Nanjing Liming Bio-products Co., Ltd.

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REF 501070 Specification 20 Tests/Box
Detection principle Immunochromatographic assay Specimens Feces
Intended Use The StrongStep® Vibrio cholerae O1/O139 Antigen Combo Rapid Test is a rapid visual immunoassay for the qualitative, presumptive detection of Vibrio cholerae O1 and/or O139 in human fecal specimens. This kit is intended for use as an aid in the diagnosis of Vibrio cholerae O1 and/or O139 infection.
 
REF 501100 Specification 20 Tests/Box
Detection principle Immunochromatographic assay Specimens Feces
Intended Use StrongStep® Giardia lamblia Antigen Rapid Test Device (Feces) is a rapid visual immunoassay for the qualitative, presumptive detection of Giardia lamblia in human fecal specimens. This kit is intended for use as an aid in the diagnosis of Giardia lamblia infection.
 
The StrongStep®Dermatophytosis Diagnostic kit is a rapid visual immunoassay for the qualitative presumptive detection of α-1, 6 mannose in fungi belonging to dermatophytes. This kit is intended to be used as an aid in the diagnosis of Dermatophytosis.
REF  500020 Specification  20 Tests/Box
Detection principle  Immunochromatographic assay Specimens  Cervical/urethra swab
Intended Use It is suitable for qualitative detection of gonorrhoea/chlamydia trachomatis antigens in cervical secretions of women and urethral samples of men in vitro in various medical institutions for auxiliary diagnosis of the above pathogen infection.
 
REF 501050 Specification 20 Tests/Box
Detection principle Immunochromatographic assay Specimens Feces
Intended Use The StrongStep® Vibrio cholerae O1 Antigen Rapid Test Device  (Feces) is a rapid visual immunoassay for the qualitative, presumptive detection of Vibrio cholerae O1 in human fecal specimens. This kit is intended for use as an aid in the diagnosis of Vibrio cholerae O1 infection.
 
StrongStep System Device for SARS-CoV-2Antigen Rapid Test employs immunochromatography technobgy to detect the SARS-CoV-2 nucleocapsid antigen in human saliva. This test is single use only and intended for self-testing. It is recommended to use this test within 7 days of symptom onset. lt is supported by the dinical performance assessment.

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