Specification Strength/ Size Packing Size Packed In HCG Test Strip (Dipstick) 50 Tests 50 Box Pack
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
THERMAL PAPER ROLL Thermal Paper Roll For Sale. It is a special fine paper that is impregnated with a chemical that changes color when exposed to heat. We offer only premium grade Thermal Paper that extends print head life and produces black and sharp images on every copy every time and has good preservation properties. These paper rolls are used in various applications/ machinery and are offered Cash Register Paper to our buyers at economical prices. Product Features: 1. Thermal paper made from 100% raw wood pulp, paper is smooth and delicate 2. Thermal paper specifications can be customized, printed clearly, saved for a long time 3. Uniform coloring and rapid color rendering thermal paper rolls 4. Thermal paper rolls have no paper scrap, prolonging printer life 5. Thermal paper package is professional, moisture-proof, dust-proof, easy to keep 6. Thermal paper roll can be waterproof, oil and oxidation resistant, and can be used casually 7. High brightness, good in toughness, deep thermal image. Thermal Paper and filter paper manufactured are used in following areas: Blood testing Eye testing Count testing machines R&D machines ATM machines Weighing machines Offer Pre-Printed, OBM or OEM Service, Customize size for reference for Thermal Paper Roll Wholesale: Item Size Packaing Plastic /Honeycomb /Paper core Thermal Paper 80x80mm 50 Roll/CTN 13x17mm/13x19mm/13x22mm Thermal Paper 80x70mm 50 Roll/CTN 13x17mm/13x19mm/13x22mm Thermal Paper 80x60mm 50 Roll/CTN 13x17mm/13x19mm/13x22mm Thermal Paper 80x50mm 50 Roll/CTN 13x17mm/13x19mm/13x22mm Thermal Paper 80x40mm 50 Roll/CTN 13x17mm/13x19mm/13x22mm Thermal Paper 76x76mm 50 Roll/CTN 13x17mm/13x19mm/13x22mm Thermal Paper 76x70mm 100 Roll/CTN 13x17mm/13x19mm/13x22mm Thermal Paper 57x60mm 100 Roll/CTN 13x17mm/13x19mm/13x22mm Thermal Paper 57x50mm 100 Roll/CTN 13x17mm/13x19mm/13x22mm Thermal Paper 57x40mm 100 Roll/CTN 13x17mm/13x19mm/13x22mm Thermal Paper 57x30mm 100 Roll/CTN 13x17mm/13x19mm/13x22mm Thermal Paper 44x70mm 100 Roll/CTN 13x17mm/13x19mm/13x22m Packing: 5-10 rolls/shrink wrapping by plastic foil, golden foil or Silver foil if necessary, 75-100 rolls/case, or customized packing Shrink wrapping; individual packing; OEM packing; Natural packing in waterproof bag Buy Thermal Paper Wholesale (Cash Register Paper). Thermal paper (sometimes referred to as an audit roll) is a special fine paper that is coated with a material formulated to change color when exposed to heat. It is used in thermal printers, particularly in inexpensive or lightweight devices such as adding machines, cash registers, and credit card terminals. Can normal printer print on thermal paper? Using thermal paper in a regular printer is not advisable. Thermal paper is designed to work in thermal printers, which use heat instead of ink. It is also thinner and more slippery. Thus, a regular printer would probably not produce good results.
Uncut Sheet HCG Urine/Serum Rapid Test SPECIMEN: Whole Blood/ Serum/ Plasma INTENDED USE The One Step TOXO IgG/IgM Test is a rapid chromatographic immunoassay for the qualitative detection of antibodies (IgG and IgM) to Toxoplasma gondii in Whole Blood /Serum / Plasma to aid in the diagnosis of TOXO infection. Toxoplasma gondii is an obligate intracellular protozoan parasite with a worldwide distribution. Serological data indicates that approximately 30% of the population of most industrialized nations is chronically infected with the organism. A variety of serologic tests for antibodies to Toxoplasma gondii have been used as an aid in diagnosis of acute infection and to assess previous exposure to the organism. These tests are the Sabin-Feldman dye test, direct agglutination, indirect hemagglutination, latex agglutination, indirect immunofluorescence, and ELISA. Recently, lateral flow chromatographic immunoassay, such as The Toxo IgM/IgG Rapid Test (Whole Blood/Serum/Plasma) was introduced into the clinic for the serodiagnosis of Toxoplasma gondii infection. One step TOXO IgG/IgM Test is a simple, visual qualitative test that detects TOXO antibodies in human Whole Blood/serum/plasma. The test is based on immunochromatography and can give a result within 15 minutes. Storage and Stability Store as packaged in the sealed pouch at room temperature or refrigerated (4-30â?? or 40-86â??). The test device is stable through the expiration date printed on the sealed pouch. The test must remain in the sealed pouch until use.
Application For the detection of eye / nose / stool / rectal secretions or blood pathogens The most convenient and rapid diagnostic tool for canine distemper / canine parvovirus Feature High accuracy for monoclonal antibody capture target Good tools for antibody detection and disease diagnosis Easiest reagent to operate the test Quickly present the result Low testing cost Technical specification Technical Parameters for Rapid Canine Distemper Ag Test Kit Principle: colloidal gold lateral chromatography Test samples: eye / nasal secretions or blood Interpretation of time: 10-15 minutes Sensitivity: 98% Specificity: 97% Shelf life: 24 months Storage temperature: 4-28 Packing: 10 Test/ box Technical Parameters for Rapid Feline Parvovirus Ag Test Kit Principle: colloidal gold lateral chromatography Test samples: rectal / feces Interpretation of time: 10-15 minutes Sensitivity: 99% Specificity: 97% Shelf life: 24 months Storage temperature: 2-30 Packing: 10 Test / box
Self-test received notified body approved CE Marking on April 1, 2021 A home test for the rapid qualitative detection of SARS-Cov-2 virus antigen in anterior nasal swabs from individuals with or without symptoms or other epidemiological reasons to suspect COVID-19 Performance Characterisitics Sample tyep: nasal swab Time to result: 15-20 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. Specifications 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 5 Tests/Kit Catalog No.: 1N40C5-4 Kit components: 5 Rapid SARS-Cov-2 Antigen Test Card (sealed foil pouch) 5 Sterilized swabs 5 extraction tubes 5 sample extraction buffer IFU 1 tube stand 20 Tests/Kit Catalog No.: 1N40C5-6 Kit components: 20 Rapid SARS-Cov-2 Antigen Test Card (sealed foil pouch) 20 Sterilized swabs 20 extraction tubes 20 sample extraction buffer IFU 1 tube stand
Boson EUA slef testing covid antigen test card, DDP Chicago airport/DDP New York airport. Any interest pls contact us!
Till now we already exported 20 million tests and we can promise you very high quality. 25 tests/box, CE Mark and ISO, Clinical report, Certificate of analysis (COA) available Clinical specify >98.89% Accuracy: 93.41% Specimen: whole blood/serum, 10 minutes to get results
INTENDED USE The neisseria gonorrhoeae antigen test card is a rapid visual immunoassay for the qualitative detection of neisseria gonorrhoeae in female endocervical swab and male urethral swab specimens. This kit is intended for use as an aid in the diagnosis of neisseria gonorrhoeae infection. PRINCIPLE The neisseria gonorrhoeae antigen test kit is designed to detect N. Gonorrhoeae through visual interpretation of the color development in the internal strip. The membrane was immobilized with gonococcal Antigen-specific polychonal antibody on the test region (T) and related antibodies on the control region(C). During testing, the specimen is added to the sample region (S) and reacts with anti-gonococcus antibodies conjugated to colored particles and precoated onto the sample pad of the test. Then, the mixture migrates through the membrane by capillary action and interacts with reagents on the membrane. If there is sufficient gonococcus antigens in the specimen, a colored band will form at the test region (T) of the membrane. The presence of this colored band indicates a positive result, while its absence indicates a negative result. The appearance of a colored band at the control region serves as a procedural control, indicating that the proper volume of specimen has been added and membrane wicking has occurred.
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
Product Details: Brand J.Mithra Kit Type HIV Test Kit (Rapid) (Tri Dot) Sensitivity 100% WHO Evaluation Specificity 100% WHO Evaluation Result Time Within 3 Minutes Cat. No IR130100 Intended Use:The HIV TRI-DOT test is a visual, rapid, sensitive and accurate immunoassay for the differential detection of HIV-1 & HIV-2 antibodies (IgG,IgM & IgA) in human serum or plasma using HIV-1 & HIV-2 Antigens immobilized on an immunofiltration membrane. The test is a screening test for Anti HIV-1 and HIV-2 and is for in vitro diagnostic use only. Salient Features: Rapid visual test ,based on Flow Through Technology. Differential detection of HIV-1 & HIV-2. Detection of group O & subtype C. Use of envelop antigens gp41& C terminus of gp120 for HIV-1 & gp36 for HIV-2. 100% sensitivity & 100% specificity as per WHO Evaluation. Shelf life 24 months at 2-8C Available in convenient pack sizes- 50 Tests and 100 Tests. Results within 3 minutes. No instrument required. In built quality control dot. Evaluations: WHO Evaluation: Evaluation report from UNAIDS (WHO), CH-1211Geneva,Switzerland Aug 1999 the Sensitivity and Specificity of HIV TRI-DOT is 100 % .The panel used for evaluation of HIV TRI-DOT by Institute of Tropical Medicine, WHO Collaborating Centre in AIDS, Belgium also included HIV-O virus, which was found reactive with HIV TRI-DOT. NIMHANS BANGALORE: Evaluation report from National HIV Reference Laboratories of Government of India , claiming Sensitivity and Specificity of HIV TRI-DOT to be 100 %. CMC VELLORE: Evaluated by Department of Clinical Virology, Christian Medical College & Hospital, Vellore and published in JCM, vol. 38, Issue 2000,claiming 99.5% sensitivity and 99.9% specificity. NARI PUNE: Evaluation Report from National AIDS Research Institute(NARI-Pune) claiming sensitivity & Specificity to be 100 %. Approved by Drug Controller General of India( DCGI) for the usage in Blood Banks.
Product Details: Number of Reactions(Preps)/Kit 25 T Brand Premier Result Time (Rapid Kits) 20 -30 MIN Certified WHO Aproved CAT No; PI13FRC25 First Response Malaria Antigen P.falciparum (HRP2) Card Test is intended to be performed by trained users (In either laboratory or point of care settings) as qualitative screening in vitro diagnostic test for detection of P. falciparum specific HRP2 antigen. Sensitivity - 100% Specificity - 100% Rapid Result time within 20 - 30 Minutes. Detects Histidine Rich protein(HRP2) of Plasmodium P.falciparum Storage at 1 40 C. Specimen Type- Whole Blood
Product Details: Number of Reactions(Preps)/Kit 25 T Brand Premier Result Time (Rapid Kits) 20 - 30 Min Certified WHO Aproved CAT No; PI16FRC25 First Response Malaria Ag. pLDH/HRP2 Combo Card Test is intended to be performed by trained users (In either laboratory or point of care settings) as qualitative screening test for detection of P.falciparum, P. vivax, P. ovale and P. malariae. 100% - Specificity 100% - Sensitivity Rapid Result time within 20 - 30 Minutes. Storage at 1 40 C. Detects P.falciparum, P. vivax, P. ovale and P. malariae. Specimen - Whole Blood
Product Details: Brand : Abbott ICMR Approved ; Yes Sample Type : Nasal Swab Packaging Size : 25 Test Kits/Box Cat. No: 195000 The BinaxNOWTM COVID-19 Ag Card is a lateral flow immunoassay intended for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2 in direct anterior nasal (nares) swabs from individuals suspected of COVID-19 by their healthcare provider within the first seven days of symptom onset
BOSON - Rapid SARS-CoV-2 Antigen Test - Pack of 5 Available at 0.75 EUR Plus VAT and Transport per test IFU - Swedish, Finissh, Norwagian, English, Danish Product Descirption : "A home test for the rapid qualitative detection of SARS-CoV-2 virus antigen in anterior nasal swabs from individuals with or without symptoms or other epidemiological reasons to suspect COVID-19 Performance Characteristics: Sample type: nasal swab Time to result: 15-20 min Sensitivity - 97.70% Specificity - 99.84% Accuracy - 98.97% UK MHRA - DHSC Approved for Self Test Approved in Germany, France, Italy, Belgium, Netherlands, Greece, Spain, Portugal. 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 Test Kit Specifications: 5 Tests / Kit Catalog No.: 1N40C5-4 Kit Components: 5 Rapid SARS-CoV-2 Antigen Test Card (sealed foil pouch) 5 sterilized swabs 5 extraction tubes 5 sample extraction buffer IFU 1 tube stand Box / Carton Specifications : 5 Tests / Kit Box size - 202*60*37 mm Carton size - 42*42*33 cm Carton gross weight: 10 kg 500 tests (100 boxes) / carton" MOQ : 3000 FOB Price : Euro 1.03
Specification Strength/ Size Packing Size Packed In Syphilis Test Card 50 Tests 50 Box Pack
Specification Strength/ Size Packing Size Packed In Typhoid IgG/IgM 50 Tests 50 Box Pack
Specification Strength/ Size Packing Size Packed In HCV Test Cards 10 Card Test Per Pack 50 Box Pack
Format: strip, cassette, midstream Specimen: urine Sensitivity: 25 miu/ml Packing: 1 test/pouch. 25t/box , 1500t/ctn.
Initial pregnancy gold gel reagent (one step hcg pregnancy test strip) Explanation of the test One step hcg pregnancy test strip (urine) is a rapid chromatographic immunoassay for the qualitative detection of human chorionic gonadotropin (hcg) in urine to aid in the early detection of pregnancy. Human chorionic gonadotropin (hcg) is a glycoprotein hormone produced by the developing placenta shortly after fertilization. In normal pregnancy, hcg can be detected in both urine and serum as early as 7 to 10 days after conception (1-4). Hcg levels continue to rise very rapidly, frequently exceeding 100 miu/ml by the first missed menstrual period (2-4), and peaking in the 100, 000-200, 000 miu/ml range about 10-12 weeks into pregnancy. The appearance of hcg in both urine and serum soon after conception, and its subsequent rapid rise in concentration during early gestational growth, making it an excellent marker for the early detection of pregnancy. One step hcg pregnancy test strip (urine) is a rapid test that qualitatively detects the presence of hcg in urine specimens at the sensitivity of 20 miu/ml. The test utilizes a combination of monoclonal and polyclonal antibodies to selectively detect elevated levels of hcg in urine. At the level of claimed sensitivity, one step hcg pregnancy test strip (urine) shows no cross-reactivity interference from the structurally related glycoprotein hormones hfsh, hlh and htsh at high physiological levels. 50 tests pack.
