Kea u lebohela!！！"Testselabs® COVID-19 Antigen Rapid Test" e entsoeng ke Testsea e fumane Setifikeiti sa FDA Philippines ka la 25 Mmesa, 2022. Setifikeiti se supa hore lihlahisoa tsa Testsealabs® COVID-19 Antigen Rapid Test li amohetsoe ho rekisoa Mmaraka 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 ho qhoma COVID-19, Testsea e latela ka tieo ka ts'ebetso ea sistimi ea taolo ea boleng ea ISO13485 le ISO9001 ka lipatlisiso, tlhahiso, taolo ea boleng, lichelete, thekiso ea malapeng le thekiso ea machabeng joalo-joalo mme e fumane lengolo la ho itlhahloba la CE 1011/1434. ho EU, setifikeiti sa Therapeutic Goods Administration(TGA) naheng ea Australia, Thailand Food and Drug Administration(FDA) le litifikeiti tse ling tse tsoang linaheng tse fapaneng, tse bonts'ang boleng ba lihlahisoa tsa rona li amohetsoe ke litsi tse amanang le mmuso.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