Mycoplasma Pneumoniae(MP) Rapid Tests

Mycoplasma Pneumoniae (MP)-IgM Antibody Rapid Test
Catalog No.: BG1102C

Packing specification
20 test cards/ box

Intended Use
This kit is used to qualitatively detect the existence of MP -IgMantibodies in serum or plasma sample, as an auxiliary diagnostic reagent of MP infection in clinic. Mycoplasma pneumoniae(MP) is the common pathogenic microorganisms that caused the primary atypical pneumonia and other respiratory infections diseases. In addition to the respiratory tract that MP can cause other serious complication. MP infection is widespread and it can cause pharyngitis, tonsillitis, bronchitis, lung abscess, pulmonary bullae and pleurisy and multi system damage. It is not easy to identify the pneumonia is caused by MP, viruses, bacteria and other pathogens infection. And the treatment of MP infection is different to other bacterial or viral infections. MP –IgM is a specific antibody appeared first after MP infection. It can be detected in 7 days while onset.

Test Procedure
1.Test preparation: 10μL, 100μL micropipettes and matched tips
2.Test process: The temperature of the kit and the test sample should be the same with room temperature before test. Place the test card on a dry horizontal work surface. Add 10μL serum or plasma sample into the sample well, then add 100 μL of sample dilution immediately. Observe the result in 15-20 minutes after the serum or plasma samples added. The observation is invalid after 20 minutes.

Test results explain

To develop color on C line only: negative; To develop color on both C line and T line: positive; To develop color on T line only: invalid; Not to develop color on both C line and T line: invalid.
Note: Re-detection if the detection result is invalid. The invalid test cards should be dealt as infectious pollutants. The temperature of the kit and the test sample should be the same with room temperature before pre-detection.

Biovantion Inc is independent from international department of Bioneovan Co., Ltd., which established in 2 0 0 5, is an in vitro diagnostic reagents manufacturer engaged in the research, development, production, and focus on clinical testing for infectious diseases, such as Hepatitis virus, Noro virus, Parvo virus test kits, our products include rapid test cassette and Elisa kits.

All our products have been registered in National Medical Products Administration of China, in year 2020 we get Certificate of ISO 13485:2016 – QUALITY MANAGEMENT SYSTEMS FOR MEDICAL DEVICES from SGS. More importantly, we have awarded the registration certificate from National Medical Products Administration for Diagnostic Kit for IgM Antibody to COVID-19 and IgG antibody to COVID-19 during the outbreak in China, and also we developed COVID-19 Antigen test ; Neutralizing Antibody Test, these products selling well all overthe world