Cpv Ag+Ccv Ag+Giardia Ag Combo Rapid Test Kit Suppliers and Manufacturers

Specifacation: 1test/box, 5tests/box Storage temperature: 4-30C. No cold-chain Designed for qualitative detection of COVID-19 and Influenza A+B antigen test in Nasal Swab TGA has approved for self test ARTG is: 404883 ISO 13485 and ISO9001 Quality System Production Easy to operate, fast to get result within 15 minutes

1. INTENDED USE CPV + CCV +Giardia Ag Triple Test is a combined cassette to differentially diagnose the presence of Canine Parvovirus antigen, Canine Coronavirus antigen and Giardia antigen in dogâ??s feces or vomit. Assay Time: 5-10 min Sample: Feces or vomit 2. PRINCIPLE OF THE ASSAY CPV + CCV + Giardia Ag Triple Test is based on sandwich lateral flow immunochromatographic assay. The test device has three testing windows. Each testing window has an invisible T (test) zone and C (control) zone. When sample is applied into the sample hole on the device, the liquid will laterally flow on the surface of the test strip. If there is enough CPV antigen, CCV antigen or Giardia antigen in the sample, a visible T band will appear in the corresponding testing window. The C band should always appear after a sample is applied, indicating a valid result. By this means, the device can accurately indicate the presence of CPV, CCV or Giardia antigen in the sample. 3. KIT COMPONENT - 10Ã?foil pouches, each containing onecassette and a desiccant - 10Ã?assay buffer tubes (1.0 mL each) - 10Ã?pipettes - 10Ã?swab sticks - Product Manual

*Ex works price is around $5.5 per kit all in inclusive 4cents commissions for all the brokers. *Made in Korea, *Celltrion is a very well-known large corporation in Korea, and is one of the few companies that has been approved by the US FDA. *Detailed consultation is possible when submitting LOI.

The Canine Parvo Virus Antigen Rapid Test is a lateral flow immunochromatographic assay for the qualitative detection of canine Parvo virus antigen (CPV Ag) in dogs feces or vomit specimen. Assay Time: 5-10 minutes The Canine Parvo Virus Antigen Rapid Test is based on sandwich lateral flow immunochromatographic assay. The test device has a testing window for the observation of assay running and result reading. The testing window has an invisible T (test) zone and a C (control) zone before running the assay. When the treated sample was applied into the sample hole on the device, the liquid will laterally flow through the surface of the test strip and react with the pre-coated monoclonal antibodies. If there is CPV antigen in the specimen, a visible T line will appear. The C line should always appear after a sample is applied, which indicates a valid result. By this means, the device can accurately indicate the presence of Parvo virus antigen in the specimen. REAGENTS AND MATERIALS -Test devices, with disposable droppers -Assay buffer -Cotton swabs -Products Manual STORAGE AND STABILITY The kit can be stored at room temperature (4-30C). The test kit is stable through the expiration date marked on the package label. DO NOT FREEZE. Do not store the test kit in direct sunlight. TEST PROCEDURE -Collect dogs fresh feces or vomit with the cotton swab from dogs anus or from the ground. -Insert the swab into the provided assay buffer tube. Agitates it to get efficient sample extraction. -Take out the test device from the foil pouch and place it horizontally. -Suck the treated sample extraction from the assay buffer tube and place 3 drops into the sample hole â??Sâ?? of the test device. -Interpret the result in 5-10 minutes. Result after 10 minutes is considered as invalid. INTERPRETATION OF RESULTS -Positive (+): The presence of both â??Câ?? line and zone â??Tâ?? line, no matter T line is clear or vague. -Negative (-): Only clear C line appear. No T line. -Invalid: No colored line appears in C zone. No matter if T line appears. PRECAUTIONS -All reagents must be at room temperature before running the assay. -Do not remove test cassette from its pouch until immediately before use. -Do not use the test beyond its expiration date. -The components in this kit have been quality control tested as standard batch unit. Do not mix components from different lot numbers. -All specimens are of potential infection. It must be strictly treated according to the rules and regulations by local states. LIMITATION Canine Parvo Virus Antigen Rapid Test is for in vitro veterinary diagnosis use only. All result should be considered with other clinical information available with veterinarian. It is suggested to apply a further confirmative method when positive result was observed.

The Canine Parvo Virus Antigen Rapid Test is a lateral flow immunochromatographic assay for the qualitative detection of canine Parvo virus antigen (CPV Ag) in dogâ??s feces or vomit specimen. Assay Time: 5-10 minutes The Canine Parvo Virus Antigen Rapid Test is based on sandwich lateral flow immunochromatographic assay. The test device has a testing window for the observation of assay running and result reading. The testing window has an invisible T (test) zone and a C (control) zone before running the assay. When the treated sample was applied into the sample hole on the device, the liquid will laterally flow through the surface of the test strip and react with the pre-coated monoclonal antibodies. If there is CPV antigen in the specimen, a visible T line will appear. The C line should always appear after a sample is applied, which indicates a valid result. By this means, the device can accurately indicate the presence of Parvo virus antigen in the specimen. REAGENTS AND MATERIALS -Test devices, with disposable droppers -Assay buffer -Cotton swabs -Products Manual STORAGE AND STABILITY The kit can be stored at room temperature (4-30�°C). The test kit is stable through the expiration date marked on the package label. DO NOT FREEZE. Do not store the test kit in direct sunlight. TEST PROCEDURE -Collect dogâ??s fresh feces or vomit with the cotton swab from dogâ??s anus or from the ground. -Insert the swab into the provided assay buffer tube. Agitates it to get efficient sample extraction. -Take out the test device from the foil pouch and place it horizontally. -Suck the treated sample extraction from the assay buffer tube and place 3 drops into the sample hole â??Sâ?? of the test device. -Interpret the result in 5-10 minutes. Result after 10 minutes is considered as invalid. INTERPRETATION OF RESULTS -Positive (+): The presence of both â??Câ?? line and zone â??Tâ?? line, no matter T line is clear or vague. -Negative (-): Only clear C line appear. No T line. -Invalid: No colored line appears in C zone. No matter if T line appears. PRECAUTIONS -All reagents must be at room temperature before running the assay. -Do not remove test cassette from its pouch until immediately before use. -Do not use the test beyond its expiration date. -The components in this kit have been quality control tested as standard batch unit. Do not mix components from different lot numbers. -All specimens are of potential infection. It must be strictly treated according to the rules and regulations by local states. LIMITATION Canine Parvo Virus Antigen Rapid Test is for in vitro veterinary diagnosis use only. All result should be considered with other clinical information available with veterinarian. It is suggested to apply a further confirmative method when positive result was observed.

Intended Use Package Storage Specimen Type Shelf life Time to result Detection of SARS-CoV2 antigen 20 Tests / kit 1 - 40 Nasopharynx / Nasopharyngeal 24 months from manufacture date 5 - 8 minutes

BIOMETRO is an in-vitro diagnostic device manufacturer serving to improve the health and well-being of people around the world. Our effort for the development of medical IVD device based on proprietary Cathodic Electrochemiluminescence (C-ECL) technology, resulted in better clinical and personal healthcare outcomes globally

General Information One-Step Dengue Rapid Test is to detect the NS1 antigens in serum, plasma or whole blood. Sensitivity : 99.9% , Specificity : 99.5% Specimen : Serum , Plasma and Whole Blood Reading Time : 10 min

General Information One-Step Adenovirus Rapid Test (Feces) is a rapid visual immunoassay for the qualitative presumptive detection of adenovirus in human fecal specimens. Sensitivity: 98.7% , Specificity: 98.0% Detection limit:1.37s/CO Specimen: Feces Reading Time : 10min

General Information One-Step Rotavirus Rapid Test (Feces) is a rapid visual immunoassay for the qualitative presumptive detection of rotavirus in human fecal specimens. Sensitivity: 99.1% , Specificity: 99.9% Detection limit:103.5TCID50/ml Specimen: Feces Reading Time : 10min

General Information One-Step H.Pylori Ag Rapid Test is to detect the antigens in stool. For H.Pylori Ag Rapid tests: Sensitivity: 98.9 %, Specificity: 98.5%, Specimen: Stool Reading Time: 10 min

Canine Distemper Virus Ag Test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of canine Distemper virus (CDV Ag) in dog secretions or serum. Assay Time: 5-10 min Sample: secretions or serum 25PCS/BOX

CTK BioTech's, CE certified, Utilizes recombinant chimeric dengue virus licensed from the US CDC Detects all four dengue serotypes Duo test format minimizes processing time IgM detection indicates recent infection IgG detection indicates recent or previous infections Ag detection indicates a current infection Individually sealed foil pouches containing: One cassette device One desiccant 5 �µL Capillary tubes (for Dengue IgG/IgM test) Plastic droppers (for Dengue Ag test) Sample diluent (REF SB-R0062, 5 mL/bottle) One package insert (instruction for use)

CAT No : R0063C. Utilizes recombinant chimeric dengue virus licensed from the US CDC Detects all four dengue serotypes Duo test format minimizes processing time IgM detection indicates recent infection IgG detection indicates recent or previous infections Ag detection indicates a current infection Individually sealed foil pouches containing: One cassette device One desiccant 5 uL Capillary tubes (for Dengue IgG/IgM test) Plastic droppers (for Dengue Ag test) Sample diluent (REF SB-R0062, 5 mL/bottle) One package insert (instruction for use)

INTENDED USE Canine Parvovirus Ag Test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of canine Parvovirus (CPV Ag) in dog��s feces or vomit. Assay Time: 5-10 min Sample: Feces or vomit 25 PCS/BOX

This kit is used to detect RBV antigen in saliva secretion of dogs and cats, and can be used for screening of RBV infection and auxiliary diagnosis. test time: 10- 15min Package specification:20 tests/kit

Product Details: Number of Reactions(Preps)/Kit ; 25T Brand : CTK BioTech Result Time (Rapid Kits) : 10 min Sample Type : Blood Test Type : Rapid Test CAT No : R0192C Clinical accuracy: 96.7% sensitivity, 93.8% specificity Analytical sensitivity: 100% positive detection rate at 1 ng/mL of pylori lysate antigen in fecal specimens Cross reactivity: no cross reactivity with the following organisms at â?¥ 1 x 108 org/mL: Acinetobacter calcoaceticus, Neisseria gonorrheae, Adenovirus, Neisseria meningitides, Enterococcus faecalis, Proteus mirabilis, Escherichia coli, Proteus vulgaris Hauser, Gardnerella vaginalis, Pseudomonas aeruginosa, Geotrichum candidum, Rotavirus, Haemophilus influenza, Salmonella Paratyphi A, �±-haemolytics streptococcus, Salmonella Paratyphi B, �²-haemolytic streptococcus, Salmonella Paratyphi C, Klebsiella pneumonia, Salmonella typhi, Moraxella catarrhalis Interference: No interference was seen with 5 mg/mL Tums�® Antacid, 1:20 Pepto-Bismol�® Antacid, 5 mg/mL Tagamet�® Antacid, 5% Barium sulfate, 5 mg/mL Prilosec Antacid, 12.5% Hemoglobin (tarry stool), or 1:20 Mylanta�® Antacid Shelf life: 24 month Individually sealed foil pouches containing: One cassette device One desiccant Stool collection devices, each containing 2 mL extraction buffer Plastic droppers for transferring watery stool 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)