Mayeso a antigen a Testsealabs® COVID-19 ovomerezedwa ndi Philippine FDA

Zabwino!！！"Testselabs® COVID-19 Antigen Rapid Test" yopangidwa ndi Testsea yalandira Chiphaso cha FDA ku Philippines pa Epulo 25, 2022. Chitsimikizochi chikuwonetsa kuti zinthu za Testsealabs® COVID-19 Antigen Rapid Test ndizololedwa kugulitsa mu Msika waku Philippines wopangidwa ndi boma.

Zogulitsa zathu zitha kugwiritsidwa ntchito ngati akatswiri komanso kunyumba (kudziyesa). Ndikosavuta kuti mabungwe, anthu ndi mabanja azindikire zitsanzo za nasal / nasopharyngeal / oropharyngeal swab mwachangu komanso munthawi yake.

 chifukwa cha kutchuka kwake:

* Kukhazikika kwakukulu komanso chidwi

* Zotsatira zaposachedwa pa mphindi 15-20

* Zosavuta kutolera zitsanzo* Palibe zida zofunika* Zotsatira zikuwonekera bwino

* Yoyenera korona wamkulu wamkulu* Dziwani matenda oyamba

Chiyambire kufalikira kwa COVID-19, Testsea ikutsatira mosamalitsa ndi ISO13485 ndi ISO9001 kasamalidwe kabwino kachitidwe ka kafukufuku, kupanga, kuwongolera bwino, ndalama, malonda apakhomo ndi malonda apadziko lonse lapansi ndi zina zambiri. ku EU, satifiketi ya Therapeutic Goods Administration(TGA) ku Australia, Thailand Food and Drug Administration(FDA) ndi ziphaso zina zochokera kumayiko osiyanasiyana, zomwe zikuwonetsa mtundu wazinthu zathu zimavomerezedwa ndi mabungwe aboma ogwirizana nawo. Komanso, malonda athu ali ndi mbiri yabwino komanso chikoka chamtundu wochokera kumisika yakunja. Testsea ipitiliza kufufuza ndi kupanga zinthu zoyesa mwachangu za COVID-19 ndikuthandizira polimbana ndi mliri wa COVID-19 padziko lonse lapansi.