Covid-19 Antibody Rapid Test
COVID-19 IgG / IgM rapid antibody test
J.A.M. Swiss Medical is an authorized reseller of the COVID-19 IgG / IgM rapid antibody test (PoC Point-of-Care or With-Patient type), produced by Zhejiang Orient Gene Biotech Co., Ltd. and Healgen Scientific LLC.
The serological Coronatest for detecting antibodies is CE, EUA and approved by the researchers of the Swedish UPPSALA University. It is a high precision accuracy test, comparable to laboratory analyzes and each batch is numbered and produced with quality control.
Deliveries of the covidtest are made worldwide, from small to large volumes (up to millions), at competitive prices and without intermediaries, with delivery times within 10 working days. We are direct partners of Orient Gene and the Healgen manufacturer and millions of tests have already been sold worldwide (including Europe and the United States).
In line with the Public Health Authorities, we want to ensure the dissemination of guaranteed quality antibody tests, which can demonstrate the passage of the Covid-19 infection. In this way, the return to work can be accelerated with a lower risk of contagion and employers can be given better conditions to plan their business.
Public health authorities are mandated by governments to develop a national strategy for extensive sampling of contagion. According to the strategy, one of the objectives is to rapidly increase the spread of antibody tests in the country. Some, but not all, of these tests are tested and considered of good quality. The Orient Gene and Healgen IgG / IgM rapid tests provided by J.A.M. Swiss Medical are quality tested and have high accuracy.
To reduce the spread of the infection in society, we recommend reading the advice of the national public health authority on how to protect yourself and how to reduce the spread of the infection in the community.
The Orient Gene IgG / IgM test (from Zhejiang Orient Gene Biotech Co. Ltd) and the identical Healgen IgG / IgM test (from Healgen Scientific LLC) is performed by taking a very small blood sample or alternatively serum or plasma. The blood (serum or plasma) is aspirated with an accompanying pipette, and is then dropped into the square cavity in the center of the cartridge. Then two drops of the buffer solution are dropped into the special round cavity. The result should be read after 10-15 minutes, using a timer.
The analysis must be carried out within a healthcare facility by personnel trained in sampling and interpreting the results. The assessment and quality assurance of SARS-CoV-2 antibody tests must be performed in consultation with clinical microbiological experience. The legal aspects to ensure patient safety must be considered, as well as the safety requirements for management systems, record keeping. Staff must be licensed, including doctors. The operations carried out must be reported to the inspection and control bodies for national health and healthcare.