Imikhiqizo
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I-SARS-CoV-2 & Influenza A/B Multiplex Real-Time PCR Kit
REF 510010 Ukucaciswa 96 Izivivinyo/Ibhokisi Umgomo wokutholwa I-PCR Izibonelo Ikhala / i-Nasopharyngeal swab / i-Oropharyngeal swab Ukusetshenziswa Okuhlosiwe I-StrongStep® SARS-CoV-2 & Influenza A/B Multiplex Real-Time PCR Kit ihloselwe ukutholwa kwekhwalithi kanye kanye nokuhlukaniswa kwe-SARS-CoV-2, igciwane loMkhuhlane A kanye negciwane le-RNA le-Influenza B kumhlinzeki wezempilo eqoqwe i-swab yamakhala kanye ne-nasopharyngeal. noma izibonelo ze-oropharyngeal swab kanye nezibonelo ze-swab zamakhala noma ze-oropharyngeal oziqoqele zona (eziqoqwe endaweni yokunakekelwa kwezempilo ngokuyalelwa umhlinzeki wezempilo) ezivela kubantu okusolwa ukuthi banegciwane lokuphefumula elihambisana ne-COVID-19 ngumhlinzeki wabo wezempilo.
Ikhithi ihloselwe ukusetshenziswa ngabasebenzi abaqeqeshwe elabhorethri
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I-Vibrio cholerae O1 Antigen Rapid Test
REF 501050 Ukucaciswa 20 Izivivinyo/Ibhokisi Umgomo wokutholwa Ukuhlolwa kwe-Immunochromatographic Izibonelo Indle Ukusetshenziswa Okuhlosiwe I-StrongStep® Vibrio cholerae O1 Antigen Rapid Test Device (Indle) iyisivivinyo esisheshayo esibonakalayo sokutholwa kwekhwalithi, okucabangelayo kwe-Vibrio cholerae O1 ezifanekisweni zendle yomuntu.Le kit ihloselwe ukusetshenziswa njengosizo ekuxilongweni kwe-Vibrio cholerae O1 ukutheleleka. -
Ukuhlolwa Okusheshayo kwe-bacterial vaginosis
REF 500080 Ukucaciswa 50 Izivivinyo/Ibhokisi Umgomo wokutholwa PH inani Izibonelo Ukukhipha isitho sangasese sowesifazane Ukusetshenziswa Okuhlosiwe Isinyathelo Esiqinile®I-Bacterial vaginosis(BV) Idivayisi Yokuhlola Okusheshayo ihlose ukukala i-pH yesitho sangasese sowesifazane ukuze uthole usizo ekuxilongweni kwe-Bacterial vaginosis. -
Ukuhlolwa kweProcalcitonin
REF 502050 Ukucaciswa 20 Izivivinyo/Ibhokisi Umgomo wokutholwa Ukuhlolwa kwe-Immunochromatographic Izibonelo I-Plasma / Serum / Igazi Eliphelele Ukusetshenziswa Okuhlosiwe Isinyathelo Esiqinile®Ukuhlolwa kwe-Procalcitonin ukuhlola okusheshayo kwe-immune-chromatographic kokutholwa kwe-semi-quantitative ye-Procalcitonin ku-serum yomuntu noma ku-plasma.Isetshenziselwa ukuxilonga nokulawula ukwelashwa kokutheleleka okunzima, okubangelwa amagciwane kanye ne-sepsis. -
Ukuhlolwa Okusheshayo kwe-SARS-CoV-2 IgM/IgG Antibody
REF 502090 Ukucaciswa 20 Izivivinyo/Ibhokisi Umgomo wokutholwa Ukuhlolwa kwe-Immunochromatographic Izibonelo Igazi Eliphelele / I-Serum / Plasma Ukusetshenziswa Okuhlosiwe Lokhu ukuhlola okusheshayo kwe-immuno-chromatographic kokutholwa ngasikhathi sinye kwamasosha omzimba e-IgM ne-IgG kugciwane le-SARS-CoV-2 egazini lomuntu lonke, i-serum noma i-plasma. Ukuhlola kukhawulelwe e-US ukuthi kusakazwe ezindaweni zokucwaninga ezigunyazwe yi-CLIA ukuze zenze ukuhlola okuyinkimbinkimbi.
Lokhu kuhlolwa akuzange kubuyekezwe yi-FDA.
Imiphumela engemihle ayikuvimbeli ukutheleleka okukhulu kwe-SARS-CoV-2.
Imiphumela yokuhlolwa kwe-antibody akufanele isetshenziselwe ukuxilonga noma ukukhipha ukutheleleka kwe-SARS-CoV-2 okuyingozi.
Imiphumela emihle ingase ibe ngenxa yokutheleleka kwangaphambilini noma kwamanje ngezinhlobo ze-coronavirus ezingezona ze-SARS-CoV-2, njenge-coronavirus HKU1, NL63, OC43, noma 229E.
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Neisseria gonorrhoeae/Chlamydia trachomatis Antigen Combo Rapid Test
REF 500050 Ukucaciswa 20 Izivivinyo/Ibhokisi Umgomo wokutholwa Ukuhlolwa kwe-Immunochromatographic Izibonelo I-Cervical/urethra swab
Ukusetshenziswa Okuhlosiwe Lena i-lateral-flow immunoassay esheshayo yokutholwa kwekhwalithi ye-Neisseria gonorrhoeae/Chlamydia trachomatis antigens ku-urethral yesilisa kanye ne-swab yomlomo wesibeletho yesifazane. -
I-Neisseria Gonorrhoeae Antigen Rapid Test
REF 500020 Ukucaciswa 20 Izivivinyo/Ibhokisi Umgomo wokutholwa Ukuhlolwa kwe-Immunochromatographic Izibonelo I-Cervical/urethra swab Ukusetshenziswa Okuhlosiwe Ifanele ukutholwa kwekhwalithi ye-gonorrhoea/chlamydia trachomatis antigens ekusithekeni komlomo wesibeletho kwabesifazane kanye namasampula e-urethral yamadoda e-in vitro ezikhungweni zezokwelapha ezihlukahlukene ukuze kuhlonzwe usizo lokutheleleka kwe-pathogen okungenhla. -
Idivayisi ye-Cryptococcal Antigen Rapid Test
REF 502080 Ukucaciswa Izivivinyo/Ibhokisi ezingama-20;50 Izivivinyo/Ibhokisi Umgomo wokutholwa Ukuhlolwa kwe-Immunochromatographic Izibonelo Uketshezi lwe-Cerebrospinal/Serum Ukusetshenziswa Okuhlosiwe I-StrongStep®Cryptococcal Antigen Rapid Test Device iwukuhlola okusheshayo kwe-immune-chromatographic ukuze kutholwe ama-antigen e-capsular polysaccharide e-Cryptococcus species complex (Cryptococcus neoformans ne-Cryptococcus gattii) ku-serum, i-plasma, igazi lonke kanye noketshezi lwe-cerebral spinal (CSF) -
I-Candida Albicans Antigen Rapid Test
REF 500030 Ukucaciswa 20 Izivivinyo/Ibhokisi Umgomo wokutholwa Ukuhlolwa kwe-Immunochromatographic Izibonelo I-Cervical/urethra swab Ukusetshenziswa Okuhlosiwe I-StrongStep® Candida albicans Antigen Rapid Test iyisivivinyo se-immunochromatographic esithola ama-antigen e-pathogen ngokuqondile kuma-swabs wesitho sangasese sowesifazane.
