Product Details: Number of Reactions(Preps)/Kit : 10 Brand : CTK BioTech Result Time (Rapid Kits): 15 min Sample Type : Blood Test Type Rapid Test CAT No : R0090C Single test for identifying acute infection and protective immunity by detecting and differentiating IgG and IgM anti-HAV Indicates protective immunity by detecting HAV IgG titers â?¥70 mIU/mL High confidence as it is traceable to the 2nd WHO International Standard for HAV, and IgM is in agreement with market leading ELISA test: Sensitivity: 94.8%; Specificity: 96.7% Flexible specimen types including serum, plasma, or whole blood which allows testing at any time without special specimen preparation Small sample volume (5 �µL) enables multiple testing on the same specimen without having to re-draw the patient. Initial patient care action can begin during the patientâ??s visit as test results are available in 15 minutes. Easily transported, and can be stored for 24 months at 2-30oC Individually sealed foil pouches containing: One cassette device One desiccant 5 aUL capillary tubes Sample diluent (REF SB-R0092, 5 mL/bottle) Package insert (instruction for use)
Product Details: Number of Reactions(Preps)/Kit:10T Brand : CTK BioTech Result Time (Rapid Kits): 15 min Sample Type : Blood Test Type : Rapid Test CAT No : R0095C Single test for identifying acute infection and protective immunity by detecting and differentiating IgG and IgM anti-HAV Indicates protective immunity by detecting HAV IgG titers â?¥70 mIU/mL High confidence as it is traceable to the 2nd WHO International Standard for HAV, and IgM is in agreement with market leading ELISA test: Sensitivity: 94.8%; Specificity: 96.7% Flexible specimen types including serum, plasma, or whole blood which allows testing at any time without special specimen preparation Small sample volume (5 �µL) enables multiple testing on the same specimen without having to re-draw the patient. Initial patient care action can begin during the patientâ??s visit as test results are available in 15 minutes. Easily transported, and can be stored for 24 months at 2-30oC Individually sealed foil pouches containing: One cassette device One desiccant 5 AUL capillary tubes Sample diluent (REF SB-R0092, 5 mL/bottle) Package insert (instruction for use).
Product Details: Number of Reactions(Preps)/Kit : 10 Brand : CTK BioTech Result Time (Rapid Kits) : 20Min Sample Material ; Serum / Plasma / Whole Blood Cat. No : R0063c The OnSite Dengue Ag rapid Test CE is a lateral flow chromatographic immunoassay for the qualitative detection of dengue NS1 antigen (DEN1, 2, 3, 4) in human serum, plasma or whole blood. The test is designed to be used by professionals as a screening test and provides a preliminary test result to aid in the diagnosis of infection with dengue virus. Any use or interpretation of this preliminary test result must also rely on other clinical findings and the professional judgment of health care providers. Alternative test method(s) should be considered to confirm the test result obtained by this device. Recommended for use: Any person presenting with clinical signs or symptoms within 9 days consistent with acute dengue infection or dengue fever including: high fever, severe headaches, severe pain behind the eyes, severe joint and muscle pain, fatigue, nausea, vomiting, and/or skin rash. Dengue NS1 antigen is detectable in human blood from the first day after the onset of fever up to 9 days, which allows early detection and prompt treatment of infection with dengue virus. As mild dengue fever symptoms can overlap with acute clinical manifestations of other arbovirus infections, such as Zika virus and chikungunya virus infections, correct diagnosis of dengue infection during early disease onset is critical for guiding clinical patient management. Product Specification: Individually sealed foil pouches containing: One cassette device One desiccant Plastic droppers Sample diluent (REF SB-R0063, 5 mL/bottle) One package insert (instruction for use)
Product Details: Number of Reactions(Preps)/Kit 10 T Brand CTK BioTech Test Type Rapid test Sample human serum, plasma, or whole blood Test time 10 Min Cat No : R0253C The OnSite TORCH Panel Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection and differentiation of antibodies (IgG and IgM) to Toxoplasma gondii (T. gondii), rubella virus, cytomegalovirus (CMV), herpes simplex virus 1 (HSV-1), and herpes simplex virus 2 (HSV-2) in human serum, plasma, or whole blood. This test is intended to be used by professionals as a screening test and provides a preliminary test result to aid in the diagnosis of infection with T. gondii, rubella virus, CMV, HSV-1 and HSV-2. Any interpretation or use of this preliminary test result must also rely on other clinical findings as well as on the professional judgment of health care providers. Alternative test method(s) should be considered to confirm the test result obtained by this device. Recommended for use: Any person presenting with clinical signs or symptoms consistent with TORCH infection. Women who are pregnant or who are planning to become pregnant Individuals with a compromised immune system The OnSite TORCH Panel Rapid Test detects and differentiates IgG and IgM antibodies for all 5 TORCH infections. In general, a negative test result indicates that the individual is at risk for acquiring a primary infection. A positive IgM result only indicates acute infection, a positive IgM and IgG test indicate acute, late phase infection, and a positive IgG test result only indicates past or chronic infection. The presence of IgM anti-rubella virus or high titers of IgG anti-rubella virus (> 200 IU/mL) are suggestive of acute rubella infection. Lower titers of IgG anti-rubella virus (â?¥ 10-15 IU/mL) are suggestive of previous exposure and protective immunity. An individual with an IgG anti-rubella virus titer less than 10-15 IU/mL is considered to be at risk of acquiring a rubella virus infection. The TORCH Panel Rapid test also differentiates between HSV-1 and HSV-2 antibodies using HSV-1 specific glycoprotein G1 and HSV-2 specific glycoprotein G2. Product Specification : Individually sealed foil pouches containing: One cassette device Two desiccants Plastic droppers Sample diluent (REF SB-R0253, 5 mL/bottle) One package insert (instruction for use)
Product Details: Brand SD Country of Origin Made in India Specimen Serum Shelf Life 24 Months Temperature Storage 30 Degree Celsius Sensitivity 97.6% Specificity 98.0% H.Pylori Helicobacter pylori (H.pylori) is a spiral shaped bacterium and is found in the gastric mucous layer or adherent to epithelial lining of the stomach. H.pylori causes more than 90% of duodenal ulcers and up to 80% of gastric ulcers. Approximately two thirds of the world's population is infected with H.pylori. The immuno- chronomatographic techinques for the detection of antibodies specific to H.pylori has substantially resolved these problems. General Information: SD BIOLINE H.pylori test is a rapid test for the qualitative detection of antibodies of all isotypes (IgG, IgM, IgA etc) specific to Helicobacter pylori in human serum plasma or whole blood. Detection of all isotype (IgG, IgM, IgA) antibodies against H.pylori High Accuracy Sensitivity: 95.9%, Specificity: 89.6% Specimen: Serum. Plasma, Whole blood Material provided with this kit are as follows: SD BIOLINE H.pylori test device multi-device Assay diluent
Product Details: Number of Reactions(Preps)/Kit 40 Brand Abon Result Time (Rapid Kits) 15 mins The Syphilis Rapid Test Cassette (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay for the qualitative detection of antibodies (IgG and IgM) to Treponema Pallidum (TP) in whole blood, serum or plasma to aid in the diagnosis of Syphilis.
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: BIOCREDIT One Step, rapid, immunochromatographic assay for the qualitative detection of SARS- CoV-2 antigen from nasopharyngeal swab Quality: Applicable Standarts: EN ISO 13485:2016; EN ISO 9001:15 (QMS). Tests meets the provisions of the Directive 98/79/EC of the European Parliament and of the Council on In-Vitro Diagnostic Medical Devices Quantity: 15 200 in warehouse in Vilnius, Lithuania, EU. Packing: 20 test kits/ inner box, 800 tests/carton, Price: 1,20 EUR OTG Vilnius, Lithuania (EU) Delivery terms: OTG Vilnius, Lithuania (EU);
Want to Sell: Lepu Rapid Covid Test 5er/5 Pack 20.000 Pack of 5: Total: 100.000 Test Stock ready to inspect in The Netherlands
TBG SARS-CoV-2 Neutralizing Antibody Qualitative Rapid Test(colloidal gold) Now with the detection before and after vaccination, TBG''s company has a neutralizing antibody detection reagent, that it can be used as the effective rate detection of antibody before and after vaccination. No matter how the vaccine is administered, The Neutralizing Antibody Qualitative Rapid Test will be used. Our test kits for COVID-19 as below are still effective to detect the infection of new COVID-19 variant B.1.1.7and The new variant has no effect on the detection performance of products
We can provide Covid-19 Rapid Antigen Test. Test with reliable results within minutes. Made in the USA. Lateral flow assay, No equipment required, Results within 10 minutes, minimally invasive specimen collection, nasal swab, POC (in patient care setting). Detects SARS-CoV2 nucleocapsid protein antigen with ultra high performance. Identifies acute infection with 88.4% sensitivity and 100% specificity. Complies with FDA. Principals or Buyer's Mandates only. No broker chains. FOB or CIF. Minimum order 500000 test please.
10,000 Rapid Antigen Test 500 Boxes 20 Test Per Box CE CERTIFICATION
Covid-19 - Antigen - Schnelltests
Rapid Influenza A + B Test Card Intended Use Influenza A+B Test is an in vitro immunochromatographic assay for the qualitative detection of influenza type A and type B nucleoprotein antigens in nasopharyngeal swab, nasal swab and nasal aspirate samples. The identification is based on the monoclonal antibodies specific for the nucleoprotein of Influenza virus A. It is intended to aid in the rapid diagnosis of influenza infection. Negative results should be confirmed by other methods, such as cell culture. Contents of Kit Flu A + B Test Card 20 ea Sample Extraction Buffer 1 ea Extraction Tube 20 ea Nozzle With Filter 21 ea Sterilized Swab 20 ea Tube Stand 1 ea Instructions For Use 1 ea Storage And Stability Store the Influenza A+B Rapid Test at room temperature or refrigerated (2-30ípC). Do not freeze. All reagents are stable until the expiration dates marked on their outer packaging and buffer vial. Pre Cautions 1. For in vitro diagnostic use only. 2. Do not use after the expiration date. 3. The test device should remain in the sealed pouch until use. 4. If the Influenza A+B Rapid Test kit was kept refrigerated, let all the reagents warm up to room temperature (15ípC -30ípC) before proceeding with the test. 5. Wear gloves when handing the samples, avoid touching the reagent membrane with your fingers. 6. Discard gloves, swabs, test tubes, and test devices in accordance with the local regulation. 7. Visibly bloody samples should not be used for the testing. 25 tests/kit, 40 kits/carton
Rapid antigen test kit for detection of COVID-19 . Easy,safe and accurate
European CE Certified 15 Minutes Detection Time Format 25T/Kit Colloidal Gold Method Detection Substance: Antibody Type of Sample : Serum/Plasma/Whole Blood No instruments needed
Beright brand, oral fluid with CE1434 and self-testing certificate. Stock EU, shipping 3-6 days with DHL economy to any country of Europe.
CareStarfTM COVID-19 ANTIGEN RAPID TESTS Why CareStartTM COVID-19 Live infection 10 minutes Diagnostic Tests dose not require a machine reader! Abbott, Quidel, and BD require readers, that are in short supply. â?¢ EASY TO USE CareStart â?¢ AVAILABILE Rapid Tests on the shelf available products (in inventory) with We offer CareStartTM reliable production and delivery schedules. Abbott, Quidel and BD testing cassettes are in short supply with unreliable availability. â?¢ FDA EUA is currently the only Point-Of-Care rapid antigen test registered authorized under the FDA EUA. CareStart TM CareStarfTM COVID-19 ANTIGEN RAPID TESTS Features Identify individual's current infection status to COVID-19 Fast and easy to use in Point-of-Care setting Qualitatively detect the SARS-CoV-2 nucleocapsid protein Use nasopharyngeal (NP) swab specimens Reliable results only in 1O minutes No special equipment or training required All-in-one package including collection swabs High sensitivity (88.4�°/o) and specificity (100�°/o) Kit Components 20 test devices 20 extraction vials and caps 20 NP swabs 1 positive and 1 negative controls Package insert Quick reference Instructions (QRI)
Malaria P.f /P.f,P.v / P.f,P.v,P.o,P.m Rapid Test Antige (Uncut Sheet) Specimen: Whole Blood/Serum/Plasma Format:2.5mm 3.0mm 4.0mm Accuracy:99.8% Cut-off:200 parasites/uL Sensitivity:98.6% Specificity:99.8% Package: in bulk or unit box package for your options Delivery date:7-10 days after receipt of the payment Pouch design: white pouch / netrual/ OEM design/CE Marked Payment:Westren Union,T/T
Quicking canine coronavirus ag rapid test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of canine coronavirus (ccv ag) in dog's feces or vomit. Assay time: 5-10 min Sample: feces or vomit Shelf life: 18 months Storage temperature: room temperature. Packing size: 10 tests/kit Gross weight:170g/kit
