Makorokoto!！！"Testselabs® COVID-19 Antigen Rapid Test" yakagadzirwa neTestsea vakawana FDA Certification muPhilippines musi wa25 Kubvumbi 2022. Chitupa chinoratidza kuti Testsealabs® COVID-19 Antigen Rapid Test zvigadzirwa zvakatenderwa kutengeswa mumusika wePhilippines nehurumende yeko.
Chigadzirwa chedu chinogona kushandiswa zvese kushandiswa kwehunyanzvi uye kushandisa pamba (kuzviyedza). Zvakanakira masangano, vanhu uye mhuri kuona nasal / nasopharyngeal / oropharyngeal swab samples nekukurumidza uye nenguva.
chikonzero chekuzivikanwa kwayo:
* Yakanyanya kujeka uye kunzwa
* Instant mhedzisiro pa15-20 maminetsi
* Zviri nyore kuunganidza sampuli * Hapana michina inodikanwa * Mibairo inooneka zvakajeka
* Inokodzera makona makuru makuru* Ziva hutachiona hwekutanga
Kubva pakatanga COVID-19, Testsea iri kunyatso kutevedzera ISO13485 uye ISO9001 quality management system kushanda nekutsvaga, kugadzira, kutonga kwemhando, mari, kutengesa mudzimba uye kutengesa kune dzimwe nyika nezvimwewo uye vakawana CE 1011/1434 self-testing certification muEU, iyo Therapeutic Goods Management System (TGA) imwe Dhipatimendi Yezvekudya uye FDA nyika dzakasiyana, dzinoratidza kunaka kwezvigadzirwa zvedu zvinotenderwa nemasangano ehurumende ane hukama. Zvakare, zvigadzirwa zvedu zvine mukurumbira wakanaka uye pesvedzero yemhando kubva kumisika yemhiri kwemakungwa. Testsea icharamba ichitsvaga nekuvandudza zvigadzirwa zvekuyedza zveCCIDID-19 uye kubatsira mukurwisa denda reCOVID-19 pasi rese.
Nguva yekutumira: Kubvumbi-29-2022