Nanjing Liming Bio-products Co., Ltd.

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

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REF	502010	Specification	20 Tests/Box
Detection principle	Immunochromatographic assay	Specimens	Whole Blood/Serum / Plasma
Intended Use	StrongStep® H. pylori Antibody Rapid Test is a rapid visual immunoassay for the qualitative presumptive detection of specific IgM and IgG antibodies to Helicobacter pylori with human whole blood/serum/plasma as specimen.

Vibrio Cholerae O1 Antigen Rapid Test

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.

Rotavirus Antigen Rapid Test

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.

Candida albicans/Trichomonas Vaginalis/Gardnerella Vaginalis Antigen Combo Rapid Test

For the qualitative detection of Trichomonas and/or Candida and/or Gardnerella Vaginalis antigens from vaginal swabs or from the saline solution prepared when making wet mount from vaginal swabs. This kit is intended to be used as an aid in the diagnosis of Candida albicans and/or Trichomonas Vaginalis andlorGardnerella Vaginalis infection.

Trichomonas Vaginalis Antigen Rapid Test

REF	500040	Specification	20 Tests/Box
Detection principle	Immunochromatographic assay	Specimens	Vaginal discharge
Intended Use	StrongStep® Trichomonas vaginalis antigen rapid test is a rapid lateral-flow immuno assay for the qualitative detection of Trichomonas vaginalis antigens in vaginal swab.

SARS-CoV-2 IgM/IgG Antibody Rapid Test

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.