Ngwaahịa
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SARS-CoV-2 & Influenza A/B Multiplex PCR ezigbo oge
REF 510010 Nkọwapụta 96 Nnwale/igbe Ụkpụrụ nchọpụta PCR Ụdị Ize imi / Nasopharyngeal swab / Oropharyngeal swab Ezubere iji StrongStep® SARS-CoV-2 & Influenza A/B Multiplex Real-Time PCR Kit bụ maka nchọpụta qualitative n'otu oge na ọdịiche nke SARS-CoV-2, Influenza A virus na Influenza B virus RNA na ndị na-ahụ maka ahụike-anakọtara imi na nasopharyngeal swab. ma ọ bụ oropharyngeal swab ụdị na-anakọta onwe ya imi ma ọ bụ oropharyngeal swab ụdị (anakọtara na ọnọdụ ahụike yana ntuziaka nke onye na-ahụ maka ahụike) sitere n'aka ndị mmadụ na-enyo enyo na ha nwere ọrịa nje iku ume kwekọrọ na COVID-19 site n'aka onye na-ahụ maka ahụike ha.
Ezubere ngwa a maka ndị ọrụ zụrụ azụ nke ụlọ nyocha
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Vibrio cholerae O1 Antigen Rapid Test
REF 501050 Nkọwapụta 20 Nnwale/igbe Ụkpụrụ nchọpụta Immunochromatographic nyocha Ụdị Mpekere Ezubere iji Ngwa StrongStep® Vibrio cholerae O1 Antigen Rapid Test Device (Feces) bụ ngwa ngwa immunoassay anya maka njirimara qualitative, nke echere na Vibrio cholerae O1 n'ime ihe nlere anya fecal mmadụ.Ezubere ngwa a ka ọ bụrụ ihe enyemaka na nyocha nke ọrịa Vibrio cholerae O1. -
Nlere ngwa ngwa nke vaginosis nje
REF 500080 Nkọwapụta 50 ule/igbe Ụkpụrụ nchọpụta PH uru Ụdị Ọpụpụ nke ikpu Ezubere iji Nzọụkwụ siri ike®Ihe nlere ngwa ngwa nke nje bacteria (BV) bu n'obi tụọ pH ikpu maka enyemaka na nchọpụta nke vaginosis nje. -
Nyocha Procalcitonin
REF 502050 Nkọwapụta 20 Nnwale/igbe Ụkpụrụ nchọpụta Immunochromatographic nyocha Ụdị Plasma / Serum / Ọbara dum Ezubere iji Nzọụkwụ siri ike®Nnwale Procalcitonin bụ nyocha chromatographic na-alụso ọrịa ọgụ ngwa ngwa maka nchọpụta ọkara nke Procalcitonin na ọbara mmadụ ma ọ bụ plasma.A na-eji ya maka ịchọpụta na ịchịkwa ọgwụgwọ ọrịa siri ike, nje bacteria na sepsis. -
Nnwale ngwa ngwa SARS-CoV-2 IgM/IgG Antibody
REF 502090 Nkọwapụta 20 Nnwale/igbe Ụkpụrụ nchọpụta Immunochromatographic nyocha Ụdị Ọbara dum / Serum / Plasma Ezubere iji Nke a bụ nyocha ngwa ngwa immuno-chromatographic maka nchọpụta otu oge nke ọgwụ mgbochi IgM na IgG na nje SARS-CoV-2 n'ọbara mmadụ dum, serum ma ọ bụ plasma. Nnwale a nwere oke na US maka ikesa na ụlọ nyocha nke CLIA kwadoro iji mee nnwale mgbagwoju anya dị elu.
FDA enyochabeghị ule a.
Nsonaazụ ọjọọ anaghị egbochi nnukwu ọrịa SARS-CoV-2.
E kwesịghị iji nsonaazụ sitere na nnwale mgbochi iji chọpụta ma ọ bụ wepu nnukwu ọrịa SARS-CoV-2.
Nsonaazụ dị mma nwere ike ịbụ n'ihi ọrịa gara aga ma ọ bụ ugbu a nwere ụdị coronavirus na-abụghị SARS-CoV-2, dị ka coronavirus HKU1, NL63, OC43, ma ọ bụ 229E.
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Neisseria gonorrhoeae/Chlamydia trachomatis Antigen Combo Nnwale ngwa ngwa.
REF 500050 Nkọwapụta 20 Nnwale/igbe Ụkpụrụ nchọpụta Immunochromatographic nyocha Ụdị Cervical/urethra swab
Ezubere iji Nke a bụ immunoassay n'akụkụ mpụta ngwa ngwa maka nchọpụta elele anya nke Neisseria gonorrhoeae/Chlamydia trachomatis antigens na swab uretral nwoke na nwanyị. -
Neisseria Gonorrheae Antigen Rapid Test
REF 500020 Nkọwapụta 20 Nnwale/igbe Ụkpụrụ nchọpụta Immunochromatographic nyocha Ụdị Cervical/urethra swab Ezubere iji Ọ dabara maka nchọpụta qualitative nke gonorrhea / chlamydia trachomatis antigens na nzuzo nzuzo nke ụmụ nwanyị na urethra n'ụdị ụmụ nwoke na vitro n'ụlọ ọrụ ahụike dị iche iche maka nyocha inyeaka nke ọrịa nje a dị n'elu. -
Ngwa ule Cryptococcal Antigen ngwa ngwa
REF 502080 Nkọwapụta 20 Nnwale / Igbe;50 ule/igbe Ụkpụrụ nchọpụta Immunochromatographic nyocha Ụdị Mmiri Cerebrospinal/Serum Ezubere iji Ngwa nyocha ngwa ngwa nke StrongStep®Cryptococcal Antigen Rapid bụ nyocha ngwa ngwa mgbochi-chromatographic maka nchọpụta capsular polysaccharide antigens nke ụdị Cryptococcus (Cryptococcus neoformans na Cryptococcus gattii) na serum,plasma, ọbara dum na mmiri ụbụrụ ụbụrụ (CSF) -
Candida Albicans Antigen Ngwa ngwa ule
REF 500030 Nkọwapụta 20 Nnwale/igbe Ụkpụrụ nchọpụta Immunochromatographic nyocha Ụdị Cervical/urethra swab Ezubere iji StrongStep® Candida albicans Antigen Rapid Test bụ nyocha nke immunochromatographic nke na-achọpụta antigens pathogen ozugbo site na swabs ikpu.
