Product Details: Number of Reactions(Preps)/Kit 22T Brand Abbott Result Time (Rapid Kits) 15 Min Cat. No 852-000 BinaxNOW Legionella Urinary Antigen Card is a rapid assay for the qualitative detection of Legionella pneumophila serogroup 1 antigen in urine samples from patients with symptoms of pneumonia. It is intended to aid in the presumptive diagnosis of Legionnaires disease caused by L. pneumophila serogroup 1 in conjunction with culture and other methods. Sample Type: Urine Time to Result: 15 minutes Kit Size: 22 tests Performance Data: Sensitivity/Specificity: 95%/95%
Product Details: Brand Abbott ICMR Approved Yes Test Method Antigen Test Result Time (Rapid Kits) 15 min Packaging Size 25 Test Kits/Box Cat. No 41FK10 Panbio COVID-19 Ag Rapid Test Device is an in vitro diagnostic rapidtest for the qualitative detection of SARS-CoV-2 antigen (Ag) in humannasopharyngeal swab specimens from individuals who meet COVID-19clinical and / or epidemiological criteria. Panbio COVID-19 Ag RapidTest Device is for professional use only and is intended to be used asan aid in the diagnosis of SARS-CoV-2 infection
Product Details: Number of Reactions(Preps)/Kit ; 25 Brand : Cellex Test Method : (SARS-CoV-2) IgM/IgG Rapid Antibody Result Time (Rapid Kits) 30 minutes Time To Result 15 mins Cat. No : 5513C COVID-19 serology test.Cellex qSARS-CoV-2 IgG/IgM Rapid Test.qSARS-CoV-2 IgG/IgM Rapid Test Cassette.FDA Grants Emergency Authorization for First Rapid Antibody Test for COVID-19
AbChek (SARS-CoV-2) IGM/IGG Corona Rapid Antibody Test Kit Product Details: Number of Reactions(Preps)/Kit : 50 Brand : AbChek ICMR(Govt) Approved : Yes Test Method : (SARS-CoV-2) IgM/IgG Rapid Antibody Result Time (Rapid Kits) : 5-10 minutes Sample Type : Blood Type : Rapid Test Kit Sensitivity : 98 Packaging Size : 50 Tests/ Box Country of Origin : Made in India Corona viruses are enveloped RNA viruses that are distributed broadly among humans, birds and other mammals, that cause respiratory, enteric, hepatic, and neurologic disease. SPECIFICATIONS: Whole blood/serum/plasma may be used for testing. Results available in only 15 minutes. Easy to use. Result can be read visually. No need for an analyser. Cost effective method for assisting in screening COVID-19 disease. Additional Information: Item Code: RapidTestcov19 Production Capacity: 100000 Delivery Time: 10 days Packaging Details: Carton Box
Product Details: Number of Reactions(Preps)/Kit ; 2 Brand ; iHEALTH Test Method : Antigen Test Result Time (Rapid Kits) : 15mins Sample Type : Nasal Swab Cat. No : ICO-3000 iHealth COVID-19 Antigen Rapid Test is the simplest way to detect SARS-CoV-2 nucleocapsid protein antigen. It only takes 4 steps and 15 minutes to complete the test. The test is also non-invasive. You won't need to collect a sample from deep in your nasal cavity to get accurate results.
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
Product Details: Number of Reactions(Preps)/Kit : 25 Brand : Roche ICMR Approved : Yes Test Method : Antigen Test Result Time (Rapid Kits) : 10-15 mins Cat. No : 9901-NCOV-01G Reliable, rapid chromatographic immunoassay for the qualitative detection of specific antigens of SARS-CoV-2 The SARS-CoV-2 Rapid Antigen Test is a reliable, rapid chromatopgraphic immunoassay for the qualitative detection of specific antigens of SARS-CoV-2 present in the human nasopharynx. This test is an aid in detecting antigen from the SARS-CoV-2 virus in individuals suspected of COVID-19. This product is strictly intended for professional use in laboratory and Point of Care environment
Ethicon (W9922) Sutures Vicryl Rapide Und 4-0 19mm 3/8 R/C PS-2 75cm
Vicryl Rapide Sutures USP 2-0, 1/2 Circle Tapercut W9962 Material:Polyglactin910 Absorbable Colour:Undyed Braided
Flowflex antigen kits
Bacterial Vaginosis Rapid Test Kit core Chromogenic Ingredient IBX-4041 IBX-4041 Testing vessel BV Blue active ingredient BVBlue active ingredient BVBlue substrates BV Blue substrates Chromogenic substrate IBX-4041 chromogenic substrate of sialidase enzyme Detection reagent for bacterial vaginosis (sialidase two-step method) Shenzhen BST Science & Technology Co., Ltd sells and exports chromogenic substrate of sialidase enzyme IBX-4041. Specification: Appearance: Light yellow solid powder Purity: 95% min Application: Two-step chromogenic substrates of neuraminidase (sialidase) BVBLUE Test Kit Component 1)BVBLUE Developer Solution: Water and Sodium hydroxide 2) BVBLUE Testing Vessel: Water, Potassium acetate, IBX-4041 (chromogenic substrate compound). IBX-4041 is the key ingredient of BVBLUE test kit, BVBLUE test is a rapid sialidase test for bacterial vaginosis. BVBLUE test method is currently the only test method approved by the FDA for testing Bacterial Vaginosis(BV), The BV BLUE Test contains a chromogenic substrate of sialidase enzyme, IBX-4041. BV Blue test is a commercially available test, it detects sialidase activity, an enzyme produced by BV-associated bacteria such as Gardnerella vaginalis, Bacteroides spp., Prevotella spp., and Mobiluncus spp. In the test procedure, a vaginal fluid sample is placed in the test vessel which contains a chromogenic substrate for sialidase. After incubation, a developer solution is added, and If the sample contained a high level of sialidase, a blue or green color is seen. Samples containing no sialidase, or low levels of this enzyme, will generate a yellow color in the reaction. The BV test has high specificity and sensitivity. The BVBlue test enables rapid detection of BV in a physician's office, and can thereby provide advantages over the Amsel methods and other methods requiring extensive laboratory testing. Advantage of BVBLUE Test Kit Compared to other diagnostic test methods for BV such as Amsel criteria, Nugent Gram-stain scoring system, Affirm�® Microbial Identification Test, BVBLUE Test Kit has following advantage: 1, BVBLUE Test is currently the only test method approved by the FDA for testing Bacterial Vaginosis(BV). 2, BVBLUE Test just take 10 minutes to 15 minutes to get the result. 3, High purity sialidase substrate with high specificity can reduce the occurrence of false positive. 4. Comparing with the gold standard, the coincidence rate is high, the relative sensitivity is 93%, and the specificity is 95%. 5. Easy to operate, do not need equipment. 6. The specimen does not need to pretreat.
Rapid Antigen Test Card Self-test received notified body approved CE marking on Apr.1,2021 A home test for the rapid qualitative detection of antigen in anterior nasal swabs within 7days of symptom onset â?¢Sample type: nasal swab â?¢Time to result: 15-20 min â?¢Sensitivity: 96.77%Specificity: 99.20%Accuracy: 98.72% â?¢Layperson study statistics: 99.10% of non-professionals carried out the test without requiring 97.87% 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 250 tests (boxes) / carton Carton gross weight - 9.9 kg Price and Minumum Quantity Price FOB in USD: -Minimum Order Qty: 2000 Pieces Production Capacity: 10 Million Units A MonthPackaging: Pack Of 1, 5, 20 Product Model And Origin: Xiamen China Brand: BOSON
nasal or throat swab, 25 tests per box, it has CE certificate
It has CE certificate, 1T per box, 540 tests per carton; 25T per box, 1000T per carton. high accuracy
25 tests per box, CE certificate
It has CE certificate, 25 tests per box, 40 boxes per carton, high accuracy
For the newly discovered new coronavirus mutant strain Omicron(B.1.1.529),our conducts the sequence comparison analysis of its 32 mutation sites. All mutation sites are outside the epitope region recognized by the new crown paired monoclonal antibody selected by our company.Therefore,according to known academic opinions,the effective production strain for Omicron(B.1.1.529)can still be detected by our product"SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold Immunochromatography)" Next,our will continue to follow up on the mutation of Covid-19perform sequence alignment analysis in timeand evaluate and verify the detection ability of key mutation sites to ensure the sensitivity and specificity of the kit.
ALL OTG PO from Buyer CI from Seller Buyer signs and returns the CI Seller's Attorney prepared LOA and submits to Buyer Escrow Agreement from Seller is signed Buyer escrows funds for full purchase SGS inspection is performed at buyer's expense Logistics details are exchanged Upon confirmed report, escrowed funds are released simultaneous with title transfer
The 2019-nCoV Ag Saliva Rapid Test is a lateral flow immunoassav intended for the qualitative detection of nucleocapsid protein antigen from2019-nCoV in saliva specimens directly collected from individuals who are suspected of COVID-19 by their healthcare provider within the first 7 days of symptom onset
Green Spring Box size: 400 pieces in a box (individual packaging) Size: 70.3*44.9*32.4cm Weight: 15.5kg TGA certification
