FDA iri kumisikidza yakasarudzika mudziyo wekuzivisa sisitimu yekuziva zvakakwana michina yekurapa kuburikidza nekugovera uye kushandiswa kwayo.Kana yaitwa zvizere, iyo label yemidziyo mizhinji inosanganisira yakasarudzika mudziyo identifier (UDI) mumunhu- uye nemuchina-inoverengeka fomu.Vanyoreri vemidziyo vanofanirwawo kuendesa rumwe ruzivo nezve mudziyo wega wega kuFDA's Global Unique Chishandiso Chiziviso Database (GUDID).Veruzhinji vanogona kutsvaga nekudhawunirodha ruzivo kubva kuGUDID paAccessGUDID.
Iyo yakasarudzika yedhisheni yekuzivikanwa sisitimu, iyo inozoiswa mukati memakore akati wandei, inopa akati wandei mabhenefiti ayo anozove akazadzikiswa nekutorwa uye kubatanidzwa kweUDIs muhutano hwekupa hutano.Kuitwa kweUDI kuchavandudza kuchengetedzeka kwevarwere, kugadziridza kutariswa kwechishandiso postmarket, uye kufambisa hunyanzvi hwekurapa.
Kana uine mubvunzo kana chinokunetsa chaungade kugovera nechikwata cheUDI, tapota taura neFDA UDI Help Desk.
