Família AFIAS Ustekinumab

Ustekinumab · class II · Valid

Registration no.
10350840494
Process no.
25351058618202657
Status
Valid
Device type
Ustekinumab (USTEKINUMAB)
Risk class
II
Registration holder
BIOSYS LTDA CNPJ 02.220.795/0001-79 · 506 registrations
Manufacturer
BODITECH MED INC. · South Korea
Published
04/05/2026
Valid until
No expiry (VIGENTE)
Last updated by ANVISA
2026-10-12
Official record
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