\u3010Tikimas naudojimas\u3011<\/p>\n
Testas skirtas naudoti vienu metu greitai in vitro nustatant ir diferencijuojant<\/p>\n
A gripo viruso, B gripo viruso ir COVID-19 viruso nukleokapsidinio baltymo antigeno, bet ne<\/p>\n
neatskiria SARS-CoV ir COVID-19 virus\u0173 ir n\u0117ra skirtas SARS-CoV ir COVID-19 virusams aptikti.<\/p>\n
gripo C antigenai. Veikimo charakteristikos gali skirtis prie\u0161 kitus naujus gripo virusus.<\/p>\n
virusai.<\/p>\n
A, B ir COVID-19 gripo virus\u0173 antigenai paprastai aptinkami vir\u0161utini\u0173 kv\u0117pavimo tak\u0173 m\u0117giniuose \u016bmios infekcijos faz\u0117s metu. Teigiami rezultatai rodo, kad yra viruso antigen\u0173, ta\u010diau infekcijos b\u016bklei nustatyti b\u016btina klinikin\u0117 koreliacija su paciento anamneze ir kita diagnostine informacija.<\/p>\n
Teigiami rezultatai neatmeta bakterin\u0117s infekcijos ar koinfekcijos su kitais virusais galimyb\u0117s. Veiksnys<\/p>\n
aptiktos ligos prie\u017eastis gali b\u016bti neabejotina.<\/p>\n
Neigiami COVID-19 rezultatai pacientams, kuriems simptomai pasirei\u0161k\u0117 po penki\u0173 dien\u0173, tur\u0117t\u0173 b\u016bti<\/p>\n
laikomas numanomu ir, jei reikia, patvirtinamas molekuliniu tyrimu.<\/p>\n
valdymas, gali b\u016bti atliekamas. Neigiami rezultatai neatmeta COVID-19 ir netur\u0117t\u0173 b\u016bti<\/p>\n
naudojami kaip vienintelis gydymo ar paciento valdymo sprendim\u0173 pagrindas, \u012fskaitant infekcijos<\/p>\n
kontrol\u0117s sprendimus. Neigiami rezultatai tur\u0117t\u0173 b\u016bti vertinami atsi\u017evelgiant \u012f paciento neseniai<\/p>\n
poveikis, anamnez\u0117 ir klinikiniai po\u017eymiai bei simptomai, atitinkantys COVID-19.<\/p>\n
Neigiami rezultatai neatmeta galimyb\u0117s u\u017esikr\u0117sti gripo virusu ir netur\u0117t\u0173 b\u016bti naudojami kaip vienintelis<\/p>\n
gydymo ar kit\u0173 paciento valdymo sprendim\u0173 pagrindas.<\/p>\n
\u3010Sertifikatas\u3011<\/p>\n
CE, ISO9001, ISO13485<\/p>","protected":false},"excerpt":{"rendered":"
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