-compromised recipients. The Cytomegalovirus Rapid Test Device (Serum/Plasma) has been designed to detect CMV through visual interpretation of color development in the internal strip. The membrane was immobilized with antigens of CMV on the test region. During the test, the specimen is allowed to react with colored recombinant mouse anti-human IgM latex conjugates, which were precoated on the sample pad of the test. The mixture then moves on the membrane by a capillary action, and interact with reagents on the membrane. If there were enough CMV antibodies in specimens, a colored band will from at the test region of the membrane. Presence of this colored band indicates a positive result, while its absence indicates a negative result. Appearance of a colored band at the control region serves as a procedural control. This indicates that proper volume of specimen has been added and membrane wicking has occurred.

General Information One-Step Chloramphenicol Rapid Test is a competitive immunoassay for the semi-quantitative detection of the presence of Chloramphenicol residue in milk, Honey,Tissue extract and Aquatic products. Detection limit: Milk 0.3ppb ,Honey 0.3ppb , Tissue extract 0.3ppb , Aquatic products 0.3ppb Specimen: Defatted milk, Honey, Tissue extract, Aquatic products Reading Time : 5-10min

General Information One-Step Streptomycin Rapid Test is a competitive immunoassay for the semi-quantitative detection of the presence of Streptomycin residue in milk,honey and aquatic product . Detection limit:Milk 100ppb , Honey 10ppb , Aquatic product 100ppb Specimen: Defatted Milk, Honey,Aquatic products Reading Time : 5-10 min

General Information One-Step Sulfonamides Rapid Test is a competitive immunoassay for the semi-quantitative detection of the presence of Sulfonamides residue in Milk,Honey,Tissue extract and Aquatic products. Specimen: Milk, Honey, Tissue extract, Aquatic products Reading Time : 5-10 min

INTENDED USE Giardia Ag Feces Rapid Test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of Giardia antigen in feces. Assay Time: 5-10 min Sample: Feces 25PCS/BOX

INTENDED USE THE ONE STEP ANTI-DENGUE (IGM & IGG) TRI-LINE TEST IS A COLLOIDAL GOLD ENHANCED, RAPID IMMUNOCHROMATOGRAPHIC ASSAY FOR THE QUALITATIVE DETECTION OF ANTIBODIES (IGM & IGG) TO DENGUE VIRUS (DV) IN HUMAN WHOLE BLOOD, SERUM OR PLASMA. THIS TEST IS A SCREENING TEST, AND ALL POSITIVES MUST BE CONFIRMED USING AN ALTERNATE TEST SUCH AS WESTERN BLOT. THE TEST IS INTENDED FOR HEALTHCARE PROFESSIONAL USE ONLY. 25PCS/BOX

MOR Test SUMMARY AND EXPLANATION OF THE TEST The MOR Gold Rapid Screen Test Strip is a fast and easy to read membrane chromatographic immunoassay with no need for instrument. The method employs a unique combination of monoclonal and polyclonal antibodies to specifically identify Morphine in urine with a high degree of sensitivity. Morphine, one of opiates�¢?? derivatives, is central nervous system stimulants that produce alertness, wakefulness, increased energy, reduced hunger, and an overall feeling of well-being. Morphine has been the preferred drug for the management of pain in cases of advanced cancer and other severe conditions. Morphine and other Opiates�¢?? metabolites may be detected in urine as a result of heroin morphine, codeine, or poppy seed intake. Administration of large doses of Morphine can cause tolerance and physiological dependence in users, and can lead to substance abuse. D-Morphine is controlled substances. GC/MS or immunoassay method has been developed for the determination of 300ng/ml for Morphine. MOR Test PRINCIPLE During a test labeled antibody-dye conjugate mixes with urine specimen and binds to the free drug if it is presented in the sample, to form an antibody-antigen complex. This complex prevents the formation of pink color bands in the test zone of the dip-stick if drug to be detected in specimen is above the detection levels (300ng/ml for Morphine). In case of absent of drug and its metabolites, unbound dye conjugate will bind to the antigens immobilized in the test zone to form a pink reaction line. To serve as a quality control for the assay, another pink line will always appears in the test zone regardless positive or negative result. Packaging Details: Pouch+Box+Carton packaging (1) With our company's Logo (2) With the natural package (3) With OEM package (4) ODM

Product Name: Coronavirus (COVID-19) Antigen Rapid Test Cassette (Swab), COVID-19 Antigen Test Kit, SARS COV 2 Variant Test Kits Sample type Throat OR nasal swab Detection type Qualitative Method: Colloidal Gold Rapid Test Function: Diagnose Certificate: ISO9001/ ISO13485/CE Format: Strip, Cassette, Midstream Sensitivity: 96.23% Specificity: 99.11% Accuracy: 98.56% Reading time: 15 minutes Packaging Details: Pouch+Box+Carton packaging (1) With our company's Logo (2) With the natural package (3) With OEM package (4) ODM

Product Name: Coronavirus (COVID-19) Antigen Rapid Test Cassette (Swab), COVID-19 Antigen Test Kit, SARS COV 2 Variant Test Kits Sample type Throat OR nasal swab Detection type Qualitative Method: Colloidal Gold Rapid Test Function: Diagnose Certificate: ISO9001/ ISO13485/CE Format: Cassette Sensitivity: 96.23% Specificity: 99.11% Accuracy: 98.56% Reading time: 15 minutes Packaging Details: Pouch+Box+Carton packaging (1) With our company's Logo (2) With the natural package (3) With OEM package (4) ODM

From as little as $1.00 FoB per test - including IFU in Language of your choice! COVID Rapid Test / Lateral Flow - SARS-CoV-2 Antigen Kit Self Test Kit - Nasal Swab based - Qualitative - IVD (Invitro diagnostic medical device) - Rapid immunochromatographic assay - 12 Minutes to result - Shelf Life 18 months - EU common list approved. - In use: BE, BG, CY, FR, RO, SI, ES - Validation Completed: - FR, DE, ES UK DHSC Approved. - Validation completed & In use - Specificity 100.0% - Sensitivity 93.0% Certifications: EU HSC Approved UK DHSC Approved (included in JRC database) CE Directive 98/79/EC EN ISO 13485:2016 BS EN 13612:2002 ISO 14971:2019 EN ISO 23640:2015 ISO 15223-1:2016 EN ISO 18113-1:2011 EN ISO 18113-4:2011 EN 62366-1:2015 More Information is available at our website. Please contact us directly, visit our website, follow us on LinkedIn and/or Instagram. @fiigureofficial in = fiigureofficial

Great for Kids. From as little as $1.00 FoB per test - including IFU in Language of your choice! COVID Rapid Test / Lateral Flow - SARS-CoV-2 Antigen Kit Self Test Kit - Saliva based - Lollipop Style - Qualitative - IVD (Invitro diagnostic medical device) - Rapid immunochromatographic assay - 15 Minutes test to result - Shelf Life 18 months - EU common list approved. - In use: BE, BG, CY, FR, RO, SI, ES - Validation Completed: - FR, DE, ES UK DHSC Approved. - Validation completed & In use - Specificity 100.0% - Sensitivity 93.0% Certifications: EU HSC Approved UK DHSC Approved (included in JRC database) CE Directive 98/79/EC EN ISO 13485:2016 BS EN 13612:2002 ISO 14971:2019 EN ISO 23640:2015 ISO 15223-1:2016 EN ISO 18113-1:2011 EN ISO 18113-4:2011 EN 62366-1:2015 More Information is available at our website. Please contact us directly, visit our website, follow us on LinkedIn and/or Instagram. @fiigureofficial in = fiigureofficial

Assay+ COVID-19 antigen rapid test is authorized with CE marker, the sensitivity is 90%, the specificity is 98.5%. Assay+ Covid 19 antigen rapid test is a lateral flow immunochromatographic assay intended for the qualitative detection of the nucleocapsid protein of SARS-CoV-2 from the nasopharyngeal swab from the suspected COVID-19 patients within five days of symptom onset. This test is an aid to differentiate Covid 19 virus infection from other respiratory tract infection caused by coronavirus 229E, NL63, OC43 and HKU1, or severe acute respiratory syndrome caused by SARS-CoV and MERS-CoV. The test should be performed in moderate, high or waived complexity tests. This test can also perform for the Point of Care (POC) purpose.