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ANVISA registration 10350840495Active

GOLIMUMAB

ANVISA Registration Number: 10350840495BIOSYS LTDABODITECH MED INC.Risk Class II
Verified
Device names
Technical name
GOLIMUMAB
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Commercial name
Família AFIAS Golimumab
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Risk class
Class II
Registration details
Registration Number
10350840495
Process Number
25351058651202687
CNPJ
02220795000179
Company information
Registration Holder
BIOSYS LTDA
Manufacturer
BODITECH MED INC.
Manufacturing Country
South Korea
PT: CORÉIA DO SUL
Dates and status
Publication Date
May 04, 2026
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for GOLIMUMAB in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10350840495 and manufactured by BODITECH MED INC.. The registration is held by BIOSYS LTDA with validity until currently active (VIGENTE).

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.