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I-High Sensitivity Covid19/influenza A+B Antigen Combo Rapid Test Iphumelele i-TGA

Incazelo emfushane:

 

  • I-Austria TGA ARTG No. 404883
  • I-Hong kang MDD HKMD No. 230344
  • I-ISO 13485 kanye ne-ISO9001 Quality System Production
  • Isitifiketi se-CE
  • Isifanekiso: I-Nasal Swab
  • Ukucaciswa: 1/5test/box


  • :
  • Imininingwane Yomkhiqizo

    Omaka bomkhiqizo

    ESITOKWENI I-COVID-19/Influenza A+B Antigen Combo Rapid Test Cassette Austrilia ARTG No. 404883 HKMD No. 230344

    UKUSETSHENZISWA OKUHLOSIWE

    I-COVID-19/Influenza A+B Antigen Combo Rapid Test Cassette iyi-lateral flow immunoassay ehloselwe ukutholwa kwekhwalithi ye-SARSCoV-2, umkhuhlane A kanye ne-influenza B viral nucleoprotein antigens ku-nasopharyngeal swab evela kubantu okusolwa ukuthi banegciwane lokuphefumula elihambisana ne-COVID. -19 ngomhlinzeki wabo wezempilo.I-COVID-19/Influenza A+B Antigen Combo Rapid Test Cassette ihloselwe ukusetshenziswa izisebenzi zaselabhorethri eziqeqeshiwe ezifundiswe futhi eziqeqeshwe ngezinqubo zokuxilonga i-in vitro.

     

    新冠和流感A+B宣传页单页_1 

     

     


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