Nanjing Liming Bio-products Co., Ltd.

StrongStep System Device for SARS-CoV-2 Antigen Rapid Test

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REF 500090 Specification 20 Tests/Box
Detection principle Immunochromatographic assay Specimens Female vaginal swab
Intended Use StrongStep® Strep B antigen Rapid Test is a rapid visual immunoassay for the qualitative presumptive detection of Group B Streptococcal antigen in female vaginal swab.
 
REF 500160 Specification 20 Tests/Box
Detection principle Immunochromatographic assay Specimens Cervicovaginal secretions
Intended Use StrongStep® Fetal Fibronectin Rapid Test is a visually interpreted immunochromatographic test intended to be used for the qualitative detection of fetal fibronectin in cervicovaginal secretions.
REF 501010 Specification 20 Tests/Box
Detection principle Immunochromatographic assay Specimens Feces
Intended Use StrongStep® Rotavirus antigen Rapid Test is a rapid visual immunoassay for the qualitative, presumptive detection of rotavirus in human fecal specimens.
 
This is a rapid immuno-chromatographic assay for the simultaneous detection of IgM and IgG antibodies to SARS-CoV-2 virus in human whole blood, serum or plasma.
REF 501080 Specification 20 Tests/Box
Detection principle Immunochromatographic assay Specimens Feces
Intended Use The StrongStep® Salmonella Antigen Rapid Test is a rapid visual immunoassay for the qualitative, presumptive detection of Salmonella typhimurium, Salmonella enteritidis, Salmonella choleraesuis in human fecal specimens. This kit is intended for use as an aid in the diagnosis of Salmonella infection.
 
REF 500010 Specification 20 Tests/Box
Detection principle Immunochromatographic assay Specimens

Cervical/urethra swab

Intended Use This is a rapid lateral-flow immunoassay for the qualitative presumptive detection of Chlamydia trachomatis antigen in male urethral and female cervical swab.
 
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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