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.
CE Approved Singclean COVID-19Test Kit (Colloidal Gold Method) is a solid phase immunochromatographic assay for the rapid,qualitative detection of antigen from COVID-19 in human nasal swab specimen.This test provides only a preliminarytest result. Therefore, any reactive specimen with the COVID-19 Test Kit (Colloidal Gold Method) must be confimed with alternative testing method(s) and clinical findings. This rapid antigen test kit is the second test kit developed by Singclean Medical for COVID-19 testing on the basis of Colloidal Gold Method after Singclean COVID-19 lgG/IgM Test Kit, an antibody test, was launched globally in March. Advantage Results ready in 15 minutes Accurate diagnostic tool for active infection Easy to administer and read results Affordable, no need for instrument, highly portable Enable testing on a massive scale For healthcare workers use only Sensitivity 98.56% Sensitivity 99.03% Accuracy 98.84% Warnings 1. This test is not for at home testing, and should only be operated by healthcare workers. 2. Optimal assay performance requires strict adherence to the assay procedure described in this insert sheet. Inadequate or inappropriate sample collection, storage, and transport may cause false test results.
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.
Korean made Gmate COVID-19 Saliva Antigen Test Kit is a rapid chromatographic immunoassay for the qualitative detection of specific antigens to SARS-CoV-2 present in human saliva specimens. This test is an aid to early diagnosis of SARS-CoV-2 infection in patients with clinical symptoms with SARS-CoV-2 infection. â?¢ 90.9% Sensitivity, 100% Specificity â?¢ Made in Korea â?¢ Easy to Use â?¢ Currently the only imported brand approved and fully registered with governments and medical / health agencies for professional and home use. Provides initial screening result only Disclaimer: Reactive specimens must be confirmed with alternative testing method(s)
10,000 Rapid Antigen Test 500 Boxes 20 Test Per Box CE CERTIFICATION
The CareStart COVID-19 Antigen Test is a lateral flow immunochromatographic assay for the detection of extracted nucleocapsid protein antigens specific to SARS-CoV-2 in swab specimens directly collected from symptomatic individuals who are suspected of COVID-19 by their healthcare providers. Kit Includes 20 Test Devices 20 Assay Buffer 20 Extraction Vials and Caps 20 Specimen Collection Swabs 1 Positive and 1 Negative Control Swabs 1 Instructions for Use
[CONTENTS] (25) Test Kits (25) Individual Test Kits (25) Serum Pipets (1) Instruction For Use SENSITIVITY 100% | SPECIFICITY 97.3%
PRODUCT CONTENTS : 3ML Media in 15ml Sterile Tubes. Nylon Flocked Nasal Swabs, Sterile Individually Packed. Nylon Flocked Oral Swabs, Sterile Individually Packed. PRODUCT SPEC: Life: 12 Months. Sterility :No Microbial Growth in Incubation of 14 days. Appearance: Light Yellow / Clear Solution. Osmolality: 500-600 mOsm/KG Storage: 15 - 30 Celsius. Packaging :50 VTM kits / box
One-step real-time-PCR test for qualitative detection of genetic material of SARS-CoV-2 virus in upper and lower respiratory specimens collected from individuals suspected of COVID-19 infection. Targets the RdRp gene and E gene. Products with high specificity and sensitivity for accurate and reliable results.
Standard Q Covid 19 Ag is a rapid chromatographic immunoassay for the qualitative detection of antigens specific to SARS-CoV-2 in swab samples collected from a human nasopharynx. Fast results within 15~30 mins Easy to useSpecimen : Nasopharyngeal swab All necessary reagents provided & no equipment needed
Used for collection, transport and long term storage of clinical specimens for molecular analysis. Collected samples can be stored at ambient temperature (25-30 Degree C) . Specially formulated for inactivation of viral material, ensures safety of handling personnel involved. Screw caps with o-ring for zero leakage. Externally sealed with parafilm. Extra film provided with each test. Skirted, self standing 15 ml collection tubes with nasal & throat swabs.
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 .
We offer antigenic tests saliva and nasal. Product free of EU customs clearance. Shipment according to quantities averages 2-3weeks.
Lateral flow assay No equipment required Rapid results within 10 minutes Minimally invasive specimen collection (nasopharyngeal swabs) POC setting (i.e. in patient care settings) by medical professionals Detects SARS-CoV-2 nucleocapsid protein antigen with ultra high performance Identify acute infection wit 88.4% sensitive and 100% specificity 20 test/box 20 test devices 20 assay buffer 20 extraction vials and caps 20 specifimen collection swabs 1 positive and 1 negative control swabs 1 instructions for use
Catalog Number: HSN01 Type: Point of Care Test Technical Details: Rapid antibody test kit made with blood sample Sample Types: Blood Plasma Sensitivity Rate: Sensitivity: 97%, Specifity: 97% Contents: Lancet, Pipette, Silica Gel, Alcohol Swab, Test cassette Number of Kits in a Box: 15 tests Storage Condition: Room Temperature Shipping Type: Shipping storage condition Room temperature Analysis Time: 15 Min < In short: In the IgG or IgM test line area, it reacts with locally bound anti-human IgG or IgM, respectively and forms a colored line. If sample does not contain any COVID-19 antibodies, a colored line showing a negative result will not appear in any of the Test Line Areas. As a positive check for the correct performance of the tape's procedure and operation, a colored line should always be appearing in the Control Line Area. If Control Line area is empty, then the test is invalid.
Catalog Number: FRT02 Type: FAMEX SARS-CoV-2 Saliva Antigen Rapid Test Kit Technical: Rapid Antigen Test Kit Specimen Types: Sputum Claim: Sensitivity .4 Specifity ,3 Contents: Pipette, Test Cassette, Specimen Tube, Medical Waste Bag, Silica Gel Storage: 2 C -30 C Shipment Type: 2 C -3 C Analysis Time: 15 Minutes Shortly : This kit is used for the qualitative detection of SARS-CoV-2 antigen in vitro environment. It is a lateral flow sandwich assay designed for the qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 directly in saliva.Packaging, package leaflet and manual customized for various markets.
