Find Verified Diagnostic Kits Suppliers, Manufacturers and Wholesalers

Minimum order - 5000 units Port - Shanghai, Ningbo Payment - T/T, L/C 25 pieces * One step test for the Novel Corona-virus (COVID19) (2019nCov) lg

Minimum order - 5000 units. Port - Shanghai, Ningbo Payment - T/T, L/C Coronavirus Ag rapid test cassette (swab) * Rapid testing for SARS-Cov-2 antigen within 15 minutes * Facilitates patient treatment decisions quickly * Simple time saving procedure * All necessary reagents provided & no equipment needed * High sensitivity and specificity 20 tests per kit. Storage - 2 to 30 degrees C. Shelf life - 24 months Specimen type - Nasal or throat swab.

Medical Sterile Cotton Swab to collect specimen of corona virus VTM (Viral Transport medium) to deliver the specimen samples to testing place

Product name:FIV Ab/FeLV Ag Combo Rapid Test Kit MOQ: 1PCS Use: Vet Diagnosis Assay Time:  5 - 10 minutes Shelf life: 18-24 Months Specimen: Serum Plasma Feces, vomit Sensitivity: 99.8% Storage: 2-30 Degree Certification: ISO9001 Packing: 10pcs/box

Product name:Canine Heartworm Antigen Rapid Test (CHW Ag) MOQ: 1PCS Use: Vet Diagnosis Assay Time:  5 - 10 minutes Shelf life: 18-24 Months Specimen: Serum Plasma Feces, vomit Sensitivity: 99.8% Storage: 2-30 Degree Certification: ISO9001 Packing: 10pcs/box

Product name:CPV Ag+CCV Ag+Giardia Ag Combo Rapid TestC MOQ: 1PCS Use: Vet Diagnosis Assay Time:  5 - 10 minutes Shelf life: 18-24 Months Specimen: Serum Plasma Feces, vomit Sensitivity: 99.8% Storage: 2-30 Degree Certification: ISO9001 Packing: 10pcs/box

Product name:Canine Pregnancy@Relaxin Rapid Test (Relaxin) MOQ: 1PCS Use: Vet Diagnosis Assay Time:  5 - 10 minutes Shelf life: 18-24 Months Specimen: Serum Plasma Feces, vomit Sensitivity: 99.8% Storage: 2-30 Degree Certification: ISO9001 Packing: 10pcs/box

Product name:Giardia Antigen Rapid Test (Giardia Ag) MOQ: 1PCS Use: Vet Diagnosis Assay Time:  5 - 10 minutes Shelf life: 18-24 Months Specimen: Serum Plasma Feces, vomit Sensitivity: 99.8% Storage: 2-30 Degree Certification: ISO9001 Packing: 10pcs/box

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.

Dr. Guard is space sterilization and deodorant using pure chlorine dioxide. [Dr. Guard] * Sterilization test against COVID-19 showed a high result of 99.99% effectiveness * Registered as a disinfectant for general disinfection in the Central Defense Countermeasures Headquarters of Korean government * Corona 19 self-disinfecting environment approved product * Completed safety check test and the only product certified by the Ministry of Environment * Registered with the FDA. Safety verification completed in WHO. * With proven technical skills, Dr. Guard has been recognized for its effectiveness in removing germs and odors. * Obtained certifications from honorable global health institutions such as CE, FDA, PFDA and KEMENKES [ClO2 Chlorine Dioxide] * Chlorine Dioxide (ClO2) is a World Health Organization (WHO) recognized safety class A-1 safety material. As a sanitary disinfectant already in Korea under the Drinking Water Management Act of 1999. It is soluble in chlorine dioxide. This is because there is no problem even when used for drinking water. * The fatal drawback is that it is difficult to commercialize because it vaporizes quickly and is not easy to manufacture in gaseous form. However, since the sterilizing and deodorizing power is strong, manufacturers have added additional additives (sulfur, surfactant, etc.) for long-term storage. * So, to make pure chlorine dioxide, special and difficult differentiated technology is required. Dr. Guard is a pure chlorine dioxide product made by a purely Korean technology by an honest company. [Germs that can be sterilized by Dr. guard] COROPNA-19 virus, N1N1, Pneumococcus, Dermatophyte, Norovirus, Pseudomonas aeruginosa, Fungi, Salmonella typhi, Staphyococcus aureus, Legionella [Applications of Dr. Guard] Using pure silicon dioxide chlorine sterilizing and deodorizing agent, we use the best technology in producing Dr. Guard for variety of purposes. Bedroom, Bathroom, Refrigerator, Kitchen No alcohol, No cancerous agents, No preservatives Air purification, Antivirul action [How to use Dr. Guard] The stick contains main solution�?� and an ample (secondary solution) 1. Bend central part of the stick. 2. Once the ample inside the stick cracks, shake it enough to mix the power with the solution well. 3. As it turns yellow, the active ingredients are released to the surface of the stick. 4. After 3~4 weeks of usage, dispose stick into normal trash bag once solution inside turns transparent.

Strengths of antigen rapid test: FAST & EASY (Compared with PCR test) People could RAPIDLY & EASILY be tested as a prerequisite to school attendance, work, or travel. FAST --PCR test - the swab test looks for viral RNA - may take days to perform. --Antigen test might take only 15-30 minutes to complete. EASY --PCR test swabs must be sent to laboratory to be performed by experienced technicians, it requires expensive and specialized equipment and can take days to get result. -- Antigen test can be run in an office or at home in about 15-30 minutes. The sampling process is FAST & EASY and requires very little expertise. Similar tests are done routinely in clinics for influenza all the time.

Viral transport medium is used to carry the patient samples to test in RTPCR testing.

RTPCR testing kits are used for testing golden test processes to detect Covid19 viruses in patients.

Rapid Antibody kit used for testing to detect the neutralized Antibodies in Patrons.

Covid19 Antigen testing kit is used for test patrons on Covid19 symptoms.

For in vitro qualitative detection of SARS-CoV-2 nucleocapsid antigen in nasal (NS) swab specimens directly from individuals who are suspected of COVID-19 by their healthcare provider within the first 5 days after onset of symptoms. This test is only provided for use by clinical laboratories or to healthcare workers for point-of-care testing, not for at-home testing. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2, or 2019-nCoV) is an enveloped non-segmented positive-sense RNA virus. It is the cause of coronavirus disease (COVID-19), which is contagious in humans. SARS-CoV-2 has several structural proteins including spike (S), envelope (E), membrane (M), and nucleocapsid (N). The antigen is generally detectable in upper respiratory samples during the acute phase of infection. Positive results indicate the presence of viral antigens, but the clinical correlation with patient history and other diagnostic information is necessary to determine infection status. Positive results do not rule out a bacterial infection or co-infection with other viruses. The agent detected may not be the definite cause of disease. Negative results should be treated as presumptive, which do not rule out SARS-CoV-2 infection and should not be used as the sole basis for treatment or patient management decisions, including infection control decisions. Negative results should be considered in the context of a patient's recent exposures, history, and the presence of clinical signs and symptoms consistent with COVID-19, and confirmed with a molecular assay, if necessary, for patient management. For in vitro diagnostic use only. For professional use only .

COVID-19 (2019-nCoV) Coronavirus IgG/IgM Rapid Test Kit Principle: based on Colloidal Gold Method, to detect COVID-19 IgG/IgM Antibody in serum, plasma, whole blood qualitatively. Easy to operate, results can be obtained in 15 minutes. Component: 25 tests cassttes/ 25 dropper/ 25 tubes of dilution buffer/25 Alcohol pad/ 25 Lancet/ 1 manual Certificate: CE, ISO13485, ISO9001

1. Nasopharynx swab specimen, non-invasive 2. Very simple to use 3. Convenient, no devices required 4. Rapid, results within 20 minutes 5. Cost-efficient 6:Listed on German BfArm ,got approval by PEI Clinical report from local CDC Sensitivity is 97.14%, Specificity is 100%, total accuracy rate is 99.68%.

Coivd Rapid Antigent Test kit Covid Rapid Antibody (Neutralizing) Test Kits CE certified For more discussion, please contact me