Família AFIAS Golimumab

Golimumab · class II · Valid

Registration no.
10350840495
Process no.
25351058651202687
Status
Valid
Device type
Golimumab (GOLIMUMAB)
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
View on ANVISA ↗