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The Influenza A+B Rapid Test Device is a rapid chromatographic immunoassay for the qualitative detection of influenza A and B antigens in nasal swab or throat swab or nasal aspirate specimens. It is intended to aid in the rapid differential diagnosis of influenza A and B viral infections. |
Suitable for the collection , transportation and storage of various types of virus specimens include Covid-19, Influenza virus, bird flu, hand-foot-month disease, leprosy etc. Certificate by Chinese NMPA, European CE , have FSC. Various specification: Non-Inactivated, Inactivated/10ml/5ml/with one swab or two swabs. |
Dectect SARS-CoV-2 antigen within 10-15 mins, shorter the window period. All necessary reagents provided, no equipment needed; Simple, time-saving procedure. High sensitivity and specificity. Nasopharyngeal or Oropharyngeal swab samples. Certificate by CE, ISO13485 |
Recommended by <The Lancet>, Sensitivity is 93.4%, Specificity is 99%. Certified by CE, ISO13485, approval by South Korea KFDA, Singapore HSA, Philippines PFDA, France ANSM, Ecuador import license, Estonia import license, United Kingdom import license etc. WHO,FDA EUA, ANVISA are ongoing. Exported to more than 21 countries with 8 millions tests, verified by the laboratories from USA, Germany, Iran,Noway, UK, Korea, Philippines, Croatia, France. |
Mycoplasma cultivation/Identification/ Enumeration/ Susceptibility Test Kit is intended for cultivation, identification, enumeration and antibiotic susceptibility tests of UU and MH in human urogenital tract in one step. |
Adeno/Rota Combo Test is an in vitro qualitative immunochromatographic assay for the rapid detection of adenovirus rotavirus antigens in human stool specimen. The test results are intended to aid in the diagnosis of rotavirus infection and to monitor the effectiveness of therapeutic treatment. |
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