FDA hian medical devices te chu an sem darh leh hman dan hmangin a dik taka hriat theihna turin device identification system danglam tak a din mek a ni. A taka hman a nih chuan device tam zawk label-ah hian mihring leh machine-in a chhiar theih angin unique device identifier (UDI) a awm ang. Device labelers te hian device tin chungchang information thenkhat chu FDA’s Global Unique Device Identification Database (GUDID) ah an thehlut tur a ni bawk. Mipui chuan -ah GUDID aṭangin information an zawng thei a, an download thei bawk AccessGUDID .
Kum eng emaw zat chhunga hman ṭan tur, unique device identification system hian hlawkna engemaw zat a pe a, chu chu UDI-te chu health care delivery system-a hman leh inzawmkhawm a nih chuan a taka tihhlawhtlin a ni ang. UDI kalpui hian damlote himna a tichangtlung ang a, device postmarket surveillance pawh a tichangtlung ang a, medical device thar siamna a ti awlsam bawk ang.
UDI team hnena zawhna emaw, ngaihtuahna emaw i sawi duh chuan FDA UDI Help Desk hnenah zawhfiah theih a ni.
