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
For in vitro qualitative detect of Covid-19 antigen in nasal(NS) swab specimens directly from individuals who are suspected of COVID-19 by their healthcare provider within the first 5 days of the onset of the symptoms. This test is only provided for use by clinical laboratories or to healthcare workers for point-of-care testing, and not for at home testing.
1.Easy to collect samples simple operation without professional equipment.
2.The test results are available in 15 minutes, and the test results are clearly visible. 3.Convenient transportation and low price, higher accuracy.
4.Suitable for large-scale rapid screening.
Shelf life: 24 Months
Test Result time: 10 Mins
Packing: 25 Pieces per Box
Our Rapid Typhoid Testing Kit is a cutting-edge solution for swift and accurate diagnosis of typhoid fever. This advanced kit is designed for quick detection of the Salmonella Typhi bacteria, streamlining the diagnostic process for healthcare professionals.
With a user-friendly approach, it requires a small blood sample and delivers results within minutes, enabling rapid treatment decisions. The kit exhibits exceptional sensitivity and specificity, ensuring reliable diagnoses even in low-infection scenarios. Its compact, portable design makes it ideal for remote and resource-limited areas. Trust our Rapid Typhoid Testing Kit for fast, dependable, and life-saving typhoid fever diagnosis, enhancing patient care and containment of this infectious disease.
The self testing product is transformed from the professional testing product
CLUNGENE COVID 19 Antigen Rapid Test manufactured by Clongene
The BfArM has granted the first special approvals according to 11 paragraph 1
of the German Medical Devices Act ( of antigen tests for self administration by laypersons (self tests) for the detection of SARS CoV 2 Our self testing product can be sold and
used in Germany Overview of CLUNGENE COVID 1
Product Name -
Realy Tech" Rapid Coronavirus Antigen Test (sars-cov-2) -
Product Description -
Specifications
Test duration: 15 minutes
Sample type: nasopharyngeal swab.
Storage: at room temperature or refrigerated (2-30 C)
Expiration: 24 months ex works
Key Specifications/Special Features -
25 test boxes: Each test box is packed in an aluminum foil bag with desiccant.
25 extraction reagents: vial with 0.3 ml extraction reagent
25 sterilized swabs: disposable swabs for sample collection
25 extraction tubes
25 dropper tips
1 work station
1 leafle
Product Name -
REALY TECH" Rapid Coronavirus Antigen Test (SARS-Cov-2)
Product Description -
Specifications
Test duration: 15 minutes
Sample type: nasopharyngeal swab.
Storage: at room temperature or refrigerated (2-30A' C)
Expiration: 24 months ex works
Price of product ( USD price or FOB price) - DEPENDS ON QUANTITY
Product origin -
China
Key Specifications/Special Features -
5 test boxes: Each test box is packed in an aluminum foil bag with desiccant.
5 extraction reagents: vial with 0.3 ml extraction reagent
5 sterilized swabs: disposable swabs for sample collection
5 extraction tubes
5 dropper tips
1 work station
1 leaflet
Minimum Order Size and Packaging details -
MOQ 30000 units
Health Canada Authorised Rapid Test
The COVID-19 antigen rapid test device is a lateral flow in-vitro immunoassay intended to be used for the qualitative detection of the SARS-CoV-2 viral nucleoprotein. This device will detect both viable and nonviable virus in both nasopharyngeal and oropharyngeal secretions.
This test had been authorized for point of care use by Health Canada and is available for immediate dispatch
MediGuard Systems of Canada is an Authorised distributor of the Assuretech Rapid Antigen test.
Support documentation and details available on request
The HIV-1/2 Rapid Screen Test (RST) is a qualitative test for the detection of antibodies to Human Immunodeficiency Virus type 1 and 2(HIV-1/2) in human serum/plasma and whole blood. It is considered as an initial screening test for HIV-1/2 antibodies. All positive specimens must be confirmed with Western Blot or other qualified EIA.
Precaution
1.For in vitro diagnostic uses only.
2.All patient samples should be treated as if capable of transmitting diseases.
3.Do not use test kit beyond expiration date.
4.Icteric, lipemic, hemolysed, heat treated and contaminated sera may cause erroneous results.
Summary And Explanation Of The Test
It has been shown that the acquired immunodeficiency syndrome (AIDS) is caused by viruses transmitted by sexual contact, transfusion, use of contaminated blood products and sharing contaminated needles. HIV-1 and HIV-2 viruses have been isolated from patients with AIDS and AIDS-related complex (ARC), high-risk persons for AIDS. HIV-1 and HIV-2 viruses delete T helper cells, a subpopulation of T cells for body defense, thus causing AIDS patients susceptible to opportunistic infections and developing malignant tumors. The incidence of specific antibodies to HIV-1/2 is high in AIDS, ARC and persons with high risk for AIDS. The HIV-1/2 Rapid Screen Test is designed to detect antibodies to HIV-1/2 in AIDS patients, ARC or high risk persons and identify any potential donors carrying these antibodies in serum specimens.
Principle
HIV-1/2 RST is a chromatographic immunoassay (CIA) for the detection of antibodies to HIV-1/2 in human serum/plasma and whole blood. HIV-1/2 specific antigens are precoated onto membrane as a capture reagent on the test region. During the test, specimen is allowed to react with the colloidal gold particles, which have been labeled with HIV-1/2 specific antigens. Antibodies to HIV-1/2, if present, a red colored band will develop on the membrane in proportion to the amount of HIV-1/2 antibodies present in the specimen. Absence of this red colored band in the test region suggests a negative result. To serve as a procedural control, red colored band in the control region will always appear regardless the presence of antibodies to HIV-1/2.
A rapid test for the qualitative detection of Strep A antigen in throat swab specimens.For professional in vitro diagnostic use only.
Intended Use
The Strep A Rapid Test Strip (Throat Swab) is a rapid chromatographic immunoassay for the qualitative detection of Strep A antigen from throat swab specimens to aid in the diagnosis of Group A Streptococcal infection.
Summary
Streptococcus pyogenes is non-motile gram-positive cocci, which contains the Lancefield group A antigen that can cause serious infections such as pharyngitis, respiratory infection, impetigo, endocarditis, meningitis, puerperal sepsis, and arthritis.1 Left untreated, these infections can lead to serious complications, including rheumatic fever and peritonsillar abscess.2 Traditional identification procedures for Group A Streptococci infection involve the isolation and identification of viable organisms using techniques that require 24 to 48 hours or longer.3,4
The Strep A Rapid Test Strip (Throat Swab) is a rapid test to qualitatively detect the presence of Strep A antigen in throat swab specimens, providing results within 5 minutes. The test utilizes antibodies specific for whole cell Lancefield Group A Streptococcus to selectively detect Strep A antigen in a throat swab specimen.
PRINCIPLE
The Strep A Rapid Test Strip (Throat Swab) is a qualitative, lateral flow immunoassay for the detection of Strep A carbohydrate antigen in a throat swab. In this test, antibody specific to Strep A carbohydrate antigen is coated on the test line region of the test. After the test strip is immersed into a specimen, the extracted throat swab specimen reacts with an antibody to Strep A that is coated onto particles. This mixture migrates up the membrane to react with the antibody to Strep A on the membrane and generate a colored line in the test line region. The presence of this colored line in the test line region indicates a positive result, while its absence indicates a negative result. To serve as a procedural control, a colored line will always appear at the control line region, indicating that proper volume of specimen has been added and membrane wicking has occurred.
The Influenza A +B Test is a rapid chromatographic immunoassay for the qualitative detection of influenza type A and B nucleoprotein antigens in nasopharyngeal swab and nasal aspirate specimens. This kit is intended to be used as an aid in the diagnosis of influenza A and influenza B virus in nasal swab specimens.
Principle
The Influenza A +B Test is a qualitative membrane strip based immunoassay for the detection of influenza type A and B nucleoprotein antigens in nasopharyngeal swab and nasal aspirate specimens. In this test procedure, influenza type A antibody is immobilized in the A line, influenza type B antibody is immobilized in the B line. After a specimen is placed in the specimen well, it reacts with influenza type A antibody and/or B antibody coated particles that have been applied to the specimen pad. This mixture migrates chromatographically along the length of the test strip and interacts with the immobilized antibody. If the specimen contains influenza type A, a colored line will appear in the A line region indicating a influenza type A positive result. If the specimen contains influenza type B, a colored line will appear in the B line region indicating a influenza type B positive result. Absence of any T lines (A and B) suggests a negative result. To serve as a procedural control, a colored line will always appear at the control line region indicating that proper volume of specimen has been added and membrane wicking has occurred.
Storage and Stability
1.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.
2.The test must remain in the sealed pouch until use.
The mor gold rapid screen test strip is a fast and easy to read membrane chromatographic immunoassay with no need for instrument. The method employs a unique combination of monoclonal and polyclonal antibodies to specifically identify morphine in urine with a high degree of sensitivity.
Morphine, one of opiates derivatives, is central nervous system stimulants that produce alertness, wakefulness, increased energy, reduced hunger, and an overall feeling of well-being. Morphine has been the preferred drug for the management of pain in cases of advanced cancer and other severe conditions. Morphine and other opiates metabolites may be detected in urine as a result of heroin morphine, codeine, or poppy seed intake. Administration of large doses of morphine can cause tolerance and physiological dependence in users, and can lead to substance abuse. D-morphine is controlled substances. Gc/ms or immunoassay method has been developed for the determination of 300ng/ml for morphine.
Mor test principle
During a test labeled antibody-dye conjugate mixes with urine specimen and binds to the free drug if it is presented in the sample, to form an antibody-antigen complex. This complex prevents the formation of pink color bands in the test zone of the dip-stick if drug to be detected in specimen is above the detection levels (300ng/ml for morphine). In case of absent of drug and its metabolites, unbound dye conjugate will bind to the antigens immobilized in the test zone to form a pink reaction line. To serve as a quality control for the assay, another pink line will always appears in the test zone regardless positive or negative result.
The helicobacter-pylori antigen rapid test kit (stool) is a rapid visual immunoassay for the qualitative detection of helicobacter pylori antigen in human stool specimens. This kit is used as an aid in the diagnosis of h. Pylori infection.
Introduction
Helicobacter pylori (also known as campylobacter pylori) as a spiral-shaped gram negative bacteria which infects the gastric mucosa. H. Pylori to causes several gastro-enteric diseases such as non-ulcerous dyspepsia, gastric and duodenal ulcer, active gastritis and can even increase the risk of stomach adenocarcinoma.
The epidemiologic study shows that more than 50% of the world's population is infected by h. Pylori strains. Infection is more prevalent in developing countries. The lowest infection rate is 20%, and the highest infection rate can be 90% in developing countries. H. Pylori strains is the major reason to cause chronic gastritis and gastric ulcers, 80%-90% chronic gastritis patients and 95%-100% gastric ulcers patients are infected by h. Pylori strains. So the detection and treatment of h. Pylori strains infection is very important.
At present several invasive and non-invasive approaches are available to detect this infection state. Invasive methodologies require endoscopy of the gastric mucosa with histologic, cultural and urease investigation, which are expensive and require some time for diagnosis. Alternatively, non-invasive methods are available such as breath tests, which are extremely complicated and not highly selective, and classical elisa and immunoblot assays. This kit belongs to non-invasive approach.
Intended use
Canine distemper virus ag test is a sandwich lateral flow immunochromatographic assay for the qualitative
Detection of canine distemper virus (cdv ag) in dogs secretions or serum.
Assay time: 5-10 min
Sample: secretions or serum
Principle
Canine distemper virus ag test is based on sandwich lateral flow immunochromatographic assay. The test
Device has a testing window. The 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 distemper antigen in the sample, a visible t band will appear. 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 canine distemper antigen in the sample.
One-Step Canine Influenza Virus Ag Test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of canine Influenza virus (CIV Ag) in dogs secretions.
Sensitivity: 94.7% , Specificity: 100%
Specimen: Secretions
Reading Timen:5-10 min
General Information
Method: Double Antibodies Sandwich Method
Sensitivity : 99.8%
Specificity : 99.6%
Specimen : Canine feces or vomit
Detection limit: 103 TCID50 / mL
No cross reaction against CDV, CCV, CRV, CAV - I, Giardia
Reading Time : 5- 10 min
One-Step the D-Dimer Rapid Test Device is a chromatographic immunoassay for the qualitative detection of D-Dimer in human blood.
Specimen : Serum, Plasma or Whole Blood
Reading Time : 10 -15min
General Information
One-Step FOB Rapid Test is qualitative test for the detection of human blood hemoglobin in human stool specimens and early diagnosis for Colon Cancer by Fecal Occult Blood screening with double methods, immunology and chemistry No Cross reactivity :(Bovine, Hemoglobin, Swine hemoglobin, Horse hemoglobin, Bililrubin, Bovine serum albumin, Vitamin C) Analytical sensitivity : 20ng/ml of FOB (immunology) ,100ng/ml of FOB (chemistry)
Specimen : Stool
General Information
One-Step Leishmania IgG/IgM Rapid Test is detection antibodies IgG and IgM to the subspecies of the Leishmania donovani (L. donovani), the Visceral leishmaniasis causative protozoans in human blood.
Sensitivity: 91.2 % , Specificity: 99.5%
Specimen : Serum, Plasma or Whole Blood
Reading Time : 10 min
General Information
One-Step Chagas IgG/IgM Rapid Test is detection of IgG anti-Trypanosoma cruzi (T. cruzi) in human blood.
Sensitivity: 92.9% , Specificity: 100%
Specimen : Serum, Plasma or Whole Blood
Reading Time : 10 min
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