Kea u leboha!！！"Testselabs® COVID-19 Antigen Rapid Test" e entsoeng ke Testsea e fumane Setifikeiti sa FDA naheng ea Philippines ka la 25 Mmesa, 2022. Setifikeiti se supa hore lihlahisoa tsa Testsealabs® COVID-19 Antigen Rapid Test li amohetsoe ho rekisoa 'marakeng oa Philippines ke mmuso oa lehae.
Sehlahisoa sa rona se ka sebelisoa ka bobeli bakeng sa ts'ebeliso ea litsebi le ts'ebeliso ea lapeng (ho itlhahloba). Ho bonolo hore litsi, batho ka bomong le malapa a bone lisampole tsa nasal / nasopharyngeal / oropharyngeal swab kapele le ka nako.
* Boiphihlelo bo phahameng le kutloisiso
* Sephetho sa hang-hang ka metsotso e 15-20
* E loketse meqhaka e mecha ea boholo-holo* Lemoha tšoaetso ea pele
Ho tloha ha COVID-19 e qala, Testsea e latela ka tieo ka ts'ebetso ea tsamaiso ea boleng ba ISO13485 le ISO9001 ka lipatlisiso, tlhahiso, taolo ea boleng, lichelete, thekiso ea lapeng le thekiso ea machabeng joalo-joalo 'me ba fumane lengolo la ho itlhahloba la CE 1011/1434 EU, Therapeutic Goods Management (TGA) ho tsoa ho Tsamaiso ea Lijo le Lithethefatsi tse ling (TGA) Australia. linaha tse fapaneng, tse bonts'ang boleng ba lihlahisoa tsa rona li amohetsoe ke litsi tse amanang le 'muso. Hape, lihlahisoa tsa rona li na le botumo bo botle le tšusumetso ea brand ho tsoa limmarakeng tsa mose ho maoatle. Testsea e tla tsoelapele ho etsa lipatlisiso le ho nts'etsapele lihlahisoa tsa tlhahlobo tse potlakileng tsa COVID-19 le ho kenya letsoho ntoeng khahlanong le seoa sa COVID-19 lefatšeng ka bophara.
Nako ea poso: Apr-29-2022