FDA chuan damdawi hmanrua te chu an sem leh hman dan hmanga an hriat chian theih nan device identification system danglam tak a siam mek a ni. A taka hman a nih chuan, device tam zawk label-ah chuan mihring leh machine-a chhiar theih form-a device identifier (UDI) danglam bik a awm ang. Device labeler te pawhin device tin chungchanga information thenkhat chu FDA’s Global Unique Device Identification Database (GUDID) ah an thehlut tur a ni. Mipuiin Gudid hnen atangin AccessGudid 2019 ah information an zawng thei a, an download thei bawk..
Kum engemaw zat chhunga phase hrang hranga hman tur device identification system danglam tak hian hlawkna engemaw zat a pe a, chu chu UDI-te chu health care delivery system-a hman leh inzawmkhawm a nih chuan a takin a thleng thei ang. UDI kalpui hian damlote himna a tichangtlung ang a, device postmarket surveillance chu a tichangtlung ang a, medical device innovation a ti awlsam bawk ang.
Zawhna emaw, ngaihtuahna emaw i neih chuan UDI team-te hnena i sawi duh chuan FDA UDI Help Desk-ah zawhfiah theih a ni.
