Nā huahana
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ʻO SARS-CoV-2 a me ka Influenza A/B Multiplex PCR Kikoʻo Manawa maoli
REF 510010 Hōʻike 96 Hoao/Pahu Kumuʻike ʻike PCR Nā mea hoʻohālike Nasal / Nasopharyngeal swab / Oropharyngeal swab Hoohana Manao ʻO StrongStep® SARS-CoV-2 & Influenza A/B Multiplex Real-Time PCR Kit i manaʻo ʻia no ka ʻike like ʻana a me ka hoʻokaʻawale ʻana o SARS-CoV-2, Influenza A virus a me Influenza B virus RNA i loko o ka mea mālama ola kino i hōʻiliʻili ʻia i ka ihu a me ka nasopharyngeal swab a i ʻole nā hiʻohiʻona oropharyngeal swab a me nā hōʻailona nasal a i ʻole oropharyngeal swab i hōʻiliʻili ponoʻī ʻia (i hōʻiliʻili ʻia ma kahi hoʻonohonoho mālama olakino me ke aʻo ʻana e kahi mea mālama ola) mai nā poʻe i manaʻo ʻia he maʻi maʻi hanu e like me COVID-19 e kā lākou mea mālama ola.
Hoʻohana ʻia ka pahu e nā limahana i hoʻomaʻamaʻa ʻia
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ʻO Vibrio cholerae O1 Antigen Rapid Test
REF 501050 Hōʻike 20 Hoao/Pahu Kumuʻike ʻike Immunochromatographic assay Nā mea hoʻohālike Feces Hoohana Manao ʻO ka StrongStep® Vibrio cholerae O1 Antigen Rapid Test Device (Feces) he immunoassay ʻike wikiwiki no ka qualitative, presumptive detection of Vibrio cholerae O1 i loko o nā ʻano fecal kanaka.Hoʻohana ʻia kēia pahu i mea kōkua i ka ʻike ʻana i ka maʻi Vibrio cholerae O1. -
ʻO ka hoʻāʻo wikiwiki ʻana i ka vaginosis bacteria
REF 500080 Hōʻike 50 Hoao/Pahu Kumuʻike ʻike Waiwai PH Nā mea hoʻohālike ʻO ka hoʻoheheʻe ʻana Hoohana Manao ʻO ka StrongStep®Ua manaʻo ʻia ʻo Bacterial vaginosis(BV) Rapid Test Device e ana i ka pH vaginal no ke kōkua ʻana i ka ʻike ʻana i ka maʻi bacterial vaginosis. -
Ho'āʻo Procalcitonin
REF 502050 Hōʻike 20 Hoao/Pahu Kumuʻike ʻike Immunochromatographic assay Nā mea hoʻohālike Plasma / Serum / Koko holoʻokoʻa Hoohana Manao ʻO ka StrongStep®ʻO ka hoʻāʻo ʻo Procalcitonin kahi hoʻomaʻamaʻa immune-chromatographic wikiwiki no ka ʻike semi-quantitative o Procalcitonin i ka serum kanaka a i ʻole ka plasma.Hoʻohana ʻia ia no ka ʻike ʻana a me ka mālama ʻana i ka mālama ʻana i ka maʻi koʻikoʻi, bacterial a me sepsis. -
ʻO SARS-CoV-2 IgM/IgG Antibody Rapid Test
REF 502090 Hōʻike 20 Hoao/Pahu Kumuʻike ʻike Immunochromatographic assay Nā mea hoʻohālike Koko holoʻokoʻa / Serum / Plasma Hoohana Manao He hōʻike immuno-chromatographic wikiwiki kēia no ka ʻike like ʻana o nā antibodies IgM a me IgG i ka maʻi SARS-CoV-2 i ke koko holoʻokoʻa o ke kanaka, serum a i ʻole plasma. Ua kaupalena ʻia ka hoʻāʻo ma US no ka hāʻawi ʻana i nā laboratories i hōʻoia ʻia e CLIA e hana i ka hoʻāʻo paʻakikī kiʻekiʻe.
ʻAʻole i loiloi ʻia kēia hoʻokolohua e ka FDA.
ʻAʻole ʻae nā hopena maikaʻi ʻole i ka maʻi maʻi SARS-CoV-2.
ʻAʻole pono e hoʻohana ʻia nā hopena mai ka hoʻāʻo ʻana i ka antibody no ka hoʻopaʻa ʻana a haʻalele paha i ka maʻi maʻi SARS-CoV-2.
Loaʻa nā hopena maikaʻi ma muli o ka maʻi i hala a i ʻole i kēia manawa me nā kānana coronavirus non-SARS-CoV-2, e like me ka coronavirus HKU1, NL63, OC43, a i ʻole 229E.
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ʻO Neisseria gonorrhoeae/Chlamydia trachomatis Antigen Combo Rapid Test
REF 500050 Hōʻike 20 Hoao/Pahu Kumuʻike ʻike Immunochromatographic assay Nā mea hoʻohālike ʻAi ʻāʻī/urethra
Hoohana Manao He immunoassay wikiwiki loa kēia no ka ʻike manaʻo kūpono o Neisseria gonorrhoeae/Chlamydia trachomatis antigens i loko o ka urethral kāne a me ka swab cervical wahine. -
ʻO Neisseria Gonorrhoeae Antigen Rapid Test
REF 500020 Hōʻike 20 Hoao/Pahu Kumuʻike ʻike Immunochromatographic assay Nā mea hoʻohālike ʻAi ʻāʻī/urethra Hoohana Manao He kūpono ia no ka qualitative detection of gonorrhoea/chlamydia trachomatis antigens in cervical secretions of women and urethral samples of men in vitro in other medical institutions for auxiliary diagnostics of the above pathogen infection. -
Mea ho'āʻo wikiwiki ʻo Cryptococcal Antigen
REF 502080 Hōʻike 20 Ho'āʻo / pahu;50 Hoao/Pahu Kumuʻike ʻike Immunochromatographic assay Nā mea hoʻohālike ʻO ka wai cerebrospinal/Serum Hoohana Manao ʻO StrongStep®Cryptococcal Antigen Rapid Test Device kahi hoʻāʻo wikiwiki immune-chromatographic no ka ʻike ʻana i nā antigens capsular polysaccharide o Cryptococcus species complex (Cryptococcus neoformans a me Cryptococcus gattii) i ka serum, plasma, ke koko holoʻokoʻa a me ka cerebral spinal fluid (CSF) -
ʻO Candida Albicans Antigen Rapid Test
REF 500030 Hōʻike 20 Hoao/Pahu Kumuʻike ʻike Immunochromatographic assay Nā mea hoʻohālike ʻAi ʻāʻī/urethra Hoohana Manao ʻO ka StrongStep® Candida albicans Antigen Rapid Test kahi hōʻike immunochromatographic e ʻike pololei ana i nā antigen pathogen mai nā swabs vaginal.
