Sivuyisana nawe!！！”I-Testselabs® COVID-19 Antigen Rapid Test” eyenziwe yi-Testsea ifumene iSatifikethi se-FDA ePhilippines nge-25 ka-Epreli 2022. Isiqinisekiso sibonisa ukuba iimveliso ze-Testselabs® COVID-19 Antigen Rapid Test zivunyiwe ukuba zithengiswe Imarike yakwiiPhilippines ngurhulumente wasekhaya.
Imveliso yethu ingasetyenziselwa zombini ukusetyenziswa kobuchwephesha kunye nokusetyenziswa kwekhaya (ukuzivavanya). Kukulungele ukuba amaziko, abantu kunye neentsapho bafumane iisampuli ze-nasal / nasopharyngeal / oropharyngeal swab ngokukhawuleza nangexesha.
* Ukuchaneka okuphezulu kunye novakalelo
* Iziphumo ezikhawulezayo kwimizuzu eyi-15-20
* Kulula ukuqokelela iisampulu* Akukho sixhobo sifunekayo* Iziphumo zibonakala ngokucacileyo
• Ifanele izithsaba ezinkulu ezitsha* Chonga usulelo lwakwangoko
Ukusukela ekuqhambukeni kwe-COVID-19, i-Tessea ilandela ngokungqongqo nge-ISO13485 kunye ne-ISO9001 yokusebenza kwenkqubo yokulawula umgangatho ngophando, imveliso, ulawulo lomgangatho, imali, intengiso yasekhaya kunye neentengiso zamazwe ngamazwe njl.njl. kwi-EU, isiqinisekiso soLawulo lweeMpahla zoNyango (TGA) e-Australia, eThailand Ulawulo lokuTya kunye neDrugs (FDA) kunye nezinye izatifikethi ezivela kumazwe ahlukeneyo, ezibonisa umgangatho weemveliso zethu ezivunyiweyo ngamaziko karhulumente anxulumeneyo. Kwakhona, iimveliso zethu zinegama elihle kunye nefuthe lophawu oluvela kwiimarike zaphesheya. I-Tessea iya kuqhubeka nokuphanda kunye nokuphuhlisa iimveliso zovavanyo olukhawulezayo lwe-COVID-19 kwaye ifake isandla kumlo ochasene nobhubhani we-COVID-19 kwihlabathi jikelele.
Ixesha lokuposa: Apr-29-2022