Specification Strength/ Size Packing Size Packed In Filariasis Kit Includes One test Strip, Desiccant and Dropper 50 Strip Test Per Pack 50 Box Pack
BOSON RAPID SARS CoV-2 Antigen Test Card (Self Test) Manufactured by Xiamen Boson Biotech Co., Ltd. DHSC - UK Approved - 3rd Phase Approved. NASAL TEST CE & ISO Approved Full Home Test - Self Test Approval for UK and Europe Test Result in 15 Minutes. Sensitivity 97.70% Specificity 99.84% Accuracy 98.97% Layperson study statistics 99.84% of non-professionals carried out the test without requiring assistance 99.82% of different types of results were interpreted correctly Each Test have Unique Identifier Number - Easy to track Approved By - UK, Germany, France, Spain, Netherlands, Greece, Belgium, Italy, Portugal. 1 Test / Kit Catalog No.: 1N40C5-2 Kit Components: 1 Rapid SARS-CoV-2 Antigen Test Card (sealed foil pouch) 1 sterilized swab 1 extraction tube 1 sample extraction buffer IFU Tube holder on back of box Box / Carton Specifications : 1 Test / Kit Box size - 190*60*15 mm Carton size - 42*42*33 cm Carton gross weight - 9.9 kg 250 tests (boxes) / carton Euro 1.12
The Pathocatch Coviself Covid - 19 Rapid Antigen test (RAT) is an in vitro diagnostic test for the qualitative detection of covid - 19 antigen in nasal swab specimens directly from individuals with or without symptoms or other epidemiological reasons to suspect COVID-19.
Product Name - REALY TECH" Rapid Coronavirus Antigen Test (SARS-Cov-2) Product Description - Specifications Test duration: 15 minutes Sample type: nasopharyngeal swab. Storage: at room temperature or refrigerated (2-30A' C) Expiration: 24 months ex works Performance characteristics Sensitivity: 96.72%. Specificity: 99.22%. Accuracy: 98.74%. Price of product ( USD price or FOB price) - DEPENDS ON QUANTITY Product origin - China Key Specifications/Special Features - 5 test boxes: Each test box is packed in an aluminum foil bag with desiccant. 5 extraction reagents: vial with 0.3 ml extraction reagent 5 sterilized swabs: disposable swabs for sample collection 5 extraction tubes 5 dropper tips 1 work station 1 leaflet Minimum Order Size and Packaging details - MOQ 30000 units
Product Name - Realy Tech" Rapid Coronavirus Antigen Test (sars-cov-2) - Product Description - Specifications Test duration: 15 minutes Sample type: nasopharyngeal swab. Storage: at room temperature or refrigerated (2-30 C) Expiration: 24 months ex works Performance characteristics Sensitivity: 96.72%. Specificity: 99.22%. Accuracy: 98.74%." Product origin - China Key Specifications/Special Features - 25 test boxes: Each test box is packed in an aluminum foil bag with desiccant. 25 extraction reagents: vial with 0.3 ml extraction reagent 25 sterilized swabs: disposable swabs for sample collection 25 extraction tubes 25 dropper tips 1 work station 1 leafle
Rapid Tests Kits OTG USA COVID-19 Rapid Urine Antibody Test (World's First and Only) COVID-19 IgG / IgM Rapid Antibody Detection Test COVID-19 Saliva Antigen Rapid POC Test COVID-19 Antigen Rapid POC Test (Nasal Swab Collection)
Covid-19 Rapid Test Kits Results in 15 Min - MOQ 100,000- $9.15 USD Each Test -FOB-Abbott Antigen BinaxNOW Covid-19 Self Test (Nasal) (No Blood-No Saliva)
Hotgen Covid 19 Rapid Test Kits-LOI for Pricing Outfront Marketing Medical LLC-MOQ 10K-Worldwide Shipping
General Information One-Step Syphilis Rapid Test is to detect the antibodies against syphilis in serum, plasma or whole blood. Advantage: No need diluent for whole blood test Method; Double Antigens Sandwich Method Sensitivity : 100% , Specificity : 100% Specimen: Serum , Plasma or Whole Blood Reading Time : 10 min
General Information One-Step Chikungunya IgG/IgM Rapid Test is detection of IgG and IgM anti-chikungunya virus CHIK in human blood. Sensitivity: 90.3% , Specificity: 100% Specimen : Serum, Plasma or Whole Blood Reading Time : 10 min
General Information One-Step Influenza A/B Test is detection influenza type A and type B nucleoprotein antigen extracted from the nasal swab specimen. Sensitivity : 91.3% , Specificity : 95.7% Detection limit:5.1x105TCID50/ml Specimen: Nasal Swab Reading Time : 15-20min
General Information One-Step Chagas IgG/IgM Rapid Test is detection of IgG anti-Trypanosoma cruzi (T. cruzi) in human blood. Sensitivity: 92.9% , Specificity: 100% Specimen : Serum, Plasma or Whole Blood Reading Time : 10 min
General Information One-Step Leishmania IgG/IgM Rapid Test is detection antibodies IgG and IgM to the subspecies of the Leishmania donovani (L. donovani), the Visceral leishmaniasis causative protozoans in human blood. Sensitivity: 91.2 % , Specificity: 99.5% Specimen : Serum, Plasma or Whole Blood Reading Time : 10 min
General Information One-Step H.Pylori Ab Rapid Test is to detect the antibodies against H. pylori in serum, plasma or whole blood. For H.Pylori Ab Rapid tests: Sensitivity: 98.9 %, Specificity: 98.5%, Specimen: Serum, Plasma or Whole Blood Reading Time: 10 min
General Information One-Step Cow Ovulation Rapid Test is to detect the Beta-LH in milk. Analytical sensitivity : 10mIU/ml Sensitivity : 90% , Specificity : 90% Specimen : Milk Reading Time : 5 min No cross-reactivity: FSH (500ng/mL), Beta-E2(500ng/mL), PRL(500ng/mL), ASA(20µg/mL), DHT(20¼g/mL), tetraborane(20g/mL) and 0.01nol/mL pH 7.3 PBS
General Information One-Step the D-Dimer Rapid Test Device is a chromatographic immunoassay for the qualitative detection of D-Dimer in human blood. Specimen : Serum, Plasma or Whole Blood Reading Time : 10 -15min
General Information The CRP C-Reactive Protein 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
Uncut Sheet Strep A IgG/IgM Rapid Test Format:Cassette/Strip Uncut Sheet A rapid test for the qualitative detection of Strep A antigen in throat swab specimens.For professional in vitro diagnostic use only. INTENDED USE The Strep A Rapid Test Strip (Throat Swab) is a rapid chromatographic immunoassay for the qualitative detection of Strep A antigen from throat swab specimens to aid in the diagnosis of Group A Streptococcal infection. SUMMARY Streptococcus pyogenes is non-motile gram-positive cocci, which contains the Lancefield group A antigen that can cause serious infections such as pharyngitis, respiratory infection, impetigo, endocarditis, meningitis, puerperal sepsis, and arthritis.1 Left untreated, these infections can lead to serious complications, including rheumatic fever and peritonsillar abscess.2 Traditional identification procedures for Group A Streptococci infection involve the isolation and identification of viable organisms using techniques that require 24 to 48 hours or longer.3,4 The Strep A Rapid Test Strip (Throat Swab) is a rapid test to qualitatively detect the presence of Strep A antigen in throat swab specimens, providing results within 5 minutes. The test utilizes antibodies specific for whole cell Lancefield Group A Streptococcus to selectively detect Strep A antigen in a throat swab specimen. PRINCIPLE The Strep A Rapid Test Strip (Throat Swab) is a qualitative, lateral flow immunoassay for the detection of Strep A carbohydrate antigen in a throat swab. In this test, antibody specific to Strep A carbohydrate antigen is coated on the test line region of the test. After the test strip is immersed into a specimen, the extracted throat swab specimen reacts with an antibody to Strep A that is coated onto particles. This mixture migrates up the membrane to react with the antibody to Strep A on the membrane and generate a colored line in the test line region. The presence of this colored line in the test line region indicates a positive result, while its absence indicates a negative result. To serve as a procedural control, a colored line will always appear at the control line region, indicating that proper volume of specimen has been added and membrane wicking has occurred.
Uncut Sheet Influenza A/B Rapid Test Specimen:nasal swab Intended Use The Influenza A +B Test is a rapid chromatographic immunoassay for the qualitative detection of influenza type A and B nucleoprotein antigens in nasopharyngeal swab and nasal aspirate specimens. This kit is intended to be used as an aid in the diagnosis of influenza A and influenza B virus in nasal swab specimens. Principle The Influenza A +B Test is a qualitative membrane strip based immunoassay for the detection of influenza type A and B nucleoprotein antigens in nasopharyngeal swab and nasal aspirate specimens. In this test procedure, influenza type A antibody is immobilized in the A line, influenza type B antibody is immobilized in the B line. After a specimen is placed in the specimen well, it reacts with influenza type A antibody and/or B antibody coated particles that have been applied to the specimen pad. This mixture migrates chromatographically along the length of the test strip and interacts with the immobilized antibody. If the specimen contains influenza type A, a colored line will appear in the A line region indicating a influenza type A positive result. If the specimen contains influenza type B, a colored line will appear in the B line region indicating a influenza type B positive result. Absence of any T lines (A and B) suggests a negative result. To serve as a procedural control, a colored line will always appear at the control line region indicating that proper volume of specimen has been added and membrane wicking has occurred. Storage and Stability 1.Store as packaged in the sealed pouch at room temperature or refrigerated (4-30 or 40-86). The test device is stable through the expiration date printed on the sealed pouch. 2.The test must remain in the sealed pouch until use.
General Information Items : MOR/MET/THC/AMP/MDMA/MTD/COC/TCA/BAR/BZO, up to 15 kinds of Drug Tests Format: Strip, Cassette, Cup,and Panel Specimen: Urine Packaging Details: Pouch+Box+Carton packaging (1) With our companyâ??s Logo (2) With the natural package (3) With OEM package (4) ODM Anna Lee Int'l Market Executive SPANBIO T