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ANVISA registration 10158120751Active

COMBINED PARAMETERS IN THE SAME PRODUCT - CLASS II

ANVISA Registration Number: 10158120751BIOMERIEUX BRASIL COMERCIO DE PRODUTOS LABORATORIAIS LTDABIOMERIEUX SARisk Class II
Device names
Technical name
COMBINED PARAMETERS IN THE SAME PRODUCT - CLASS II
PT: PARÂMETROS COMBINADOS NO MESMO PRODUTO - CLASSE II
Commercial name
VIDAS® TBI (GFAP, UCH-L1)
Risk class
Class II
Registration details
Registration Number
10158120751
Process Number
25351397013202417
CNPJ
33040635000171
Company information
Manufacturer
BIOMERIEUX SA
Manufacturing Country
France
PT: FRANÇA
Dates and status
Publication Date
Oct 07, 2024
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for COMBINED PARAMETERS IN THE SAME PRODUCT - CLASS II in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10158120751 and manufactured by BIOMERIEUX SA. The registration is held by BIOMERIEUX BRASIL COMERCIO DE PRODUTOS LABORATORIAIS 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.