● Packing size: 1 test/kit
● Specimen type: Nasal swabs, Throat swabs, BALF
● Instrumentation: not required
● Detection time: 15-20 minutes
● Storage: Room temperature (2-30°C)
● Shelf life: 24 months
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]]>Medomics – SARS-CoV-2 Antigen Test Kit (LFIA) determines if someone is infected by detecting the presence of viral material.
How does the virus infect the cell
- For the virus to invade the human cells, it needs to attach to the ACE2 receptor with the receptor binding domain (RBD) of the Spike protein.
- Colloidal gold-labeled anti-SARS-CoV-2 antibody and quality control antibody are sprayed on conjugation pad.
- Test line is fixed with anti-SARS-CoV-2 antibody for detecting the novel coronavirus and the quality control antibody is fixed on the Control line.
Advantage of Medomics – SARS-CoV-2 Antigen Test Kit (LFIA)
- It is easy to use
- It show accurate result
- Show result in just 15 minutes
Tests to detect SARS-CoV-2 infection
There are several types of tests used to detect SARS-CoV-2,1 and their performance characteristics vary.
- Tests can provide results quickly (within minutes); others require processing time.
- Several tests require specialized training in a laboratory, while others can be performed at the point of care or at home.
- It is possible for some tests to identify SARS-CoV-2 without a false-negative result; other tests can identify SARS-CoV-2 without a false-positive result; and some tests can identify both.
- Because some tests are less expensive and easier to perform, and supplies are readily available, they can be performed frequently.
More Medomics are Medomics – SARS-CoV-2
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]]>Deliveries will be done in 72 hours.
For business/wholesale inquiries please email us at info@h4healthcare.co.uk
Postage Charges will be £5.00 on each case and above £10,000 for Free delivery.
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]]>The COVID-19 IgG/IgM (Whole Blood/Serum/Plasma) Helegen Rapid Test Cassette For COVID-19 utilizes lateral flow technology for the qualitative, differential detection of both anti-SARS-CoV-2 IgM and IgG antibodies. In general, antibodies can be detected 1-3 weeks after infection. This test is intended to screen patients for SARS-CoV-2 antibodies. Coronaviruses are enveloped RNA viruses that are distributed broadly among humans, other mammals, and birds that cause respiratory, enteric, hepatic, and neurologic diseases. Four viruses – 229E, OC43, NL63, and HKU1 are prevalent and typically cause common cold symptoms in immunocompromised individuals. Three other strains SARS-CoV, MERS-CoV, and SARS-CoV-2 (COVID-19) can be transmitted from non-human vertebrates to humans.
Warning:-
- This product has not been FDA cleared or approved, but has been authorized for emergency use by FDA under a EUA for use by authorized laboratories.
- This product has been authorized only for detecting the presence of IgG and IgM antibodies to SARS-CoV-2, not for any other viruses or pathogens.
- The emergency use of this product is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for the detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug, and Cosmetic Act, 21 U.S.C. § 360bbb-3(b)(1) unless the declaration is terminated or authorization is revoked sooner.
- This product is intended for professional use and not for home use.
- Not for the screening of donated blood.
Instructions for Use
1. Remove the test cassette from the sealed foil pouch and use it as soon as possible.
2. Lay the device on a flat surface and add specimen (see specific instructions for each specimen type below):
a. For Serum or Plasma Specimen: With the plastic dropper provided, draw serum/plasma specimen to exceed the specimen line, as shown in the diagram below. Hold the dropper vertically and transfer the drawn serum/plasma specimen into the sample well (S). Immediately add 2 drops (about 80 μL) of sample buffer to the buffer well (B) ensuring that the buffer vial tip does not touch the sample. Avoid air bubbles.
b. For Whole Blood Specimen: Hold the plastic dropper vertically and transfer 1 drop of whole blood (about 10 μL) to the sample well (S) of the test device. Immediately add 2 drops (about 80 μL) of sample buffer to the buffer well (B) ensuring that the buffer vial tip does not touch the sample. Avoid air bubbles.
3. Wait for the control line (C) to change from blue to a red color. If, after 2 minutes, the sample has not moved across the test window or if blood is still present in the sample well (S), add 1 additional drop of sample buffer to the buffer well (B).
4. The results should be read in 10 minutes. Do not interpret the result after 15 minutes.
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]]>Deliveries will be done in 72 hours.
For business/wholesale enquiries please email us at info@h4healthcare.co.uk
Postage Charges will be £5.00 on each case and above £10,000 Free delivery.
The post FLOWFLEX COVID-19 ANTIGEN RAPID TEST KIT – 1 Piece appeared first on H4 HealthCare.
]]>The FlowFlex Rapid Test Kit uses the latest patented technology in detecting proteins ensuring that it can detect new strains of the COVID-19 virus. Using a simple nasal swab within 2cm of the nose makes it extremely easy to administer an accurate test as shown in the Porton Down. The FlowFlex Rapid Test Kit is currently the most accurate and affordable test on the market.
U.K. GOVERNMENT VALIDATED AT PUBLIC HEALTH ENGLAND, PORTON DOWN LABORATORIES
- U.K.GOVERNMENT VALIDATED
- DETECTS NEW VIRUS STRAINS
- MHRA REGISTERED
- NASAL ONLY TEST
- 98.8% ACCURACY
- CE APPROVED AND ISO CERTIFIED
- SELF TEST APPROVED
- 2 YEAR SHELF LIFE
- RESULTS IN 15 MINUTES
IF YOU TEST NEGATIVE:-
Take another test, following the manufacturer’s instructions (usually within two to three days). The same goes if you test negative and aren’t experiencing any symptoms—especially if you’ve been to a gathering with several people. As per the CDC, it’s possible the sample was collected too early in the infection and may show up positive after a few days. If it’s still negative, then it’s possible any symptoms you have aren’t Covid.
IF YOU TEST POSITIVE:-
Take another test to verify the result. If both results are positive, you should quarantine for 10 days and wear a mask around others. You should also make sure to contact your primary care physician as well as friends and family that may have been exposed. Those experiencing severe symptoms should seek medical attention as soon as possible. Many of these tests rely on the honor system—mask up and stay home.
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]]>Minimum 1 box
The Coronavirus Ag Rapid Test Cassette (Swab) is an in vitro immunochromatographic assay for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2 in nasopharyngeal (NP) swab specimens directly or after the swabs have been added to viral transport media from individuals who are suspected of COVID-19 by their healthcare provider. It is intended to aid in the rapid diagnosis of SARS-CoV-2 infections.
Deliveries will be done in 72 hours.
For business/wholesale enquiries please email us at info@h4healthcare.co.uk
Postage Charges will be £5.00 on each case and above £10,000 Free delivery.
The post ANTIGEN RAPID TEST CASSETTE (SWAB) appeared first on H4 HealthCare.
]]>The Coronavirus Ag Rapid Test Cassette (Swab) is an in vitro lateral flow test assay for. The qualitative detection of nucleocapsid protein antigen from SARS-CoV-2 in (NP). Swab specimens directly or after the swabs have been add to viral transport. Media from individuals who are suspect of COVID-19 by their healthcare provider. It is intend to aid in the rapid diagnosis of CoV-2 infections.
Scientific Description
CoV-2 is a single strand RNA coronavirus. Coronaviruses are compos of several proteins. Including the spike ,envelope , membrane and nucleocapsid. The spike glycoprotein of CoV-2 is a trimeric protein with each 180. Monomer consisting of 2 subunits which facilitate attachment and binding to the target cell.
Key Features and Values
- Qualitative detection of CoV-2 nucleocapsid antigen
- Fast and easy to use in point of care. Setting and near patient testing
- For use with nasal swab samples
- No special equipment needed
- Rapid determination of current infection with CoV-2
- Result within 15 minutes
- Sensitivity: 98.32%
- Specificity: 99.60%
- Recognize by the European Commission as an acceptable test method for member states
Complementary Products
- SARS-CoV-2 Antigen Rapid Test
- ErbaLisa COVID-19 IgG
- ErbaLisa COVID-19 IgM
- TGS COVID-19 IgM
- COVID-19 IgG
- TGS COVID-19 Control Set
Contents:
Each kit contains all the components required to run 20 tests:
- 20 Individually sealed test cassettes
- Sterile swabs
- 20 Extraction Tubes and Tips
- 2 Extraction Buffer Vials
- 1 Workstation
- 1 Instruction manual
What does it do?
The novel coronaviruses belong to the genus. COVID-19 is an acute respiratory infectious disease. People are generally susceptible. Currently, the patients infected by the novel. Coronavirus are the main source of infection. Asymptomatic infected people can also be an infectious source. Based on the current (EI). The incubation period is 1 to 14 days. Mostly 3 to 7 days. The main manifestations include fever. And dry cough. Nasal congestion runny nose, sore throat, myalgia, and diarrhea are found in a few cases. This test is for the detection of CoV-2 nucleocapsid protein antigen. Antigen is generally detectable in upper respiratory specimens during the acute phase of infection. Rapid diagnosis of SARS-CoV-2 infection will help healthcare professionals to treat patients and control the disease more efficiently and effectively.
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]]>Minimum 1 box
The Rapid COVID-19 Innova Antigen Test is an in vitro immunochromatographic assay for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2 in direct nose and/or throat swab from individuals who are suspected of COVID-19 by their healthcare provider.
Deliveries will be done in 72 hours.
For business/wholesale enquiries please email us at info@h4healthcare.co.uk
Postage Charges will be £5.00 on each case and above £10,000 Free delivery.
The post Innova IVD Covid Testing Kits appeared first on H4 HealthCare.
]]>- Easy to Use: It is easy to use because special equipment needed and intuitive visual interpretation.
- Rapid: Quick sampling with results in 15 min.
- Convenient: All necessary reagents provide and because of this no other equipment needed.
- German Registration: Registered with the German equivalent of the MHRA – the Federal Institue for Drugs and Medical Devices.
- EU Manufactured: Manufactured and evaluated in Germany by MöLab.
- CE Marked: For professional use.
- Accurate: >99.9% Specificity, 97.3% Sensitivity and 99.0% Accuracy.
- ISO13485: Healgen manufacture in accordance with their ISO13485 Quality Management accreditation. They are held many additional ISO accreditations.
This antigen test is intended for use by clinical professionals.
The Rapid Innova IVD Covid Testing Kits. The test is an in vitro lateral flow. The test assay for the qualitative. Detection of nucleocapsid protein antigen from SARS-CoV-2 indirect nose. The throat swab from individuals. Who is suspected of COVID-19 by their healthcare provider?
It is intended to aid in the rapid diagnosis of SARS-CoV-2 infections.
The novel coronaviruses belong to the β genus. COVID-19 is an acute respiratory infectious disease. Currently, the individuals infected by SARS-CoV-2 are the main source of transmission. Asymptomatic carriers are called sources of transmission. Based on the current epidemiological information. Symptoms include fever or chills, cough, shortness of breath, fatigue, muscle or body aches, headache. New loss of taste or smell, sore throat, runny nose, nausea or vomiting, and diarrhea.
These rapid lateral flow tests generate accurate results, usually within 15 minutes. This Antigen test has 100% specificity, 98.98% overall accuracy.
- Qualitative, visually read results in 15 minutes.
- No instrument require.
- Room temperature storage or refrigerate.
- Procedural internal control include.
- Sterile Swabs, Extraction Buffer, and Extraction Tubes include.
- Dispose of used test components according to the IFU.
Box Content:
Each box contains everything to perform 25 tests, and comprises of:
- Test device – individual foil wrapped with desiccant x 25 cassettes.
- Extraction buffer solution x 2 bottles.
- Sterile swabs x 25.
- Extraction tubes x 25.
- Instructions for use and Quick Reference Guide.
Test Procedure:
- Specimen Collection (Nasal Swab Collection).
- Specimen Collection (Throat Swab Collection).
- Sample preparation.
- Interpretation of Results.
Test results:
- POSITIVE – The presence of two lines as control line (C) and test line (T) within the result window indicates a positive result.
- NEGATIVE – The presence of only control line (C) within the result window indicates a negative result.
- INVALID – If the control line (C) is not visible within the result window after performing the test. The result is consider invalid. It is recommend that the specimen be re-test using a new test.
Note:
The intensity of color in the test line region (T) may vary depending on the concentration of analytes present in the specimen. Insufficient specimen volume, incorrect operating procedure, or expired tests are the most likely reasons for control band failure.
The Government is report considering buying 200 million of the “lateral flow” tests, of which 60 million would be available in January.
Leaked documents seen by the Daily Telegraph. Suggest that a deal would be sign next month to acquire 192 million lateral flow tests, which cost about £5 each, by next March.
This would pave the way for people who tested negative in the morning to be allow to attend football matches, theatres, and pubs.
Official sources said the figures were “indicative only and may be subject to change” but confirm plans for a “massive increase” in testing capacity — the so-call Moonshot strategy.
London boroughs that were left off an initial government list of priority areas said this had been an “oversight” and that tests would now be made available.
But it came as experts today cast doubt on the accuracy of the tests, warning that between one in four and one in two asymptomatic people with covid may not have the virus detect.
The Government claims the Innova antigen test that is being used in the two-week mass screening pilot in Liverpool detects 76.8 percent of cases of covid — and up to 95 percent in people who have a higher “viral load” and thus are more likely to be infectious.
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