Kunze kwekugamuchira FDA (EUA) mvumo!

Makorokoto kuBeyond Medical: yakagamuchirwa FDA (EUA) mvumo!

Chii chinonzi EUA?
United States FDA yagadzira mamwe mafirita, gasi michina yakagadziridzwa kuti ishandiswe semhepo inofefetedza, uye nemidziyo yekufemera inovandudzwa kuti ishandiswe sevhenefeta (pamwe chete inonzi "ma ventilator"), zvinongedzo zvevacilator, uye zvishongedzo zvemhepo zvinowanika pasi pechimbichimbi kuwana mashandiro anonzi Emergency Use Authorization (EUA). EUA inotsigirwa nemunyori wezve Hutano neHuman Service's (HHS) kuzivisa kuti mamiriro ezvinhu aripo ekururamisa kushandiswa kwechimbichimbi kwemidziyo yezvokurapa, kusanganisira mamwe majaira anoshandiswa semidziyo yezvokurapa, nekuda kwekushomeka panguva yedenda re COVID-19.

Ko Beyond Medical yakawana iyo FDA (EUA) chitupa?
Ehe, isu takawana iyo FDA (EUA) chitupa chedu B-30 P uye C-20A mupepeti, ndokumbira utarise seinotevera!

Kubva ikozvino, Beyond Medical yakava kambani yehunyanzvi iyo ine FDA chitupa, CE chitupa uye ISO chitupa, Kunze kwaizvozvo, isu takaverengerwawo mune chena rondedzero yemhepo yekubuditsa kunze kweHurumende Drug Administration. Isu tese tinotenda kuti tichaita zvirinani uye zvirinani muzuva rinouya.