I-FDA isungula uhlelo oluhlukile lokuhlonza idivaysi ikhomba ngokwanele ukubona amadivaysi ezokwelapha ngokwanele ngokusatshalaliswa nokusetshenziswa kwawo. Uma kusetshenziswe ngokuphelele, ilebula yamadivayisi amaningi izofaka isikhombi sedivayisi esiyingqayizivele (i-UDI) kwifomu elifundeka lomuntu nelomshini. Ababhali bedivaysi kumele futhi balethe imininingwane ethile mayelana nedivaysi ngayinye kuya ku-Fatabase Provice Divice Divice Divice Diffenethi Ye-FDA's Valavice Stabase (Gudid). Umphakathi ungasesha futhi ulande imininingwane evela ku-gudid e -accessgudid.
Uhlelo oluhlukile lokuhlonza idivaysi, elizofakwa ngezigaba eminyakeni eminingana, linikeza nezinzuzo eziningi ezizotholwa ngokuphelele ngohlobo lokutholwa kanye nokuhlanganiswa kwe-UDIS ohlelweni lokulethwa kwezidingo zezempilo. Ukuqaliswa kokuqalisa kwe-UDI kuzothuthukisa ukuphepha kweziguli, ukubhekwa kwe-posturket yedatha yesimanjemanje, kanye nokwenza lula ukwenziwa kwemininingwane yedivayisi yezokwelapha.
Uma unombuzo noma ukukhathazeka ongathanda ukuwabelana ngethimba le-UDI, sicela uxhumane nedeski losizo lwe-FDA UDI.
