Human Diagnostics
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Screening Test for Cervical Pre-cancer and Cancer
REF 500140 Specification 20 Tests/Box Detection principle Immunochromatographic assay Specimens Cervical swab Intended Use The Strong Step® Screening test for cervical pre-cancer and cancer boasts of the strength of more accurate and cost-effective in cervical pre-cancer and cancer screening than DNA method. -
Trichomonas/Candida Antigen Combo Rapid Test
REF 500060 Specification 20 Tests/Box Detection principle Immunochromatographic assay Specimens Vaginal discharge Intended Use The StrongStep® StrongStep® Trichomonas/ Candida rapid test Combo is a rapid lateral-flow immunoassay for the qualitative presumptive detection of trichomonas vaginalis /candida albicans antigens from vaginal swab. -
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. -
Candida Albicans Antigen Rapid Test
REF 500030 Specification 20 Tests/Box Detection principle Immunochromatographic assay Specimens Cervical/urethra swab Intended Use The StrongStep® Candida albicans Antigen Rapid Test is an immunochromatographic assay that detects pathogen antigens directly from vaginal swabs. -
Neisseria Gonorrhoeae Antigen Rapid Test
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. -
Neisseria gonorrhoeae/Chlamydia trachomatis Antigen Combo Rapid Test
REF 500050 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 Neisseria gonorrhoeae/Chlamydia trachomatis antigens in male urethral and female cervical swab -
Chlamydia Trachomatis Antigen Rapid Test
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. -
Candida albicans/Trichomonas Vaginalis/Gardnerella Vaginalis Antigen Combo Rapid Test
REF 500340 Specification 20 Test/box Detection principle Immunochromatographic assay Specimens Vulvovaginal candidiasis/Trichomonal vaginitis/Bacterial vaginosis Intended Use 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. -
PROM Rapid Test
REF 500170 Specification 20 Tests/Box Detection principle Immunochromatographic assay Specimens Vaginal discharge Intended Use StrongStep® PROM rapid test is a visually interpreted, qualitative immunochromatographic test for detection of IGFBP-1 from amniotic fluid in vaginal secretions during pregnancy. -
Gardnerella Vaginalis Antigen Rapid Test
REF 500330 Specification 20 Test/box Detection principle Immunochromatographic assay Specimens Vaginal discharge Intended Use For the qualitative detection of Gardnerella Vaginalis 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 Gardnerella Vaginalis infection. -
SARS-CoV-2 Antigen Rapid Test（Professional Use）
REF 500200 Specification 25 Tests/box Detection principle Immunochromatographic assay Specimens Anterior nasal swab Intended Use StrongStep® SARS-CoV-2 Antigen Rapid Test Cassette employs immunochromatography technology to detect the SARS- CoV-2 nucleocapsid antigen in human anterior nasal swab specimen. This testis single use only and intended for self-testing. It is recommanded to use this test within 5 days of symptom onset. It is supported by the clinical performance assessment.
