I-FDA iseka inkqubo yokuchonga isixhobo esisodwa ukuze ichonge ngokwaneleyo izixhobo zonyango ngokusasazwa kunye nokusetyenziswa kwazo. Xa iphunyezwe ngokupheleleyo, ileyibhile yezixhobo ezininzi iya kubandakanya isichongi sesixhobo esisodwa (UDI) ngohlobo olufundeka ngabantu kunye nomatshini. Iilebhile zesixhobo kufuneka kwakhona zingenise ulwazi oluthile malunga nesixhobo ngasinye kwi-FDA's Global Unique Device Identification Database (GUDID). Uluntu lunokukhangela kwaye lukhuphele ulwazi kwi-GUDID kwi -AccessGUDID.
Inkqubo yokuchongwa kwesixhobo esisodwa, esiza kufakwa ngezigaba kwiminyaka emininzi, inika inani leenzuzo eziya kufezekiswa ngokupheleleyo ngokwamkelwa kunye nokuhlanganiswa kwee-UDIs kwinkqubo yokunikezelwa kwezempilo. Ukuphunyezwa kwe-UDI kuya kuphucula ukhuseleko lwesigulana, ukwenza uphononongo lwe-postmark yesixhobo, kunye nokuququzelela ukusungulwa kwesixhobo zonyango.
Ukuba unombuzo okanye inkxalabo ongathanda ukwabelana ngayo neqela le-UDI, nceda uqhagamshelane neDesika yoNcedo ye-FDA UDI.
